Skip to content

Magnesium

by Thermo Fisher Scientific Oy

Ref 981905

Active European Union

CE IVDR CE IVDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR NumberB-16438153004377 Basic UDI-DIDate5 Aug 2022RegisteredStatusActive
European UnionCE/IVDD NumberB-16438153004377 Basic UDI-DIDate5 Aug 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR, CE/IVDD Active

Specification

EUDAMED

Model / Reference
981905
Primary DI / UDI-DI
16438153004377
Basic UDI-DI
B-16438153004377, 6438153BU00163BW
Direct Marketing DI
16438153004377
EMDN Code
W01010306 Magnesium
Device Class
Class IVD General
Class B
Market of Registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000001479

Other devices from Thermo Fisher Scientific Oy

See all devices from Thermo Fisher Scientific Oy →

Properties

  • Reagent
  • Professional Testing

Other properties (9)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No