Careturner A/S
DK-MF-000020149 · Denmark · Karlslunde
Careturner A/S is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 17 |
|---|
Devices declared under this manufacturer
- Careturner - Vendesystem til OPUS 1
- Careturner - Vendesystem til OPUS 7
- Careturner 3.0
- Careturner 3.1 Opus 1 &7
- Careturner 3.2
- GDV® Careturner 2.0 for Völker 5384
- GDV® Careturner 2.2 for Stiegelmeyer Elvido-Movo 817422
- GDV® Careturner 2.2 for wissner-bosserhoff Sentida 6
- Soft Tilt 2.0 for Invacare® Etude Plus
- Soft Tilt 2.0 for Invacare® Etude Plus UK version
- Soft Tilt 2.0 for Invacare® SB 755
- Soft Tilt 2.0 for Invacare® SB 755 UK version
Showing 12 of 17 declared devices.
Catalogue references include ABLOPUS7200821, CTUUNIVE301122, GDVSTM81221019, GDVVO84200320, GDVWIBOS220620, IVC SB755 2 2 0519.
European nomenclature codes declared: V08068099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| 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 | 17 |
|---|---|
| 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. Careturner A/S was not found in either the U.S. or the Canadian register.