Home › India › Meril Diagnostics Pvt. Ltd.
Manufacturer of medical devices registered in the European database in Vapi, India.
| Registration number (SRN) | IN-MF-000028158 |
|---|---|
| Short name | Meril Diagnostics |
| Role | Manufacturer |
| Status | Active |
| Country | India |
| City | 396191 Vapi |
| Address | Meril Diagnostics Private Limited, No. 135/139, Bilakhia House,Muktanand Marg, Chala. Vapi, Valsad, Gujarat (India) - 396191, 396191 Vapi |
| Registered on | 2022-09-06 |
| FDA establishment register | Registered with the U.S. FDA |
|---|---|
| Matched entry | MERIL DIAGNOSTICS PVT. LTD. (IN) · FDA 3013124221 |
| Certificate | Status | Expiry | Type | Body |
|---|---|---|---|---|
2025-IVDR/TD-001/A | amended | 2028-09-09 | Technical documentation | NB 2265 |
2025-IVDR/QS-001/A | amended | 2028-09-09 | Quality management system | NB 2265 |
2024-IVDR/TD-010/A | amended | 2029-11-11 | Technical documentation | NB 2265 |
2024-IVDR/TD-009 | amended | 2029-11-11 | Technical documentation | NB 2265 |
2024-IVDR/TD-003/A | amended | 2028-09-09 | Technical documentation | NB 2265 |
2024-IVDR/QS-010/A | amended | 2029-11-11 | Quality management system | NB 2265 |
2024-IVDR/QS-009/A | amended | 2029-11-11 | Quality management system | NB 2265 |
2024-IVDR/QS-003/A | amended | 2028-09-09 | Quality management system | NB 2265 |
2023-IVDR/TD-004/B | amended | 2028-09-09 | Technical documentation | NB 2265 |
2023-IVDR/TD-003/B | amended | 2028-09-09 | Technical documentation | NB 2265 |
2023-IVDR/TD-002/B | amended | 2028-09-09 | Technical documentation | NB 2265 |
2023-IVDR/QS-004/B | amended | 2028-09-09 | Quality management system | NB 2265 |
2023-IVDR/QS-003/B | amended | 2028-09-09 | Quality management system | NB 2265 |
2023-IVDR/QS-002/B | amended | 2028-09-09 | Quality management system | NB 2265 |
⚠️ State of the register on 2026-08-20. EUDAMED shows only the current version of a certificate — earlier versions are not published, by the Commission or by anyone. A certificate shown as valid here may have changed since. For a legally binding check, consult EUDAMED directly.
The SRN is the registration number assigned by the European Commission. It has been mandatory since 28 May 2026 for any operator placing a medical device on the Union market. Contact details are published in the official register; we do not reproduce them here.
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