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cerascreen® COVID-19-Impfung Antikörper Test

by Cerascreen GmbH EUDAMED

Withdrawn No longer placed on the EU market

Ref 99010441

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number42516207002JR Basic UDI-DIDate19 Oct 2023RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Probenahme- und Einsende-Kit Trockenblut
Model / Reference
99010441
Primary DI / UDI-DI
04251620706445
Basic UDI-DI
42516207002JR
Direct Marketing DI
04251620706445
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

  • Professional Testing
  • New Device

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