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Hem-O-Lok Open Remover Medium /Medium Large/Large 11" Refurbished

by Teleflex Medical LLC. EUDAMED

Active European Union

Ref 544123R

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08019020000000000000092KP Basic UDI-DIDate19 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

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.

Specification

EUDAMED

Device Name
Weck® Hem-o-lok® Ligating Clip Removers, various s
Model / Reference
544123R
Primary DI / UDI-DI
14026704928924
Basic UDI-DI
08019020000000000000092KP
Direct Marketing DI
24026704760927
EMDN Code
L21 Clip removal surgical forceps, reusable
Device Class
Class I
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
US-MF-000023660
Authorised representative
Teleflex Medical IE-AR-000015869

Other devices from Teleflex Medical, LLC

See all devices from Teleflex Medical, LLC →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No