McKesson Sterile Skin Marker Prep-Resistant Dual Tip (EA)

McKesson Sterile Skin Marker Prep-Resistant Dual Tip (EA)
The McKesson Skin Marker (MPN 19-0771) is a sterile, full-size skin marker designed for clinical marking workflows. It uses prep-resistant gentian violet ink and features a dual tip design with regular and fine tip options to support different marking needs during patient preparation.

Prep-resistant ink is commonly selected for procedure workflows where maintaining visible markings through skin prep is important. The dual tip design provides flexibility—use the fine tip for more precise marking and the regular tip for broader, more visible lines. This marker is supplied sterile to support use in clinical environments following facility protocol.

This MQ Healthcare listing is configured for EA purchasing to support flexible ordering and stocking. Manufacturer packaging is provided as BX/50EA for bulk replenishment.

Key Features:
•Sterile skin marker
•Prep-resistant gentian violet ink
•Full size marker format
•Dual tip design with regular and fine tips

Benefits:
•Supports clear patient marking workflows in clinical environments
•Prep-resistant ink helps maintain visibility during prep processes
•Dual tip design supports both precision marks and broader lines
•Sterile format supports procedure use per facility protocol

Specifications:
•Brand: McKesson
•Product Type: Skin Marker
•Ink Type: Gentian Violet Ink
•Ink Feature: Prep-Resistant
•Sterility: Sterile
•Tip Style: Dual Tip
•Tip Options: Regular / Fine
•Size: Full Size
•Minimum Selling/Purchasing Unit: EA
•Minimum Package Qty: 1 EA
•Packaging (Factual): 50 EA per BX (BX/50EA reference)
•MPN: 19-0771

Application:
Designed for patient skin marking in clinical environments where prep-resistant, dual-tip marking is preferred.
•Use for procedure site marking and related clinical marking needs per facility protocol
•Select regular or fine tip based on the marking requirement

Warnings:
•For use by trained medical professionals
•Single-patient use only if required by facility protocol
•Do not use if sterile packaging is damaged prior to use