Oy Diagnostic Devices Development
FI-MF-000017197 · Finland · Kuopio
Oy Diagnostic Devices Development is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|
Most frequent device types declared: CardioMobile-12, CardioMobile-3.
Among these devices, 3 are declared active, 5 with a measuring function.
Devices declared under this manufacturer
- Cardio Mobile
- CardioMobile
- CloudHolter
- TeleCardio
- Web-ECG
Catalogue references include 01, 02, 03, 04, 05.
European nomenclature codes declared: C020599, Z12050301, Z12050403, V92.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| Country of registration | Finland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. Oy Diagnostic Devices Development was not found in either the U.S. or the Canadian register.