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Aorfix™ AAA Endovascular Stent Graft with Intelliflex™ Low Profile Delivery System

by Lombard Medical Limited 493 variants

Ref MB-24-81-63-16

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05055715632492 Basic UDI-DI 05055715632492UDI-DIDate8 Nov 2022RegisteredStatusActive

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  • Withdrawn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
Aorfix™ AAA Endovascular Stent Graft with Intelliflex™ Low Profile Delivery System
Model / Reference
MB-24-81-63-16
Primary DI / UDI-DI
05055715632492
Basic UDI-DI
B-05055715632492
EMDN Code
C019009 Aortic occlusion systems
Device Class
Class III
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
GB-MF-000014515
Authorised representative
Medical Device Management Ltd IE-AR-000002496

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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