电子肌动描记器及诱发反应设备检测

📅 发布时间:2024-05-27 👤 来源:北检院 👁 阅读:

KS C IEC 60601-2-40:2008 医用.第2-40部分:安全专用要求

KS C IEC 60601-1의 1.1에 따르는 외에 다음 사항을 추가한다.이 표준

Electromyographs and evoked response equipment

IEC 60601-2-40:1998 医用 第2-40部分:安全专用要求

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

JJF 1896-2021 校准规范

Calibration Specification for Electromyographs and Evoked Response Equipments

BS EN 60601-2-40:1998 医疗.详细安全性要求.仪和规范

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

JIS T 0601-2-40:2005 医用.第2-40部分:安全专用要求

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

YY 0896-2013 医用第2部分:安全专用要求

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

UNE-EN 60601-2-40:1999 医疗 第 2-40 部分:安全的特殊要求

MEDICAL ELECTRICAL EQUIPMENT. PART 2-40: PARTICULAR REQUIREMENTS FOR THE SAFETY OF ELECTROMYOGRAPHS AND EVOKED RESPONSE EQUIPMENT.

AS/NZS 3200.2.40:1999 医用第 2.40 部分:特殊安全要求 图和

Medical Electrical Equipment Part 2.40: Particular Requirements for Safety - Electromyographs and Evoked Response Equipment

YY 9706.240-2021 医用 第2-40部分:的基本安全和基本性能专用要求

Medical electrical equipment Part 2-40: Special requirements for basic safety and basic performance of myoelectric and induced response equipment

JIS T 1150:1986

Electromyographs

DS/EN 60601-2-40:1998 医用 第 2-40 部分:图仪和安全的特殊要求

This Particular Standard applies to ELECTROMYOGRAPHS as defined in 2.101 and EVOKED RESPONSE EQUIPMENT as defined in 2.102

Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment

CAN/CSA-C22.2 NO.60601-2-40-2001 医用 第 2-40 部分:图仪和安全的特殊要求(第一版)

Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment (First Edition)

LST EN 60601-2-40-2000 医疗 第 2-40 部分:图和安全的特殊要求(IEC 60601-2-40:1998)

Medical electrical equipment. Part 2-40: Particular requirements for the safety of electromygraphs and evoked response equipment (IEC 60601-2-40:1998)

AS/NZS IEC 60601.2.40:2022 医用 第 2.40 部分:图和基本安全和基本性能的特殊要求

AS/NZS IEC 60601.2.40:2022 identically adopts IEC 60601 2 40:2016 (ED.2.0) which specifies requirements for the basic safety and essential performance

Medical electrical equipment, Part 2.40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment

BS EN 60601-2-40:2019 跟踪更改 医疗 图和基本安全和基本性能的特殊要求

Tracked Changes. Medical electrical equipment. Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment

KS C IEC 60601-2-40:2008 医用.第2-40部分:安全专用要求

KS C IEC 60601-1의 1.1에 따르는 외에 다음 사항을 추가한다.이 표준

Electromyographs and evoked response equipment

IEC 60601-2-40:1998 医用 第2-40部分:安全专用要求

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

JJF 1896-2021 校准规范

Calibration Specification for Electromyographs and Evoked Response Equipments

BS EN 60601-2-40:1998 医疗.详细安全性要求.仪和规范

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

JIS T 0601-2-40:2005 医用.第2-40部分:安全专用要求

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

YY 0896-2013 医用第2部分:安全专用要求

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

UNE-EN 60601-2-40:1999 医疗 第 2-40 部分:安全的特殊要求

MEDICAL ELECTRICAL EQUIPMENT. PART 2-40: PARTICULAR REQUIREMENTS FOR THE SAFETY OF ELECTROMYOGRAPHS AND EVOKED RESPONSE EQUIPMENT.

