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McKesson 100122

by Mckesson Medical-Surgical Inc.

McKesson 100122 is a wound irrigation kit (FDA Class I; FDA product code KDD, Kit, Surgical Instrument, Disposable) made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 19 Oct 2023 (UDI-DI 10612479205854), 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 Number10612479205854 UDI-DI Date19 Oct 2023ListedStatusListed 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  • Withdrawn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
Wound irrigation kit
Model / reference
100122
Primary DI / UDI-DI
10612479205854
FDA product code
KDD
GMDN term
Wound irrigation kit
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Wound irrigation kit

Similar devices

Other devices filed under FDA product code KDD (Kit, Surgical Instrument, Disposable).

Other devices from Mckesson Medical-Surgical Inc.

See all devices from Mckesson Medical-Surgical Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)