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Pilling IPN004235

by Teleflex Incorporated

Pilling IPN004235 (200121) is a neurosurgical sponge (FDA unclassified; FDA product code EFQ, Gauze/Sponge, Internal) made by Teleflex Incorporated, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 04026704599394), 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 Number04026704599394 UDI-DI Date16 Sep 2016ListedStatusListed 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  • Withdrawn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
Neurosurgical sponge
Model / Ref / Catalog
IPN004235, 200121
Primary DI / UDI-DI
04026704599394
FDA product code
EFQ
GMDN term
Neurosurgical sponge
Device class
U
GUDID distribution status
In Commercial Distribution
Size
Width — 6 Inch
Length — 0.5 Inch

Similar devices

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

Other devices from Teleflex Incorporated

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  • 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
Other properties (10, all answered No)