MEDE Technik GmbH
DE-MF-000005564 · Germany · Emmingen
MEDE Technik GmbH is registered in the European database on medical devices as a manufacturer, with 6 661 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 6 661 |
|---|
Most frequent device types declared: Cerclagedrähte (1.4441), Cerclagedrähte (Titan), Kirschner Bohrdrähte (1.4441), Kirschner Bohrdrähte (Titan), Knochendrähte (1.4441).
Among these devices, 6 661 are declared implantable.
Catalogue references include 33.0130.400, 33.0135.175, 33.0222.220, 33.0245.400, 33.0322.200, 33.1365.180.
European nomenclature codes declared: P09120301, P09120299, P09120302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 661 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 6 661 |
|---|---|
| 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. MEDE Technik GmbH was not found in either the U.S. or the Canadian register.