REBOTEC Rehabilitationsmittel GmbH
DE-MF-000009447 · Germany · Quakenbrück
REBOTEC Rehabilitationsmittel GmbH is registered in the European database on medical devices as a manufacturer, with 656 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 656 |
|---|
Most frequent device types declared: Arthritisstützen, Dusch-Toilettenrollstühle, Duschstühle, Gehgestelle, Gehstöcke.
Among these devices, 16 are declared active.
Devices declared under this manufacturer
- Anatom
- Berlin
- Bonn
- Hemi
- Magic-Soft
- Magic-Soft-Anatom
- Magic-Twin
- Magic-Twin Überlänge
- Oslo
- Phoenix
- Safe-In-Anatom-Soft
- Walk-On
Showing 12 of 656 declared devices.
Catalogue references include 10280, 10460, 1073020, 1212010, 17440, 3440300.
European nomenclature codes declared: Y091203, Y12030601, Y120399, Y180918, Y12030602, Y120318.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | REBOTEC REHABILITATIONSMITTEL GMBH (DE) · FDA 3006481901 |
| Devices in EUDAMED | 656 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 656 |
|---|---|
| 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: United States only. REBOTEC Rehabilitationsmittel GmbH is registered in the United States but was not found in the Canadian register.