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McKesson 1721

by Mckesson Medical-Surgical Inc. 2 variants

McKesson 1721 is a Class I device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 9 Apr 2020 (UDI-DI 00612479193284), 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 Number00612479193284 UDI-DI Date9 Apr 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  • Withdrawn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
Wound hydrogel dressing, non-sterile
Model / reference
1721
Primary DI / UDI-DI
00612479193284
FDA product code
NAE
GMDN term
Wound hydrogel dressing, non-sterile
Device class
Class I
Regulation number
878.4022
GUDID distribution status
In Commercial Distribution

Related devices

Category: Wound hydrogel dressing, non-sterile

Similar devices

Other devices filed under FDA product code NAE (Dressing, Wound, Hydrogel Without Drug And/Or Biologic).

Other devices from Mckesson Medical-Surgical Inc.

See all devices from Mckesson Medical-Surgical Inc. →

Properties

  • Single use
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)