FRANCEHOPITAL SAS
FR-MF-000038034 · France · Erstein
FRANCEHOPITAL SAS is registered in the European database on medical devices as a manufacturer, with 26 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 26 |
|---|
Most frequent device types declared: CbPlus, EssentialPlus, PerlaPlus, PersocarPlus, PersolifePlus.
Devices declared under this manufacturer
- Cb
- Essential
- Perla
- Persocar
- Persolife
- Pi-Nero
- Preciso
- Presto
- Trs
Showing 12 of 26 declared devices.
Catalogue references include CB20DMXXXX, HK6DMXXXX, PC4DMXXXX, PNDM-XXXX, PREIDMXXXX, TRSDDMXXXX.
European nomenclature codes declared: V0899.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 26 |
| 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 | 26 |
|---|---|
| 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. FRANCEHOPITAL SAS was not found in either the U.S. or the Canadian register.