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Weck ME05LGTL

by Teleflex Incorporated

Ref ME05LGTL

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08019020000000000000011JV Basic UDI-DI 04026704943838UDI-DIDate19 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04026704943838 UDI-DI Date8 Apr 2026ListedStatusListed GUDID: in commercial distribution

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

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
Hol Purpleplus L 5mm Endo App 45cm Tap EUDAMED
Weck GUDID
Generic Name
Open-surgery ligation clip applier
Device Name
Weck® Hem-o-lok® Take Apart Endoscopic Ligating Cl
Model / Ref / Catalog
ME05LGTL
Primary DI / UDI-DI
04026704943838
Basic UDI-DI
08019020000000000000011JV
Direct Marketing DI
14026704943835
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
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Teleflex Incorporated

See all devices from Teleflex Incorporated →

Properties

  • Reusable
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (18)

  • 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