购物车
400-168-0010
- 您的位置：
- 快3网下载安装到手机 >>
- 全部标准分类 >>
- 国际标准 >>
- 11.040.01 >>
- IEC 60601-1-8:2006+AMD1:2012+AMD2:2020 CSV EN-FR 820fa3d2 Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
【国际标准】 Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
本网站 发布时间：
2025-01-04
开通会员免费在线看70000余条国内标准，赠送文本下载次数，单本最低仅合13.3元！还可享标准出版进度查询、定制跟踪推送、标准查新等超多特权！
查看详情>>
标准简介适用范围：
暂无
标准号：
IEC 60601-1-8:2006+AMD1:2012+AMD2:2020 CSV EN-FR
标准名称：
Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
英文名称：
Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems标准状态：
现行-
发布日期：
2020-07-23 -
实施日期：
出版语种：
EN-FR
- 其它标准
- 上一篇： IEC 60601-1-8:2006+AMD1:2012+AMD2:2020 CSV EN dc51edae Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
- 下一篇： IEC 60601-1-8:2006/Amd 1:2012 EN/FR 9fe5b470 Medical electrical equipment — Part 1-8: General requirements for basic safety and essential performance — Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems — Amendment 1
- 推荐标准
- IEC 80601-2-30:2018 EN-FR 5db8028e Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers
- IEC 80601-2-60:2019 EN-FR 4f041135 Medical electrical equipment - Part 2-60: Particular requirements for the basic safety and essential performance of dental equipment
- IEC 80601-2-78:2019 EN-FR 011bdd6a Medical electrical equipment - Part 2-78: Particular requirements for basic safety and essential performance of medical robots for rehabilitation, assessment, compensation or alleviation
- IEC 80601-2-78:2019 EN/FR c567d8b5 Medical electrical equipment — Part 2-78: Particular requirements for basic safety and essential performance of medical robots for rehabilitation, assessment, compensation or alleviation
- IEC 80601-2-78:2019/Amd 1:2024 EN/FR 8a99442b Medical electrical equipment — Part 2-78: Particular requirements for basic safety and essential performance of medical robots for rehabilitation, assessment, compensation or alleviation — Amendment 1
- IEC 80601-2-78:2019/AMD1:2024 EN-FR b970c006 Amendment 1 - Medical electrical equipment - Part 2-78: Particular requirements for basic safety and essential performance of medical robots for rehabilitation, assessment, compensation or alleviation
- IEC TR 60601-4-3:2018 EN 8d3a8bcf Medical electrical equipment - Part 4-3: Guidance and interpretation - Considerations of unaddressed safety aspects in the third edition of IEC 60601-1 and proposals for new requirements
- IEC TR 60601-4-3:2018 RLV EN 5bf1033e Medical electrical equipment - Part 4-3: Guidance and interpretation - Considerations of unaddressed safety aspects in the third edition of IEC 60601-1 and proposals for new requirements
- IEC TR 61289:2011 EN d80edb95 High frequency surgical equipment - Operation and maintenance
- IEC TR 61289:2019 RLV EN 146a5d6a High frequency surgical equipment and high frequency surgical accessories - Operation and maintenance
- IEC TR 80001-2-2:2012 EN 677792ac Application of risk management for IT-networks incorporating medical devices - Part 2-2: Guidance for the disclosure and communication of medical device security needs, risks and controls
- ISO 14971:2007 EN 239205d0 Medical devices - Application of risk management to medical devices
- ISO 14971:2007 FR e0526c5f Medical devices - Application of risk management to medical devices
- ISO 14971:2019 EN 11855628 Medical devices - Application of risk management to medical devices
- ISO 14971:2019 EN c0676a75 Medical devices — Application of risk management to medical devices
