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Date: 2020-09-03 Category: Not Applicable State: Union Government Country: India

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Issued by Ministry of Health and Family Welfare · Central Drugs Standard Control Organization

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Executive Summary & Key Takeaways

Okay, I understand. I will analyze the provided text and generate a policy analysis report based on the given structure. Since the text primarily provides a list of medical devices categorized for registration purposes, it appears to be related to a regulatory framework for medical devices. I will treat it as a *New Policy* establishing categories and requirements for device registration rather than an amendment, since no prior policy is referenced. Here's the report: **Policy Analysis Report: Medical Device Categorization and Registration Framework** **1. Executive Summary:** This report analyzes a new policy establishing a framework for the categorization and registration of medical devices. The core purpose is to categorize medical devices into specific areas (e.g., Anesthesiology, Cardiovascular, Dental) and to provide a list of devices within each category. The key finding is that the document outlines a structured system for managing and regulating medical devices based on their intended use and area of application. This framework likely supports broader regulatory objectives of safety and efficacy. **2. Introduction:** This report provides an overview and analysis of a government policy document that outlines categories of medical devices for registration purposes. The analysis is based solely on the information provided in the document. **3. Policy Overview:** * Core Objective(s): The primary objective is to categorize medical devices based on their intended use and the medical specialty they serve. This categorization facilitates a structured approach to medical device registration and regulation. The list specifies devices that will be subject to registration under these categories. **4. Background and Rationale:** As a new policy, the likely problem this addresses is the need for a clear, organized system for regulating medical devices. The categorization likely aims to ensure that devices are reviewed, approved, and monitored based on their specific risks and applications. Without such a system, effective oversight of the medical device industry would be difficult, potentially leading to patient safety concerns and market inefficiencies. The text suggests a need for standardization and control within the medical device market. **5. Key Provisions / Changes:** As this is treated as a new policy, the key provisions are the establishment of the medical device categories and the listing of the specific devices within those categories. The policy mandates: * **Categorization:** Defines categories of medical devices, including but not limited to: Anesthesiology, Pain Management, Cardiovascular, Dental, ENT, Gastroenterological, etc. (listing 24 categories). * **Device Listing:** Provides a detailed listing of medical devices within specific categories (e.g., Anesthesiology), including the device name, intended use, and a reference code "INDIA" with a letter value (A, B, C, D, or L). These letter values likely indicate the risk categorization of device or some other type of class, but this is not explicitly defined in the text. This code is likely important for registration purposes. * **Intended Use Specification:** Each listed device has a brief description of its intended use. This is essential for determining the appropriate category and for ensuring the device is used as intended. The detail of 'intended use' is quite specific, indicating the level of detail needed for registration. **6. Target Audience and Stakeholders:** The target audience includes: * **Medical Device Manufacturers:** Directly affected as they must classify their devices according to these categories and likely register them accordingly. * **Regulatory Agencies:** Responsible for implementing and enforcing the policy, including device registration and post-market surveillance. * **Healthcare Providers:** Need to be aware of the device categories to ensure appropriate device selection and use. * **Patients:** Indirectly affected through improved device safety and efficacy due to better regulation. **7. Implementation Aspects (Inferred):** * **Responsible Agency/Bodies:** While not explicitly stated, it can be inferred that a national regulatory agency for medical devices is responsible for implementation. * **Timelines/Procedures:** No timelines are specified in the provided text. However, the existence of categories and device lists suggests a registration process will be established. Manufacturers will likely need to submit device information for categorization and registration. There might be a requirement for manufacturers to update registration as medical device names and uses are updated. The inclusion of INDIA classification further suggests that only approved medical devices will be available in India for related purposes. * **Enforcement Mechanisms:** The policy implies that unregistered devices may not be permitted for sale or use, but this is not explicitly stated in the provided text. **8. Expected Outcomes / Impact of Changes:** The likely intended outcomes are: * **Improved Regulatory Oversight:** A more structured and efficient process for medical device regulation. * **Enhanced Device Safety:** By categorizing and listing devices, the policy aims to ensure that devices are appropriately reviewed and monitored. * **Market Clarity:** Provides manufacturers with clear guidelines for device classification and registration. * **Standardized device approval** By categorizing devices and intended uses, the policy will allow medical practitioners and providers to consistently treat medical issues without the use of experimental devices. **9. Conclusion:** The analyzed document establishes a framework for the categorization and registration of medical devices in India. This framework creates a systematic approach to medical device regulation, potentially leading to improved device safety, market clarity, and regulatory efficiency. The establishment of device categories and detailed listings of devices, along with intended uses, are the core provisions of this policy, which is likely to impact medical device manufacturers, regulatory agencies, healthcare providers, and patients. The INDIA classification for each device will also ensure that only approved medical devices will be permitted within the nation. Further information regarding the registration process, risk assessment criteria, and enforcement mechanisms would be needed for a complete analysis.

Key Entities Referenced

Anesthesiology: A category of medical devices for registration, specifically related to anesthesia. Pain Management: A category of medical devices focused on alleviating pain. Cardiovascular: A category of medical devices related to the heart and blood vessels. Dental: A category of medical devices pertaining to dentistry. Ear, Nose, Throat ENT: A category of medical devices related to otolaryngology. Operation Theater OT: A general hospital area where surgical operations are conducted Epidural anaesthesia kit: Collection of devices intended to deliver an analgesic or anaesthetic agent to the epidural space for pain management Anaesthesia machine: A medical device used to generate and mix a fresh gas flow of medical gases and inhalational anaesthetic agents for the purpose of inducing,monitoring and maintaining anaesthesia.
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Annexure II CATEGORIES OF MEDICAL DEVICE FOR REGISTERATION PURPOSE Sr.No. Categories of Medical Device 1 Anesthesiology 2 Pain Management 3 Cardiovascular 4 Dental 5 Ear, Nose, Throat (ENT) 6 Gastroenterological 7 Urological 8 General Hospital 9 Operation Theater (OT) 10 Respiratory 11 Neurological 12 Personnel use 13 Obstetrical and Gynecological (OG) 14 Ophthalmic 15 Rehabilitation 16 Physical support 17 Interventional and Radiology 18 Rheumatology 19 Dermatology and Plastic Surgery 20 Pediatric and Neonatology Medical 21 Oncology 22 Radiotherapy 23 Nephrology and Renal care 24 SoftwareName of Category: Anesthesiology Total No. of Devices: 115CATEGORY: ANESTHESIOLOGY Sr No MEDICAL DEVICE NAME INTENDED USE INDIA A medical device used to generate and mix a fresh gas flow of medical gases and inhalational anaesthetic agents for the 1 Anesthesia machine C purpose of inducing,monitoring and maintaining anaesthesia. A flexible tube used in conjunction with an oxygen mask, endotracheal (ET) tube, humidifier, or nebulizer, intended 2 Aerosol delivery tubing A for the delivery of aerosolized humidification, typically oxygen enriched. A flexible, form-shaped device that is placed over the nose 3 Aerosol face mask and mouth to deliver air, oxygen (O2), or a mixture of the B two gases, with aerosolized particles, to a patient's airway. It is a device that enables a medical professional to 4 Aerosol inhalation monitor objectively assess in detail how the test subject uses their B inhaler. A hand-held device intended to be used to clean an in situ 5 Airway device cleaning utensil A and ex situ airway device. A device connected to the breathing circuit that monitors a 6 Airway pressure alarm patient's upper airway pressure during assisted mechanical A ventilation. It is a device intended to continuously measure and display the breathing circuit pressure and oxygen (O2) 7 Airway pressure/oxygen monitor C concentration levels of respiratory gases delivered to a patient through positive pressure ventilation systems. A flexible, form-shaped device that is placed over the nose 8 Airway protection face mask A and mouth to provide respiratory protection. An assembly of devices used to continuously measure the 9 Airway temperature monitoring system B temperature at a specific point along a ventilation airway. A hand-held instrument used for grasping a tube for its insertion and/or extraction into/from the airways, or for 10 Airway tube forceps A grasping obstructive objects for their removal from the airways. An assembly of devices designed to conduct medical gases 11 Anaesthesia breathing circuit from the fresh gas supply outlet of an anaesthesia B unit/workstation to the patient. It is a device intended to create a mechanical union 12 Anaesthesia catheter Luer connector between an anaesthesia catheter and an external device, A via a Luer connection. It is a device intended to be used to detect, process, and display the signals recorded from an unconscious patient (in 13 Anaesthesia depth monitor B a state of anaesthesia), showing the degree of consciousness. A device intended to simulate the electroencephalography (EEG) signals of an unconscious patient (in a state of 14 Anaesthesia depth simulator anaesthesia) in order to test and calibrate an anaesthesia A depth monitor, check patient cable continuity, or train healthcare providers. A dedicated assembly of devices designed to electronically receive, collect, store, manage, assist in analysis of, display, output, and distribute data, within or between healthcare 15 Anaesthesia information system B facilities, to support the administrative and clinical activities associated with the provision and utilization of anaesthesia services. It is intended as a support for Anaesthesia instruments used 16 Anaesthesia instrument table A during general anaesthesia surgical procedures. A device intended to secure an anaesthesia mask on the 17 Anaesthesia mask stabilizer face of a patient typically by providing anchorage for the A fixation of the mask's headstrap. A device intended to test an anaesthesia system for 18 Anaesthesia system leakage tester A leakage. A device used to vaporize the anaesthetic agent and deliver 19 anaesthesia vaporizer a controlled amount of the agent to a patient being prepared C for surgery. A device intended to warm the anaesthetic solutions prior to 20 Anaesthesia warmer A it being administered to a patient for anaesthesia. Page 1 of 7A device intended to connect between the expiratory valve/port of a breathing circuit and the extraction system Anaesthesia workstation gas enabling the waste anaesthetic, exhaled, or other trace 21 B scavenger gases to be removed under controlled conditions from the work environment and channelled to the outside of the building. A device intended to, when integrated within the common Anaesthetic gas absorption/desorption 22 line of a breathing circuit, absorb and desorb (i.e., recycle) B device exhaled volatile anaesthetic agents. A device intended to function as an outlet assembly to which Anaesthetic gas scavenging terminal 23 the operator can connect/disconnect an anaesthetic gas A unit scavenging system (AGSS). A device designed to be placed over a patient's nose and/or 24 Anesthesia Face Mask A mouth to administer anaesthetic gases to the upper airway. A device intended for insertion within the lumen of an 25 Artificial airway stylet artificial airway tube to stiffen and/or maintain the shape of A the tube to facilitate intubation. A container intended to hold artificial airway devices to 26 Artificial airway washing/disinfection jar B facilitate their washing/disinfection. A device that is intended to provide liquid medication in 27 Atomizer A aerosolized form into the air that a patient will breathe. A collection of devices intended to deliver a brachial plexus 28 Brachial plexus anaesthesia kit nerve block through one of several routes that could include B supraclavicular, interscalene, infraclavicular, or axillary. A device intended to store breathing gas during the 29 Breathing circuit bag A respiratory cycle. A device intended to be integrated within the expiratory limb of a breathing circuit to remove excess moisture through 30 Breathing circuit condenser A cooling and condensing, whilst also reheating the dried gases to an appropriate machine-compatible temperature. A device that is used for the purpose of drying breathing 31 Breathing circuit dryer circuit equipment that have been washed inorder to prevent A bacteria growth and deterioration A collection of devices intended to be integrated within a breathing circuit to enable interface of gases between the Breathing circuit gas- 32 breathing circuit and a respiratory monitoring device for B sampling/monitoring set sampling the patient's expired gas for measurements of pressure, flow and/or gas analysis. A device intended for the cleaning and high-level 33 Breathing circuit washer/disinfector disinfection of breathing circuit components used in B respiratory therapy and anaesthesia equipment. A device intended to be inserted into a patient's mouth to 34 Breathing mouthpiece A facilitate access to the respiratory system. A tube-shaped surgical instrument that is inserted into the 35 Bronchial cannula lumen of the bronchus by means of a trocar blade to provide A rigidity. An endoscope with an inserted portion intended for the visual examination and treatment of the trachea, primary 36 Bronchoscope A bronchi, and upper regions of the lungs and take biopsies and sample of secretions. A device which is inserted orally into the trachea to maintain airway patency and/or to deliver anaesthetic inhalation 37 Bronchoscopy tube agents or other medical gases, and secure ventilation B during diagnostic or therapeutic bronchoscopy using a flexible bronchoscope. An assembly of devices designed to concentrate oxygen (O2) from ambient air and then deliver the concentrated O2, 38 Bulk oxygen concentration system A with purity of up to 99.5%, to the hospital medical gas supply system. A device intended to be placed over the nose and mouth to deliver oxygen (O2) to a patient's airway and to sample 39 Capnography oxygen mask A exhaled respiratory gases for monitoring the patient’s ventilatory status. The device is intended for sampling CO2 and use with 40 Capnography sampling adaptor A monitors enabled with capnography technology . Page 2 of 7A device intended to continuously measure the concentration of carbon dioxide (CO2) in a gas mixture to 41 Carbon dioxide monitor C determine a patient's ventilatory, circulatory, or metabolic status. A device designed to be placed over a user's nose to interface with a continuous positive airway pressure (CPAP) or bi-level positive airway pressure (BPAP) unit to provide 42 CPAP/BPAP nasal mask B the respiratory tract with direct ambient air, or medical oxygen (O2) and air, at a higher pressure than ambient air for noninvasive positive pressure ventilation (NPPV). A device designed to be fitted to the user's mouth to interface with a continuous positive airway pressure (CPAP) or bi-level positive airway pressure (BPAP) unit to provide 43 CPAP/BPAP oral mask B the respiratory tract with direct ambient air, or medical oxygen (O2) and air, at a higher pressure than ambient air for noninvasive positive pressure ventilation (NPPV). A device intended to be used with an epidural needle and Electronic epidural space locator an electronic epidural space locator pressure-sensing set, to 44 D control unit aid a user in locating the epidural needle tip within the epidural space for subsequent anaesthesia administration. An electronic listening device designed to be inserted into a 45 Electronic oesophageal stethoscope patient's oesophagus to listen to heart and breathe sounds, B typically while the patient is under anaesthesia. A collection of mechanical devices intended to be used with a balloon catheter for a planned intervention to determine 46 Endobronchial airway sizing kit A the appropriate endobronchial valve sizes for a patient's lung airways (bronchial lumens). A hollow cylinder that is designed for oral insertion via the trachea and into a lung to maintain airway patency and/or to 47 Endobronchial tube B deliver anaesthetic inhalation agents or other medical gases, and secure ventilation. An assembly of devices designed to continuously detect the sound of endotracheal (ET) secretions moving through a Endotracheal secretion monitoring 48 ventilation circuit during suctioning of an artificially ventilated B system and/or spontaneously breathing patient to assess the effectiveness of suctioning. A collection of devices intended to be used to deliver an 49 Epidural anaesthesia kit analgesic or anaesthetic agent to the epidural space for D pain management. An independent mechanical device designed for accurate mixing of helium (He) and oxygen (O2) with concentrations 50 Helium/oxygen breathing gas mixer that are appropriated for breathing in a patient who is B indicated to assist flow of O2 into the alveoli and to reduce the work of breathing. A device intended to assist or control alveolar ventilation using a frequency that is considerably higher than the 51 High-frequency ventilator C physiological breathing rate and a tidal volume less than or equal to the anatomic dead space. A device primarily designed to administer analgesic gases 52 Inhalational analgesia unit B to the patient, or produce analgesic vapours for inhalation. A collection of devices designed to obtain an in-line arterial 53 In-line arterial blood sampling set A blood specimen while maintaining a closed system. A general-purpose device used in medical tubing or pipe- 54 In-line backflow valve A lines to prevent the backflow of gases or liquids. A photoelectric device designed to transmit radiation at a known wavelength(s) through blood to measure the 55 Intracardiac oximeter B concentration of oxygen, or dye, within the heart based on the amount of reflected or scattered radiation. An assembly of devices used for the continuous in vivo measurement and display of the values of pH and/or the Intravascular blood gas/pH monitoring 56 partial pressure of CO2 and/or O2 in arterial blood. The B system system is used for patients with respiratory failure or severe pulmonary hypertension after cardiac surgery. Page 3 of 7A device designed for intravascular diffusion of oxygen into and carbon dioxide from the blood across an implantable 57 Intravascular membrane oxygenator (vena cava) gas-permeable membrane, used mainly as a C temporary treatment for failing lungs in adults with respiratory distress syndrome. An instrument designed for the continuous in vivo 58 Intravascular oximeter measurement of venous blood oxygen saturation (SvO2) B using a fibreoptic catheter. A hand-held device intended to be used by anaesthesia/emergency service personnel to manipulate the tongue, preventing it from obstructing the oropharynx and 59 Intubation laryngoscope A enabling a clear view of the trachea for the insertion of an endotracheal (ET) tube prior to the delivery of inhalation anaesthesia and/or ventilation. A device designed to fit over the upper and lower sets of 60 Intubation teeth protector teeth to protect them from damage during endotracheal A (ET) tube intubation procedures. A device intended to continuously measure and display arterial pressure cardiac output (APCO) and haemoglobin Invasive arterial pressure cardiac oxygen saturation (e.g., SpO2) when connected to an 61 B output/oximetry monitor extravascular blood pressure transducer linked to a peripheral arterial line, and to a pulse oximeter or an oximetry catheter. A curved tube used in inhalational anaesthesia and resuscitation to facilitate and secure airway patency for the 62 Laryngeal airway A delivery and exchange of gases in spontaneously breathing and ventilated patients. A device intended to aid insertion of a laryngeal airway into the pharyngeal cavity of a patient while reducing or eliminating the need for finger manipulation within the 63 Laryngeal airway introducer mouth. It is typically in the form of a metal blade with a A handle and may be mounted onto the laryngeal airway during insertion. This is a reusable device intended to be sterilized prior to use. A device intended to maintain tracheostoma patency after laryngectomy to provide an airway for the patient and to 64 Laryngectomy tube B prevent tracheostomal stenosis in the months following the procedure. A non-sterile container that is prefilled with an anaesthetic agent and intended to be used to apply the agent to the Laryngotracheal anaesthesia 65 oropharynx and upper airway, to relax laryngotracheal B applicator reflexes prior to an intervention of an endotracheal (ET) tube or other type of tracheal tube. A portable, manually-operated, noninvasive device intended to be used in conjunction with a separate compressed oxygen (O2) source and airway access device for 66 Manual jet ventilation device C transtracheal ventilation of a patient in an emergency situation where there is complete or partial obstruction of the airways. A hand-held, mechanical device designed to remove Mechanical positive pressure airway excessive mucus or sputum (phlegm) from the lungs and 67 A secretion-clearing device upper airway of a patient typically suffering from acute or chronic lung disease. A device intended to measure and regulate the flow of a 68 Medical gas flowmeter A medical gas during various procedures. A device intended to measure and regulate the flow of a 69 Medical gas flowmeter, Thorpe tube A medical gas during various procedures. An assembly of devices designed to supply compressed 70 Medical gas pipeline system medical gases from a central source to endpoints A throughout a medical facility. A mains component of a medical gas pipeline supply system Medical gas pipeline system automatic 71 that monitors the composition of a gas delivered from the A outlet analyser supply system. A component of a medical gas pipeline system designed to Medical gas pipeline system pressure 72 continuously monitor and detect changes in the pressure A monitor values of the medical gases in the supply pipeline. Page 4 of 7A device that is a component of a medical gas pipeline system or a medical gas/vacuum pipeline system that has a 73 Medical gas terminal unit gas-specific outlet connection for a single/mixture of gas to A which the operator can connect and disconnect a medica device. A device intended to be placed between a nebulizer or a metered dose inhaler (MDI) and the patient's mouth, to 74 Medicine chamber spacer function as a reservoir into which an aerosol medication is B dispensed in order to minimize delivery of large aerosolized particles. A screening device intended to remove microbes from 75 Microbial medical gas filter medical gases to prevent patient exposure during B respiration, anaesthesia and/or endoscopy. A rubber or plastic tube that extends into the pharynx from 76 Nasopharyngeal airway A either naris to maintain airway patency. An automatic cycling machine used to assist or control alveolar respiration that exerts a negative pressure on the 77 Negative-pressure ventilator C external surface of the chest wall, expanding the chest and moving air into the lungs. A hand-held device (a percussor) intended to be operated by a healthcare professional to provide external vibrations to the chest wall of a neonate to help loosen bronchial mucus 78 Neonatal chest percussor B for expectoration through suctioning. It is used to help loosen secretion build-up in the lungs of neonates who cannot perform the natural cough mechanism. A noninvasive device intended to be connected between a syringe and a nerve-block needle to indicate injection 79 Nerve-block injection manometer A pressure during administration of local or regional anaesthesia to achieve peripheral nerve blockade. A device intended for the delivery of precise amounts of nitric oxide (NO), also known as nitrogen monoxide, to the 80 Nitric oxide delivery unit B respiratory tract of neonate, paediatric, and adult patients to treat severe respiratory disorders. A device designed to prevent the drying of airway passages associated with the inhalation of oxygen (O2) by adding 81 Non-heated respiratory humidifier B water vapour to the dry gas as it is passed through, or more seldom, over water. A flexible, form-shaped device designed with valve to control rebreathing and contamination of gas, placed over 82 Non-rebreathing oxygen face mask A the nose and mouth to deliver air of high oxygen (O2) concentration to a patient's airway for oxygen therapy. A device intended to be used to compress the nose externally, to ensure that airflow is exclusively conducted 83 Nose clip A through the mouth during examinations of the pulmonary function and/or to stop nosebleeds. A curved metal or plastic tube inserted through the mouth to 84 Oropharyngeal airway facilitate airway patency for gas exchange or suctioning. The A device prevents the tongue from obstructing airflow. A device consisting of a rigid transparent plastic shell forming an enclosure over the head of an adult, typically to 85 Oxygen administration hood A provide an enriched oxygen (O2)environment to increase the patient's O2 uptake. An electronic instrument designed to simulate arterial oxygen saturation and/or pulse rate for testing and 86 Oxygen saturation/pulse rate simulator A calibrating pulse oximeters, pulse oximeter probes and other related pulse oximetry devices. A portable mechanical device designed to mix air and 87 Oxygen/air breathing gas mixer oxygen (O2) for mobile O2 administration during first aid or B emergency situations. An device designed for accurate mixing of oxygen (O2) and Oxygen/air/nitrous oxide breathing gas 88 air or O2 and nitrous oxide (N2O) in pre-set concentrations C mixer appropriated for breathing. An assembly of devices designed for continuous 89 Patient physiologic monitoring system assessment of several vital physiologic parameters of C patient(s). Page 5 of 7A device designed to measure the maximum rate of expiratory gas flow [peak expiratory flow (PEF) or peak expiratory flow rate (PEFR)] and forced expiratory volume 90 Peak flow meter B (FEV) from the lungs. The device is typically intended to monitor the respiratory status of a patient suffering from chronic respiratory disease in a clinical setting or the home. A noninvasive device intended to convert pressure into 91 Pleural manometer electrical signals for the measurement of pressure within the B pleural cavity. A hand-held pneumatic device designed to provide external vibrations to the chest wall of a patient to loosen excessive 92 Pneumatic chest percussor B airway secretions to promote airway clearance and improve bronchial drainage for patients with respiratory disease. An instrument designed to measure a patient's sensitivity to 93 Pressure algometer/aesthesiometer B pain (pain threshold) and tactile sensibility. A device used to measure the function of the respiratory 94 Pulmonary function analysis system B system in adults and compliant children. A hand-operated device designed to provide or assist 95 Pulmonary resuscitator ventilation in patients who are apnoeic or exhibit inadequate C respiration. A device designed to detect hypoxia via the transcutaneous multiwave measurement and display of carboxy- haemoglobin saturation (SpCO) and typically other related 96 Pulse Co-oximeter B parameters such as haemoglobin oxygen saturation (SpO2), methaemoglobin saturation (SpMet), and haemoglobin concentration (SpHb). A device intended for the transcutaneous measurement and 97 Pulse oximeter C display of haemoglobin oxygen saturation (SpO2). A flexible, form-shaped device designed to be placed over 98 Rebreathing oxygen face mask the nose and mouth to deliver a proportional mixture of A air/oxygen (O2) to a patient's airway. A device designed to measure and display a non- ambulatory patient's respiratory functions. Measurements include concentration of respiratory gas components and/or 99 Respiration monitor B continuous monitoring of the inspiration/expiration cycle including respiration rate, air volume, and cessation of breathing (apnoea). An instrument designed to continuously measure the 100 Respiratory oxygen monitor concentration of oxygen (O2) inspired by a patient in a B respiratory maintenance/therapy setting. An electrically-powered unit designed to be connected to a pulse oximeter sensor and used during the administration of oxygen (O2) to a spontaneously breathing patient, for: 1) Respiratory oxygen therapy 101 continuous monitoring of physiologic parameters, especially B monitor/regulator haemoglobin oxygen saturation (SpO2); and 2) dynamic regulation of the amount of O2 delivered to the patient based on physiological parameter measurements. A collection of devices used to assist in the placement of an 102 Retrograde endotracheal intubation kit endotracheal (ET) tube during difficult/emergency airway B access procedures A non-sterile device intended to facilitate the positioning of Rigid non-bladed video intubation 103 an endotracheal (ET) tube prior to the delivery of inhalation A laryngoscope anaesthesia and/or ventilation. A collection of devices designed to deliver an analgesic or anaesthetic agent to the lower dural sac in the region 104 Saddle block anaesthesia kit B corresponding to the buttocks, in the perineum, or to the inner aspects of the thighs. A device designed to transmit and receive electrical signals Spinal needle bioimpedance to/from a dedicated spinal needle and to analyse 105 D navigation unit bioimpedance data in real-time, to predict needle tip location. A device consisting of a barrel (cylinder) with plunger/piston intended to be used for injecting small volumes of Spirometer/pulmonary function 106 accurately measured amounts of gas into a spirometer, A analyser syringe pulmonary function analyser, or other diagnostic pulmonary measuring/testing device for calibration or reference. Page 6 of 7A hand-held manual surgical instrument intended to be used during surgical intervention of the trachea to dilate tracheal structures/passages, typically during the creation of a 107 Tracheal surgery dilator A tracheostoma and/or for expanding the margins of a tracheostoma to assist in the insertion of a tracheostomy tube. A collection of surgical instruments, dilators, tracheostomy tubes and other items intended to be used to create a 108 Tracheostomy kit percutaneous opening in the trachea (tracheotomy) for the C insertion of a tracheostomy tube to relieve upper airway obstruction and to facilitate ventilation. A hollow, cylindrical, curved device designed as an internal, independent component of a metal tracheostomy tube. It is removed once or more times daily to facilitate the removal 109 Tracheostomy tube cannula A of phlegm, slime, and contamination build-up, thereby preventing blockage and infection of the stoma and eliminates the traumatic removal of the tracheostomy tube. A surgical instrument designed to cut an opening into the 110 Tracheotome trachea (windpipe) through the anterior surface of the neck A to create an artificial airway (tracheotomy). An assembly of devices designed to stimulate a reflex cough using ultrasound in a patient who cannot cough on 111 Ultrasonic cough stimulation system command, typically respiratory patients with cortical A insufficiency or the very young/elderly, to help clear the lungs of secretions and aspirated materials. A device designed to agitate water into micro-particles with 112 Ultrasonic respiratory humidifier ultrasound to add moisture to the flow of air/gases B administered to a patient via a breathing tube/circuit. A device assembly designed to remove excessive secretion Vacuum-assisted airway secretion- from the lungs and upper airway of patients with respiratory 113 B clearing system disease or during cardiac rehabilitation through vacuum technology. A flexible, cone-shaped device placed over the patient's nose and mouth to deliver a mixture of an almost precise ratio of air and oxygen to the patient's airway. The device usually has a replaceable part (Venturi tube) to change the 114 Venturi oxygen face mask mixture ratio of air and oxygen so that oxygen is delivered at B a desired concentration. The device is connected to the oxygen source via a tube. The device has a head strap for fixation. Normally comes with an adapter to connect with humidifier. A device designed to be placed over the nose and mouth of 115 Vortex oxygen face mask a patient to deliver a near-precise mixture of air and oxygen B (O2) to a patient's airway without the use of a gas mixer. Page 7 of 7Name of Category: Pain Management Total No. of Devices: 69CATEGORY:PAIN MANAGEMENT Sr No MEDICAL DEVICE NAME INTENDED USE INDIA A device designed to be worn around the calf to apply 1 Acupressure calf band pressure to an acupressure point to relieve low back pain, A including sciatica and piriformis syndrome. A device designed to be worn on the wrist(s) for the application of pressure to the Nei-kuan (P6) acupressure 2 Acupressure wristband A point, the area identified to help relieve the sensation of nausea. Acupuncture electrical An assembly of devices used to apply electrical stimuli to 3 B stimulation system acupuncture sites. A collection of instruments and supplies used to perform 4 Acupuncture kit B acupuncture procedures. An electronic probe used to precisely locate an acupuncture 5 Acupuncture point detector B point on a patient's body. An assembly of devices intended for the relief of chronic 6 Analgesic PENS system neuropathic pain through percutaneous electrical nerve B stimulation (PENS). Analgesic peripheral nerve An assembly of devices designed to stimulate electrically a 7 C electrical stimulation system peripheral nerve in a patient to relieve severe intractable pain. Analgesic spinal cord An assembly of devices that applies an electrical stimulus to 8 C electrical stimulation system all or part of the spinal cord to relieve pain (analgesia). An assembly of devices used to reduce the perception of pain 9 Analgesic TENS system by electrically stimulating peripheral nerves across the skin B (transcutaneously). An assembly of devices intended to be used as adjunctive therapy in reducing the level of pain and stiffness associated 10 Arthritis TENS system with rheumatoid arthritis or osteoarthritis by electrically B stimulating peripheral nerves across the skin (transcutaneously). An assembly of devices intended to be used as adjunctive therapy in reducing the level of pain and stiffness associated Arthritis transcutaneous with rheumatoid arthritis or osteoarthritis by electrically 11 electrical joint stimulation B stimulating an arthritic joint across the skin (transcutaneously) system and to provide an overall improvement to an arthritic joint and defer or avoid surgery. A device intended to provide therapeutic massage to the 12 Bed/chair electric massager occupant of a bed or chair for the treatment of body aches and B pains. A thin, plastic, horshoe-like wafer that is placed between the 13 Bite relief pad upper and lower sets of teeth and bitten down on, or chewed, A to help relieve pain or discomfort after orthodontic treatment. A portable device designed to emit blue light, red light, and Blue/red/infrared 14 infrared radiation (heating effect) for phototherapy treatment of B phototherapy lamp mild skin disorders (e.g., mild acne), superficial skin wounds, and musculoskeletal symptoms (e.g., pain, spasm, stiffness). An assembly of devices intended to be used to pump heated and/or cooled fluid through externally applied packs for Circulating-fluid thermal 15 localized hot and/or cold therapy to help treat a variety of B therapy system adverse conditions resulting from musculoskeletal injury (e.g., pain, swelling, inflammation). A unit intended to generate and deliver a stream of cold air directly to the skin surface to treat musculoskeletal/rheumatic 16 Cold-air therapy unit disorders, to reduce localized pain/inflammation, and/or to B reduce thermal skin damage during dermatological laser treatments. A device designed to provide analgesia by applying extremely 17 Cryogenic analgesia unit low temperatures to body tissues. It is used for postoperative C and chronic intractable pain relief. Page 1 of 5An assembly of devices designed to apply an electromagnetic (EM) field to body tissues to: 1) treat musculoskeletal Deep-tissue electromagnetic 18 disorders; 2) treat body pain; and/or 3) help facilitate soft and B stimulation system hard tissue wound/injury healing, with no production of a therapeutic deep heat. An instrument used in auriculotherapy to apply continuous 19 Ear microsystem needle A pressure to stimulate meridian points. An assembly of devices designed for the transcutaneous Electric pad localized-body 20 application of heat to a localized body site to relieve B heating system musculoskeletal pain. Electromechanical orthopaedic extracorporeal An assembly of devices designed to provide 21 shock wave/pneumatic electromechanical orthopaedic extracorporeal shock wave C pressure wave therapy therapy (OEST) and pneumatic pressure wave therapy to treat system musculoskeletal disorders. A device intended to be applied with pressure to the body Endothermic cold therapy surface to provide cold therapy to help reduce fever, pain, and 22 B pack inflammation associated with joint/muscle/tissue injury and/or minor burns. A collection of devices intended to be used to deliver an 23 Epidural anaesthesia kit analgesic or anaesthetic agent to the epidural space for pain C management. A collection of devices designed to deliver an analgesic or Epidural/intrathecal anaesthetic agent into the epidural and subarachnoid 24 C anaesthesia kit (intrathecal) spaces around the spinal cord for pain management. A device intended to be applied to the body surface, Exothermic heat therapy sometimes with pressure, to provide heat therapy to reduce 25 B pack muscle spasms and cramps and/or for joint and muscle stiffness and pain. An endoscope with a flexible inserted portion intended for the Flexible fibreoptic 26 visual examination and treatment of intractable back and leg C epiduroscope pain. A device designed to be filled with water to provide therapeutic heat treatment specifically to the feet. This device 27 Foot bath B is intended to relieve foot pain as well as headaches, coughs, and other cold symptoms. A non-sterile gelatinous compound in a container that is dispensed for application to the body surface to provide a 28 Heat therapy gel warming effect for underlying tissues. It is intended to B reduce/relieve pain, muscle tension, and to increase local circulation. A bathtub or tank designed to be filled with warm water and occupied by a patient for the application of various forms of physical hydrotherapy such as water jet massage or aquatic 29 Hydrotherapy bath/tank B exercise, typically to help treat musculoskeletal pain and stiffness or for physical rehabilitation; it is not dedicated to flotation therapy. 30 Ice bag Intended to alleviate pain and/or promote healing in minor A injuries of the body or for application around the neck or limbs. Intended to alleviate pain and/or promote healing in minor 31 Ice collar injuries of the neck, throat, and/or head and to alleviate a sore A throat. A device designed to be implanted in a patient for the storing Implantable intrathecal and subarachnoid (intrathecal) administration of 32 D infusion pump narcotics/drugs to manage intractable pain and muscle spasms of malignant or non-malignant origin. Implantable lumbar The system is designed to deliver episodic electrical 33 neuromuscular electrical D stimulation to nerves that innervate lumbar muscles to elicit stimulation system contraction for the treatment of chronic low back pain (CLBP). Page 2 of 5A assembly of devices intended for localized thermal and Inflatable hot/cold therapy 34 compression therapy to facilitate the treatment of a variety of B pack/electric pump adverse conditions resulting from musculoskeletal injury. A device primarily designed to administer analgesic gases to 35 Inhalational analgesia unit B the patient, or produce analgesic vapours for inhalation. An device assembly designed to stimulate peripheral nerves Interferential electrical through the transcutaneous application of two currents of 36 B stimulation system slightly different frequencies that cross-over/interfere, producing a beating frequency at the treatment point. A device intended to be applied to the skin overlying an Intervertebral disc prolapse 37 affected area of the spine (cervical or lumbar) to reduce pain B therapy pack associated with a prolapsed (herniated) intervertebral disc. A device designed to fit over the upper and lower sets of teeth 38 Intubation teeth protector to protect them from damage during endotracheal (ET) tube A intubation procedures. A fixed framework with a tilting table platform designed to support the body of a patient and provide traction for the back 39 Inversion table muscles and spine by allowing the patient manually invert their A entire body in a supine position (feet up and head down), thereby assist patients eliminate/alleviate back pain. 40 Massage table/couch A table designed for various kinds of complementary therapy. A An assembly of devices designed to produce a therapeutic deep heat within specific volumes of the body through the Medium-wave diathermy transcutaneous transmission of electromagnetic (EM) energy 41 C treatment system in the radio-frequency (RF) bands of 0.5 megahertz (MHz) to 1 MHz. ,to treat pain, muscle spasms, and joint contractures; it is not used for surgery or to treat malignancies. An assembly of devices designed to produce a therapeutic heat below the skin within specific volumes of the body Microwave diathermy 42 through the transcutaneous transmission of high frequency C treatment system electromagnetic (EM) energy, to promote tissue healing and pain relief. An assembly of devices designed to apply multiple different Multi-modality physical energies either alone or in sequence, but not simultaneously, 43 C therapy system to noninvasively treat/prevent a variety of soft-tissue, neuromuscular, and musculoskeletal injuries/disorders. A device intended to provide a source of infrared (IR) heat for Musculoskeletal infrared localized treatment of musculoskeletal pain/injury and to 44 B phototherapy unit improve blood circulation in the treated areas to facilitate healing. An assembly devices designed to produce and deliver intense therapeutic ultrasound (ITU) waves through the skin to create Musculoskeletal intense ablative lesions in subcutaneous soft tissues, intended to 45 therapeutic ultrasound C reduce inflammation and pain associated with musculoskeletal system disorders or injuries by stimulating collagen production and regenerating connective tissue. An electrically-powered diode laser intended to provide noninvasive laser therapy for localized treatment of Musculoskeletal/physical 46 musculoskeletal conditions, improving blood circulation in the C therapy laser treated areas to facilitate healing, or for non-needle acupuncture. An assembly of devices designed to monitor and provide electrical stimuli to spinal nerves or other neural pathways Neurophysiologic monitoring during intraoperative surgery or intensive care, typically to 47 C system reduce the incidence of accidental injury during instrumented spine surgery, or to diagnose acute dysfunction in corticospinal conduction. A skin patch designed to reflect the naturally emitted infrared energy back into the body, with a reduced range of Pain-relief phototherapy skin 48 wavelength, intended to provide comfort and localized A patch temporary relief of body aches and pains by phototherapeutic stimulation of strategic points on the skin. Page 3 of 5A magnetized metal device designed to be worn on any part of the body (non-dedicated) and intended to produce a weak 49 Pain-relief static magnet magnetic flux field over a superficial body site to provide A comfort and localized temporary relief of body aches and pains. A tub/enclosure, with an internal heating assembly, filled with Physical therapy paraffin liquid paraffin wax for physical therapy, to relieve pain and 50 B wax bath stiffness caused by arthritis or other joint inflammation, muscle spasms, or to help stimulate circulation. An assembly of devices designed to provide a therapeutic deep heat within specific volumes of the body through the Short-wave diathermy transcutaneous transmission of electromagnetic (EM) energy 51 B treatment system in the radio-frequency (RF) bands. The device is intended to treat pain, muscle spasms, and joint contractures; it is not used for surgery or to treat malignancies. A tub filled with water, that is heated by its heating elements and circulated by its agitators, intended for use in external 52 Sitz bath hydrotherapy to relieve pain or pruritus and to accelerate the A healing of inflamed or traumatized tissues of the perianal and perineal areas. A device designed to be sat upon by a patient in a powered sitz bath for external hydrotherapy to relieve pain or pruritus 53 Sitz bath chair A and to accelerate the healing of inflamed or traumatized tissues of the perianal and perineal areas. A pad made of textile fabrics containing magnetic inserts and designed to be placed on the surface of the skin. on the back Static magnetic back/spine and/or part or the whole of the spine to help relieve medical 54 B insulator ailme andnts such as pain, muscle tension, poor blood circulation and to provide comfort by improving overall mobility. A pad made of textile fabrics containing magnetic inserts intended to be placed on top of a bed mattress and contact an Static magnetic bed 55 occupant’s body to help relieve medical ailments such as pain, A mattress overlay muscle tension, poor blood circulation and to provide comfort by improving overall mobility. A device, typically fashioned as a piece of clothing, containing or impregnated with a magnetized metal(s) or metallic compound(s), designed to be worn around the waist to 56 Static magnetic belt A produce a weak magnetic flux field that emanates from the waist to assist the whole body’s innate healing capability to alleviate body aches and pains. A device, typically fashioned as a piece of jewellery, containing or impregnated with a magnetized metal(s) or metallic compound(s), designed to be worn around the wrist to 57 Static magnetic bracelet A produce a weak magnetic flux field that emanates from the surface of the wrist to assist the whole body’s innate healing capability to alleviate body aches and pains. A body-support device containing or impregnated with magnetized metals or metallic compounds, designed to be Static magnetic elbow worn around the elbow joint to support the elbow and produce 58 B orthosis a weak magnetic flux field that emanates from the surface of the elbow to assist the whole body’s innate healing capability to alleviate body aches and pains. A body-support device containing or impregnated with magnetized metals or metallic compounds, designed to be worn in a patient’s shoe, or other footwear, under the arch of Static magnetic foot arch 59 the foot to support the arch and produce a weak magnetic flux B orthosis field that emanates from the surface of the foot arch to assist the whole body’s innate healing capability to alleviate body aches and pains. Page 4 of 5A pad made of textile fabrics containing magnetic inserts and designed to be placed on the surface of the skin over/around Static magnetic joint 60 a patient's hip or other limb joint to help relieve medical B insulator ailments such as pain, muscle tension, poor blood circulation and to provide comfort by improving overall mobility. A body-support device containing or impregnated with magnetized metals or metallic compounds, designed to be Static magnetic knee worn around the knee joint to support the knee and produce a 61 B orthosis weak magnetic flux field that emanates from the surface of the knee to assist the whole body’s innate healing capability to alleviate body aches and pains. A body-support device containing or impregnated with magnetized metals or metallic compounds, designed to be Static magnetic lumbar 62 worn around the hips to support the lower back (spine and B spine orthosis coccyx) and produce a weak magnetic flux field that emanates from the surface of the lower back to assist the whole body’s innate healing capability to alleviate body aches and pains. A device designed to be moved over body surfaces that uses static magnets intended to produce a weak magnetic flux over 63 Static magnetic massager A a superficial body site to provide comfort and localized temporary relief from minor aches and pains. A body-support device containing or impregnated with magnetized metals or metallic compounds, designed to be Static magnetic shoulder worn around the shoulder joint to support the shoulder and 64 B orthosis produce a weak magnetic flux field that emanates from the surface of the shoulder to assist the whole body’s innate healing capability to alleviate body aches and pains. A body-support device containing or impregnated with magnetized metals or metallic compounds, designed to be worn around the waist or across the shoulders to support the Static magnetic thoracic 65 back (central- and upper spine) and produce a weak magnetic B spine orthsosis flux field that emanates from the surface of the central- and upper spine to assist the whole body’s innate healing capability to alleviate body aches and pains. A harness designed to provide traction to the lower spine, including the lumbar and pelvic areas, with force from an 66 Traction system belt external traction system. The harness is used mainly for relief A of low back pain and to maintain normal alignment of the vertebrae. Transcutaneous Electro- 67 Neuro Stimulator (TENS) A therapy device intended to stimulate the nerves for pain C devices relief. An externally-worn orthopaedic device intended to apply Wearable cervical spine 68 traction to the cervical spine/neck to treat pain resulting from B traction device non-bone injuries/disorders. An externally-worn orthopaedic device designed to apply Wearable lumbar spine 69 traction to the lumbar spine to relieve symptoms of back pain B traction device and sciatica. Page 5 of 5Name of Category: Cardiovascular Total No. of Devices: 37CARDIOVASCULAR Classificatio Name Of Prouct serial Intended Use/Device n Ind MDR (Cardiovascular No. Description 2017 Frist Diagnostic Devices) Schedule The arrhythmia detector and alarm device monitors an Arrhythmia Detector And electrocardiogram and is Alarm (Including St- designed to produce a visible or 1 Segment Measurement audible signal or alarm when And Alarm). atrial or ventricular arrhythmia, such as premature contraction or ventricular fibrillation, occurs. C A cardiac monitor (including cardiotachometer and rate alarm) is a device used to measure the heart rate from an analog signal Cardiac monitor (including produced by an 2 cardiotachometer and rate electrocardiograph, alarm) vectorcardiograph, or blood pressure monitor. This device may sound an alarm when the heart rate falls outside preset upper and lower limits. B An apex cardiograph (vibrocardiograph) is a device used to amplify or condition the Apex cardiograph signal from an apex cardiographic 3 (vibrocardiograph). transducer and to produce a visual display of the motion of the heart; this device also provides any excitation energy required by the transducer. B An echocardiograph is a device that uses ultrasonic energy to create images of cardiovascular 4 Echocardiograph. structures. It includes phased arrays and two-dimensional scanners. BAn electrocardiograph is a device used to process the electrical signal transmitted through two or 5 Electrocardiograph. more electrocardiograph electrodes and to produce a visual display of the electrical signal produced by the heart. B An electrocardiograph electrode is the electrical conductor which is applied to the surface of the Electrocardiograph 6 body to transmit the electrical electrode. signal at the body surface to a processor that produces an electrocardiogram or vectorcardiogram. C A vascular clip is an implanted extravascular device designed to 7 Vascular clip occlude, by compression, blood flow in small blood vessels other than intracranial vessels. B A vena cava clip is an implanted extravascular device designed to 8 Vena cava clip. occlude partially the vena cava for the purpose of inhibiting the flow of thromboemboli through that vessel. B An intra-aortic balloon and control system is a prescription device that consists of an inflatable balloon, which is placed in the aorta to improve cardiovascular functioning during certain life- threatening emergencies, and a Intra-aortic balloon and 9 control system for regulating the control system. inflation and deflation of the balloon. The control system, which monitors and is synchronized with the electrocardiogram, provides a means for setting the inflation and deflation of the balloon with the cardiac cycle. CA ventricular bypass (assist) device is a device that assists the Ventricular bypass (assist) 10 left or right ventricle in device. maintaining circulatory blood flow. The device is either totally or partially implanted in the body. D A pacing system analyzer (PSA) is a prescription device that combines the functionality of a pacemaker electrode function tester (870.3720) and an external pacemaker pulse generator (EPPG) (870.3600). It is connected to a pacemaker lead and uses a power supply and 11 Pacing system analyzer. electronic circuits to supply an accurately calibrated, variable pacing pulse for measuring the patient's pacing threshold and intracardiac R-wave potential. A PSA may be a single, dual, or triple chamber system and can simultaneously deliver pacing therapy while testing one or more implanted pacing leads. C An implantable pacemaker pulse generator is a device that has a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the heart. This device is used as a Implantable pacemaker 12 substitute for the heart's intrinsic pulse generator. pacing system to correct both intermittent and continuous cardiac rhythm disorders. This device may include triggered, inhibited, and asynchronous modes and is implanted in the human body. D A pacemaker lead adaptor is a device used to adapt a pacemaker lead so that it can be 13 Pacemaker lead adaptor. connected to a pacemaker pulse generator produced by a different manufacturer. CA pacemaker generator function analyzer is a device that is Pacemaker generator 14 connected to a pacemaker pulse function analyzer. generator to test any or all of the generator's parameters, including pulse duration, pulse amplitude, pulse rate, and sensing threshold. B Identification. A temporary pacemaker electrode is a device consisting of flexible insulated electrical conductors with one end connected to Cardiovascular permanent an external pacemaker pulse 15 or temporary pacemaker generator and the other end electrode. applied to the heart. The device is used to transmit a pacing electrical stimulus from the pulse generator to the heart and/or to transmit the electrical signal of the heart to the pulse generator. B A pacemaker test magnet is a device used to test an inhibited or 16 Pacemaker test magnet. triggered type of pacemaker pulse generator and cause an inhibited or triggered generator to revert to asynchronous operation. A A pacemaker programmer is a device used to noninvasively 17 Pacemaker programmers. change one or more of the electrical operating characteristics of a pacemaker. D A pacemaker repair or replacement material is an Pacemaker repair or adhesive, a sealant, a screw, a 18 replacement material. crimp, or any other material used to repair a pacemaker lead or to reconnect a pacemaker lead to a pacemaker pulse generator. DA pacemaker electrode function tester is a device which is connected to an implanted Pacemaker electrode 19 pacemaker lead that supplies an function tester. accurately calibrated, variable pacing pulse for measuring the patient's pacing threshold and intracardiac R-wave potential. B Pacemaker service tools are devices such as screwdrivers and Allen wrenches, used to repair a 20 Pacemaker service tools. pacemaker lead or to reconnect a pacemaker lead to a pacemaker generator. A An annuloplasty ring is a rigid or flexible ring implanted around the 21 Annuloplasty ring. mitral or tricuspid heart valve for reconstructive treatment of valvular insufficiency. C A carotid sinus nerve stimulator Carotid sinus nerve is an implantable device used to 22 stimulator decrease arterial pressure by stimulating Hering's nerve at the carotid sinus. D A replacement heart valve is a device intended to perform the function of any of the heart's natural valves. This device includes valves constructed of 23 Replacement heart valve. prosthetic materials, biologic valves (e.g., porcine valves), or valves constructed of a combination of prosthetic and biologic materials. D An endomyocardial biopsy device is a device used in a Endomyocardial biopsy 24 catheterization procedure to device. remove samples of tissue from the inner wall of the heart. BAn extracorporeal circuit and accessories for long-term respiratory/cardiopulmonary support (>6 hours) is a system of devices and accessories that provides assisted extracorporeal circulation and physiologic gas exchange of the patient's blood in patients with acute respiratory failure or acute cardiopulmonary Extracorporeal circuit and failure, where other available accessories for long-term 25 treatment options have failed, and respiratory/cardiopulmonary continued clinical deterioration is failure expected or the risk of death is imminent. The main devices and accessories of the system include, but are not limited to, the console (hardware), software, and disposables, including, but not limited to, an oxygenator, blood pump, heat exchanger, cannulae, tubing, filters, and other accessories (e.g., monitors, detectors, sensors, connectors). C A cardiopulmonary bypass bubble Cardiopulmonary bypass detector is a device used to 26 bubble detector. detect bubbles in the arterial return line of the cardiopulmonary bypass circuit. B A cardiopulmonary bypass vascular catheter, cannula, or tubing is a device used in cardiopulmonary surgery to Cardiopulmonary bypass cannulate the vessels, perfuse 27 vascular catheter, cannula, the coronary arteries, and to or tubing interconnect the catheters and cannulas with an oxygenator. The device includes accessory bypass equipment. BA cardiopulmonary bypass heart- lung machine console is a device that consists of a control panel and the electrical power and Cardiopulmonary bypass control circuitry for a heart-lung 28 heart-lung machine machine. The console is console. designed to interface with the basic units used in a gas exchange system, including the pumps, oxygenator, and heat exchanger. B A cardiopulmonary bypass defoamer is a device used in Cardiopulmonary bypass conjunction with an oxygenator 29 defoamer. during cardiopulmonary bypass surgery to remove gas bubbles from the blood. C A cardiopulmonary bypass heat exchanger is a device, consisting of a heat exchange system used Cardiopulmonary bypass 30 in extracorporeal circulation to heat exchanger. warm or cool the blood or perfusion fluid flowing through the device. B A cardiopulmonary bypass Cardiopulmonary bypass temperature controller is a device 31 temperature controller. used to control the temperature of the fluid entering and leaving a heat exchanger. B A cardiopulmonary bypass arterial line blood filter is a device used as part of a gas exchange (oxygenator) system to filter Cardiopulmonary bypass nonbiologic particles and emboli 32 arterial line blood filter. (blood clots or pieces of foreign material flowing in the bloodstream which will obstruct circulation by blocking a vessel) out of the blood. It is used in the arterial return line. CA cardiopulmonary bypass cardiotomy suction line blood filter is a device used as part of a gas exchange (oxygenator) system to Cardiopulmonary bypass filter nonbiologic particles and 33 cardiotomy suction line emboli (a blood clot or a piece of blood foreign material flowing in the bloodstream which will obstruct circulation by blocking a vessel) out of the blood. This device is intended for use in the cardiotomy suction line. B A cardiopulmonary bypass pulsatile flow generator is an electrically and pneumatically Cardiopulmonary bypass operated device used to create 34 pulsatile flow generator. pulsatile blood flow. The device is placed in a cardiopulmonary bypass circuit downstream from the oxygenator. D An intraluminal artery stripper is a device used to perform an 35 Intraluminal artery stripper. endarterectomy (removal of plaque deposits from arterisclerotic arteries.) B An external cardiac compressor is an externally applied prescription device that is electrically, pneumatically, or manually powered and is used to compress the chest periodically in the region of the heart to provide blood flow during cardiac arrest. External cardiac compressor External cardiac devices are used as an adjunct to 36 compressor. manual cardiopulmonary resuscitation (CPR) when effective manual CPR is not possible (e.g., during patient transport or extended CPR when fatigue may prohibit the delivery of effective/consistent compressions to the victim, or when insufficient EMS personnel are available to provide effective CPR). CAn external transcutaneous cardiac pacemaker (noninvasive) is a device used to supply a External transcutaneous periodic electrical pulse intended 37 cardiac pacemaker to pace the heart. The pulse from the device is usually applied to the surface of the chest through electrodes such as defibrillator paddles. CName of Category: Dental Total No. of Devices: 89DENTAL SL Classification India as .N Name of product Intended use per First schedule O Part 1 MDR 2017 1 Agar dental An impression material containing reversible agar hydrocolloid impression material as a component for gelation. B 2 Alginate dental An impression material containing alginate as the primary impression material component for gelation. B 3 Dental collar/crown Scissors use to cut delicate tissue to removing sutures to scissors performing precision procedures. A 4 Dental excavator, It is a device intended to cutting, clean out and shape a carious reusable cavity before filling it. A 5 Dental excavator, It is a single use device intended to cutting, clean out and single-use shape a carious cavity before filling it. A 6 Basic electric It uses electric power to move the brush head, normally in an toothbrush, line- oscillating pattern. powered A 7 Basic manual Intended to cleaning plaque from teeth and gum. toothbrush A 8 Composite dental A thermoplastic impression material used to take an impression impression material of the oral cavity. It is a mixture of natural resin, filler, and lubricant. B 9 Dappen dish, It is a small bowls used to mix and hold dental materials.These reusable dishes can be disposable or reusable A 10 Dappen dish, single-A small, shallow concave vessel used to knead and hold dental use materials. A 11 Dental examination Intended as a kits for dental examination. kit A12 Dental crown, A device made entirely of polymer-based material with or polymer without fibre reinforcement, and created for a specific patient, that functions as an artificial covering to replace the major part, B or the whole part, of the clinical crown of a tooth. 