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Zenith

by William Cook Europe ApS United States EUDAMED

Ref ZDES-36-180

EMDN P07040199

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00827002342583 Basic UDI-DIDate19 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Zenith TX2 Dissection Endovascular Graft and Zenith TX2 Dissection Endovascular Stent
Model / Reference
ZDES-36-180
Primary DI / UDI-DI
00827002342583
Basic UDI-DI
B-00827002342583
EMDN Code
P07040199 Vascular endoprostheses - other
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DK-MF-000000911

Other devices from William Cook Europe Aps

See all devices from William Cook Europe Aps →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 00827002342583|B-00827002342583 61 fields · synced 24 Oct 2026