McKesson 241

by Mckesson Medical-Surgical Inc.

McKesson 241 is a Class I device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 25 Jun 2020 (UDI-DI 10612479205892), 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	Number10612479205892 UDI-DI	Date25 Jun 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10612479205892

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: McKesson
Generic name: Skin staple remover, single-use
Model / reference: 241

Primary DI / UDI-DI: 10612479205892
FDA product code: MCZ
GMDN term: Skin staple remover, single-use

Device class: Class I
Regulation number: 878.4800
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
Prescription use
Convenience kit
Premarket exempt
Lot / batch number
Expiration date

Other properties (8, all answered No)