HERDEGEN SAS
FR-MF-000002425 · France · CHELLES
HERDEGEN SAS is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 13 |
|---|
Most frequent device types declared: 304723, 570806, Contact Plus neo, Contact plus neo, REHAUSSE WC CLIPPER II.
Devices declared under this manufacturer
- CHAISE PERCÉE BEST UP ROULETTES AVEC BOUCHON - OCÉAN
- CLIPPER II
- Clipup
- Contact Plus neo
- Contact plus neo
- Slid Plus
- clipup grey
Showing 12 of 13 declared devices.
Catalogue references include 410172, 500001, 500001anis, 500001blanc, 500200n, 500300n.
European nomenclature codes declared: Y091215, Y091203, Y091299, Y0999.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 13 |
| 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 | 13 |
|---|---|
| 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. HERDEGEN SAS was not found in either the U.S. or the Canadian register.