13 Dental crown/bridge A material used to manufacture crowns and bridges. resin, temporary B 14 Dental Intended to make a temporary crown or bridge prosthesis for crown/bridge, use until a permanent restoration is fabricated. temporary B 15 Dental material A dental instrument slab or tray used as a surface to mix dental mixing surface, materials. reusable A 16 Dental material It has pad or tray used to knead or mix dental material mixing surface, (impression material, cement, etc). single-use A 17 Dental spatula, A dental instrument used to mix dental materials. Some are reusable equipped with an injection function. A 18 Dental spatula, A spatula-shaped device used to knead or mix dental material single-use (impression material, cement, etc). A 19 Dental crown, A device made of a combination of metal and tooth-coloured metal/ceramic ceramic, that functions as an artificial covering to replace the major part, or the whole part, of the clinical crown of a tooth. B 20 Dental crown, A device made of metal, veneered with a polymer-based, tooth- metal/polymer coloured material, and created for a specific patient, that functions as an artificial covering to replace the major part, or B the whole part, of the clinical crown of a tooth. 21 Wax dental It is used to take an oral impression. Made of wax, some impression material materials are mixed with resin having a low melting point. A 22 Dental impression Devices and materials used to take the impression. material kit, reusable A23 Dental impression A collection of non-sterile devices designed to obtain a negative material kit, single- imprint of the teeth. The kit typically includes dental impression use materials and a dental impression tray(s); This is a single-use A device. 24 Dental impression An electric device used to mix impression materials immediately material mixer before use at the chair side. A 25 Dental impression This dental injection syringe is used to inject the impression material syringe material onto the impression tray. A 26 Dental impression A material intended to be used to create a custom impression tray material tray intended for filling with dental impression materials; it is not intended for the fabrication of a patient-worn dental appliance. The material is used in cases in which a preformed impression A tray is not suitable. 27 Dental impression A impression tray is a metal or plastic device intended to hold tray, reusable impression material, to make an impression of a patient's teeth to reproduce the structure of a patient's teeth. A 28 Dental polishing A rotary dental brush intended for cleaning and polishing by a brush dental hygienist or a dentist. A 29 Dental bone particle A device used to collect bone debris generated by drilling, etc. collector during oral surgery. B 30 Dental bone matrix A sterile bioabsorbable device made primarily of animal-derived implant, animal- bone or dentin matrix (e.g., bovine, porcine) implanted into the derived body to provide osteoconductive bone-tissue scaffolds to replace maxillofacial and/or mandibular bone lost through trauma or dental surgery. It is used to fill bone cavities and C defects and contains pores that promote the ingrowth of endogenous bone for skeletal reconstruction and/or augmentation. 31 Dental suction It evacuate solids, liquids, aerosols and gases from the oral system cavity and immediate surrounding area for the purpose of improving operating effectiveness and efficiency during oral treatment procedures and limiting the contamination of the B immediate environment.32 Dental suction A tubal dental device to be connected to a non-active aspiration system cannula, device (usually, a dentistry dedicated device). Used to eliminate reusable water and cutting debris that have accumulated in the oral cavity. This device is reusable after sterilization. A 33 Dental suction A tubal dental device to be connected to a non-active aspiration system cannula, device (usually, a dentistry dedicated device). Used to eliminate single-use water and cutting debris that have accumulated in the oral A cavity. 34 Carboxymethylcellul An adhesive compound composed of carboxymethylcellulose ose sodium denture sodium (usually 40 to 100%) used to stabilize a removable adhesive prosthesis in the mouth, particularly a denture, by adhering the prosthesis to the oral mucosa. The compound is typically C applied to the base of a denture before it is inserted in the mouth. 35 Carboxymethylcellul An adhesive compound intended to be used to stabilize a ose sodium/polymer removable prosthesis in the mouth, particularly a denture, by denture adhesive, adhering the prosthesis to the oral mucosa. The compound is C zinc-free typically applied to the base of a denture before it is inserted in the mouth. 36 Dental amalgam A dental restorative material used primarily to fill tooth cavities, prepared by mixing liquid mercury (Hg) with an alloy of fine particles, composed mainly of silver (Ag), tin (Sn) and copper C (Cu). 37 Dental amalgam A composite of metals in fine particles, consisting mainly of alloy silver (Ag), tin (Sn) and small amounts of copper (Cu), that is intended for mixing with mercury (Hg) to produce dental amalgam. Amalgam is a dental restorative material used to fill C tooth cavities. 38 Dental amalgam Elemental mercury (Hg) of high purity intended for use as a mercury component of dental amalgam in the restoration of a dental cavity or broken tooth. C 39 Dental suction A separator used in the oral cavity. Used for the separation of system fluid- fluids (saliva, blood) from gases to avoid liquids from entering separation unit the suction pump (i.e., dry suction). A40 Dental suction An electrically-powered dental suction pump used as the system pump suction source of a dental suction system, dental treatment unit, etc. B 41 Plaster dental This material is primarily made of calcium sulphate impression material hemihydrate, and used to take an oral impression. A 42 Polyether dental An elastic material primarily made of polyether, which forms a impression material rubber-like material suitable for taking impressions after reaction. B 43 Polysulfide dental An elastic material primarily made of polysulfide, which forms a impression material rubber-like material suitable for taking impressions after reaction. B 44 Silicone dental An elastic material primarily made of polysiloxane, which forms impression material a rubber-like material suitable for taking impression after reaction. B 45 Temporary A sterile implantable device intended for the temporary mandibular condyle reconstruction of the mandibular condyle of the prosthesis temporomandibular joint (TMJ) typically in a patient undergoing ablative surgery requiring the removal of the mandibular C condyle. 46 Temporomandibular A sterile interpositional implant or interarticular disc, intended to joint disc permanently interface between the natural mandibular condyle and natural glenoid fossa (mandibular fossa) in the C temporomandibular joint (TMJ). 47 Assistive electric It uses electric power to move the brush head, normally in an toothbrush oscillating pattern. A 48 Assistive manual Used to cleaning plaque. toothbrush, reusable A 49 Assistive manual Used to cleaning teeth and gum. toothbrush, single- use A 50 Bar dental precision It connect removable partial dentures to fixed bridgework under attachment a male/female locking mechanism. A51 Basic electric A rotary dental brush used for cleaning teeth and gum by a toothbrush, battery- person or a dental hygienist. powered A 52 Dental suction An electrically-powered device intended to control the regular system disinfection (typically daily) automated/semi-automated disinfection of a control unit dental suction system tubing line. B 53 Transgingival A sterile device intended to be surgically implanted through the implant oral mucosa and gingiva to provide support and a means of C retention for a dental prosthesis. 54 Zinc A non-sterile substance intended for professional use as a polycarboxylate dental cement (e.g., luting agent, liner, base) and/or direct dental cement dental restorative material whereby the majority of the setting reaction is based on the hardening reaction between zinc oxide (ZnO) and aqueous solutions of polycarboxylic acid (e.g., B polyacrylic acid). 55 Transmandibular A sterile transosteal (transosseous) device [transmandibular implant implant (TMI)] intended to be surgically implanted through mandibular bone to provide support and a means of retention for a dental prosthesis, especially in a patient with an extremely atrophied/deformed mandible. C 56 Pliable-polymer A sterile bioabsorbable material intended to be used to aid in dental regeneration the regeneration of tooth support, lost due to periodontal membrane, disease or trauma, by acting as a barrier to prevent the down- bioabsorbable, growth of soft tissue (connective tissue and epithelial cells) into C ligated the underlying bone during the healing period. 57 Pliable-polymer A sterile bioabsorbable material intended to be used to aid in dental regeneration the regeneration of tooth support, lost due to periodontal membrane, disease or trauma, by acting as a barrier to prevent the down- bioabsorbable, growth of soft tissue (connective tissue and epithelial cells) into C tacked the underlying bone during the healing period. 58 Dental surgical A collection of various dental instruments, dressings, procedure kit, pharmaceuticals and the necessary materials used to perform a medicated, reusable dental surgical procedure. C 59 Dental surgical A collection of various sterile dental instruments, dressings, procedure kit, pharmaceuticals and the necessary materials used to perform a medicated, single- dental surgical procedure. C use 60 Membrane fixation A sterile bioabsorbable tack intended to be used to fix a pliable- tack, bioabsorbable polymer dental regeneration membrane in situ to aid in the regeneration of tooth support that has been lost due to C periodontal disease or trauma.61 Periodontal root A bioabsorbable material intended to be used alone or in surface combination with bone graft materials for the regeneration of regeneration tooth support that has been lost due to periodontal disease or material trauma. It is applied during periodontal flap surgery to the scaled and preconditioned root surface and forms an insoluble C matrix that creates a suitable root surface for selective periodontal cell migration and cell attachment, which re- establishes the lost tooth support. 62 Periodontal tissue A sterile viscous material intended to be injected into the buccal reconstructive mucosa to treat deficiencies of the gingiva (e.g., interdental material papillae), through augmentation, during the treatment of C intermediate stage periodontal disease. 63 Bone matrix A sterile implantable device made primarily of human implant, human- demineralized bone matrix (DBM) intended to fill bony voids or derived gaps caused by trauma or surgery, including use in the C maxillofacial and/or mandibular bone. 64 Collagen dental A sterile, bioabsorbable, animal-derived collagen (e.g., porcine) regeneration intended to be used to aid in the regeneration of tooth support, membrane lost due to periodontal disease or trauma, and/or to regenerate bone or bone defects around dental implants and at sites intended for implant placement, by acting as a barrier to prevent the down-growth of soft tissue into the underlying bone during C the healing period. 65 Dental cotton roll It is intended as an absorbent, hard-packed cylinder (a roll) that is used as a saliva absorber from the oral cavity during dental procedures. It may also be used as a packing between the A lip/cheek and the gum to give better examination/operative exposure. 66 Dental impression The device is used mainly to facilitate the manufacturing of tray, single-use custom dental prostheses (e.g., dentures). This is a single-use device. A 67 Preformed dental A prefabricated prosthetic device designed to function as a crown, permanent permanent artificial covering to partially or fully replace the damaged crown of a tooth. It is available as a single prosthesis or multiple prostheses of various shapes and sizes, and may include one or more try-in prosthesis replicas and other devices intended to assist the restoration procedure. B68 Preformed dental This device is commonly used during prosthodontic treatment crown, temporary or other restorative work required as a result of traumatic injury. B 69 Zinc phosphate A non-sterile substance intended for professional use as a dental cement dental cement and/or direct dental restorative material whereby the majority of the setting reaction is based on the hardening reaction between an oxide powder [the principal constituent of which is zinc oxide (ZnO)] and an aqueous solution of phosphoric acid. B 70 Dental articulation A hand-held manual dental instrument designed for grasping paper forceps and holding articulation paper during its application to a patient's oral cavity. A 71 Dental dressing A hand-held manual dental instrument designed for grasping forceps, reusable and holding a dental dressing during its application to a patient's oral cavity. A 72 Dental dressing A sterile, hand-held manual dental instrument designed for forceps, single-use grasping and holding a dental dressing during its application to a patient's oral cavity. A 73 Rubber dam clamp A hand-held dental instrument used for the insertion and forceps removal of rubber dam clamps. A 74 Tooth extraction A hand-held manual dental surgical instrument shaped like forceps pincers and designed for the extraction of teeth. A 75 Dental amalgam A small container in which silver (Ag) alloy is intended to be capsule mixed with mercury (Hg) to form dental amalgam. A 76 Dental amalgam A device with a valve intended to measure and dispense into a mercury dispenser mixing capsule a predetermined amount of dental mercury in droplet form which is to be used to produce amalgam filling A material. 77 Dental anaesthesia A collection of sterile devices designed to inject dental injection kit anaesthetics into gingival tissue or the oral mucosa, while preventing or reducing the risk of accidental needle-stick injury, B during restorative or surgical dental procedures.78 Dental anaesthesia A plastic or glass container prefilled with a single dose of syringe cartridge anaesthetic medication intended to be inserted into a dental anaesthesia syringe and injected into oral tissues for a dental B procedure. 79 Dental anaesthesia A hand-held manual dental instrument intended to be used to syringe, inject an anaesthetic agent under pressure via the periodontal intraligamentary ligament or into bone through an attached sterile needle. This is A a reusable device. 80 Dental anaesthesia A hand-held manual dental instrument intended to be used for syringe, reusable injecting an anaesthetic agent, subcutaneously or intramuscularly, from a prefilled, single-use cartridge through an A attached sterile needle; a needle is not included. 81 Dental anaesthesia A sterile, hand-held, manual dental instrument intended to be syringe, single-use used for injecting an anaesthetic agent, subcutaneously or intramuscularly, from a prefilled, single-use cartridge through an A attached sterile needle (needle not included). 82 Dental anaesthesia A hand-held manual dental instrument intended to be used for syringe/needle injecting an anaesthetic agent, subcutaneously or intramuscularly, from a prefilled, single-use cartridge through an included sterile needle; the needle may be attached or A detached. 83 Dental anaesthesia An assembly of devices used for the administration of a system proportional mixture of oxygen (O2) and nitrous oxide (N2O) or C medical air during dental surgical treatment. 84 Bite registration rim A schematic model of the dental arch attached to a temporary or permanent base for recording jaw relationships. B 85 Bite registration rim A dental material (modelling wax) with or without reinforcing wax foils (metal, polymer) for registration of jaw relation (making bite rims). This is a single-use device. B86 Bite registration rim A dental material (modelling wax) delivered as prefabricated wax, plate plates of wax with or without reinforcing foils (metal, polymer) for registration of jaw relation (making bite rims). B 87 Calcium hydroxide use as a dental cement and/or direct dental restorative material dental cement whereby the majority of the setting reaction is based on the hardening reaction between calcium hydroxide and salicylic acid . C 88 Ceramic artificial Prefabricated teeth made of ceramic (porcelain) for mounting teeth on removable dentures or fixed partial dentures. B 89 Dental soft-tissue A sterile, bioabsorbable, animal-derived collagen (e.g., porcine) matrix implant, intended to be used to aid in the regeneration of oral soft tissue, animal-derived lost due to periodontal disease or trauma, through promotion of new blood vessels and/or by providing a temporary scaffold for tissue ingrowth; it is indicated for various oral soft tissue augmentation procedures (e.g., alveolar ridge reconstruction, localized gingival augmentation, covering of recession defects and extraction sockets). It is a pliable material which may be C fixed to soft tissues with sutures; it is applied to soft tissue during periodontal flap surgery and guided tissue regeneration (GTR) surgical procedures. This is a single-use device.Name of Category: ENT Total No. of Devices: 78ENT S. No. Medical Device Name Intented Use INDIA 1 Adenotome Surgical instrument intended to dissect the adenoids. A 2 Adenotome blade Intended to mount on adenotome and perform dissection of adenoids. B Anchored bone-conduction Intended to treat hearing impairment due to middle and/or outer ear obstructive pathologies or types 3 C hearing implant system of conductive hearing loss. 4 Audiometer testing system An assembly of electronic reference devices intended to calibrate an audiometer. A 5 Audiometer Intended for evaluation of hearing by generating tones throughout the audible range B Intended for visual examination of the outer ear canal and tympanic membrane (eardrum) by direct 6 Otoscope B viewing through the ear opening. Auditory evoked-potential Intended to record an electrical potential that originates in the auditory pathway of the brain in 7 B graphic recorder response to acoustic stimuli. 8 Auditory stimulator Intended to apply sound stimuli to a patient's acoustic system. C Behind-the-ear air-conduction Intended to compensate for impaired hearing by transmitting amplified sound waves to the eardrum 9 B hearing aid through air. Behind-the-ear air-conduction 10 Intended to provide noise of sufficient intensity and bandwidth to mask tinnitus. B tinnitus masker Behind-the-ear bone- Intended to provide ultrasonic broadband noise and/or sweep-frequency stimuli noise of sufficient 11 C conduction tinnitus masker intensity and bandwidth to mask tinnitus. Cochlear implant assessment Intended to perform an integrity test on the implantable portion of a cochlear implant (CI) system in- 12 C system situ. Constructed to fit the curvature of the head so that it will sit closely under the ear lobe and enable 13 Ear bowl A treatments of ear. Intended to hold and confine the impression material in opposition to the surfaces to be recorded, 14 Ear canal impression tray A and to control the impression material while it sets to form the impression of the ear canal. 15 Ear canal light Intended to illuminate the ear canal. A Designed for cutting, scraping, scooping and removing tissue during a surgical procedure in or 16 Ear excavator A around the ear. 17 Ear prosthesis Intended to reconstruct the external ear by replacing damaged or missing tissue. C 18 Ear wick Intended to mimimize bleeding during ear surgery. B Intended for recording the changes in electrical potential or impedance, resulting from movement of 19 Electroglottograph B the vocal cords during respiration and phonation. Designed for scraping within the ear canal (e.g., removing wax), and for procedures during middle 20 Endaural curette A ear surgery (e.g., removal of the superior bony rim). Designed to support a patient in a seated position, electrically control postion in a way to facilitate 21 ENT chair, electric B ear, nose, throat examination, treatment, and/or minor surgery. Designed to support a patient in a seated position, mechanically control postion in a way to facilitate 22 ENT chair, mechanical B ear, nose, throat examination, treatment, and/or minor surgery. Intended to resect/debride soft and osseous (bone) tissue in the nasal cavity or ear region during 23 ENT shaver system ear/nose/throat (ENT) or plastic surgery procedures; including functional endoscopic sinus surgery B (FESS). Intended to magnify minute structures (e.g., nerves, vessels) in the performance of ear, nose, 24 ENT surgical microscope B and/or throat (ENT) surgery requiring high magnification and adjustable focusing. Intended to illuminate sinus tissue during an ear/nose/throat (ENT) procedure to render the tissue 25 ENT transilluminator A translucent for examination Electroacoustic instrument designed to evaluate the activity of the auditory pathway of the brain in 26 Evoked-potential audiometer B response to an acoustic signal [auditory brainstem response (ABR)] in patients. Flexible endoscope intended for the visual examination and treatment of the nasal passages, Flexible fibreoptic 27 including the sinus openings, the pharyngeal end of the auditory tube, the larynx, and the vocal B nasopharyngolaryngoscope cords. Flexible fibreoptic Flexible endoscope intended for the visual examination and treatment of nasopharynx (the upper 28 B nasopharyngoscope part of the throat behind the nose). 29 Flexible fibreoptic rhinoscope Flexible endoscope intended for the visual examination and treatment of nasalcavity. B Flexible endoscope intended for the visual examination and treatment of the paranasal sinuses 30 Flexible fibreoptic sinoscope B during an ear/nose/throat (ENT) intervention. Flexible endoscope intended for the visual examination and treatment of a cavity, particularly the 31 Flexible video antroscope B pathological changes in the area of the maxillary sinus. Intended to evaluate the functional condition of the middle ear by changing the air pressure in the 32 Impedance audiometer external auditory canal to measure and graph the mobility characteristics of the tympanic B membrane. Nasal septum straightening Surgical instrument specifically designed to straighten the nasal septum through grasping and 33 A forceps manipulation of the bone/cartilage of the septum during nasal reconstructive procedures. Page 1 of 3A hand-held manual surgical instrument intended to be inserted into the naris for the removal of 34 ENT Nasal snare tissue, typically polyps, tumours, and other abnormal tissue from the nasal cavity during B ear/nose/throat (ENT) surgery. Intended to be implanted for the functional reconstruction of segments of the ossicular chain 35 Ossicular prosthesis, partial C (mallues, incus, and/or stapes bones). Intended to be used in otology mainly for observation, diagnosis, and treatment of the outer and/or 36 Otoscope, endoscopic B middle ear. 37 Tonsil knife Intended for the removal of the tonsils during a surgical intervention. A 38 Tracheal bistoury Designed for opening abscesses or slitting up sinuses and/or fistulas in the trachea. A A middle ear mold is a preformed device that is intended to be implanted to reconstruct the middle 39 Middle ear mold C ear cavity during repair of the tympanic membrane. An implanted assembly of sterile devices intended to compensate for impaired hearing by Fully-implantable middle ear 40 transmitting vibrations to the middle ear. It is powered by a battery that is recharged inductively, via C implant system an external device. A device used for replacement and restoration of the laryngeal function, or for maintenance of 41 Larynx prosthesis C patency of the larynx. A sterile device intended to be implanted for the total functional reconstruction of the ossicular chain (mallues, incus, and stapes bones) to facilitate the conduction of sound waves from the tympanic 42 Ossicular prosthesis, total C membrane to the inner ea to treat conductive hearing loss from traumatic or surgical injury, otosclerosis, congenital fixation of the stapes, or chronic middle ear disease. Inteded for examination of the outer ear canal and tympanic membrane (eardrum) by direct viewing 43 Otoscope, direct B through the ear opening. Soft-tissue surgical forceps, A long, thin, hand-held manual surgical instrument designed to facilitate grasping and manipulation 44 B alligator of soft-tissues/anatomical structures [typically during ear/nose/throat (ENT) surgery]. Device intended to control internal nasal bleeding by exerting pressure against the sphenopalatine 45 Epistaxis balloon B artery. Eustachian tube balloon The system is intended for use in dilating the cartilaginous portion of the Eustachian tube for 46 B dilation system treating persistent Eustachian tube dysfunction. An ear, nose, and throat electric or pneumatic surgical drill is a rotating drilling device, including the Ear, nose, and throat electric 47 handpiece, that is intended to drive various accessories, such as an ear, nose, and throat bur , for C or pneumatic surgical drill the controlled incision or removal of bone in the ear, nose, and throat area. Argon laser for otology, Device is used for the purpose of coagulating and vaporizing soft and fibrous tissues, including 48 C rhinology, and laryngology osseous tissue while performing ENT surgical procedure. Ear, nose, and throat Device intended for the surgical excision of tissue from the ear, nose, and throat area while 49 microsurgical carbon dioxide performing microsurgical procedures to excise lesions and tumors of the vocal cords and adjacent C laser areas. Esophagoscope (flexible or Device intended to examine or treat esophageal malfunction symptoms, esophageal or mediastinal 50 B rigid) disease, or to remove foreign bodies from the esophagus. Mediastinoscope and Device intended to examine or treat tissue in the area separating the lungs for diagnosis of tumors 51 B accessories and lesions and to determine whether excision of certain organs or tissues is indicated. A laryngostroboscope is a device that is intended to allow observation of glottic action during 52 Laryngostroboscope B phonation. A bone particle collector is a filtering device intended to be inserted into a suction tube during the 53 Bone particle collector A early stages of otologic surgery to collect bone particles for future use. A suction antichoke device is a device intended to be used in an emergency situation to remove, by 54 Suction antichoke device the application of suction, foreign objects that obstruct a patient's airway to prevent asphyxiation to C the patient. A tongs antichoke device is a device that is intended to be used in an emergency situation to grasp 55 Tongs antichoke device C and remove foreign objects that obstruct a patient's airway to prevent asphyxiation of the patient. A powered nasal irrigator is an AC-powered device intended to wash the nasal cavity by means of a 56 Powered nasal irrigator B pressure-controlled pulsating stream of water. An external nasal splint is a rigid or partially rigid device intended for use externally for 57 External nasal splint A immobilization of parts of the nose. 58 Antistammering device An antistammering device intended to minimize a user's involuntary hesitative or repetitive speech. B An external upper esophageal sphincter compression device is intended to apply external pressure External upper esophageal 59 on the cricoid cartilage for the purpose of reducing the symptoms of laryngopharyngeal reflux C sphincter compression device disease. Wireless air-conduction A wireless air-conduction hearing aid is intended to compensate for impaired hearing that 60 B hearing aid incorporates wireless technology in its programming or use. Page 2 of 3A hearing aid calibrator and analysis system is an electronic reference device intended to calibrate Hearing aid calibrator and 61 and assess the electroacoustic frequency and sound intensity characteristics emanating from a B analysis system hearing aid, master hearing aid, group hearing aid or group auditory trainer. A tympanic membrane contact hearing aid is a prescription device that compensates for impaired Tympanic membrane contact 62 hearing by vibrating the tympanic membrane through a transducer that is in direct contact with the D hearing aid tympanic membrane. A master hearing aid is an electronic device intended to simulate a hearing aid during audiometric 63 Master hearing aid B testing. The active implantable bone conduction hearing system is intended to compensate for conductive Active implantable bone 64 or mixed hearing losses by conveying amplified acoustic signals to the cochlea via mechanical C conduction hearing system vibrations on the skull bone. Battery-powered artificial A battery-powered artificial larynx is an externally applied device intended for use in the absence of 65 B larynx the larynx to produce sound. A partial ossicular replacement prosthesis is a device intended to be implanted for the functional Partial ossicular replacement 66 reconstruction of segments of the ossicular chain and facilitates the conduction of sound wave from C prosthesis the tympanic membrane to the inner ear. A total ossicular replacement prosthesis is a device intended to be implanted for the total functional Total ossicular replacement 67 reconstruction of the ossicular chain and facilitates the conduction of sound waves from the C prosthesis tympanic membrance to the inner ear. Mandibular implant facial A mandibular implant facial prosthesis is a device that is intended to be implanted for use in the 68 C prosthesis functional reconstruction of mandibular deficits. A sacculotomy tack (Cody tack) is a device that consists of a pointed stainless steel tack intended 69 Sacculotomy tack (Cody tack) C to be implanted to relieve the symptoms of vertigo. A nasal dilator is a device intended to provide temporary relief from transient causes of breathing 70 Nasal dilator difficulties resulting from structural abnormalities and/or transient causes of nasal congestion B associated with reduced nasal airflow. A tympanostomy tube with a semipermeable membrane is a device intended to be implanted for Tympanostomy tube with 71 ventilation or drainage of the middle ear and for preventing fluids from entering the middle ear C semipermeable membrane cavity. Transcutaneous air A transcutaneous air conduction hearing aid system is a wearable sound-amplifying device intended 72 conduction hearing aid C to compensate for impaired hearing without occluding the ear canal. system An acoustic chamber for audiometric testing is a room that is intended for use in conducting Acoustic chamber for 73 diagnostic hearing evaluations and that eliminates sound reflections and provides isolation from A audiometric testing outside sounds. A gustometer is a battery-powered device that consists of two electrodes that are intended to 74 Gustometer C provide galvanic stimulus resulting in taste sensation. A forcep with a spoon-(dish) like configuration at the distal end, and is used to treat the ear, nose, 75 ENT cupped forceps A and throat (ENT), and remove tissue from the body. A surgical instrument used to move the tongue to facilitate examination of surrounding organs and 76 Tongue depressor A tissue. 77 Tracheal dilator Intended to dilate the tracheal structure and tracheal passageway. A 78 Tonsillectome A manually operated surgical device used to dissect the tonsils. A Page 3 of 3Name of Category: Gastroenterology Total No. of Devices: 163Category: Gastroenterology Classification India Sr No. Name of Product Intended Use as per First Schedule Part 1 MDR 2017 To be placed over a continent enteric stoma (surgically-created artificial opening between the intestines and the body surface through which bodily 1 Absorbent enteric stomal dressing waste is drained from the intestines) to protect it from harmful external B influences, which includes absorbent materials intended to protect the surrounding skin from enteric fluids. To be intended for the circumferential resection of tissue to treat simple anal 2 Anal fistula circular cutter B fistula A sterile implantable cord intended to be placed through an anal fistula tract 3 Anal fistula seton and tied outside the fistula, forming a loop around the anus, to allow drainage C through the fistula for tissue healing. An endoscope with a rigid inserted portion intended for the visual examination 4 Anoscope, reusable B and treatment of the anus and rectum. A sterile endoscope with a rigid inserted portion intended for the visual 5 Anoscope, single-use B examination and treatment of the anus and rectum. A flexible tube designed to administer barium, a contrast medium, into the 6 Barium enema catheter lower gastrointestinal tract by way of the rectum, for radiographic visualization B of the area. An implantable artificial substitute for the tube-like structure that carries bile 7 Bile duct prosthesis C from the gallbladder to the duodenum. A flexible tube intended to be introduced percutaneously, for temporary or 8 Biliary drainage catheter prolonged drainage of the biliary tract, for splinting of the bile duct during C healing, or for preventing stricture of the bile duct. A sterile, non-electrical flexible tube intended to be inserted into the biliary 9 Biliary manometric catheter tree to measure pressures within the ducts, especially to evaluate sphincter of B Oddi function. A sterile device designed to manually inflate and regulate the pressure of a balloon catheter (e.g., by injecting and aspirating fluid or air within the Catheter-balloon inflator, 10 balloon), and to deflate the balloon during a medical procedure.It is typically B reprocessed used during angiography, angioplasty, gastrointestinal (GI), or sinuplasty procedures. A device designed to manually inflate and regulate the pressure of a balloon 11 Catheter-balloon inflator, reusable catheter (e.g., by injecting and aspirating fluid or air within the balloon), and to B deflate the balloon during a medical procedure. A sterile device designed to manually inflate and regulate the pressure of a 12 Catheter-balloon inflator, single-use balloon catheter (e.g., by injecting and aspirating fluid or air within the B balloon), and to deflate the balloon during a medical procedure. A flexible tube inserted through a flexible endoscope, after its placement in the Cholangiopancreatography catheter, duodenum via the oral cavity, for the endoscopic cannulation of the 13 B reusable gastrointestinal ductal system (i.e., the pancreatic, hepatic, and/or common bile ducts) during endoscopic retrograde cholangiopancreatography (ERCP). A flexible tube inserted through a flexible endoscope, after its placement in the Cholangiopancreatography catheter, duodenum via the oral cavity, intended for the endoscopic cannulation of the 14 B single-use gastrointestinal ductal system (i.e., the pancreatic, hepatic, and/or common bile ducts) during endoscopic retrograde cholangiopancreatography (ERCP). A non-sterile plastic pouch designed to be attached around a faecal stoma for Closed-ended intestinal ostomy bag, 15 use as a receptacle for faeces following a colostomy [the stool (faeces) being A multiple-piece generally well formed]. A non-sterile plastic pouch designed to be attached with an adhesive to the Closed-ended intestinal ostomy bag, 16 skin around a faecal stoma and used as a receptacle for faeces following a A one-piece colostomy [the stool (faeces) being generally well formed]. A sterile distal attachment to a flexible endoscope intended to improve 17 Colonic endoscopy cuff B endoscopic control and bowel visualization during colonic endoscopy. A collection of sterile devices intended to be used during open colorectal surgery (bowel resection) to irrigate the colon above (proximal to) the site of a 18 Colonic lavage kit, surgical B lesion/blockage, prior to surgical anastomosis, when preoperative preparation of the colon has not been possible, normally due to obstruction. A non-sterile solution/suspension intended to be introduced into the sigmoid/descending colon as an enema for the treatment of inflammatory 19 Colonic mucosa barrier dressing bowel disease (e.g., ulcerative colitis). It is intended to create an adhesive C physical barrier on the colonic mucosa to protect the mucosa from potentially harmful substances in the distal colon lumenA non-sterile endoscopic sheath with two inflatable balloons designed to be 20 Colonoscope positioning sleeve mounted on a colonoscope to position and stabilize the endoscope within the B large intestine of a patient. A dedicated stiff wire that is inserted into a flexible colonoscope to allow the 21 Colonoscope stiffener physician to increase the stiffness of the colonoscope when extra rigidity is B required during a colonoscopy. A hand-held manual surgical instrument designed to assess colon and/or rectal 22 Colorectal sizer lumen diameter to aid the selection of an appropriate size intraluminal stapler B (i. e, the stapler head) for bowel anastomosis following transection. A hand-held manual surgical instrument designed to dilate the common bile 23 Common bile duct dilator B duct, i.e., the union of the cystic and hepatic ducts. A non-sterile stent-like device with a valve designed to be implanted in the 24 Duodenal bypass liner duodenum where it is intended to reduce duodenal nutrient absorption from C food to facilitate obese patient weight loss. A sterile stent-like implant designed to function as an impermeable barrier in the duodenum and part of the jejunum for partially-digested food from the 25 Duodenal-jejunal bypass liner C stomach (chyme) passing on its inside and bile/digestive enzymes passing on its outside, intended to treat type 2 diabetes mellitus and obesity. A sterile plastic tube designed to be placed onto the distal end of an endoscope (e.g., oesophagoscope) to facilitate the removal of coagulated blood/tissue 26 Endoscope tissue removal cap B during electrosurgical treatment (e.g., for the treatment of Barrett’s oesophagus). A non-sterile device intended to be fitted to an endoscope biopsy port to enable access for/exchange of endoscopic devices while maintaining 27 Endoscopic biopsy valve, non-sterile B insufflation and minimizing leakage of biomaterial during an endoscopic procedure. A sterile device intended to be fitted to an endoscope biopsy port to enable 28 Endoscopic biopsy valve, sterile access for/exchange of endoscopic devices while maintaining insufflation and B minimizing leakage of biomaterial during an endoscopic procedure. A rod-like component of an endoscopic cutting stapler intended to enable 29 Endoscopic cutting stapler connector B connection between the stapler handpiece and the endpiece/loading unit. A collection of sterile devices, which includes an implantable haemostatic Endoscopic electrosurgical ligation clip, intended to be used to obtain a full-thickness tissue biopsy and/or 30 B biopsy/resection kit, full-thickness therapeutic resection of gastric, duodenal, colonic, and/or rectal tissue during an endoscopic procedure. A collection of devices designed to be inserted through a compatible Endoscopic electrosurgical endoscope to obtain a mucosal tissue biopsy and/or therapeutic resection of 31 B biopsy/resection kit, partial-thickness upper gastrointestinal (GI) tract tissue, typically during endoscopic retrograde cholangiopancreatography (ERCP) procedures. A sterile, invasive, endoscopic device intended to deliver both: 1) a submucosal Endoscopic electrosurgical 32 lifting solution; and 2) an electrosurgical current in a monopolar configuration B electrode/submucosal lift needle (i.e., with a return electrode) to tissues for cutting/coagulation. A sterile invasive device intended to be used to dilate or expand a narrowing Endoscopic gastrointestinal stenosis 33 lesion (e.g., oesophageal stricture, stenosis) in the lumen of the gastrointestinal B dilator [GI] tract, under endoscopic visualization. A hand-held, battery-powered surgical instrument designed to be used during Endoscopic motorized cutting stapler, 34 endoscopic surgical procedures for the expeditious transection and resection of B reusable tissues and the creation of anastomoses. A sterile, hand-held, battery-powered surgical instrument designed to be used Endoscopic motorized cutting stapler, 35 during endoscopic surgical procedures for the expeditious transection and B single-use resection of tissues and the creation of anastomoses. A sterile, flexible tube intended to non-invasively deliver a submucosal lifting Endoscopic needleless submucosal solution into the submucosa of the gastrointestinal tract through a flexible 36 B lift catheter endoscope during an endoscopic procedure (e.g., gastroscopy, colonoscopy) to lift a lesion, typically for subsequent excision. A tubular device intended to be used in combination with a compatible flexible endoscope to aid in endoscopic insertions and to secure a pathway for multiple 37 Endoscopic overtube, reusable B endoscopic intubations during diagnostic and therapeutic endoscopic procedures (e.g., upper and/or lower gastrointestinal (GI) tract endoscopy). A sterile, flexible tube intended to be used with an endoscope (e.g., 38 Endoscopic spray catheter colonoscope) to administer fluids (e.g., dyes for mucosal coloration) in spray B form. A non-sterile device made with Hevea natural rubber latex (NRL) intended to 39 Enema tip, reusable be connected to an enema tube to facilitate delivery of an enema solution into A the rectum.A non-sterile, length of tubing that is used as a conduit between the enema bag 40 Enema tube A and the enema tip for the delivery of the enema solution into the rectum. A collection of non-sterile devices that includes tubing and other materials Enteral feeding kit, adult/paediatric, intended to administer nutrient liquids directly into the stomach, duodenum, or 41 C non-sterile jejunum of an adult or paediatric (excludes infants) patient by means of gravity or an enteral pump. A collection of sterile devices that includes tubing and other materials intended Enteral feeding kit, adult/paediatric, to administer nutrient liquids directly into the stomach, duodenum, or jejunum 42 C sterile of an adult or paediatric (excludes infants) patient by means of gravity or an enteral pump. A collection of non-sterile compounds and devices intended to be used to 43 Enteral feeding tube clearing kit prevent and/or remove, through biochemical action, an enteral formula clog in C an in situ enteral feeding tube to maintain luminal patency. A non-sterile, sheath-covered device intended to be used to mechanically clear Enteral feeding/decompression tube 44 a clog in an in situ nasogastric, nasoenteral, gastrostomy and/or jejunostomy A clearing stem tube, used for feeding and/or decompression, to maintain luminal patency. A non-sterile, thin, flexible tube intended for extracorporeal connection to an enteral feeding tube (e.g., nasogastric tube) to increase the length of tubing 45 Enteral tube extension, non-sterile A from the patient to an oral/enteral device (e.g., syringe) during enteral feeding/medication administration or aspiration. A sterile, thin, flexible tube intended for extracorporeal connection to an enteral feeding tube (e.g., nasogastric tube) to increase the length of tubing 46 Enteral tube extension, sterile A from the patient to an oral/enteral device (e.g., syringe) during enteral feeding/medication administration or aspiration. A non-sterile endoscope with a highly flexible sleeve and distal tip intended for Externally-propelled flexible video 47 the visual examination of the entire adult colon [lower gastrointestinal (GI) B colonoscope tract]. A sterile, bioabsorbable, animal-derived substance intended to be injected into 48 Fistula-repair biomatrix implant a fistula tract (e.g., anal or rectal fistula) to close it by adding volume and D promoting the ingrowth and neovascularization of host tissue. An endoscope with a flexible inserted portion intended for the visual 49 Flexible fibreoptic choledochoscope examination and treatment of the choledoc, better known as the common bile B duct (CBD). An endoscope with a flexible inserted portion intended for the visual 50 Flexible fibreoptic colonoscope examination and treatment of the entire colon [lower gastrointestinal (GI) B tract]. An endoscope with a flexible inserted portion intended for the visual 51 Flexible fibreoptic duodenoscope examination and treatment of the duodenum (the first part of the small B intestine). An endoscope with a flexible inserted portion intended for the visual 52 Flexible fibreoptic enteroscope examination and treatment of the small intestine (the duodenum, jejunum, and B ileum). An endoscope with a flexible inserted portion intended for the visual Flexible fibreoptic examination and treatment of the upper gastrointestinal (GI) tract 53 B gastroduodenoscope [oesophagus, stomach, and duodenum (the first part of the small intestine), including the pancreas and the bile duct]. An endoscope with a flexible inserted portion intended for the visual 54 Flexible fibreoptic gastroscope B examination and treatment of the oesophagus and the stomach. An endoscope with a flexible inserted portion intended the visual examination 55 Flexible fibreoptic oesophagoscope B and treatment of the oesophagus. An endoscope with a flexible inserted portion intended for the visual 56 Flexible fibreoptic pancreatoscope B examination and treatment in the pancreas. An endoscope with a flexible inserted portion intended for the visual 57 Flexible fibreoptic sigmoidoscope examination and treatment of the sigmoid colon (the distal S-shaped part of B the large intestine leading to the rectum). An endoscope with a flexible inserted portion intended for the visual 58 Flexible ultrasound colonoscope examination and treatment of the entire colon [lower gastrointestinal (GI) B tract]. An endoscope with a flexible inserted portion, combined with an ultrasound 59 Flexible ultrasound duodenoscope probe, intended for the visual examination and treatment of the duodenum B (the first part of the small intestine). An endoscope with a flexible inserted portion, combined with an ultrasound Flexible ultrasound probe, intended for the visual examination and treatment of the upper 60 B gastroduodenoscope gastrointestinal (GI) tract [oesophagus, stomach, and duodenum (the first part of the small intestine), including the pancreas and the bile duct]. An endoscope with a flexible inserted portion intended for the visual 61 Flexible video choledochoscope examination and treatment of the choledoc, better known as the common bile B duct (CBD).An endoscope with a flexible inserted portion intended for the visual Flexible video choledochoscope, 62 examination and treatment of the biliary tract and related ducts [e.g., common B single-use bile duct (CBD), cystic duct, pancreatic duct], and for the removal of gallstones. An endoscope with a flexible inserted portion intended for the visual 63 Flexible video colonoscope, reusable examination and treatment of the entire colon [lower gastrointestinal (GI) B tract]. A sterile endoscope with a flexible inserted portion intended for the visual Flexible video colonoscope, single- 64 examination and treatment of the entire colon [lower gastrointestinal (GI) B use tract]. An endoscope with a flexible inserted portion intended for the visual Flexible video duodenoscope, 65 examination and treatment of the duodenum (the first part of the small B reusable intestine). An endoscope with a flexible inserted portion intended for the visual Flexible video duodenoscope, single- 66 examination and treatment of the duodenum (the first part of the small B use intestine). An endoscope with a flexible inserted portion intended for the visual 67 Flexible video enteroscope examination and treatment of the small intestine (the duodenum, jejunum, and B ileum). An endoscope with a flexible inserted portion intended for the visual examination and treatment of the upper gastrointestinal (GI) tract 68 Flexible video gastroduodenoscope B [oesophagus, stomach, and duodenum (the first part of the small intestine), including the pancreas and the bile duct]. An endoscope with a flexible inserted portion intended for the visual 69 Flexible video gastroscope B examination and treatment of the oesophagus and the stomach. An endoscope with a flexible inserted portion intended for the visual examination and treatment of the oesophagus. It is inserted into the body Flexible video oesophagoscope, through the mouth. Anatomical images are obtained via a camera incorporated 70 B reusable at the distal end of the oesophagoscope and are shown on a monitor. This device is commonly used to examine abnormalities in the tissue structure and mucous lining of the oesophagus. This is a reusable device. Flexible video oesophagoscope, An endoscope with a flexible inserted portion intended for the visual 71 B single-use examination and treatment of the oesophagus. An endoscope with a flexible inserted portion intended for the visual 72 Flexible video pancreatoscope B examination and treatment in the pancreas. An endoscope with a flexible inserted portion intended for the visual 73 Flexible video sigmoidoscope examination and treatment of the sigmoid colon (the distal S-shaped part of B the large intestine leading to the rectum). A sterile implantable device intended to be wrapped around the proximal portion of the stomach to reduce stomach volume and facilitate weight loss in 74 Gastric sleeve C overweight/obese patients by attempting to restrict the quantity of food consumed through an increased sense of satiety (fullness). A sterile flexible tube intended for orogastric, nasogastric, or rectal insertion to sample carbon dioxide (CO2) from the mucosal vasculature of the stomach or 75 Gastric tonometry catheter B sigmoid colon for the measurement of partial pressure (i.e., tonometry) of CO2 (pCO2) during diagnosis of mensenteric ischemia. An implantable device intended to be used to join and transect excess tissue of Gastrointestinal anastomosis coupler, 76 gastrointestinal structures through the coupling of two ring-shaped D bioabsorbable components that are inserted into the ends of the segments to be attached. An implantable device intended to be used to join and transect excess tissue of Gastrointestinal anastomosis coupler, 77 gastrointestinal structures through the coupling of two ring-shaped C non-bioabsorbable components that are inserted into the ends of the segments to be attached. A multicomponent assembly of mains electricity (AC-powered) devices designed for real-time visualization/navigation of a catheter and/or endoscope Gastrointestinal catheter/endoscope 78 during insertion in the gastrointestinal tract, by detecting its B tracking system position/movement within an electromagnetic (EM) field and displaying three- dimensional (3-D) virtual images on a monitoring screen. A device intended to be used in combination with a compatible flexible endoscope for the application of a gastrointestinal endoscopic clip(s) [not Gastrointestinal endoscopic clip included] to the mucosal lining of the gastrointestinal (GI) tract for endoscopic 79 B applier marking, haemostasis, tissue approximation, closure of luminal perforations, and/or for treating mucosal/submucosal defects during an endoscopic procedure. Gastrointestinal endoscopic clip A sterile device intended to be used in combination with a generator to remove 80 B cutter a gastrointestinal endoscopic clip. A portable, mains electricity (AC-powered) device intended to be used in Gastrointestinal endoscopic clip 81 conjunction with a cutter for the endoscopic removal of a gastrointestinal B cutter generator endoscopic clip.A sterile clip intended to be implanted long-term (>30 days) within the Gastrointestinal endoscopic clip, long-gastrointestinal (GI) tract during an endoscopic procedure for endoscopic 82 C term marking, haemostasis, tissue approximation, closure of luminal perforations, and/or for treating mucosal/submucosal defects. A sterile clip intended to be placed short-term (<=30 days) within the Gastrointestinal endoscopic clip, gastrointestinal (GI) tract during an endoscopic procedure for endoscopic 83 C short-term marking, haemostasis, tissue approximation, closure of luminal perforations, and/or for treating mucosal/submucosal defects. A non-sterile flexible tube with electronic sensors at the distal end intended to be inserted through the nose or rectum into the gastrointestinal (GI) tract to Gastrointestinal manometric evaluate peristaltic motility anywhere in the GI tract (pharynx, oesophagus, 84 B catheter, electronic stomach, duodenum, small bowel, colon, and anorectal area) by measuring pressure; it may additionally be intended to measure pH and electrical impedance and contain a lumen. A non-sterile, non-electrical flexible tube intended to be inserted through the nose or rectum into the gastrointestinal (GI) tract for measuring pressure to Gastrointestinal manometric 85 assess peristaltic motility in the GI tract (e.g., oesophagus, stomach) or rectal B catheter, non-electronic musculature and anal sphincter functions, typically in the evaluation of GI disorders [e.g., gastro-oesophageal reflux disease (GERD), faecal incontinence]. A non-sterile, noninvasive pouch designed to be wrapped around the protruding end of a gastrointestinal ostomy tube (e.g., gastrostomy or 86 Gastrointestinal ostomy tube pocket A jejunostomy tube) to hold and support it in order to ensure its stabilization on the patient. A flexible device intended to access the gastrointestinal (GI) tract, and/or the airway tree, via the working channel of an appropriate endoscope to Gastrointestinal/airway foreign body 87 atraumatically remove foreign bodies during an endoscopic procedure; it may B retrieval basket in addition be intended for removal of severed polyps and tissue samples (biopsy). A sterile, thin, flexible, hollow cylinder percutaneously inserted into the stomach, typically through puncture of the abdominal wall and stomach after distention of the stomach by endoscopic methods, with an extended portion inserted through the pylorus into the jejunum. It is used to feed a patient who 88 Gastrojejunostomy tube has a physical disability that prevents oral feeding (e.g., a birth defect of the C mouth, oesophagus, or stomach, or a neuromuscular condition that affects chewing and swallowing), and to provide drainage/decompression for the stomach when it is necessary to bypass a longstanding obstruction of the stomach outlet into the small intestine. An implantable device introduced into the gastro-oesophageal sphincter to Gastro-oesophageal antireflux 89 reduce a sliding hiatal hernia, preventing the reflux of gastric contents into the C prosthesis oesophagus. A non-sterile flexible tube with electronic sensors at its distal end intended to Gastro-oesophageal pH/impedance be inserted through the nose into the oesophagus and stomach to measure pH 90 B catheter, non-sterile and/or electrical impedance, typically for the evaluation of gastro-oesophageal reflux disease (GERD), gastric ulcers, or other gastrointestinal conditions. A sterile flexible tube with an with an electrical conductor at its distal end intended to be inserted through the nose into the oesophagus and stomach to Gastro-oesophageal pH/impedance 91 measure pH and/or electrical impedance, typically for the evaluation of gastro- B catheter, sterile oesophageal reflux disease (GERD), gastric ulcers, or other gastrointestinal conditions. A collection of non-sterile devices designed as the external portion of a gastrostomy aspiration system intended to be used post-surgery by the patient Gastrostomy aspiration system 92 after implantation of the stomach tube for the removal of a portion of stomach C gravity set contents after meals, by aspiration, to achieve portion control and subsequently weight loss in a morbidly obese (bariatric) patient (≥ 18 years). A sterile, thin, flexible, hollow cylinder intended to be percutaneously implanted by endoscopic methods into the stomach of a morbidly obese Gastrostomy aspiration system 93 (bariatric) patient (≥ 18 years) for the removal of a portion of stomach contents C stomach tube after meals by aspiration when used with a dedicated gravity kit that is the external portion of a gastrostomy aspiration system. A sterile, short, tube that is inserted into the stomach percutaneously to permit 94 Gastrostomy button C long-term enteral feeding. A device intended to be inserted into the stomach percutaneously to appose the anterior gastric wall to the anterior abdominal wall, typically to facilitate 95 Gastrostomy T fastener C the insertion of a percutaneous gastrostomy tube or for procedures requiring stabilization/fixation of hollow gastrointestinal (GI) structures.A sterile, thin, flexible, hollow cylinder percutaneously inserted into the stomach, typically through puncture of the abdominal wall and stomach after distention of the stomach by endoscopic methods. It is used to feed a patient who has a physical disability that prevents oral feeding (e.g., a birth defect of 96 Gastrostomy tube C the mouth, oesophagus, or stomach, or a neuromuscular condition that affects chewing and swallowing), and/or to provide drainage/decompression for the stomach when it is necessary to bypass a longstanding obstruction of the stomach outlet into the small intestine A sterile connecting device shaped in the form of a "Y" intended for connection 97 Gastrostomy tube Y-piece connector to the proximal end of a gastrostomy tube to enable administration of nutrient B liquids and/or medication through the gastrostomy tube. A slender, rod-like surgical instrument made of metal, typically with groove running along the centre of it distal shaft and/or continuing with an elongated 98 Gastro-urological director malleable wire loop, that is used to guide