OLFA
FR-MF-000010359 · France · SIGNY LE PETIT
OLFA is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 15 |
|---|
Most frequent device types declared: BASSIN MALADE, BOCAL URINE, BOCK INJECTION, CRACHOIR, CUVETTE HARICOT.
Devices declared under this manufacturer
- Bassin malade blanc
- Bocal urine 2L translucide
- Bock injection 2L blanc
- Couvercle bassin malade blanc
- Crachoir blanc
- Cuvette haricot blanc
- Inhalateur Naturactive Vert P343
- Inhalateur blanc
- Pharmex Inhalator / Inhalateur CNK 0626598
- Seau hygiénique adulte 306 blanc
- Urinal femme 1L
- Urinal homme 1L avec bouchon
Showing 12 of 15 declared devices.
Catalogue references include 6502100, 6507100, 6507150, 6509100, 6509201, 6509201M.
European nomenclature codes declared: V0812, R0699, V0499, V0402, A99.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 15 |
| 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 | 15 |
|---|---|
| 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. OLFA was not found in either the U.S. or the Canadian register.