Wilhelm Weisweiler GmbH & Co. KG
DE-MF-000021416 · Germany · Münster
Wilhelm Weisweiler GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 234 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 234 |
|---|
Among these devices, 56 are declared sterile.
Devices declared under this manufacturer
- BONA Mulltupfer 6 K haselnuss
- DC Wattekügelchen 7 mm
- DC Watterollen Pure 10 mm
- HS Mulltupfer Größe XL
- Mullkompressen 12-fach, 10 x 10 cm
- Orbis Wattekügelchen 5,5 mm
- abc Wattekügelchen 4 mm
- selbsthaftende elastische Binde 10 cm x 4,5m, orange
- selbsthaftende elastische Binde 2,5 cm x 4,5m, dunkelgrün
- selbsthaftende elastische Binde 7,5 cm x 4,5m, purple
- selbsthaftende elastische Binde latexfrei 10 cm x 4,5m, blau
- selbsthaftende elastische Binde latexfrei 2,5 cm x 4,5m, rot
Showing 12 of 234 declared devices.
Catalogue references include 00372860, 00704342, 00704354, 00SEB25g, 900-8744, SEBFL50r.
European nomenclature codes declared: M020199, M0199, M04010201, M04010101, T04010299, M0202030102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 234 |
| 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. Wilhelm Weisweiler GmbH & Co. KG was not found in either the U.S. or the Canadian register.