Laboratoires Anios
FR-MF-000011756 · France · Lezennes
Laboratoires Anios is registered in the European database on medical devices as a manufacturer, with 277 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 237 |
|---|---|
| Class IIb | 40 |
Devices declared under this manufacturer
- ANIOSYME SYNERGY 5
- ANIOSYME SYNERGY WD
- ANIOSYME X3
- ANIOXYDE 1000 LD
- Aniospray Surf 29
- Aniosyme XL3
- BANDELETTES ANIOXYDE 1000 LD
- BANDELETTES OPASTER ANIOS
- Bandelettes Anioxyde 1000LD
- INCIDIN OXYFOAM NG
- SURFA SAFE PREMIUM
- SURFANIOS PREMIUM
Showing 12 of 277 declared devices.
Catalogue references include 100110T3, 100120YL, 1917431, 23810366C, 2387038EM, 2419544TB.
European nomenclature codes declared: D0901, V0799, V80, D0599, D0701, D050103.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 277 |
| 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 | 277 |
|---|---|
| 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. Laboratoires Anios was not found in either the U.S. or the Canadian register.