Baumann Ed.
FR-MF-000049737 · France · Cléon
Baumann Ed. is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 12 |
|---|
Devices declared under this manufacturer
- CHAJA
- FAVA
- KAGARA
- PABAMA
- SAZA
- TADANALA
Catalogue references include CHAJA T1, FAVA T1, FAVA T2, KAGARA T1, KAGARA T2, PABAMA T1.
European nomenclature codes declared: Y0599.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| 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 | 12 |
|---|---|
| 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. Baumann Ed. was not found in either the U.S. or the Canadian register.