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Pilling IPN007743

by Teleflex Incorporated 2 variants

Pilling IPN007743 (502275) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 22 Oct 2018 (UDI-DI 14026704630742), 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 Number14026704630742 UDI-DI Date22 Oct 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  • Withdrawn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
Endoscopic bite block, basic, single-use
Model / Ref / Catalog
IPN007743, 502275
Primary DI / UDI-DI
14026704630742
FDA product code
KBN
GMDN term
Endoscopic bite block, basic, single-use
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic bite block, basic, single-use

Similar devices in this category

Other devices filed under Endoscopic bite block, basic, single-use.

Other devices from Teleflex Incorporated

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    Class II

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    Class II

See all devices from Teleflex Incorporated →

Properties

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