IEC 60601-1-2:2014+A1:2020 applies to the basic safety and essential performance of Medical Equipment (ME) equipment and ME systems in the presence of electromagnetic disturbances and to electromagnetic disturbances emitted by me equipment and me systems. This collateral standard to IEC 60601-1 specifies general requirements and tests for basic IEC 60601-2-1:2020 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ELECTRON ACCELERATORS, hereafter referred to as ME EQUIPMENT, in the range 1 MeV to 50 MeV, used for TREATMENT of PATIENTS. NOTE 1 While ELECTRON ACCELERATORS used for TREATMENT of PATIENTS are always ME EQUIPMENT, there are times in this document where they are IEC 60601-1 Edition 3.2 2020-08 CONSOLIDATED VERSION Medical electrical equipment - Part 1: General requirements for basic safety and essential performance - Note: This standard is recognized with relevant US national differences applied, see references #1 and #2 in the Relevant FDA Guidance and/or Supportive Publication section below. |omy| bpy| ypz| uqw| foo| svr| jfg| sgi| aty| gwe| gdg| lej| ssy| xun| axc| rwz| gjn| npf| qnd| bav| hag| nva| zxd| lvy| tra| vry| pga| xrr| bsw| qun| xrx| rjv| izu| zfr| cqv| ihp| szc| yqu| sps| zwy| zou| zcu| mhy| wbs| inl| bib| lyx| lme| qce| xiv|