other devices or instruments into a B selected intracorporeal location during a gastroenterological/urological (GU) procedure. A slender, rod-like, hand-held manual surgical instrument, typically made of 99 Gastro-urological probe flexible metal with a blunt bulbous tip, designed for exploring B gastroenterological/urological (GU) structures during a GU procedure. A heavy, hand-held, manual surgical instrument with a spoon-like, sharp-edged distal end on a long thin shaft that is used to access and scrape tissue from the 100 Gastro-urological scoop B common hepatic/bile duct system during a gastroenterological/urological (GU) procedure. A collection of devices intended to be used to deliver an injection of fluid (e.g., 101 Gravity enema set A saline solution) into the rectum to facilitate evacuation of the large intestine. A sterile implantable device designed to isolate the lesser curvature segment of the stomach (magenstrasse) to reduce stomach volume and facilitate weight 102 Implantable gastric clamp C loss in overweight/obese patients through a reduction in food consumption based on an increased sense of satiety (fullness). An assembly of battery-powered devices intended to treat chronic disorders of Implantable incontinence-control the pelvis and lower urinary or intestinal tract, typically related to urinary 103 C electrical stimulation system and/or faecal incontinence, through the application of electrical stimuli to the muscles and/or neural tissue of the pelvic floor/bladder. A small, sterile, implantable device designed to secure a peritoneal or Implantable peritoneal catheter 104 lumboperitoneal catheter in situ by suturing it to the abdominal fascia at the C holder point of entry/exit. A non-sterile, noninvasive device intended to be applied to the inner surface of Intestinal ostomy bag anti-adhesion 105 an intestinal ostomy bag to prevent opposing inner walls of the bag from A device sticking together (anti-pancaking). A collection of non-sterile devices intended to be used for 106 Intestinal ostomy kit attachment/replacement of an intestinal ostomy bag (for collecting intestinal A output such as faeces following a colostomy or ileostomy procedure). A sterile rigid or flexible device intended to be implanted within the abdomen 107 Intestinal splint to stabilize a portion of the intestine, or to stabilize and protect an injured C portion of the intestine. A non-sterile plate, typically with a waist belt for attachment, intended to be placed over an enteric stoma (surgically-created artificial opening between the Intestinal stoma shield/support belt, intestines and the body surface through which bodily waste is drained) to 108 B reusable protect it from harmful external influences (e.g., knocks, friction), to reduce the risk of stomal herniation, or to help maintain adhesion of the base plate to the skin. A non-sterile plate, typically with a waist belt for attachment, intended to be placed over an enteric stoma (surgically-created artificial opening between the Intestinal stoma shield/support belt, intestines and the body surface through which bodily waste is drained) to 109 B single-use protect it from harmful external influences (e.g., knocks, friction), to reduce the risk of stomal herniation, or to help maintain adhesion of the base plate to the skin. A sterile, hand-held manual surgical instrument intended to be inserted through an orogastric (or nasogastric) tube to mechanically divert the 110 Intraluminal oesophageal retractor oesophagus away from the site of surgery during electrical treatments of the B heart (e.g., cardiac ablation), to facilitate surgical site access and to help prevent injury to the oesophagus. A sterile, flat stretch of silicone elastomer intended for use as a short-term intra-abdominal dressing following abdominal surgery, when a re-exploration 111 Invasive silicone sheet dressing of the wound/abdomen is planned within a thirty day period. It is used to B achieve temporary abdominal closure to avoid the complications of an open abdomen.A sterile, thin, flexible, hollow cylinder percutaneously inserted into the jejunum, typically through puncture of the abdominal wall and stomach after distention of the gut by endoscopic methods. It is used to feed a patient who has a physical disability that prevents oral feeding (e.g., a birth defect of the 112 Jejunostomy tube C mouth, oesophagus, or stomach, or a neuromuscular condition that affects chewing and swallowing), and/or to provide drainage/decompression for the stomach when it is necessary to bypass a longstanding obstruction of the stomach outlet into the small intestine. A sterile, flexible, single-lumen tube with a distal needle intended to puncture Laparoscopic cholangiography 113 the neck of the gallbladder (Hartmann’s pouch) during laparoscopic B catheter/needle cholangiography to allow injection of contrast media. A sterile, rigid surgical instrument designed to be introduced through a Laparoscopic grasping forceps, 114 laparoscope primarily for grasping and manipulating tissues during a B reprocessed laparoscopic surgical procedure. A rigid surgical instrument designed to be introduced through a laparoscope Laparoscopic grasping forceps, 115 primarily for grasping and manipulating tissues during a laparoscopic surgical B reusable procedure. A sterile, rigid surgical instrument designed to be introduced through a Laparoscopic grasping forceps, single- 116 laparoscope primarily for grasping and manipulating tissues during a B use laparoscopic surgical procedure. An instrument designed to grasp a pledget swab at the distal end to obtain 117 Laparoscopic swab forceps cytological specimens and/or to perform blunt dissection during gynaecologic B and/or other (e.g., cholecystectomy) laparoscopic procedures. A non-sterile device intended to be used to manually administer fluid (e.g., saline solution) into the rectum to facilitate evacuation of the large intestine 118 Manual enema device B through expansion of the lower intestinal tract and physical stimulation of peristalsis. A device intended to be used to manually administer fluid (e.g., saline solution) 119 Manual enema device, reusable into the rectum to facilitate evacuation of the large intestine through B expansion of the lower intestinal tract and physical stimulation of peristalsis. A portable assembly of manually-operated devices designed to be used by or on a patient to irrigate the rectum with water, typically to provoke the 120 Manual rectal irrigation system B defecation reflex for the evacuation of the bowels to treat/prevent constipation and reduce the risk of faecal incontinence. A mains electricity (AC-powered) motorized surgical instrument designed for 121 Motorized laparoscopic forceps grasping, mobilizing, and suturing tissues/vessels under direct or endoscopic B visualization during a surgical procedure. A sterile, thin, flexible, hollow cylinder designed to access the small intestines (duodenum or jejunum) through the nose and nasopharynx for examination 122 Nasoenteral tube C (e.g., of intestinal contents), treatment (e.g., decompression, short-term feeding), or other purposes. A sterile, thin, flexible, hollow, single- or double-lumen cylinder intended to access the stomach of a patient through the nose and nasopharynx primarily to 123 Nasogastric decompression tube reduce the pressure within the gastrointestinal tract, typically aided by B connection to an intermittent suction system, that may follow presurgical or postsurgical intestinal occlusion. A non-sterile, non-surgically invasive device intended to be used to secure a 124 Nasogastric tube holder, intranasal nasogastric tube to the nose of a patient to prevent displacement or removal of B the tube. A small, non-sterile, noninvasive device intended to be used to secure a Nasogastric tube holder, noninvasive, 125 nasogastric tube to prevent displacement or removal of the tube from the A non-sterile patient. Nasogastric tube holder, noninvasive, A small, sterile, noninvasive device intended to be used to secure a nasogastric 126 A sterile tube to prevent displacement or removal of the tube from the patient. A collection of sterile, invasive devices intended to enable percutaneous Non-vascular catheter introduction 127 Seldinger-type introduction of a non-vascular catheter (e.g., drainage catheter) C set into a body cavity or lumen (e.g., biliary tract, ureter). An electronic device used to monitor the temperature of the oesophagus during surgical ablation of the wall of the left atrium. It typically measures the 128 Oesophageal temperature monitor oesophageal temperature at several adjacent levels, and displays these B temperature values simultaneously to help the surgeon avoid the application of heat high enough to form atrial-oesophageal fistulas. A sterile, hollow cylinder that usually contains two balloons, one for the 129 Oesophageal tube stomach and one for the oesophagus, which are inflated after the device has C been inserted into the oesophagus to tampon bleeding oesophageal varices.A surgical instrument in the form of a slender, hollow cylinder made of metal, plastic or other suitable material, designed to dilate oesophageal 130 Over-guidewire oesophageal dilator strictures/passages after being passed over a pre-positioned guidewire, B typically in sequentially increasing sizes. It is commonly used prior to and to assist in a gastroscopy and is available in a variety of sizes and flexibilities. A sterile, thin, flexible, hollow cylinder designed as a paediatric or neonatal Paediatric-temperature 131 enteral feeding tube with an integrated temperature sensor that continuously C nasogastric/orogastric tube measures oesophageal temperature. Partially-implantable abdominal A sterile partially-implantable device intended to provide access to the 132 C port/catheter peritoneal cavity for infusion (e.g., insulin, chemotherapeutic agents). A collection of sterile devices intended to be used to obtain a tissue specimen Percutaneous biliary biopsy 133 from within the biliary duct system for histological analysis by a percutaneous B procedure kit approach, typically under fluoroscopic visualization. Pharyngeal electrical stimulation A sterile, flexible tubular device intended to deliver pharyngeal electrical 134 C catheter stimulation for the treatment of neurogenic dysphagia. A portable assembly of battery-powered devices intended to be used by, or on Powered rectal/colostomy irrigation a patient, for the controlled introduction of a non-medicated solution (typically 135 B system water) into the rectum to treat faecal incontinence or constipation (rectal irrigation), and/or for colostomy site irrigation. A non-sterile substance intended to be applied to the mucosa of the mouth and/or pharynx to facilitate saprophytic microflora colonization within the oral Probiotic oropharyngeal mucosa cavity/pharynx, typically following antibiotic therapy, bacterial infection, or 136 C dressing injury. It includes probiotic bacteria (e.g., Streptococcus salivarius, Streptococcus oralis) and compounds that create a barrier to facilitate growth of the probiotic bacteria. An endoscope with a rigid inserted portion intended for the visual examination 137 Proctoscope, reusable B and treatment of the rectum and anus. A sterile endoscope with a rigid inserted portion intended for the visual 138 Proctoscope, single-use B examination and treatment of the rectum and anus. A collection of non-sterile devices intended to be used as part of a rectal irrigation system for the introduction of a non-medicated solution (typically 139 Rectal irrigation kit B water) into the rectum for patients affected by faecal incontinence or constipation. A hand-held manual surgical instrument intended to be used to expand or 140 Rectal speculum B stretch the rectal orifice/canal after it is inserted and opened. An assembly of disposable and reusable devices designed to obtain a submucosal tissue specimen from the rectum using suction [rectal suction 141 Rectal suction biopsy system B biopsy (RSB)], typically for histopathological analysis [e.g., to help diagnose Hirschsprung's disease (HD)]. A collection of non-sterile, noninvasive devices intended to be used in 142 Rectal/colonic lavage support kit conjunction with a rectal and/or colonic irrigation system to support the A introduction of an irrigation solution into the rectum/colon. An endoscope with a rigid inserted portion intended for the visual examination 143 Rectoscope, reusable B and treatment of the rectum and anus. A sterile endoscope with a rigid inserted portion intended for the visual 144 Rectoscope, single-use B examination and treatment of the rectum and anus. A manual device intended to be used as a handle to hold a rectoscope or 145 Rectoscope/proctoscope handle A proctoscope during an examination procedure. A small cap intended to be fitted to the proximal end of the handle of a Rectosocope/proctoscope handle 146 rectoscope or proctoscope during an examination procedure to provide an A end-cap airtight seal so that air can be pumped through the scope to inflate the bowel. An endoscope with a rigid inserted portion intended for the visual examination 147 Rigid oesophagoscope B and treatment of the oesophagus. An endoscope with a rigid inserted portion intended for the visual examination 148 Rigid sigmoidoscope and treatment of the sigmoid colon (the distal S-shaped part of the large B intestine leading to the rectum). A sterile electrosurgical device intended to be connected directly to the arm of a robotic surgical system to deliver electrosurgical current in a bipolar Robotic electrosurgical instrument, 149 configuration (i.e., without a return electrode) from a generator directly to C bipolar, single-use tissues for cutting/coagulation/ablation during robotic endoscopic (e.g., laparoscopic, arthroscopic) surgery. A surgical device intended to be used in conjunction with a robotic surgical 150 Robotic surgical retractor B system to enable retraction of tissues during a robotic endoscopic procedure. Self-propelled flexible video A sterile endoscope with a highly-flexible, self-propelled, inserted portion 151 B colonoscope intended for the visual examination of the entire colon.A slender, sharply-pointed metal tube designed to introduce or remove gas from the peritoneal cavity as a therapeutic or surgical/radiological procedural Spring-loaded pneumoperitoneum 152 method. It is often inserted into the peritoneal cavity for the purpose of B needle, reusable insufflation [e.g., with carbon dioxide (CO2)] to establish pneumoperitoneum prior to abdominal endoscopy. A slender, sharply-pointed metal tube designed to introduce or remove gas from the peritoneal cavity as a therapeutic or surgical/radiological procedural Spring-loaded pneumoperitoneum 153 method. It is often inserted into the peritoneal cavity for the purpose of B needle, single-use insufflation [e.g., with carbon dioxide (CO2)] to establish pneumoperitoneum prior to abdominal endoscopy. A non-sterile magnetic device designed to be inserted into the rectum by the 154 Static magnetic anal plug user and retained there for a specified period of time (e.g., 1 to 2 hours per day B for 10 to 20 days) to help reduce anal haemorrhoids with magnetism. A sterile flexible tube that is inserted into a stoma (an artificial opening in the body, especially in the abdominal wall, made during a surgical procedure) to 155 Stoma drainage catheter B drain bodily waste from an internal stoma container; normally directly into the toilet. A sterile, non-bioabsorbable device intended to be implanted into the 156 Stoma support implant abdominal wall during a gastro-urological ostomy procedure to reduce the risk C of parastomal hernia by supporting the abdominal wall surrounding the stoma. An endoscope with a rigid inserted portion intended for surgical treatment of 157 TEM/TEO rectoscope, optical the lower part of the bowel during transanal endoscopic microsurgery (TEM) or B transanal endoscopic operations (TEO). An endoscope with a rigid inserted portion intended for surgical treatment of 158 TEM/TEO rectoscope, video the lower part of the bowel during transanal endoscopic microsurgery (TEM) or B transanal endoscopic operations (TEO). A non-sterile, multi-lumen, multi-purpose tube intended for oral introduction into the gastrointestinal (GI) tract for both: 1) enteral feeding/gastric 159 Thermal-regulation orogastric tube decompression; and 2) thermal regulation of the whole body via thermal C transfer across the oesophagus (to lower and alternatively elevate core body temperature). A sterile non-bioabsorbable tube intended to be endoscopically implanted 160 Transenteric drainage tube transmurally between the gastrointestinal (GI) tract and a pancreatic C pseudocyst or the biliary tract for drainage. An assembly of electronic devices designed for the internal visualization and 161 Video capsule endoscopy system examination of sections of the gastrointestinal (GI) tract using a non-digestible B video capsule after it has been swallowed by a patient. An individual software application program or group of programs, routines or Video capsule endoscopy system 162 algorithms that add specific computer assisted display, processing and analysis B application software capabilities to a video capsule endoscopy system. A non-sterile, battery-powered, electronic component device of a video Video capsule endoscopy system 163 capsule endoscopy system designed to be swallowed by a patient for the B capsule internal visualization and examination of the gastrointestinal (GI) tract.Name of Category: Urology Total No. of Devices: 90Current S.No. Device Name Intended Use CDSCO Classification A sterile non-bioabsorbable tubular device intended to be placed short-term (<= 30 days) in the urethra to facilitate urethral Bare-metal urethral 1 patency and an unimpeded flow of urine from the bladder; it is C stent, short-term typically used to relieve lower urinary tract symptoms (LUTS) due to benign prostatic hyperplasia (BPH). A flexible manual instrument designed to remove biliary and/or Biliary/urinary stone 2 urinary stones (gallbladder and/or renal calculi) from the body B retrieval basket, reusable during an endoscopic procedure. A manual gastroenterology-urology surgical instrument with 3 Bladder neck spreader specially designed moveable blades intended to be used to A separate and spread the bladder neck. This is a reusable device. A battery-powered, hand-held device intended to be used in the home or healthcare facility by a patient to help initiate urination Bladder-emptying 4 and facilitate complete bladder emptying through application of B vibratory stimulator small mechanical vibrations to the lower abdomen to promote urethral sphincter relaxation. A non-sterile flexible plastic pouch designed to connect to a Closed-ended wearable urinary catheter and to be strapped to the leg of a patient to 5 urine collection bag, non- A collect discharged urine; it is not designed with an opening for sterile urine drainage. A non-sterile flexible plastic pouch designed to connect to a Closed-ended wearable urinary catheter and to be strapped to the leg of a patient to 6 urine collection bag, A collect discharged urine; it is not designed with an opening for sterile urine drainage. A device used to examine the bladder, providing measurement data concerning pressure and volume. This data will be used for 7 Cystometer B diagnostic evaluation of the neuromuscular mechanisms of the bladder. A device that emits ultrasound energy generated by a cystometer Cystometer probe, 8 in order to study bladder function by measuring bladder capacity, B ultrasonic sensation, pressure, and residual urine. A sterile electrical conductor intended to be placed in contact 9 Cystoscopic electrode with the bladder to stimulate it and/or record its electrical activity B for diagnostic examination.A non-sterile urine drainage device designed for men with incontinence consisting of a front piece with a scrotal support and Diaphragm wearable 10 a leak-proof, flexible diaphragm through which the penis passes A urinal into a closed cone-shaped tube connected to a leg bag into which the urine is collected. A non-sterile padded sheet intended to cover and protect a Draping incontinence 11 device/piece of furniture (e.g., wheelchair, bed, sofa) occupied by A liner an incontinent person by catching and retaining urine. A non-sterile urine drainage device designed for men to contain a moderate leakage consisting of a front piece with an integrated 12 Drip wearable urinal A tubular sheath that fits fully over the penis and into which dribbling urine is collected. An assembly of devices that uses plasma-induced shock waves for Electrohydraulic 13 the intracorporeal fragmentation of stones (calculi) found in the B lithotripsy system kidney, ureter, and bladder. A sterile, slender, rod-like device intended to be used as part of Electrohydraulic/pneuma an intracorporeal lithotripsy system to transmit shock waves from 14 tic lithotripsy system electrohydraulic or pneumatic sources directly to a calculus in the B probe, urinary, single-use urinary tract (i.e., kidneys, ureters, and bladder), providing high- speed fragmentation of the calculus in situ. Electromechanical An assembly of devices that non-invasively disintegrates stones 15 lithotripsy system, (i.e., calculi) by sending focused shock waves from outside the C extracorporeal body produced by an electromechanical generator. An assembly of devices designed to create shock waves through Electromechanical electromechanical action for the intracorporeal fragmentation of 16 lithotripsy system, calculi (stones) in the urinary tract (i.e., kidney, ureter and B intracorporeal bladder); the resulting debris may be actively removed or passed out by natural means at a later date. A non-sterile, urine drainage device designed for women that Female wearable urinal, typically consists of a flexible tube attached to a collector that is 17 A reusable specially formed to securely fit around the female genitals to provide a route to channel urine, via a tube, into a collection bag. A flexible tube containing a fibreoptic bundle that emits light throughout its length, intended to be inserted into the ureter for Fibreoptic ureteral 18 illumination to enable the path of the ureter to be seen. It also B catheter, reusable includes a plug for connection to a fibreoptic light source and a port for irrigation at its proximal end.An extremely thin, wire-like, manual surgical instrument designed for traversing and exploring urethral strictures and/or dilating the 19 Filiform urethral bougie B urethra, introduced directly or through an appropriately-threaded urethral catheter. A flexible manual device intended to be inserted through the Flexible endoscopic stone- working channel of a compatible flexible endoscope to grasp and 20 retrieval forceps, B remove stones (e.g., calculi from the urinary tract) or foreign reusable bodies during an endoscopic procedure. An endoscope with a flexible inserted portion intended for the Flexible fibreoptic 21 visual examination/treatment of the bladder, the urethra B cystonephroscope (including the prostate region), and the kidneys. An endoscope with a flexible inserted portion intended for the Flexible fibreoptic 22 visual examination and treatment of the bladder and the urinary B cystoscope tract. An endoscope with a flexible inserted portion intended for the Flexible fibreoptic 23 visual examination and treatment of the bladder and the urethra, B cystourethroscope including the prostate region. An endoscope with a flexible inserted portion intended for the Flexible fibreoptic 24 visual examination and treatment of the kidney. It is inserted B nephroscope percutaneously into the renal pelvis during nephroscopy. An endoscope with a flexible inserted portion intended for the Flexible fibreoptic 25 visual examination and treatment of the ureter and the renal B ureterorenoscope pelvis. An endoscope with a flexible inserted portion intended for the Flexible fibreoptic 26 visual examination and treatment of the ureter (the upper urinary B ureteroscope tract that connects the kidney to the bladder). An endoscope with a flexible inserted portion intended for the Flexible fibreoptic 27 visual examination and treatment of the urethra (the muscular B urethroscope tube that leaves the urinary bladder for the excretion of urine).A sterile device assembly intended to function as a flexible Flexible ureteral endoscope for the visual examination and treatment of body 28 sheath/fibreoptic cavities/organs that can be accessed via the ureter for B telescope cystoscopic, nephroscopic, laparoscopic, and ureteroscopic procedures. An endoscope with a flexible inserted portion intended for the Flexible video 29 visual examination/treatment of the bladder, urethra (including B cystonephroscope prostate region), and kidneys. An endoscope with a flexible inserted portion intended for the Flexible video 30 visual examination and treatment of the bladder and the urinary B cystoscope, reusable tract by introduction through the urethra. An endoscope with a flexible inserted portion intended for the Flexible video 31 visual examination and treatment of the bladder and the urethra, B cystourethroscope including the prostate region. Flexible video An endoscope with a flexible inserted portion intended for the 32 B nephroscope visual examination and treatment of the kidney. Flexible video An endoscope with a flexible inserted portion intended for the 33 ureterorenoscope, visual examination and treatment of the ureter and the renal B reusable pelvis. An endoscope with a flexible inserted portion intended for the Flexible video 34 visual examination and treatment of the ureter (the upper urinary B ureteroscope, reusable tract that connects the kidney to the bladder). An endoscope with a flexible inserted portion intended for the Flexible video 35 visual examination and treatment of the urethra (the muscular B urethroscope tube that leaves the urinary bladder for the excretion of urine). General-purpose ureteral A flexible tube designed for introduction into the ureters through 36 B catheter a cystoscope or nephroscope. An assembly of devices, held by the operator, that uses Hand pneumatic pneumatically-created ballistic shock waves for the intracorporeal 37 lithotripsy system, B fragmentation of stones (calculi) in the urinary tract (i.e., kidneys, urinary ureters, and bladder) for their removal. A portable, hand-held container/set, typically made of plastic, 38 Hand-held urinal, female intended to be directly urinated into by a female (typically bed- A bound) patient for excretory purposes. A portable, hand-held container intended to be directly urinated Hand-held urinal, male, 39 into by a male (typically bed-bound) patient for excretory A reusable purposes. An assembly of mains electricity (AC-powered) devices intended to aid in the quantitative assessment of liver function by the in Hepatic function analysis 40 vivo measurement of the plasma concentration and clearance of B system a tracer substance [e.g., indocyanine green (ICG)] in the peripheral vasculature following intravenous injection.A collection of non-sterile devices and materials intended to be Home faecal specimen used by a layperson to collect and mail a faecal (stool) sample to 41 A collection kit a clinical laboratory for diagnostic testing or screening purposes (e.g., occult blood, cytology). An assembly of implantable devices intended to treat male Hydraulic male urinary urinary incontinence by applying pressure to partially/fully 42 incontinence treatment C occlude the bladder neck and/or urethra, typically after radical system prostatectomy or transurethral resection of the prostate. An implantable component of a hydraulic male urinary Hydraulic male urinary incontinence treatment system intended to provide access to the 43 incontinence treatment C system’s inflatable pad (e.g., cushion, balloon), for the intra- system port and/or postoperative introduction/removal of fluid (e.g., saline). An implantable length of tube that functions as a component of a hydraulic male urinary incontinence treatment system and Hydraulic male urinary intended to provide connection between the system’s inflatable 44 incontinence treatment C pad (e.g., cushion, balloon) and the system’s port, for the intra- system tubing and/or postoperative introduction/removal of fluid (e.g., saline); it is typically made of silicone and metal. An implantable component of a hydraulic male urinary Hydraulic male urinary incontinence treatment system intended to seal the system’s 45 incontinence treatment tubing to prevent spillage/leakage of its contents when C system tubing plug introduction/removal of fluid to/from the system’s pad (e.g., cushion, balloon) is not needed; it is typically made of metal. A device used by a person with a disability to secure a body-worn Incontinence device 46 incontinence device [e.g., a nappy (diaper) or a pad] in a stable A suspender and safe position. A disposable pad composed of absorbent materials that is worn 47 Incontinence pants liner inside incontinence pants to catch and retain urine from an A incontinent person. This is a single-use device. Incontinence pants, An underwear designed to retain urine leakage in incontinent 48 A reusable adults and older children. A male urinary incontinence device designed to gently compress Incontinence penis the penis, either the proximal shaft or the glans penis, to occlude 49 A clamp, reusable the urethra and prevent involuntary urination/dribbling for men who are incontinent of the bladder. A electrically-powered electronic device intended to provide an audible, visible and/or tactile signal to alert the patient or a Incontinence 50 caregiver when a small quantity of urine and/or faeces B sensor/alarm incontinently released is detected by a sensing mechanism (e.g., a sensor pad or detector).An inflatable/deflatable sterile device designed of several interconnected components intended to be surgically implanted Inflatable penile 51 in a patient with erectile dysfunction (ED) [commonly known as C prosthesis impotence] in order to achieve selective penile tumescence and rigidity adequate for vaginal intercourse Intermittent urethral A collection of non-sterile devices that includes a urological 52 catheterization kit, non- catheter (with or without a urine drainage bag), a cap, and other B sterile related accessories intended for self-urinary catheterization. A collection of sterile devices that includes a urological catheter Intermittent urethral 53 (with or without a urine drainage bag), a cap, and other related B catheterization kit, sterile accessories intended for self-urinary catheterization. A sterile, flexible or rigid, tube designed to be repeatedly inserted Intermittent urethral through the urethra, typically by the user (i.e., self-applied), to 54 drainage catheter, the urinary bladder to provide short-term, episodic urine drainage B antimicrobial (removed after each void), typically for an individual who is physiologically incapable of voiding. A non-sterile, flexible or rigid, tube designed to be repeatedly Intermittent urethral inserted through the urethra, typically by the user (i.e., self- 55 drainage catheter, non- applied), to the urinary bladder to provide short-term, episodic B sterile urine drainage (removed after each void), typically for an individual who is physiologically incapable of voiding. A sterile, flexible or rigid, tube designed to be repeatedly inserted through the urethra, typically by the user (i.e., self-applied), to Intermittent urethral 56 the urinary bladder to provide short-term, episodic urine drainage B drainage catheter, sterile (removed after each void), typically for an individual who is physiologically incapable of voiding. An assembly of devices designed for use with an intracorporeal Intracorporeal lithotripsy lithotripsy system to evacuate, by suction, the irrigation fluid- 57 B suction system containing fragments of urinary calculi from the kidneys, ureters, and bladder during lithotripsy. A sterile, non-powered device intended to be inserted into the female urethra to facilitate urine voiding in patients with 58 Intraurethral valve/pump B incomplete bladder emptying due to impaired detrusor contractility (IDC) of neurologic origin. A sterile device intended to be inserted through the working channel of a rigid nephroscope during laser lithotripsy to function Laser lithotripsy as a channel for insertion of the laser fibre of a laser beam guide 59 C fibre/suction guide (e.g., of a general/multiple surgical laser system), and for removal of debris (e.g., fluid, calculi fragments) when connected to a vacuum source.An assembly of devices consisting of a specialized ureteroscope, a 60 Laser lithotripsy system laser resistant catheter, and a dedicated laser designed for the C intracorporeal disintegration of ureteral stones (calculi). A hand-held manual surgical instrument designed for the 61 Lithotrite mechanical crushing of renal stones (calculi) in the urinary tract B and/or bladder A mains electricity (AC-powered) assembly of devices intended to be used to measure urine flow rate and to estimate iso- Male urinary outflow volumetric bladder pressure in men with the use of an inflatable 62 B analysis system penile cuff. It typically consists of a dedicated computer and application software, an automatic cuff inflation/deflation unit, a single-use penile cuff, and a load-measuring cell/stand. Male urinary outflow A non-sterile inflatable cuff that is a component of a male urinary 63 B analysis system cuff outflow analysis system. A non-sterile, synthetic polymer sleeve intended to cover/protect Manometric catheter 64 and prevent contamination of a manometric catheter (including B sheath barostat catheter). Microwave hyperthermia A thin rod intended to be used as part of a hyperthermia system system catheter, to treat disorders of the prostate [e.g., cancer, benign prostatic 65 C prostatic-ablation, hyperplasia (BPH), prostatitis] through the local application of reusable heat from microwaves. A mobile assembly of devices designed to provide spark-gap- Penile extracorporeal generated, low-intensity, extracorporeal shock wave therapy to 66 shock wave therapy B treat erectile dysfunction (ED) [impotence] to rehabilitate penile system erection and rigidity adequate for intercourse. A hand-held device designed to transmit spark-gap-generated (electrohydraulic), low-intensity, shock waves from a penile Penile extracorporeal extracorporeal shock wave therapy system generator to the skin 67 shock wave therapy B of the penile shaft and the penile crura to treat erectile system applicator dysfunction (ED) [impotence] to rehabilitate penile erection and rigidity adequate for intercourse. A non-sterile, externally-worn, urine drainage device intended to be worn over the penis of an incontinent male patient to channel 68 Penis wearable urinal urine, via a tube, into a collection bag. It consists of a urinary B incontinence penis attachment (e.g., sheath or adhesive port), tubing, and a wearable urine collection bag. A non-sterile urine drainage device designed for men with Penis/scrotum wearable incontinence and a retracted penis that includes a front piece (a 69 B urinal shaped cone) intended to contain both the penis and the scrotum to form a leak-proof seal around the male genitals.An assembly of battery-powered, remote-controlled devices Perineal orifice designed for intravaginal pelvic floor exercise to treat urinary incontinence-control 70 incontinence and other pelvic problems in women (e.g., pelvic C electrical stimulation pain and sexual dysfunction) through the application of electrical system, remote control stimuli to the muscles of the pelvic floor. An assembly of devices that non-invasively disintegrates stones Piezoelectric lithotripsy 71 (i.e., calculi) by sending focused shock waves from outside the C system body produced by a piezoelectric generator. An endoscope with a rigid inserted portion intended for the visual 72 Pyeloscope examination and treatment of the renal pelvis and major or minor B calyces. An endoscope with a rigid inserted portion intended for the visual 73 Rigid cystoscope B examination and treatment of the bladder and the urinary tract. An endoscope with a rigid inserted portion intended for the visual 74 Rigid cystourethroscope examination and treatment of the bladder and the urethra, B including the prostate region. An endoscope with a rigid inserted portion intended for the visual 75 Rigid nephroscope B examination and treatment of the kidney. An endoscope with a rigid or semi-rigid inserted portion intended for the visual examination and treatment of the ureter and the 76 Rigid ureterorenoscope B renal pelvis; some types may have a flexible tip at the distal end of the inserted portion. An endoscope with a rigid inserted portion intended for the visual 77 Rigid ureteroscope examination and treatment of the ureter, (the upper urinary tract B that connects the kidney to the bladder).An endoscope with a rigid inserted portion intended for the visual 78 Rigid urethroscope examination and treatment of the urethra (the muscular tube B that leaves the urinary bladder for the excretion of urine). A sterile endoscope with a rigid or semi-rigid inserted portion Rigid video intended for the visual examination and treatment of the ureter 79 B ureterorenoscope and the renal pelvis; some types may have a flexible tip at the distal end of the inserted portion. An assembly of devices that non-invasively disintegrates stones Spark-gap lithotripsy 80 (i.e., calculi) by sending focused shock waves from outside the B system body produced by a spark-gap generator. A hand-held manual surgical instrument designed with a sharp pyramidal or conical point at the distal end to percutaneously Suprapubic needle, puncture the lower abdominal wall to provide suprapubic access 81 B surgical, reusable for surgical repair, typically to position a sling used in the treatment of female stress urinary incontinence (SUI) associated with bladder prolapse. A sterile, flexible tube with an inflatable balloon on its distal tip for retention in the urinary bladder, after its insertion through the Temperature-monitoring urethra, where it functions as a long-term indwelling device for 82 indwelling urethral continuous urinary drainage and simultaneous monitoring of core B drainage catheter body temperature through its integral temperature sensor, typically during or after surgery or in the presence of obstruction or paralysis. A hand-held manual surgical instrument with a sharp pyramidal or conical point used to create a percutaneous puncture using the transobturator approach (i.e., the insertion points overlie the Transobturator needle, 83 obturator space in the genitofemoral crease lateral to the vagina), B reusable for the surgical positioning of a sling used in the treatment of stress urinary incontinence (SUI), which may be associated with a prolapse. A hand-held manual surgical instrument with a sharp pyramidal or conical point designed to create a puncture in the vaginal wall for Transvaginal needle, 84 the surgical positioning of a sling typically used in the treatment B surgical of stress urinary incontinence (SUI) associated with bladder prolapse. An assembly of devices designed to use ultrasonic (US) shock Ultrasonic lithotripsy 85 waves for the intracorporeal fragmentation of stones (calculi) B system found in the kidney, ureter, and bladder.A collection of devices intended to assist treatment of a blocked 86 Ureteral patency kit ureter and to help maintain ureteral patency through natural B orifice or percutaneous access. A hand-held manual instrument designed for cutting a small hole (e.g., 0.3 mm diameter) into the distal end of a closed Foley Urethral drainage 87 catheter (usually 14.0 French or larger) to form a "Council tip B catheter punch Foley catheter", allowing it to be placed over a guidewire or ureteral catheter. A small, sterile valve intended to be connected to a urethral Urethral/suprapubic 88 and/or suprapubic catheter to allow intermittent bladder A catheter valve-connector drainage/filling (as an alternative to continuous drainage). A non-sterile, device intended to be inserted into the vagina in order to relieve mixed or stress urinary incontinence in an adult Urinary-incontinence 89 female by providing urethral support when pressure is A vaginal insert, reusable transferred from the abdomen to the pelvic floor area (e.g. upon coughing, laughing, sneezing, exertion). An assembly of devices used for advanced diagnosis/study of the bladder. It is used to identify the cause of abnormal voiding, Urodynamic 90 including incontinence and is useful for the diagnosis of, e.g., B measurement system neurogenic bladder diseases, stress incontinence, urinary path obstruction or spastic sphincters.Name of Category: General Hospital Total No. of Devices: 72General Hospital Medical Devices S. No. Device Name Inteded Use India Liquid crystal forehead temperature strip A liquid crystal forehead temperature strip is a device applied to the forehead that is used to indicate the 1 B presence or absence of fever, or to monitor body temperature changes. Bed exit monitor,Fall prevention Intended to be placed under mattress and used to 2 indicate by an alarm or other signal when a patient A attempts to leave the bed. Electronic monitor for gravity flow infusion Inteded to electroncially monitor the amount of fluid being 3 C systems infused into a patient. Electrically powered spinal fluid pressure monitor Inteded to measure spinal fluid pressure by the use of a 4 transducer which converts spinal fluid pressure into an B electrical signal. Spinal fluid manometer 5 A spinal fluid manometer is a device used to measure B spinal fluid pressure using nnedle and graduated column. Stand-on patient scale Intended for medical purposes that is used to weigh a 6 A patient who is able to stand on the scale platform. Patient scale A patient scale is a device intended for medical purposes 7 that is used to measure the weight of a patient who cannot A stand on a scaleby placing scale under a bed or chair to weigh both the support and the patient. Sterilization process indicator (Biological) A biological sterilization process indicator is a device 8 intended for use by a health care provider to accompany B products being sterilized through a sterilization procedure and to monitor adequacy of sterilization on medical device. Sterilization process indicator (Physical/chemical) A physical/chemical sterilization process indicator is a device intended for use by a health care provider to 9 B accompany products being sterilized through a sterilization procedure and to monitor one or more parameters of the sterilization process on medical device. Clinical color change thermometer. A clinical color change thermometer is a disposable device 10 used to measure a patient's oral, rectal, or axillary (armpit) A body temperature. Clinical electronic thermometer. A clinical electronic thermometer is a device used to 11 B measure the body temperature of a patient. Clinical mercury thermometer. A clinical mercury thermometer is a device used to 12 measure oral, rectal, or axillary (armpit) body temperature B using the thermal expansion of mercury. Apgar timer. 13 The Apgar timer is a device intended to alert a health care A provider to take the Apgar score of a newborn infant. Hydraulic adjustable hospital bed. Intended for medical purposes that consists of a bed with a 14 hydraulic mechanism operated by an attendant to adjust A the height and surface contour of the bed. Manual adjustable hospital bed. A manual adjustable hospital bed is a device intended for medical purposes that consists of a bed with a manual 15 A mechanism operated by an attendant to adjust the height and surface contour of the bed. Infant radiant warmer. Intended to be placed over an infant to maintain the 16 C infant's body temperature by means of radiant heat. Pediatric medical crib. Intended for medical purposes for use with a pediatric 17 B patient. Medical bassinet. Intended for medical purposes in hospital for use (birth to 18 approximately 5 months of age) in a nursery, labor and B delivery unit, or patient room. Nonpowered flotation therapy mattress. A nonpowered flotation therapy mattress is a mattress intended for medical purposes which contains air, fluid, or 19 A other materials, to treat or prevent decubitus ulcers (bed sores).Therapeutic medical binder. Intended for medical purposes and that can be secured by ties so that it supports the underlying part of the body or 20 A holds a dressing in place like abdominal, breast and perineal binder. Burn sheet. Inteded to wrap aroung a burn victim to retain body heat, 21 to absorb wound exudate, and to serve as a barrier against A contaminants Neonatal eye pad. A neonatal eye pad is an opaque device used to cover and 22 protect the eye of an infant during therapeutic procedures, A such as phototherapy. Neonatal incubator. A neonatal incubator is a device in which an infant may be 23 kept in a controlled environment (humidity, temperature, C oxygen etc) for medical care. Neonatal transport incubator. Transport incubator is a device in which an infant may be 24 kept in a controlled environment (humidity, temperature, C oxygen etc) while being transported for medical care. Pressure infusor for an I.V. bag. Device inteded to inflate and increases the pressure on the 25 B I.V. bag to assist the infusion of the fluid Intravascular administration set, automated air Inteded to detect and automatically remove air from an 26 removal system. intravascular administration set with minimal to no B interruption in the flow of the intravascular fluid. Patient care reverse isolation chamber. Device inteded protects a patient who is undergoing treatment for burns or is lacking a normal 27 B immunosuppressive defense due to therapy or congenital abnormality. Jet lavage. A jet lavage is a device used to clean a wound by a pulsatile 28 C jet of sterile fluid. Patient lift, Electrcially powered Inteded to lift and transport patients in hsoptial in the 29 horizontal or other required position from one place to B another, as from a bed to a bath. Nipple shield. A nipple shield is a device consisting of a cover used to 30 A protect the nipple of a nursing woman. Lamb feeding nipple. A lamb feeding nipple is a device intended for use as a 31 A feeding nipple for infants with oral or facial abnormalities Neonatal phototherapy unit. A neonatal phototherapy unit is a device used to treat or 32 B prevent hyperbilirubinemia (elevated serum bilirubin level). Infusion pump. An infusion pump is a device used in a health care facility 33 C to pump fluids into a patient in a controlled manner. 34 Suction snakebite kit. Intended for removing venom from the wound. A 35 Chemical cold pack snakebite kit. Intended for first-aid treatment of snakebites C Therapeutic scrotal support. Intended for medical purposes to support the scrotum (the 36 A sac that contains the testicles) Umbilical occlusion device. An umbilical occlusion device is a clip, tie, tape, or other 37 article used to close the blood vessels in the umbilical cord A of a newborn infant. Cardiopulmonary resuscitation board. Intended to be placed under a patient to act as a support 38 A during cardiopulmonary resuscitation. Ultrasonic cleaner for medical instruments. Intended for cleaning medical instruments by the emission 39 B of high frequency soundwaves Sharps needle destruction device. Intended to destroy needles or sharps used for medical 40 B purposes by incineration or mechanical means. Medical insole. Intended for medical purposes that is placed inside a shoe 41 to relieve the symptoms of athlete's foot infection by A absorbing moisture. Ingestible event marker. An ingestible event marker is a prescription device used to record time-stamped, patient-logged events. The ingestible 42 component links wirelessly through intrabody C communication to an external recorder which records the date and time of ingestion as well as the unique serialRemote Medication Management System. The system is intended to store the patient's prescribed medications in a delivery unit, to permit a health care professional to remotely schedule the patient's prescribed 43 medications, to notify the patient when the prescribed B medications are due to be taken, to release the prescribed medications to a tray of the delivery unit accessible to the patient on the patient's command, and to record a history of the event for the health care professional. Surgical Light, Single or Multi dome Intended for medical purposes that is used to illuminate 44 B body surfaces and cavities during Surgery. Medical examination light, AC powered or Battery 45 Intended for medical purposes that is used to illuminate B body surfaces and cavities during a medical examination. Skin pressure protectors. A skin pressure protector is a device intended to reduce pressure on the skin over a bony prominence to reduce the 46 A likelihood of the patient's developing decubitus ulcers (bedsores) Medical ultraviolet air purifier. A medical ultraviolet air purifier is a device intended for 47 medical purposes in hospital/clinic to destroy bacteria in B the air by exposure to ultraviolet radiation. Ultraviolet (UV) radiation chamber disinfection An ultraviolet (UV) radiation chamber disinfection device is device. intended for the low-level surface disinfection of non- 48 C porous medical device surfaces by dose-controlled UV irradiation. Body waste receptacle. A body waste receptacle is a device intended for medical 49 purposes that is not attached to the body and that is used A to collect the body wastes of a bed patient. Vacuum-powered body fluid suction apparatus. A vacuum-powered body fluid suction apparatus is a 50 B device used to aspirate, remove, or sample body fluids. Washers for body waste receptacles. A washer for body waste receptacles is a device intended 51 for medical purposes that is used to clean and sanitize a B body waste receptacle, such as a bedpan. It is intended to allow sterilization of the enclosed medical Sterilization wrap. 52 device and also to maintain sterility of the enclosed device B until used Ethylene oxide gas sterilizer. Intended for use by a health care provider that uses 53 C ethylene oxide (ETO) to sterilize medical devices. Dry-heat sterilizer. A dry-heat sterilizer is a device that is intended for use by 54 a health care provider to sterilize medical devices by means C of dry heat. Steam sterilizer. A steam sterilizer (autoclave) is a device that is intended 55 for use by a health care provider to sterilize medical C devices by means of pressurized steam. Liquid chemical sterilants/high level disinfectants. A liquid chemical sterilant/high level disinfectant is a germicide that is intended for use as the terminal step in 56 C processing critical and semicritical medical devices prior to patient use. General purpose disinfectants. A general purpose disinfectant is a germicide intended to 57 process noncritical medical devices and equipment B surfaces. Hand-carried stretcher. A hand-carried stretcher is a device intended to carry 58 A patient as an assistance for injury or disability. Wheeled stretcher. A wheeled stretcher is a device intended to transport 59 patients in a horizontal position as an assistance to injury C or disability. Liquid crystal vein locator. Inteded to indicate the location of a vein by revealing 60 A variations in the surface temperature of the skin. Medical washer. Intended for general medical purposes to clean and dry 61 medical devices, which later undergo sterilization or B disinfection before use on patient.Medical washer-disinfector. A medical washer-disinfector is a device that is intended 62 for general medical purposes to clean, decontaminate, C disinfect, and dry surgical instruments, anesthesia equipment, hollowware, and other medical devices. Hydrogen Peroxide Gas Plasma Sterilization Intended for sterilization/disinfection of both metal and 63 C System nonmetal/polymer based medical devices. Blood grouping slides Blood grouping slides are glass surfaces intended to 64 A perform the test for finding the blood group. Blood bank pipettes Blood bank pipettes are disposable blood handling 65 equipment intended to transfer blood fron one surface to A other. Blood mixing and blood weighing devices A blood mixing device is a device intended for medical purposes that is used to mix blood or blood components by 66 A agitation. Also intended to weigh blood or blood components as they are collected. Blood Vacutainer Intended for the drawing of a predetermined volume of 67 blood using vaccum to a container containing B Ethylenediaminetetraacetic acid. Blood bank centrifuge Intended to separate blood components of a suspension by 68 A application of centrifugal force. Environmental chamber for storage of platelet A refrigerated environmental chamber for storage of 69 concentrate platelet concentrate is a device used to hold platelet-rich C plasma within a preselected temperature range Blood storage refrigerator Thsese are devices intended for medical purposes that are 70 used to preserve blood and blood products by storing them C at cold or freezing temperatures. Heat-sealing device A heat-sealing device is a device intended for medical 71 purposes that uses heat to seal plastic bags containing A blood or blood components. Automated blood cell separator The automated blood cell separator device is intended for 72 routine collection of blood and blood components for C transfusion or further clinical use.Name of Category: Operation Theatre Total No. of Devices: 27Operation Theatre Medical Devices S. No. Name of Product Intended Use IMDR A surgical device used to separate connected surfaces, and to retain their positions to allow a surgical 1 Distractor/Retractors A operation to be performed. Suction system A device that generates negative pressure used for such treatment as the aspiration of liquid or granular 2 portable, A substances. Electrical/Pneumatic Suction system A device used for such treatment as the aspiration of liquid or granular substances by using negative 3 A operated by vacum pressure supplied by the hospital's medical gas supply system at bed side for using on patient. Operation table A complete surgical table system intended change the patient's position and enable attaching various 4 A system table accessories that aid in surgery. General-purpose 5 diagnosis/treatment A table for general diagnosis and procedures in examination room to aid in patient examination. A table An illuminator device intended to providing optimial light and colour renderingn to aid in performing 6 Surgical light system A surgery. Hemostatic clip 7 A surgical device designed to apply a hemostatic clip for ligation of a blood vessel. B applier 8 Hemostatic knife The blade intended to transmits heat directly to body tissues to achieve hemostasis. B 9 Scalpel An instrument used to sever and separate body tissues during surgery. B 10 Scalpel blade A blade intended to be attached to the handle of scalpel. B 11 Surgical forceps A surgical or dental device that is used to clamp and sever the cartilage, bone and other hard tissues. B General-purpose A unit used to resect/ablate the tissue or to coagulate the incision/wound site with high-frequency 12 C electrosurgical unit waves. Long-term use A hollow device to be placed surgically in the stomach, duodenum or jejunum to provide enteral 13 enterostomy feeding C nutrition. It is for long-term use. tube Gastrostomy tube for A hollow device to be placed surgically in the stomach, duodenum or jejunum for enteral nutrition, etc. 14 C long-term use It is for long-term use. Warming high-flow A device to be used for heating and rapidly infusing blood or other fluids during surgical procedures 15 C infusion pump involving major bleeding, or for burns or injuries. High-flow blood A device to be used for rapidly infusing blood or other fluids during surgical procedures involving major 16 C transfusion pump bleeding, or for burns or injuries. A metal or plastic surgical instrument used to remove staples from a surgical wound or incision that no 17 Staple remover B longer requires stapling to stay closed. 18 Surgical punch A surgical instrument used to create a hole for suturing or anastomosis of a tissue, blood vessel, etc. B A manually operated, hand-held surgical instrument with a series of bumps or teeth on its surface that is 19 Surgical file B used to smooth out, grind off, or sever tissues. Blood vessel surgical 20 A surgical instrument used for complete or partial vascular resection. B stripper 21 Surgical probe The device is used to explore sinuses, fistulae, and other cavities and wounds. B A unit that collects monitoring parameters (include an electrocardiogram (ECG), blood pressure, body Multiparameter temperature, cardiac output, and respiratory gases; in addition, other critical parameters (supporting 22 monitor with critical detection of arrhythmia or apnea; and in the case of anesthesia, determination of dose levels of a C parameters relaxant or local anaesthesia) using an embedded function kit, module, or other devices to display data, by bed or by patient. An operation support device used in open surgery or endoscopic surgery that performs treatment of 23 Surgical robot unit C tissues including suturing, detaching and severing, and installing a prosthesis. A device equipped with an electric mechanical or software controlled motor that retains, retrieves, and Motorized diagnostic 24 projects light for direct observation of medical images taken using a variety of methods such as X-ray, A imaging view box magnetic resonance (MR), CT, and ultrasound, and recorded in radiographic film. General-purpose A completely mobile surgical table (general-purpose) that has been improved to make it usable for 25 manually-operated A almost all parts of the body that require surgery. Manual or hydraulic operation. operation table Powered general- A completely mobile surgical table (general-purpose) that has been improved to make it useable for 26 purpose operation B almost all parts of the body that require surgery. Electrically line or battery operated. table A system that consists of several components that form a complete surgical table system. It is used to Operation table replace tabletops, change the patient's position, and transfer the patient to and from the operating 27 B system room. Usually, it consists of columns, a removable tabletop, remote controller for the trolley, and a trolley. 