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Weck IPN008536

by Teleflex Incorporated

Weck IPN008536 (523140) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 15 Sep 2018 (UDI-DI 24026704429466), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number24026704429466 UDI-DI Date15 Sep 2018ListedStatusListed GUDID: in commercial distribution

Official records

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  • Withdrawn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
Open-surgery ligation clip applier
Model / Ref / Catalog
IPN008536, 523140
Primary DI / UDI-DI
24026704429466
FDA product code
GDO
GMDN term
Open-surgery ligation clip applier
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 6 Inch
Width — 3.599 Inch

Related devices

Category: Open-surgery ligation clip applier

Similar devices in this category

Other devices filed under Open-surgery ligation clip applier.

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See all devices from Teleflex Incorporated →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)