BS EN 60601-2-36:2015 applies to BASIC SAFETY and ESSENTIAL PERFORMANCE of equipment for EXTRACORPOREALLY INDUCED LITHOTRIPSY as defined in 201.3.206 including equipment for other medical applications of therapeutic extracorporeally induced focused PRESSURE PULSES, hereafter referred to as ME EQUIPMENT. The applicability of this particular standard is limited to components directly involved in the LITHOTRIPSY treatment, such as, but not limited to, the generator of the PRESSURE PULSE, PATIENT support device, and their interactions with imaging and monitoring devices. Other devices, such as PATIENT treatment planning computers, X-ray and ultrasonic devices, are excluded from this standard, because they are treated in other applicable IEC standards.


Cross References:
IEC 60601-1-2:2007
IEC 60601-1:2005
IEC 60601-1:2005+A1:2012
IEC 60601-2-5:2009
IEC 61846:1998
EN 60601-1-2:2007
EN 60601-1-2:2007+Ac:2010
EN 60601-1:2006
EN 60601-1:2006+Ac:2010
EN 60601-1:2006+Ac:2014
EN 60601-1:2006+A11:2011
EN 60601-1:2006+A1:2013
EN 61846:1998
IEC 60601-2-5:2009
IEC 60601-2-62
IEC 61689:2013
IEC 62555
IEC/TS 62556
EN 10002/AC 1
DIN 50 100/02.78
EN 61689:2013
EN 62555


Replaces BS EN 60601-2-36:1997 which remains current

All current amendments available at time of purchase are included with the purchase of this document.