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Hol Purpleplus L 5mm Endo Remover 45cm

by Teleflex Medical LLC.

Ref ME05RVLGL

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08019020000000000000007K6 Basic UDI-DI 14026704921666UDI-DIDate19 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number14026704921666 UDI-DI Date10 Mar 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  • Withdrawn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 Remover 45cm EUDAMED
Weck GUDID
Generic Name
Surgical clip remover, reusable
Device Name
Weck® Hem-o-lok® Endoscopic Clip Removers, various sizes
Model / Ref / Catalog
ME05RVLGL
Primary DI / UDI-DI
14026704921666
Basic UDI-DI
08019020000000000000007K6
Direct Marketing DI
24026704921663
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
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

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
  • 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