ORTHO-REHA Neuhof GmbH
DE-MF-000008438 · Germany · Nürnberg
ORTHO-REHA Neuhof GmbH is registered in the European database on medical devices as a manufacturer, with 40 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 40 |
|---|
Most frequent device types declared: 201B09, 202B36=1, 202Z09=6, 202Z09=8, 204D27.
Devices declared under this manufacturer
- Frottee-Stumpfstrumpf
- Modular Clutchlock Blackline
Showing 12 of 40 declared devices.
Catalogue references include 201B09=L, 201B09=M, 201B09=S, 203B, 204D27=22L, 204D27=25R.
European nomenclature codes declared: Y062403, Y06120601, Y062409, Y120399, Y062499, Y060312.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 40 |
| 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 | 40 |
|---|---|
| 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. ORTHO-REHA Neuhof GmbH was not found in either the U.S. or the Canadian register.