MECCELLIS BIOTECH
FR-MF-000002452 · France · LA ROCHELLE
MECCELLIS BIOTECH is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 23 |
|---|
Most frequent device types declared: C55E.
Among these devices, 23 are declared sterile, 23 implantable.
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 | 23 |
| 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.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
1434-MDR-013/2026 | issued | 2031-04-23 |
1434-MDR-012/2026 | issued | 2031-04-23 |