Vebasan OÜ
EE-MF-000043782 · Estonia · Tallinn
Vebasan OÜ is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Devices declared under this manufacturer
- BodyNeutrAll 5 L
- BodyNeutrAll S 100 ml
- C-Gel
- NeutralAll 100 ml
- NeutralAll 2 x 300 ml
- NeutralAll 5 Liter
- SkinNeutrAll 2 x 300 ml
Catalogue references include EST 00100, EST 00300, EST 00310, EST 00400, EST 0100 Bottle 2, EST 0100 x 4.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | Estonia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| 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. Vebasan OÜ was not found in either the U.S. or the Canadian register.