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Medium Hemolok Takeapart Applier

by Teleflex Medical LLC. EUDAMEDGUDID

Active European Union

Ref 544945T

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number14026704928689 UDI-DIDate21 Aug 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number08019020000000000000011JV 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  • Withdrawn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
Medium Hemolok Takeapart Applier EUDAMED
Weck GUDID
Generic Name
Open-surgery ligation clip applier
Device Name
Weck® Hem-o-lok® Take Apart Endoscopic Ligating Cl
Model / Ref / Catalog
544945T, IPN930280
Primary DI / UDI-DI
14026704928689
Basic UDI-DI
08019020000000000000011JV
Direct Marketing DI
44026704727474
FDA Product Code
GDO
EMDN Code
L020802 Multiple applicators of clips for video surgery, reusable
GMDN Term
Open-surgery ligation clip applier
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
Height — 5.1 Inch
Length — 18.3 Inch
Width — 1.4 Inch

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
544945T
GUDID
IPN930280

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