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Buchanan Hand Pluggers 974-0059

by Kerr Corporation

Buchanan Hand Pluggers 974-0059 is a Class I device made by Kerr Corporation, listed in FDA GUDID since 11 Jan 2024 (UDI-DI 00195062032745), 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 Number00195062032745 UDI-DI Date11 Jan 2024ListedStatusListed 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  • Withdrawn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
Buchanan Hand Pluggers
Generic name
Endodontic plugger
Model / reference
974-0059
Primary DI / UDI-DI
00195062032745
FDA product code
EKR
GMDN term
Endodontic plugger
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Endodontic plugger

Other devices from Kerr Corporation

See all devices from Kerr Corporation →

Properties

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