novacare gmbh
DE-MF-000007623 · Germany · Bad Dürkheim
novacare gmbh is registered in the European database on medical devices as a manufacturer, with 193 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 193 |
|---|
Most frequent device types declared: Alternating Pressure Chushion, Alternating pressure mattress, Non active anti-decubitus medical mattress, Patient Lift, ProLift.
Among these devices, 103 are declared active.
Devices declared under this manufacturer
- APM 440X
- ASX Digital 5inch 88
- ASX Digital FR 88x220
- ASX Digital Junior 70x140
- ASX Digital Junior UK 60x120
- Angle-adjustable legrest (left) for VarioXX²
- Hemi kit for VARIOXX2 with drum brakes
- Highsupport Sling, Polyester, XS, 200kg
- LAS 500N, Low Air Loss System 90 cm
- Smartline Pro Steuergerät
- Smartline Turn 7\
- Smartline plus 5 Matratzenauflage komplett
Showing 12 of 193 declared devices.
Catalogue references include 102206, 103799 / 996851, 96110113, 982196, 991230UK, 991240.
European nomenclature codes declared: V080701, V0805038002, V080702, Y122103, V0805030102, V0805030101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 193 |
| 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 | 193 |
|---|---|
| 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. novacare gmbh was not found in either the U.S. or the Canadian register.