AS/NZS 3200.2.40:1999 医用第 2.40 部分:特殊安全要求 图和

Medical Electrical Equipment Part 2.40: Particular Requirements for Safety - Electromyographs and Evoked Response Equipment

YY 9706.240-2021 医用 第2-40部分:的基本安全和基本性能专用要求

Medical electrical equipment Part 2-40: Special requirements for basic safety and basic performance of myoelectric and induced response equipment

JIS T 1150:1986

Electromyographs

DS/EN 60601-2-40:1998 医用 第 2-40 部分:图仪和安全的特殊要求

This Particular Standard applies to ELECTROMYOGRAPHS as defined in 2.101 and EVOKED RESPONSE EQUIPMENT as defined in 2.102

Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment

CAN/CSA-C22.2 NO.60601-2-40-2001 医用 第 2-40 部分:图仪和安全的特殊要求(第一版)

Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment (First Edition)

LST EN 60601-2-40-2000 医疗 第 2-40 部分:图和安全的特殊要求(IEC 60601-2-40:1998)

Medical electrical equipment. Part 2-40: Particular requirements for the safety of electromygraphs and evoked response equipment (IEC 60601-2-40:1998)

AS/NZS IEC 60601.2.40:2022 医用 第 2.40 部分:图和基本安全和基本性能的特殊要求

AS/NZS IEC 60601.2.40:2022 identically adopts IEC 60601 2 40:2016 (ED.2.0) which specifies requirements for the basic safety and essential performance

Medical electrical equipment, Part 2.40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment

BS EN 60601-2-40:2019 跟踪更改 医疗 图和基本安全和基本性能的特殊要求

Tracked Changes. Medical electrical equipment. Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment

编辑:北检院编辑部

我们的优势

选择北检院的六大理由

📚

CMA/CNAS 双认证

旗下实验室具备国家认证认可监督管理委员会CMA资质认定及中国合格评定国家认可委员会CNAS实验室认可,检测报告具有国际公信力。

🔬

1000+ 台套先进设备

配备扫描电镜、气质联用仪、电感耦合等离子体质谱仪等国际先进检测仪器,确保数据精准可靠。

🏢

15000+ 平米实验室

拥有规模化专业检测基地,涵盖材料、化工、食品、环境等多个专业实验室,满足多领域检测需求。

👥

资深技术团队

汇聚材料科学、化学分析、环境工程等领域专家,拥有10年+行业经验,提供专业可靠的检测分析服务。

快速响应机制

标准检测周期短至3个工作日,加急服务24小时出具报告,全程一对一工程师跟进,确保高效交付。

🌎

全国服务网络

总部位于北京,山东设立分部,服务覆盖全国,为20万+客户提供便捷的一站式检测解决方案。

荣誉资质

旗下实验室资质荣誉

CMA 检验检测机构资质认定

CMA 检验检测机构资质认定

国家认证认可监督管理委员会颁发,具备向社会出具具有证明作用数据的资质。

CNAS 实验室认可证书

CNAS 实验室认可证书

中国合格评定国家认可委员会认可,检测结果获国际互认,具有国际公信力。

ISO 质量管理体系认证

ISO 质量管理体系认证

通过ISO 质量管理体系认证,管理体系实现规范化、标准化。

绿色低碳诚信示范创建企业

绿色低碳诚信示范创建企业

荣获绿色低碳诚信示范创建企业称号,践行可持续发展理念,推动绿色低碳转型,助力"双碳"目标实现。

北京市创新型中小企业

北京市"创新型"中小企业

经北京市经济和信息化局认定的创新型中小企业,具备较强创新能力与较高专业化水平,是优质中小企业梯度培育体系的重要基础力量。

北京市专精特新中小企业

北京市"专精特新"中小企业

经北京市经济和信息化局认定的专精特新中小企业,具备专业化、精细化、特色化、新颖化发展特征,在细分领域具有较强竞争优势。

查看全部资质

仪器设备

国际先进检测仪器,确保检测数据精准可靠

查看全部设备

检测流程

标准化流程,高效交付

01

需求沟通

客户提交检测需求,技术顾问一对一沟通,明确检测项目与标准。

02

样品寄送

客户按照规范要求寄送样品,实验室确认样品状态与数量。

03

实验检测

专业工程师按照标准方法进行检测分析,全程质量控制。

04

数据审核

检测数据经多级审核,确保结果准确、可靠、可追溯。

05

报告出具

出具检测报告,支持电子版与纸质版,快递送达。