Alber GmbH
DE-MF-000005502 · Germany · Albstadt
Alber GmbH is registered in the European database on medical devices as a manufacturer, with 356 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 356 |
|---|
Most frequent device types declared: SMOOV O10, e-fix E35, e-fix E36, e-motion M25, e-motion M25 DuoDrive.
Among these devices, 356 are declared active.
Devices declared under this manufacturer
- VIA GO
- e-fix
- e-motion
- e-motion DuoDrive
- e-pilot
- scalacombi
- scalacombi S36
- scalacombi S39
- scalamobil S38
- smoov
- twion
- viamobil
Showing 12 of 356 declared devices.
Catalogue references include 1592654, 1592666, 1592677, 1592897, 1594196, 1594227.
European nomenclature codes declared: Y122410, Y183012.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | ALBER GMBH (DE) · FDA 3004730072 |
| Devices in EUDAMED | 356 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 356 |
|---|---|
| Found in the U.S. device database | 142 |
| Share | 39.9 % |
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: United States only. Alber GmbH is registered in the United States but was not found in the Canadian register.