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Citotest

by Citotest Labware Manufacturing Co., Ltd EUDAMED

Active European Union

Ref 2120-0029-02Model Transport

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697079159TSW1000A00RZH Basic UDI-DIDate11 Apr 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Transport swabs
Model / Reference
Transport, 2120-0029-02
Primary DI / UDI-DI
06975085646266
Basic UDI-DI
697079159TSW1000A00RZH
EMDN Code
A1101 Sample collection neutral swabs
Device Class
Class I
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

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No