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Biopsy Foam Pad Black Q Path

by Vwr International SAS France EUDAMED

Ref 720-2255 EMDN W05030580

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number731205W008BB Basic UDI-DIDate2 Mar 2026RegisteredStatusActive

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  • Withdrawn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 · synced 22 Oct 2026

Device Name
Q Path Biopsy Pad
Model / Reference
720-2255
Primary DI / UDI-DI
07312056607700
Basic UDI-DI
731205W008BB
Unit of Use DI
07312052222228
EMDN Code
W05030580 Devices for patology tests - accessories
Device Class
Class A
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000016509

Other devices from Vwr International SAS

See all devices from Vwr International SAS →

Properties & raw data

Show properties, registry sources and raw records
  • Professional Testing
Other properties (10)
  • 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
  • New Device: No

Sources (1)

  • EUDAMED b065f6cf-9b5e-4c7a-bc87-0007c7e8f335 61 fields · synced 22 Oct 2026