EUROS SAS
FR-MF-000000605 · France · La Ciotat
EUROS SAS is registered in the European database on medical devices as a manufacturer, with 2 047 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 1 487 |
|---|---|
| Class I | 536 |
| Class IIb | 24 |
Most frequent device types declared: BONE SCREWS, COSYX, EUROP MODULAR, HEXAGON, Instruments IIa.
Among these devices, 560 are declared sterile, 560 implantable, 1 487 reusable.
Devices declared under this manufacturer
- BONE SCREWS
- COSYX
- EUROP MODULAR
- HEXAGON
- Têtes fémorales
Showing 12 of 2 047 declared devices.
Catalogue references include A110202031, A282812041, A311525151, B2526121, B280455613, B282461091.
European nomenclature codes declared: L091199, L091104, P090903020201, L091102, L091001, P090905020202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 2 047 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 2 047 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. EUROS SAS was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
D1447900036 | reissued | 2031-07-24 |
D1447900035 | reissued | 2031-07-24 |