NEVEON Austria GmbH
AT-MF-000003497 · Austria · Kremsmünster
NEVEON Austria GmbH is registered in the European database on medical devices as a manufacturer, with 143 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 143 |
|---|
Most frequent device types declared: Care mattress, Deku Bariatric, Deku Bio, Deku Care, Deku Duo.
Devices declared under this manufacturer
- MP Deku Care 1980x840x150 Bez. Slipy/Ant
- MP Deku Care 2000x890x150 PU210 blau
- MP Deku Care 2000x900x150 Orto petrol PU
- MP Deku Care 2000x900x150 PU210 dklboAnt
- MP Deku Foam 2000x900x140 PU210 blau
- MP Deku Foam 2200x900x140 PU210 beig
- MP Deku MAX 2000x900x170 PU210 LOR Druck
- MP Deku MAX 2200x1100x170 PU210 Druck
- MP Deku Mono PU210 blau 2000x880x140
- MP Deku Vienna 1980x850x140 Slipy/Anti
- MP DekuCare 2000x1100x150 PU210 ohne Ant
- MP DekuStar RZ 2000x900x140 Pflegebett
Showing 12 of 143 declared devices.
Catalogue references include 3000013428, 3000076725, 3000230981, 3000328362, 3000341405, 3000375465.
European nomenclature codes declared: V080702, V0880.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 143 |
| Country of registration | Austria |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 143 |
|---|---|
| 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. NEVEON Austria GmbH was not found in either the U.S. or the Canadian register.