VILGO
FR-MF-000009712 · France · Creysse
VILGO is registered in the European database on medical devices as a manufacturer, with 2 641 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 2 641 |
|---|
Among these devices, 43 are declared active.
Devices declared under this manufacturer
- 471 VIOLET POURPRE
- 571 GRIS PASTEL
- 771 LILAS
- CANDY 200 (LAGON/NOIR)
- CANDY 250 (LAGON/BLEU)
- CANDY 600 (ROUGE/NOIR)
- GR 101 (NOIR/BORDEAUX)
- GR 32 FORTISSIMO (BLANC/BORDEAUX)
- GR 52 FORTISSIMO (BLEU VERT/BORDEAUX)
- HYSEA 200 AMANDE
- NOUMEA 100 VERT
- OMEGA GRIS PASTEL
Showing 12 of 2 641 declared devices.
Catalogue references include 1020012S22, 1020016S6, 2010007S6, 2010046S12, 2010140S23, 2040016S7.
European nomenclature codes declared: Y091203, Y12030601, V080202, Y120606, Y120603, Y120399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 2 641 |
| 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 | 2 641 |
|---|---|
| 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. VILGO was not found in either the U.S. or the Canadian register.