CLErmont RAyonnement Détection
FR-MF-000033379 · France · CLERMONT-FERRAND
CLErmont RAyonnement Détection is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 4 |
|---|---|
| Class IIb | 2 |
Most frequent device types declared: GAMMA-AM, GAMMA-SUPII, Générateur PAPILLON +.
Among these devices, 6 are declared reusable, 5 active.
Devices declared under this manufacturer
- GAMMA-AM
- GAMMA-SUPII
- PAPILLON +
Catalogue references include 87-1-1, GS II 5000 RAD 5001 RAD 5002 RAD 5003 RAD 5004, GSIIBT, GSIIDEC2, GSIIDECGSIIDEC, GSIIMULTI.
European nomenclature codes declared: Z110206, Z11010301,Z11029001, Z11010301.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 6 |
|---|---|
| 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. CLErmont RAyonnement Détection was not found in either the U.S. or the Canadian register.