Weiss Tex GmbH
DE-MF-000008101 · Germany · Miltenberg
Weiss Tex GmbH is registered in the European database on medical devices as a manufacturer, with 125 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 125 |
|---|
Among these devices, 125 are declared sterile.
Catalogue references include M0000033, M0000145, M0000239, M0000311, M0000314, M0000370.
European nomenclature codes declared: T020199, T020199,T020401, T020401, T020402, T020199,T020401,T020402, T020401,T020402.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 125 |
| 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 | 125 |
|---|---|
| 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. Weiss Tex GmbH was not found in either the U.S. or the Canadian register.