Wieds Ecochem AG
DE-MF-000006539 · Germany · Freudenberg
Wieds Ecochem AG is registered in the European database on medical devices as a manufacturer, with 80 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 80 |
|---|
Devices declared under this manufacturer
- A-Silikonspray
- A-Silikonspray Sodimed
- Elektrodengel GE 102
- Elektrodenklebegel 5060
- Elektrodenkontakspray
- Elektrodenkontaktspray
- Kalt Warm Kompresse
- Kalt Warm Kompresse Braun
- Kontaktgel
- Kühlspray
- Medispray
- Pumpe, Spender-, für Cubitainer 5 und 10 Liter
Showing 12 of 80 declared devices.
Catalogue references include M 60091901 FOD, M 600920919 BMF, M 60092194A BAC, M 60093792 TID, M 60093793 TIH, M 7019371.
European nomenclature codes declared: Z11049085, V0899, V9007, V0999, V0799,V0999, Z11040185,Z11049085.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 80 |
| 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. Wieds Ecochem AG was not found in either the U.S. or the Canadian register.