magtivio B.V.
NL-MF-000023114 · Netherlands · Nuth
magtivio B.V. 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
Devices declared under this manufacturer
- MagSi-DX Blood
- MagSi-DX Pathogen Plus
Catalogue references include MDDX00020096, MDDX00020960, MDDX00030005K, MDDX00030096, MDDX0003025K, MDDX00030960.
European nomenclature codes declared: W0105900101, W0580.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | Netherlands |
⚠️ 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. magtivio B.V. was not found in either the U.S. or the Canadian register.