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Weck IPN010797

by Teleflex Incorporated

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None ongoing

1 closed

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number14026704553126 UDI-DI Date30 Sep 2016ListedStatusListed GUDID: in commercial distribution

Recalls

1 recall · FDA

    • Terminated Z-0083-2018 FDA Class II initiated 5 Oct 2017

    The product has a non-conformity that may cause clips to mislead, jam or fall out of the applier.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Weck
Generic Name
Laparoscopic clip applier
Model / Ref / Catalog
IPN010797, AE05ML
Primary DI / UDI-DI
14026704553126
510(k) Number
FDA Product Code
FZP
GMDN Term
Laparoscopic clip applier
Device Class
Class II
Regulation Number
878.4300
GUDID distribution status
In Commercial Distribution
Size
Length — 35 Centimeter

Related devices

Category: Laparoscopic clip applier

Similar devices

Also classified as Laparoscopic clip applier.

Other devices from Teleflex Incorporated

See all devices from Teleflex Incorporated →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No