Stryker Altrix Operation Manual page 4

In accordance with European Directive 2012/19/EU on Waste Electrical and Electronic
Equipment (WEEE) as amended, this symbol indicates that the product should be collected
separately for recycling. Do not dispose of as unsorted municipal waste. Contact local distributor
for disposal information. Ensure infected equipment is decontaminated prior to recycling.
Medical Equipment Classified by Underwriters Laboratories Inc. with Respect to Electric Shock,
Fire, Mechanical and Other Specified Hazards Only in Accordance with IEC 60601-1:20 05 (3rd
edition), ANSI/AAMI ES60601-1 (2005, 3rd edition), CAN/CSA C22.2 No. 60601-1:20 08, IEC
80601-2-35:2009, CAN/CSA C22.2 NO 80601-2-35:12, ISO 80601-2-56:2009, CAN/CSA C22.2
87VL Medical NO 80601-2-56:12, IEC 60601-1-8:2007, CAN/CSA C22.2 NO 60601-1-8-08, IEC 60601-1-
Electrical Equipment 10:2008, CAN/CSA C22.2 NO 60601-1-10-09, IEC 60601-1-6, CAN/CSA-C22.2 No. 60601-1-
6:11
Liquid level indicator
CE Mark
2797
Authorized representative in the European Community
European medical device
Fragile, handle with care
Keep dry
Do not stack
This way up
EN 8001-109-001 Rev C.0