標(biāo)準(zhǔn)號(hào)：IEC 60601-2-10-2012
中文標(biāo)準(zhǔn)名稱：醫(yī)用電氣設(shè)備.第2-10部分:神經(jīng)和肌肉刺激器安全詳細(xì)要求
英文標(biāo)準(zhǔn)名稱：Medical electrical equipment. Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators
標(biāo)準(zhǔn)類型：C42
發(fā)布日期：1999/12/31 12:00:00
實(shí)施日期：1999/12/31 12:00:00
中國標(biāo)準(zhǔn)分類號(hào)：C42
國際標(biāo)準(zhǔn)分類號(hào)：11.040.60
引用標(biāo)準(zhǔn)：IEC 60601-1-2-2007;IEC 60601-1-2005
適用范圍：Replacement:This International Standard specifies the requirements for the safety of nerve and muscle STIMULATORS, defined in subclause 201.3.204, for use in the practice of physical medicine,hereinafter referred to as ME EQUIPMENT. This includes transcutaneous electrical nerveSTIMULATORS (TENS) and electrical muscle STIMULATORS (EMS).The following ME EQUIPMENT is excluded:- ME EQUIPMENT intended to be implanted or to be connected to implanted electrodes;- ME EQUIPMENT intended for the stimulation of the brain (e.g. electroconvulsive therapy MEEQUIPMENT);- ME EQUIPMENT intended for neurological research;- external cardiac pacemakers (see IEC 60601-2-31);- ME EQUIPMENT intended for averaged evoked potential diagnosis (see IEC 60601-2-40);- ME EQUIPMENT intended for electromyography (see IEC 60601-2-40);- ME EQUIPMENT intended for cardiac defibrillation (see IEC 60601-2-4).