Fysiotech OÜ
EE-MF-000007651 · Estonia · Viimsi vald
Fysiotech OÜ is registered in the European database on medical devices as a manufacturer, with 16 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 16 |
|---|
Most frequent device types declared: 2, 20103, 846A, BX2, CX1.
Among these devices, 15 are declared active.
Devices declared under this manufacturer
- Fysiotech Medistar X1 examination table
- Syntropy Tables
- Treat
Showing 12 of 16 declared devices.
Catalogue references include 10203, 10603, 10606, 10802, 20201, 20204.
European nomenclature codes declared: V080603.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 16 |
| 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 | 16 |
|---|---|
| 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. Fysiotech OÜ was not found in either the U.S. or the Canadian register.