Tieto Finland Oy
FI-MF-000002445 · Finland · Espoo
Tieto Finland Oy is registered in the European database on medical devices as a manufacturer, with 22 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 18 |
|---|---|
| Class IIb | 4 |
Among these devices, 22 are declared active.
Devices declared under this manufacturer
- DynamicHealth
- Effica Kertomus
- Effica Laboratorio
- Effica Patologia (QPati)
- Effica Perioperatiivinen hoito
- Effica Äitiyshuolto
- Lifecare Dental SWE
- Lifecare EHR
- Lifecare Kasvun ja kehityksen seuranta
- Lifecare Kirjausalusta
- Lifecare Lääkitys
- Lifecare Patologia (QPati)
Showing 12 of 22 declared devices.
Catalogue references include 111031, 111403, 111918, 113520, 113947, 120436.
European nomenclature codes declared: V92, Z12040192.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 22 |
| 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 | 22 |
|---|---|
| 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. Tieto Finland Oy was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
CR-03-1226-911-26 | supplemented | 2028-08-11 |