Dansac A/S
DK-MF-000001514 · Denmark · Kongens Lyngby
Dansac A/S is registered in the European database on medical devices as a manufacturer, with 912 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 912 |
|---|
Devices declared under this manufacturer
- Dansac
Showing 12 of 912 declared devices.
Catalogue references include 1155-40, 1215-55, 1219-36, 901-10, 931-37, 932-20.
European nomenclature codes declared: A1001010202, A1001010102, A10020202, A1002010402, A1002010401, A1001030202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 912 |
| 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 | 912 |
|---|---|
| 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. Dansac A/S was not found in either the U.S. or the Canadian register.