VUILLET VEGA
FR-MF-000015806 · France · MOREZ
VUILLET VEGA is registered in the European database on medical devices as a manufacturer, with 814 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 814 |
|---|
Most frequent device types declared: 1693.35.03, 1808.51.27, 1824.54.02, 1848.46.01.
Devices declared under this manufacturer
- VUILLET VEGA
Showing 12 of 814 declared devices.
Catalogue references include 1918.48.03, 1953.1.21, 2286.52.05, PL1028.52.13, PL495.56.06, PL835.47.02.
European nomenclature codes declared: Q02100201, Q02100203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 814 |
| 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 | 814 |
|---|---|
| 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. VUILLET VEGA was not found in either the U.S. or the Canadian register.