Timoteos Oy
FI-MF-000011749 · Finland · Espoo
Timoteos Oy is registered in the European database on medical devices as a manufacturer, with 28 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 28 |
|---|
Devices declared under this manufacturer
- ELLA STANDER
- ODE INDOOR BASE
- ODE OUTDOOR BASE
- ODE SEAT
Showing 12 of 28 declared devices.
Catalogue references include 5500, 5520, 66111, 9311+, 9321, 9341.
European nomenclature codes declared: Y050202, Y180918.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 28 |
| Country of registration | Finland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 28 |
|---|---|
| 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. Timoteos Oy was not found in either the U.S. or the Canadian register.