VILLARD
FR-MF-000002454 · France · NEUVILLE SUR SARTHE
VILLARD is registered in the European database on medical devices as a manufacturer, with 74 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 74 |
|---|
Most frequent device types declared: BERCEAU, CARDIAC BOARD, Divan d'examen, Lit parc, PORTE SERUM.
Catalogue references include 1500.23, 317.03, 317.13, 317.14, 317.34, 505.52.
European nomenclature codes declared: Z12030399, V080602, V0809, V080202, C020299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 74 |
| 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 | 74 |
|---|---|
| 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. VILLARD was not found in either the U.S. or the Canadian register.