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Ankura

by LifeTech Scientific (Europe) B.V. Netherlands EUDAMED

Ref LE-TAA4040B200

EMDN P070401020102

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08720214002639 Basic UDI-DIDate25 Jul 2023RegisteredStatusActive

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 25 Oct 2026

Device Name
Ankura™ TAA Stent Graft System
Model / Reference
LE-TAA4040B200
Primary DI / UDI-DI
08720214002639
Basic UDI-DI
B-08720214002639
EMDN Code
P070401020102 Ptfe vascular endoprostheses, straight - thoracic
Device Class
Class III
Market of Registration
Estonia

Manufacturer details

EUDAMED SRN
NL-MF-000005742

Other devices from LifeTech Scientific (Europe) B.V.

See all devices from LifeTech Scientific (Europe) B.V. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
  • Reprocessed
Other properties (8)
  • Reusable: No
  • Contains Latex: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 93f74c0e-dec9-4f8a-9a65-47e85f55c88d 61 fields · synced 25 Oct 2026