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Weck IPN028190

by Teleflex Incorporated

Weck IPN028190 (237111) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 2 Oct 2017 (UDI-DI 34026704622727), 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 Number34026704622727 UDI-DI Date2 Oct 2017ListedStatusListed 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  • Withdrawn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
IPN028190, 237111
Primary DI / UDI-DI
34026704622727
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 — 11 Inch
Width — 5.12 Inch

Related devices

Category: Open-surgery ligation clip applier

Similar devices in this category

Other devices filed under Open-surgery ligation clip applier.

Other devices from Teleflex Incorporated

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    Class II

  • Arrow IPNB00826 Open recall

    Class II

  • Arrow IPNB00822 Open recall

    Class II

  • Arrow IPNB00827 Open recall

    Class II

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)