MP Medical Product GmbH
DE-MF-000008853 · Germany · Geestland
MP Medical Product GmbH is registered in the European database on medical devices as a manufacturer, with 156 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 156 |
|---|
Among these devices, 92 are declared implantable, 2 reusable.
Devices declared under this manufacturer
- CAVITYLINER KDM
- Diamond Rapid set
- Lichthärtendes Löffelmaterial
- MP Ceramic Repair
- Nano-Ceramic LC
- OMNICERAM BULK FILL
- OMNIFILL C AKTIVATOR
- OMNIFILL C APPLIKATOR
- OMNITEMP KB
- ORBIS Cem SE DC
- Orbis Cavity Liner LC
- TOP DENT SC TEMP C&B MATERIAL
Showing 12 of 156 declared devices.
Catalogue references include 102980, 216465, 604049, 829609, 8477, FLU404.
European nomenclature codes declared: Q01010103, Q01020605, Q0101010201, Q010503, Q01010106, Q01010105.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 156 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. MP Medical Product GmbH was not found in either the U.S. or the Canadian register.