Vitabalans Oy
FI-MF-000005080 · Finland · Hämeenlinna
Vitabalans Oy is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|
Devices declared under this manufacturer
- Asept antiseptinen liuos
- Gynolacta
- ICE GEL
- MacroBalans
- NaFDent
Catalogue references include FI-CA01-2009-0025, FI-CA01-2015-0884, FI-CA01-2016-0743, FI-CA01-2019-0276, FI/CA01/03989643-0002.
European nomenclature codes declared: V9099, G0499, Q010499, U0803.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| Country of registration | Finland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. Vitabalans Oy was not found in either the U.S. or the Canadian register.