欢迎来到寰标网! 客服QQ:772084082 加入会员
当前位置: 首页 > 标准详情页

IEC 60601-1-3:2008+AMD1:2013+AMD2:2021 CSV现行

Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment

出版:

获取原文 如何获取原文?问客服 获取原文,即可享受本标准状态变更提醒服务!

专家解读视频

基本信息
标准编号: IEC 60601-1-3:2008+AMD1:2013+AMD2:2021 CSV
标准类别:Standard
出版单位:
标准页数:0
标准简介

IEC 60601-1-3:2008+A1:2013+A2:2021 applies to X-ray equipment and to subassemblies of such equipment, where radiological images of a human patient are used for diagnosis, planning or guidance of medical procedures. The object of this collateral standard is to establish general requirements for protection against X-radiation in X-ray equipment, in order that the irradiation of the human patient, the operator, staff and members of the public can be kept as low as reasonably achievable, without jeopardizing the benefit of the radiological procedure. Particular standards may specify their appropriate values and/or measures for general requirements specified in this collateral standard. The implementation of the general requirements or the reference to the particular standard instead, shall be justified in the risk management process. This collateral standard considers radiation protection aspects related to X-radiation only. Requirements for the control of the electrical energy used to generate X-radiation, which is also an important aspect of radiation protection, are included in IEC 60601-1 and in particular standards for the safety and essential performance of the equipment concerned. This document cancels and replaces the first edition of IEC 60601-1-3, published in 1994 (which replaced IEC 60407 issued in 1973). It constitutes a technical revision. This edition has been restructured and aligned to IEC 60601-1(2005) and focussed on general requirements for RADIATION PROTECTION that apply to all diagnostic X-RAY EQUIPMENT. Requirements particular to specific equipment have been removed and will be covered in particular standards. For a description of the changes, see the mapping in Annex C. This consolidated version consists of the second edition (2008), its amendment 1 (2013) and its amendment 2 (2021). Therefore, no need to order amendments in addition to this publication.