APOL
FR-MF-000001707 · France · Champagnole
APOL is registered in the European database on medical devices as a manufacturer, with 274 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 274 |
|---|
Most frequent device types declared: APOLSYSTEME, APOLSYSTEME A&B, COFFRET APOLSYSTEME, DIADEME, FIBREGLASS.
Among these devices, 2 are declared sterile, 91 implantable.
Devices declared under this manufacturer
- Alésoir Ø 1,8
- COURONNES DIADEME N°100 - 5 PIECES
- COURONNES DIADEME N°200 - 5 PIECES
- COURONNES DIADEME N°29 - 5 PIECES
- COURONNES DIADEME N°50 - 5 PIECES
- Clavettes Pivocolor Rouge 1,4
- Q010105\tYes\tTi topaze Opal Evo / Ø 1,6 / L 10,5
- Screw. Fibre Jaune Ø1,6 L11,5
- Série Fibreglass L19 Ø 1.4
- Série Fibreglass L19 Ø 1.6
- Tenons Fibreglass Jaune Ø1,6 L15
- Ti PIVOCOLOR ROUGE Ø 1,4 / L 13,55
Showing 12 of 274 declared devices.
Catalogue references include E99100, E99200, P20155, P25135, P25570, P65150.
European nomenclature codes declared: Q010299, Q010105, Q01010199, Q010207.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 274 |
| 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 | 274 |
|---|---|
| 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. APOL was not found in either the U.S. or the Canadian register.