Skip to content

Ankura

by LifeTech Scientific (Europe) B.V. 198 variants

Ref LE-TAA2626B120, LE-TAA3026B080, LE-TAA3434B080, LE-TAA4234B200, LE-TAA3030B140, LE-TAA4040B080, LE-cuff1216C120, LE-cuff1418C100, LE-TAA3226B160, LE-TAA4436B120, LE-cuff1412C090, LE-TAA4646B100, LE-AAA2010B130, LE-AAA3412B110, LE-TAA3838B200, LE-TAA4242B180, LE-AAA3412B160, LE-cuff1614C040, LE-TAA3232B140, LE-TAA4640B180, LE-TAA4032B140, LE-AAA2812B160, LE-TAA3030B160, LE-TAA3030B040, LE-TAA2822B200, LE-cuff1214C100, LE-AAA2412B110, LE-TAA3430B200, LE-TAA4040B100, LE-TAA2824B120, LE-TAA4646B120, LE-TAA3636B160, LE-cuff1410C090, LE-TAA3632B180, LE-TAA2622B160, LE-cuff1410C120, LE-TAA2420B100, LE-cuff1010C060, LE-TAA3636B120, LE-AAA3012B160, LE-cuff1410C060, LE-TAA3630B120, LE-TAA2824B160, LE-TAA3228B200, LE-cuff1420C100, LE-TAA3632B140, LE-TAA4642B200, LE-AAA2210B140, LE-TAA4236B160, LE-TAA4036B200, LE-cuff1618C120

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08720214000925 Basic UDI-DI Date20 Jul 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Ankura™ TAA Stent Graft System
Ankura™ Cuff Stent Graft System
Ankura™ AAA Stent Graft System
Model / Reference
LE-TAA2626B120, LE-TAA3026B080, LE-TAA3434B080, LE-TAA4234B200, LE-TAA3030B140, LE-TAA4040B080, LE-cuff1216C120, LE-cuff1418C100, LE-TAA3226B160, LE-TAA4436B120, LE-cuff1412C090, LE-TAA4646B100, LE-AAA2010B130, LE-AAA3412B110, LE-TAA3838B200, LE-TAA4242B180, LE-AAA3412B160, LE-cuff1614C040, LE-TAA3232B140, LE-TAA4640B180, LE-TAA4032B140, LE-AAA2812B160, LE-TAA3030B160, LE-TAA3030B040, LE-TAA2822B200, LE-cuff1214C100, LE-AAA2412B110, LE-TAA3430B200, LE-TAA4040B100, LE-TAA2824B120, LE-TAA4646B120, LE-TAA3636B160, LE-cuff1410C090, LE-TAA3632B180, LE-TAA2622B160, LE-cuff1410C120, LE-TAA2420B100, LE-cuff1010C060, LE-TAA3636B120, LE-AAA3012B160, LE-cuff1410C060, LE-TAA3630B120, LE-TAA2824B160, LE-TAA3228B200, LE-cuff1420C100, LE-TAA3632B140, LE-TAA4642B200, LE-AAA2210B140, LE-TAA4236B160, LE-TAA4036B200, LE-cuff1618C120
Primary DI / UDI-DI
08720214000925, 08720214001281, 08720214001854, 08720214002684, 08720214001403, 08720214002578, 08720214004466, 08720214004695, 08720214001519, 08720214002882, 08720214004145, 08720214003308, 08720214003391, 08720214003797, 08720214002394, 08720214002868, 08720214003834, 08720214004350, 08720214001649, 08720214003209, 08720214002417, 08720214003650, 08720214001410, 08720214001359, 08720214000994, 08720214004275, 08720214003490, 08720214001823, 08720214002585, 08720214001038, 08720214003315, 08720214002134, 08720214004022, 08720214002059, 08720214000871, 08720214004046, 08720214000710, 08720214003919, 08720214002110, 08720214003711, 08720214004008, 08720214001977, 08720214001052, 08720214001588, 08720214004817, 08720214002035, 08720214003261, 08720214003469, 08720214002714, 08720214002547, 08720214004763
Basic UDI-DI
B-08720214000925, B-08720214001281, B-08720214001854, B-08720214002684, B-08720214001403, B-08720214002578, B-08720214004466, B-08720214004695, B-08720214001519, B-08720214002882, B-08720214004145, B-08720214003308, B-08720214003391, B-08720214003797, B-08720214002394, B-08720214002868, B-08720214003834, B-08720214004350, B-08720214001649, B-08720214003209, B-08720214002417, B-08720214003650, B-08720214001410, B-08720214001359, B-08720214000994, B-08720214004275, B-08720214003490, B-08720214001823, B-08720214002585, B-08720214001038, B-08720214003315, B-08720214002134, B-08720214004022, B-08720214002059, B-08720214000871, B-08720214004046, B-08720214000710, B-08720214003919, B-08720214002110, B-08720214003711, B-08720214004008, B-08720214001977, B-08720214001052, B-08720214001588, B-08720214004817, B-08720214002035, B-08720214003261, B-08720214003469, B-08720214002714, B-08720214002547, B-08720214004763
EMDN Code
P070401020102, P070401020101, P0704010202
Device Class
Class III
EU market of registration
Belgium
Austria
France
Hungary
Germany
Cyprus
Finland
Estonia
Denmark

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

  • 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