RehaNorm GmbH & Co. KG
DE-MF-000006643 · Germany · Bingen-Kempten
RehaNorm GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 12 |
|---|
Most frequent device types declared: BRHAR/3001, BRMAX/1000, BRMTS/5002.
Devices declared under this manufacturer
- Harlekin Lagerungskeil
- Mannheimer Toiletten- und Duschsitzschalen-stuhl (MTS)
- Mannheimer Toiletten- und Duschsitzschalenstuhl (MTS)
- Max Therapiestuhl
- Multiroller Rehabuggy
Catalogue references include BRHAR/3002, BRMAX/1000, BRMTS/5004, BRMTS/5005, BRMTS/5006, BRMTS/5042.
European nomenclature codes declared: Y091203, Y180939, Y122703, Y180918.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| 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 | 12 |
|---|---|
| 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. RehaNorm GmbH & Co. KG was not found in either the U.S. or the Canadian register.