BAG Diagnostics GmbH
DE-MF-000024383 · Germany · Lich
BAG Diagnostics GmbH is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- DaraEx GO
Catalogue references include 69311, 69501, 726110, 728198, 728201, 728208.
European nomenclature codes declared: W01030399, W0106010499, W010699, W0106010401, W02060199, W010399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| 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 | 7 |
|---|---|
| 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. BAG Diagnostics GmbH was not found in either the U.S. or the Canadian register.