80601国际标准的本部分适用于201.3.204中定义的脑电图仪的基本安全和基本性能，以下也称为医用电气设备或医用电气系统。本文件适用于专业医疗机构、急救医疗服务环境或家庭医疗环境中使用的脑电图仪。交叉引用:EN 60601-1-2:2015EN 60601-1:2006/A12:2014EN 60601-1:2006EN IEC 60601-2-2:2018IEC 60601-1-6:2013IEC 60601-1-11:2015IEC 60601- 1:2005EN 60601-1:2006/更正2010年3月EN 60601-1:2006/A11:2011IEC 60601-2-2017IEC 60601-1-2:2014IEC 60601-1-12:2014EN 60601-1-11:2015IEC 60601-1-10EN 60601-1-9EN 60601-1-10IEC 60601-1-1-3EN 60601-1-3IEC 60601-1-1-1-9EN 62366-1:2015IEC 62366-1-1:2015IEC 62366-1:2015购买本文件时可提供的所有现行修订内容均包含在购买本文件中。

This part of the 80601 International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ELECTROENCEPHALOGRAPHS as defined in 201.3.204, hereafter also referred to as ME EQUIPMENT or ME SYSTEM. This document is applicable to ELECTROENCEPHALOGRAPHS intended for use in professional healthcare facilities, the EMERGENCY MEDICAL SERVICES ENVIRONMENT or the HOME HEALTHCARE ENVIRONMENT.Cross References:EN 60601-1-2:2015EN 60601-1:2006/A12:2014EN 60601-1:2006EN IEC 60601-2-2:2018IEC 60601-1-6:2013IEC 60601-1-11:2015IEC 60601-1:2005EN 60601-1:2006/corrigendum Mar. 2010EN 60601-1:2006/A11:2011IEC 60601-2-2:2017IEC 60601-1-2:2014IEC 60601-1-12:2014EN 60601-1-11:2015IEC 60601-1-10EN 60601-1-9EN 60601-1-10IEC 60601-1-3EN 60601-1-3IEC 60601-1-9EN 62366-1:2015IEC 62366-1:2015All current amendments available at time of purchase are included with the purchase of this document.