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Pilling IPN928137

by Teleflex Incorporated

Pilling IPN928137 (532237) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 3 Nov 2023 (UDI-DI 14026704916785), 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 Number14026704916785 UDI-DI Date3 Nov 2023ListedStatusListed 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  • Withdrawn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
Rigid optical laryngopharyngoscope
Model / Ref / Catalog
IPN928137, 532237
Primary DI / UDI-DI
14026704916785
FDA product code
CCW
GMDN term
Rigid optical laryngopharyngoscope
Device class
Class I
Regulation number
868.5540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Rigid optical laryngopharyngoscope

Similar devices in this category

Other devices filed under Rigid optical laryngopharyngoscope.

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Properties

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