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EUDAMED last updated this device on Oct 8, 2025
37017008MGXB00BCMAGNESIUM XB is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class B. Manufactured by VitalScientific. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0370170082510437017008MGXB00BCMGXB-0600(01)03701700825104
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W01010306MAGNESIUM1 warning recorded — scroll inside the panel to see all entries.
CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Sep 30, 2024 | Still on market |
FR-MF-000004722No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.