VIDAL FRANCE
FR-MF-000004612 · France · Issy-les-Moulineaux
VIDAL FRANCE is registered in the European database on medical devices as a manufacturer, with 251 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 224 |
|---|---|
| Class IIa | 27 |
Most frequent device types declared: VIDAL SECURISATION, VIDAL SENTINEL.
Among these devices, 251 are declared active.
Devices declared under this manufacturer
- VIDAL SECURISATION
- VIDAL SENTINEL
- Vidal Sécurisation FR
- Vidal sécurisation
Showing 12 of 251 declared devices.
Catalogue references include 2025.09, 2025.11.1, 2025.12.2, 2025.12.5, 2025.12.6, 2025.12.7.
European nomenclature codes declared: Z12040292.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 251 |
| 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 | 232 |
|---|---|
| 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. VIDAL FRANCE was not found in either the U.S. or the Canadian register.