Sanavita Pharmaceuticals GmbH
DE-MF-000005463 · Germany · Hamburg
Sanavita Pharmaceuticals 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
| Class IIa | 4 |
|---|
Among these devices, 1 are declared sterile, 2 active.
Devices declared under this manufacturer
- Enelbin® Paste
- WariActiv® N
Catalogue references include (01)4033033508058, 20220328, 506115, COMBIPACK, OVULATIONTEST, PREGNANCYTEST.
European nomenclature codes declared: V9099, W0102050205, W0102160399, A0299, W0102050105.
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 | 2 |
|---|---|
| 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. Sanavita Pharmaceuticals GmbH was not found in either the U.S. or the Canadian register.