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RealAccurate® Quadruplex Influenza PCR Kit

by PathoFinder B.V. EUDAMED

Withdrawn No longer placed on the EU market

Ref PF0970-R

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD Number87193265699PF0970-R5M Basic UDI-DIDate26 Oct 2022RegisteredStatusWithdrawn No longer placed on the EU market
European UnionCE/IVDR Number87193265699PF0970-R5M Basic UDI-DIDate26 Oct 2022RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDD, CE/IVDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Model / Reference
PF0970-R
Primary DI / UDI-DI
08719326569901
Basic UDI-DI
87193265699PF0970-R5M, B-08719326569901
Direct Marketing DI
08719326569901
EMDN Code
W0105040504, W0105040604
Device Class
Class B
Class IVD General
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000002704

From the manufacturer

Manufacturer's product page: RealAccurate® technologyQuadruplex real-time PCR

Other devices from PathoFinder B.V.

See all devices from PathoFinder B.V. →

Properties

  • Animal Tissues
  • Reagent
  • Professional Testing

Other properties (8)

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