Schupp GmbH & Co. KG
DE-MF-000010127 · Germany · Dornstetten-Aach
Schupp GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 37 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 37 |
|---|
Most frequent device types declared: Therapy Table.
Among these devices, 16 are declared active.
Devices declared under this manufacturer
- ACHAT
- BOLANI
- EisPack 17x20cm
- EisPack 25*30cm
- EisPack 30x37 cm
- EisPack 30x52 cm
- Gymnastikhocker
- OPAL
- OPAL PLUS
- PHOENIX
- TEDAVI
- TEDAVI ELLE
Showing 12 of 37 declared devices.
Catalogue references include 124099, 131035, 136435, 138635, 139435, 139935.
European nomenclature codes declared: Z120602.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 37 |
| 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 | 37 |
|---|---|
| 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. Schupp GmbH & Co. KG was not found in either the U.S. or the Canadian register.