Kaniedenta Produktionsgesellschaft mbH
DE-MF-000005873 · Germany · Herford
Kaniedenta Produktionsgesellschaft mbH is registered in the European database on medical devices as a manufacturer, with 48 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 48 |
|---|
Among these devices, 37 are declared implantable.
Catalogue references include 1550, 1961, 40380, 42503, 42551, 42602.
European nomenclature codes declared: Q01010103, Q01010106, Q01020102, Q010503, Q0102050102, Q01010104.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 48 |
| 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. Kaniedenta Produktionsgesellschaft mbH was not found in either the U.S. or the Canadian register.