2021.02.05_Draft GSR 98(E) ASTM Standards.pdf2021.12.31GSR918 Ammendment of Rule 46.pdf2022.02.09_Draft GSR 104(E) STocking of MD for sale.pdf2022.05.18_Final GSR 356(E) Suspension-cancellation of MD.pdf2022.09.20_Draft_GSR 710(E)_Exemption of certain Class A medical device from licensing regime.pdfDCGI-dt-10-12-2021-List-of-the-certified-Medical-Device-Testing-Laboratory-under-MDR-2017.pdfDCGI-Notice-dated-03-06-2022-Classification-of-MD-For Dental.pdfDRAFT-MDR-2019.pdfFinal notifi 4 exempt of non steril cat A MDR.pdfG.-S.-R.-30-E-dt.-15-01-2019-Medical-Devices-Amendment-Rules-2019-2.pdfG.-S.-R.-224-E-dt.-18-03-2019-Medical-Devices-Second-Amendment-Rules-2019-2.pdfG.-S.-R.-318-E-dt.-18-04-2019-Medical-Devices-Third-Amendment-Rules-2019-2.pdfG.-S.-R.-652-E-dt.-13-09-2019-Medical-Devices-Fourth-Amendment-Rules-2019-2.pdfG.-S.-R.-729-E-dt.-01-08-2018-Medical-Devices-Amendment-Rules-2018-2.pdfG.S.R-78-E-dt.-31-01-17-Medical-Device-Rules-2017-2.pdfG.S.R-No.-787E-dt.-16-10-2019-MDR-Govt.-Testing-Labs-exempted-for-accraditation-from-NABL-for-two-years.pdfG.S.R.-102E-dt-11-02-2020-Medical-Devices-Amandment-Rules-2020.pdfG.S.R.-1074-E-dt.-30-10-2018-Section-10A-Prohibited-Rapid-Diagnostic-Tests-for-diagnosis-of-malaria-2.pdfG.S.R.-No.-499E-dt.-17-07-2019-Medical-Devices.pdfGSR-98E-05-02-2021-Draft-notification-American-Standard-Test-Method-ASTM-in-the-product-standards-for-Medical-Devices-under-Rule-7-of-MDR-2017.pdfGSR-104E-dt-09-02-2022-Draft-notification-to-amend-Medical-Devices-Rules-2017-regarding-Rule-34-87-insertion-of-Form-MD-41-42-43.pdfGSR-157E-dt-01-03-2023-Draft-Medical-Device-Rule-2023-State-Medical-DEvice-Testing-Laboratory.pdfGSR-174E-dt-04-03-2022-Amendment-of-Rule-363-MDR-to-include-United-Kingdom-under-MDR-2017.pdfGSR-450E-dt-15-06-2022-Final-notification-to-amend-Fourth-Schedule-wrt-TSE-or-BSE-certificate-under-MDR (1).pdfGSR-450E-dt-15-06-2022-Final-notification-to-amend-Fourth-Schedule-wrt-TSE-or-BSE-certificate-under-MDR (2).pdfGSR-450E-dt-15-06-2022-Final-notification-to-amend-Fourth-Schedule-wrt-TSE-or-BSE-certificate-under-MDR.pdfGSR-710E-dt-20-09-2022-Draft-notification-Exemption-of-certain-Class-A-medical-device-from-licensing-regime.pdfGSR-729E-dt-12-10-2021-Draft-of-Medical-Devices-Amendment-Rules-2021-ISO-13485.pdfGSR-754E-dt-30-09-2022-Sale-of-medical-device-by-means-of-retail-and-wholesale.pdfGSR-777E-dt-14-10-2022-Registration-of-Class-A-Medical-Devices-Medical-Devices-Sixth-Amendment-Rules-2022.pdfGSR-850E-dt-10-12-2021-Draft-Amendment-of-Rule-363-MDR-to-include-United-Kingdom-1.pdfGSR-918E-dt-31-12-2021-Medical-Device-Amandment-Rules-2021-Unique-device-identification-of-medical-device (1).pdfGSR-918E-dt-31-12-2021-Medical-Device-Amandment-Rules-2021-Unique-device-identification-of-medical-device.pdfGSR-No.