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-SUPII, GAMMA-AM, Générateur PAPILLON +.
Among these devices, 6 are declared reusable, 5 active.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | France |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.