GAIA AG
DE-MF-000006280 · Germany · Hamburg
GAIA AG is registered in the European database on medical devices as a manufacturer, with 21 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 21 |
|---|
Among these devices, 21 are declared active.
Devices declared under this manufacturer
- alivis
- attexis
- autimia
- calisda
- covivio
- deprexis
- levidex
- libraderm
- lipodia
- priovi
- reviga
- somnovia
Showing 12 of 21 declared devices.
Catalogue references include 16, 28, 33, 6, 72, 84.
European nomenclature codes declared: V92.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 21 |
| 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 | 21 |
|---|---|
| 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. GAIA AG was not found in either the U.S. or the Canadian register.