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.
Devices declared under this manufacturer
- CELLIS
- CELLIS BREAST
- CELLIS DENTAL
- CELLIS RECTOPEXY
Showing 12 of 23 declared devices.
Catalogue references include CELLIS BREAST CB1923MF, CELLIS BREAST CB2124MF, CELLIS C1015E, CELLIS C1825E, CELLIS C2030E, CELLIS DENTAL NP1520E.
European nomenclature codes declared: P900299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 23 |
| 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 | 23 |
|---|---|
| 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. MECCELLIS BIOTECH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
1434-MDR-013/2026 | issued | 2031-04-23 |
1434-MDR-012/2026 | issued | 2031-04-23 |