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DiaTrust

by DiaTrust Medical Co., Ltd EUDAMED

Active European Union

Ref PT01-0017Model FT10,FT11,FT12,FT14,FT16,FT17,FT20,FT21,FT22,FT24,FT26,FT27,FT50,FT51,FT52,FT53,FT54,FT56,FT57,FT58,FT60,FT61,FT62,FT63,FT64,FT66,FT67,FT68,FT914,FT924,FT954,FT964,PT01,PT02,PT04,PT05,PT07,PT08,PT09,PT11,PT12,PT13,PT14,PT15,PT16,PT17,PT18,PT20,PT22,PT26

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number6974570461041BP Basic UDI-DIDate28 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Non-Sterile Pipette Tip
Model / Reference
FT10, FT11, FT12, FT14, FT16, FT17, FT20, FT21, FT22, FT24, FT26, FT27, FT50, FT51, FT52, FT53, FT54, FT56, FT57, FT58, FT60, FT61, FT62, FT63, FT64, FT66, FT67, FT68, FT914, FT924, FT954, FT964, PT01, PT02, PT04, PT05, PT07, PT08, PT09, PT11, PT12, PT13, PT14, PT15, PT16, PT17, PT18, PT20, PT22, PT26, PT01-0017
Primary DI / UDI-DI
06936700742039
Basic UDI-DI
6974570461041BP
Direct Marketing DI
06936700742039
EMDN Code
W0503020202 Pipettes, tips without filter
Device Class
Class A
Market of Registration
Northern Ireland

Manufacturer details

EUDAMED SRN
CN-MF-000009279
Authorised representative
Wellkang Ltd XI-AR-000001836

Other devices from DiaTrust Medical Co., Ltd

See all devices from DiaTrust Medical Co., Ltd →

Properties

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