Rehadapt GmbH
DE-MF-000008141 · Germany · Kassel
Rehadapt GmbH is registered in the European database on medical devices as a manufacturer, with 270 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 270 |
|---|
Among these devices, 6 are declared active.
Devices declared under this manufacturer
- CC BM Nightstand E20x20 / 25x10
- Custom Monty 3D Plus
- FS TeleFloat QP
- FS VarioFloat Light QP
- Hybrid 3D Long SLS Sturdy
- Hybrid 3D Long UDS Sturdy
- Hybrid 3D Short UDS
- L3D 10-Base R14
- M3D RKL 30
- M3D RKL Cross 6
- M3D RKL-T 22
- M3D RKL-T 27
Showing 12 of 270 declared devices.
Catalogue references include 11.1051, 11.1130, 11.1197, 11.1422, 11.3312CM, 13.4311.
European nomenclature codes declared: Y214299, V0880.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Rehadapt GmbH (DE) · FDA 3008931108 |
| Devices in EUDAMED | 270 |
| Country of registration | Germany |
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: United States only. Rehadapt GmbH is registered in the United States but was not found in the Canadian register.