Ahmedabad, Gujarat
GST No. 24AAJHJ4621D1ZN
Call 07942830998 80% Response Rate
Send Enquiry
| Service Location | India |
| Service Charges | Yes |
| Type of Services | Guidance Documents Medical Devices Validation For Canada |
| Type of Service Provider | Consultant |
| Payment mode | Online/offline |
| Language | English |
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:
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.
View Complete details