標(biāo)準(zhǔn)號(hào)：DIN EN 60601-2-33-2017
中文標(biāo)準(zhǔn)名稱：醫(yī)療電氣設(shè)備.第2-33部分:醫(yī)療診斷用磁共振設(shè)備的基本安全和主要性能的特殊要求(IEC 60601-2-33-2010+COR1-2012+A1-2013+A2-2015+COR2-2016);德文版本EN 60601-2-33-2010 +Cor.-2010+A11-2011+A1-2015+A2-2015+AC-2016+A12-2016
英文標(biāo)準(zhǔn)名稱：Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis(IEC 60601-2-33:2010 + COR1:2012 + A1:2013 + A2:2015 + COR2:2016); German version EN 6060
標(biāo)準(zhǔn)類型：C43
發(fā)布日期：1999/12/31 12:00:00
實(shí)施日期：2017/11/1 12:00:00
中國(guó)標(biāo)準(zhǔn)分類號(hào)：C43
國(guó)際標(biāo)準(zhǔn)分類號(hào)：11.040.55;35.240.80
引用標(biāo)準(zhǔn)：DIN EN 45502-2-1-2004;DIN EN 60601-1-2013;DIN EN 60601-1 Beiblatt 2-2009;DIN EN 60601-1-1-2002;DIN EN 60601-1-2-2016;DIN EN 60601-1-3-2014;DIN EN 60601-1-4-2001;DIN EN 60601-1-6-2016;DIN EN 60601-1-8-2014;DIN EN 60601-1-9-2014;DIN EN 60601-1-10-2016;DIN E
適用范圍：This International Standard addresses technical aspects of the medical diagnostic MR-SYSTEM and the MR-EQUIPMENT therein related to the safety of PATIENTS examined with this system, the safety of the MR-WORKER involved with its operation and the safety of the MR-WORKER involved with the development, manufacturing, installation, and servicing of the MR-SYSTEM.