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McKesson 59820

by Mckesson Medical-Surgical Inc.

McKesson 59820 is a Class I device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 3 Feb 2022 (UDI-DI 00612479259126), 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 Number00612479259126 UDI-DI Date3 Feb 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  • Withdrawn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
McKesson
Generic name
Colour-indication patient thermometer
Model / reference
59820
Primary DI / UDI-DI
00612479259126
FDA product code
PXC
GMDN term
Colour-indication patient thermometer
Device class
Class I
Regulation number
880.6250
GUDID distribution status
In Commercial Distribution

Other devices from Mckesson Medical-Surgical Inc.

See all devices from Mckesson Medical-Surgical Inc. →

Properties

  • Over-the-counter
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)