Cizeta Medicali France
FR-MF-000000604 · France · SAINT-AMAND-MONTROND
Cizeta Medicali France is registered in the European database on medical devices as a manufacturer, with 289 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 289 |
|---|
Most frequent device types declared: SL 500.
Catalogue references include 3701126302340, 3701126307833, 3701126309080, 3701126312950, 3701126316910, 3701126318945.
European nomenclature codes declared: Y061209, Y06120601, Y060308, Y060312, Y060613, Y060612.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 289 |
| 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 | 289 |
|---|---|
| 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. Cizeta Medicali France was not found in either the U.S. or the Canadian register.