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McKesson 43-1-102

by Mckesson Medical-Surgical Inc.

McKesson 43-1-102 is a Class I device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 12 Nov 2018 (UDI-DI 00612479234314), 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 Number00612479234314 UDI-DI Date12 Nov 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  • Withdrawn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
McKesson
Generic name
Tuning fork
Model / reference
43-1-102
Primary DI / UDI-DI
00612479234314
FDA product code
GWX
GMDN term
Tuning fork
Device class
Class I
Regulation number
882.1525
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Tuning fork

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Other devices filed under Tuning fork.

Other devices from Mckesson Medical-Surgical Inc.

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Properties

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