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Zenith TX2

by William Cook Europe ApS EUDAMED

Active European Union

Ref ZDEG-PT-40-32-205-PF

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00827002231818 Basic UDI-DIDate19 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Zenith TX2 Dissection Endovascular Graft and Zenith TX2 Dissection Endovascular Stent
Model / Reference
ZDEG-PT-40-32-205-PF
Primary DI / UDI-DI
00827002231818
Basic UDI-DI
B-00827002231818
EMDN Code
P07040199 Vascular endoprostheses - other
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DK-MF-000000911

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Properties

Show properties
  • Sterile
  • Implantable
Other properties (9)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No