Helavo GmbH
DE-MF-000035224 · Germany · Seeheim-Jugenheim
Helavo 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: H2010, Rollator.
Among these devices, 2 are declared active.
Devices declared under this manufacturer
- Helavo Electric Wheelchair (H2010)– Heavy Duty_Dual Side Battery
- Helavo Electric Wheelchair (H2320)- Magnesium Lightweight
Showing 12 of 29 declared devices.
Catalogue references include H1010, H1012, H1013, H1060, H1142, H1170.
European nomenclature codes declared: Y120606, Y122127.
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. Helavo GmbH was not found in either the U.S. or the Canadian register.