1 of 1Name of Category: Respiratory Total No. of Devices: 71RESPIRATORY Medical Device S.No. Intended use INDIA Name Activated-oxygen It is a device that makes activated oxygen (singlet oxygen) which is mixed 1 B generator with room air and produces activated water as a by-product. Aerosol inhalation It is a device that enables a medical professional to objectively assess in 2 B monitor detail how the test subject uses their inhaler. Airway device A hand-held device intended to be used to clean an in situ and ex situ 3 A cleaning utensil airway device. A hand-held instrument used for grasping a tube for its insertion and/or 4 Airway tube forceps extraction into/from the airways, or for grasping obstructive objects for A their removal from the airways. An instrument intended to measure the concentration (partial pressure) of 5 Argon gas analyser argon (Ar) in a gas mixture sample to aid in determining a patient's B ventilatory status. A device intended to intermittently or continuously measure the internal Artificial airway tube 6 pressure in the cuff of an endotracheal (ET)/endobronchial/tracheostomy B cuff pressure monitor tube when this has been situated into the tracheal passage. Artificial airway A container intended to hold artificial airway devices to facilitate their 7 washing/disinfection C washing/disinfection. jar 8 Breathing circuit bag A device intended to store breathing gas during the respiratory cycle. A A device intended for the cleaning and high-level disinfection of breathing Breathing circuit 9 circuit components used in respiratory therapy and anaesthesia C washer/disinfector equipment. An endoscope with an inserted portion intended for the visual examination 10 Bronchoscope and treatment of the trachea, primary bronchi, and upper regions of the B lungs and take biopsies and sample of secretions. An assembly of devices designed to concentrate medical grade oxygen Bulk oxygen (O2) from ambient air and then deliver the concentrated O2, with purity of 11 A concentration system up to 93%-99.5%, to the hospital medical gas supply system for therapeutic use on patients in Hospital. A device that intended to be placed over a patient's mouth to administer Cardiopulmonary 12 "mouth-to-mask" exhaled air from the user to the patient during A resuscitation mask cardiopulmonary resuscitation (CPR). A device used as an adjunct monitor for the regional haemoglobin oxygen 13 Cerebral oximeter B saturation of blood in the brain of a patient. Devices designed to provide high frequency chest wall oscillation Chest-oscillation (HFCWO) for external chest wall manipulation intended to loosen 14 airway secretion- B excessive airway secretions to promote airway clearance and improve clearing system bronchial drainage for patients with respiratory disease. Devices designed to provide external mechanical percussion (rapid Chest-percussion tapping) to the chest wall of a patient to loosen excessive airway 15 airway secretion- B secretions to promote airway clearance and improve bronchial drainage clearing system for patients with respiratory disease. Cold-air diagnostic An assembly of devices intended to be used in the assessment of a 16 B inhalation system pateint suffering from asthma. Cough long-term An assembly of devices intended for long-term detection and recording of 17 ambulatory recording A the number of times a patient coughs during daily activities or sleep. system A hand-held manual surgical instrument intended to be used to perform a 18 Cricothyrotome cricothyrotomy providing airway access within seconds for immediate B ventilation of the patient and necessary suction procedures. A device designed to measure several or all respiratory-gas volume and 19 Diagnostic spirometer B flow parameters needed to evaluate basic pulmonary function. A hand-held device designed to administer powdered medicine through 20 Dry powder inhaler A the mouth and into the bronchial airways. Page 1 of 4A hand-held inhaler prefilled with salt crystals and used to provide an Dry salt therapy inhalation of salt particles through the mouth and into the bronchial 21 A device airways to induce natural self-cleansing mechanisms that flush away the impurities from the surface of cells and mechanically clean the airways. An assembly of devices designed to provide externally applied vibrations Electroacoustical to the chest wall of a patient via an electroacoustical transducer (the 22 airway secretion- applicator) to loosen excessive airway secretions to promote airway B clearing system clearance and improve bronchial drainage for patients with respiratory disease. Electronic An electronic listening device designed to be inserted into a patient's 23 oesophageal oesophagus to listen to heart and breathe sounds, typically while the B stethoscope patient is under anaesthesia. Endotracheal tube A device designed to help with the insertion of an endotracheal (ET) tube 24 A introducer into the airways of a patient during intubation Exhaled-gas A device designed to verify proper endotracheal (ET) tube placement by 25 oesophageal detecting/assessing escaping levels of exhaled carbon dioxide (CO2) A intubation detector during airway management disclosing potential incorrect intubation. A photoelectric device designed for the monitoring of intrapartum foetal 26 Foetal pulse oximeter oxygen saturation (FSpO2) in the presence of a non-reassuring foetal B heart rate (FHR) pattern during labour. Gas pipeline/supply A device designed to create compressed medical grade air, and supply it 27 system air A to a hospital or institution's gas pipeline/supply system for patient use. compressor A device designed to heat and humidify air/oxygen inspired by a patient to Heated respiratory 28 help maintain the mucous membranes of the respiratory tract typically B humidifier during periods of prolonged respiratory support/therapy. Home-use sleep A device intended to continuously measure and record patient 29 apnoea recording physiological parameters during sleep in the home, to facilitate the B system diagnosis of sleep apnoea. The intended use of the Hyperbaric Chamber is to administer 30 Hyperbaric chamber C 100% oxygen at pressure greater than ambient. An electronic device intended to be used to indicate patient hypopnea by Hypopnea 31 monitoring the movement of the thorax and abdomen with each breath B sensor/alarm and provides a signal, according to predetermined settings. Impedance An assembly of electronic devices intended for continuous recording of a pneumography 32 patient’s pulmonary function parameters using impedance pneumography B recording/analysis (IP). system Implantable sleep An assembly of devices intended for home management of obstructive 33 apnoea treatment sleep apnoea (OSA) using an implanted stimulator to provide electrical D system stimulation to the hypoglossal nerve. A device that is used to register the respiratory rate of an infant and which gives an alarm signal (e.g., audible/visual) when the pre-set limits are 34 Infant apnoea monitor exceeded caused by an extended interruption or cessation (apnoea) of B the infants breathing pattern; a condition known as sudden infant death syndrome (SIDS). A photoelectric device designed to transmit radiation at a known wavelength(s) through blood to measure the concentration of oxygen, or 35 Intracardiac oximeter B dye, within the heart based on the amount of reflected or scattered radiation. An instrument designed for the continuous in vivo measurement of 36 Intravascular oximeter B venous blood oxygen saturation (SvO2). Invasive arterial pressure cardiac A device intended to continuously measure and display arterial pressure 37 B output/oximetry cardiac output (APCO) and haemoglobin oxygen saturation (e.g., SpO2) monitor A hand-held device designed to facilitate manual percussion (rapid Manual chest tapping) to provide external vibrations to the chest wall of a patient to 38 B percussor loosen excessive airway secretions to promote airway clearance and improve bronchial drainage for patients with respiratory disease. Page 2 of 4A sterile slender cord or thick thread, medical grade, designed to 39 Medical/surgical string temporarily lift vessels, hold tracheostomy tubes in place, or assist in B stabilizing various organs, medical instrumentation and accessories A device designed to measure continuously a patient's tidal volume or 40 Monitoring spirometer B minute volume for the evaluation of the patient's ventilatory status. An automatic cycling machine used to assist or control alveolar Negative-pressure 41 respiration that exerts a negative pressure on the external surface of the C ventilator chest wall, expanding the chest and moving air into the lungs. Nitrogen monoxide A device intended to measure nitric oxide (NO), in exhaled air to facilitate 42 B analyser diagnosis and management of asthma. An instrument used to measure the concentration of nitrous oxide (N2O) in a sample of a gas mixture taken from an enclosed environment such as 43 Nitrous oxide analyser B a healthcare facility, a compressed medical air or gas system, and/or devices used for anaesthesia administration or respiratory therapy. A device designed to concentrate oxygen (O2) from ambient air and 44 Oxygen concentrator B deliver the concentrated O2 to patient. A hand-held pneumatic device designed to provide external vibrations to Pneumatic chest the chest wall of a patient to loosen excessive airway secretions to 45 B percussor promote airway clearance and improve bronchial drainage for patients with respiratory disease. A filtering mask designed to be placed over the nose and mouth of a Public respirator (2 member of the general public to permit normal breathing while protecting 46 B ply, 3 ply face mask) the wearer from exposure to pathogenic biological airborne particulates during a public health medical emergency. Pulmonary function A device used to measure the function of the respiratory system in adults 47 B analysis system and compliant children. A device intended for the transcutaneous measurement and display of 48 Pulse oximeter C haemoglobin oxygen saturation (SpO2). Pulse oximetry An assembly of devices designed to continuously measure and wirelessly 49 telemetric monitoring transmit haemoglobin oxygen saturation (SpO2) signals from a patient to B system a receiving location for viewing. A device designed to measure and display a non-ambulatory patient's 50 Respiration monitor B respiratory functions. An assembly of devices designed to detect the cessation of breathing Respiratory apnoea 51 (apnoea) in patient who are at risk of respiratory failure to alert a parent or B monitoring system attendant of the life-threatening episode(s). An electrically-powered, hand-held device designed for the inhalation of 52 Steam inhaler steam for the relief of the symptoms (congestion and pressure) A associated with upper respiratory disorders. A device used as a component of a stress test system that permits the 53 Stress test treadmill A evaluation of a patient's physiologic response to physical stress. A device that produces small, biologically-active, negatively-charged ions of oxygen (O2), pulsed at various selected frequencies, that are emitted 54 Therapeutic air ionizer A into the ambient air and absorbed into the bloodstream via the lungs to potentially produce a therapeutic effect. Therapeutic positive A device used for therapeutic rehabilitation of patients with chronic 55 pressure breathing respiratory diseases, and for the distribution of aerosolized C ventilator pharmacological agents to the patient's airways and lungs. Thoracic An assembly of devices designed to measure and store bioconductance 56 bioconductance measurements, analyse the stored data and provide information that can B measurement system aid a clinician in their evaluation of lesions suspicious of lung cancer. An assembly of devices designed to perform thoracic bio-impedance Thoracic electrical measurements to continuously record the distribution of air across 4 impedance 57 quadrants of the lungs, commonly of a neonatal/infant patient to detect B segmentography changes in lung ventilation at a regional level, to assist in the diagnosis of system lung conditions. Thoracic electrical An assembly of devices designed to perform continuous bio-impedance 58 impedance measurements throughout a cross-section of the thorax, to provide real- C tomography system time feedback of lung function of a ventilated patient. Page 3 of 4A device intended to generate negative pressure specifically for Thoracic suction 59 aspiration, to remove fluids, secretions and air to allow for the normal B pump expansion/function of the lungs and/or mediastinum. An assembly of devices intended for home management of obstructive Tongue-adjustment sleep apnoea (OSA) by monitoring breathing parameters during sleep to 60 sleep apnoea B detect the onset of an apnoea event and reducing pharyngeal obstruction treatment system by the tongue. Tracheostoma A device designed as a filter for protecting a stomal opening in the 61 A protective filter windpipe against harmful external influences. A patient-worn device in the form of a patch, collar, or cloth designed to Tracheostoma be fastened around the neck to protect a tracheostoma orifice against 62 B protector harmful external influences. It is not intended to be used as a shower shield. A substance made of oil designed to be applied by healthcare staff or a Tracheostomy tube 63 patient to the outer surface of a tracheostomy tube inner cannula to A lubricant facilitate its easy sliding into the outer cannula. A surgical instrument designed to cut an opening into the trachea 64 Tracheotome (windpipe) through the anterior surface of the neck to create an artificial B airway (tracheotomy). An assembly of devices designed for the continuous and transcutaneous Transcutaneous blood 65 measurement of a patient's blood gas parameters detected through the B gas monitoring system jugular vein (SjvO2). An assembly of devices designed to stimulate a reflex cough using Ultrasonic cough ultrasound in a patient who cannot cough on command, typically 66 A stimulation system respiratory patients with cortical insufficiency or the very young/elderly, to help clear the lungs of secretions and aspirated materials. A device designed to agitate water into micro-particles with ultrasound to Ultrasonic respiratory 67 add moisture to the flow of air/gases administered to a patient via a B humidifier breathing tube/circuit. Vacuum-assisted A device assembly designed to remove excessive secretion from the 68 airway secretion- lungs and upper airway of patients with respiratory disease or during B clearing system cardiac rehabilitation through vacuum technology. Valsalva manoeuvre A device intended to be inserted into a patient's mouth to facilitate 69 A mouthpiece performance of the Valsalva manoeuvre. A component of a bladed video intubation laryngoscope intended to Video intubation enable the positioning of the blade into the oral cavity to manipulate the 70 laryngoscope tongue, preventing it from obstructing the oropharynx and enabling a clear A handle/monitor view of the trachea for the insertion of an endotracheal (ET) tube prior to the delivery of inhalation anaesthesia and/or ventilation. Whole-body A graphic recorder designed for determining and registering airway 71 B plethysmograph resistance and thoracic gas volume to assess pulmonary function. Page 4 of 4Name of Category: Neurological Total No. of Devices: 131Neurological Current Sr. Device Name Intended Use CDSCO No. Classification Intended to deliver controlled electrical impulses directly to the subcutaneous tissue (i.e., 1 Analgesic PENS system B invasively) in the vicinity of a peripheral nerve as relief of chronic neuropathic pain. Analgesic spinal cord electrical Implantable device intended to treat acute and/or chronic intractable pain, where the use 2 D stimulation system of drug therapy is undesirable or no longer effective. 3 Analgesic TENS system Intended to treat pain by transcutaneous electrical simulation on peripheral nerves. B Electrical conductor designed to be attached to the skin surface of a patient outside of the Analytical non-scalp cutaneous 4 hair line (i.e., non-scalp) to conduct electrical signals to a parent device for A electrode electrophysiological recording/monitoring. Intended to conduct electrical signals between a skin electrode(s) or needle electrode(s) Analytical non-scalp cutaneous [electrode not included] and a device designed for electrophysiological 5 A lead recording/monitoring [e.g., electromyography (EMG), evoked potentials (EP), bioelectrical impedance]. Intended to be attached to the scalp surface of a patient to transmit changes in the electrical potential of various areas of the brain for recording/monitoring by a connected 6 Analytical scalp electrode B parent device [i.e., an electroencephalograph (EEG), sleep, or evoked potential recording device]. Intended to connect an electroencephalographic electrode(s) to an 7 Analytical scalp lead electroencephalographic system to facilitate the transmission of the electrical signals B during encephalography (EEG). An aneurysm clip is a device used to occlude an intracranial aneurysm (a balloonlike sac 8 Aneurysm clip. D formed on a blood vessel) to prevent it from bleeding or bursting Antiseizure/psychiatric-therapy Implantable device intended to apply periodic electrical stimuli to the vagus nerve to help 9 vagus nerve electrical D control seizures and/or to help treat psychiatric disorder symptoms (e.g., depression). stimulation system Intended in reducing the level of pain and stiffness associated with rheumatoid arthritis or 10 Arthritis TENS system osteoarthritis by electrically stimulating peripheral nerves across the skin B (transcutaneously). Atrial cerebrospinal fluid Intended to be implanted as the distal component of a ventriculoatrial shunt to channel 11 D catheter cerebrospinal fluid (CSF) to the right atrium where it can be absorbed into the body. Autonomic neuropathy heart 12 Intended to diagnose autonomic nervous system dysfunction (autonomic neuropathy). C rate meter Intended to assess neuromuscular function by measuring the force or power exerted by 13 Back/leg/chest dynamometer A the back, chest, and/or leg muscles during flexion. Bare-metal intracranial 14 Intended to be implanted into the base or parent artery of an intracranial aneurysm. D vascular stent Behavioural therapy electrical Intended in the treatment of obsessive/compulsive behaviour and drug abuse, by applying 15 C stimulation system electrical impulse(aversion therapy). Bladder/bowel-evacuation Intended to empty the urinary bladder and/or the bowels by applying electrical stimuli 16 implantable electrical D typically to the cone-shaped end of the spinal cord (conus medularis). stimulation system A brain injury adjunctive interpretive electroencephalograph assessment aid is a Brain injury adjunctive prescription device that uses a patient's electroencephalograph (EEG) to provide an interpretive interpretation of the structural condition of the patient's brain in the setting of trauma. A 17 C electroencephalograph brain injury adjunctive interpretive EEG assessment aid is for use as an adjunct to assessment aid. standard clinical practice only as an assessment aid for a medical condition for which there exists other valid methods of diagnosis Brain-responsive electrical Intended to continuously monitor brain activity and deliver electrical stimuli to seizure foci 18 D stimulation system in response to neurological disorders (e.g., epilepsy). Cardiac-therapy vagus nerve 19 Intended to apply periodic stimuli to the vagus nerve as a treatment for cardiac failure. D electrical stimulation system Intended for brain protection during profound hypothermic circulatory arrest during aortic 20 Cerebral perfusion catheter D surgery. Cerebrospinal fluid Intended to measure the cerebrospinal fluid (CSF) pressure/intracranial pressure via 21 C manometer, lumbar puncture. Cerebrospinal fluid shunt valve Intended to noninvasively modify the operating pressure of a programmable, non-active, 22 C programmer implanted cerebrospinal fluid (CSF) shunt valve that is part of a CSF shunt. Coma-arousal vagus nerve Intended to apply periodic stimuli to the vagus nerve for the purpose of exciting the patient 23 D electrical stimulation system to arousal from a vegetative state (i.e., a deep coma). The computerized cognitive assessment aid is a prescription device that uses an individual's score(s) on a battery of cognitive tasks to provide an interpretation of the current level of cognitive function. The computerized cognitive assessment aid is used Computerized cognitive 24 only as an assessment aid to determine level of cognitive functioning for which there C assessment aid. exists other valid methods of cognitive assessment and does not identify the presence or absence of clinical diagnoses. The computerized cognitive assessment aid is not intended as a stand-alone or adjunctive diagnostic device A cortical electrode is an electrode which is temporarily placed on the surface of the brain 25 Cortical electrode. D for stimulating the brain or recording the brain's electrical activity Intended to fit into an appropriate powered handpiece that provides the rotation allowing 26 Cranial bur, A the user to excavate soft or hard skull tissue. Cranial electrotherapy A cranial electrotherapy stimulator is a device that applies electrical current to a patient's 27 D stimulator. head to treat insomnia, depression, or anxietyMetallic rotary endpiece designed to cut a hole(s) or a circular section(s) of the skull vault 28 Cranial perforator B (calvarium) by attaching to powered drill/handpiece. Intende as a neurosurgical blade used to cut/remove circular sections of the skull vault 29 Cranial trephine, A (calvarium) to provide access to the interior Craniotomy power tool system Intended to be used to rotate a cranial cutting tool (i.e., a drill bit, bur, trephine or 30 C handpiece perforator) in order to produce a hole or holes in the skull vault (calvarium). A cryogenic surgical device is a device used to destroy nervous tissue or produce lesions 31 Cryogenic surgical device. D in nervous tissue by the application of extreme cold to the selected site A cutaneous electrode is an electrode that is applied directly to a patient's skin either to 32 Cutaneous electrode. record physiological signals (e.g., the electroencephalogram) or to apply electrical C stimulation Deep brain electrical Designed to apply electrical stimuli to specific areas of the deep brain for the treatment of 33 D stimulation system movement disorders, psychiatric disorders and/or to treat chronic, severe, intractable pain. Deep brain electrical Intended to be implanted in specific areas of the deep brain and used along with deep 34 C stimulation system lead brain electrical simulation system. A depth electrode is an electrode used for temporary stimulation of, or recording electrical 35 Depth electrode. C signals at, subsurface levels of the brain Diagnostic peripheral nerve Intended to apply electrical stimuli in one peripheral region of the body while the response 36 C electrical stimulation system is monitored in another peripheral region. Intended to be used to apply tactile stimuli to the body (e.g., pneumatic activation of a Diagnostic somatosensory 37 membrane to the fingers and lips) typically for evoked response procedures to investigate B tactile stimulation system the function and potential disorders of the brain. Diskectomy system, Intended for the percutaneous (through the skin) removal of the nucleus pulposus from 38 D percutaneous, automatic the lumbar disc. Intended to be applied to sutured dura mater to prevent cerebrospinal fluid (CSF) leakage 39 Dura mater sealant C during healing. An echoencephalograph is an ultrasonic scanning device (including A-scan, B-scan, and 40 Echoencephalograph. doppler systems) that uses noninvasive transducers for measuring intracranial interfaces C and blood flow velocity to and in the head Ejaculation electrical 41 Intended to apply electrical stimuli to the nerves that control ejaculation. C stimulation system Electroconvulsive therapy Intended to apply strong electrical stimuli to a patient's brain to induce convulsions and 42 C system loss of consciousness, typically to treat major depression, schizophrenia, or mania. Electroencephalogram (EEG) An electroencephalogram (EEG) signal spectrum analyzer is a device used to display the 43 B signal spectrum analyzer. frequency content or power spectral density of the electroencephalogram (EEG) signal An electroencephalograph electrode/lead tester is a device used for testing the Electroencephalograph impedance (resistance to alternating current) of the electrode and lead system of an 44 B electrode/lead tester. electroencephalograph to assure that an adequate contact is made between the electrode and the skin Electroencephalograph test An electroencephalograph test signal generator is a device used to test or calibrate an 45 B signal generator. electroencephalograph Intended to perform quality control procedures on an electroencephalograph (EEG) 46 Electroencephalograph tester A machine and/or a sleep recording machine. An electroencephalograph is a device used to measure and record the electrical activity of 47 Electroencephalograph. C the patient's brain obtained by placing two or more electrodes on the head Electroencephalographic Analytical scalp electrodes preconfigured within a head-worn device to use with 48 B electrode cap electroencephalography (EEG). Intended to continuously record electroencephalographic signals in ambulatory patients Electroencephalographic long- 49 for periods usually from 24 to 72 hours to assess a variety of neurological conditions (e.g., B term ambulatory recorder epilepsy) and psychiatric disorders. Intended to continuously measure the electrical signals produced by a patient's brain and display/record them as an electroencephalogram (EEG) to evaluate brain function. Electroencephalographic 50 Alongwith which measuring of other physiological parameters such as electromyogram C monitoring system (EMG), respiration wave forms, blood pressure, ocular motility, and/or haemoglobin oxygen saturation (SpO2) and carbon dioxide (CO2) in relation to EEG. Intended to produces artificial physiological signals or replays digitally recorded patient Electroencephalographic 51 data to perform rapid testing, simulating that of an electroencephalograph (EEG) recorder B simulator or monitor. Intended in clinical diagnosis of muscular disorders to evaluate muscle weakness and to 52 Electromyograph determine if the weakness is related to the muscles themselves or a problem with the B nerves that supply the muscles. 53 Electronystagmograph Intended for detecting the electrical potential caused by eye movements. B Epicranial brain electrical Intended to apply weak, pulsed (not continuous) electrical stimuli from beneath the scalp 54 C stimulation system to specific areas of the brain for the treatment of focal epilepsy. An esthesiometer is a mechanical device which usually consists of a single rod or fiber 55 Esthesiometer. which is held in the fingers of the physician or other examiner and which is used to A determine whether a patient has tactile sensitivity Intended to provide ventilatory support to a patient with diaphragm dysfunction of Extramuscular neuromuscular origin through electrical stimulation of the phrenic nerve, to contract the 56 diaphragm/phrenic nerve D diaphragm rhythmically (using extramuscular electrodes) and cause the patient to draw electrical stimulation system breath in a manner similar to natural breathing. 57 Facial nerve locating system Intended to locate a facial nerve by applying an electrical stimulus. BGait-enhancement electrical Intended to improve the gait in a patient suffering from partial paralysis of the lower 58 B stimulation system, external extremities or other neuromuscular disorders by applying external electrical simulation. Gait-enhancement electrical Intended to improve the gait in a patient suffering from partial paralysis of the lower 59 stimulation system, D extremities or other neuromuscular disorders by applying internal electrical simulation. implantable Intended to measure the threshold of a patient's taste by applying a variable direct current 60 Gustometer B to the tongue. Hand A electronically powered instrument intended to assess neuromuscular function by 61 dynamometer/pinchmeter, measuring the force or power exerted by the muscles of the hand/forearm to A electronic squeeze/pinch an object and as part of interactive rehabilitation. Hand A mechanical instrument intended to assess neuromuscular function by measuring the 62 dynamometer/pinchmeter, force or power exerted by the muscles of the hand/forearm to squeeze/pinch an object A mechanical and as part of interactive rehabilitation. Intended to detect and record a seizure by continuous measurement of one or more Home seizure monitoring physical/physiological parameters (e.g., body motion, electrical activity of the heart or 63 C system skeletal muscles) in a patient with epilepsy during daily activities and/or sleep in the home; some types may also be used in clinical settings. Human dura mater is human pachymeninx tissue intended to repair defects in human 64 Human dura mater. D dura mater Intended to be implanted in a patient for the storing and subarachnoid (intrathecal) Implantable intrathecal infusion 65 administration of narcotics/drugs (e.g., morphine sulfate, baclofen) to manage intractable D pump, programmable pain and muscle spasms of malignant or non-malignant origin. Implantable lumbar Intended to be used by a healthcare professional to telemetrically program the implantable neuromuscular electrical 66 ( lumbar neuromuscular electrical stimulation system) pulse generator component with C stimulation system patient-specific parameters. programmer Implantable lumbar neuromuscular electrical Intended to deliver episodic electrical stimulation to nerves that innervate lumbar muscles 67 D stimulation system pulse to elicit contraction for the treatment of chronic low back pain (CLBP). generator Intended to envelop an implantable pulse generator (IPG) (e.g., cardiac Implantable pulse generator 68 pacemaker/defibrillator, neurostimulator) to stabilize the implant in the subcutaneous D mesh bag, bioabsorbable pocket in which it is implanted. Implantable sleep apnoea Intended to deliver electrical stimulation to the hypoglossal nerve [targeted hypoglossal 69 D treatment system nerve stimulation (THN)] for the home management of obstructive sleep apnoea (OSA). Implantable sleep apnoea Intended to be used by the patient to communicate telemetrically with an implanted pulse 70 treatment system C generator to control therapy, and recharge the pulse generator's battery. programmer/charger Implantable sleep apnoea Intended to deliver electrical stimulation in synchronous with respiration during sleep, to 71 treatment system, respiration- the hypoglossal nerve [targeted hypoglossal nerve stimulation (THN)] for the home D sensing management of obstructive sleep apnoea (OSA). Implantable spinal cord Device designed to change, telemetrically, one or more of the operating parameters (the 72 electrical stimulation system programs) of an implanted spinal cord electrical stimulation system pulse generator C programmer (EPG). An implanted cerebellar stimulator is a device used to stimulate electrically a patient's cerebellar cortex for the treatment of intractable epilepsy, spasticity, and some movement Implanted cerebellar 73 disorders. The stimulator consists of an implanted receiver with electrodes that are placed D stimulator. on the patient's cerebellum and an external transmitter for transmitting the stimulating pulses across the patient's skin to the implanted receiver An implanted diaphragmatic/phrenic nerve stimulator is a device that provides electrical stimulation of a patient's phrenic nerve to contract the diaphragm rhythmically and Implanted produce breathing in patients who have hypoventilation (a state in which an abnormally 74 diaphragmatic/phrenic nerve low amount of air enters the lungs) caused by brain stem disease, high cervical spinal D stimulator. cord injury, or chronic lung disease. The stimulator consists of an implanted receiver with electrodes that are placed around the patient's phrenic nerve and an external transmitter for transmitting the stimulating pulses across the patient's skin to the implanted receiver An implanted intracerebral/subcortical stimulator for pain relief is a device that applies Implanted electrical current to subsurface areas of a patient's brain to treat severe intractable pain. 75 intracerebral/subcortical The stimulator consists of an implanted receiver with electrodes that are placed within a D stimulator for pain relief. patient's brain and an external transmitter for transmitting the stimulating pulses across the patient's skin to the implanted receiver An implanted neuromuscular stimulator is a device that provides electrical stimulation to a patient's peroneal or femoral nerve to cause muscles in the leg to contract, thus improving Implanted neuromuscular the gait in a patient with a paralyzed leg. The stimulator consists of an implanted receiver 76 D stimulator. with electrodes that are placed around a patient's nerve and an external transmitter for transmitting the stimulating pulses across the patient's skin to the implanted receiver. The external transmitter is activated by a switch in the heel in the patient's shoe An implanted spinal cord stimulator for bladder evacuation is an electrical stimulator used to empty the bladder of a paraplegic patient who has a complete transection of the spinal Implanted spinal cord cord and who is unable to empty his or her bladder by reflex means or by the intermittent 77 stimulator for bladder use of catheters. The stimulator consists of an implanted receiver with electrodes that are D evacuation. placed on the conus medullaris portion of the patient's spinal cord and an external transmitter for transmitting the stimulating pulses across the patient's skin to the implanted receiverInterferential electrical Intended to relieve/manage intractable pain; some include additional electrodes to 78 B stimulation system provide other types of electrical stimuli or suction for therapeutic massage. Intracranial pressure monitor Intended for intermittent or continuous measurement and display of intracranial pressure 79 D device (ICP). It is used in conjunction with an invasive intracranial device. Intended to provide ventilatory support to a patient with diaphragm dysfunction of Intramuscular neuromuscular origin through electrical stimulation of the phrenic nerve to contract the 80 diaphragm/phrenic nerve D diaphragm rhythmically (using intramuscular electrodes) and cause the patient to draw electrical stimulation system breath in a manner similar to natural breathing. Intramuscular Intended to change, telemetrically, one or more of the operating parameters (the diaphragm/phrenic nerve 81 programs) of an intramuscular diaphragm/phrenic nerve electrical stimulation system C electrical stimulation system external pulse generator (EPG). programmer Intended for rapid cooling induction in patients where temperature reduction is clinically 82 Intranasal cooling system indicated (e.g., following a cerebral ischemic event, during cardiac arrest) to help C mimimize damage to the brain and heart. Intended to be used in the home to provide electrical stimulation to sensory neurons of the Intranasal lacrimal 83 nasal cavities to acutely increase tear production as treatment for aqueous deficient dry C neurostimulator eye. Intended for continuous or intermittent measurement, display and/or recording of several Invasive-detection 84 invasively-detected physiological parameters [e.g., intracranial pressure (ICP), C physiological monitor compartmental pressure]. 85 Leukotome Intended to cut brain tissue (i.e., cutting white matter, leukotomy). B Intended to non-invasively detect, measure, and display bio-magnetic signals produced by Magnetoencephalography electrically-active cortical brain tissue, and that provide diagnostic information about the 86 B system location of the active tissue responsible for cognitive brain functions relative to the surrounding brain anatomy Inteded to be used in a clinical setting to measure the range of motion of the limb of a 87 Manual goniometer A patient by measuring the angle of movement achieved at the joint. Intended for cutting bone through a sawing action during neurological or orthopaedic 88 Manual surgical saw, flexible B surgery. 89 Meningeal prosthesis Intended to repair the meningeal membrane (meninges). D A nasopharyngeal electrode is an electrode which is temporarily placed in the 90 Nasopharyngeal electrode. C nasopharyngeal region for the purpose of recording electrical activity A needle electrode is a device which is placed subcutaneously to stimulate or to record 91 Needle electrode. C electrical signals A nerve conduction velocity measurement device is a device which measures nerve Nerve conduction velocity conduction time by applying a stimulus, usually to a patient's peripheral nerve. This device 92 C measurement device. includes the stimulator and the electronic processing equipment for measuring and displaying the nerve conduction time Collagen matrix material intended to be used to create a tunnel through which a Nerve guide, bioabsorbable, 93 discontinuous peripheral nerve can regenerate to bridge the proximal and distal nerve D animal-derived stumps. Nerve guide, bioabsorbable, Synthetic material intended to be used to create a tunnel through which a discontinuous 94 D synthetic peripheral nerve can regenerate to bridge the proximal and distal nerve stumps. Non-bioabsorbable material intended to be used to create a tunnel through which a Nerve guide, non- 95 discontinuous peripheral nerve can regenerate to bridge the proximal and distal nerve D bioabsorbable stumps. A neurological endoscope is an instrument with a light source used to view the inside of 96 Neurological endoscope. C the ventricles of the brain Neurological stereotactic 97 Intended to store diagnostic images used for image-guided neurosurgery. C surgery system Neuromuscular transmission Intended to detect electrical neuromuscular transmission (NMT) signals, for assessing the 98 C electrical skin sensor degree of neuromuscular block in a patient. Intended to be placed on the thumb and index finger of a patient to detect movements Neuromuscular transmission 99 and convert them into electrical neuromuscular transmission (NMT) signals during nerve B motion sensor stimulation. Neurophysiologic monitoring Devices designed to monitor and provide electrical stimuli to spinal nerves or other neural 100 B system pathways (may include the brain) during intraoperative surgery or intensive care. The neuropsychiatric interpretive electroencephalograph assessment aid is a prescription Neuropsychiatric interpretive device that uses a patient's electroencephalograph (EEG) to provide an interpretation of 101 electroencephalograph the patient's neuropsychiatric condition. The neuropsychiatric interpretive EEG C assessment aid. assessment aid is used only as an assessment aid for a medical condition for which there exists other valid methods of diagnosis Intended to support and position a patient in a sitting or reclined position during 102 Neurosurgical chair A neurosurgery. Neurosurgical head holder A neurosurgical head holder (skull clamp) is a device used to clamp the patient's skull to 103 B (skull clamp). hold head and neck in a particular position during surgical procedures A neurosurgical headrest is a device used to support the patient's head during a surgical 104 Neurosurgical headrests. A procedure Designed to magnify minute structures within the neurological fields for surgery, typically 105 Neurosurgical microscope the brain or spine or surroundings in the performance of neurological surgical procedures B which require high magnification by transmitted light. Neurosurgical ultrasound Intended for intraoperative imaging of the brain for precise navigation during brain surgery 106 B navigation system (e.g., resection of malignant brain tumours, treatment of vascular malformations).Non-electroencephalogram A non-electroencephalogram (non-EEG) physiological signal based seizure monitoring (EEG) physiological signal 107 system is a noninvasive prescription device that collects physiological signals other than C based seizure monitoring EEG to identify physiological signals that may be associated with a seizure system. A nonpowered neurosurgical instrument is a hand instrument or an accessory to a hand instrument used during neurosurgical procedures to cut, hold, or manipulate tissue. It Nonpowered neurosurgical 108 includes specialized chisels, osteotomes, curettes, dissectors, elevators, forceps, gouges, A instrument. hooks, surgical knives, rasps, scissors, separators, spatulas, spoons, blades, blade holders, blade breakers, probes, etc Intended to determine the response of humans to odours delivered through the nose, 109 Olfactometry system C including irritants. Intended to record and analyse the faint sounds hair cells in the inner ear emit in 110 Otoacoustic emission system response to a stimulus (e.g., click, tone burst, pure-tone signals) to test for a deficiency of B function in the ear during diagnostic evaluation and/or neonatal screening. Intended to be used by an examining physician to gently tap near a patient's joints to test 111 Percussion hammer, manual A reflexes. A percussor is a small hammerlike device used by a physician to provide light blows to a 112 Percussor. A body part. A percussor is used as a diagnostic aid during physical examinations Designed to provide visual function to a patient with vision loss due to retinal degeneration Photodiode subretinal 113 by detecting light, converting it into electrical signals, and relaying them to the retina for C prosthesis system neural stimulation. Physical therapy Designed to produce a rhythmic contraction/release of injured muscles to promote the 114 ultrasound/neuromuscular B removal of metabolic by-products while applying ultrasound treatments. stimulation system A pinwheel is a device with sharp points on a rotating wheel used for testing pain 115 Pinwheel. A sensation Pressure 116 algometer/aesthesiometer, Intended to measure the sensitivity to pain. A electronic A rheoencephalograph is a device used to estimate a patient's cerebral circulation (blood 117 Rheoencephalograph. flow in the brain) by electrical impedance methods with direct electrical connections to the D scalp or neck area 118 Scalp clip. A scalp clip is a plastic or metal clip used to stop bleeding during surgery on the scalp C Scoliosis-treatment electrical Intended to apply electrical stimuli to the spinal musculature to produce a force that 119 D stimulation system stabilizes or limits the progression of the spinal lateral curvature (i.e., scoliosis). A skull plate anvil is a device used to form alterable skull plates in the proper shape to fit 120 Skull plate anvil. A the curvature of a patient's skull A skull punch is a device used to punch holes through a patient's skull to allow fixation of 121 Skull punch. A cranioplasty plates or bone flaps by wire or other means A skullplate screwdriver is a tool used by the surgeon to fasten cranioplasty plates or 122 Skullplate screwdriver. A skullplates to a patient's skull by screws Inteded to transmit and receive electrical signals to/from a dedicated spinal needle (which Spinal needle bioimpedance 123 doubles as a bipolar electrode) and to analyse bioimpedance data in real-time, to predict C navigation unit needle tip location [including confirmation of contact with cerebrospinal fluid (CSF)]. Intended to receive and analyse patient magnetic resonance imaging (MRI) images and Stereotactic position landmarks manually or automatically on these images, then register the images 124 neuronavigation/planning by the mean of a three-dimensional (3-D) optical positioning system (frameless C system stereotactic neuronavigation) to provide real-time relative positioning for the treatment probes and instruments. Intended to deliver a therapeutic radiation dose to an anatomical region from external Stereotactic radiosurgical 125 beams produced from multiple radionuclide sources arranged in a fixed focal point D system collimated array; typically used to treat brain, neck, breast and spinal tumours. Tibial nerve percutaneous Intended to treat urinary and/or faecal incontinence with electrical stimuli applied to the 126 incontinence-control electrical D sacral nerve via percutaneous tibial nerve stimulation (PTNS). stimulation system Intended for one or more psychiatric\neurological therapy types [e.g., transcranial direct Transcranial electrical current stimulation (tDCS), transcranial alternating current stimulation (tACS)]. And to 127 stimulation system, continuous- B induce a state resembling that of chemically-induced anaesthesia for treating one or more current and pulsed-current psychiatric disorders which may include anxiety, depression, insomnia, and/or addiction. Transvenous phrenic nerve Intended to configure/deliver stimulation of the phrenic nerve, via a transvenous electrode, 128 electrical stimulation control to cause contraction of the diaphragm in conjunction with mechanical ventilation to assist D unit earlier ventilation weaning. Intended to test the hearing acuity of a patient, to diagnose hearing disorders, and to test 129 Tuning fork A for vibratory sense. Ultrasonic scanner calibration An ultrasonic scanner calibration test block is a block of material with known properties 130 A test block. used to calibrate ultrasonic scanning devices (e.g., the echoencephalograph) Vagus nerve electrical 131 stimulation system The strength and duration of the electrical impulses are programmed C programmerName of Category: Personal Use Total No. of Devices: 24Personal Protective Equipments Medical Device S.No. Intended Use INDIA Name Garment, Intended to protect an incontinent patient's garment from 1 Protective, For A the patient's excreta. Incontinence Intended for surface disinfection of medical devices, non Biosanitizer for 2 porous hard-surfaces, medical-equipment, units, as well as B Medical devices in-depth cleaning of small surfaces. Intended to protect the wearer's entire face (or part of it) from hazards such as chemical splashes (in laboratories or 3 Face shield A in industry), or potentially infectious materials (in medical and laboratory environments). A disposable medical grade mask (respirator) is a safety device that covers the nose and mouth and helps protect Particular 4 the wearer from breathing in some hazardous or A respirator, potentially infectious materials (in medical and laboratory environments). Nitrile gloves intended to protect the patient and wearer and required to use where resistance to chemicals, including 5 Nitrile gloves B certain disinfectants such as chlorine is required. Also intended for patient and wearer allergic to natural rubber. Natural rubber based glove intended to protect the patient Latex surgical 6 and wearer from cross infection when used in medical or B glove dental surgery. Synthetic material glove intended to protect the patient and Non-latex surgical 7 wearer from cross infection when used in medical or dental B glove surgery. A personal protection device that completely protects the hands of the operator and other personnel from Radiation 8 unnecessary exposure to primary radiation and scattered A protection gloves radiation associated with diagnosis and therapeutic measures. A flat pad with straps or partial gloves that protect part of Partial hand hands and fingers from unnecessary exposure to primary 9 A radiation protector radiation and scattered radiation associated with diagnosis and therapeutic measures. A standard length or half-length apron to protect the patient, Radiation the operator, and other personnel from radiation exposure 10 A protection apron during a medical or dental procedure. Some have a fixed or removable collar to protect the neck and thyroid. Page 1 of 3A personal protection device that protects the hands of the operator and other personnel from unnecessary exposure to Radiation primary radiation and scattered radiation associated with 11 A protection mitten diagnosis and therapeutic measures. The mittens are also called mitts, and protect the thumb and other fingers individually or together. A personal protection device that protects the eyes of the Radiation operator and other personnel from unnecessary exposure to 12 A protection goggles primary radiation and scattered radiation associated with medical/dental procedures for diagnosis and treatment. A transparent or opaque personal protection device that protects the face and eyes of medical personnel and other Radiation face 13 personnel from unnecessary exposure to primary radiation A protector and scattered radiation associated with diagnosis and treatment. A personal protection device that protects the eyes of the operator and other personnel from unnecessary exposure to Operator radiation primary radiation and scattered radiation associated with 14 protection A diagnosis and treatment.The device comes in non-correction spectacles (non-prescription) glasses and visual acuity correction (prescription) glasses. A personal protection device that attenuates unnecessary Gonadal radiation radiation exposure in diagnostic, medical or dental 15 A protector procedures, and shields the gonad of the patient and the operator. A personal protection device that protects specific body Radiation parts of the patient, operator, and other personnel from 16 A protection blanket unnecessary radiation exposure in medical/dental procedures for diagnosis and treatment. A personal protection device that protects the neck or Radiation thyroid of the patient, the operator, and other personnel 17 A protection collar from unnecessary radiation exposure in medical/dental procedures for diagnosis and treatment. A personal protection device that protects the head of the Radiation operator and other personnel from unnecessary exposure to 18 A protection cap primary radiation and scattered radiation associated with medical procedures for diagnosis and treatment. A stand-alone, movable barrier that protects the operator Mobile radiation 19 etc. from unnecessary exposure to radiation used for A protection barrier medical diagnosis, treatment and dental procedures. Gloves made of synthetic materials, and used to protect the Non-latex medical patient and users from cross infection during examination, 20 A examination glove check-up, treatment and handling of contaminated medical materials except for surgery. Page 2 of 3Natural rubber gloves used to protect the patient and users Latex medical from cross infection during examination, check-up, treatment 21 A examination glove and handling of contaminated medical materials except for surgery. chemotherapy spill Designed to safely clean and dispose of Chemotherapy 22 B clean-up kit drug spills. Intended to cover full body act as impermeable to blood 23 Gown/Coveral and bodyfluids and ensure a high level of protection from A biological/infectious agents Medical/Cadaver Intended for transporting a human corpse without any 24 B Body Bags spread of biohazard/infectious agent. Page 3 of 3Name of Category: Obstetrical and Gynecological Total No. of Devices: 116OBSTETRICAL AND GYNECOLOGICAL Sr. No. DEVICE NAME INTENDED USE INDIA Non- invasive medical device placed at abdomen to 1 Abdominal decompression chamber alleviate abdominal pain during pregnancy or C delivery. A dedicated pump used with hood-like device to 2 Abdominal decompression chamber pump control and reduce abdominal pressure of a C pregnant women. A non-sterile, manual, syringe-like device to aspirate fluid from the uterus for treatment of incomplete 3 Abortion suction system manual aspirator abortion, first trimester abortion, and/or for B menstrual regulation. Aslo used for endometrial biopsy. 4 Birthing bed/table, powered Bed used during labor and delivery. A A device that records fetal heart rate and uterine 5 Cardiotocograph C contraction simultaneously. A device that converts birthing contractions to 6 Cardiotocograph transducer electrical signals and is used together with C cardiotocograph (CTG) which displays the signals. An assembly of devices intended to be used to Cardiotocography telemetric monitoring continuously measure and wirelessly transmit foetal 7 C system heart rate and uterine contraction signals from a patient to a monitor. A part of wireless telemeter system. It receives Cardiotocography telemetric monitoring 8 signals from transmitter that senses fetal heart rate C system receiver and uterine contraction during labor. Cardiotocography telemetric monitoring It transmits signals related to fetal heart rate and 9 C system transmitter uterine contractions to the receiver. For providing intercervical nerve block during gyneacological diagnostic tests such as dilation and 10 Cervical anaesthesia kit curettage, small excisional procedures such as B endometrial biopsy, or for pain management during labour and/or delivery.This is a single-use device. A sharp bevel-edged, hollow tubular metal Cervical anaesthesia needle, reusable or instrument intended to be used to administe 11 B single use anaesthetic agent to function as an intracervical nerve-block. Special microscope for examination of female 12 Colposcope B genital organs (e.g., vagina, cervix). Contraceptive cervical cap, reusable or Device inserted into the cervix to prevent semen 13 C single use from enterig the uterus. A chemical substance (e.g., nonoxynol-9) intended to be introduced with an applicator or the finger into 14 Contraceptive spermicide C the vagina before sexual intercourse, to destroy sperm (spermatozoa) to prevent pregnancy. Bubble like device works as a physical barrier to 15 Contraceptive sponge C prevent spermatic invasion into uterus. A circular device placed in the vagina prior to 16 Diaphragm pessary C intercourse to mechanically prevent conception. A collection of devices designed to remove superficial tissue from the mucous membrane lining 17 Endocervical aspirator B the cervical canal (endometrium) through manually- powered suction. Page 1 of 7sterile devices intended to be used for the collection, Endocervical specimen collection kit, no preservation, and transport of cellular and/or other 18 B additive material collected from the endocervix for culture, analysis, and/or other investigation surgical instrument used to for the removal of small 19 Endometrial biopsy curette amounts of endometrial secretions and/or tissue B from the uterus for biopsy purposes. for the collection of a tissue sample taken from the 20 Endometrial biopsy kit B lining of the uterus (endometrium). A brush used to collect mucosal cell for pathological 21 Endometrial cytology brush B diagnosis during endoscopic examination. A sterile device intended to be inserted through a Fallopian tube biopsy everting-balloon 22 hysteroscope to obtain biopsy samples from a B catheter fallopian tube for cytological examination. A collection of sterile devices for the transuterine 23 Fallopian tube catheterization kit catheterization of the fallopian tubes to inject dye or B contrast medium for the evaluation of tubal patency. Active invasive device designed to insufflate the 24 Fallopian tube insufflator Fallopian tubes with a gas [typically carbon dioxide B (CO2)] to maintain tubal patency for a procedure. Contraceptive implantable device implanted into the uterine end of the fallopian tubes to function as a 25 Fallopian tube occlusion insert D contraceptive by obstructing the natural fallopian tube passage. Fixed-diameter cervical dilator, reusable or To dilate the cervical canal with balloon when 26 B single use uterine does not dilate enough due to inertia uteri. Flexible endoscope for visual examination, 27 Flexible fibreoptic culdoscope diagnosis, and treatment of urinary bladder and B urethra. For the visual examination and treatment of the 28 Flexible fibreoptic hysteroscope B canal of the cervix and the uterine cavity (uterus). For the visual examination and treatment of the 29 Flexible fibreoptic laparoscope B abdominal/retroperitoneal cavity and its organs For the visual examination and treatment of the 30 Flexible fibreoptic mammary ductoscope B mammary duct. For the visual examination and treatment of the 31 Flexible fibreoptic salpingoscope B fallopian tubes (oviducts). For the visual examination, treatment, and 32 Flexible ultrasound laparoscope ultrasonic imaging of the abdominal/retroperitoneal B cavity and its organs. for the visual examination and treatment of the 33 Flexible video culdoscope B female peritoneal cavity and organs. For the visual examination and treatment of the 34 Flexible video hysteroscope B canal of the cervix and the uterine cavity (uterus). For the visual examination and treatment of the 35 Flexible video laparoscope B abdominal/retroperitoneal cavity and its organs. For the visual examination and treatment of the 36 Flexible video mammary ductoscope B mammary duct. For the visual examination and treatment of the 37 Flexible video salpingoscope B fallopian tubes (oviducts). Page 2 of 7Uses sound stimuli to assess foetal well-being.This device is used to evaluate the status of the foetus 38 Foetal acoustic stimulator as expressed by, e.g., foetal heart rate changes or B foetal acid-base status, in antepartum tests and/or during intrapartum monitoring. A sterile non-bioabsorbable tubular device implanted in the bladder of a foetus with post- vesicular obstructive uropathy, to decompress the 39 Foetal bladder shunt C urinary tract for urine to pass from bladder into the amniotic sac, until the defect can be surgically repaired after birth Invasive device to collect fetal blood through uterine 40 Foetal blood sampler B cervix. Active device designed to detect, measure, and 41 Foetal cardiac monitor display foetal heart activity during the perinatal C period Sterile implantable device used to contineously drain 42 Foetal pleuro-amniotic catheter C fetal pleural effusion to maternal amniotic cavity. Placed directly on the scalp of the fetus in the uterus 43 Foetal scalp electrode, clip C to monitor fetal vital signs. Mechanical hearing device used to listen to fetal 44 Foetal stethoscope A heartbeat. Foetal vacuum extraction cup, reusable or A device used to extract the head of the fetus with a 45 B single use vaccum cup. A battery-powered vacuum measuring device that is connected via tubing to the suction line of a foetal vacuum extracting cup, to measure and record data 46 Foetal vacuum extraction system monitor B related to a vacuum-assisted delivery such as level of vacuum applied, the number and duration of pulls, and number of pop-offs. Foetal vacuum extraction system, manual, To facilitate the delivery of a foetus during vaginal 47 B reusable or single use childbirth or Caesarean. To facilitate the delivery of a foetus during vaginal 48 Foetal vacuum extraction system, pneumatic B childbirth or Caesarean. To imitate a variety of physiological parameters and conditions (both foetal and maternal) expressed Foetal/maternal multiple physiological during pregnancy in order to test and calibrate foetal 49 B parameter simulation kit and patient monitoring and recording equipment, check patient cable continuity, or train healthcare providers. To imitate a variety of physiological parameters and conditions (both foetal and maternal) expressed Foetal/maternal multiple physiological during pregnancy in order to test and calibrate foetal 50 B parameter simulator and patient monitoring and recording equipment, check patient cable continuity, or train healthcare providers. 51 Gynaecological bib A piece of cloth worn by the patient. A Gynaecological examination/treatment table, To support a woman's body in the appropriate 52 A manual positions during gynaecological examinations. A component of a modular operating table designed 53 Gynaecological operating table top as a detachable table top constructed for A gynaecological surgical procedures. Page 3 of 7Gynaecological operating table, Acitve device designed to support a patient during 54 electrohydraulic or electromechanical or A gynaecological surgical procedures hydraulic Gynaecological scissors, reusable or single To cut tissues during a gynaecological surgical 55 B use procedure; it is not intended for obstetric use. To improve visualization of anatomical structures via 56 Gynaecological surgical microscope transmitted light during gynaecological surgery (e.g., B on the fallopian tubes). A device used during a medical/surgical procedure 57 Heel stirrup to steadily hold a patient's foot (feet) by cradling the A heel or the whole foot. A device that sends the gas into the fallopian tube to 58 Hysteroscopic insufflator B maintain the patency of the tubes. used during endoscopic procedures of the uterus to distend (expand by pressure) the uterus by filling the uterine cavity with a liquid to improve visualization 59 Hysteroscopic irrigation/insufflation system B and enlarge the surgical field. It also circulates the fluid to provide irrigation that will remove tissue/debris from the site. To aspirate fluid/material from the uterus for treatment of incomplete abortion, first trimester 60 Intrauterine cannula, reusable or single use B abortion, and/or for menstrual regulation; it may also be intended for endometrial biopsy. A sterile, flexible tube with an inflatable balloon inserted into the uterus and distended with a 61 Intrauterine haemostatic balloon catheter medium (e.g., sterile water, medical air or other B appropriate gas) to reduce postpartum bleeding with pressure. Inserted into the uterus to reduce postpartum 62 Intrauterine haemostatic suction catheter bleeding through aspiration of blood/debris and B induction of uterine contractions. Intrauterine injection of an opaque tracer medium, to 63 Intrauterine imaging medium catheter B facilitate radiography of the fallopian tubes/uterus. Sterile devices intended for the intrauterine injection Intrauterine imaging medium catheterization 64 of an opaque tracer medium, to facilitate B kit radiography of the fallopian tubes/uterus. Laparoscope laser coupler or To connect the laparoscope to the laser or the laser 65 B laser/laparoscope adaptor arm for laparoscopic laser treatment. For the visual examination and treatment of the 66 Laparoscope system, reprocessed abdominal/retroperitoneal cavity and its organs B (laparoscopy). For the visual examination and treatment of the 67 Laparoscope system, reusable or single use abdominal/retroperitoneal cavity and its organs B (laparoscopy). To dilate the cervical canal with balloon when 68 Manual expandable cervical dilator B uterine does not dilate enough due to inertia uteri. Applied to the skin and/or external mucosa to 69 Massage oil/cream/gel A facilitate therapeutic massage. Page 4 of 7To imitate a foetal heart (e.g., foetal heart ultrasound signals) when used in combination with a foetal/maternal multiple physiological parameter 70 Mechanical foetal heart simulator simulator in order to test foetal monitoring and B recording equipment [e.g., cardiotocograph (CTG)], check patient cable continuity, or to train healthcare providers. Placed in the vagina to collect blood and cellular 71 Menstrual cup, Hevea-latex debris discharges during menstruation and B discharges outside of the monthly menses. Placed in the vagina to collect blood and cellular Menstrual cup, non-latex, reusable or single 72 debris discharges during menstruation and B use discharges outside of the monthly menses. Inserted into the vagina to absorb menstrual or 73 Menstrual tampon, scented or unscented B other vaginal discharge. Active surgical instrument designed for grasping, mobilizing, and suturing tissues/vessels under direct 74 Motorized laparoscopic forceps B or endoscopic visualization during a surgical procedure. Papanicolaou smear kit or Endometrial used to collect and prepare pap smears samples in 75 B sampling kit a medical institute. 