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QFT-Plus HA tubes

by QIAGEN GmbH

Ref 623526

Active European Union

CE IVDR

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number4053228RTBQFT0000000002WA Basic UDI-DI 14053228015922UDI-DIDate15 May 2026RegisteredStatusActive

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  • Withdrawn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 Active

Specification

EUDAMED

Device Name
QuantiFERON-TB Gold Plus (QFT-Plus) Blood Collection Tubes
Model / Reference
623526
Primary DI / UDI-DI
14053228015922
Basic UDI-DI
4053228RTBQFT0000000002WA
EMDN Code
W050101010201 Blood collection, tubes with additives or serum separator
Device Class
Class C
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
DE-MF-000004949

Other devices from QIAGEN GmbH

See all devices from QIAGEN GmbH →

Properties

  • Sterile
  • Animal Tissues
  • Reagent
  • Professional Testing

Other properties (7)

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