medi GmbH & Co. KG
DE-MF-000007092 · Germany · Bayreuth
medi GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 658 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 658 |
|---|
Devices declared under this manufacturer
- Lumbamed pro
- doumed basic
- duomed basic
- mediven thrombexin 18
Showing 12 of 658 declared devices.
Catalogue references include 214C105007, 2210502007, 2240112007, 2240505007, 2240514007, 2240517007.
European nomenclature codes declared: M030405, Y060308.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 658 |
| 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 | 658 |
|---|---|
| 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. medi GmbH & Co. KG was not found in either the U.S. or the Canadian register.