Tukimet Oy
FI-MF-000006700 · Finland · Rauma
Tukimet Oy is registered in the European database on medical devices as a manufacturer, with 137 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 137 |
|---|
Most frequent device types declared: 3000, 3020, 3030, 3070, 4000.
Devices declared under this manufacturer
- Koroketyyny 5 cm 40 x 40, sametti
- Mauno
- Mauno Matala
- Nousutuki, kääntyvä, sormiruuvikiinnitys, matalalla lattiatuella
- Paavo Iso
- Pyörätuolityyny 40 cm x 46 cm x 5 cm visko, muovitettu polyester
- Pyörätuolityyny 42 cm x 46 cm x 5 cm visko, muovitettu polyester
- Pyörätuolityyny 42 x 50 x 4, tarralla, muovitettu polyester
- Pyörätuolityyny 44 cm x 48 cm x 5 cm visko, muovitettu polyester
- Pyörätuolityyny 46 cm x 44 cm x 5 cm visko, muovitettu polyester
- Pyörätuolityyny 48 cm x 40 cm x 5 cm visko, muovitettu polyester
- Sauli Matala
Showing 12 of 137 declared devices.
Catalogue references include 338700i, 339600M, 650129S, 654220S, 660105, 674250T.
European nomenclature codes declared: V080399, Y180999, Y181899, Y120609, Y1899, Y181803.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 137 |
| 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 | 137 |
|---|---|
| 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. Tukimet Oy was not found in either the U.S. or the Canadian register.