McKesson 1210767

by Mckesson Medical-Surgical Inc.

McKesson 1210767 is a Class II device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 19 May 2022 (UDI-DI 10612479263137), 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	Number10612479263137 UDI-DI	Date19 May 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10612479263137

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: McKesson
Generic name: Wound dressing kit, non-medicated
Model / reference: 1210767

Primary DI / UDI-DI: 10612479263137
FDA product code: QMT
GMDN term: Wound dressing kit, non-medicated

Device class: Class II
Regulation number: 880.5570
GUDID distribution status: In Commercial Distribution

Other devices from Mckesson Medical-Surgical Inc.

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Properties

Single use
Convenience kit
Premarket exempt
Lot / batch number
Expiration date

Other properties (10, all answered No)