PROTEOR SAS
FR-MF-000001711 · France · Saint-Apollinaire
PROTEOR SAS is registered in the European database on medical devices as a manufacturer, with 128 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 128 |
|---|
Devices declared under this manufacturer
- EXONEO Core P2 Droit Clair - 23 cm
- EXONEO Core P2 Droit Clair - 24 cm
- EXONEO Core P2 Gauche Foncé - 21 cm
- EXONEO Core P2 Gauche Foncé - 23 cm
- EXONEO Core P3 Droit Clair - 23 cm
- EXONEO Core P3 Droit Clair - 24 cm
- EXONEO Core P3 Droit Foncé - 21 cm
- EXONEO Core P3 Gauche Clair - 28 cm
- EXONEO Core P3 Gauche Clair - 29 cm
- EXONEO Core P3 Gauche Foncé - 27 cm
- EXONEO Core P4 Droit Clair - 24 cm
- EXONEO Core P4 Droit Foncé - 27 cm
Showing 12 of 128 declared devices.
Catalogue references include 05CDC1-P2-24, 05CDC1-P3-23, 05CDC1-P4-24, 05CDC2-P3-21, 05CDC2-P4-27, 05CGC1-P3-28.
European nomenclature codes declared: Y062409.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | PROTEOR (FR) · FDA 3004134478 |
| Devices in EUDAMED | 128 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 128 |
|---|---|
| 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: United States only. PROTEOR SAS is registered in the United States but was not found in the Canadian register.