Mekalasi Oy
FI-MF-000003102 · Finland · Helsinki
Mekalasi Oy is registered in the European database on medical devices as a manufacturer, with 52 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 52 |
|---|
Devices declared under this manufacturer
- Idocare Visel istuintyyny
- Idocare Visel istuintyyny 46 x 46 x 6 cm
- Idocare Visel istuintyyny 52 x 45 x 6 cm
- Idocare Visel patja 119 x 58 x 13 cm
- Idocare Visel patja 160 x 70 x 13 cm, sisältää evakuointisuojuksen
- Idocare Visel patja 160 x 80 x 13 cm, sisältää evakuointisuojuksen
- Idocare Visel patja 160 x 80 x 13 cm, viskoelastinen vaahto 5 cm + PU
- Idocare Visel patja 200 x 78 x 13 cm, sisältää evakuointisuojuksen
- Idocare Visel patja 200 x 85 x 13 cm, sisältää evakuointisuojuksen
- Idocare Visel patja 205 x 78 x 13 cm, sisältää evakuointisuojuksen
- Idocare Visel patja 205 x 85 x 13 cm, sisältää evakuointisuojuksen
- Idocare Visel patja 205 x 90 x 13 cm, sisältää evakuointisuojuksen
Showing 12 of 52 declared devices.
Catalogue references include 281000, 2810462, 2810526, 2868013, 2927813, 2957813.
European nomenclature codes declared: V080702, Q030499, Q03040199, U089006, V0399, U089010.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 52 |
| 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 | 52 |
|---|---|
| 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. Mekalasi Oy was not found in either the U.S. or the Canadian register.