METEK Köber & Michalski OHG
DE-MF-000039613 · Germany · Königswartha
METEK Köber & Michalski OHG is registered in the European database on medical devices as a manufacturer, with 54 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 54 |
|---|
Most frequent device types declared: Zureichtisch.
Devices declared under this manufacturer
- METEK Köber & Michalski OHG
- MRT-Rollsessel
- artosy
Showing 12 of 54 declared devices.
Catalogue references include 11430011, 12200116, 12200122, 12200522, 12211001/2, 12221100.
European nomenclature codes declared: V80, Y122199, V080299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 54 |
| 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 | 54 |
|---|---|
| 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. METEK Köber & Michalski OHG was not found in either the U.S. or the Canadian register.