Is Omaolo certified as a medical device?
Omaolo by DigiFinland Oy is listed in EUDAMED as a CE class IIb medical device. The manufacturer holds a valid notified body certificate under the MDR in EUDAMED. We found no FDA authorisation.
At a glance
| Product | Omaolo |
|---|---|
| Maker | DigiFinland Oy |
| Care area | Other |
| What it does | Finnish public symptom checker and self-care service that directs people to the right care |
| FDA | No FDA authorisation found |
| EU (CE) | Class IIb |
| EU certificate | Manufacturer certificate from a notified body (MDR) in EUDAMED (checked 18 October 2026) |
| Website | omaolo.fi |
| Status | CE verified |
| Last checked | 7 October 2026 |
Need the evidence behind this entry?
Certified Health Apps Pro gives you the FDA reference number, decision date and a direct link to the official record, plus the EU certificate and notified body, for every app. See Pro · Free guide: how to check a health app in two minutes
Certified Health Apps Pro gives you the FDA reference number, decision date and a direct link to the official record, plus the EU certificate and notified body, for every app. See Pro · Free guide: how to check a health app in two minutes
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