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Weck IPN931083

by Teleflex Incorporated

Ref 523120

Weck IPN931083 (523120) is a Class I device made by Teleflex Incorporated, registered in EUDAMED on 22 Jul 2026 (Basic UDI-DI 08019020000000000000014K3) and listed in FDA GUDID since 6 Feb 2026 (UDI-DI 14026704935670), active as of 7 Nov 2026.

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

CE MDR

Valid until

No date given

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

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08019020000000000000014K3 Basic UDI-DI 14026704935670UDI-DIDate22 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number14026704935670 UDI-DI Date6 Feb 2026ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08019020000000000000014K3 registered 22 Jul 2026 Active
  • FDA GUDID UDI-DI 14026704935670 listed 6 Feb 2026 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 14026704935670
  2. Registered EUDAMED 08019020000000000000014K3

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  • Withdrawn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
Metal Clip Removing Forceps 6.5" EUDAMED
Weck GUDID
Generic name
Surgical clip remover, reusable
Device name
Weck(R) Metal Clip Removing Forceps, various sizes (Open)
Model / Ref / Catalog
523120, IPN931083
Primary DI / UDI-DI
14026704935670
Basic UDI-DI
08019020000000000000014K3
Direct marketing DI
44026704726842
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 registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 6.25 Inch

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
523120
GUDID
IPN931083

Similar devices

Other devices filed under FDA product code GDO (Applier, surgical, clip).

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See all devices from Teleflex Incorporated →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)