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Pilling IPN002066

by Teleflex Incorporated

Pilling IPN002066 (025165) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 15 Sep 2018 (UDI-DI 24026704505498), 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 Number24026704505498 UDI-DI Date15 Sep 2018ListedStatusListed 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  • Withdrawn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
Ear speculum, reusable
Model / Ref / Catalog
IPN002066, 025165
Primary DI / UDI-DI
24026704505498
FDA product code
EPY
GMDN term
Ear speculum, reusable
Device class
Class I
Regulation number
878.1800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 43 Millimeter

Related devices

Category: Ear speculum, reusable

Other devices from Teleflex Incorporated

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    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)