W.Söhngen GmbH
DE-MF-000026580 · Germany · Taunusstein
W.Söhngen GmbH is registered in the European database on medical devices as a manufacturer, with 208 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 208 |
|---|
Among these devices, 1 are declared active.
Devices declared under this manufacturer
- Dreiecktuch V, schwarz, einzeln
- Nachfüllset detectable Strips, stab., blau, 40 Strips
- Nachfüllset detectable Strips, stab., blau, gefüllt mit 40 Strips á 2
- aluderm+ Dreiecktuch V Kinder, groß, einzeln
- aluderm+ Kalt/Warm Kompresse, 2 Stk.
- aluderm+ Pflasterspender, elastisch, gefüllt mit 115 Pflastern
- aluderm+ Pflasterverband elastisch, Strips, 30 Stück
- aluderm+ Pflasterverband stabil, Fingerkuppenverband, 50 Stück
- aluderm+ Pflasterverband stabil, Fingerkuppenverband, wasserfest, 10 S
- aluderm+ Pflasterverband stabil, Fingerverband, 50 Stück
- aluderm+ Rettungsdecke Kinder, gold/silber, mit Box, einzeln
- aluderm+ Wundpflaster Mix, transparent, wasserfest, 20 Stück
Showing 12 of 208 declared devices.
Catalogue references include 1008212, 1008300, 1008305, 1008325, 1009984, 1010006.
European nomenclature codes declared: M04010101, M04010102, M03050299, T0399, M050101, V080603.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 208 |
| 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 | 208 |
|---|---|
| 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. W.Söhngen GmbH was not found in either the U.S. or the Canadian register.