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Weck IPN010798

by Teleflex Incorporated

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number14026704553133 UDI-DI Date12 Dec 2016ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

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  • Withdrawn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
IPN010798, AE10LG
Primary DI / UDI-DI
14026704553133
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
MRI Safety
MR Safe
Size
Length — 35 Centimeter
Outer Diameter — 10 Millimeter

Related devices

Category: Laparoscopic clip applier

Cleared under the same submission (K161758)

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