Biotechni S.A.S
FR-MF-000013608 · France · La Ciotat
Biotechni S.A.S is registered in the European database on medical devices as a manufacturer, with 347 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 347 |
|---|
Among these devices, 347 are declared sterile, 347 implantable, 1 with a measuring function.
Devices declared under this manufacturer
- APOGEE acetabular cup to be cemented, size 44
- APOGEE acetabular cup to be cemented, size 46
- APOGEE acetabular cup to be cemented, size 50
Showing 12 of 347 declared devices.
Catalogue references include CI6038-22, CI6047, FI04316, FI04412, FIC04015, QH18-105.
European nomenclature codes declared: P090804030201, P090804010201, P09080302, P0901040204, P090803010201, P09088007.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 347 |
| 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 | 347 |
|---|---|
| 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. Biotechni S.A.S was not found in either the U.S. or the Canadian register.