Danrehab A/S
DK-MF-000024162 · Denmark · Tørring
Danrehab A/S is registered in the European database on medical devices as a manufacturer, with 25 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 25 |
|---|
Most frequent device types declared: ERGOtip.
Among these devices, 15 are declared active.
Devices declared under this manufacturer
- BUZZ 1
- ERGOtip 10 (M)
- ERGOtip 5 (M) Anytoilet
- ERGOtip 6 (L)
- ERGOtip 7 (XL)
- ERGOtip 8 (S)
- ERGOtip Butterfly Large (L)
- ERGOtip Tall (M)
- MAJ
- PullAid
- SOLI 7
- SOLI 8
Showing 12 of 25 declared devices.
Catalogue references include 100206, 109630, 125729, 1400, 25178, 2780.
European nomenclature codes declared: Y093303, V08068099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 25 |
| Country of registration | Denmark |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 25 |
|---|---|
| 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. Danrehab A/S was not found in either the U.S. or the Canadian register.