Aacurat GmbH
DE-MF-000019560 · Germany · Hüttlingen
Aacurat GmbH is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|
Most frequent device types declared: CURATOR, HEBIXmobil, genius UniversalLift, pulla.
Among these devices, 2 are declared active.
Devices declared under this manufacturer
- CURATOR WandLift
- HEBIXmobil
- HEBIXstarr
- genius
- pulla - transportierendes Bettlaken
- transit
Catalogue references include 7700000, 7800000, 8235001, 8266001, 8275001, 8805000.
European nomenclature codes declared: Z12069001, Y0999,Y1299, V0805030101, Y0999.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| 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. Aacurat GmbH was not found in either the U.S. or the Canadian register.