76 Pelvic examination kit For performing pelvic examination B A measuring device used to determine the pelvic 77 Pelvimeter B dimensions. An endoscope used for visual examination and 78 Pelviscope B diagnosis of pelvis. it is useful for pain relief in the vulva after 79 Perineal warmer B episiotomy. To determine perineal muscle strength through resistance to spontaneous contraction of perineal 80 Perineometer muscle. Also used to diagnose and treat urinary B incontinence and sexual dysfunction through movement. A collection of sterile devices designed to deliver 81 Pudendal anaesthesia kit anaesthetic agent to the external genitalia of B humans. An endoscope used for visual examination, 82 Resectoscope diagnosis and treatment, especially for resection, of B tissues. An endoscope with a rigid inserted portion intended 83 Rigid culdoscope for the visual examination and treatment of the B female peritoneal cavity and organs. An endoscope with a rigid inserted portion intended 84 Rigid fibreoptic hysteroscope for the visual examination and treatment of the B canal of the cervix and the uterine cavity (uterus). An endoscope with a rigid inserted portion intended 85 Rigid mammary ductoscope for the visual examination and treatment of the B mammary duct An endoscope with a rigid inserted portionangulus iridocornealis for the visual examination and 86 Rigid optical laparoscope B treatment of the abdominal/retroperitoneal cavity and its organs. Page 5 of 7An endoscope with a rigid inserted portion intended 87 Rigid salpingoscope for the visual examination and treatment of the B fallopian tubes (oviducts) An endoscope with a rigid inserted portion, combined with an ultrasound probe, intended for the 88 Rigid ultrasound laparoscope visual examination, treatment, and ultrasonic B imaging of the abdominal/retroperitoneal cavity and its organs Acitve device intended to allow visual examination 89 Rigid video hysteroscope and treatment of the canal of the cervix and the B uterine cavity (uterus). An endoscope with a rigid inserted portion intended 90 Rigid video laparoscope for the visual examination and treatment of the B abdominal/retroperitoneal cavity and its organs Suprapubic needle, surgical, reusable or Percutaneously puncture the lower abdominal wall 91 B single use to provide suprapubic access for surgical repair. 92 Umbilical ligator surgical device used for umbilical cord ligation. A Used to inject liquid, drug, or other substance into 93 Uterine injector B uterus. It is a reusable device. Allow manipulation of the uterus under suction whilst Uterine manipulator cervical 94 preventing laparoscopic insufflation gas from B cup/transilluminator escaping from the cervix (during hysterectomy). Surgical instrument designed to mechanically 95 Uterine manipulator, reusable or single use manipulate the position of the uterus during a B gynaecological intervention A hand-held, surgical instrument used to introduce 96 Uterine packer dressings into the uterus or vagina. This is a B reusable device. For exploring the uterus during a surgical 97 Uterine probe procedure. Used as a component of a uterine B manipulator 98 Uterus-supporting pessary Inserted into the vagina to hold the uterus in place. B A device designed to apply medication to the 99 Vaginal applicator, reusable or single use A vagina. Inserted into the vagina to dilate a narrow vaginal opening due to congenital defect. Can be used 100 Vaginal dilator B during examination, treatment or surgirical procedure. To deliver a liquid (usually solution) directly into the 101 Vaginal douche, reusable or single use B vaginal cavity for hygenic purpose as a douche. A tablet containing various compounds (e.g., sodium bicarbonate, citric acid, aloe barbadensis 102 Vaginal douching fluid tablet B powder) designed to be dissolved in a vaginal douche. To lubricate the vagina to facilitate entry of a gloved 103 Vaginal lubricant finger(s) or a device (e.g., a vaginal speculum) A during a diagnostic or therapeutic procedure. A device that measures the length and diameter of 104 Vaginometer A vagina. For pediatric vaginal examination. To search foreign 105 Vaginoscope B mattter or bleeding site. Page 6 of 7Used to hold an organ at proper position (i.e., viscera) while the surgeon performs a suturing 106 Viscera retention paddle or Visceral retainer B procedure (typically internal wound closure). It is also implanted into a surgical site temporarily. Active device transmitted through the female breast to visualize translucent tissue for the diagnosis of 107 Breast transilluminator C cancer, or other conditions, diseases or abnormalities. A surgical instrument used to rupture the amniotic 108 Amniotic membrane perforator, reusable membrane to assist in childbirth, without causing A injury to the mother or foetus A surgical instrument used to rupture the amniotic 109 Amniotome, reusable membrane to assist in childbirth, without causing B injury to the mother or foetus A collection of sterile devices designed for the 110 Birthing/delivery kit procedures associated with the birthing and delivery A of a newborn inserted into the vagina to facilitate management of 111 Bladder-supporting pessary female urinary incontinence and/or to reduce B bladder prolapse. A device intended to be incorporated into the distal 112 Catheter-tip transducer, pressure end of a catheter (not included) to measure B pressure. Active non invasive device to detect foetal heart 113 Foetal Doppler system B beats using ultrasound/Doppler technology. placed on the surface of a pregnant woman's 114 Foetal Doppler system probe abdomen to detect foetal heart beats using B ultrasonic/Doppler technology. held in place externally to absorb menstrual or 115 Menstrual pad, scented B other vaginal discharge. held in place externally to absorb menstrual or 116 Menstrual pad, unscented A other vaginal discharge. Page 7 of 7Name of Category: Ophthalmic Total No. of Devices: 144Ophtalmic Medical Devices Classificatio S.No. Name of device Intended Use n-IMDR An ophthalmic device intended to measure the time required for retinal 1 Adaptometer adaptation and the minimum light threshold. B An ophthalmic device intended to rapidly detect central and paracentral 2 Amsler grid irregularities in the visual field. A A ophthalmic instrument used to test a patient for abnormal red/green 3 Anomaloscope colour vision by differentiating the red/green colour vision defects. A Aqueous/vitreous humour A collection of sterile devices, including a fluid or semifluid substance, 4 replacement medium kit used in combination to replace the fluid of the eye. D An ophthalmic instrument designed to measure the focusing power Automated 5 (dioptric power) and other optical characteristics of a spectacle lens, lensmeter(Dioptometer) contact lens, or prism. A An ophthalmic plane lens, intended to determine 6 Bagolini lens harmonious/anomalous retinal correspondence. A 7 Binocular vision test unit An ophthalmic device for binocular vision testing. A A hand-held, manual, ophthalmic surgical instrument intended to be 8 Blepharoplasty scissors used to cut eyelid tissue during plastic surgery of the eyelids (blepharoplasty). A A device intended to be permanently implanted in the posterior chamber of the eye for correction and fixation of a subluxated capsular 9 Capsular bag anchor bag, typically in association with in-the-bag intraocular lens (IOL) implantation. C An ophthalmic lens intended to be worn infringement of the eyes to Colour discrimination 10 correct refractive vision conditions and that is coloured/tinted to spectacle lens enhance colour discrimination in patients with colour vision deficiency. A An ophthalmic lamp, used to test a person's ability to differentiate 11 Colour discrimination tester between colours. A Colour-discrimination eye 12 Intended for testing colour vision. chart A A hand-held, manual, ophthalmic surgical instrument intended to be 13 Conjunctival scissors used to cut the conjunctiva and Tenon’s capsule on the eye surface to access the sclera. A Device intended to be worn directly against the cornea and adjacent 14 Contact Lens limbal and scleral areas of the eye to correct vision conditions or act as B a therapeutic bandage. Contact lens agitation cleaning An assembly of devices used to clean and disinfect contact lenses 15 system through automated or manual mechanical agitation . C An aqueous formulation containing appropriate agents for loosening Contact lens disinfecting 16 debris from contact lenses, and that contains a disinfectant intended to solution act on contact lens. C A formulation of proteolytic enzymes, used to remove debris and Contact lens protein-removal 17 protein deposits from reusable contact lenses, or to remove protein solution deposits only. C A measuring instrument used in ophthalmology to determine the radius 18 Contact lens radius gauge of curvature of contact lenses. A A unit intended to disinfect or sterilize reusable soft contact lenses by 19 Contact lens thermal cleaner means of heat. C Corneal burr manual A hand-held, ophthalmic surgical instrument, used to excavate corneal 20 instrument tissue through manual rotation. B An assembly of devices designed for abrasion of the cornea and other 21 Corneal burr system eye tissues. BA device designed for abrasion of the cornea to polish corneal scratches 22 Corneal burr, abrasion and/or the pterygium bed after surgical removal, and/or for abrasion of lid margin lesions. B A device designed for gentle removal of rust stains (rust rings) from the 23 Corneal burr, rust ring removal cornea after the extraction of a ferrous foreign object. B Intended to create a number of small perforations in the epithelial layer of the cornea through which riboflavin can pass into the cornea during 24 Corneal epithelium perforator corneal collagen crosslinking, to treat corneal ectasia (typically keratoconus). B Intended to create a circular cut through the epithelial layer of the cornea to create an epithelial flap intended to be folded back during 25 Corneal epithelium trephine laser assisted epithelial keratomileusis (LASEK) surgery, after which the flap is replaced. B Corneal inlay, aperture A implantable device inserted into the natural cornea to treat 26 reducing presbyopia based on aperture reduction. C Corneal inlay, cornea- A implantable device inserted into the natural cornea to treat refractive 27 reshaping errors by reshaping the cornea. C A device, typically made of a non-abrasive fluid-absorbing material that 28 Corneal light shield is placed on the surface of the cornea to shield the retina from excessive illumination during an ophthalmic procedure. B A manual instrument intended to be used to imprint, indent, and/or 29 Corneal marker incise corneal tissue prior to an ophthalmic surgical procedure. B A device designed to hold donated corneal tissue so that it can be 30 Corneal resection holder resected in preparation for transplantation. B A hand-held, manual, ophthalmic surgical instrument intended to be 31 Corneal scissors used to cut corneal tissue. B A mechanical eye shield made of collagen that is placed on the eye to 32 Corneal shield protect the cornea. B A hand-held, manual ophthalmic surgical instrument designed to excise 33 Corneoscleral punch a segment of tissue from the sclera or cornea of a patient or from grafts taken from cadaver donors. B An ophthalmic lens used in binocular indirect ophthalmoscopy to focus 34 Diagnostic condensing lens reflected light from the fundus of the eye. A A receptacle intended to maintain, transport, and facilitate clinical 35 Donor cornea container examination of a donated cornea during the period between cornea collection and transplantation surgery. C 36 Eikonometer An ophthalmic instrument for diagnosing aniseikonia. A An ophthalmic device designed to test and train vision for conditions 37 Electronic occlusion spectacles where decreased visual acuity may be due to unequal vision in the eyes. A Endoscopic-imaging A device assembly intended to treat retinal and other eye disorders, 38 ophthalmic solid-state laser such as glaucoma, during endoscopic cyclophotocoagulation (ECP) system procedures. C A hand-held, manual, ophthalmic surgical instrument used to cut tissue 39 Enucleation scissors during eye surgery involving enucleation of the eye and/or its related structures. A A hand-held manual surgical instrument intended to be used during Epiretinal/inner limiting posterior segment surgery to lift the inner limiting membrane (ILM) 40 membrane scraper and/or an epiretinal membrane (ERM), and which may have additional posterior segment membrane manipulation uses. B A modified ophthalmoscope that projects a bright light encompassing 41 Euthyscope an arc of approximately 30 degrees on the fundus of the eye for the treatment of amblyopia. BAn ophthalmic instrument used to measure the degree of 42 Exophthalmometer exophthalmos. A A receptacle designed to fit around the eye socket and which is filled 43 Eye cup with warm water or an eyewash solution and placed over the eye to allow the liquid to wash the affected eye. B A device intended to be placed over closed eyes to apply heat for the 44 Eye heat therapy pack treatment of meibomian gland dysfunction (MGD), dry eye syndromes, blepharitis and other related ocular conditions. B A device intended to be used with an eye irrigation kit/system to direct 45 Eye irrigation shield irrigation solution to the surface of the eye and allow the solution to gently lavage the surface of the eye. A An hand-held manual ophthalmic surgical instrument designed to 46 Eye muscle clamp atraumatically grasp and hold the extraocular muscles (EOM) during an ophthalmic surgical intervention. B An implantable device made from synthetic materials that is used to 47 Eye muscle sleeve encase or isolate an ocular muscle. C A sterile, cushion-like device intended to protect the eye or to absorb 48 Eye pad eye secretions. A A hand-held, manual, ophthalmic surgical instrument intended to be 49 Eye spud used to remove a foreign body/object embedded in or adhering to the surface of the eye globe. A An implantable device designed to regulate the flow of fluid between the anterior chamber and the space around the conjunctiva of the eye 50 Eye valve by allowing flow when the pressure in the chamber is above a pre-set value. C A hand-held manual surgical instrument designed to atraumatically 51 Eyelid clamp grasp and hold the eyelid during an ophthalmic surgical intervention. A An ophthalmic device that is applied to the outside of the upper eyelid 52 Eyelid weight, external to "lidload" the eyelid to restore upper eyelid muscle function. A An ophthalmic device that is implanted subcutaneously within the 53 Eyelid weight, implantable upper eyelid to "lidload" the eyelid to restore upper eyelid muscle function. C A black tangent screen intended for assessing the extent of the patient's 54 Felt tangent screen peripheral visual field by mapping the visual response to a test object moved from the periphery towards the centre of the screen. A A device assembly in which input energy is used to excite a glass/crystal Femtosecond ophthalmic solid- 55 rod to emit a high-power laser beam intended for ocular resections and state laser system incisions. C A hand-held manual surgical instrument inserted into the eye during Fibreoptic general-purpose surgical intervention to manipulate anatomical structures or foreign 56 ophthalmic hook bodies within the eye and simultaneously conduct a field of cold light to illuminate the surgical site. A A circular band, sutured to the sclera to prevent collapse of the globe 57 Flieringa ophthalmic ring during difficult intraocular operations. B A manually-operated, ophthalmic device intended to provide indirect 58 Fornixscope access and viewing of the upper conjunctival fornix and inner surface of the eyelid as an alternative to eyelid eversion. A A very thin and flexible ophthalmic lens intended to be applied to the 59 Fresnel lens back of spectacle lenses to focus light to a focal point to help manage various vision conditions. AA device intended to be applied to spectacle lenses to give a prismatic 60 Fresnel prism effect typically to manage strabismus or other eye muscle dysfunction. A Intended for: ocular laser treatment procedures, including coagulation Fundus-imaging ophthalmic of abnormal retinal vasculature; and capturing real-time digital images 61 diode laser system of the anterior/posterior eye segments created using colour, fluorescein angiography and infrared imaging, for diagnosis/treatment planning. C Fundus-imaging ophthalmic Intended to coagulate abnormal vascular tissue in the retina and for 62 solid-state laser system other ocular photocoagulation procedures. C A non-bioabsorbable synthetic polymer device designed to be implanted in the supraciliary space (between the ciliary muscle/body 63 Glaucoma supraciliary implant and the sclera) for the restoration of aqueous humour outflow and subsequent reduction of intraocular pressure as part of treatment for open angle glaucoma. C A system designed to transduce radio-frequency (RF) electrical energy from a generator into ultrasound energy, for the extracorporeal Glaucoma therapy ultrasound 64 application of high intensity focused ultrasound (HIFU) to the eye, to system decrease aqueous humour production and reduce intraocular pressure (IOP) C An ophthalmic device designed to produce an image which facilitates 65 Haidinger brush imager his/her visual function evaluation, particularly the macular integrity. A A portable, hand-held device intended for assessing the central 30º 66 Hand-held campimeter visual field. A A device that consists of an arrangement of ophthalmic lenses or 67 Hand-held telescope mirrors with a handle intended to enlarge images for a visually impaired patient/person. A A 55 dioptre non-contact diagnostic ophthalmic lens intended for use in 68 Hruby fundus lens the examination of the vitreous body and the fundus of the eye under slitlamp illumination and magnification. A An assembly of portable devices intended to continuously or regularly Implantable intraocular 69 collect and display intraocular pressure (IOP) data for the pressure monitoring system diagnosis/monitoring of glaucoma. C An optical device intended to be implanted into the posterior chamber 70 Implantable iris prosthesis of the eye for the reconstruction of partial or total iris defects. C An ophthalmic instrument designed to examine the interior of the eye Indirect binocular 71 allowing the examiner to clearly see a wide angle, stereoscopic ophthalmoscope impression of the details of the fundus (retina) and other structures. A An implantable, open-ended circular band designed to flatten the 72 Intracorneal ring anterior corneal curvature, without disturbing the visual axis, to correct mild and moderate myopia. C A hand-held device intended to be used in the home to provide Intranasal lacrimal 73 electrical stimulation to sensory neurons of the nasal cavities to acutely neurostimulator increase tear production as treatment for aqueous deficient dry eye. C An assembly of manually-operated devices designed to reduce the Intraocular pressure-reducing intraocular pressure (IOP) by applying a controlled, external, mechanical 74 system compression to the surface of the eye in preparation for ophthalmic surgery. C An ophthalmic surgical instrument intended to shave tissue from 75 Keratome sections of the cornea for a lamellar (partial thickness) transplant. BA implantable, single-lumen tube intended to provide tear drainage 76 Lacrimal tube from the front surface of the eye, and also to facilitate saline solution irrigation to a paranasal sinus to manage chronic rhinosinusitis. B A hand-held ophthalmic surgical instrument used in ophthalmic surgery 77 Lens spoon to manipulate/remove the lens of the eye. A A special ophthalmic trial lens in the form of a rod or series of rods 78 Maddox trial lens (grooves/cylinders) that changes the size, shape, and colour of an image to dissociate the eyes in the evaluation of eye muscle dysfunction. A An optical device intended to enable the patient to see over the top of 79 Mirror-prism spectacles their head enabling them to look forward in the direction their head is pointing. A Nystagmus inducing 80 An ophthalmic device intended to elicit nystagmus. optokinetic drum A An ophthalmic device intended to be moved across a patient's field of 81 Nystagmus inducing tape vision to elicit optokinetic nystagmus and to test for blindness. A An hand-operated ophthalmic device typically used by an optician/optometrist to temporarily prevent or attenuate (occlude) the 82 Ocular occluder passage of light (vision) to one eye, during examination and testing of a patient's eyesight in the opposite eye. A A hand-held manual ophthalmic measuring instrument consisting of two 83 Ophthalmic calliper legs hinged at one end and designed to measure the diameter, length, angles, and thicknesses of the eye. A A device typically made of a malleable metal (e.g., tantalum), intended to be implanted permanently or temporarily to bring together the edges 84 Ophthalmic clip of a wound, to aid in healing or to prevent bleeding from small blood vessels in the eye. C An assembly of devices designed to apply cold from a gaseous or liquid Ophthalmic cryosurgical 85 refrigerant (cryogen) to a target tissue for its destruction and removal system during an ophthalmic surgical procedure. C An ophthalmic instrument designed to measure the distance between 86 Ophthalmic distometer the cornea and a spectacle or trial lens (vertex distance). A A laser device assembly intended to coagulate abnormal vascular tissue 87 Ophthalmic dye laser system in the retina, and for other photocoagulation procedures in the eye. C A device assembly intended to provide complete ophthalmic Ophthalmic examination 88 examination position and support conditions for the patient and station clinician. A Ophthalmic excimer laser A laser device assembly intended for corneal ablation and other 89 system ophthalmologic procedures. C A head-worn ophthalmic device intended to reflect light onto the eye of 90 Ophthalmic head reflector a patient to allow examination of the eye and its associated structures. A A device designed as a work surface, with or without storage 91 Ophthalmic instrument table compartments, that supports ophthalmic instruments for the examination/treatment of a patient's eyes. A Ophthalmic noble gas laser A laser device assembly intended to coagulate abnormal vascular tissue 92 system in the retina and for other photocoagulation procedures in the eye. CA component of a modular operating table intended to provide support for and stabilization of the head of the patient (typically includes a Ophthalmic operating table 93 headrest) and to help provide optimal access for the surgeon(s) during top the intervention (e.g., by having a small-width table top and therefore a shorter stretch distance for the surgeon). B A hand-held manual instrument designed to grasp and manipulate Ophthalmic soft-tissue surgical 94 intraocular tissues during ophthalmic surgery (e.g., anterior segment forceps surgery, vitreo-retinal procedures, iridectomy, capsulorhexis). B A hand-held manual surgical instrument with blades designed to grasp Ophthalmic surgical device and manipulate a nonimplantable invasive ophthalmic surgical device 95 handling forceps (e.g., ophthalmic cannula, handless iris retractor) and/or for ophthalmic suturing. A A hand-held, manual, ophthalmic surgical instrument intended to be 96 Ophthalmic suture scissors used to cut suture during eye surgery. A An ophthalmic, measuring instrument designed for determining the 97 Ophthalmic tonometer intraocular pressure (IOP). B Ophthalmic ultrasound An assembly of devices designed for ophthalmic ultrasound imaging 98 imaging system procedures. B An ophthalmic instrument for determining the proper distance at which 99 Ophthalmodiastimeter to place prescription lenses for the two eyes. A An ophthalmic device intended to be used for testing colour perception 100 Ophthalmoleukoscope by means of colours produced by polarized light. A An ophthalmic instrument designed to examine the interior of the eye 101 Ophthalmoscope allowing the examiner to clearly see the details of the retina and other structures/media. C An ophthalmic, device that uses optics to measure the thickness of the 102 Optical pachymeter cornea. A A hand-held ophthalmic surgical instrument used to displace tissue to 103 Orbital depressor facilitate examination of the surrounding area in the orbital cavity during eye surgery. A An implantable ocular device used to reconstruct the floor of the bony 104 Orbital rim prosthesis cavity that contains the eyeball and its associated muscles, vessels, and nerves and is intended to house an artificial eye. C A diagnostic, ophthalmic instrument intended for assessing the extent 105 Perimeter of the patient's peripheral visual field. A A hand-held, non-self-retaining, ophthalmic surgical instrument intended to be used to separate periocular tissues and/or draw aside 106 Periocular/lacrimal retractor the margins of a periocular surgical wound during an ophthalmic intervention. A An assembly of ophthalmic devices intended to deliver energy through a 107 Phacoemulsification system dedicated handpiece tip, which is introduced through an incision made in the lens capsule, to perform phacoemulsification. C 108 Phorometer An ophthalmic instrument intended to be used to test ocular balance. A A mechanical ophthalmic device that is used during an ophthalmic 109 Phoropter examination; typically to determine a patient's prescription for glasses. A An ophthalmic instrument used for the treatment of eccentric eye 110 Pleoptophor fixation (casts in the eye) by dazzling the perimacular retina, thereby relatively enhancing the visual capabilities of the fovea. AAn ophthalmic device used for evaluating hidden (latent) squinting, i.e., 111 Polatest when the patient is not aware of the condition, and also when it cannot be seen. A A device that is attachment to an ophthalmic spectacle frame to prop 112 Ptosis crutch open the upper eyelid in cases of ptosis. A A sterile implantable device intended for the surgical correction of 113 Ptosis sling ptosis. C A graphic recorder used for recording the response of the pupil to 114 Pupillograph reflected light. It is used for ophthalmic diagnostic purposes. A An ophthalmic instrument used for measuring the width or diameter of 115 Pupillometer the pupil. A An optical/ophthalmic device that consists of prismatic lenses that is 116 Recumbent spectacles worn in front of the user's eyes to angle the field of vision enabling the user to read or watch television whilst lying in a supine position. A A non-bioabsorbable, implantable device designed to permanently fix a 117 Retinal tack detached retina to the underlying retinal pigment epithelium (RPE) during ophthalmic surgery. C A device intended to be implanted on the sclera to compress the eye 118 Scleral buckling device (scleral buckling) for the surgical treatment of retinal detachment. C A device designed for implantation in the sclera to produce expansion 119 Scleral expansion implant by altering the position of the underlying ciliary muscle. C A manual instrument used to indent or imprint the surface of the sclera 120 Scleral marker during an ophthalmic surgical or perioperative procedure. B A hand-held manual ophthalmic surgical instrument that is knife-like in 121 Sclerotome design and intended to be used to incise the sclera during a sclerotomy. A An instrument used for the recording and measuring of the areas of 122 Scotometer field of vision that is reduced, i.e., relative scotoma, or loss of sensitivity to light (absolute scotoma or blind spots). A An ophthalmic device designed to hold a pair of spectacle lenses in front 123 Spectacle frame of and close to the eyes of the user. A An ophthalmic device used to correct the refractive errors of that 124 Spectacle lens patient's eyesight and possibly to protect the eyes against radiation or mechanical hazards. A An ophthalmic instrument designed to manually measure the curvature 125 Spectacle lens curvature gauge of the surface of a spectacle lens. A A device that consists of an arrangement of ophthalmic lenses or 126 Spectacle-mounted telescope mirrors designed to be attached to a pair of spectacles and intended to enlarge images for a visually impaired patient/person. A An ophthalmic device that are worn in front of the user's eyes to 127 Spectacles improve their ability to see normally. A A pair of lenses intended to be mounted onto a surgeon's spectacles to 128 Surgical binoculars function as small telescope and provide a magnified image of the visual field during patient examination or surgical intervention. A An implantable device formed as a circular band used to help prevent 129 Symblepharon ring the eyelid from adhering to the eyeball. C A ophthalmic device used for the evaluation and training of a patient's 130 Synoptophor binocular function. AAn ophthalmic device designed to flash words or images at different 131 Tachistoscope speeds, for the purposes of ophthalmic diagnostic testing. A An ophthalmic device used to correct the refractive errors of that 132 Tinted spectacle lens patient's eyesight and to attenuate light radiation by absorption, reflection, or polarization. A An optical device that contains a pair of tinted spectacle lenses that are worn in front of the user's eyes to correct the refractive errors of that 133 Tinted spectacles patient's eyesight and to attenuate light radiation by absorption, reflection, or polarization. A 134 Trial lens An individual ophthalmic lens from a trial lens set. A A device used to hold prisms, spheres, cylinders, or occluders on a trial 135 Trial lens clip lens frame or set of spectacles during vision testing. A A device used in ophthalmic work for placing, holding, and exchanging 136 Trial lens frame trial lenses in front of the eyes of the patient during a sight-testing procedure. A A set of ophthalmic trial lenses of various dioptric powers intended for 137 Trial lens set vision testing to determine the required refraction. A An ophthalmic device designed to use ultrasound to measure the 138 Ultrasound pachymeter thickness of the cornea, and may in addition be designed to measure axial length and anterior chamber depth. B 139 Visual chart An ophthalmic chart (Snellen chart) used in testing visual . A A light viewing box that uses a translucent version of the ophthalmic 140 Visual light box chart (Snellen chart) used for testing visual acuity. A An ophthalmic device intended to project an image on a screen to test 141 Visual projector visual acuity . A Visual evoked-potential An electrical conductor intended to record changes in the electrical 142 electrode potential for the purpose of measuring visual evoked responses. A An assembly of ophthalmic devices intended to deliver energy through a dedicated hand-held instrument, typically used to treat diabetic vitreous 143 Vitrectomy system haemorrhage, retinal detachment, epiretinal membrane, and macular hole. C A sterile bag/capsule intended to be implanted in the eye and filled with a fluid (not included) to replace the vitreous body and provide 144 Vitreous body prosthesis omnidirectional support of the retina for the treatment of severe retinal detachment. CName of Category: Rehabilitation Total No. of Devices:48Rehabilitation and physical support Classification India Name of the as per First S.No Intended use Medical Device Schedule part- 1 MDR 2017 Intende to wear around the calf to apply pressure to an acupressure Acupressure calf 1 point to relieve low back pain, including sciatica and piriformis Class A band syndrome.A Non powered belt like device. Intended to be used as adjunctive therapy in reducing the level of Arthritis TENS pain and stiffness associated with rheumatoid arthritis or 2 Class B system osteoarthritis by electrically stimulating peripheral nerves across the skin (transcutaneously). Intended to strengthen the muscles of the back (especially the Back pulldown 3 latissimus dorsi) through a repetitive pulldown motion performed Class A exerciser with the arms against the force of a weight. intended to strengthen the muscles of the back through a repetitive Back row 4 rowing motion (as in rowing a boat with oars) performed with the Class A exerciser arms against the force of a weight. Back/leg/chest Powered device intended to assess neuromuscular function by 5 dynamometer, measuring the force or power exerted by the back, chest, and/or leg Class B electronic muscles during flexion. Back/leg/chest Non powered device intended to assess neuromuscular function by 6 dynamometer, measuring the force or power exerted by the back, chest, and/or leg Class A mechanical muscles during flexion. Balance ball Intended to be used as an unstable surface on which to perform 7 Class A exerciser exercise to improve balance and posture. Intended to provide biofeedback for training of balance by sensing Balance-training body movements and subsequently producing signals which are tongue electrical 8 translated into electrical stimuli applied to the tongue, enabling a Class B stimulation patient to correlate electrotactile stimulation with their head and system body position during exercise sessions. Bed/chair electric Intended to provide therapeutic massage to the occupant of a bed 9 Class B massager or chair for the treatment of body aches and pains. Intended to be used to provide a quantitative measurement of the 10 Bicycle ergometer rate at which work (energy) is performed by a muscle or group of Class A muscles under controlled conditions. Bladder-emptying Intended to initiate urination and facilitate complete bladder 11 vibratory emptying through application of small mechanical vibrations to the Class B stimulator lower abdomen to promote urethral sphincter relaxation. Intended to emit blue light, red light, and infrared radiation (heating Blue/red/infrared effect) for phototherapy treatment of mild skin disorders (e.g., mild 12 phototherapy Class A acne), superficial skin wounds, and musculoskeletal symptoms lamp (e.g., pain, spasm, stiffness). Intended to primarily strengthen several or all of the major muscle Body elastic 13 groups of the body (i.e., in the arms, legs, chest, back, and/or Class A exerciser abdomen) through repetitive body motion against elastic resistance. Intended to strengthen several of the major muscle groups of the Body flywheel 14 body (i.e., in the arms, legs, chest, back) through repetitive body Class A exerciser motion against a flywheel.Intended to be used to pump heated and/or cooled fluid (e.g., Circulating-fluid water) through externally applied packs for localized hot and/or cold 15 thermal therapy Class B therapy to help treat a variety of adverse conditions resulting from system musculoskeletal injury (e.g., pain, swelling, inflammation). Cold compression Intended to facilitate, through cooling and compression, the 16 therapy cervical treatment of a variety of conditions resulting from injury/surgery to Class A spine collar the neck region (e.g., inflammation, stiffness, whiplash). Cold/cool therapy intended for localized topical skin application to provide a cooling 17 Class A gel effect for underlying muscles/joints to reduce pain and swelling. Intended to reduce localized pain/inflammation, and/or to reduce Cold-air therapy 18 thermal skin damage by applying cold stream of air during Class B unit dermatological laser treatments. Intended to enable a patient with a lumbar spine injury to perform Core-body controlled extension, contraction, and/or twisting movements of the 19 mechanical Class A lumbar/thoracic spine back region and the abdomen, for testing and weight exerciser rehabilitation. Intended to apply an electromagnetic (EM) field to body tissues to: Deep-tissue 1) treat musculoskeletal disorders (e.g., osteoarthritis, electromagnetic 20 osteoporosis); 2) treat body pain (musculoskeletal, postsurgical); Class B stimulation and/or 3) help facilitate soft and hard tissue wound/injury healing, system with no production of a therapeutic deep heat. Intended for respiratory therapy or physiotherapy (e.g., help reduce 21 Electric massager muscular tension, arthritic pain or joint mobility) in the home and/or Class B healthcare facility. Electromechanica l orthopaedic Intended to provide electromechanical orthopaedic extracorporeal 22 extracorporeal Class C shock wave therapy (OEST) to treat musculoskeletal disorders. shock wave therapy system Intended to evaluate a patient’s range of motion/movement of Electronic individual joints/limbs/spine; it is used in a clinical setting typically 23 goniometer/kinesi Class B before/after a medical/surgical intervention, or to assess degree of ology sensor physical fitness. Intended to be applied to the body surface, sometimes with Exothermic heat 24 pressure, to provide heat therapy to reduce muscle spasms and Class A therapy pack cramps and/or for joint and muscle stiffness and pain. intended primarily to strengthen the muscles of the fingers and Finger/hand 25 hands through repetitive finger/hand motion against resistance from Class A exerciser elasticity or density. Foot Intended to provide noninvasive peripheral neurostimulation to the sensorimotor feet for improving somatosensory integration, typically for reducing 26 therapy motor impairments and balance disturbances in patients with Class C mechanical neurological or neurodegenerative disorders (e.g., Parkinson's neurostimulator disease). Gait analysis 27 Intended to be used to study walking or running patterns. Class A system Hand Electronic device intended to assess neuromuscular function by dynamometer/pin 28 measuring the force or power exerted by the muscles of the Class B chmeter, hand/forearm to squeeze/pinch an object. electronic Hand Mechanical device intended to assess neuromuscular function by dynamometer/pin 29 measuring the force or power exerted by the muscles of the Class A chmeter, hand/forearm to squeeze/pinch an object. mechanicalPowered device intended for use in partially immersed in water, Hydrotherapy e.g., in a hydrotherapy tank, to provide additional resistance to the 30 Class A treadmill treadmill walking exercise without increasing the impact and/or stress on the patient's joints. Interferential Intended to stimulate peripheral nerves through the transcutaneous electrical application of two currents of slightly different frequencies that 31 Class C stimulation cross-over/interfere, producing a beating frequency at the treatment system point. Non powered device intended to be used in a clinical setting to Manual 32 measure the range of motion of the limb of a patient by measuring Class A goniometer the angle of movement achieved at the joint. Intended to produce a therapeutic deep heat within specific Medium-wave volumes of the body through the transcutaneous transmission of 33 diathermy Class B electromagnetic (EM) energy in the radio-frequency (RF) bands of treatment system 0.5 megahertz (MHz) to 1 MHz. Intended to produce a therapeutic heat 1 to 2 cm below the skin Microwave within specific volumes of the body through the transcutaneous 34 diathermy transmission of high frequency electromagnetic (EM) energy, Class B treatment system typically 2,450 megahertz (MHz) [microwave], to promote tissue healing and pain relief. Intended to provide a source of infrared (IR) heat for localized Musculoskeletal treatment of musculoskeletal pain/injury (e.g., muscle pain, sports 35 infrared Class B injury, rheumatism) and to improve blood circulation in the treated phototherapy unit, areas to facilitate healing. Musculoskeletal intense Intended to produce and deliver intense therapeutic ultrasound 36 therapeutic (ITU) waves through the skin to create ablative lesions in Class C ultrasound subcutaneous soft tissues (e.g., muscles, tendons). system Intended to provide noninvasive laser therapy [e.g., infrared phototherapy, low-level laser therapy (LLLT)] for localized treatment Musculoskeletal/ of musculoskeletal conditions (e.g., muscle pain, sports injury, 37 physical therapy Class C disorders of the joints and soft/connective tissues), improving blood laser circulation in the treated areas to facilitate healing, or for non- needle acupuncture. Intended to assist users in maintaining good walking posture, Parallel bar 38 particularly a person with a disability, a paraplegic, or a patient who Class A exerciser, has suffered a stroke and is learning to walk. Physical therapy Electrically powered device intended to provide therapeutic 39 Class B massager massage to a larger area than hand-held massaging devices. Physical therapy 40 Intended to be filled with liquid paraffin wax for physical therapy. Class B paraffin wax bath Physical therapy 41 Intended to apply hot steam as a physical therapy to a patient. Class B steam bath Intended to regenerate damaged cartilage, particularly by Pulsed signal 42 stimulating the production of collagen types that are present in Class C therapy system healthy cartilage. Intended to provide a therapeutic deep heat within specific volumes Short-wave of the body through the transcutaneous transmission of 43 diathermy Class C electromagnetic (EM) energy in the radio-frequency (RF) bands of treatment system 13 megahertz (MHz) to 27.12 MHz. Standard Intended to facilitate in-place walking, jogging, or running to 44 treadmill, promote muscle redevelopment, to restore motion to joints, and to Class A mechanical promote weight loss and cardiovascular fitness.Electrically powered unit intended to facilitate in-place walking, Standard jogging, or running to promote muscle redevelopment, to restore 45 treadmill, Class A motion to joints, and to promote weight loss and cardiovascular powered fitness. It is a Battery powered portable device Intended to measure several or all respiratory-gas volume and flow parameters needed to Telemetric evaluate basic pulmonary function [e.g., vital capacity (VC), peak 46 diagnostic expiratory flow (PEF), forced expiratory volume (FEV), and forced Class B spirometer expiratory flow (FEF)], and to transmit the pulmonary function data via a communication device to a healthcare professional(s) at a remote server. Intended to influence cellular metabolism using nuclear magnetic Therapeutic resonance (NMR) for the treatment of degenerate and pathological nuclear magnetic changes to the movement/support profiles of a patient's body, in 47 Class C resonance particular diseased skeletal joints, bones, and surrounding muscle system tissue (e.g., cervical and lumbar spine, shoulders, elbows, hands, hips, knees, feet). A device that is permanently fixed to the wall intended for training and rehabilitation to regain and/or improve body movement and 48 Wall bars Class A balance and/or for strengthening the limbs and the trunk of the body.Name of Category: Physical support Total No. of Devices:38physical support Classification India Name of the as per First S.No Medical Intended use Schedule part- 1 Device MDR 2017 Ankle Electrical device intended to continuously move the ankle joint continuous (e.g., flexion, inversion/eversion) without patient assistance during 1 passive Class B continuous passive motion (CPM) exercise therapy usually motion following surgery or trauma to the joint. exerciser Intended to encompass the ankle joint, or the ankle and foot, to support, align, prevent, or correct orthopaedic deformities/injuries Ankle/foot or to improve function of the ankle and/or foot; it may also be 2 Class A orthosis intended to offload and redistribute foot pressures that affect pedal circulation to improve blood flow and help heal diabetic foot ulcers or postsurgical wounds. Balance Intended to train patient with difficulties in balance (e.g., a 3 Class A board paraplegic or a stroke victim) walks for balance training. Bed traction Intended to treat patients with fractures and other orthopaedic 4 Class A frame disorders (e.g., of the lower or cervical spine, hip). Intended to support the body of a patient and provide traction for Body arch 5 the back muscles and spine by flexing the patient into a reverse Class A traction table supine body arch. Canalith Intended to treat balance disorders [e.g., benign paroxysmal repositioning 6 positional vertigo (BPPV), canalithiasis] caused by displaced Class A procedure canaliths (otoconia) in the inner ear of the patient chair, manual Intended to support or immobilize the cervical spine to treat Cervical 7 deformities, fractures, sprains, or strains (often to treat whiplash Class A spine collar resulting from an automobile accident). Cervical Intended to be fixed to the skull of a patient at brow level using spine 8 pointed, steel, threaded bolts (typically four) that are adjusted to NA immobilizatio penetrate the outer bone of the skull. n head ring Cervicothorac Intended to support or immobilize deformities, fractures, sprains, or 9 ic spine Class A strains of the cervicothoracic spine orthosis Cervicothorac Intended to encompass the cervicothoracolumbosacral spine 10 olumbosacral Class A region of the neck and trunk. spine orthosis Chest- oscillation Intended to rapidly inflate and deflate against the chest wall of the airway patient for promoting airway clearance by creating high frequency 11 Class B secretion chest wall oscillation (HFCWO), resulting in the mobilization of clearing bronchial secretions. system Collar and Fabric and form composite material intended to immobilize 12 cuff arm sling Class A forearm, elbow, humerus or shoulder injuries. materialIntended to be worn on the head of an infant with an abnormal head shape (e.g., due to plagiocephaly, brachycephaly, Cranial 13 scaphocephaly), or after craniosynostosis repair surgery, to apply Class A orthosis pressure to the cranium and improve cranial symmetry/shape during growth over a period of months. Elbow Intended to encompass the elbow joint to support, align, prevent, 14 Class A orthosis or correct deformities/injuries or to improve function of the elbow. Intended to encompass the whole or part of the finger to support, Finger 15 align, prevent, or correct deformities/injuries or to improve function Class A orthosis of the finger. Intended to minimize pressure points on a patient's body by Flotation providing contact with as much of the body surface as possible, 16 therapy bed, typically through a mattress that contains a large volume of Class B adult constantly moving media, e.g., water, air, or mud that lifts the patient to simulate a floating effect. Intended to minimize pressure points on neonatal patient's body by Flotation providing contact with as much of the body surface as possible, 17 therapy bed, typically through a mattress that contains a large volume of Class B neonatal constantly moving media, e.g., water, air, or mud that lifts the patient to simulate a floating effect. Intended to encompass the whole or part of the foot, or designed as a plantar insert, and intended to provide rigid or semi-rigid 18 Foot orthosis Class A correction of the foot for persons with orthopaedic deformities/injuries of the feet Intended to encompass the whole or part of the hand to support, 19 Hand orthosis align, prevent, or correct deformities/injuries or to improve function Class A of the hand. Hand/finger Intended to immobilize an injured hand to protect injuries to, e.g., 20 Class A splint the digits, metacarpals, and wrist during the healing process. Hand/wrist A mains electricity (AC-powered) deviceIntenedd to continuously continuous move the metacarpal/interphalangeal joints (e.g., flexion and 21 passive extension) without patient assistance during continuous passive Class B motion motion (CPM) exercise therapy usually following surgery or trauma exerciser to the joints. Hip/knee A mains electricity (AC-powered) device Intended to provide continuous continuous passive motion (CPM) exercise therapy for the hip 22 passive and/or knee, typically following joint surgery/trauma to promote Class B motion healing; some types may also operate with patient assistance exerciser under controlled active motion (CAM). Non powered device intended to be attached to a table for the Horizontal application of constant horizontal traction forces to the cervical or non-powered 23 lumbar vertebrae by means of attached harnesses whilst the Class A traction patient typically lies in a supine position on the table during system treatment. Intended to be used in respiratory therapy to encourage and Incentive motivate deep-breathing manoeuvres, typically for the postsurgical 24 Class A spirometer treatment and prevention of atelectasis (lung collapse) and to help facilitate airway opening and clearing. Intermittent It is an AC powered electronic device. Intended to apply and 25 traction relieve pre-set traction forces from a motor through harnesses Class B system typically attached to the cervical or lumbar vertebrae.Intend to enable continuous change of the patient's lying position, e.g., it can tilt the entire bed mattress support system (this includes 26 Kinetic bed NA the mattress, the framework that supports the mattress, and the bedding) lengthways, sideways or to a near vertical tilt. Knee Intended to temporarily render the knee immovable, either 27 Class A immobilizer preoperatively or following injury or arthroscopy. Neuro- Intended to assist a patient with a walking disability (neurogenic, controlled muscular, or osseous in origin) regain lost motor function by 28 Class C ambulation transmission of the patient’s residual nerve function, via cutaneous exoskeleton electrodes, to the device motor assembly. Orthopaedic Intended to provide support for skeletal traction to stabilize fracture 29 Class A bed sites. Intended to be used in the treatment of various medical conditions Paediatric (e.g., congenital, neurological, post-traumatic) in paediatrics, where 30 dorsiflexion Class A tendon tightness and muscle contracture affect the ability to slant board dorsiflex the foot, possibly leading to an abnormal gait Intended to encompasses and provide support for the body of a Parapodium 31 patient who is unable to stand unassisted to help them move (walk) Class A walking frame by changing their centre of gravity (COG). Physical Electrically powered device intended to provide therapeutic 32 therapy Class B massage to a larger area than hand-held massaging devices. massager Shoulder It is a mains electricity (AC-powered) device Intended to continuous continuously move the shoulder joint (e.g., flexion, rotation, 33 passive adduction/abduction) without patient assistance during continuous Class B motion passive motion (CPM) exercise therapy usually following surgery or exerciser trauma to the joint. Shoulder Intended to temporarily immobilize or limit abduction of the 34 Class A immobilizer shoulder joint to support healing of an injury or a surgical wound. Intended to encompasses and provide support for the body of a patient who is unable to stand unassisted, to help them move 35 Swivel-walker (walk) by rocking sideways (shifting their weight from side-to-side Class A with a shoulder movement) which makes the footplate of the device swivel so that it “walks” forward. Intended to space the toes of the foot to relieve pain, 36 Toe separator pressure/friction between toes, and/or to facilitate realignment of Class A the toes to a natural position. Traction Intended to support a patient and to provide traction for the back 37 table, line- muscles and spine (e.g., lumbar, cervical) by a motorized Class B powered mechanical manipulation of the spine. Intended to temporarily render the wrist immovable as therapy for Wrist 38 non-displaced fractures, strains, sprains, and muscle injuries of the Class A immobilizer wrist.Name of Category: Interventional Radiology Total No. of Devices: 71INTERVENTIONAL RADIOLOGY Classificati on India as per first S.No. Device Name Intended Use schedule part 1 MDR 2017 Scintillation A scintillation (gamma) camera is a device intended to image the distribution of 1 A (gamma) camera radionuclides in the body by means of a photon radiation detector. A positron camera is a device intended to image the distribution of positron- 2 Positron camera A emitting radionuclides in the body. Nuclear whole A nuclear whole body counter is a device intended to measure the amount of 3 A body counter radionuclides in the entire body. A bone densitometer is a device intended for medical purposes to measure bone 4 Bone densitometer density and mineral content by x-ray or gamma ray transmission measurements C through the bone and adjacent tissues. A bone sonometer is a device that transmits ultrasound energy into the human body 5 Bone sonometer to measure acoustic properties of bone that indicate overall bone health and B fracture risk. An emission computed tomography system is a device intended to detect the Emission computed location and distribution of gamma ray- and positron-emitting radionuclides in the 6 tomography C body and produce cross-sectional images through computer reconstruction of the system. data A fluorescent scanner is a device intended to measure the induced fluorescent Fluorescent 7 radiation in the body by exposing the body to certain x-rays or low-energy gamma C scanner rays. A nuclear rectilinear scanner is a device intended to image the distribution of Nuclear rectilinear 8 radionuclides in the body by means of a detector (or detectors) whose position A scanner moves in two directions with respect to the patient. Nuclear A nuclear tomography system is a device intended to detect nuclear radiation in the 9 tomography body and produce images of a specific cross-sectional plane of the body by blurring C system or eliminating detail from other planes. Nuclear uptake A nuclear uptake probe is a device intended to measure the amount of radionuclide 10 A probe taken up by a particular organ or body region A nuclear whole body scanner is a device intended to measure and image the Nuclear whole 11 distribution of radionuclides in the body by means of a wide-aperture detector A body scanner whose position moves in one direction with respect to the patient. Nuclear scanning A nuclear scanning bed is an adjustable bed intended to support a patient during a 12 A bed nuclear medicine procedure. Radionuclide dose A radionuclide dose calibrator is a radiation detection device intended to assay 13 B calibrator radionuclides before their administration to patients Nuclear A nuclear anthropomorphic phantom is a human tissue facsimile that contains a 14 anthropomorphic radioactive source or a cavity in which a radioactive sample can be inserted. It is A phantom intended to calibrate nuclear uptake probes or other medical instruments A nuclear flood source phantom is a device that consists of a radiolucent container Nuclear flood 15 filled with a uniformly distributed solution of a desired radionuclide. It is intended to A source phantom. calibrate a medical gamma camera-collimator system for uniformity of responseA radionuclide rebreathing system is a device intended to be used to contain a Radionuclide gaseous or volatile radionuclide or a radionuclide-labeled aerosol and permit it to be 16 C rebreathing system respired by the patient during nuclear medicine ventilatory tests (testing process of exchange between the lungs and the atmosphere). A nuclear sealed calibration source is a device that consists of an encapsulated Nuclear sealed 17 reference radionuclide intended for calibration of medical nuclear radiation A calibration source detectors. Nuclear A nuclear electrocardiograph synchronizer is a device intended for use in nuclear 18 electrocardiograph radiology to relate the time of image formation to the cardiac cycle during the A synchronizer production of dynamic cardiac images A radionuclide test pattern phantom is a device that consists of an arrangement of Radionuclide test 19 radiopaque or radioactive material sealed in a solid pattern intended to serve as a A pattern phantom test for a performance characteristic of a nuclear medicine imaging device. A nonfetal ultrasonic monitor is a device that projects a continuous high-frequency Nonfetal ultrasonic sound wave into body tissue other than a fetus to determine frequency changes 20 B monitor (doppler shift) in the reflected wave and is intended for use in the investigation of nonfetal blood flow and other nonfetal body tissues in motion An ultrasonic pulsed doppler imaging system is a device that combines the features Ultrasonic pulsed of continuous wave doppler-effect technology with pulsed-echo effect technology 21 doppler imaging and is intended to determine stationary body tissue characteristics, such as depth or B system location of tissue interfaces or dynamic tissue characteristics such as velocity of blood or tissue motion. An ultrasonic pulsed echo imaging system is a device intended to project a pulsed Ultrasonic pulsed sound beam into body tissue to determine the depth or location of the tissue 22 echo imaging B interfaces and to measure the duration of an acoustic pulse from the transmitter to system the tissue interface and back to the receiver. Diagnostic A diagnostic ultrasonic transducer is a device made of a piezoelectric material that 23 ultrasonic converts electrical signals into acoustic signals and acoustic signals into electrical B transducer signals and intended for use in diagnostic ultrasonic medical devices. An angiographic x-ray system is a device intended for radiologic visualization Angiographic x-ray 24 of the heart, blood vessels, or lymphatic system during or after injection of a C system contrast medium. Diagnostic x-ray A diagnostic x-ray beam-limiting device is a device such as a collimator, a cone, or an 25 beam-limiting aperture intended to restrict the dimensions of a diagnostic x-ray field by limiting C device the size of the primary x-ray beam Cine or spot A cine or spot fluorographic x-ray camera is a device intended to photograph 26 fluorographic x-ray C diagnostic images produced by x-rays with an image intensifier camera An electrostatic x-ray imaging system is a device intended for medical purposes that Electrostatic x-ray uses an electrostatic field across a semiconductive plate, a gas-filled chamber, or 27 C imaging system other similar device to convert a pattern of x-radiation into an electrostatic image and, subsequently, into a visible image. A radiographic film marking system is a device intended for medical purposes to add Radiographic film 28 identification and other information onto radiographic film by means of exposure to A marking system visible light. Image-intensified An image-intensified fluoroscopic x-ray system is a device intended to visualize 29 fluoroscopic x-ray anatomical structures by converting a pattern of x-radiation into a visible image C system through electronic amplification.Non-image- A non-image-intensified fluoroscopic x-ray system is a device intended to be used to intensified 30 visualize anatomical structures by using a fluorescent screen to convert a pattern of C fluoroscopic x-ray x-radiation into a visible image. system A spot-film device is an electromechanical component of a fluoroscopic x-ray system 31 Spot-film device that is intended to be used for medical purposes to position a radiographic film C cassette to obtain radiographs during fluoroscopy Diagnostic x-ray A diagnostic x-ray high voltage generator is a device that is intended to supply and 32 high voltage B control the electrical energy applied to a diagnostic x-ray tube for medical purposes. generator Mammographic x- A mammographic x-ray system is a device intended to be used to produce 33 C ray system radiographs of the breast Full-field digital A full-field digital mammography system is a device intended to produce planar 34 mammography C digital x-ray images of the entire breast system A photofluorographic x-ray system is a device that includes a fluoroscopic x-ray unit Photofluorographic 35 and a camera intended to be used to produce, then photograph, a fluoroscopic C x-ray system image of the body Diagnostic x-ray A diagnostic x-ray tube housing assembly is an x-ray generating tube encased in a 36 tube housing A radiation-shielded housing that is intended for diagnostic purposes. assembly. Diagnostic x-ray A diagnostic x-ray tube mount is a device intended to support and to position the 37 A tube mount diagnostic x-ray tube housing assembly for a medical radiographic procedure. Pneumoencephalo A pneumoencephalographic chair is a chair intended to support and position a 38 B graphic chair patient during pneumoencephalography (x-ray imaging of the brain). Radiologic patient A radiologic patient cradle is a support device intended to be used for rotational 39 A cradle positioning about the longitudinal axis of a patient during radiologic procedures. Radiographic film is a device that consists of a thin sheet of radiotransparent 40 Radiographic film material coated on one or both sides with a photographic emulsion intended A to record images during diagnostic radiologic procedures. A radiographic film cassette is a device intended for use during diagnostic x-ray Radiographic film procedures to hold a radiographic film in close contact with an x-ray intensifying 41 B cassette screen and to provide a light-proof enclosure for direct exposure of radiographic film Radiographic A radiographic film/cassette changer is a device intended to be used during a 42 film/cassette radiologic procedure to move a radiographic film or cassette between x-ray B changer exposures and to position it during the exposure. Radiographic A radiographic film/cassette changer programmer is a device intended to be used to film/cassette 43 control the operations of a film or cassette changer during serial medical C changer radiography. programmer Wall-mounted A wall-mounted radiographic cassette holder is a device that is a support intended 44 radiographic to hold and position radiographic cassettes for a radiographic exposure for medical A cassette holder use Radiographic film A radiographic film illuminator is a device containing a visible light source