BIOMED Labordiagnostik GmbH
DE-MF-000010310 · Germany · Oberschleissheim
BIOMED Labordiagnostik GmbH is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Hemafix® Blau
- Hemafix® Fixierlösung
- Hemafix® Puffer pH 7.2
- Hemafix® Rot
Catalogue references include 102301, 102302, 102304, 102305, 102307, 102308.
European nomenclature codes declared: W0103010302, W01030799, W01030705.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| 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. BIOMED Labordiagnostik GmbH was not found in either the U.S. or the Canadian register.