发布时间:2024-05-27 17:49:26 - 更新时间:2024年06月29日 15:22
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Calibration Specification for Electromyographs and Evoked Response Equipments
增补:本专用标准规定了2.1.101所定义的肌电图设备和2.1.102所定义的诱发反应设备,下文统称设备。替换:本专用标准的目的是建立在2.1.101所定义的肌电图设备和2.1.102所定义的诱发反应设备安全专用要求
Medical electrical equipment.Part 2:Particular requirments for the safety of electromyograohs and evoked response equipment
KS C IEC 60601-1의 1.1에 따르는 외에 다음 사항을 추가한다.이 표준
Electromyographs and evoked response equipment
Addition: This Particular Standard applies to ELECTROMYOGRAPHS as defined in 2.1.101 and EVOKED RESPONSE EQUIPMENT as defined in 2.1.102, hereinafter
Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment
To be read in conjunction with BS EN 60601-1:1990
Medical electrical equipment - Particular requirements for safety - Specification for electromyographs and evoked response equipment
この規格は,2.1.101で定義する筋電計及び2.1.102で定義する誘発反応機器(以下,これらを機器という。)に適用する
Medical electrical equipment -- Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment
Medical electrical equipment — Part 2-40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment
Medical electrical equipment - Part 2-40 : particular requirements for the safety of electromyographs and evoked response equipments.
Replacement: This particular standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ELECTROMYOGRAPHS and EVOKED RESPONSE EQUIPMENT
Medical electrical equipment - Part 2-40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment
Covers emergency lighting and power equipment for use in unclassified locations and intended for connection to branch circuits of 600 volts or less
Emergency Lighting and Power Equipment
本标准规定了肌电生物反馈仪的术语、要求、试验方法、检验规则和标志、包装、运输、贮存。 本标准适用于肌电生物反馈仪(以下简称“肌反仪
Myoelectric biofeedback equipment
Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment
Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromygraphs and evoked response equipment (IEC 60601-2-40:1998); German version EN 60601-2-40:1998
本标准规定了肌电生物反馈仪(以下简称肌反仪)的术语和定义、分类、要求、试验方法。本标准适用于3.1规定的肌反仪。本标准不适用于使用针电极记录肌电信号的仪器和肌电诱发电位仪
Myoelectric biofeedback equipment
Calibration Specification for Electromyographs and Evoked Response Equipments
增补:本专用标准规定了2.1.101所定义的肌电图设备和2.1.102所定义的诱发反应设备,下文统称设备。替换:本专用标准的目的是建立在2.1.101所定义的肌电图设备和2.1.102所定义的诱发反应设备安全专用要求
Medical electrical equipment.Part 2:Particular requirments for the safety of electromyograohs and evoked response equipment
KS C IEC 60601-1의 1.1에 따르는 외에 다음 사항을 추가한다.이 표준
Electromyographs and evoked response equipment
Addition: This Particular Standard applies to ELECTROMYOGRAPHS as defined in 2.1.101 and EVOKED RESPONSE EQUIPMENT as defined in 2.1.102, hereinafter
Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment
To be read in conjunction with BS EN 60601-1:1990
Medical electrical equipment - Particular requirements for safety - Specification for electromyographs and evoked response equipment
この規格は,2.1.101で定義する筋電計及び2.1.102で定義する誘発反応機器(以下,これらを機器という。)に適用する
Medical electrical equipment -- Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment
Medical electrical equipment — Part 2-40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment
Medical electrical equipment - Part 2-40 : particular requirements for the safety of electromyographs and evoked response equipments.
Replacement: This particular standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ELECTROMYOGRAPHS and EVOKED RESPONSE EQUIPMENT
Medical electrical equipment - Part 2-40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment
Covers emergency lighting and power equipment for use in unclassified locations and intended for connection to branch circuits of 600 volts or less
Emergency Lighting and Power Equipment
本标准规定了肌电生物反馈仪的术语、要求、试验方法、检验规则和标志、包装、运输、贮存。 本标准适用于肌电生物反馈仪(以下简称“肌反仪
Myoelectric biofeedback equipment
Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment
Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromygraphs and evoked response equipment (IEC 60601-2-40:1998); German version EN 60601-2-40:1998
本标准规定了肌电生物反馈仪(以下简称肌反仪)的术语和定义、分类、要求、试验方法。本标准适用于3.1规定的肌反仪。本标准不适用于使用针电极记录肌电信号的仪器和肌电诱发电位仪
Myoelectric biofeedback equipment