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Guidance Documents Medical Devices Validation For Canada

Guidance Documents Medical Devices Validation For Canada
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CDSCO Certification Types for Medical Devices
2. Form MD-3 – Application for Manufacturing License for Class A & B Devices
3. Form MD-5 – Manufacturing License for Class A & B Devices Apply to State Licensing Authority (SLA).For domestic manufacturers of low to medium risk medical devices.

4. Form MD-7 – Application for Manufacturing License for Class C & D Devices

5. Form MD-9 – Manufacturing License for Class C & D Devices

Apply to CDSCO Head Office (Central Licensing Authority).
For domestic manufacturing of high-risk devices (e.g., cardiac stents, catheters).

6. Form MD-4 – Application for Loan License for Class A & B

7. Form MD-6 – Loan License for Class A & B Devices

When a manufacturer uses another licensed facility to manufacture.
8. Form MD-8 – Application for Loan License for Class C & D
9. Form MD-10 – Loan License for Class C & D Devices Similar purpose as MD-4/6 but for high-risk categories.1
10. Form MD-11 – Application for Import License for Medical Devices
11. Form MD-15 – Import License for Medical Devices For foreign manufacturers.

Requires appointment of an Authorized Indian Agent.

Requires:

  • Free Sale Certificate (FSC)
  • ISO 13485
  • Device Master File (DMF)
  • Plant Master File (PMF)

 

12. Form MD-12 – Application for Import License for IVDs

13. Form MD-16 – Import License for IVD Devices

Specifically for in-vitro diagnostics.

14. Form MD-14 – Application for Testing License

15. Form MD-18 – Testing License to Manufacture for Test or Evaluation

Required for clinical evaluation, R&D, or stability studies.
16. Form MD-17 – Application for Test License for Import
17. Form MD-19 – Test License for Import of Medical Device for Testing/Evaluation
For imported samples not for commercial sale.

18. Form MD-20 – Application for Registration of Notified Body
19. Form MD-21 – Notified Body Registration Certificate

For certification bodies performing audit of Class A & B manufacturers.
20. Form MD-22 / MD-23 – Application for Clinical Investigation of Medical Device

21. Form MD-24 / MD-25 – Permission for Clinical Investigation Applicable for new or investigational medical devices.

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