SIS SS IEC 601-2-10-1988
医疗电气设备.神经肌肉刺激器安全细则

Medical electrical equipment — Particular requirements for the safety ofnerve andmuscle s tim u la tors


SIS SS IEC 601-2-10-1988 发布历史

Addition: This Particular Standard specifies the requirements for the safety of nerve and musc u: stimulators, as defined in Sub-clause 2.1.101, for use in the practice of physical medicine, hereinafter referred to as stimulator(s). The following equipment is excluded: — equipment intended to be implanted or to be connected to implanled electrodes, — equipment intended for the stimulation of the brain (e.g. electroconvulsive therapy equipment), — equipment intended for neurological research, — cardiac pacemakers, — body-worn equipment, — stimulators intended for use during surgical procedures, — equipment intended for averaged evoked potential diagnosis, — equipment intended for electromyography, — equipment intended for cardiac defibrillation, — equipment intended only as a transcutaneous nerve and muscle stimulator for pain relief.

SIS SS IEC 601-2-10-1988由SE-SIS 发布于 1988-11-15。

SIS SS IEC 601-2-10-1988的历代版本如下:

 

 

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标准号
SIS SS IEC 601-2-10-1988
发布日期
1988年11月15日
实施日期
废止日期
发布单位
SE-SIS
适用范围
Addition: This Particular Standard specifies the requirements for the safety of nerve and musc u: stimulators, as defined in Sub-clause 2.1.101, for use in the practice of physical medicine, hereinafter referred to as stimulator(s). The following equipment is excluded: — equipment intended to be implanted or to be connected to implanled electrodes, — equipment intended for the stimulation of the brain (e.g. electroconvulsive therapy equipment), — equipment intended for neurological research, — cardiac pacemakers, — body-worn equipment, — stimulators intended for use during surgical procedures, — equipment intended for averaged evoked potential diagnosis, — equipment intended for electromyography, — equipment intended for cardiac defibrillation, — equipment intended only as a transcutaneous nerve and muscle stimulator for pain relief.




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