BS EN 60601-2-11:2015适用于伽马射线的基本安全和基本性能 束治疗设备，包括多源立体定向放射治疗设备， 以下简称医用电气设备。如果某条款或子条款专门适用于医用电气设备，或 仅适用于ME系统，该条款或子条款的标题和内容将说明这一点。如果不是这样的话 在这种情况下，本条款或子条款适用于医用电气设备和医用电气系统（视情况而定）。医用电气设备或医用电气系统预期生理功能中固有的危险 在本标准的范围内，本标准的具体要求不包括 通用标准7.2.13和8.4.1中的规定除外。交叉引用:IEC 60601-1-3:2008EN 60601-1-3:2008EN 60601-1-3:2008/勘误表1:2010IEC 61217EN 61217IEC/TR 60788:200493/42/EEBS EN 60601-2-11:1998（保持最新状态）购买本文件时，包括所有当前可用的修改件。

BS EN 60601-2-11:2015 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of GAMMA BEAM THERAPY EQUIPMENT, including MULTI-SOURCE STEREOTACTIC RADIOTHERAPY equipment, hereafter referred to as ME EQUIPMENT.If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant.HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the general standard.Cross References:IEC 60601-1-3:2008EN 60601-1-3:2008EN 60601-1-3:2008/Corrigendum 1:2010IEC 61217EN 61217IEC/TR 60788:200493/42/EECReplaces BS EN 60601-2-11:1998 which remains currentAll current amendments available at time of purchase are included with the purchase of this document.