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Anchor™

by Dongguan TT Medical, Inc. 378 variants

Ref SST22520Model Anchor™ SST Balloon Catheter Series

Active European Union

CE MDR

Valid until

10 Feb 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

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

Certificates

1 certificate · EUDAMED

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

    Technical documentation EU MDR

    Certifier
    UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş. 2292
    Issued
    30 Sep 2026
    Expires
    10 Feb 2031
    Reason
    Add device or group

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Anchor™ SST Coronary Dilatation Balloon Catheters
Model / Reference
Anchor™ SST Balloon Catheter Series, SST22520
Primary DI / UDI-DI
06934184045721
Basic UDI-DI
069341840SSTLP
EMDN Code
C010401020101 Ptca balloon dilation catheters
Device Class
Class III
Market of Registration
Spain

Manufacturer details

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

Other devices from Dongguan Tt Medical, Inc.

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    Class III

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    Class III

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    Class III

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    Class III

  • VesTraveler®

    Class III

  • VesTrek™

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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