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McKesson 73-SSI1000

by Mckesson Medical-Surgical Inc.

McKesson 73-SSI1000 is a Class II device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 9 Dec 2016 (UDI-DI 20612479159024), 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 Number20612479159024 UDI-DI Date9 Dec 2016ListedStatusListed 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  • Withdrawn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
Chemical/physical sterilization process indicator
Model / reference
73-SSI1000
Primary DI / UDI-DI
20612479159024
FDA product code
JOJ
GMDN term
Chemical/physical sterilization process indicator
Device class
Class II
Regulation number
880.2800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Chemical/physical sterilization process indicator

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Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)