Cardia International A/S
DK-MF-000002223 · Denmark · Roskilde
Cardia International A/S 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 IIb | 5 |
|---|
Most frequent device types declared: BM0207RF, CA-10ES, CR-13P, CT0207RF, CT0207RS.
Among these devices, 5 are declared active, 5 with a measuring function.
Devices declared under this manufacturer
- BLOSTRUPMOEN®
- CardiAid®
Catalogue references include F/BRO/01, F/BRO/02.
European nomenclature codes declared: C020401, Z12030503, Z12030501.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 5 |
|---|---|
| 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. Cardia International A/S was not found in either the U.S. or the Canadian register.