CAHOUET
FR-MF-000009778 · France · Montreuil
CAHOUET is registered in the European database on medical devices as a manufacturer, with 597 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 597 |
|---|
Most frequent device types declared: VA7001 D, VE1402 I, VF3320 B, VF8601 C.
Among these devices, 597 are declared active.
Devices declared under this manufacturer
- CENTRALE A INVERSION AUTOMATIQUE T2m50
- DISPOSITIF DE SORTIE DE LA SOURCE DE SECOURS SS2m
- FLEXIBLES HAUTE PRESSION
- POTELET
Showing 12 of 597 declared devices.
Catalogue references include VA7016 A, VC5013 C, VC6138, VF3359 A, VF3391 A, VF3457.
European nomenclature codes declared: Z120309, Z12159099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 597 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. CAHOUET was not found in either the U.S. or the Canadian register.