医疗器械行业标准的制定 第1部分:阶段划分、代码和程序
Development of medical devices industrial standards—Part 1:Stage division,code and procedure
2005-07-18
AAMI/ISO 16142-2-2017
Medical devices - Recognized essential principles of safety and performance of medical devices - Part 2: General essential principles and additional specific essential principles for all IVD medical devices and guidance on the selection of standards
医疗器械.医疗器械安全和性能的公认基本原则.第2部分:所有IVD医疗器械的一般基本原则和附加特定基本原则及标准选择指南
2017-07-31
AAMI/IEC TIR80001-2-8-2016
Application of risk management for IT networks incorporating medical devices - Part 2-8: Application guidance Guidance on standards for establishing the security capabilities identified in IEC 80001-2-2
包含医疗设备的IT网络风险管理的应用第2-8部分:IEC 80001-2-2中确定的安全能力建立标准的应用指南
2016-11-18
IEC/TR 80001-2-8-2016
Application of risk management for IT-networks incorporating medical devices — Part 2-8: Application guidance — Guidance on standards for establishing the security capabilities identified in IEC 80001-2-2
风险管理应用于包含医疗设备的网络 - 第2-8部分:应用指南 - 建立Iec 80001-2-2中确定的安全功能标准的指导
2016-05-19
IEC TR 80001-2-8-2016
Application of risk management for IT-networks incorporating medical devices - Part 2-8: Application guidance - Guidance on standards for establishing the security capabilities identified in IEC TR 80001-2-2
包含医疗设备的IT网络的风险管理应用第2-8部分:应用指南IEC TR 80001-2-2中确定的安全能力建立标准指南