-19E-dt-18-01-2022-Draft-notification-Registration-number-for-Medical-Devices-Medical-Devices-Rules-2017.pdfGSR-No.-356-E-Dt-18-05-2022-Inserted-rule-43A-for-Suspension-and-cancellation-of-license-in-MDR-2017.pdfGSR-No.-409E-dt-02-06-2023-Amendment-of-Rule-18-19-for-Medical-Devices-Testing-Laboratory-Medical-Devices-Amendment-Rules-2023.pdfGSR-No.-1232-E-dt-31-03-2020-All-Medical-devices-under-DPCO.pdfMDR_G.S.R. 777(E) dt_14.10.2022_exemption of non sterile and non measuring Class A medical devices from licensing regime.pdfMinistry-of-Health-Dt-08-07-2022-Draft-of-New-Drugs-Medical-Devices-and-Cosmetics-Bill-2022.pdfnon sterile and non measuring Class A medical devices from licensing regime.pdfNPPA-Dt-09-06-2021-Office-Memorandum-Revised-MRP-for-Oxygen-Concentrators.pdfNPPA-Office-Memorandum-03-08-2021-Submission-of-price-related-information-for-Knee-Implants..pdfNPPA-Office-Memorandum-dt-04-06-2021-In-pursuance-to-the-Notification-dated-03.06.2021-for-Oxygen-Concentrators.pdfNPPA-Office-Memorandum-dt-15-05-2021-for-call-of-MRP-Data-for-Pulse-Oximeter-Oxygen-Concentrator-2021.pdfNPPA-Office-Memorandum-dt-23-07-2021-–-for-Revised-MRPs-in-pursuance-to-the-TMR-Notification-for-5-Medical-Devices.pdfNPPA-order-dt-03-06-2021-Price-Cap-for-Oxygen-Concentrator-through-Trade-Margin-Rationalisation-Approach.pdfNPPA-S.O.-2808-dt-13-07-2021-Trade-Margin-Rationalisation-TMR-of-5-Medical-Devices.pdfS.-O.-775-E-dt.-08-02-2019-Devices-declared-drug-under-Section-3-b-iv-2.pdfS.-O.-2237-E-dt.-01-06-2018-Designated-Central-Medical-Device-Testing-Laboratory-2.pdfS.-O.-5980-E-dt.-03-12-2018-Medical-Devices-for-human-use-declared-as-Drug-2.pdfS.O-1352-E-dt.-23-03-18-Section-26A-Banned-Malria-Rapid-test-kits-2.pdfS.O-1468-dt.-06-10-2005-List-of-10-sterile-devices-intended-for-external-or-internal-use-in-human-beings-as-drugs.pdfS.O.-648E-dt-11-02-2020-Medical-Device-Definition-Instruments-apparatus-etc-are-drugs.pdfS.O.-3400-E-dt.-11-07-18-Medical-devices-MDTO-2.pdfS.O.-3596-dt-02-09-2021-Notification-of-Amar-Jyoti-Dilip-Sarkar-Rinku-Kalita-Arun-Kr-Das-as-MDTO.pdfS.O.-3739E-dt-02-08-2022-Notification-of-Medical-Devices-Testing-Officer-for-CMDTL.pdfS.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..pdfS.O.-4573E-dt-28-09-2022-Notification-for-designation-of-RDTL-Chandigarh-also-as-CMDTL-as-per-MDR-2017.pdfS.O.-4574E-dt-28-09-2022-Designation-of-Government-Analysts-at-RDTL-Chandigarh-as-MDTO-as-per-MDR-2017.pdfS.O.-NO.-3721E-dt.-16-10-2019-Notification-Ultrasound-equipment-as-drug-w.e.f.-01-11-2020.pdfS.O.-No.-4671-E-dt.-27-12-2019-Devices-for-human-use-date-extended-Nebulizer-BP-Apparatus-Thermometer-Glucometer.pdfS.O.-No.-4672-E-dt-27-12-2019-Devices-for-human-use-date-extended-CT-Scan-MRI-X-Ray-etc..pdfsale of medical device retail and wholesale.pdfUltrasound MD as Drug.pdf