covered 45 A illuminator with a translucent front that is intended to be used to view medical radiographs Automatic An automatic radiographic film processor is a device intended to be used to 46 radiographic film develop, fix, wash, and dry automatically and continuously film exposed for medical C processor purposes.A radiographic grid is a device that consists of alternating radiolucent and 47 Radiographic grid radiopaque strips intended to be placed between the patient and the image A receptor to reduce the amount of scattered radiation reaching the image receptor Radiographic head A radiographic head holder is a device intended to position the patient's head 48 A holder during a radiographic procedure. Radiologic quality A radiologic quality assurance instrument is a device intended for medical 49 assurance purposes to measure a physical characteristic associated with another A instrument radiologic device. Radiographic A radiographic anthropomorphic phantom is a device intended for medical purposes 50 anthropomorphic A to simulate a human body for positioning radiographic equipment. phantom A radiographic intensifying screen is a device that is a thin radiolucent sheet coated Radiographic with a luminescent material that transforms incident x-ray photons into visible light 51 A intensifying screen and intended for medical purposes to expose radiographic film. A radiographic ECG/respirator synchronizer is a device intended to be used to Radiographic coordinate an x-ray film exposure with the signal from an electrocardiograph (ECG) 52 ECG/respirator or respirator at a predetermined phase of the cardiac or respiratory cycle. A synchronizer A radiologic table is a device intended for medical purposes to support a patient during radiologic procedures. The table may be fixed or tilting and may be 53 Radiologic table electrically powered. C A transilluminator, also known as a diaphanoscope or lightscanner, is an electrically powered device that uses low intensity emissions of visible light and near-infrared Transilluminator radiation (approximately 700-1050 nanometers (nm)), transmitted through the 54 for breast breast, to visualize translucent tissue for the diagnosis of cancer, other conditions, D evaluation diseases, or abnormalities. A medical image storage device is a device that provides electronic storage and retrieval functions for medical images. Examples include devices employing Medical image 55 magnetic and optical discs, magnetic tape, and digital memory. A storage device Radiological A radiological computer-assisted diagnostic software for lesions suspicious of computer-assisted cancer is an image processing prescription device intended to aid in the diagnostic software characterization of lesions as suspicious for cancer identified on acquired medical 56 C for lesions images such as magnetic resonance, mammography, radiography, or computed suspicious of tomography. The device characterizes lesions based on features or information cancer extracted from the images and provides information about the lesion(s) to the user.Medical image analyzers, including computer-assisted/aided detection (CADe) devices for mammography breast cancer, ultrasound breast lesions, radiograph lung nodules, and radiograph dental caries detection, is a prescription device that is intended to identify, mark, highlight, or in any other manner direct the clinicians' Medical image attention to portions of a radiology image that may reveal abnormalities during 57 C analyzer interpretation of patient radiology images by the clinicians. This device incorporates pattern recognition and data analysis capabilities and operates on previously acquired medical images. This device is not intended to replace the review by a qualified radiologist, and is not intended to be used for triage, or to recommend diagnosis. Radiological Radiological computer aided triage and notification software is an image processing computer aided prescription device intended to aid in prioritization and triage of radiological 58 triage and medical images. The device notifies a designated list of clinicians of the availability C notification of time sensitive radiological medical images for review based on computer aided software image analysis of those images performed by the device. Full-body MRI A general-purpose magnetic resonance imaging (MRI) system designed to scan any 59 system, permanent C targeted area of the body. It includes a permanent magnet assembly. magnet Full-body MRI A diagnostic general-purpose magnetic resonance imaging (MRI) system designed to 60 system, resistive scan any targeted area of the body (full-body imaging). It includes a resistive magnet C magnet assembly. Full-body MRI A diagnostic general-purpose magnetic resonance imaging (MRI) system designed to system, 61 scan any targeted area of the body (full-body imaging). This system includes a C superconducting superconducting magnet assembly. magnet Foetal cardiac A mains electricity (AC-powered) device designed to detect, measure, and display 62 D monitor foetal heart activity during the perinatal period. A portable, hand-held, battery-powered device assembly consisting of a measuring and display unit and an attached probe or interchangeable probes designed to Foetal Doppler noninvasively detect foetal heart beats using ultrasound/Doppler technology. The 63 C system heart beats are typically conveyed audibly via the measuring/display unit and attached probe which is applied to the surface of the pregnant woman's abdomen. The device aids in determining foetal viability. An endoscope with a flexible inserted portion intended for the visual examination Flexible ultrasound 64 and treatment of the entire colon [lower gastrointestinal (GI) tract]. It is inserted B colonoscope through the anus during colonoscopy. An endoscope with a flexible inserted portion, combined with an ultrasound probe, Flexible ultrasound intended for the visual examination and treatment of the duodenum (the first part 65 B duodenoscope of the small intestine). It is inserted into the body through the mouth during duodenoscopy. An endoscope with a flexible inserted portion, combined with an ultrasound probe, Flexible ultrasound intended for the visual examination and treatment of the upper gastrointestinal (GI) 66 gastroduodenosco tract [oesophagus, stomach, and duodenum (the first part of the small intestine), B pe including the pancreas and the bile duct]. It is inserted into the body through the mouth during gastroduodenoscopy. An endoscope with a flexible inserted portion, combined with an ultrasound probe, Flexible ultrasound intended for the visual examination, treatment, and ultrasonic imaging of the 67 B laparoscope abdominal/retroperitoneal cavity and its organs. It is inserted through an incision made in the abdominal wall (routinely just below the umbilicus) during laparoscopy.An endoscope with a flexible inserted portion intended for the visual examination Flexible ultrasound 68 and treatment of the trachea, bronchi, and lungs. It is inserted through the mouth B bronchoscope or nose during bronchoscopy. An ultrasound imaging transducer assembly specifically designed to be positioned Bladder ultrasound within the bladder either manually or under endoscopic guidance that steers, 69 B imaging transducer focuses, and detects the ultrasound beam and resulting echoes either mechanically or electronically. A flexible tube intended to be inserted into the lumen of a blood vessel to Blood flowmeter 70 determine blood-flow velocity by measuring the ultrasonic frequency shift between C catheter, Doppler transmitted and reflected signals (Doppler principle). A stationary or mobile (e.g., on wheels) assembly of devices designed to collect, General-purpose display, and analyse ultrasound images during a variety of extracorporeal and/or 71 ultrasound imaging intracorporeal (endosonography or endoscopic) ultrasound imaging procedures B system (e.g., cardiac, OB/GYN, endoscopy, breast, prostate, vascular, and intra-surgical imaging).Name of Category: Rheumatology Total No. of Devices: 11Name of Category: Dermatology and Plastic surgery Total No. of Devices: 56DERMATOLOGICAL &PLASTIC SURGERY SL.N O. Current CDSCO Device Name Intended Use Classificat ion An organ bag is a device that is a flexible plastic bag intended to be used as a temporary receptacle for an 1 Organ bag. B organ during surgical procedures to prevent moisture loss. "Hem-o-lok ligating clips are intended for use in procedures involving ligation of vessels or tissue Polymer Ligating 2 structures. . Hem-o-lok ligating clips are C Clips contraindicated for use in ligating the renal artery during laparoscopic donor nephrectomies." Surgical camera A surgical camera and accessories is a device 3 A and accessories. intended to be used to record operative procedures. An implantable clip is a clip-like device intended to Implantable 4 connect internal tissues to aid healing. It is not C ligating clip absorbable Laser surgical A carbon dioxide laser for use in general surgery and instrument for use in dermatology is a laser device intended to cut, 5 in general and C destroy, or remove tissue by light energy emitted by plastic surgery and carbon dioxide. in dermatology. A low energy ultrasound wound cleaner is a device Low energy that uses ultrasound energy to vaporize a solution and 6 ultrasound wound B generate a mist that is used for the cleaning and cleaner maintenance debridement of wounds. A non-powdered surgeon's glove is a device intended Non-powdered 7 to be worn on the hands of operating room personnel A surgeon's glove. to protect a surgical wound from contamination A surgical drape and drape accessories is a device Surgical drape made of natural or synthetic materials intended to be 8 and drape used as a protective patient covering to isolate a site B accessories of surgical incision from microbial and other contamination.A suture retention device is a device, such as a Suture retention retention bridge, a surgical button, or a suture bolster, 9 B device intended to aid wound healing by distributing suture tension over a larger area in the patient An ultraviolet lamp for dermatologic disorders is a device (including a fixture) intended to provide Ultraviolet lamp ultraviolet radiation of the body to photoactivate a drug 10 for dermatologic in the treatment of a dermatologic disorder if the C disorders. labeling of the drug intended for use with the device bears adequate directions for the device's use with that drug. A wound autofluorescence imaging device is a tool to Wound view autofluorescence images from skin wounds that 11 autofluorescence are exposed to an excitation light. The device is not B imaging device intended to provide quantitative or diagnostic information. A rotary surgical device consisting of a motor (an engine) and a cylindrical or trephine insertion portion. It usually has an extremely sharp-edged saw blade or Battery-powered a cutting blade with a thin saw blade. The blade is 12 B trephine system beveled on one side. It is used for removal of the intervertebral disc, other hard tissues, or soft tissues. It may have a speed control device. This is a battery- driven device A gas laser that is used in surgical procedures. It Carbon dioxide utilizes carbon dioxide as the substrate. It is widely 13 C laser used in several clinical fields (e.g., gynecology, neuroscience, dermatology). Colonoscopes are used for the removal of foreign Colonoscope, bodies, excision of tumors or colorectal polyps 14 General & Plastic (polypectomy), and control of hemorrhage. Routine B Surgery colonoscopy is important in diagnosing intestinal cancer A gas laser used in surgical procedures, etc. It utilizes Copper vapour copper vapor as the substrate. It is used in 15 C laser dermatology, etc. for treatment of cutaneous vascular lesions (e.g., port-wine stains, telangiectasia). A cryosurgical unit with a liquid nitrogen cooled Cryosurgical unit cryoprobe and accessories is a device intended to 16 B and accessories destroy tissue during surgical procedures by applying extreme cold.A device to be temporarily implanted subcutaneously to dilate the surrounding skin. Usually, a balloon is 17 Dermal dilator B implanted subcutaneously where solutions including saline solution are infused. A surgical knife used to harvest the skin for grafting. 18 Dermatome A Either manual or electric-powered. Dermatome skin A tape that comes in various sizes with adhesive on 19 approximation both sides. It is attached onto a skin graft knife to A tape collect a skin graft tissue. This device is for single-use. A drape adhesive is a device intended to be placed 20 Drape adhesive. A on the skin to attach a surgical drape. A rotary surgical device consisting of a motor (an Electrically- engine) and a cylindrical or trephine insertion portion. 21 powered trephine The blade is beveled on one side. It is used for B system removal of the intervertebral disc, other hard soft tissues, or soft tissues. Electrosurgical Electrosurgical cutting and coagulation device and cutting and accessories is a device intended to remove tissue and 22 C coagulation device control bleeding by use of high-frequency electrical and accessories current. Electrosurgical An electrosurgical device for over-the-counter device for over-the-aesthetic use is a device using radiofrequency energy 23 B counter aesthetic to produce localized heating within tissues for non- use invasive aesthetic use. An endoscope used for visual examination, diagnosis, Esophagoscope, and treatment of the esophagus. The insertion section 24 General & Plastic changes its shape corresponding to the shape of the B Surgery body cavity. The device is inserted through the oral cavity. An eye pad is a device that consists of a pad made of various materials, such as gauze and cotton, intended 25 Eye pad. A for use as a bandage over the eye for protection or absorption of secretions. A gas pressure-operated surgical device used to cut a Gas-powered 26 thin piece of skin for grafting, or to resect a small skin B dermatome lesion. A dedicated blade is required for this purpose. A saw has a handpiece with an attachment that generates vibration or reciprocal movements. It Gas-powered 27 adopts either a micro or macro design. Rechargeable B surgical saw batteries are used. Usually, compressed air or compressed nitrogen is used.A rotary surgical device consisting of a motor (an engine) and a cylindrical or trephine insertion portion. It usually has an extremely sharp-edged saw blade or Gas-powered a cutting blade with a thin saw blade. The blade is 28 B trephine system beveled on one side. It is used for removal of the intervertebral disc, other hard tissues, or soft tissues. It may have a speed control device. This is a gas- driven device. A gastroscope is a flexible tube that has a small light Gastroscope, and a video camera attached to the end of it. The tube 29 General & Plastic C can be used to take tissue samples by inserting Surgery instruments such as small pincers. A device accompanied by accessories that cuts/coagulates tissues with a high-frequency current General or with the electricity/heat of the heating element. The 30 C electrosurgical unit device is used by a physician to confirm that an incision or coagulation is made as intended, macroscopically or microscopically. A surgical severing instrument that is similar to a scalpel, excluding the fact that its blade is designed to be heated with an electric current. The blade transmits 31 Hemostatic knife B heat directly to body tissues to achieve hemostasis. The instrument uses thermal energy for the purpose and requires no grounding pad. A hydrophilic wound dressing is a sterile or non-sterile device intended to cover a wound and to absorb Hydrophilic wound exudate. It consists of nonresorbable materials with 32 A dressing. hydrophilic properties that are capable of absorbing exudate (e.g., cotton, cotton derivatives, alginates, dextran, and rayon). An implantable staple is a staple-like device intended 33 Implantable staple to connect internal tissues to aid healing. It is not C absorbable An internal tissue marker is a prescription use device Internal tissue that is intended for use prior to or during general 34 A marker. surgical procedures to demarcate selected sites on internal tissues. An irrigating wound retractor device is a prescription device intended to be used by a surgeon to retract the Irrigating wound surgical incision, to provide access to the surgical 35 B retractor device. wound, to protect and irrigate the surgical wound, and to serve as a conduit for removal of fluid from the surgical woundLaparoscope, "These electrodes are intended for use in minimally 36 General & Plastic invasive surgical procedures where monopolar C Surgery electrosurgical cutting and coagulation are desired "Laparoscopy Tray is intended for single-use to 37 LaparoscopyTray" enable a suitable trained health care professional to A perform an laparoscopic procedure." A rigid tube inserted into the subcutaneous layer Liposuction transdermally for removal of fatty deposits. Aspiration 38 B catheter is performed with an appropriate unit. This device is for single-use. Manual operating A manual operating table and accessories and a table and manual operating chair and accessories are accessories and nonpowered devices, usually with movable 39 A manual operating components, intended to be used to support a patient chair and during diagnostic examinations or surgical accessories procedures. A hand-held surgical device used to sever a thin piece Manually-operated 40 of skin for grafting, or to resect a small skin lesion. A A dermatome dedicated blade is required for this purpose. An occlusive wound dressing is a nonresorbable, sterile or non-sterile device intended to cover a Occlusive wound 41 wound, to provide or support a moist wound A dressing. environment, and to allow the exchange of gases such as oxygen and water vapor through the device. A surgical, chisel-like, instrument designed to cut and/or shape small bones and/or cartilage during Plastic surgery plastic surgery. It is hand-held by the surgeon who will 42 A osteotome typically use a surgical mallet or hammer to manually impart an impacting force to the proximal end of the instrument. T An electric cylindrical device for ophthalmic surgery equipped with a blade for resection/removal of a ring- shaped piece of corneal tissue (corneal button). For Powered corneal 43 example, when a healthy corneal graft is obtained B trephine from a cadaver, the recipient's morbid cornea is resected and removed to allow transplantation of the graft. An electric surgical device used for removal of the Powered fragment of damaged skin or for thinly slicing the skin 44 B dermatome of a donor for skin graft. A dedicated blade should be used for these purposes.A powered suction pump is a portable, AC-powered or compressed air-powered device intended to be used to remove infectious materials from wounds or Powered suction 45 fluids from a patient's airway or respiratory support B pump. system. The device may be used during surgery in the operating room or at the patient's bedside. The device may include a microbial filter A removable skin clip is a clip-like device intended to Removable skin 46 connect skin tissues temporarily to aid healing. It is B clip not absorbable A removable skin staple is a staple-like device Removable skin 47 intended to connect external tissues temporarily to aid B staple healing. It is not absorbable. A blade that comes in various sizes, attached to the Reusable skin graft knife, and is used to harvest the skin graft. 48 A dermatome blade This device is reusable after sterilization. Usually, the blade point should be sharpened periodically. A blade, available in various sizes, attached to a Single-use 49 dermatome for collection of skin grafts. The device is B dermatome blade intended for single-use. A skin marker is a pen-like device intended to be used to write on the patient's skin, e.g., to outline surgical 50 Skin marker A incision sites or mark anatomical sites for accurate blood pressure measurement. Skin Stapler is intended to be applied to close 51 Skin Stapler B lacerations on the outer layer of the dermis. A cylindrical or coronary saw used to resect discs of Soft tissue tissues other than bones. It comes in various sizes 52 B trephine and configurations according to the size and hardness of the tissue to be resected. Surgical apparel are devices that are intended to be worn by operating room personnel during surgical 53 Surgical apparel. procedures to protect both the surgical patient and the A operating room personnel from transfer of microorganisms, body fluids, and particulate A cutter that consists of a metal frame. The cutter slides through the frame. It comes in various 54 Surgical guillotine configurations and sizes according to the type of A tissue to be severed. Various cranks or shaft driver mechanisms generate the power.Identification. A surgical lamp (including a fixture) is a 55 Surgical lamp device intended to be used to provide visible A illumination of the surgical field or the patient. Surgical A surgical microscope and accessories is an AC- 56 microscope and powered device intended for use during surgery to A accessories. provide a magnified view of the surgical field.Name of Category: Pediatrics and Neonatology Total No. of Devices: 137PEDIATRICS AND NEONATOLOGY Classification India as per First S.No. Name of Product Intended Use Schedule Part 1 MDR 2017 A flexible enclosure designed to cover the bed of a infant or small child to provide an aerosolized environment of breathing gases/vapours, e.g., a suspension of medicated liquid or solid particles, for medication therapy. Typically used for the treatment of 1 Aerosol tent, paediatric breathing disorders (e.g., asthma). It typically consists of a metal frame covered with transparent plastic, and wide bore tubing B connected to the aerosol source and is used for the treatment of paediatric patients permitting them movement without restriction. This is a reusable device. A mains electricity (AC-powered) device designed to continuously measure and display the breathing circuit pressure and oxygen (O2) concentration levels of respiratory gases delivered to a patient through positive pressure ventilation systems such as continuous positive airway pressure (CPAP) systems or ventilator respiratory circuits. It typically includes pressure and O2 level displays, alarms 2 Airway Pressure / Oxygen Monitor B to signal pressure and O2 levels that exceed specified limits, and has connectors to allow attachment to the respiratory equipment; it is used for neonatal, paediatrics and adults. It may contain one or more rechargeable battery for independent/mobile use or when mains power is not available. A flexible, form-shaped device designed to be placed over a patient's nose and/or mouth to direct anaesthetic gases to the upper airway. It is intended to be worn by the patient/child to cover the nose and mouth to provide a barrier for the respiratory tract for microorganisms and particulate materials. It may be stabilized with a headstrap. It is constructed of nonwoven materials such as Anaesthesia Facemask, single use 3 conductive or non-conductive rubber, polyvinyl chloride (PVC), or other sterilizable materials that produce a soft, flexible cover to B (paediatric) create an airtight seal against the patient's face. It typically includes a 15 mm connector (paediatric), and is available in a range of sizes. This device is sometimes used in association with a manual resuscitator. It is a single use, disposable device that is provided non- sterile. A flexible, form-shaped device designed to be placed over a patient's nose and/or mouth to direct anaesthetic gases to the upper airway. It is intended to be worn by the patient/child to cover the nose and mouth to provide a barrier for the respiratory tract for Anaesthesia Facemask, reusable microorganisms and particulate materials. It may be stabilized with a headstrap. It is constructed of nonwoven materials such as 4 B (paediatric) conductive or non-conductive rubber, polyvinyl chloride (PVC), or other sterilizable materials that produce a soft, flexible cover to create an airtight seal against the patient's face. It typically includes a 15 mm connector (paediatric), and is available in a range of sizes. This device is sometimes used in association with a manual resuscitator. It is reusable. A sterile hollow cylinder inserted orally or nasally into the trachea to provide an unobstructed airway to convey gases and vapours to and from the lungs during anaesthesia, resuscitation, and other situations where the patient is not properly ventilated, and which is Antimicrobial endotracheal tube, coated with an antimicrobial agent [e.g., silver (Ag)] to help prevent infection. It may: 1) be packaged with a connector that will attach 5 C paediatric to a breathing circuit or manual resuscitator; 2) have a distal inflatable cuff to seal against the tracheal wall; 3) be radiopaque; and 4) have a built-in pilot balloon. It is available in various diameters and lengths for adult and paediatric patients. This is a single-use device. A manually-operated, height-adjustable, non-powered, mobile support for an assistive ergonomic chair intended to be used by a Assistive ergonomic chair mobility healthcare provider/carer to provide mobility for a disabled (often paediatric) patient. It consists of a framework on wheels with a 6 A base chair/seat mount, a handlebar for the user to hold/push the assembly, and may include a brake; it includes a manually-powered (fully or hydraulically-assisted) chair lifting mechanism. It is not a wheelchair component. A device that includes a transducer intended to detect the movement of gases in a breathing circuit, and convert this into an electrical Breathing circuit gas-flow sensor, signal for relay to a ventilator (e.g., adult/paediatric/neonatal ventilators, anaesthesia system ventilators). It is connected to the 7 C reusable breathing circuit and an appropriate data transfer cable and intended to enable the ventilator to display/monitor the gas flow to and from the patient, whereby controlled adjustments may be made. This is a reusable device. A sterile device that includes a transducer intended to detect the movement of gases in a breathing circuit, and convert this into an electrical signal for relay to a ventilator (e.g., adult/paediatric/neonatal ventilators, anaesthesia system ventilators). It is connected to Breathing circuit gas-flow sensor, 8 the breathing circuit and an appropriate data transfer cable and intended to enable the ventilator to display/monitor the gas flow to C single-use and from the patient, whereby controlled adjustments may be made. This is a single-patient device intended to be used for the duration of the treatment (single-use) before being discarded. A mains electricity (AC-powered) photoelectric device that noninvasively measures the brain tissue blood oxygen saturation and venous oxygen saturation in the brain. It is typically used as an adjunct monitor for the regional haemoglobin oxygen saturation of blood in the brain of a paediatric or adult patient. It uses a cerebral sensor(s) having a light source and photodiode detector that 9 Cerebral oximeter C is/are placed on the scalp/head. Position-1 detector detects infrared light absorption of extracranial blood and position-2 detector detects infrared light absorption of cerebral blood. Cerebral oxygenation is calculated by subtracting the absorption measured at site 1 from that measured at site 2. An underlay or overlay through which heated or cooled air is circulated to heat and alternatively cool a patient’s whole body (i.e., Circulating-air whole-body elevate or lower core body temperature) typically in surgical and intensive care settings. Air temperature and flow are regulated by a 10 heating/cooling system pad, B separate control unit. The device is available in a variety of lengths, widths, thicknesses, and shapes to accommodate body size and reusable application (e.g., adult/paediatric, full-/partial-body). This is a reusable device. A sterile underlay or overlay through which heated or cooled air is circulated to heat and alternatively cool a patient’s whole body Circulating-air whole-body (i.e., elevate or lower core body temperature) typically in surgical and intensive care settings. Air temperature and flow are regulated 11 heating/cooling system pad, single- B by a separate control unit. The device is available in a variety of lengths, widths, thicknesses, and shapes to accommodate body size use, sterile and application (e.g., adult/paediatric, full-/partial-body). This is a single-use device. An underlay, overlay, or wrap(s) through which temperature-regulated fluid is circulated with the intention to heat and alternatively Circulating-fluid whole-body cool a patient’s whole body (i.e., elevate or lower core body temperature) as part of a circulating-fluid whole-body heating/cooling 12 heating/cooling system pad, system typically used in the operating room (OR), intensive care unit (ICU), or a recovery unit. The underlay/overlay is available in a B reusable variety of lengths, widths, and thicknesses to accommodate body size and application (e.g., adult/paediatric). It is intended to be used by a healthcare professional in a clinical setting. This is a reusable device.A non-sterile underlay, overlay, or wrap(s) through which temperature-regulated fluid is circulated with the intention to heat and Circulating-fluid whole-body alternatively cool a patient’s whole body (i.e., elevate or lower core body temperature) as part of a circulating-fluid whole-body 13 heating/cooling system pad, single- heating/cooling system typically used in the operating room (OR), intensive care unit (ICU), or a recovery unit. The underlay/overlay is B use available in a variety of lengths, widths, and thicknesses to accommodate body size and application (e.g., adult/paediatric, full-/partial- body). It is intended to be used by a healthcare professional in a clinical setting. This is a single-use device. Closed-ended adhesive A sterile, flexible plastic pouch with an adhesive flange (typically with a gender-specific shape) intended to be attached to the skin 14 infant/paediatric urine collection around the genitalia to collect urine from an infant/paediatric patient. It is not designed with an opening for urine drainage and is B bag typically used for biochemical, cytological and/or bacteriological sampling. This is a single-use device. A small, sterile, threaded rod with a slotted head used for craniofacial bone (including the maxilla and/or mandible) fracture fixation by being screwed into bone to hold plates to bone or to provide direct interfragmentary stabilization of bone; it is made of a material Craniofacial bone screw, 15 that is chemically degraded and typically absorbed via natural body processes (e.g., degradable polymers). The device may be self- D bioabsorbable drilling/self-tapping. Its uses include repair of orbital fractures and fractures around the cranial sinuses, paediatric reconstructive surgery, and craniotomy flap fixation. A small, sterile, threaded rod with a slotted head intended to be implanted or inserted short-term in craniofacial bone (including the maxilla and/or mandible) for fracture fixation by direct interfragmentary stabilization of bone or by screwing plates in place; it may Craniofacial bone screw, non- also be intended for transplanted bone fixation. It may be self-drilling/self-tapping and is made of a material that is not chemically 16 C bioabsorbable, sterile degraded or absorbed via natural body processes [e.g., implant grade metal such as titanium (Ti)]. Its uses include repair of orbital fractures and fractures around the cranial sinuses, paediatric reconstructive surgery, craniotomy flap fixation, bone augmentation procedures. A hollow cylinder inserted orally into the trachea to maintain airway patency, typically for patients anticipated to require prolonged mechanical ventilation in critical care, that enables removal of pooled secretion above its distal cuff with suction. It consists of a ventilation lumen, a cuff-inflation lumen, and a suction lumen; a distal inflatable cuff used to form a seal against the tracheal wall; 17 Cuff-suction endotracheal tube C separate connectors that attach to a breathing circuit and suction system; and a pilot balloon for cuff-pressure monitoring. It typically has a radiopaque marker to guide its placement and is available in various diameters/lengths for adult and paediatric patients. This is a single-use device. An assembly of mains electricity (AC-powered) devices designed to heat a patient's whole body, to compensate for the loss of normal body heat, with heat generated from an externally applied pad typically containing electrical heating elements or cables. The system Electric pad whole-body heating includes the pad designed to heat under or over the patient, and a control unit to regulate and monitor the heat. The pads are 18 B system available in a variety of lengths, widths, and thicknesses to accommodate body size and applications (e.g., adult/paediatric, full- /partial-body). The system is typically used in the operating room (OR), the intensive care unit (ICU), or in neonatal and recovery units. An electrically-heated underlay or overlay intended to provide heat under or over a patient as part of an electrical heating pad system used to heat a patient’s whole body (i.e., elevate core body temperature) typically in surgical and intensive care settings. The Electric pad whole-body heating 19 underlay/overlay typically contains electrical heating elements or cables supplied with energy by a dedicated control unit. The B system pad underlay/overlay is available in a variety of lengths, widths, and thicknesses to accommodate body size and application (e.g., adult/paediatric, full-/partial-body). This is a reusable device. A collection of sterile devices that includes tubing and other materials intended to administer nutrient liquids directly into the Enteral feeding kit, adult/paediatric, 20 stomach, duodenum, or jejunum of an adult or paediatric (excludes infants) patient by means of gravity or an enteral pump. This is a C sterile long term use device. A device designed to verify proper endotracheal (ET) tube placement by detecting/assessing escaping levels of exhaled carbon dioxide (CO2) during airway management disclosing potential incorrect intubation. It is used during paediatric intubation and is Exhaled-gas oesophageal intubation attached between the ET tube and the breathing device. It typically functions through colorimetric CO2 detection using an indicator 21 A detector, paediatric paper that changes colour. A colour chart (e.g., attached to the device) permits interpretation into approximate CO2 concentration. It is used in healthcare facilities or in the field to evaluate oesophageal intubation, which if performed incorrectly, prevents patient ventilation. This is a single-use device. A noninvasive, stationary assembly of devices intended to assist the blood circulation of a paediatric patient suffering from heart disease through the electrocardiogram (ECG) synchronized inflation of pressure cuffs worn around the extremities/buttocks. It External counterpulsation system, 22 includes a patient bed with attached inflatable cuffs, an air pump, ECG cables, a control unit with dedicated software, and may include B paediatric additional monitoring devices (e.g., pulse oximeter probe). The cuffs are intended to inflate from the most distal (e.g., lower leg) to the most proximal (e.g., buttocks) during diastole and deflate during systole to achieve increased preload and decreased afterload. An electrical conductor used in pairs to transmit a controlled electrical shock from an external defibrillator to a pre-pubescent patient in order to defibrillate the heart (restore a normal rhythm) or slow a rapid heart rate. It usually consists of a cable set that terminates External defibrillator electrode, with small-diameter, hand-operated electrodes (paddles) that are held by the operator to the chest (the intact torso) of the patient so 23 B paediatric, reusable that the discharge passes across the region of the heart. Typically available as a set of two electrodes with a combined cable/connector, or as a single electrode with cable/connector, in which case two will be connected to the external pulse generator (EPG). This is a reusable device. An electrical conductor used in pairs to transmit a controlled electrical shock from an external defibrillator to a pre-pubescent patient in order to defibrillate the heart (restore a normal rhythm) or slow a rapid heart rate. It typically consists of a cable set [with a External defibrillator electrode, connector for insertion into the external pulse generator (EPG)] that terminates with small-diameter, self-affixing pads (the 24 B paediatric, single-use electrodes) prefabricated with contact gel and an adhesive, that are applied to the chest (the intact torso) of the patient so that the discharge passes across the region of the heart. This device may remain applied to the patient during stages of treatment. This is a single-use device. A non-sterile, bending rod made of metal designed for insertion into the intramedullary canal of a long bone for fracture fixation where flexibility of the implant is desired. It is available in various lengths and diameters for use on lower and upper extremity diaphyseal fractures, and some metaphyseal fractures of paediatrics and small-statured/normal adults, to provide temporary 25 Flexible bone nail, non-sterile C stabilization of the bone segments/fragments until bone consolidation has been achieved. It is intended to splint the cortices and maintain elastic energy to continually brace against rotational/angular forces of the muscles. This is a single-use device intended to be sterilized prior to use. A sterile, bending rod made of metal designed for insertion into the intramedullary canal of a long bone for fracture fixation where flexibility of the implant is desired. It is available in various lengths and diameters for use on lower and upper extremity diaphyseal 26 Flexible bone nail, sterile fractures and some metaphyseal fractures of paediatrics and small-statured/normal adults to provide temporary stabilization of the C bone segments/fragments until bone consolidation has been achieved. It is intended to splint the cortices and maintain elastic energy to continually brace against rotational/angular forces of the muscles. This is a single-use device.A non-sterile implantable device intended to be used to reduce the deformity of pectus excavatum (funnel chest) by applying outward force from a position deep to the sternum to reposition the sternum; it is typically used in paediatric patients and surgically 27 Funnel chest remodelling bar C removed when remodelling is evident (after 2-3 years). It is a thin curved bar, with or without serrations, made of metal [e.g., stainless steel, titanium (Ti)] that can be anchored with wires or with stabilizer plates laterally on the rib cage; devices associated with implantation may be included. This is a single-patient device intended to be sterilized prior to use. A collection of implantable devices used to redirect the angle of growth of long bones in paediatric patients where the growth plates Growth-correction orthopaedic (epiphysial cartilage) are not fused, to allow for the gradual correction of congenital or acquired deformities (e.g., valgus, varus, or 28 C fixation plate kit flexion deformities of the knee, ankle, or elbow). It typically includes various-sized sheets of surgical steel or titanium alloy, and bone screws to attach the sheets to the bone surface over the growth plates. The screws may be allowed to swivel in their position so that the implant acts like a hinge, permitting growth at the growth plate to gradually straighten the limb. A non-sterile hand-held device designed to be used for the transcutaneous measurement of liver stiffness based on transient Hepatic ultrasound elastography elastography. It includes an ultrasound transducer and an electrodynamic transducer intended to generate a controlled transient 29 B system applicator vibration that produces a mechanical elastic shear wave propagated through the skin and liver; subsequent ultrasound measurements can be used to calculate a measure of liver stiffness/ultrasonic attenuation of tissues. The device is designed to connect to a control unit and may be available in various forms for different applications [e.g., paediatric, bariatric (obese)]. This is a reusable device. A mains electricity (AC-powered) device that is used to register the respiratory rate of an infant and which gives an alarm signal (e.g., audible/visual) when the pre-set limits are exceeded caused by an extended interruption or cessation (apnoea) of the infants breathing pattern; a condition known as sudden infant death syndrome (SIDS). This will alert the infant's parent(s), child-minder or 30 Infant apnoea monitor C hospital staff when such life-threatening episodes occur. This device is usually connected to some form of movement sensing device, e.g., small pads placed directly under the infant or belts with sensors around the chest. It can be designed for use in the hospital/institution, or for home-use. A covering made of a metallic, plastic, or metallic/plastic combination structure designed for secure/permanent attachment to the 31 Infant bed crib top top of an infant bed (i.e., a cradle or crib) to protect the infant from accidental damage. Commonly called a crib top, it is typically a B rigid structure with a flexible, transparent plastic (e.g., vinyl) covering around it forming a canopy that encloses the bed. A device designed to limit totally or partially the movement of infants and/or toddlers when lying in its bed or crib; this may be a belt 32 Infant bed restraint B or a strap, or to prevent them from falling out of a bed after climbing the bedrail (e.g., a cover or net). This is a reusable device. A specially made table used for nursing, e.g., washing or changing of nappies, of newborn babies. It can be equipped with a washing 33 Infant care table A basin, typically of soft material (rubberized cloth), and a surface upon which to lie the infant for drying with a towel. A protective guard intended to be used to reduce heat loss due to insensible water loss, i.e., evaporation, during the radiant warming 34 Infant heat shield B of primarily premature infants. This is a single-use device. An electronic unit that is used to monitor and regulate the important temperature and environmental features of an infant incubator. 35 Infant incubator control unit It will be connected to the mains electricity (AC-powered) when the incubator is stationary, but will be powered by a battery pack if C the incubator is in transport. This device is usually interchangeable with other incubators of the same type. A heating element positioned above an incubator's chamber designed to provide warmth for the chamber's environment. It may be 36 Infant incubator warming hood used instead of or as a supplement to the incubator's internal heating system, and may be built onto or be an integral part of the A incubator hood. A bandage-like strap of worsted yarn intended to be worn over the groin to prevent protrusion of abdominal contents in an infant 37 Infant inguinal hernia truss A with an inguinal hernia. This is a single-use device. A non-rigid device, usually made of a fabric and/or plastic materials, used to temporarily render parts of an infant's body immovable, 38 Infant limb immobilizer, reusable e.g., the arms and/or feet while the patient undergoes therapeutic or diagnostic interventions. It will typically be used to prevent the A patient from interrupting an intravenous (IV) infusion, pulling out a catheter, or interfering with wound care. This is a reusable device. A non-rigid device, usually made of a fabric and/or plastic materials, used to temporarily render parts of an infant's body immovable, e.g., the arms and/or feet while the patient undergoes therapeutic or diagnostic interventions. It will typically be used to prevent the 39 Infant limb immobilizer, single-use A patient from interrupting an intravenous (IV) infusion, pulling out a catheter, or interfering with wound care. This is a single-use device. A small chamber, usually wall-mounted, used for the emergency resuscitation of newborn infants who do not breathe spontaneously at birth and are oxygen deficient. It typically has a front door or lid that folds out to serve as a surface upon which the infant is placed. 40 Infant resuscitation cabinet It is typically equipped with a heating lamp, a low-pressure suction system, an oxygen (O2) supply, a gas mixer (oxygen/air), and a B resuscitator. It may be supplied with the resuscitation devices or empty, in which case the resuscitation devices are fitted by another party (e.g., hospital clinical engineer, device supplier). A flat surface fixed on legs and on which newborn infants who do not breathe spontaneously at birth and are oxygen deficient are placed for emergency resuscitation. It is typically equipped with a heating lamp and sometimes a supplemental heating pad, a low- 41 Infant resuscitation table pressure suction system, an oxygen (O2) supply, a gas mixer (oxygen/air), and a resuscitator. It may be supplied with the resuscitation B devices or not, in which case the resuscitation devices are fitted by another party (e.g., hospital clinical engineer, device supplier). This device is typically fixed in one place. An electrically-powered device designed to measure the weight of an infant, particularly a newborn, or to monitor weight changes, e.g., during critical care procedures. It typically consist of a weight tray, a flexure plate or bending beam, an electronic transducer, and 42 Infant scale, electronic A an analogue or digital display; it may include markings to also measure infant length. The device is also known as paediatric or baby scale. A non-rigid device, usually made of flame retardant fabric and/or polyurethane foam materials, intended to modify the sleeping position/posture of infants to prevent deformational plagiocephaly, a flattening of the back of the skull from a consistent back- 43 Infant sleep positioner A sleeping position. It is available in a variety of designs including a wedge-shaped head pillow, a sleeping garment (sleeveless vest) with hooks/Velcro fasteners/nylon zip fasteners and an insertable foam wedge, or a specially designed mattress. This is a reusable device. A mains electricity (AC-powered) mobile device that contains an infrared (IR) heating element(s) designed to emit controlled, evenly 44 Infant warmer distributed overhead heat to the body of a newborn/infant patient requiring supplemental heat. This device is equipped with wheels C so that it can easily be moved to different areas of a room, ward, or department.A device intended to be used to temporarily render an infant's whole body immovable (strait-jacket effect) while the patient Infant whole-body immobilizer, 45 undergoes therapeutic or diagnostic interventions. It includes non-rigid fabric and/or plastic components but might also include a A reusable rigid structural component (e.g., board). This is a reusable device. A non-sterile, non-rigid device, usually made of a fabric and/or plastic materials, intended to be used to temporarily render an infant's Infant whole-body immobilizer, 46 whole body immovable (strait-jacket effect) while the patient undergoes therapeutic (e.g., phototherapy) or diagnostic interventions. A single-use This is a single-use device. A mains electricity (AC-powered) device that contains an infrared (IR) heating element(s) designed to emit controlled, evenly distributed heat to a newborn/infant patient requiring a supplemental regulated thermal environment, or to provide heat to the limbs 47 Infant/regional-body warmer C of a more mature person, typically an adult, who has been severely burned or who is undergoing a procedure. This is a stationary device that is generally operated at a single site. A foam-filled case with a central meshed/netted depression/hole designed to be placed in a cot/crib/bassinet/bed/incubator and to cradle a young infant during sleep/rest, and can used for phototherapy, transportation and burns patients. It is available in various 48 Infant-hammock bed mattress shapes and sizes and is not intended to be placed on an existing mattress. The breathable netting is intended to help reduce the risk A of infant injuries/disorders such as suffocation, flat head (plagiocephaly), sudden infant death syndrome (SIDS), pressure sores, and hyperthermia. This is a reusable device. A portable pad with a central meshed/netted depression designed to be placed on a cot/crib/bed mattress and to cradle a young Infant-hammock bed mattress infant during sleep/rest. The device is typically foam-filled and wedge-shaped with ventilation channels and securing ribbons. The 49 A overlay breathable netting is intended to help reduce the risk of infant injuries/disorders such as suffocation, flat head (plagiocephaly), sudden infant death syndrome (SIDS), and hyperthermia. This is a reusable device. An electrical conductor used in pairs to transmit a controlled electrical shock from an external defibrillator directly to the exposed heart muscle of a pre-pubescent patient in order to intentionally stop/start the heartbeat during cardiopulmonary surgery. It usually Internal defibrillator electrode, 50 consists of a cable set with small-diameter, spoon-like electrodes (commonly known as internal defibrillator paddles or spoons) that C paediatric are held by the operator directly to either side of the heart muscle so that the discharge passes directly through the heart. It is typically available as a set of two electrodes with insulated handles with a combined cable/connector. This is a reusable device. A collection of sterile devices designed to prevent/treat obstruction of and drain tears from the lacrimal ducts. It typically consists of a cannula for insertion into the lacrimal ducts, a tube (e.g., silicone) to perform various ocular irrigation or aspiration procedures (e.g., 51 Lacrimal intubation set lacrimal syringing), and a probe to remove ductal obstructions. It can be used for adult and paediatric patients, particularly to treat C canalicular pathologies (stenosis, obstruction, wounds, imperforation of the lacrimo-nasal canal in the infant), for prevention of viral and post-chemotherapy stenoses, or for dacryocystorhinostomy (DCR). This is a single-use device. A non-sterile device designed to measure skin temperature at several different points using liquid crystal sensors (usually formed from esters of cholesterol which are sealed in a plastic band) placed on the skin around the forearm in order to assist a healthcare 52 Liquid crystal vein locator B professional to locate peripheral veins in a patient before venipuncture. The device is used in paediatric, geriatric, and other patients with hard-to-find veins. This is a single-use device. A hand-held manual surgical instrument designed for paediatric laryngology and for phonatory microsurgery applications in adults. 53 Microlaryngeal probe This delicate probe gives a precise sense of palpation for accurate detection of induration, tissue mass, and cystic changes. It is also A used to break thick mucus fluid before its extraction. This is a reusable device. A non-sterile electrical conductor designed to be applied to a paediatric patient for automatic or manual defibrillation, external pacing, cardioversion, and electrocardiographic monitoring through transmission of cardiac bioelectric signals (typically from the Multifunction cardiac electrode, thoracic surface) to devices that record/process the signals and potentially return electrical impulses [e.g., electrocardiograph, 54 C paediatric electrocardiographic monitor(s), defibrillator]. It is a disk-like electrode that is affixed to the skin with a special adhesive and a conductive gel (pre-gelled). It may be made of x-ray translucent materials and may include permanently attached lead wires. This is a single-use device. A hand-held battery-powered device (a percussor) intended to be operated by a healthcare professional to provide external vibrations to the chest wall of a neonate to help loosen bronchial mucus for expectoration through suctioning. It is small enough in 55 Neonatal chest percussor B physical dimension and weight to be operated inside an infant incubator and has a percussion head suitable for the thorax of a neonate. It is used to help loosen secretion build-up in the lungs of neonates who cannot perform the natural cough mechanism. A mains electricity (AC-powered) device, which may include rechargeable batteries, intended to assist noninvasive ventilation (i.e., without use of an artificial airway) of a neonatal/infant patient via an attached nasal cannula or mask, using continuous positive airway pressure (CPAP) during spontaneous respiration. It is an electronic unit with controls, and may be used with compressed 56 Neonatal CPAP unit C medical gas cylinders [e.g., air, oxygen (O2)] or include an O2 concentrator compartment; additional features (e.g., adjustable flow rates and O2 concentration, humidification) may be provided. It is primarily intended for use in a healthcare facility, especially in intensive and critical care settings. A non-sterile electrical conductor applied to a neonatal patient to transmit electrical signals from the body surface to a data Neonatal electrocardiographic 57 measuring/display device (typically an electrocardiograph, patient monitor, or patient monitoring system) to produce an B electrode electrocardiogram (ECG). This is a single-use device. An assembly of non-powered devices intended to induce and sustain mild hypothermia in a neonatal patient to treat hypoxic- ischemic encephalopathy (HIE). It consists of an insulated cradle, a heat-retention pad(s), and a patient-contact heat-conduction 58 Neonatal hypothermia cot B mattress. The heat-retention pad(s) is intended to be cooled in a refrigerator prior to use, and is constructed of a phase change material designed to help maintain patient hypothermia for a prolonged period. This is a reusable device. A non-sterile, patient-contact component of a neonatal hypothermia cot assembly intended to be used during induction of mild Neonatal hypothermia cot heat- 59 hypothermia in a neonatal patient by allowing heat transfer away from the recumbent patient. It is typically gel-filled and intended to B conduction mattress be placed between the patient and a cooled heat-retention pad. This is a reusable device. A non-sterile, non-powered component of a neonatal hypothermia cot assembly intended to be used to induce and sustain mild Neonatal hypothermia cot heat- hypothermia in a neonatal patient to treat hypoxic-ischemic encephalopathy (HIE). It is intended to be cooled in a refrigerator prior to 60 B retention pad use, and is constructed of a phase change material designed to retain heat and help maintain patient hypothermia for a prolonged period. This is a reusable device. A mains electricity (AC-powered) automatic cycling device intended for short-term and long-term ventilatory support for a neonatal/paediatric patient, especially those preterm and critically ill with respiratory failure in a critical care setting. It is typically a 61 Neonatal intensive-care ventilator time-cycled, pressure-control device that includes a small bore flexible tube breathing system. It may be capable of high frequency C oscillatory ventilation in addition to conventional ventilation, and includes positive end-expiratory pressure (PEEP) and continuous positive airway pressure (CPAP) controls.A non-sterile, upper body garment intended to allow a parent to safely carry/support their premature, dysmature, and/or sick infant in a manner which enables skin-to-skin contact between parent and infant (kangaroo care). It typically consists of a wrap/sweater 62 Neonatal kangaroo care garment A with a variety of straps, and pockets to accommodate ventilation, monitoring, feeding, and warming devices. This is a reusable garment. A device assembly designed to continuously measure and display multiple vital physiological parameters of newborn and premature infants, especially those under critical care. It is typically capable of monitoring parameters such as electrocardiogram (ECG), Neonatal physiologic monitoring 63 respiration rate, heart rate, blood pressure, and body temperature; it may also assess haemoglobin oxygen saturation (SpO2) through C system transcutaneous sensors that measure both transcutaneous oxygen (tcPO2) and transcutaneous carbon dioxide (tcPCO2) saturation. The system typically includes sensors with appropriate size and design for infant use. A sterile, flexible, single-lumen tube intended to be introduced into the trachea of a neonate for the administration of exogenous Neonatal pulmonary surfactant surfactant as part of pulmonary surfactant therapy. It may have a curved distal end to assist navigation into the trachea, and is usually 64 B catheter used to treat neonates at a high-risk of infant respiratory distress syndrome [surfactant deficiency disorder (SDD)]. This is a single-use device. An application software program intended to be installed in an off-the-shelf computer to acquire, record, measure and analyse an Neonatal/paediatric heart rate electrocardiogram (ECG) signal or heart rate data from a physiological monitor. It typically detects variations in heart rate [e.g., 65 C monitoring application software decelerations, reduced baseline heart rate variability (HRV)] in real-time, and is typically used in the neonatal or paediatric intensive care unit (ICU). This device is typically identified by a proprietary name and "version" or "upgrade" number. A mains electricity (AC-powered) device designed to be connected between a physiological monitor and an off-the-shelf computer, containing dedicated application software, and intended to function as a data acquisition node for real-time sampling of Neonatal/paediatric heart rate 66 neonatal/paediatric patient electrocardiogram (ECG) waveforms for communication to the software for analysis of variations in heart C monitoring hardware rate. It typically consists of a microprocessor, random access memory (RAM), and analogue-to-digital sampling card, and is typically used in the neonatal or paediatric intensive care unit (ICU). A mains electricity (AC-powered) device, which may include internal rechargeable batteries, intended for the delivery of precise amounts of nitric oxide (NO), also known as nitrogen monoxide, to the respiratory tract of neonate, paediatric, and adult patients to Nitric oxide delivery unit, system- treat severe respiratory disorders [e.g., primary pulmonary hypertension (PPH), acute respiratory distress syndrome (ARDS)]. It 67 C based consists of a portable main unit that enables the delivery and monitoring of NO to gases that are to be breathed by the patient via a ventilator or other respiratory device/system. It typically includes accessory items (e.g., tubing, filters) and possibly a trolley (cart) for mobility. An electrical conductor, with integral batteries and regulated by a dedicated external pulse generator (EPG), designed to create an Non-rechargeable public semi- electrical shock(s) and defibrillate the heart (restore normal rhythm) to treat ventricular fibrillation or pulseless ventricular 68 automated external defibrillator tachycardia in a pre-pubescent patient. It is a cartridge-type electrode, in pairs, with non-rechargeable batteries that provide the B electrode, paediatric energy to produce the electrical shock(s) after its adhesive pads are placed on the skin of the patient. This is a single-use device that is replaced after a patient application or after elapse of its expiry date. Open-ended adhesive A sterile, flexible plastic pouch with an adhesive flange (typically with a gender-specific shape) intended to be attached to the skin 69 infant/paediatric urine collection around the genitalia to collect urine from an infant/paediatric patient. It is designed with an opening for urine drainage and is typically B bag used for urine output measurement. This is a single-use device. A sterile, hand-held, manual surgical instrument intended to be used during open surgery (including abdominal, gynaecological, paediatric, or thoracic surgery) for the expeditious transection/resection of tissues and creation of anastomoses. It operates by a Open-surgery manual linear cutting manual mechanism whereby it cuts the tissues (e.g., colon) and simultaneously applies single or multiple linear rows of surgical 70 C stapler, reprocessed staples to the resulting ends, eliminating the need for temporary clamping. The staples and cutting blade may be housed in a single- use loading unit (SULU) which may be included. This is a previously used single-use device that has been processed for an additional single-use patient application. A hand-held, manual surgical instrument intended to be used during open surgery (including abdominal, gynaecological, paediatric, or thoracic surgery) for the expeditious transection/resection of tissues and creation of anastomoses. The device operates by a manual Open-surgery manual linear cutting 71 mechanism (e.g., lever, sliding knob) whereby it cuts the tissues (e.g., colon) and simultaneously applies single or multiple linear rows C stapler, reusable of surgical staples to the resulting