Serumwerk Bernburg Vertriebs GmbH
DE-MF-000005002 · Germany · Bernburg
Serumwerk Bernburg Vertriebs GmbH is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 9 |
|---|---|
| Class IIa | 5 |
Among these devices, 5 are declared sterile.
Devices declared under this manufacturer
- DiaCart
- Eye-Lotion Balanced salt solution
Showing 12 of 14 declared devices.
Catalogue references include 1342, 1500, 1510, 1515, 1518, 1560.
European nomenclature codes declared: F040201, Q02030203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. Serumwerk Bernburg Vertriebs GmbH was not found in either the U.S. or the Canadian register.