OBRO
FR-MF-000019841 · France · Beziers
OBRO is registered in the European database on medical devices as a manufacturer, with 59 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 59 |
|---|
Most frequent device types declared: Accessoires, Châssis, Porte tablette, Repose Pied, Têtière.
Devices declared under this manufacturer
- Articulation libre déportée
- CS300
- Châssis CS65
- Coulisse
- Manette indexable femelle M10
- Molette papillon M8x12
- Paire de repose pied simple 16mm
- Paire de repose pied à noix crantée avec palette basculable 16 mm
- Plaquette inox longue
- Rallonge aluminium 350
- Têtière basculante et coulissante à tête plate
- Têtière à tête plate déportée sur l’arrière
Showing 12 of 59 declared devices.
Catalogue references include CS210, CS300, CS316-16, CS32-20, CS51-AR, CS51-AV.
European nomenclature codes declared: Z12130280, Z12130202, Y1299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 59 |
| 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 | 59 |
|---|---|
| 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. OBRO was not found in either the U.S. or the Canadian register.