NOAO SA
FR-MF-000022232 · France · PARIS
NOAO SA is registered in the European database on medical devices as a manufacturer, with 24 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 24 |
|---|
Most frequent device types declared: Artiflex - Tube souple 100 ml, Ceinture dorsale, Chaussette de compression - 2 unités, Couvre épaules, Mitaine.
Devices declared under this manufacturer
- Ceinture dorsale - Form'Vital - Taille 3
- Ceinture dorsale - Form'Vital - Taille 5
- Chaussettes de compression - Form'Vital - Taille 43/46
- Couvre-épaules - Form Vital - Taille M
- Couvre-épaules - Form'Vital - Taille S
- Mitaine - Form'Vital - Taille M
- Mitaine - Form'Vital - Taille S
- Panty - Form'Vital - Taille L/XL
- Panty - Form'Vital - Taille S/M
- Protège cervicales - Form'Vital
- Protège cheville - Form'Vital - Taille S/M
- Protège coude-genou - Form'Vital - taille 1
Showing 12 of 24 declared devices.
Catalogue references include BE4782, BE4785, BE4787, BE4791, BE4792, BE4799.
European nomenclature codes declared: M9001, M9002, Y061203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 24 |
| 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 | 24 |
|---|---|
| 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. NOAO SA was not found in either the U.S. or the Canadian register.