McKesson 4893

by Mckesson Medical-Surgical Inc.

McKesson 4893 is a Class I device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 12 Sep 2018 (UDI-DI 00612479224018), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00612479224018 UDI-DI	Date12 Sep 2018Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00612479224018

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: McKesson
Generic name: Wound-nonadherent dressing, absorbent, non-antimicrobial
Model / reference: 4893

Primary DI / UDI-DI: 00612479224018
FDA product code: NAD
GMDN term: Wound-nonadherent dressing, absorbent, non-antimicrobial

Device class: Class I
Regulation number: 878.4020
GUDID distribution status: In Commercial Distribution

Other devices from Mckesson Medical-Surgical Inc.

See all devices from Mckesson Medical-Surgical Inc. →

Properties

Supplied sterile
Single use
Over-the-counter
Premarket exempt
Lot / batch number
Expiration date

Other properties (9, all answered No)