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Pilling IPN004276

by Teleflex Incorporated

Pilling IPN004276 (200403) is a dissection sponge (FDA unclassified; FDA product code EFQ, Gauze/Sponge, Internal) made by Teleflex Incorporated, listed in FDA GUDID since 15 Sep 2018 (UDI-DI 04026704417896), 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 Number04026704417896 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  • Withdrawn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
Pilling
Generic name
Dissection sponge
Model / Ref / Catalog
IPN004276, 200403
Primary DI / UDI-DI
04026704417896
FDA product code
EFQ
GMDN term
Dissection sponge
Device class
U
GUDID distribution status
In Commercial Distribution
Size
Width — 58 Millimeter
Length — 86 Millimeter

Similar devices

Other devices filed under FDA product code EFQ (GAUZE/SPONGE, INTERNAL).

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

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)