DHCare Suomi Oy
FI-MF-000009089 · Finland · Helsinki
DHCare Suomi Oy is registered in the European database on medical devices as a manufacturer, with 60 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 60 |
|---|
Most frequent device types declared: CaseSlow, CaseSupport, CaseTop, Exact7040, ExactQ.
Among these devices, 12 are declared active.
Devices declared under this manufacturer
- CaseSlow
- CaseSupport
- CaseTop
- ExactQ
- Mega18040
- Mega7040
- MegaMemorest
- MegaT
- Opera II
- OptimaCot
- ProKuutio
- ProRelax
Showing 12 of 60 declared devices.
Catalogue references include 10TS2L68P170K13, 20CSL503313, 20CSU30308, 30EXQL42S42K7, 40MEG7040, 40MET806032.
European nomenclature codes declared: V080702, V080701, V080302, Y1899, V08030102, V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 60 |
| 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 | 60 |
|---|---|
| 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. DHCare Suomi Oy was not found in either the U.S. or the Canadian register.