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Citotest

by Citotest Labware Manufacturing Co., Ltd China EUDAMED

Ref 4020-2906-13Model Plastic

EMDN W05020199

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697079159ASCA002A00NA3 Basic UDI-DIDate23 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Specimen Container
Model / Reference
Plastic, 4020-2906-13
Primary DI / UDI-DI
06942826220047
Basic UDI-DI
697079159ASCA002A00NA3
EMDN Code
W05020199 Samples transport, containers - other
Device Class
Class A
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000017214
Authorised representative
Wellkang Ltd XI-AR-000001836

Other devices from Citotest Labware Manufacturing Co., Ltd

See all devices from Citotest Labware Manufacturing Co., Ltd →

Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No

Sources (1)

  • EUDAMED 06942826220047|697079159ASCA002A00NA3 61 fields · synced 24 Oct 2026