A/S Aabentoft
DK-MF-000034597 · Denmark · Skødstrup
A/S Aabentoft is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 7 |
|---|
Most frequent device types declared: Poweradapter.
Among these devices, 5 are declared active.
Devices declared under this manufacturer
- Aabentoft
- Poweradapter LiNX GP 19V
- Poweradapter R-net GP 12V
- Poweradapter R-net GP 19V
- Unitrack Bracket Left
- Unitrack Bracket Right
Catalogue references include ABTIMJD, AMTPUTRL, AMTPUTRR, HPSUSB12072LX, HPSUSB12072RN, HPSUSB19072LX.
European nomenclature codes declared: Y122499, Y122499,Y210906.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| 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 | 7 |
|---|---|
| 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. A/S Aabentoft was not found in either the U.S. or the Canadian register.