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corQC Test System

by Immucor, Inc.

Ref 0002410

corQC Test System (0002410) is an in vitro diagnostic device (EU IVDR Class D; EMDN category immunohaematology controls) made by Immucor, Inc., registered in EUDAMED on 1 May 2026 (Basic UDI-DI 08882340004LDK), active as of 7 Nov 2026.

Active European Union

CE IVDR

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number08882340004LDK Basic UDI-DI 10888234002123UDI-DIDate1 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Model / reference
0002410
Primary DI / UDI-DI
10888234002123
Basic UDI-DI
08882340004LDK
EMDN code
W0103030499 Immunohaematology controls - other
Device class
Class D
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000011568
Authorised representative
IMMUCOR Medizinische Diagnostik GmbH DE-AR-000007083

Similar devices in this category

Other devices filed under IMMUNOHAEMATOLOGY (BLOOD GROUPING).

Other devices from Immucor, Inc.

See all devices from Immucor, Inc. →

Properties

  • Contains human tissues or cells
  • Contains animal tissues or cells
  • Contains substances of microbial origin
  • Reagent
  • IVD kit
  • Professional testing
Other properties (7, all answered No)