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StorAX Cerba

by Axon Biotech GmbH Germany EUDAMED

Ref AL0320CER EMDN W05020199

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number425173790367 Basic UDI-DIDate27 Aug 2025RegisteredStatusWithdrawn 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  • Withdrawn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European Union — CE/IVDR Withdrawn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 · synced 25 Oct 2026

Device Name
Transportgefäss Stuhlprobe
Model / Reference
AL0320CER
Primary DI / UDI-DI
04251737900675
Basic UDI-DI
425173790367
EMDN Code
W05020199 Samples transport, containers - other
Device Class
Class A
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
DE-MF-000027334

Other devices from Axon Biotech GmbH

See all devices from Axon Biotech GmbH →

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 a9b78abc-9be2-4874-a997-342c9968a976 61 fields · synced 25 Oct 2026