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Section 2017 in The Medical Devices Rules, 2017 [Entire Act]

Government Hospital or Statutory Medical Institution) hereby apply for a licence to import small quantities of investigational medical device specified below manufactured ... imported     |- | 2. | The prescription from a registered medical practitioner prescribing the need for the said medical device is attached. |- | 3. | The particular of the patients
Union of India - Section Cites 0 - Cited by 0

Section 3 in The Medical Devices Rules, 2017 [Entire Act]

relating to such device, which is as per approval obtained from the Central Licensing Authority; (w) "invasive device" means a device which, in whole ... analyze information gained from medical device that have been placed in the market; (zm) "predicate device" means a device, first time and first
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Section 38 in The Medical Devices Rules, 2017 [Entire Act]

Section 38 in The Medical Devices Rules, 2017 38. Conditions to be complied with by Licence holder. (1) The licencee shall comply with the following ... conditions, namely:- (i) licence shall be produced when requested by the Medical Device Officer or any other senior officer under the control of Central Licensing
Union of India - Section Cites 0 - Cited by 0
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