Download the Latest Notifications: Medical Devices

Govt. of India issues Notifications time to time which are published by Department of Publication and are printed by the Government of India Printing Presses regularly.

We have provided some of the notifications relevant to the above said topic, Click below links for more information:

2022

GSR-710E-dt-20-09-2022-Draft-notification-Exemption-of-certain-Class-A-medical-device-from-licensing-regime

S.O.-3758E-dt-10-08-2022-To-authorize-director-incharge-Dr.-Saroj-Kumar-Ghosh-of-CDL-Kolkata-for-signing-report-of-test-of-MD-samples-sent-by-Court-of-Laws.

S.O.-3739E-dt-02-08-2022-Notification-of-Medical-Devices-Testing-Officer-for-CMDTL

Ministry-of-Health-Dt-08-07-2022-Draft-of-New-Drugs-Medical-Devices-and-Cosmetics-Bill-2022

GSR-450E-dt-15-06-2022-Final-notification-to-amend-Fourth-Schedule-wrt-TSE-or-BSE-certificate-under-MDR

GSR-No.-356-E-Dt-18-05-2022-Inserted-rule-43A-for-Suspension-and-cancellation-of-license-in-MDR-2017

GSR-228E-dt-29-03-2022-To-amend-Fourth-Schedule-wrt-TSE-or-BSE-certificate-under-MDR

GSR-174E-dt-04-03-2022-Amendment-of-Rule-363-MDR-to-include-United-Kingdom-under-MDR-2017

GSR-104E-dt-09-02-2022-Draft-notification-to-amend-Medical-Devices-Rules-2017-regarding-Rule-34-87-insertion-of-Form-MD-41-42-43

GSR-No.-23E-dt-18-01-2022-Draft-Notification-Rule-43-Suspension-and-cancellation-of-license-of-Medical-Devices

GSR-No.-19E-dt-18-01-2022-Draft-notification-Registration-number-for-Medical-Devices-Medical-Devices-Rules-2017

2021

GSR-918E-dt-31-12-2021-Medical-Device-Amendment-Rules-2021-Unique-device-identification-of-medical-device

GSR-850E-dt-10-12-2021-Draft-Amendment-of-Rule-363-MDR-to-include-United-Kingdom-1

GSR-729E-dt-12-10-2021-Draft-of-Medical-Devices-Amendment-Rules-2021-ISO-13485

S.O.-3596-dt-02-09-2021-Notification-of-Amar-Jyoti-Dilip-Sarkar-Rinku-Kalita-Arun-Kr-Das-as-MDTO

NPPA-Office-Memorandum-03-08-2021-Submission-of-price-related-information-for-Knee-Implants

NPPA-Office-Memorandum-dt-23-07-2021-–-for-Revised-MRPs-in-pursuance-to-the-TMR-Notification-for-5-Medical-Devices

NPPA-S.O.-2808-dt-13-07-2021-Trade-Margin-Rationalisation-TMR-of-5-Medical-Devices

NPPA-Dt-09-06-2021-Office-Memorandum-Revised-MRP-for-Oxygen-Concentrators

NPPA-Office-Memorandum-dt-04-06-2021-In-pursuance-to-the-Notification-dated-03.06.2021-for-Oxygen-Concentrators

NPPA-order-dt-03-06-2021-Price-Cap-for-Oxygen-Concentrator-through-Trade-Margin-Rationalisation-Approach

NPPA-Office-Memorandum-dt-15-05-2021-for-call-of-MRP-Data-for-Pulse-Oximeter-Oxygen-Concentrator-2021

GSR-98E-05-02-2021-Draft-notification-American-Standard-Test-Method-ASTM-in-the-product-standards-for-Medical-Devices-under-Rule-7-of-MDR-2017

2020

S.O. -No.-1232-E-dt-31-03-2020-All-Medical-devices-under-DPCO

G.S.R.-102E-dt-11-02-2020-Medical-Devices-Amendment-Rules-2020

S.O.-648E-dt-11-02-2020-Medical-Device-Definition-Instruments-apparatus-etc-are-drugs

2019

S.O.-No.-4672-E-dt-27-12-2019-Devices-for-human-use-date-extended-CT-Scan-MRI-X-Ray-etc.

S.O.-No.-4671-E-dt.-27-12-2019-Devices-for-human-use-date-extended-Nebulizer-BP-Apparatus-Thermometer-Glucometer

S.O.-NO.-3721E-dt.-16-10-2019-Notification-Ultrasound-equipment-as-drug-w.e.f.-01-11-2020

G.S.R-No.-787E-dt.-16-10-2019-MDR-Govt.-Testing-Labs-exempted-for-accraditation-from-NABL-for-two-years

G.S.R. 797(E) dt. 18-10-19 Draft Notification-MDR-2019

G.-S.-R.-652-E-dt.-13-09-2019-Medical-Devices-Fourth-Amendment-Rules-2019

G.S.R.-No.-499E-dt.-17-07-2019-Medical-Devices

G.-S.-R.-318-E-dt.-18-04-2019-Medical-Devices-Third-Amendment-Rules-2019

G.-S.-R.-224-E-dt.-18-03-2019-Medical-Devices-Second-Amendment-Rules-2019

S.-O.-775-E-dt.-08-02-2019-Devices-declared-drug-Nebulizer-BP-Apparatus-Thermometer-Glucometer

G.-S.-R.-30-E-dt.-15-01-2019-Medical-Devices-Amendment-Rules-2019

2018

S.-O.-5980-E-dt.-03-12-2018-Medical-Devices-for-human-use-declared-as-Drug-CT-Scan-MRI-X-Ray-etc

G.S.R.-1074-E-dt.-30-10-2018-Section-10A-Prohibited-Rapid-Diagnostic-Tests-for-diagnosis-of-malaria

G.-S.-R.-729-E-dt.-01-08-2018-Medical-Devices-Amendment-Rules-2018

S.O.-3400-E-dt.-11-07-18-Medical-devices-MDTO

S.-O.-2237-E-dt.-01-06-2018-Designated-Central-Medical-Device-Testing-Laboratory

S.O-1352-E-dt.-23-03-18-Section-26A-Banned-Malaria-Rapid-test-kits

2017

G.S.R-78-E-dt.-31-01-17-Medical-Device-Rules-2017

Compiled by:Rakesh Dahiya, SDCO cum Licensing Authority, FDA Haryana

Click for more articles of the Author

Licensing procedure for Medical devices

Latest Notifications: Medical Devices

Classifications of Medical Devices under the provisions of MDR 2017

FAQs on Medical Devices Rules, 2017

FAQs – on Blood Pressure Monitoring Devices

For more Notifications on following topics, click below links:

Banned Drugs

Blood Bank / Centre

Cosmetics

COTPA

DPCO / NPPA

Drugs Act

DMROA

EC Act

General

Homoeopathic

Hospital – RMI

NDPS Act

New Drugs

Testing Laboratories
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