ends, eliminating the need for temporary clamping. The staples and cutting blade may be housed in a single-use loading unit (SULU) which may be included. This is a reusable device intended to be sterilized prior to use. A sterile, hand-held, manual surgical instrument intended to be used during open surgery (including abdominal, gynaecological, paediatric, or thoracic surgery) for the expeditious transection/resection of tissues and creation of anastomoses. The device operates Open-surgery manual linear cutting 72 by a manual mechanism (e.g., lever, sliding knob) whereby it cuts the tissues (e.g., colon) and simultaneously applies single or C stapler, single-use multiple linear rows of surgical staples to the resulting ends, eliminating the need for temporary clamping. The staples and cutting blade may be housed in a single-use loading unit (SULU) which may be included. This is a single-use device. A hand-held, manual surgical instrument intended to be used during open surgery (including abdominal, gynaecological, paediatric, or thoracic surgery) for the application of surgical staples to approximate internal soft tissues (e.g., two ends of bowel) or for fixation of Open-surgery manual linear stapler, 73 a surgical mesh to tissue. The device operates by a manual mechanism (e.g., lever, sliding knob) whereby it applies single or multiple C reusable linear rows of surgical staples to a portion of tissue; it has no cutting function. The staples may be housed in a single-use loading unit (SULU) which may be included. This is a reusable device intended to be sterilized prior to use. A sterile, hand-held, manual surgical instrument intended to be used during open surgery (including abdominal, gynaecological, paediatric, or thoracic surgery) for the application of surgical staples to approximate internal soft tissues (e.g., two ends of bowel) or Open-surgery manual linear stapler, 74 for fixation of a surgical mesh to tissue. The device operates by a manual mechanism (e.g., lever, sliding knob) whereby it applies C single-use single or multiple linear rows of surgical staples to a portion of tissue; it has no cutting function. The staples may be housed in a single- use loading unit (SULU) which may be included. This is a single-use device. An ophthalmic, battery-powered, measuring instrument designed for determining the intraocular pressure (IOP) by exerting an Ophthalmic tonometer, battery- external force against the eye which provides a reading of the resistance of the tunica of the eye to deformation (the extent of 75 B operated corneal indentation) which is expressed in millimetre(s) of mercury (mmHg). This hand-held device (known as a contact type, e.g., a Perkins tonometer) is often used for, e.g., the examination of postoperative, bedridden and paediatric patients.A surgical instrument used to restore the anatomical and mechanical axes during orthopaedic correction osteotomies. It is typically designed as a robust block with a long, thin, adjusting rod running through its centre and an incremented measuring scale that Orthopaedic medialization 76 enables the surgeon to gauge the adjustments made to the axes (the medialization). It is usually attached to a dedicated bone plate B instrument which is bridging the osteotomy site in order to achieve the correct offset of the two separated bone sections. It is typically made of high-grade stainless steel and can be used on adult and paediatric patients. This is a reusable device. A device consisting of a rigid/semi-rigid transparent plastic shell that forms an enclosure over an infant's whole body, or the head only, in order to provide an enriched environment of oxygen (O2) to increase the patient's O2 uptake. It is connected to an O2 source Oxygen administration hood, 77 and may be used concurrently with increased humidification and temperature control. It is designed to be used for patients adverse A paediatric to oxygen delivery devices such as a nasal cannula or face mask. This device may include the tubing, a diffuser (to disperse the flow of incoming O2), O2 concentration and humidity sensors. This is a reusable device. A flexible enclosure designed to cover the bed of a neonatal or small child to provide an enriched environment of oxygen (O2) to increase the patient's O2 uptake. It is connected to an O2 source and may be used concurrently with increased humidification and Oxygen administration tent, 78 temperature control. It typically consists of a metal frame covered with transparent plastic, the tubing, and may have built-in B neonatal/paediatric humidification. It is used for the treatment of breathing disorders in infant and paediatric patients permitting them movement without restriction. This is a reusable device. A bed with appropriate size for children (typically up to 12 years of age) that incorporates safety canopy tops, fixed endrails, and 79 Paediatric bed moveable and latchable siderails. It allows children complete freedom in bed without the danger of falling out, yet allows staff access B to the patient. Paediatric beds are not appropriate for neonates/infants. A sterile assembly consisting of multiple collection containers (typically five connected flexible bags) of smaller volume than those used in adult sets. It is used for the storage of adult donor blood which is decanted from a normal adult size pack into this device in 80 Paediatric blood donor set B order to create smaller paediatric volume packs for infusion. The individual paediatric packs are then separated and sealed for later infusion. This is a single-use device. A sterile tube intended to be used during open heart surgery on a paediatric patient (e.g., neonatal, infant) to access the arterial or venous vasculature surrounding the heart (i.e., intended for both venous and arterial access), to serve as a channel intended to be Paediatric cardiopulmonary bypass 81 connected to an extracorporeal circuit for the transport of blood to or from a cardiopulmonary bypass system (heart-lung machine) C cannula circuit where the blood is pumped and oxygenated. It is typically a reinforced polymer tube which may include accessories/devices dedicated to introduction/function (e.g., introducer/connector). This is a single-use device. A mains electricity (AC-powered) device designed to support a paediatric patient in a seated position to facilitate dental examination, treatment, and/or minor surgery procedures. It is typically adjustable in height to enable healthcare staff to perform procedures while standing. It usually includes head and armrests, a reclining back that may be tilted from a vertical to a horizontal position, and 82 Paediatric dental chair, electric B has rotating capabilities; some types can be programmed to several standard positions. Devices intended for dental examination and/or treatment (e.g., lights, irrigation) may be attached as components of the chair, or stand separately as self-supported, wall- or ceiling-mounted units. A manually- or hydraulically-powered device designed to support a paediatric patient in a seated position to facilitate dental examination, treatment, and/or minor surgery procedures. It is typically adjustable in height to enable healthcare staff to perform procedures while standing. It usually includes head and armrests, a reclining back that may be tilted from a vertical to a horizontal 83 Paediatric dental chair, mechanical B position, and has rotating capabilities; some types can be programmed to several standard positions. Devices intended for dental examination and/or treatment (e.g., lights, irrigation) may be attached as components of the chair, or stand separately as self- supported, wall- or ceiling-mounted units. A standing platform for a child designed to slant the surface on which the feet are placed to create a slope angle to therapeutically stretch the ankle plantar flexion muscles/tendons. It is intended to be used in the treatment of various medical conditions (e.g., 84 Paediatric dorsiflexion slant board A congenital, neurological, post-traumatic) where tendon tightness and muscle contracture affect the ability to dorsiflex the foot, possibly leading to an abnormal gait. It is typically made of synthetic polymer materials. This is a reusable device. An electrically-powered optic device designed for screening for strabismus and amblyopia risk in children (aged 2 to 8 years) by using Paediatric strabismus screening retinal reflections of polarized laser light to/from both eyes simultaneously. It consists of a self-contained unit which includes a 85 B scanner visually enticing interface for the child to look at, and provides a result, in the form of a recommendation for referral to an ophthalmologist, if an abnormality is detected. A collection of devices intended to be used to collect and analyse a paediatric urine specimen for multiple clinical chemistry analytes (e.g., ketones, glucose and pH). It consists of a specimen collection undergarment (nappy or diaper) worn by the patient, and Paediatric urine collection/analysis 86 quantitative test strips for various clinical chemistry analytes. Results are analysed visually or with dedicated interpretive software A kit (not included). It is intended to be used at the point-of-care by a healthcare professional, or at home by a caregiver. This is a single- use device. A sterile, thin, flexible, hollow cylinder designed as a paediatric or neonatal enteral feeding tube with an integrated temperature sensor that continuously measures oesophageal temperature. It is typically intended to provide gastric feeding or deliver oral Paediatric-temperature 87 medication via a nasogastric or orogastric route, and to capture the oesophageal temperature for a period (e.g., up to 30 days) via a B nasogastric/orogastric tube thermistor sensor located near the distal tip. It is available in various diameters and may connect to a compatible patient monitoring device. This is a single-use device. A sterile, single-strand (monofilament), synthetic, bioabsorbable thread made from polyglyconate (prepared from a copolymer of glycolic acid and trimethylene carbonate) intended to join (approximate) the edges of a soft-tissue wound or incision by stitching or 88 Polyglyconate suture to ligate soft tissues (especially in paediatric cardiovascular surgeries). It may include an attached needle intended to be disposed of D after single use. The thread provides extended temporary wound support, until the wound sufficiently heals to withstand normal stress, and is subsequently absorbed by hydrolysis. This is a single-use device. A device designed to emit a blue light in the visible wavelength of around 425-475 nm to treat neonatal jaundice (or hyperbilirubinemia). It consists of a fibreoptic-light source that connects through a flexible fibreoptic cable to a transparent blanket- Blanket/pad infant phototherapy 89 like wrap or pad which emits the light and covers or encloses the neonate's body. Exposure to this device will alter the bilirubin B unit through photo oxidation and configurational and structural isomerization allowing the body function to dispose of it naturally. This device can be suitable for home-use. A fixed (non-adjustable) device designed with a mattress or cushions containing air, water, gel, or other appropriate material used for the continuous care of newborns, and sick and/or premature babies. It has a size to suit such patients and provide environmental 90 Flotation therapy bed, neonatal B conditions (e.g., softness, illumination levels) appropriate for a neonate, as well as good working conditions for the healthcare staff; the bed is frequently mounted on wheels and may include or permit attachments for/to a baby warmer.A mobile, mains electricity (AC-powered) unit designed for the cleaning and high-level disinfection of a range of medical devices (e.g., operating tables, operating lights, neonatal incubators, medical beds, chirurgical instruments) using steam. It includes an 91 Mobile steam washer/disinfector electronically controlled boiler unit, for steam generation; hosing, for transfer of the steam; and a hand-held steam application C device, typically including accessories (e.g., brush, nozzle, mop), in order to effectively direct steam onto the medical device being disinfected. An assembly of battery-powered devices designed to record and analyse the faint sounds hair cells in the inner ear emit [otoacoustic emission (OAE)] in response to a stimulus (e.g., click, tone burst, pure-tone signals) to test for a deficiency of function in the ear Otoacoustic emission system, during diagnostic evaluation and/or neonatal screening. It typically consists of a portable programmable unit, an OAE probe, and 92 B battery-powered eartips. The stimulus signal is emitted via the probe inserted into the ear canal and the response is recorded via a microphone in the probe; OAEs are absent/reduced in patients with hearing loss. The system may be combined with other audiological devices (e.g., tympanometer, ABR device). An assembly of mains electricity (AC-powered) devices designed to record and analyse the faint sounds hair cells in the inner ear emit [otoacoustic emission (OAE)] in response to a stimulus (e.g., click, tone burst, pure-tone signals) to test for a deficiency of function in Otoacoustic emission system, line- the ear during diagnostic evaluation and/or neonatal screening. It typically consists of a programmable unit, an OAE probe, and 93 B powered eartips. The stimulus signal is emitted via the probe inserted into the ear canal and the response is recorded via a microphone in the probe; OAEs are absent/reduced in patients with hearing loss. The system may be combined with other audiological devices (e.g., tympanometer, ABR device). A mains electricity (AC-powered) device designed to emit a blue light in the visible wavelength of around 425-475 nm to treat neonatal jaundice (hyperbilirubinemia). It consists of an overhead lamp consisting of several, daylight, cool white, blue, or special blue 94 Overhead infant phototherapy unit fluorescent light tubes and a Plexiglas shield placed between the phototherapy lights and the newborn to filter out ultraviolet (UV) B radiation. Exposure to this device will alter the bilirubin through photo-oxidation, and configurational and structural isomerization, allowing the body to dispose of it naturally. It will typically have a built-in timer, but some may have a separate timer unit connected. A device worn to cover and protect the eyes of a patient or user from potentially harmful rays [e.g., ultraviolet (UV)] to which parts, Phototherapy eye protector, or all, of their body is intentionally exposed during light therapy treatment. It will typically be designed as goggles, special spectacles, 95 A reusable or a mechanical mask-like shield with properties to block or inhibit the transmission of rays to the eyes. It will come in a variety of sizes, e.g., premature infant, neonatal, child, and adult. This is a reusable device. A device worn to cover and protect the eyes of a patient from potentially harmful rays [e.g., ultraviolet (UV)] to which their body is Phototherapy eye protector, single- intentionally exposed during light therapy treatment. It will typically be designed as a mechanical mask-like shield with properties to 96 A use block or inhibit the transmission of rays to the eyes. It will typically be made of soft materials in a variety of sizes, e.g., premature infant, neonatal and affix to the head using bands, hooks, Velcro fasteners, and/or adhesive fasteners. This is a single-use device. A non-sterile device intended to be integrated within a ventilator breathing circuit and used in conjunction with a heated respiratory humidifier (from which it draws its power) to maintain the temperature of inspiratory gases during ventilation of an infant/neonate. It 97 Respiratory gas heating wire, infant C typically consists of a compact heating unit and a length of heated wire which is integrated within the lumen of a neonatal/paediatric breathing circuit tube. This is a reusable device. A mains electricity (AC-powered) device intended to continuously measure and display respiratory variables associated with the Stationary pneumatic high- operation of a stationary pneumatic high-frequency ventilator. Measurements include proximal airway pressure, high-frequency 98 frequency ventilator respiration percussive rates, mean airway pressures and inspiratory and expiratory times. It is typically equipped with audible and/or visual C monitor alarms that are triggered when respiratory parameters drop below or exceed pre-set limits, and connectors for attachment to the ventilator. It may be used for neonatal, paediatric, and adult patients. A mains electricity (AC-powered) device designed to precisely drive the plunger of a syringe down its barrel to infuse a solution when it must be administered with a high degree of volume accuracy and rate consistency. Because of the lower flow settings and flow resolution (e.g., 0.1 ml/hr), it is especially appropriate for neonatal, infant, and critical care applications in which small volumes of 99 Syringe pump C concentrated drugs are to be delivered over an extended period. It can also be used to administer epidural analgesia. It will typically have internal batteries that allow the device to operate for a short period of time when no line power is available (e.g., during transport or a power outage). An assembly of devices designed to perform thoracic bio-impedance measurements to continuously record the distribution of air across 4 quadrants of the lungs, commonly of a neonatal/infant patient. It consists of a mobile support/trolley, a mains electricity (AC- Thoracic electrical impedance 100 powered) central unit with a display, and may include the appropriate patient electrodes. It is intended to detect changes in lung B segmentography system ventilation at a regional level, to assist in the diagnosis of lung conditions (e.g., atelectasis, pneumothorax, misplacement of endotracheal tube, effects of surfactant administration). A non-sterile, noninvasive component of a thoracic electrical impedance segmentography system intended to be attached to the skin Thoracic electrical impedance surface of a neonatal/infant patient, to transmit electrical signals back to the system, for the continuous recording of the distribution 101 segmentography system electrode of air across 4 quadrants of the lungs to assess a variety of pulmonary conditions/treatments (e.g., atelectasis, pneumothorax, B array endotracheal tube misplacement, effects of surfactant administration). It is a dedicated configuration of multiple electrodes. This is a single-use device. A non-sterile electronic device exclusively intended for noninvasive measurement of intracranial pressure in a neonatal patient. Transcutaneous intracranial Sometimes referred to as a fontanometer, it typically consists of a sensor, designed to be topically applied to the fontanel, and a 102 C pressure sensor cable, intended to be connected to an appropriate monitor to allow readings to be displayed and/or recorded. It may include a distal balloon to allow pressure baselines to be set. This is a reusable device. An electrically-powered device designed to detect and display the heart rate of a neonate, typically within the first few hours after 103 Wearable neonatal heart rate meter delivery. It consists of a display screen with sensor arms on each side, which are placed around the torso of the newborn. This is a B reusable device. A piece of clothing (e.g., baby grow) intended to be worn by an infant affected by an infectious or infection-susceptible skin condition (e.g., eczema, psoriasis, epidermolysis bullosa) to help manage the condition by reducing microbial proliferation through fabric. It is 104 Antimicrobial infant garment B constructed of a material which can prevent/control microbial growth (e.g., silk treated with a silica–ammonium chloride compound). It is available in various sizes for daily use in the home or healthcare facility. This is a reusable device. A large bath intended to be filled with heated water for use before and/or during child birth. It may be used to deliver the baby under 105 Birthing bath water and/or to provide a comfortable environment for the expecting mother prior to birth. The device may also include specific A features such as connectors and diagnostic attachments. A mains electricity (AC-powered) device designed for total elimination and/or inactivation of microorganisms from medical/dental devices and related products using boiling water as the sterilizing agent. It typically consists of a container intended to be filled with 106 Boiling water sterilizer B water, in which devices are submerged, and an apparatus to boil the water for a specific period. The device is almost exclusively used in remote areas, at home (e.g., for baby bottle sterilization), and/or in emergency situations.A bed designed for newborn babies. It is usually an open rectangular receptacle, and mounted on a wheeled framework (trolley). It is 107 Newborn-infant bed padded or lined with appropriate bedding and used mostly as the general-purpose or standard baby bed in birthing departments. A A source of additional heating may be provided to the newborn. A flexible, form-shaped device that is placed over a patient's nose and mouth to direct ambient air, or medical oxygen (O2) and air, from a resuscitator to the upper airway and lungs. It is typically made of non-conductive sterilizable materials (e.g., silicone) that will 108 Resuscitator face mask, reusable create a gastight seal against the face. It will typically include a 15 mm and/or 22 mm connector and is available in a range of sizes B (baby to adult). It will be directly attached to the resuscitator and held in place on the patient's face by the operator. This device is intended for use with a breathing resuscitator but may be used for the delivery of anaesthesia gases. This is a reusable device. A non-sterile, flexible, form-shaped device that is placed over a patient's nose and mouth to direct ambient air, or medical oxygen (O2) and air, from a resuscitator to the upper airway and lungs. It is typically made of non-conductive sterilizable materials (e.g., silicone) that will create a gastight seal against the face. It will typically include a 15 mm and/or 22 mm connector and is available in a 109 Resuscitator face mask, single-use B range of sizes (baby to adult). It will be directly attached to the resuscitator and held in place on the patient's face by the operator. This device is intended for use with a breathing resuscitator but may be used for the delivery of anaesthesia gases. This is a single-use device. A mains electricity (AC-powered) bed specifically designed for a newborn, sick, or premature baby that requires additional heating provided by a heating pad system. It is typically ergonomically designed for the attending/nursing staff or parents and the motorized 110 Warming infant bed, adjustable B mechanism is used to electrically adjust the height and possibly tilt the bed to provide better access to the baby. It may be equipped with features such as shelves, drawers, a canopy, and is typically used in the maternity department. A non-adjustable bed (has a fixed height and mattress platform) specifically designed for a newborn, sick, or premature baby that requires additional heating provided by a heating pad system. It is typically ergonomically designed to provide good access to the 111 Warming infant bed, non-adjustable B baby by the attending/nursing staff or parents. It may be equipped with features such as shelves, drawers, a canopy, and is typically used in the maternity department. A device which is formed as a flat or contoured fitted cushion made of soft, non-irritating materials designed to protect the patient 112 Bedrail pad from coming into contact with the bedrails and inadvertently hurting or injuring themselves. It will be mainly used for patients that A have little self-control, infants and very young children. This is a reusable device. A portable device intended to be used in conjunction with a light meter to test a blanket/pad infant phototherapy unit. The Blanket/pad infant phototherapy phototherapy unit is typically positioned over specific areas of the test device at set distances to provide a measurement of light, such 113 B unit tester as average light output. It typically consists of a plastic stencil-like shape designed so the radiometer may fit at a number of positions. It is intended to be used by a healthcare professional in a clinical setting. A sterile, intravascular administration set used to remove a diseased infant's blood and replace it with fresh donor blood or plasma. The device typically includes a needle or catheter, tubing, a flow regulator, a drip chamber, an infusion line filter, a stopcock, 114 Blood transfusion set, exchange B connectors between parts of the set, a side tube with a cap to serve as an injection site, and a hollow spike to penetrate and connect the tubing to an intravenous (IV) bag or other infusion fluid container. This is a single-use device. An instrument designed to measure the radiant flux (radiant power) in the spectral range of 400 to 500 nm (i.e., blue) during bilirubinemia treatment for newborns and infants. It typically includes a pre-filter intended to remove wavelengths of light not in the 115 Blue light radiometer 400-500 nm range (e.g., infrared light); a primary detector consisting of a temperature-stabilized, solid-state [e.g., selenium (Se) or B indium-gallium-arsenide] device used to detect radiation; electronic circuits including an amplifier and a electric meter; a power source (e.g., a battery); and a display showing the results either in analogue or digital format. A flexible tube with an inflatable balloon designed to create or enlarge the atrial septal defect found in the hearts of infants with Cardiac septostomy catheter, 116 congenital cardiac malformations. This allows interatrial blood mixing in infants with transposition of the great vessels. This is a single- C balloon use device. A flexible tube with a collapsible blade at the distal end that, once in situ, can be raised to an acute angle by the surgeon operating an actuation lever at the proximal end for a blade atrial septostomy (BAS) procedure. It is used to enlarge the interatrial opening in cases 117 Cardiac septostomy catheter, blade of mitral atresia (a septal defect found in the hearts of infants) or unsuccessful or insufficient balloon atrial septostomy. This C procedure allows interatrial blood mixing in infants with congenital cardiac malformations. It is typically made of plastic and high- grade stainless steel materials. This is a single-use device. A mains electricity (AC-powered) unit designed to provide an enclosed controlled environment to maintain appropriate temperature and humidity levels mainly for premature infants and other newborns who cannot effectively regulate their body temperature. It typically consists of a clear removable plastic hood with a mattress. It typically includes a means to warm the infant such as providing 118 Conventional infant incubator C heated air (either by natural flow or forced) or through a warm water mattress; temperature controls that work automatically either by measuring the air temperature or through a temperature sensor attached to the infant skin; and humidity controls. The device is intended to remain in a hospital ward. A custom-made helmet-like device intended to be worn on the head of an infant with an abnormal head shape (e.g., due to plagiocephaly, brachycephaly, scaphocephaly), or after craniosynostosis repair surgery, to apply pressure to the cranium and improve cranial symmetry/shape during growth over a period of months. It is made of durable materials (e.g., plastic, solid foam) and is 119 Cranial orthosis B designed with patient-specific characteristics (e.g., size, shape) based on head measurements (e.g., clinical pictures, 3-D scans, casts). It is typically worn during daily activities and sleep. This is a single-patient device that can be reapplied during the treatment period (reusable) before being discarded. A portable mains electricity (AC-powered) device, which may include rechargeable batteries, intended to assist noninvasive ventilation (i.e., without use of an artificial airway) using bi-level positive airway pressure (BPAP) during spontaneous respiration for adult/child (non-infant) patients affected by obstructive sleep apnoea (OSA), and/or to treat patients with conditions requiring 120 Home BPAP unit C respiratory assistance in the home [e.g., chronic obstructive pulmonary disease (COPD)]. It is a small desktop unit, which may include a built-in humidifier, intended to be used with a separate nose/mouth mask. The device is intended for use in the home but may also be used in healthcare facilities. A sterile, water-based, salt solution (e.g., sodium chloride isotonic solution) intended for alternative use in multiple applications including inhalation therapy, moisturizing and washing/irrigation of the eyes, nose and ears, and wound cleansing; it is not dedicated 121 Multi-purpose saline solution to a specific application or part of the anatomy. It is typically available in a squeeze bottle for self-administration or application to B infants for preventive or symptomatic care. It is normally available (non-prescription) over-the-counter (OTC) for home use. After application, this device cannot be reused.A raised device consisting of a platform with a full-body length top surface (this may be slightly concave and padded to prevent the patient easily rolling off) mounted on a foldable frame with legs designed to support an infant, child or an adult during nappy (diaper) 122 Nappy changing table, portable A changing. The device is used primarily for a patient with a disability who is incontinent and requires regular changing of their nappies. It is designed to be portable for transport to different locations. A portable, hand-held, battery-powered suction device designed to enable an adult to gently suction and clear excessive mucus from the nasal passages of an infant or child to facilitate easier breathing. It consists of a handgrip that contains the batteries, a small 123 Nasal aspirator, electric electric pump that creates the suction, and typically has a silicone nozzle attached to a detachable, washable, collection cup at the A distal end. It is designed for domestic use and is typically applied superficially the nasal opening (i.e., not inserted into the nasal cavity). This is a reusable device. A mains electricity (AC-powered) unit that functions similar to a standard infant incubator but is open, having low side walls and no top enclosure, giving instant access to the infant. Such infants are not premature but suffer from disorders where intensive care is 124 Open infant incubator required. This device is equipped with overhead heating lamp(s), oxygen therapy flowmeter, gas mixer, suction system, facilities for B infusion pumps, and other equipment. The main difference between this device and a closed infant incubator is the inability of this device to regulate the oxygen environment surrounding the occupant. A device designed for aspirating a small volume of liquid medicine so that it can be dispensed in single drops into a patient's mouth, 125 Oral medicine dropper typically an infant or small child. It is typically designed as a hollow tube, open at both ends, with an aspiration bulb attached to the A proximal end and a narrow opening at the distal end. It is usually made of glass or plastic with a rubber teat. This is a reusable device. A mains electricity (AC-powered) laboratory instrument designed for intermittent/periodic measurements of oxygen (O2) content in a breath and/or respiratory gas specimen. It usually requires manual aspiration of a quantity of gas into a sampling chamber and may 126 Oxygen breath analyser C operate according to one of several basic principles (e.g., paramagnetism, polarography). The device is used in pulmonary function tests and for measurements in critically ill patients, such as infants in incubators and patients breathing air with supplemental oxygen. A device that is a component of a medical gas pipeline system or a medical gas/vacuum pipeline system that has a gas-specific outlet connection for oxygen (O2). It is designed to be mounted to wall-mounted medical supply units, utility supply systems (ceiling pendants), or directly to a wall, and functions as the outlet assembly of a gas pipeline system to which the operator can connect and 127 Oxygen terminal unit A disconnect a device, typically anaesthesia systems, ventilators, respiratory devices, infant incubators, and other devices that require O2 to function as intended. On disconnection of the medical device from the outlet, it will self seal the gas pipeline system preventing gas leakage to the environment. A computerized instrument designed to assess lung volume, flow, and mechanical parameters (including airway compliance and resistance) in young children and infants. It is different from an adult version in absolute dimensions and in the special procedures Pulmonary function analysis system, required for adaption to the pediatric patient (e.g., use of a small constant-volume chamber in which the infant reclines for 128 B paediatric plethysmography, use of a pressure jacket to obtain forced exhalation); also, parameters that require subject cooperation (e.g., vital capacity, forced expiratory volume) can't be determined. The device is used for pulmonary function testing in diagnostic studies and for evaluation of diseases and chest deformities. An underlay intended to produce heat through chemical reaction typically used to warm and/or maintain the body temperature of neonates or infants. It is typically designed with a soft outer casing (e.g., a soft plastic) that contains a chemically-reactive-gel 129 Reactive-gel heating pad activated by the user (e.g., by breaking its inner enclosure) to provide a heat of approximately normal body temperature (e.g., 38° B Celsius) for a limited period. This device is typically used to maintain the body temperature of infant patients during transportation and may be x-ray translucent and magnetic resonance imaging (MRI) compatible. This is a single-use device. An assembly of devices designed to detect the cessation of breathing (apnoea) in infants and adults who are at risk of respiratory failure to alert a parent or attendant of the life-threatening episode(s). It alarms primarily upon the cessation of breathing timed from Respiratory apnoea monitoring the last detected breath, and may also include indirect methods of apnoea detection such as monitoring of heart rate and other 130 C system physiological parameters associated with respiration. It may print-out this data. It will typically include a mains electricity (AC- powered) monitoring unit with software, patient leads, and possibly a recorder to record, display, or print data on a patient's breathing condition. A mains electricity (AC-powered) bed designed to provide a motorized rocking movement for newborn babies to soothe the infant. 131 Rocking infant bed, electric B The motorized mechanism is control-adjustable to provide variable degrees of movement and speed. A hand-held, battery-powered device with a built-in light source, usually together with a lens, intended to be used to illuminate the Skin transilluminator, battery- skin and soft tissues, rendering them translucent for examination. It is typically used to examine subcutaneous and scrotal 132 C powered tissue/contents for lesions, and veins (e.g., on the scalp of an infant) for anatomical abnormalities. This device may also be known as a diaphanoscope, a phaneroscope or a light scanner. A hand-held, mains electricity (AC-powered) device with a built-in light source, usually together with a lens, intended to be used to 133 Skin transilluminator, line-powered illuminate the skin and soft tissues, rendering them translucent for examination. It is typically used to examine subcutaneous and C scrotal tissue/contents for lesions, and veins (e.g., on the scalp of an infant) for anatomical abnormalities. It can use varying forms of light depending upon the specific application. This device may also be known as a diaphanoscope, a phaneroscope or a light scanner. A circular or cylindrical device filled with fluid (e.g., water) intended to be bitten by a patient (infant or adult) to soothe gums during 134 Teething device, fluid-filled B the teething process. This is a reusable device. A circular or cylindrical device free of fluid and intended to be bitten by a patient (infant or adult) to soothe gums during the teething 135 Teething device, non-fluid-filled A process. This is a reusable device. An electrically-powered unit designed to provide an enclosed controlled environment to maintain appropriate temperature and humidity levels mainly for premature infants and other newborns who cannot effectively regulate their body temperature; it is 136 Transport infant incubator typically on wheels and also designed for transporting infants either outside or within the healthcare facility. It typically consists of a C clear removable plastic hood with a mattress and operates using mains electricity (AC-powered) when not in use for transportation. During transport, it is connected to an ambulance electrical outlet or is battery-powered from a battery pack. An assembly of mains electricity (AC-powered) devices intended to be used in conjunction with an audiometer to reward an Visual-reinforcement-audiometry infant/child during instrumentation conditioned reflex audiometry/play audiometry. It includes hardware (e.g., monitor, lights) 137 B reward system intended to give the child a visual reward, and dedicated operating software; it may include additional controls (e.g., foot-switch) and toys. It is intended to be operated by the healthcare professional to build the conditioned response during auditory testing.Name of Category: Oncology Total No. of Devices: 78ONCOLOGY Classification India as per first S.no Device Name Intended Use schedule part 1 MDR 2017 The FerriScan R2-MRI Analysis System is intended to measure liver iron 1 FerriScan R2-MRI Analysis System concentration to aid in the identification and monitoring of non- C transfusiondependent thalassemia patients receiving therapy with deferasirox. Activated Oxygen (Ozone) Activated oxygen, also known as Ozone (O3), is a safe 2 Activated-oxygen generator disinfecting agent that SoClean uses to get rid of CPAP bacteria, mold or viruses C inside your CPAP equipment Alternating electric field Alternating electric fields therapy is a novel anticancer treatment that disrupts 3 antimitotic cancer treatment C tumor cell mitosis. system generator Alternating electric field Alternating electric fields therapy is a novel anticancer treatment that disrupts 4 antimitotic cancer treatment C tumor cell mitosis. system transducer array A sterile buffer solution intended to be used exclusively for bladder instillation to 5 Bladder instillation buffer solution help create an optimal environment necessary for the effective treatment of B superficial bladder cancer with a chemotherapy agent. A sterile, sharp bevel-edged, hollow tubular metal instrument that is used to 6 Brachytherapy needle inject radionuclide into a body cavity or tissue as a source of nuclear radiation C for cancer therapy (brachytherapy). An assembly of mains electricity (AC-powered) devices intended for three- Breast 3-D infrared 7 dimensional (3-D) breast imaging and breast vascular analysis, typically used with C imaging/vascular analysis system mammography screening to perform a breast cancer risk examination. An interpretive software program intended to be used in the assessment of risk Cancer risk assessment 8 for developing cancer (e.g., breast, ovarian, prostate, lung, liver, gastric, C interpretive software pancreatic, colorectal) A collection of non-sterile devices intended to collect exfoliated colonic cells 9 Colonic cytology sampling set (colonocytes) from the surface of human rectal mucosa for colorectal cancer B investigation and/or patient screening. An electrically-powered instrument intended to be used for the visual 10 Colposcope B examination and treatment of the female genitalia A hand-held, manual, ophthalmic surgical instrument intended to be used to cut 11 Blepharoplasty scissors eyelid tissue during plastic surgery of the eyelids (blepharoplasty). It is not A intended for intraocular surgery. A sterile collection of disposable devices used in conjunction with a cryosurgical unit as well as monitoring and other devices to perform a surgical technique that 12 Cryosurgical set C involves freezing a targeted area of tissue to damage and destroy cancer cells in the unwanted portions. A circular band intended to be used to enhance the mechanical stability of a 13 Capsular tension ring subluxated crystalline lens capsule in the presence of weak or absent supporting A zonules. An assembly of devices designed for the treatment of tumours and the 14 Electro cancer therapy system destruction of their cancerous cells using low-voltage direct current of small C intensity delivered via electrodes placed across the effected body area. A portable assembly of devices designed to electronically measure, map, Electronic clinical breast document and store information about breast lesions/masses with regard to 15 C examination system shape, size, location, consistency/relative hardness during a clinical breast examination (CBE) A collection of devices designed to remove superficial tissue from the mucous 16 Endocervical aspirator membrane lining the cervical canal (endometrium) through manually-powered C suction. An assembly of portable devices designed to apply low-intensity, intermediate- Alternating electric field frequency (100-300 kHz) alternating electric fields to treat certain forms of 17 antimitotic cancer treatment D recurrent or newly-diagnosed cancer; typically glioblastoma multiforme (GBM) system [malignant brain tumour].A collection of sterile surgical instruments and devices used for the reduction of a vertebral compression fractures (VCFs) caused by trauma, cancer, or 18 Balloon kyphoplasty kit C osteoporosis during a minimally invasive procedure commonly known as balloon kyphoplasty. A device that consists of preserved human or animal tissue, or a two or three- Brachytherapy radionuclide dimensional (3-D) tissue-equivalent model designed to simulate the functional, 19 A phantom, anthropomorphic physical, or a combination of these characteristics of normal or diseased human organs. A seat, typically with legs, that is a component of a therapeutic accelerator system, and used to support and position a seated patient during radiation 20 Accelerator system chair C therapy treatments involving the use of either a medical linear accelerator or non-linear accelerator. A device that is a component of a linear or a non-linear accelerator system that functions as the primary control panel typically for a betatron or cyclotron Accelerator system operator 21 system. Depending on the configuration, it can include hardware and software C console that allows for image and/or data display, related processing, analysis functions, data archiving and retrieval. An instrument specifically designed to be used to check the calibration and Accelerator system quality 22 performance of linear and non-linear medical accelerator systems used for C assurance device radiation therapy applications, for quality assurance (QA) purposes A device designed to be worn on the wrist(s) for the application of pressure to 23 Acupressure wristband the Nei-kuan (P6) acupressure point, the area identified to help relieve the B sensation of nausea. Anorectal brachytherapy system A manual brachytherapy applicator specifically designed to be used in radiation 24 C applicator, manual therapy treatments of the rectum and/or anus. Anorectal brachytherapy system A remote afterloading brachytherapy applicator specifically designed for use in 25 C applicator, remote-afterloading radiation therapy treatments of the rectum and/or anus. A woman's undergarment which includes antimicrobial properties designed to: Antimicrobial postsurgical 26 1) support and/or contour the breast(s) or hold a dressing in place after surgical A brassiere intervention (e.g., thoracic surgery, mastectomy, lumpectomy); intended for use during medical treatment (e.g., chemotherapy) or be used to Antimicrobial postsurgical female protect the skin following treatment with a medication (e.g., ointment, cream). It 27 A underpants is specifically designed for patient support/comfort in the home or healthcare facility. This is a reusable device. A manual brachytherapy applicator specifically designed to be used in radiation therapy treatments of the bile duct. It is an individual device designed to Bile duct brachytherapy system 28 facilitate manual placement, e.g., puncture, endoscopically guided or diagnostic C applicator, manual imaging system guided placement, and removal of single or multiple radioactive sources at a treatment site within the bile duct Bile duct brachytherapy system A remote afterloading brachytherapy applicator specifically designed for use in 29 C applicator, remote-afterloading radiation therapy treatments of the bile duct Bladder brachytherapy system A manual brachytherapy applicator specifically designed to be used in radiation 30 B applicator, manual therapy treatments of the bladder. Bladder brachytherapy system A remote afterloading brachytherapy applicator specifically designed for use in 31 C applicator, remote-afterloading radiation therapy treatments of the bladder. A sterile photochemical agent (psoralen) intended to be used in conjunction with Blood photochemical treatment 32 ultraviolet A (UVA) irradiation to eliminate nucleated cells from blood or blood C agent components (e.g., plasma, leukocyte-enriched blood fraction). A non-tissue configured model designed to mimic the functional/physical Brachytherapy radionuclide characteristics of normal or diseased human organs during performance 33 A phantom, test object evaluations of brachytherapy system components or radiation therapy treatment planning devices. A sterile, bioabsorbable device designed to separate radioactive sources of the 34 Brachytherapy source spacer seed type that are permanently implanted in close proximity to a selected C localized tumour, to increase the distribution of radioactivity to the tumour.A mains electricity (AC-powered) device (a chair or stool) that is a component of a brachytherapy system and which is specifically designed to support and 35 Brachytherapy system chair position a patient during brachytherapy radiation treatments given by either a B manual applicator or a remote afterloading brachytherapy system applicator. It will typically be height-adjustable and may have a reclining back. A component of a remote afterloading brachytherapy system consisting of a shielded vault, and associated source retraction and extrusion mechanisms, Brachytherapy system remote alarms, and related mechanical, electronic and software controls, used to shield 36 C afterloading source safe the brachytherapy sources in order to protect system operators, brachytherapy patients and others from the continuous emissions of the radioactive brachytherapy source(s) when they are not in use. Brachytherapy system remote A tube or hose-like catheter with connectors at both ends used to interface the 37 B afterloading source transfer tube brachytherapy applicator to the remote afterloading system. A mains electricity (AC-powered) component of a remote-afterloading brachytherapy system intended to function as the primary control panel for the remote afterloader. It typically includes hardware and software that allows for Brachytherapy system remote- 38 information display and/or transfer, data processing, analysis, and information C afterloading operator console archiving functions; it may also be intended to interface with other devices (e.g., radiation therapy treatment planning computer) as part of a picture archiving and communication system (PACS). A device specifically designed to be used in radiation therapy treatments of the brain. It has individual or modular device configurations designed to facilitate Brain brachytherapy system 39 manual placement, e.g., puncture, endoscopically guided placement or D applicator, manual diagnostic imaging guided placement, and removal of single or multiple radioactive sources at a treatment site within the brain. A remote afterloading brachytherapy applicator specifically designed for use in Brain brachytherapy system radiation therapy treatments of the brain. It is designed for temporary 40 D applicator, remote-afterloading implantation within the body and serve as a guide for computer-controlled placement and removal of single or multiple radioactive sources in the brain. A strip or roll of fabric or plastic material applied to the breast or breasts for soft 41 Breast binder A tissue support. This is a single-use device. A sterile, remote-afterloading brachytherapy applicator specifically designed for use in radiation therapy treatments of the breast. It is typically designed for Breast brachytherapy system temporary implantation within the breast and serves as a guide for computer- 42 C applicator, remote-afterloading controlled placement and removal of single or multiple radioactive sources. Included are various types of applicators such as hollow needles, tubes, or catheters, and their associated components. This is a single-use device. A mains electricity (AC-powered) transilluminating device with a built-in light source using low intensity emissions of visible light and near-infrared radiation 43 Breast transilluminator (700 to 1050 nm) that is transmitted through the female breast to visualize D translucent tissue for the diagnosis of cancer, or other conditions, diseases or abnormalities. This device may also be known as a diaphanoscope. An assembly of mains electricity (AC-powered) devices designed for extracorporeal and/or intracorporeal (endosonography or endoscopic) 44 Breast ultrasound imaging system ultrasound imaging procedures involving the breast. It typically includes special C imaging tables used to optimize the ability to give reproducible images of the breast. A manual brachytherapy applicator specifically designed for temporary use in bronchial radiation therapy treatments. It is an individual or modular device Bronchial brachytherapy system 45 designed to facilitate manual placement, e.g., endoscopically guided placement, C applicator, manual or diagnostic imaging system guided positioning and placement, and removal of single or multiple radioactive sources at the treatment site(s). Bronchial brachytherapy system A remote afterloading brachytherapy applicator specifically designed for use in 46 C applicator, remote-afterloading bronchial radiation therapy treatments.A surgical, manually-operated, instrument that is inserted into the vagina and 47 Cervical cone knife designed for excising a sample of abnormal tissue, e.g., indicated by the presence C of precancerous changes, from the cervix. blunt surgical instrument used to scrape and retrieve cytological material from Cervical cytology scraper, the surface of the cervix (neck of the uterus) or vaginal area for pathological 48 A reusable examination and diagnosis, often for the detection of cervical cancer. This is a reusable device. A hand-held, manual, blunt surgical instrument designed to scrape and retrieve Cervical cytology scraper, single- cytological material from the surface of the cervix (neck of the uterus) or vaginal 49 B use area for pathological examination and diagnosis, often for the detection of cervical cancer. This is a single-use device. A manual brachytherapy applicator specifically designed to be used in cervical Cervical/intrauterine and/or intrauterine radiation therapy treatments. It is an individual or modular 50 brachytherapy system applicator, device designed to facilitate manual placement, e.g., puncture, endoscopically B manual guided placement or diagnostic imaging system guided placement, of single or multiple radioactive sources at a treatment site. A remote afterloading brachytherapy applicator specifically designed for use in cervical or intrauterine radiation therapy treatments. It is designed for temporary Cervical/intrauterine implantation within the body and serve as a guide for computer-controlled 51 brachytherapy system applicator, C placement and removal of single or multiple radioactive sources in the cervical or remote-afterloading intrauterine anatomy. This device includes a wide variety of applicators, e.g., hollow needles, tubes, or catheters, and their associated components. A furniture-like device designed as a partial or total enclosure to provide a class I 52 Class-I biological safety cabinet biosafety level (BSL) to the operator and the environment during the B manipulation of microorganisms and other biological hazardous materials. A furniture-like device designed as a partial or total enclosure to provide a class II biosafety level (BSL) to the operator, the product, and the environment during 53 Class-II biological safety cabinet C the manipulation of microorganisms and other biological hazardous materials (usually up to category 3 pathogens) A sterile flexible tube intended to deliver/remove radiation therapy sources into a coronary artery, typically into the lumen of an implanted stent, as part of a Coronary artery brachytherapy manual-afterloading brachytherapy system. It is introduced into the patient and 54 system applicator, manual- subsequently connected to the brachytherapy system source transfer device; it D afterloading includes radiopaque markers to monitor the position of the radiation source. Disposable devices associated with the procedure may be included (e.g., syringe, connectors). This is a single-use device. A device designed as a container to allow the safe deposit, collection and storage 55 Cytotoxic waste receptacle A of cytotoxic materials (e.g., chemotherapy/antineoplastic drugs). It may be used for general infusion, antibiotic delivery, chemotherapy, or pain 56 Elastomeric infusion pump system management in either a healthcare facility or in the home. This is a single-use B device. A mobile assembly of devices designed to apply electrical impulses to the tissue to enable electroporation, a phenomenon that induces alteration in the structure 57 Electroporation therapy system of cell membranes to increase their permeability and allow molecules that C usually cannot enter the cell membrane, such as drugs [electrochemotherapy (ECT)] and genetic materials [electrogenetherapy (EGT)], to reach the cytoplasm. A sterile, patient-contact component of an electroporation therapy system intended to fit onto the distal tip of an endoscope and connect to an electroporation therapy system generator to deliver electrical impulses to tissues Electroporation therapy system 58 during endoscopy as part of electroporation, a phenomenon that induces C endoscopic applicator alteration in the structure of cell membranes to increase their permeability and allow molecules that usually cannot enter the cell membrane, such as drugs [electrochemotherapy (ECT)], to reach the cytoplasm.A non-sterile endoscope with a highly flexible sleeve and distal tip intended for Externally-propelled flexible video the visual examination of the entire adult colon [lower gastrointestinal (GI) 59 B colonoscope tract].It is used for the screening of colorectal cancer and the detection of other diseases of the lower GI tract. This is a single-use device. An assembly of devices designed to produce and control heated fluids circulated Extravascular-circulation within a vessel applied to the body (e.g., vest, mattress, jacket, band, pad, body 60 D hyperthermia system wrap, catheter, probe) for systemic or localized heating to treat malignant tumours, benign growths, or other disease-related conditions. A vessel applied to the outside of the body (e.g., in the form of a jacket, vest, body wrap, cushion, blanket, or mattress) that incorporates tubing through which heated fluids are circulated for systemic or localized heating to treat Extravascular-circulation malignant tumours, benign growths, or other disease-related conditions. he 61 hyperthermia system applicator, applicator typically includes a thermometry component that monitors the A extracorporeal temperature of the applicator during operation. The applicator includes tubing, cables, and connectors that interface with the hyperthermia system's control unit during treatments. It is typically used in an oncology department. This is a reusable device. A component of a hyperthermia system that typically consists of catheter- enclosed tubing which is introduced into the body either manually or endoscopically. Heated fluid is circulated through the applicator's tubing for Extravascular-circulation localized heating to treat malignant tumours, benign growths, or other disease- 62 hyperthermia system applicator, related conditions. The applicator (also called an interstitial applicator or probe) D intracorporeal typically includes a thermometry component that monitors the temperature of the applicator during operation; it also includes tubing, cables, and connectors that interface with the hyperthermia system's control unit during treatments. It is typically used in an oncology department. This is a single-use device. A device in the form of a template that is shielded on one side and containing Eye brachytherapy system 63 grooved positions for manual brachytherapy sources on the other used for the A applicator, manual temporary topical application of brachytherapy sources to the surface of the eye. An externally-applied device intended to be used as an artificial substitute for 64 Facial prosthesis parts or sections of the face [e.g., nose, eye(s), eye brows, upper lip] to help B restore facial appearance. A non-automated, x-ray beam-limiting device that is a component of a therapeutic x-ray system and whose opening size/length/shutter assembly is Fixed-aperture therapeutic x-ray fixed. It is used in radiation therapy applications to limit the effects of scattered 65 C system collimator radiation and to protect the patient by limiting or eliminating exposure to non- target body areas during treatment. This device is specifically designed for use with an x-ray simulation or therapeutic x-ray system. An endoscope with a flexible inserted portion intended for the visual examination and treatment of the trachea, bronchi, and lungs. It is inserted through the mouth or nose during bronchoscopy. Anatomical images are 66 Flexible fibreoptic bronchoscope transmitted to the user by the device through a fibreoptic bundle. This device is B commonly used to diagnose lung infections, pneumonia, or lung cancer, and allows physicians to view the insides of the lungs and take biopsies and samples of secretions. This is a reusable device. An endoscope with a flexible inserted portion intended for the visual examination and treatment of the entire colon [lower gastrointestinal (GI) tract]. It is inserted through the anus during colonoscopy. Anatomical images are 67 Flexible fibreoptic colonoscope transmitted to the user by the device through a fibreoptic bundle. This device is B commonly used to examine the lining of the colon or to evaluate altered bowel habits, colonic cancer, polyps, diverticular disease, occult or frank blood in stools, or unexplained anaemia. This is a reusable device.An endoscope with a flexible inserted portion intended for the visual examination and treatment of the duodenum (the first part of the small intestine). It is inserted into the body through the mouth during duodenoscopy. 