WH Pharmawerk Weinböhla GmbH
DE-MF-000006741 · Germany · Weinböhla
WH Pharmawerk Weinböhla GmbH is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Devices declared under this manufacturer
- Activomin®
- MOLECUSAN® Capture
- OMNi-BiOTiC® ViTAL Humin
- OMNi-LOGiC® HUMIN
Catalogue references include A000218, A000221, A000222, A000223, A000311, A000314.
European nomenclature codes declared: G0499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 11 |
|---|---|
| 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. WH Pharmawerk Weinböhla GmbH was not found in either the U.S. or the Canadian register.