Nocubi AG
CH-MF-000034743 · Switzerland · Zürich
Nocubi AG 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: Cover, Liegesystem, Topper.
Among these devices, 1 are declared active.
Authorised representative in the Union: Nocubi Deutschland GmbH.
Devices declared under this manufacturer
- Nocubi Anti-Dekubitus-Liegesystem 150 90x200
- Nocubi Cover Air 90x200
- Nocubi Cover PU 90x200
- Topper Firm 110-150 90x200
- Topper Medium 70-110 90x200
- Topper Soft 50-70 90x200
Catalogue references include 01150220920, 06065220920, 06100220920, 06125220920, 07001220920, 07002220920.
European nomenclature codes declared: V08068099, V080701.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | Switzerland |
⚠️ 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. Nocubi AG was not found in either the U.S. or the Canadian register.