PRO ACTIV Reha-Technik GmbH
DE-MF-000012881 · Germany · Dotternhausen
PRO ACTIV Reha-Technik GmbH is registered in the European database on medical devices as a manufacturer, with 29 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 29 |
|---|
Most frequent device types declared: Adaptivbike elektrisch, Adaptivbike manuell, Erwachsenenrollstuhl, Kinderrollstuhl, Kompaktbike elektrisch.
Devices declared under this manufacturer
- BUDDY
- FREAK Kompaktbike
- HUSK-E Adaptivbike mechanisch
- LIFT activ - mechanisch
- LIFT solid - elektrisch
- LITTY 4all
- SPEEDY 4teen
- SPEEDY 4you Ergo
- SPEEDY F1
- SPEEDY F2
- SPIKE Adaptivbike
- TRAVELER
Showing 12 of 29 declared devices.
Catalogue references include A901110000*, A901510000*, A901610500*, A903010000*, A904113000*, A904310000*.
European nomenclature codes declared: Y122106, Y121899, Y122410, Y122499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 29 |
| 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 | 29 |
|---|---|
| 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. PRO ACTIV Reha-Technik GmbH was not found in either the U.S. or the Canadian register.