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Pilling IPN020546

by Teleflex Incorporated

Pilling IPN020546 (P25138) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 8 Dec 2022 (UDI-DI 14026704801739), 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 Number14026704801739 UDI-DI Date8 Dec 2022ListedStatusListed 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  • Withdrawn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
Eyelid speculum, reusable
Model / Ref / Catalog
IPN020546, P25138
Primary DI / UDI-DI
14026704801739
FDA product code
HNC
GMDN term
Eyelid speculum, reusable
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Eyelid speculum, reusable

Other devices from Teleflex Incorporated

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  • Arrow IPNB00827 Open recall

    Class II

See all devices from Teleflex Incorporated →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)