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Pilling IPN056771

by Teleflex Incorporated

Pilling IPN056771 (P32423) is a Class II device made by Teleflex Incorporated, listed in FDA GUDID since 9 Nov 2020 (UDI-DI 14026704735713), 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 Number14026704735713 UDI-DI Date9 Nov 2020ListedStatusListed 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  • Withdrawn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
Freestanding patient positioner, reusable
Model / Ref / Catalog
IPN056771, P32423
Primary DI / UDI-DI
14026704735713
FDA product code
GCJ
GMDN term
Freestanding patient positioner, reusable
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

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See all devices from Teleflex Incorporated →

Properties

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