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McKesson 16-3S-672

by Mckesson Medical-Surgical Inc.

McKesson 16-3S-672 is a Class II device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 12 Sep 2018 (UDI-DI 20612479123735), 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 Number20612479123735 UDI-DI Date12 Sep 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  • Withdrawn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
Stockinette
Model / reference
16-3S-672
Primary DI / UDI-DI
20612479123735
FDA product code
PUI
GMDN term
Stockinette
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Related devices

Category: Stockinette

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Other devices filed under Stockinette.

Other devices from Mckesson Medical-Surgical Inc.

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Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)