Medical electrical equipment-Particular requirements for the basic safety and essential performance of equipment for extracorporeally induced lithotripsy
医用电气设备
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 60601-1-2:2007IEC 60601-1:2005IEC 60601-1:2005+A1:2012IEC 60601-2-5:2009IEC 61846:1998EN 60601-1-2:2007EN 60601-1-2:2007+Ac:2010EN 60601-1:2006EN 60601-1:2006+Ac:2010EN 60601-1:2006+Ac:2014EN 60601-1:2006+A11:2011EN 60601-1:2006+A1:2013EN 61846:1998IEC 60601-2-5:2009IEC 60601-2-62IEC 61689:2013IEC 62555IEC/TS 62556EN 10002/AC 1DIN 50 100/02.78EN 61689:2013EN 62555Replaces BS EN 60601-2-36:1997 which remains currentAll current amendments available at time of purchase are included with the purchase of this document.