Invacare Rea AB
SE-MF-000003772 · Sweden · Diö
Invacare Rea AB is registered in the European database on medical devices as a manufacturer, with 335 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 335 |
|---|
Among these devices, 190 are declared active.
Devices declared under this manufacturer
- Alpha Basic
- Futura™ 450
- Futura™ 600
- Futura™ 680
- Gloss® 600
- Gloss® 680
- Maxi+ 550
- Maxi+ 650
- NordBed™ Optimo
- NordBed™ Optimo Wide
- NordBed™ Ultra
- SB®910
Showing 12 of 335 declared devices.
Catalogue references include 12076-43-21, 12122-37-24, 1649849_S2, 1653831, 1654613, 1655714_S1.
European nomenclature codes declared: V08060101, Y120609, Y050201, V08060106, Y120603.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | Invacare GmbH (DE) · FDA 3007231105 |
| Devices in EUDAMED | 335 |
| Country of registration | Sweden |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 335 |
|---|---|
| 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.