QA MED Solutions
DK-MF-000001649 · Denmark · Middelfart
QA MED Solutions is registered in the European database on medical devices as a manufacturer, with 45 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 45 |
|---|
Most frequent device types declared: MP101, SS101X, WJ101.
Devices declared under this manufacturer
- CosaOP
Showing 12 of 45 declared devices.
Catalogue references include SS101X02-B/W/M, SS101X03-T/C/M, SS101XUB-06, SS101XUT-06, SS201X02-B/W, SS201X03-B/W.
European nomenclature codes declared: T0205, T0299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 45 |
| Country of registration | Denmark |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 45 |
|---|---|
| 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. QA MED Solutions was not found in either the U.S. or the Canadian register.