ANSM
Competent authority · France · Paris
A national competent authority for medical devices under the EU MDR/IVDR — market surveillance, vigilance and EUDAMED registration oversight.
A national body that oversees the application of EU medical-device regulation in its country — market surveillance, vigilance, economic-operator validation and EUDAMED registration oversight, under MDR Articles 101–108.
Explore every authority and economic operator registered in France.
A national body that oversees the application of EU medical-device regulation in its country — surveillance, vigilance, and registration oversight.
No — that's a notified body. A competent authority supervises the market; it does not issue device certificates.
Sourced directly from EUDAMED. This record was last updated Jun 25, 2026.
Operators whose registration was validated by this authority.
| Operator | Role | SRN | Country |
|---|---|---|---|
| DEXTHER | Manufacturer | FR-MF-000052364 | FR |
| Editions et Matériels Scientifiques | Manufacturer | FR-MF-000017095 | FR |
| Etablissement M GRANDET | Manufacturer | FR-MF-000038444 | FR |
| L'ATELIER BINOCL'ART | Manufacturer | FR-MF-000029329 | FR |
| MAYFAIR DEVELOPMENTS | Manufacturer | FR-MF-000001808 | FR |
| SYNERGIE INGENIERIE MEDICALE | Manufacturer | FR-MF-000001635 | FR |