Neurosurgical
This document is intended solely for the use of healthcare professionals. A surgeon must always rely on his or her
own professional clinical judgment when deciding whether to use a particular product when treating a particular
patient. We do not dispense medical advice and recommend that surgeons be trained in the use of any particular
product before using it in surgery.
The information presented is intended to demonstrate Stryker’s products. A surgeon must always refer to the
package insert, product label and/or instructions for use, including the instructions for cleaning and sterilization
(if applicable), before using any of Stryker’s products. Products may not be available in all markets because
product availability is subject to the regulatory and/or medical practices in individual markets. Please contact your
representative if you have questions about the availability of Stryker’s products in your area.
Stryker or its affiliated entities own, use, or have applied for the following trademarks or service marks: CORE, I.D.
Touch, πdrive and Stryker. All other trademarks are trademarks of their respective owners or holders.
The absence of a product, feature, or service name, or logo from this list does not constitute a waiver of Stryker’s
trademark or other intellectual property rights concerning that name or logo.
D0000023873 Rev. AA
G55/PS
Copyright © 2020 Stryker
Printed in USA
Stryker
1941 Stryker Way
Portage, MI 49002 USA
t: 269 323 7700
f: 269 323 2742
toll free: 800 253 3210
neurosurgical.stryker.com
Please refer to the current Stryker CORE 2 console
Instructions for Use (IFU Ref 5400-052-700-EN) for a
complete
list of cautions, operational details, troubleshooting
tips, cleaning protocols and duty cycles.