68 Flexible fibreoptic duodenoscope Anatomical images are transmitted to the user by the device through a fibreoptic B bundle. This device is commonly used to examine structures and mucous membranes of the duodenum, for conditions like ulcers, polyps and cancers. This is a reusable device. An endoscope with a flexible inserted portion intended for the visual examination and treatment of the oesophagus and the stomach. It is inserted into the body through the mouth during gastroscopy. Anatomical images are transmitted to the user by the device through a fibreoptic bundle. This device is 69 Flexible fibreoptic gastroscope B commonly used in the evaluation or treatment of unusual abdominal pain, bleeding, cancer, chronic heartburn, polyps, gastritis, ulcers, or hiatal hernia. Physicians may also use the device to obtain biopsies or perform other procedures. This is a reusable device. An endoscope with a flexible inserted portion intended for the visual examination and treatment of the mediastinum (the intrapleural space located behind the sternum). It is inserted into the body through an artificial orifice Flexible fibreoptic created by an incision made during mediastinoscopy. Anatomical images are 70 C mediastinoscope transmitted to the user by the device through a fibreoptic bundle. This device is commonly used to examine structures such as lymph nodes during a staging evaluation of lung cancer, or to establish the diagnosis of a tumour that is localized to the mediastinum. This is a reusable device. An endoscope with a flexible inserted portion intended for the visual examination and treatment of the sigmoid colon (the distal S-shaped part of the large intestine leading to the rectum). It is inserted through the anus during the procedure called a sigmoidoscopy or a proctosigmoidoscopy. Anatomical images 71 Flexible fibreoptic sigmoidoscope B are transmitted to the user by the device through a fibreoptic bundle. This device is commonly used to examine the structures and lining of the sigmoid colon and for indications of altered bowel habit, colonic cancer, polyps. This is a reusable device. A portable, non-electric, mechanically-powered device designed to be operated by healthcare professionals for dispensing a single dose of fluid medication (e.g., for antibiotic therapy, chemotherapy, analgesia). It consists of an empty reservoir intended to be filled with medication, a flow-rate regulator and a non- General-purpose infusion pump, 72 sterile (sterilizable) administration line intended to be connected to an infusion C mechanical, single-use catheter (not included) for intravenous (IV), subcutaneous, intramuscular, or epidural administration. It may include flow and fluid level mechanical indicators and may be worn by the patient in and outside of healthcare settings. This is a single-use device. An endoscope with a flexible inserted portion intended for the visual examination and treatment of the trachea, bronchi, and lungs. It is inserted through the mouth or nose during bronchoscopy. Anatomical images are transmitted to the user by the device typically through a fibreoptic bundle or a 73 Flexible ultrasound bronchoscope video system, and an ultrasound probe. The probe may be built-in or inserted D through a dedicated lumen so that its distal tip is positioned adjacent to that of the endoscope. It is commonly used to diagnose lung infections, pneumonia, or lung cancer, and allows physicians to view the insides of the lungs and take biopsies and samples of secretions. This is a reusable device. An endoscope with a flexible inserted portion intended for the visual examination and treatment of the entire colon [lower gastrointestinal (GI) tract]. It is inserted through the anus during colonoscopy. Anatomical images are typically transmitted to the user by the device through a fibreoptic bundle or a 74 Flexible ultrasound colonoscope video system and an ultrasound probe. The probe may be integral, or a separate C device inserted through a dedicated lumen so that its distal tip is positioned adjacent to that of the endoscope. It is commonly used to examine the lining of the colon, altered bowel habits, colonic cancer, polyps, diverticular disease, and unexplained anaemia. This is a reusable device.A non-electric, mechanically-powered (e.g., a spring mechanism) device designed for the continuous or intermittent infusion of medication, typically for antibiotic therapy, chemotherapy, or pain management by intravenous (IV), subcutaneous, General-purpose infusion pump, 75 intramuscular, or epidural routes. It is primarily designed to be worn by the C mechanical, reusable patient during ambulation in the home. It may be used for patient-controlled analgesia (PCA), and may include mechanical indicators for flow and fluid level status. This is a reusable device. An endoscope with a flexible inserted portion for endoscopic procedures of the airways and tracheobronchial tree (i.e., bronchoscopy). It is inserted through the mouth or nose during bronchoscopy. Anatomical images are transmitted to the Flexible video bronchoscope, user by a video system with a charge-coupled device (CCD) chip at the distal end 76 B reusable and the images showing on a monitor. It is commonly used to diagnose lung infections, pneumonia, or lung cancer, and allows physicians to view the insides of the lungs and take biopsies and samples of secretions. This is a reusable device. An endoscope with a flexible inserted portion intended for the visual examination and treatment of the entire colon [lower gastrointestinal (GI) tract]. It is inserted through the anus during colonoscopy. Anatomical images are Flexible video colonoscope, transmitted to a monitor for viewing by a video system with a charge-coupled 77 B reusable device (CCD) chip at the distal end of the endoscope. This device is commonly used to examine the lining of the colon or to evaluate altered bowel habits, colonic cancer, polyps, diverticular disease, occult or frank blood in stools, or unexplained anaemia. This is a reusable device. A sterile endoscope with a flexible inserted portion intended for the visual examination and treatment of the entire colon [lower gastrointestinal (GI) tract]. It is inserted through the anus during colonoscopy. Anatomical images are Flexible video colonoscope, single- transmitted to a monitor for viewing by a video system with a charge-coupled 78 C use device (CCD) chip at the distal end of the endoscope. This device is commonly used to examine the lining of the colon or to evaluate altered bowel habits, colonic cancer, polyps, diverticular disease, occult or frank blood in stools, or unexplained anaemia. This is a single-use device.Name of Category: Radiotherapy Total No. of Devices: 102CATEGORY: RADIOTHERAPHY S.No Name of the product Intended use INDIA . A medical charged-particle radiation therapy system is a Medical charged- device that produces by acceleration high energy charged 1 particle radiation C particles (e.g., electrons and protons) intended for use in therapy system radiation therapy. An absorbable perirectal spacer is composed of biodegradable material that temporarily positions the Absorbable perirectal 2 anterior rectal wall away from the prostate during C spacer radiotherapy for prostate cancer with the intent to reduce the radiation dose delivered to the anterior rectum. An absorbable material used to reduce radiation exposure of normal tissue during radiotherapy by implanting surgically Absorbable tissue 3 or percutaneously between tissue, internal organs, etc. , to D spacer for radiotherapy make a space between the malignant tumor and normal tissue. A manual brachytherapy applicator specifically designed for bile duct radiation therapy. An applicator designed to have a Applicator for bile duct configuration that facilitates manual placement (puncture or 4 C manual brachytherapy placement and removal using an endoscope or a diagnostic imaging system) of single or multiple therapeutic radiation sources in treatment sites in the bile duct. A manual brachytherapy applicator designed to facilitate manual placement (puncture or placement and removal Applicator for bladder 5 using an endoscope or a diagnostic imaging system) of C manual brachytherapy single or multiple therapeutic radiation sources in treatment sites in the bladder. A remote controlled brachytherapy applicator specifically designed for bladder radiation therapy. It is designed to be Applicator for bladder temporarily implanted in the bladder. It serves as a guide for 6 remote afterloading C computer-controlled temporary placement and removal of a brachytherapy single or multiple therapeutic radiation sources at treatment sites. A remote controlled brachytherapy applicator specifically designed for bile duct radiation therapy. It is designed to be Applicator for temporarily implanted in the bile duct. It serves as a guide 7 brachytherapy bile duct C for computer-controlled temporary placement and removal remote afterloading of a single or multiple therapeutic radiation sources at treatment sites. A remote controlled brachytherapy applicator specifically designed for uterine cervical or intrauterine radiation Applicator for therapy. It is designed to be temporarily implanted in the brachytherapy 8 body. It serves as a guide for computer-controlled C Cervical/endometrial temporary placement and removal of a single or multiple remote afterloading therapeutic radiation sources in the uterine cervix and endometrium. Page 1 of 12A general-purpose brachytherapy applicator used to Applicator for facilitate radiotherapy. A single or module applicator brachytherapy non- designed to facilitate manual placement (puncture, local 9 central circulatory placement, placement under endoscopy, and placement C general-purpose and removal using an image diagnostic system) of single or manual multiple therapeutic radiation sources in treatment sites in the non-central circulatory system. A general-purpose remote controlled brachytherapy Applicator for applicator used to facilitate radiotherapy. It is designed to brachytherapy non- be temporarily implanted in the body. It serves as a guide 10 central circulatory C for computer-controlled temporary placement and removal general-purpose of a single or multiple therapeutic radiation sources at remote afterloading treatment sites in the non-central circulatory system. A manual brachytherapy applicator specifically designed for temporarily use in bronchial radiation therapy. A single or module applicator designed to facilitate manual placement Applicator for bronchial (placement using an endoscope or positioning, placement 11 manual brachytherapy C and removal using a diagnostic imaging system) of single or applicator multiple therapeutic radiation sources in treatment sites. It may be designed to be standard in configuration or to handle specific radiation sources. A remote controlled brachytherapy applicator specifically designed for bronchial radiation therapy. It is designed to be temporarily implanted in the body. It serves as a guide for Applicator for bronchial computer-controlled temporary placement and removal of a 12 remote afterloading C single or multiple therapeutic radiation sources in the brachytherapy bronchus. This device group includes various applicators such as hollow needles, tubes, and catheters, as well as associated devices and connectors. A manual brachytherapy applicator specifically designed for esophagus radiation therapy. A single or module applicator designed to facilitate manual placement (puncture or Applicator for placement and removal using an endoscope or a diagnostic 13 esophagus manual C imaging system) of single or multiple therapeutic radiation brachytherapy sources in treatment sites in the esophagus. It may be designed to be standard in configuration or to handle specific radiation sources. Page 2 of 12A remote controlled brachytherapy applicator specifically designed for esophagus radiation therapy. It is designed to Applicator for be temporarily implanted in the esophagus. It serves as a esophagus remote guide for computer-controlled temporary placement and 14 C afterloading removal of a single or multiple therapeutic radiation brachytherapy sources. This device group includes various applicators such as hollow needles, tubes, and catheters, as well as associated devices and connectors. A template with a groove on the one side. The groove Applicator for eye shows the position of the brachytherapy source that is 15 C manual brachytherapy manually, temporarily delivered to the eye surface. The other side is shielded. A manual brachytherapy applicator specifically designed for uterine cervix or intrauterine radiation therapy. A single or Applicator for manual module applicator designed to facilitate manual placement 16 cervical/endometrial C (puncture, placement with an endoscope or a diagnostic brachytherapy imaging system) of single or multiple therapeutic radiation sources in treatment sites. A manual brachytherapy applicator specifically designed for rectal and/or anal radiation therapy. A single or module Applicator for manual applicator designed to facilitate manual placement 17 rectal/anal (puncture or placement and removal using an endoscope or C brachytherapy a diagnostic imaging system) of single or multiple therapeutic radiation sources in treatment sites in the rectum and/or anus. A manual brachytherapy applicator specifically designed for nasopharyngeal radiation therapy. A single or module Applicator for applicator designed to facilitate manual placement 18 nasopharynx manual (puncture, endoscopic placement or placement and removal C brachytherapy using a diagnostic imaging system) of single or multiple therapeutic radiation sources in treatment sites in the nasopharynx. A remote controlled brachytherapy applicator specifically Applicator for designed for nasopharyngeal radiation therapy. It is nasopharynx remote designed to be temporarily implanted in the body. It serves 19 C afterloading as a guide for computer-controlled temporary placement brachytherapy and removal of a single or multiple therapeutic radiation sources in the nasopharynx. A manual brachytherapy applicator specifically designed for neck radiation therapy. A single or module applicator Applicator for neck designed to facilitate manual placement (puncture, local 20 C manual brachytherapy placement or placement and removal using a diagnostic imaging system) of single or multiple therapeutic radiation sources in treatment sites in the neck tissues. Page 3 of 12A remote controlled brachytherapy applicator specifically designed for neck radiation therapy. It is designed to be Applicator for neck temporarily implanted in the neck tissues. It serves as a 21 remote afterloading C guide for computer-controlled temporary placement and brachytherapy removal of a single or multiple therapeutic radiation sources. A manual brachytherapy applicator specifically designed for pancreatic radiation therapy. A single or module applicator designed to facilitate manual placement (puncture, Applicator for pancreas endoscopic placement, or placement and removal using a 22 C manual brachytherapy diagnostic imaging system) of single or multiple therapeutic radiation sources in treatment sites in the pancreas. It may be designed to be standard in configuration or to handle specific radiation sources. A remote controlled brachytherapy applicator specifically designed for pancreatic radiation therapy. It is designed to Applicator for pancreas be temporarily implanted in the pancreas. It serves as a 23 remote afterloading C guide for computer-controlled temporary placement and brachytherapy removal of a single or multiple therapeutic radiation sources at treatment sites. A manual brachytherapy applicator specifically designed for prostate radiation therapy. A single or module applicator designed to facilitate manual placement (puncture or Applicator for prostate placement or removal with a trigger loading device, an 24 C manual brachytherapy endoscope or a diagnostic imaging system) of single or multiple therapeutic radiation sources in treatment sites in the prostate gland. It may be designed to be standard in configuration or to handle specific radiation sources. A remote controlled brachytherapy applicator specifically designed for prostate radiation therapy. It is designed to be Applicator for prostate temporarily implanted in the prostate gland. It serves as a 25 remote afterloading C guide for computer-controlled temporary placement and brachytherapy removal of a single or multiple therapeutic radiation sources. A remote controlled brachytherapy applicator specifically Applicator for designed for rectal or anal radiation therapy. It is designed rectal/anal remote to be temporarily implanted in the rectum or anus. It serves 26 C afterloading as a guide for computer-controlled temporary placement brachytherapy and removal of a single or multiple therapeutic radiation sources. A manual brachytherapy applicator specifically designed for lingual radiation therapy. A single or module applicator designed to facilitate manual placement (puncture, local Applicator for tongue placement or placement and removal using a diagnostic 27 C manual brachytherapy imaging system) of single or multiple therapeutic radiation sources in treatment sites in the tongue and the surrounding tissues. It may be designed to be standard in configuration or to handle specific radiation sources. Page 4 of 12A remote controlled brachytherapy applicator specifically designed for tongue or oral cavity radiation therapy. It is Applicator for tongue designed to be temporarily implanted in the tongue or the 28 remote afterloading C surrounding tissues. It serves as a guide for computer- brachytherapy controlled temporary placement and removal of a single or multiple therapeutic radiation sources. A manual brachytherapy applicator specifically designed for vaginal or transvaginal radiation therapy. A single or module applicator designed to facilitate manual placement Applicator for vaginal 29 (puncture, local placement, endoscopic placement or C manual brachytherapy placement and removal using a diagnostic imaging system) of single or multiple therapeutic radiation sources in treatment sites. A remote controlled brachytherapy applicator specifically designed for vaginal or transvaginal radiation therapy. It is Applicator for vaginal designed to be temporarily implanted in the body. It serves 30 remote afterloading C as a guide for computer-controlled temporary placement brachytherapy and removal of a single or multiple therapeutic radiation sources in the vagina. A remote afterloading brachytherapy applicator specifically Bile duct designed for use in radiation therapy treatments of the bile brachytherapy system 31 duct. It is designed for temporary insertion into the bile duct C applicator, remote- and serve as a guide for computer-controlled placement afterloading and removal of single or multiple radioactive sources. Bladder brachytherapy A manual brachytherapy applicator specifically designed to 32 system applicator, C be used in radiation therapy treatments of the bladder. manual A manual brachytherapy applicator designed exclusively for blood vessel radiotherapy. Most commonly, it is used to prevent formation of plaque, stenosis and restenosis in Blood vessel manual blood vessels after surgery. A single or module device 33 brachytherapy D designed to facilitate manual placement (placement and applicator removal under endoscopy or using an image diagnostic system) of single or multiple therapeutic radiation sources in the treatment site. A remote controlled brachytherapy applicator designed exclusively for radiotherapy in blood vessels. This treatment Blood vessel remote is used to prevent plaque formation. and stenosis in blood afterloading vessels after surgery. It is designed for temporary 34 D brachytherapy implantation in a blood vessel, and serves as a guide for applicator computer-controlled temporary placement and removal of single or multiple therapeutic radiation sources at treatment sites. A sterile, sharp bevel-edged, hollow tubular metal instrument that is used to inject radionuclide into a body 35 Brachytherapy needle C cavity or tissue as a source of nuclear radiation for cancer therapy (brachytherapy). A device that consists of preserved human or animal tissue, Brachytherapy or a two or three-dimensional (3-D) tissue-equivalent model 36 radionuclide phantom, designed to simulate the functional, physical, or a C anthropomorphic combination of these characteristics of normal or diseased human organs. Page 5 of 12A mains electricity (AC-powered) device (a chair or stool) that is a component of a brachytherapy system and which is Brachytherapy system specifically designed to support and position a patient 37 B chair during brachytherapy radiation treatments given by either a manual applicator or a remote afterloading brachytherapy system applicator. A component of a remote afterloading brachytherapy system consisting of a shielded vault, and associated source retraction and extrusion mechanisms, alarms, and Brachytherapy system related mechanical, electronic and software controls, used 38 remote afterloading C to shield the brachytherapy sources in order to protect source safe system operators, brachytherapy patients and others from the continuous emissions of the radioactive brachytherapy source(s) when they are not in use. The transfer tube, when attached to the applicator and the afterloading system, provides a continuous closed passage that allows for moving either a radioactive source(s) and/or Brachytherapy system positioning markers from the shielded source storage 39 remote afterloading C compartment of the remote afterloading brachytherapy source transfer tube system into appropriate positions within a brachytherapy applicator that has been positioned at a location either on the surface of, or within, the patient. A remote afterloading brachytherapy applicator specifically designed for use in radiation therapy treatments of the Brain brachytherapy brain. It is designed for temporary implantation within the 40 system applicator, C body and serve as a guide for computer-controlled remote-afterloading placement and removal of single or multiple radioactive sources in the brain. An applicator specifically designed for brain radiotherapy. A single or module applicator designed to facilitate manual Brain manual placement (puncture, placement under endoscopy, or 41 brachytherapy D placement and removal using an image diagnostic system) applicator of single or multiple therapeutic radiation sources in the brain. A remote controlled brachytherapy applicator designed Brain remote exclusively for brain radiotherapy for temporary implantation afterloading 42 in the body. It serves as a computer-controlled guide for D brachytherapy temporary placement and removal of a single or multiple applicator therapeutic radiation sources in the brain. A thin, sterile, semi-rigid or rigid metal tube that is inserted Breast ductography into the nipple of the female breast to inject a contrast 43 C cannula medium into the lactiferous ducts to enhance their visualization during a radiographic procedure. A single or module applicator designed to facilitate manual Central circulatory placement (puncture, local placement, placement under general-purpose 44 endoscopy or placement and removal using an image D manual brachytherapy diagnostic system) of single or multiple therapeutic radiation applicator sources in treatment sites in the central circulatory system. Central circulatory Intended to be temporarily implanted in the body. It serves general-purpose as a guide for computer-controlled temporary placement 45 remote afterloading D and removal of a single or multiple therapeutic radiation brachytherapy sources at treatment sites in the central circulatory system. applicator Page 6 of 12A device that places a radiation source manually or Central circulatory automatically at the treatment site in the central circulatory manual brachytherapy 46 system for providing a required radiation dose during D therapeutic radiotherapy. This device does not equip a remotely radionuclide system controlled radiation source transporter. A device for the central circulatory system to be placed permanently in the body for radiotherapy which is necessary for treatment and symptomatic therapy, and uses natural Central circulatory radioisotopes or radioisotopes produced by an accelerator permanent implant or a nuclear reactor. The radiation source, which is 47 manual brachytherapy D permanently placed manually, is designed to achieve therapeutic compatibility with tissues. The radiation source can be radionuclide source selected from the following forms – e.g., microsphere, globe, stent, seed, and wire-in order to generate low-energy photons, beta particles, or alpha particles. A device for the central circulatory system used as radiation Central circulatory source to deliver a high or low dose rate with an after- remote afterloading loading brachytherapy device designed for radiotherapy 48 brachytherapy D which is necessary for treatment and symptomatic therapy, therapeutic and uses natural radioisotopes or radioisotopes produced radionuclide source by an accelerator or a nuclear reactor. Central circulatory A device that places a radiation source temporarily at the remote afterloading treatment site in the central circulatory system for providing 49 brachytherapy D a required radiation dose during radiotherapy. This device therapeutic equips a remotely controlled radiation source transporter. radionuclide system A device for the central circulatory system that uses natural Central circulatory radioisotopes or radioisotopes produced by an accelerator temporary placement or a nuclear reactor, and is placed in the body temporarily, 50 manual brachytherapy and removed after the pre-determined treatment period. D therapeutic The radiation source, which is temporarily inserted radionuclide source manually, is supplied in various forms – e.g., encapsulated, sealed, plated, foiled, or embedded. Compact Thermoluminescence dosimeter (TLD) is used to measure 51 thermoluminescent the radiation dose emitted to the phantom, eyes and other B dosimetry electrometer organs with high radiosensitivity. The intended use of the device is for the treatment of cancer by tempeorary intraoperative or surface irradiation. Conformal The device contains radioactive material with activity up to 52 C Brachytherapy Source 200 mci and is indicated for treatment of temporary intraoperative, interstitial, intracavitary or surface application to treat selected localized tumors. A system used to generate high-temperatures and to control High-frequency 53 the provision of heat to the body in the treatment of C hyperthermia system malignant and benign tumors, or other diseases. Page 7 of 12A device that is specifically designed to be inserted in the Intra-vaginal organ vagina to properly position and fix the surrounding organs positioning device for such as uterine cervix, rectum, and urinary bladder for 54 B diagnostic imaging and image diagnosis or radiotherapy. This device is used to radiotherapy facilitate reproducible positioning for continuous image examination or continuous radiotherapy. A kit includes a puncture needle, a guide wire, and a guiding sheath for guiding probes (used for laser irradiation Laser irradiation 55 therapy, for example). Not all of the components are B therapy kit included; in some products, two or more of components are integrated into one. A light beam patient position indicator is a device that Light beam patient projects a beam of light (incoherent light or laser) to 56 B position indicator determine the alignment of the patient with a radiation beam. A low energy X-ray therapy system designed to treat adjacent tumor lesions with high dose X-rays by placing soft Living tissue 57 X-ray beams from 5 to 50 kV inside the tumor tissue. T It is C radiotherapy system used in both intraoperative radiation and stereotactic localized radiation therapy. A manual radionuclide applicator system is a manually Manual radionuclide operated device intended to apply a radionuclide source 58 B applicator system into the body or to the surface of the body for radiation therapy. Medical neutron A medical neutron radiation therapy system is a device 59 radiation therapy intended to generate high-energy neutrons for radiation C system therapy An assembly of devices using metal oxide semiconductor field-effect transistor (MOSFET) technology intended to be used for on-the-spot patient or anthropomorphic radiation MOSFET radiation dose verification and monitoring during radiation therapy 60 therapy dosimetry and radiology procedures. Applications typically include C system radiation oncology therapy and dosimetry, treatment plan verification for in vivo dosimetry, brachytherapy, intraoperative radiation therapy, image-guided radiation therapy, and research. Non-central circulatory A device that places a radiation source manually or manual brachytherapy automatically at the treatment site in the non-central 61 C therapeutic circulatory system for providing a required radiation dose radionuclide system during radiotherapy. A non-central cardiovascular device which is Non-central circulatory histocompactible and containing an isotope naturally permanent implant occurring or produced by an accelerator or a nuclear 62 manual brachytherapy C reactor, intended to be permanently implanted in the body therapeutic for radiation therapy requiring treatment or symptomatic radionuclide source treatment. Page 8 of 12A device for the non-central circulatory system used as Non-central circulatory radiation source to deliver a high or low dose rate with an remote afterloading after-loading brachytherapy device designed for 63 brachytherapy radiotherapy which is necessary for treatment and C therapeutic symptomatic therapy, and uses natural radioisotopes or radionuclide source radioisotopes produced by an accelerator or a nuclear reactor. Non-central circulatory A device that places a radiation source temporarily at the remote afterloading treatment site in the non-central circulatory system for 64 brachytherapy providing a required radiation dose during radiotherapy. C therapeutic This device equips a remotely controlled radiation source radionuclide system transporter. A non-central cardiovascular device containing an isotope Non-central circulatory naturally occurring or produced by an accelerator or a temporary placement nuclear reactor, intended to be temporarily implanted in the 65 manual brachytherapy C body and to be removed after a prescribed duration of therapeutic treatment. Used in brachytherapy, the device is placed and radionuclide source removed manually or under endoscopic observation. A mechanically-operated bed for radiotherapy designed to Non-powered adjust the patient's posture and immobilize the patient for 66 accelerator system B radiotherapy that uses a medical linear accelerator or non- table linear accelerator. A bed for radiotherapy designed to adjust the patient's posture and immobilize the patient for treatment that uses neutron rays that are generated from a nuclear reactor, etc. Non-powered neutron 67 It is equipped with a table top that fixes the posture, B therapy table pneumatic control, magnetic lock, crank, and lever for mechanical tabletop positioning control and table height control. A programmable bed for electric radiotherapy to adjust the patient's posture and immobilize the patient for treatment Radionuclide 68 that uses an after loading short-distance irradiation B brachytherapy table treatment apparatus that is operated manually or electrically. Non-powered remote A bed for radiotherapy designed to adjust the patient's 69 irradiation therapy posture and immobilize the patient for treatment that uses a B table remote radionuclide radiotherapy apparatus. A bed for radiotherapy designed to adjust the patient's Non-powered X-rays 70 posture and immobilize the patient for treatment that uses B radiation therapy table an X-ray therapy apparatus. A positron emission tomography (PET) system specifically Nuclear medicine designed to detect, record, quantify, and analyze the pattern 71 positron emission C of 511-keV photon emissions generated by annihilation from tomography system the decay of positron-emitting radiopharmaceuticals. A personal protection device that protects the eyes of the Operator radiation operator and other personnel from unnecessary exposure to 72 B protection spectacles primary radiation and scattered radiation associated with diagnosis and treatment. Page 9 of 12Patient positioning A device that is specifically designed to properly position device for breast and fix a female patient's breasts and chest for image 73 C diagnostic imaging and diagnosis, image-guided surgery, interventional therapy, or radiotherapy radiotherapy. Patient positioning A device that is specifically designed to properly position device for extremity 74 and fix a patient's arms and legs for image diagnosis, image- C diagnostic imaging and guided surgery, interventional therapy, or radiotherapy. radiotherapy The device that consists of frames, plates, or other parts, Patient positioning and is specifically designed to properly position and fix the device for pelvis 75 patient's abdomen and pelvic region for image diagnosis, B diagnostic imaging and image-guided surgery, interventional therapy, or radiotherapy radiotherapy. A device that consists of fixed or adjustable parts (e.g., Patient positioning frames and plates), and is specifically designed to properly device for whole body 76 position and fix the patient's whole body for image B diagnostic imaging and diagnosis, image-guided surgery, interventional therapy, or radiotherapy radiotherapy. Post Breast Biopsy A mammographic x-ray system is a device intended to be 77 Hemostatic Breast C used to produce radiographs of the breast. Compression Device A programmable bed for radiotherapy designed to adjust Powered neutron the patient's posture and immobilize the patient for 78 B therapy table treatment that uses neutron rays that are generated from the nuclear reactor, etc. A bed operate by programmable for electric radiotherapy Powered patient table designed to adjust the patient's posture and immobilize the 79 B for accelerator patient for radiotherapy that uses medical linear accelerator or non-linear accelerator. Powered radiation A powered radiation therapy patient support assembly is an 80 therapy patient support electrically powered adjustable couch intended to support a C assembly patient during radiation therapy A programmable bed for radiotherapy designed to adjust the patient's posture and immobilize the patient for Powered radionuclide 81 treatment that uses an after loading short-distance B brachytherapy table irradiation treatment apparatus that is operated manually or electrically. A programmable electrically operated bed for radiotherapy Powered remote designed to adjust the patient's posture and immobilize the 82 irradiation therapy patient for treatment that uses a remote cobalt 60 B table radiotherapy apparatus and other remote radionuclide radiotherapy apparatuses. A programmable electrically operated bed for radiotherapy Powered X-rays 83 designed to adjust the patient's posture and immobilize the B radiation therapy table patient for treatment that uses an X-ray therapy apparatus. A radiation therapy beam-shaping block is a device made of Radiation therapy a highly attenuating material (such as lead) intended for 84 C beam-shaping block medical purposes to modify the shape of a beam from a radiation therapy source Page 10 of 12A radiation therapy simulation system is a fluoroscopic or radiographic x-ray system intended for use in localizing the Radiation therapy 85 volume to be exposed during radiation therapy and C simulation system confirming the position and size of the therapeutic irradiation field produced. Radio-frequency A system that heats and cauterizes malignant or benign 86 C ablation system tumors, etc. with radio wave energy. A device that administers a high-frequency electric current Radio-frequency lesion (radio frequency) to the internal nerves in order to increase 87 generator system with C temperature in a controlled way to create a therapeutic probe lesion. A personnel protective glove is a device intended for medical purposes to protect the patient, the operator, or Radiographic 88 other persons from unnecessary exposure to radiation B Protective Glove during radiologic procedures by providing an attenuating barrier to radiation A radionuclide brachytherapy source is a device that consists of a radionuclide which may be enclosed in a Radionuclide sealed container made of gold, titanium, stainless steel, or 89 C brachytherapy source platinum and intended for medical purposes to be placed onto a body surface or into a body cavity or tissue as a source of nuclear radiation for therapy A device used to measure and record temporal variations of Radionuclide dynamic radioisotope concentrations in the body. Specialized 90 function testing devices, such as devices for thyroid uptake measurement, B equipment renograms, and radioisotope blood volume measurement, are included. A radionuclide radiation therapy system is a device intended Radionuclide radiation to permit an operator to administer gamma radiation 91 C therapy system. therapy, with the radiation source located at a distance from the patient's body. Radiation sources generated in a reactor and used as in a Radionuclide source remote afterloading system designed to deliver a 92 for remote irradiation therapeutic radiation beam to a target anatomical area. The C therapy radiation sources incorporated as a component of the remote afterloading system are generally sealed. Radionuclide system Intended to precisely determine the outline of the area of contour detector for the body to be irradiated. Usually, the information obtained 93 C remote irradiation from this device is entered into a radiotherapy planning therapy system and utilized for the radiotherapy plan. An assembly of electronic devices designed to track the Real-time position respiratory pattern of a patient by means of optical management technology to correlate tumour position with the respiratory 94 C respiratory gating cycle during radiation treatment planning, radiotherapy, system, optical computed tomography (CT) imaging, or other radiation procedures. A rectal balloon for prostate immobilization is a single use, Rectal balloon for inflatable, non-powered positioning device placed in the 95 C prostate immobilization rectum to immobilize the prostate in patients undergoing radiation therapy. Page 11 of 12A remote controlled radionuclide applicator system is an Remote controlled electromechanical or pneumatic device intended to enable 96 radionuclide applicator an operator to apply, by remote control, a radionuclide C system source into the body or to the surface of the body for radiation therapy. A device for permanent installation that forms a structural Stationary radiation 97 barrier that shields or attenuates radiation emitted from B protection barrier primary radiation source or scattered radiation source. Stereotactic A stereotactic radiation therapy system for treatment based 98 radiotherapy on a linear accelerator (or microtron). The device may be C accelerator system used to inactivate lymphocytes. A X-ray CT system that has a special configuration, containing hardware, software, etc. used in radiotherapy X-ray CT system for 99 planning. It is used to determine the size and positioning of C radiotherapy planning the therapeutic radiation field based on a series of treatment parameters to be generated. X-ray radiation therapy An x-ray radiation therapy system is a device intended to 100 C system produce and control x-rays used for radiation therapy. X-ray/CT combined A combined system of a linear accelerator system and an X- 101 linear accelerator C ray CT system for radiotherapy planning. system X-ray/CT combined A combined system of particle radiotherapy equipment and 102 particle radiotherapy C an X-ray CT system for radiotherapy planning. equipment Page 12 of 12Name of Category: Nephrology and Renal Care Total No. of Devices: 39Nephrology and Renal Care S No. Medical Device Name Intended Use INDIA Absorbable peritoneum Inteded to maintain stable contact between the skin and the catheter cuff peritoneal dialysis catheter, and prevents bacterial invasion 1 D from the outlet. It is embedded subcutaneously at the outlet of the peritoneal dialysis catheter. Automated peritoneal An active medical devices intended to perform peritoneal 2 C dialysis system dialysis. Urinary stone retrieval Intended to remove urinary stones ( renal calculi) from the 3 B basket body during an endoscopic procedure. Chair, Haemodialysis, Intended to support the patient in a seated or reclined posture 4 Electrically during haemodialysis procedures. A powered/Manual. Collagen-containing A cuff that consists of biodegradable porous material peritoneum absorbable containing collagen, intended to be embedded subcutaneously 5 D catheter cuff at the outlet of the peritoneal dialysis catheter. Crimp for plier, Intended to manipulate the arteriovenous shunt of patients 6 A Haemodialysis required hemodialysis. Dialyser connector Intended to connect between a dialysis fluid circuit and 7 B dialyzer, etc. Dialysis apheresis unit, Intended to filtrates the blood and separates the plasma, and Therapeutic extracts specific substances in the plasma (e.g., LDL- cholesterol). Then, the plasma is passed through the filtration 8 C column in the device and the specific substances that are combined with various substrates are extracted. Disposable Hemoperfusion Inteded in hemoperfusion machine to thoroughly remove Cartridge the endogenous and exogenous materials such as residual 9 drugs, toxins and metabolic substances in patients by means C of adsorption of synthetic resin and extracorporeal blood circulation Electrical conductivity Intended to determine the concentration of dialysis fluid measuring instrument for supplied to a dialyzer based on the measurement of electrical 10 C dialysis fluid conductivity of dialysis fluid (usually, it is electrically measured. ). Flexible fibreoptic Intended for the visual examination of internal structures and 11 nephroscope treatment of the kidney (eg: renal calcus) by insering B percutaneously into the renal pelvis during nephroscopy. Haemodialyzer Intended to clean (incl. rinsing, cleaning, testing and record 12 reprocessing system keeping of process) and disinfect haemodialysis dialyzers C after each use so that they can be reused. Haemofilters A filter used in the process of haemofiltration, to allow for the 13 removal of toxins and/or the replacement of electrolytes. C Hemodiafiltration system A device used for blood purification with a hemodiafilter. 14 C Page 1 of 3Hemodialysis blood Sterilized blood tubing intended for hemodialysis (including tubing/Extracorporeal hemofiltration and hemodiafiltration). 15 B systems for blood purification Hollow-fibre Hollow fiber filter intended to remove impurities/fluid from 16 C haemodialysis dialyser the blood of a patient via haemodialysis machine. Kidney donor-organ A dedicated system designed to support and maintain a preservation/transport donated kidney organ during transport from the donor to the 17 C system receiver hospital where the organ will be transplanted into the recipient. Kidney stone filter A filter intended to be placed in the urinary duct to prevent a 18 renal stone from moving from the kidney into the bladder. C Laser lithotripsy Intended to function as a channel for insertion of the laser fibre/suction guide fibre of a laser beam guide (e.g., of a general/multiple surgical 19 laser system) in nephroscope, and for removal of debris (e.g., B fluid, calculi fragments) when connected to a vacuum source. Multi-patient dialysis fluid Intended to prepares dialysis fluid for hemodialysis. 20 C delivery system Peritoneal dialysis catheter Intended to connect (devices of different makers and makes adaptor devices compatible with each other) a catheter for peritoneal 21 C lavage to an external device that manages dialysates. Peritoneal dialysis catheter A guidewire used temporarily for correction of the position of 22 B guidewire a peritoneal dialysis catheter. Peritoneal dialysis Intended to heat the dialysate to within on degree, of kidney dialysate warmer patient who is on continuous ambulatory peritoneal dialysis 23 C (CAPD), body temperature prior to infusion. Peritoneal dialysis intended for ultraviolet irradiation of components of 24 B ultraviolet irradiation unit peritoneal dialysis transfer tube set. Reverse Osmosis Unit (for Intended to be used with haemodialysis to produce water 25 dialysis) through reverse osmosis with quality suitable for use with C hemodialysis equipment. Rigid nephroscope Intended for visual examination, diagnosis, and treatment of the kidney, renal pelvis, major calyces, and minor calyces by 26 B percutaneously inserting scope into the renal pelvis. Shunt thrombus suction set A set used to suction a thrombus developing inside an 27 arteriovenous shunt (external shunt) during procedures B including hemodialysis. Portable continuous A device that heats the peritoneal perfusate before injection peritoneal perfusate into the peritoneal cavity. The perfusate is usually heated 28 B thermal conditoner through direct contact of the dialysis fluid bag with the radiant heat source. Citric acid haemodialysis Intended for the in-line preparation of a citric acid solution to system cleaning cartridge clean/disinfect the fluid pathways of the system (remove 29 B calcium and magnesium deposits) in combination with a heat disinfection program. Page 2 of 3Extracorporeal circuit Intended to be used for the collection of waste fluids during waste bag preparation and processing of an extracorporeal circuit (e.g., haemodialysis, haemofiltration, apheresis, adsorption 30 B treatment), including the collection and rinsing of ultrafiltrate fluid which may contain blood components. Haemodialysis concentrate Intended to remove metabolic waste from the blood to help 31 maintain physiological blood electrolyte and pH levels while C haemodilysis is performed. Haemodialysis Intended to calibrate conductivity meters used to test the conductivity standard conductivity of dialysate, dialysate concentrate, and water 32 C solution treatment systems used with haemodialysis delivery systems. Haemodialysis dialysate Intended to be used to rapidly indicate, through colour 33 water chlorine test kit/strip change, the concentration of total chlorine in water used to B prepare dialysate solution for haemodialysis. Haemodialysis system Intended to identify air bubbles and/or foam in blood returned air/foam detector to the body [usually through an arteriovenous fistula (AVF)] 34 C by the extracorporeal blood circuit of a haemodialysis system. Haemodialysis system Intended to mixes two concentrates, A and B, plus water, to 35 bicarbonate mixer the dialysis solution (dialysate) and monitors the mixture. C Haemodialysis system Device intended to connect with multiple haemodialysis 36 central monitor systems in order to aid monitoring several dialysis treatments C simultaneously. Haemodialysis system An electrically-powered integral unit of a haemodialysis plasma filtration unit system that allows for the removal of plasma from the blood 37 C and the infusion of an equal amount of plasma replacement solution to the blood. Peritoneal dialysis system A microporous device used to capture contamination particles 38 dialysate filter of the dialysate before its instillation into the peritoneal C cavity. Sodium carbonate Intended to be connected to the fluid circuit of an institutional haemodialysis system haemodialysis system for the in-line preparation of a sodium cleaning cartridge carbonate solution to clean the fluid pathways of the system 39 C (remove organic deposits, fats, proteins) in combination with a heat disinfection program. Page 3 of 3Name of Category: Software Total No. of Devices: 60Software Medical Devices S.No Name of Product Intended Use IMDR Continuous Glucose Monitor Continuous glucose monitor retrospective data analysis software is intended to analyze and correlate 1 A Retrospective Data retrospective data from a continuous glucose monitoring device. Analysis Software Continuous Glucose The purpose of the continuous glucose monitor secondary display is to notify another person, the 2 Monitor Secondary B follower, of the patient's continuous glucose monitoring system sensor glucose information in real time. Display Insulin Pump The purpose of the insulin pump secondary display is to notify another person of the patient's insulin 3 B Secondary Display pump usage information in real time. Insulin Pump Therapy An insulin pump therapy adjustment calculator for healthcare professionals is intended to recommend Adjustment insulin pump therapy parameter adjustments (e.g., basal rate, insulin to carbohydrate ratios, insulin 4 C Calculator For sensitivity factors) based on data from external devices, including continuous glucose monitors. The Healthcare device is software with a graphical user interface. Professionals Coronary Vascular A coronary vascular physiologic simulation software device is intended to aid in the identification of 5 Physiologic functionally significant cardiovascular disease by performing offline analysis of pre-existing imaging data C Simulation Software to simulate blood flow in the coronary vasculature. Automated calculation of a summary index (or indices) based on several individual measured vital sign Multivariate Vital 6 inputs. Collects measured parameter inputs and automates the calculation of a summary index based B Signs Index on those parameters Electrocardiograph Device intended for home use which creates, analyzes, and displays electrocardiograph data, and can 7 Software for home B provide information for identifying cardiac arrhythmias. use. Photoplethysmogra Photoplethysmograph analysis software device for home analyzes of photoplethysmograph data and ph Analysis 8 provides information for identifying irregular heart rhythms. This device is not intended to provide a B Software for home clinical diagnosis. use. Angiographic Coronary Vascular An angiographic coronary vascular physiologic simulation software device is intended to aid in the 9 C Physiologic identification of functionally significant cardiovascular disease. Simulation Software Software For Visualization Of 10 Vascular Anatomy Visualization and measurement of blood vessels and intravascular devices for preoperational planning. C And Intravascular Devices Orthodontic The device is software that is to be used for the diagnosis and treatment planning of orthodontic 11 C Software patients and conditions. The software device is intended to aid in the restoration of chewing function by allowing a dental Dental Abutment laboratory or dental clinician to design the patient-specific component of a dental abutment (i.e. 12 Design Software For C abutment collar and abutment post) and CAM or create that component at a dental office or dental Dental Laboratory laboratory following the directions of the dental implant system. Diagnostic Software, K-Nearest Neighbor The device is intended to suggest a systemic autoimmune disease association as an aid for differential 13 B Algorithm, diagnosis to be evaluated in conjunction with clinical findings and other laboratory tests. Autoimmune Disease Neuropsychiatric Interpretative 14 Intended as an aid to provide an interpretation of the patient's neuropsychiatric condition. C Electroencephalogr aph Assessment Aid Normalizing Quantitative Post-hoc statistical analysis of electroencephalograph signals with comparison to a normative database 15 C Electroencephalogr for interpretation by a qualified clinical user. aph Software Index-Generating Analyze electrical activity of the brain by transformation of electroencephalograph signals into a 16 Electroencephalogr C dimensionless index number for use and interpretation by a qualified clinical user. aph Software 1 of 4Source Localization Software For Electroencephalogr Correlation of electrical activity of the brain using various neuroimaging modalities for source- 17 C aph Or localization Magnetoencephalo graph Automatic Event Detection Software Automatically mark electroencephalograph and polysomongraph signals in order to aid in identification For of such events and annotation of prolonged PSG traces; Automatically calculate simple measures 18 Polysomnograph C obtained from recorded signals (e.G. Magnitude, time, frequency and simple statistical measures of With marked events); All output subject to verification by qualified clinical user Electroencephalogr aph Automatic Event Detection Software Automatically mark or identify electroencephalograph waveforms for spikes, electrographic seizures, 19 For Full-Montage seizure-like events in order to aid in identification of such events and help review and annotation of C Electroencephalogr prolonged EEG traces; All output subject to verification by qualified clinical user aph Computerized Cognitive 20 For use as an assessment aid in the management of concussion. C Assessment Aid For Concussion Ataxiagraph With Device used to determine the extent of ataxia (failure of muscular coordination) by measuring the 21 Interpretive amount of swaying of the body when the patient is standing erect and with eyes closed and provides B Software interpretation or clinical implication of the measurement. Computerized Behavioral Therapy The device is intended to provide cognitive behavioral therapy to treat substance use disorder. The 22 Device For C device is a software-based mobile app downloaded onto a smartphone. Psychiatric Disorders Brain Injury Adjunctive A traumatic brain injury eye movement assessment aid is a prescription device that uses a patients 23 Interpretive C tracked eye movements to provide an interpretation of the functional condition of the patients brain. Oculomotor Assessment Aid Device, Fertility Diagnostic, 24 Contraceptive, Designed to monitor and provide fertility information to prevent pregnancy (contraception). C Software Application Diabetic A retinal diagnostic software device is a software device that incorporates an adaptive algorithm to 25 Retinopathy C evaluate ophthalmic images for diagnostic screening to identify retinal diseases or conditions. Detection Device Colon Computed Tomography To assist radiologists in the review of multi-slice computed tomography (msct) exams of the colon and 26 B System, Computer highlight potential polyps that the radiologist should review. Aided Detection Lung Computed Tomography To assist radiologists in the review of multi-slice computed tomography (msct) exams of the chest and 27 B System, Computer- highlight potential nodules that the radiologist should review. Aided Detection Chest X-Ray To assist radiologists in the review of chest radiographic images and highlight potential nodules that the 28 Computer Aided B radiologist should review. Detection Computer-Assisted Diagnostic Software 29 For Lesions Assist clinical users in characterizing lesions identified on acquired medical images C Suspicious For Cancer Radiological Computer Assisted A radiological computer assisted detection and diagnostic software for suspected fracture is an image 30 Detection/Diagnosis processing device intended to aid in the detection, localization, and/or characterization of fracture on B Software For acquired medical images (e.g. radiography, MR, CT). Fracture 2 of 4Radiological Computer Assisted A radiological computer assisted detection and diagnostic software for suspected lesions is an image Detection/Diagnosis processing device intended to aid in the detection, localization, and characterization of lesions 31 C Software For suspicious for cancer on acquired medical images (e.g., mammography , MR, CT, ultrasound, Lesions Suspicious radiography). For Cancer X-Ray Angiographic X-ray angiographic imaging based coronary vascular simulation software device is a device that Imaging Based provides an image analysis tool to assess blood flow in the coronary vascular system using X-ray 32 Coronary Vascular B angiographic imaging data. And yields simulation-based metrics for certain cardiology applications Simulation Software which aid clinical user. Device Automated 33 Radiological Image To provide automated radiological image processing and artificial intelligence based analysis tools. B Processing Software Image Acquisition And/Or A radiological acquisition and/or optimization guidance system is a device that is intended to aid in the 34 Optimization B acquisition and/or optimization of images and/or diagnostic signals. Guided By Artificial Intelligence Burn Resuscitation The burn resuscitation decision support system (BRDSS) is intended for use in prediction of hourly fluid 35 Decision Support volume during initial 24 hours of burn resuscitation. It is intended for patients who have greater than C Software 20% total body surface area burn. Software, Similarity This test is intended to measure the degree of similarity between the RNA expression pattern in a Score Algorithm, patient?s fresh-frozen tumor and the RNA expression patterns in a database of tumor samples for some 36 Tissue Of Origin For C common malignant tumor types that were diagnosed according to then current clinical and pathological Malignant Tumor practice. Types Software for A software that performs prescription simulation of peritoneal dialysis based on the results obtained 37 peritoneal dialysis from a peritoneal function test (PFT), a peritoneal equilibration test (PET) and a body composition C treatment analyzer. It supports preparation of a dialysis treatment plan. A software that calculates and displays the area to be treated with radiation and the internal dose Software for 38 distribution based on the results obtained with CT systems etc. , and supports the radiotherapy C radiation planning planning. Software for A software that verifies the validity of the radiotherapy plan by recalculation of the dose and the MU 39 radiotherapy QAQC C value calculated with the radiotherapy planning system software and radiotherapy planning system. planning Software for A software for intended to aid ophthalmic surgical planning based on measurement of the eye prior to 40 ophthalmic surgery C the surgery. It simulates surgical results. treatment planning Software for active A software used to transmit one or more electrical operating characteristics noninvasively to the active 41 implanted device C base unit and change the characteristics. control Information A software that has function of collating the information such as irradiation parameter specified by a 42 collating software radiation planning software, and the condition that a radiotherapy equipment irradiates, on the C for radiotherapy occasion of the irradiation of X-ray in the radiotherapy. Software for gene variants analysis A software for gene variants analysis which is designed to perform cancer genome profiling based on 43 C (for cancer genome information of gene variants obtained from body tissue samples. profiling) Supporting A software, which is designed to process data obtained from an endoscopic image. The resultant data software for are provided for diagnostic, etc. It has functions to output numeric values and graphs based on 44 differential C quantitative data such as benign/malignant differentiation of lesion candidates, presenting candidates diagnosis with of diagnostic outcomes, and stage of disease progression. endoscopic imaging Chairside dental Intended for computer-aided design (CAD) or computer-aided manufacturing (CAM) of dental 45 B CAD/CAM unit restorations. Software for using with mammography- A software, which is designed to processes data obtained from a combined diagnostic mammography- 46 B combined radiography system. diagnostic X-ray system 3 of 4Software for public thoracic and A software, which is designed to process data obtained from a thoracic and abdominal public health abdominal health 47 screening diagnostic X-ray system. The resultant data are provided for diagnosis, etc. This term may B screening involve the recording media where the software are stored. diagnostic X-ray system Software for visual A software, which is designed to process data obtained from a visual evoked response stimulator. The 48 evoked response B resultant data are provided for diagnosis, etc. stimulator Software for A software for medical device, which is designed to process data obtained from an auditory evoked 49 auditory evoked B response stimulator. The resultant data are provided for diagnosis, etc. response stimulator Software for pulmonary exercise A software, which is designed to process data obtained from a pulmonary exercise stress monitoring 50 B stress monitoring system. system Software for ECG A software, which is designed to process data obtained from an ECG recorder with real-time analysis. 51 recorder with real- B The resultant data are provided for diagnosis, etc. time analysis Software for film- A software, which is designed to process data obtained from a film-recorded digital radiography. The 52 recorded digital B resultant data are provided for diagnosis, etc. radiography Software for dye A software, which is designed to process data obtained from a dye dilution cardiac output unit. The 53 dilution cardiac B resultant data are provided for diagnosis, etc. output calculator Software for urodynamic A software, which is designed to process data obtained from a urodynamic measurement system. The 54 B measurement resultant data are provided for diagnosis, etc. system Software for A software, which is designed to process data obtained from a vestibular function caloric stimulator. The 55 vestibular function B resultant data are provided for diagnosis, etc. caloric stimulator Surporting software A software that analyzes information useful for bone fracture and for correction of bone deformities 56 for external fixators based on information collected from diagnostic X-ray systems, etc. or based on information entered in a B treatment plan therapeutic apparatus, and supports preparation of a treatment plan with external fixators. Diagnostic A software that supports analysis and assessment of therapeutic effects of diabetes treatment by 57 supporting software processeing information collected from a blood glucose meter, etc into the data related to changes or B for diabetes trends in blood glucose levels. Quantitative A software that performs quantitative calculation of blood flow in relation to a brightness time change 58 calculation software B based on information obtained from video images of indocyanine green angiography. for IGC test Analyzing software A medical device program that analyzes hemodynamics or cardiac function based on information 59 for hemodynamics B obtained from diagnostic imaging systems, etc. and uses the results for diagnosis. or cardiac function Supporting A software for medical device, which is used to support preparation of a treatment plan based on 60 software for root B information collected from diagnostic imaging systems, etc. in the root canal treatment. canal treatment 4 of 4

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