BATEC MOBILITY
ES-MF-000000576 · Spain · Sant Quirze del Vallès
BATEC MOBILITY is registered in the European database on medical devices as a manufacturer, with 160 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 160 |
|---|
Most frequent device types declared: AIR / MINI 2 / ELECTRIC 2 / RAPID 2 / SCRAMBLER 2 / MINI 2 PLUS / ELEC, HIBRID 2.
Among these devices, 160 are declared active.
Devices declared under this manufacturer
- BATEC ELECTRIC 2 HEMI LEFT - 10 Km/h
- BATEC ELECTRIC 2 PLUS HEMI LEFT
- BATEC HIBRID 2 - 20 Km/h
- BATEC HIBRID 2- 15 Km/h
- BATEC MINI 2 HEMI LEFT - 10 Km/h
- BATEC QUAD ELECTRIC 2 - 10 Km/h
- BATEC QUAD MINI 2 - 10 Km/h
- BATEC RAPID 2
- BATEC RAPID 2 PLUS
- BATEC RAPID 2 PLUS - 15 Km/h
- BATEC RAPID 2 PLUS QUAD - 10 Km/h
- BATEC RAPID SPORT HEMI RIGHT
Showing 12 of 160 declared devices.
Catalogue references include 2511004, 2530008, 2531018, 2540016, 2557004, 2560022.
European nomenclature codes declared: Y122410.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | BATEC MOBILITY S.L (ES) · FDA 3011749761 |
| Devices in EUDAMED | 160 |
| Country of registration | Spain |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 160 |
|---|---|
| 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.