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Weck IPN008819

by Teleflex Incorporated

Weck IPN008819 (528235) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 15 Sep 2018 (UDI-DI 04026704600762), 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 Number04026704600762 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  • Withdrawn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
Skin stapler/staple, non-bioabsorbable
Model / Ref / Catalog
IPN008819, 528235
Primary DI / UDI-DI
04026704600762
FDA product code
GDT
GMDN term
Skin stapler/staple, non-bioabsorbable
Device class
Class I
Regulation number
878.4760
GUDID distribution status
In Commercial Distribution
Size
Length — 5.7 Inch

Related devices

Category: Skin stapler/staple, non-bioabsorbable

Similar devices in this category

Other devices filed under Skin stapler/staple, non-bioabsorbable.

Other devices from Teleflex Incorporated

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See all devices from Teleflex Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)