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Pilling IPN005842

by Teleflex Incorporated

Pilling IPN005842 (354430) is a Class II device made by Teleflex Incorporated, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 24026704521283), 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 Number24026704521283 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  • Withdrawn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
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Model / Ref / Catalog
IPN005842, 354430
Primary DI / UDI-DI
24026704521283
FDA product code
DXC
GMDN term
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device class
Class II
Regulation number
870.4450
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Unsafe
Size
Length — 16 Centimeter

Related devices

Category: Surgical soft-tissue manipulation forceps, scissors-like, reusable

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See all devices from Teleflex Incorporated →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)