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cerascreen® Vitamin B12 Test

by Cerascreen GmbH EUDAMED

Active European Union

Ref 99010255, 99010015, 99010159

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number42516207001JP Basic UDI-DIDate19 Oct 2023RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Probenahme- und Einsende-Kit Flüssigblut
Model / Reference
99010255, 99010015, 99010159
Primary DI / UDI-DI
04251620703864, 04251620709132, 04251620709279, 04251620709835
Basic UDI-DI
42516207001JP
Direct Marketing DI
04251620709132
04251620709279
04251620709835
EMDN Code
W0501010201 Capillary blood collection systems
Device Class
Class A
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000017602

Other devices from Cerascreen GmbH

See all devices from Cerascreen GmbH →

Properties

Show properties
  • Professional Testing
  • New Device YesEUDAMEDNoEUDAMED
Other properties (9)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No