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Traveler RX Coronary Dilatation Catheter

by Abbott Vascular EUDAMED

Withdrawn No longer placed on the EU market

Ref 1013072-06

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08717648196799 Basic UDI-DIDate19 Oct 2026RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Withdrawn

No EU certificate is linked to this device in EUDAMED.

Specification

EUDAMED

Device Name
Coronary Dilatation Catheter
Model / Reference
1013072-06
Primary DI / UDI-DI
08717648196799
Basic UDI-DI
B-08717648196799
EMDN Code
C010401020101 Ptca balloon dilation catheters
Device Class
Class III

Manufacturer details

EUDAMED SRN
US-MF-000003850
Authorised representative
Abbott Vascular International BE-AR-000002043

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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