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Hem-O-Lok Remover Large/Extra Large 11"

by Teleflex Medical LLC. EUDAMEDGUDID

Active European Union

Ref 544124

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number14026704928498 UDI-DIDate21 Aug 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number08019020000000000000008K8 Basic UDI-DIDate19 May 2026RegisteredStatusActive

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

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.

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

EUDAMED · GUDID

Trade Name
Hem-O-Lok Remover Large/Extra Large 11" EUDAMED
Weck GUDID
Generic Name
Surgical clip remover, reusable
Device Name
Weck® Hem-o-lok® Ligating Clip Removers, various s
Model / Ref / Catalog
544124, IPN930261
Primary DI / UDI-DI
14026704928498
Basic UDI-DI
08019020000000000000008K8
Direct Marketing DI
44026704727337
FDA Product Code
GDO
EMDN Code
L21 Clip removal surgical forceps, reusable
GMDN Term
Surgical clip remover, reusable
Device Class
Class I
Regulation Number
878.4800
Market of Registration
Ireland
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
MRI Safety
MR Unsafe
Size
Length — 10.5 Inch

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
544124
GUDID
IPN930261

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
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number

Other properties (19)

  • Sterile: No
  • Single Use: 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Expiration Date: No
  • Manufacturing Date: No