This document is intended solely for the use of healthcare professionals. A healthcare professional must always rely on his or her own professional clinical judgment when deciding whether to use a particular product when treating a particular patient. Stryker does not dispense medical advice and recommends that healthcare professionals be trained in the use of any particular product before using it.
The information presented is intended to demonstrate Stryker’s product offerings. A healthcare professional must always refer to operating instructions for complete directions for use indications, contraindications, warnings, cautions, and potential adverse events, 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. Specifications subject to change without notice. The products depicted are CE marked in accordance with applicable EU Regulations and Directives.
Stryker Corporation or its divisions or other corporate affiliated entities own, use or have applied for the following trademarks or service marks: LIFEPAK, LIFENET, LUCAS, HealthEMS, RevNet, CODE-STAT, Physio-Control, HeartSine, samaritan, LIFEPAK CR, TrueCPR, REDI-CHARGE, QUIK-COMBO, EDGE, cprINSIGHT, ClearVoice, QUIK-STEP, LIFEPAK TOUGH, HomeSolutions.net, RELI, REDI-PAK, Shock Advisory System, LIFELINKcentral. All other trademarks are trademarks of their respective owners or holder. The yellow and black color scheme is a registered trademark of Stryker Corporation.
LIFEPAK devices: CE Class IIb (0123)
HeartSine device: CE Class IIb (0123)
LUCAS device: CE Class IIb (2460)
EC REP: Stryker European Operations Limited | Anngrove, IDA Business & Technology Park | Carrigtwohill, Co. Cork, T45 HX08 | Ireland
Last Updated September 2020