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Absolute Pro™ LL Peripheral Self-Expanding Stent System

by Abbott Medical EUDAMED

Withdrawn Not intended for the EU market

Ref 1013016-120

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8717648PSS00037M Basic UDI-DIDate11 Sep 2026RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 751907 Supplemented

    Technical documentation EU MDR

    Notified body
    Notified body 2797
    Issued
    24 Jun 2026
    Expires
    25 Oct 2027
    Reason
    Change approved

Specification

EUDAMED

Device Name
Peripheral Self-expanding Stent System, Absolute Pro
Model / Reference
1013016-120
Primary DI / UDI-DI
08717648191589
Basic UDI-DI
8717648PSS00037M
EMDN Code
P070402020102 Non-stainless steel peripheral vascular bare metal stents
Device Class
Class IIb

Manufacturer details

EUDAMED SRN
IE-MF-000002547

Other devices from Abbott Medical

See all devices from Abbott Medical →

Properties

  • Sterile
  • Implantable
  • CMR Substance

Other properties (11)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Sutures: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No