Mediconsult Oy
FI-MF-000008741 · Finland · Helsinki
Mediconsult Oy is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|---|
| Class IIb | 5 |
Most frequent device types declared: 2021.2, Kliiniset laskurit, Lääkitys (Saga).
Among these devices, 5 are declared active.
Devices declared under this manufacturer
- Kliiniset laskurit
- Kliiniset laskurit (Mediatri)
- Lääkitys
- Mediatri
- Mediatri Siro
- Mediresepti
- Varfariinihoito
- Varfariinihoito (Mediatri)
Catalogue references include 01, 02, Kliiniset laskurit, Kliiniset laskurit (Saga), Lääkitys (Mediatri), Lääkitys (Saga).
European nomenclature codes declared: V92.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 6 |
|---|---|
| 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. Mediconsult Oy was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
FI25/0000009 | issued | 2028-02-26 |