McKesson 22-H10108

by Mckesson Medical-Surgical Inc.

McKesson 22-H10108 is a Class II device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 5 Feb 2018 (UDI-DI 20612479227426), 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	Number20612479227426 UDI-DI	Date5 Feb 2018Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 20612479227426

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: McKesson
Generic name: Electrosurgical handpiece, single-use
Model / reference: 22-H10108

Primary DI / UDI-DI: 20612479227426
FDA product code: HGI
GMDN term: Electrosurgical handpiece, single-use

Device class: Class II
Regulation number: 884.4120
GUDID distribution status: In Commercial Distribution

Other devices from Mckesson Medical-Surgical Inc.

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Properties

Supplied sterile
Single use
Prescription use
Lot / batch number
Expiration date

Other properties (10, all answered No)