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Anchor™

by Dongguan TT Medical, Inc. EUDAMED

Active European Union

Ref DST12505Model Anchor™ DST Balloon Catheter Series

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberMDR.2292-2026/0005 Date30 Sep 2026IssuedStatusActive expires 10 Feb 2031

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR.2292-2026/0005 Active Supplemented

    Technical documentation EU MDR

    Notified body
    2292
    Issued
    30 Sep 2026
    Expires
    10 Feb 2031
    Reason
    Add device or group

Specification

EUDAMED

Device Name
Anchor™ DST Coronary Dilatation Balloon Catheters
Model / Reference
Anchor™ DST Balloon Catheter Series, DST12505
Primary DI / UDI-DI
06934184041068
Basic UDI-DI
069341840DSTJC
EMDN Code
C010401020101 Ptca balloon dilation catheters
Device Class
Class III
Market of Registration
Croatia

Manufacturer details

EUDAMED SRN
CN-MF-000039087
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Dongguan Tt Medical, Inc.

  • Anchor™

    Class III

  • VesTrek™

    Class III

  • VesPenetrator®

    Class III

  • VexPander®

    Class III

  • VesTraveler®

    Class III

  • VesTrek™

    Class III

See all devices from Dongguan Tt Medical, Inc. →

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