Werkmeister GmbH + Co. KG
DE-MF-000005120 · Germany · Wanfried
Werkmeister GmbH + Co. KG is registered in the European database on medical devices as a manufacturer, with 2 180 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 2 180 |
|---|
Devices declared under this manufacturer
- BANDA
- BANDANA lang
- EcoKiss 46x43x3cm, Unterboden RutschStopp
- EcoKiss Plus Sitzkissen B&B
- EcoKiss Sitzkissen 40x43x5cm
- EcoKiss Sitzkissen 40x43x5cm Latex
- Lendenpelotte 26 cm
- Osteolind® mobil Miederbody - Mittel - mit BH Cup
- PneumoKiss Schaumstoffkissen B46xT43xH3cm RG40
- PneumoKiss Schaumstoffkissen B50xT43xH3cm RG40
- PneumoKiss Verbundschaumkissen B38xT38xH3cm V100
- Rollatorkissen SB38xST20xH5cm, mit RutschStopp
Showing 12 of 2 180 declared devices.
Catalogue references include 110438383, 13ALG, 20079/PLUS/RA, 20081/DRUCK/RA, 20291, 2177.
European nomenclature codes declared: Y060309, V080399, V08030102, M030499, Y060499, V080302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 2 180 |
| 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 | 2 180 |
|---|---|
| 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. Werkmeister GmbH + Co. KG was not found in either the U.S. or the Canadian register.