Dermanostic GmbH
DE-MF-000034712 · Germany · Solingen
Dermanostic GmbH is registered in the European database on medical devices as a manufacturer, with 24 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 24 |
|---|
Most frequent device types declared: DAPP04.
Among these devices, 24 are declared active.
Devices declared under this manufacturer
- dermanostic App
- dermanostic Webapp
Showing 12 of 24 declared devices.
Catalogue references include DAPP043670, DAPP043730, DWAPP011030, DWAPP011040, DWAPP011060, DWAPP011080.
European nomenclature codes declared: V92.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 24 |
| 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 | 24 |
|---|---|
| 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. Dermanostic GmbH was not found in either the U.S. or the Canadian register.