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McKesson 115-4

by Mckesson Medical-Surgical Inc.

McKesson 115-4 is a Class I device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 26 Jul 2021 (UDI-DI 10612479194615), 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 Number10612479194615 UDI-DI Date26 Jul 2021ListedStatusListed 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  • Withdrawn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
Cast construction material
Model / reference
115-4
Primary DI / UDI-DI
10612479194615
FDA product code
ITG
GMDN term
Cast construction material
Device class
Class I
Regulation number
890.3025
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cast construction material

Similar devices

Other devices filed under FDA product code ITG (Bandage, Cast).

Other devices from Mckesson Medical-Surgical Inc.

See all devices from Mckesson Medical-Surgical Inc. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)