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McKesson 16-028-100

by Mckesson Medical-Surgical Inc.

McKesson 16-028-100 is a Class II device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 31 Mar 2020 (UDI-DI 20612479194261), 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 Number20612479194261 UDI-DI Date31 Mar 2020ListedStatusListed 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  • Withdrawn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
Blood lancet, single-use
Model / reference
16-028-100
Primary DI / UDI-DI
20612479194261
FDA product code
FMK
GMDN term
Blood lancet, single-use
Device class
Class II
Regulation number
878.4850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood lancet, single-use

Similar devices in this category

Other devices filed under Blood lancet, single-use.

Other devices from Mckesson Medical-Surgical Inc.

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Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)