Hospidex France SAS
FR-MF-000008923 · France · Aix en Provence
Hospidex France SAS is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 17 |
|---|
Devices declared under this manufacturer
- Alco-Prep
- Alco-Swab
- Benza-Clean
Showing 12 of 17 declared devices.
Catalogue references include HOS-10-3001HD, HOS-10-4300HD, HOS-10-5201HD, HOS-610HD, HOS-7235HD, HOS-853-500HD.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| 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 | 17 |
|---|---|
| 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. Hospidex France SAS was not found in either the U.S. or the Canadian register.