Specifies the particular requirements for the electrical and mechanical safety of medical electron accelerators. It contains new sub-clauses which are additions to section one of IEC 601-2-1, and a new section three giving the electrical and mechanical safety requirements for equipment.
Establishes requirements to be complied with by manufacturers in the design and construction of electron accelerators for use in radiotherapy and defines type tests and site tests. Places limits on the degradation of equipment performance beyond which it can be presumed that a fault condition exists and where an interlock then operates to prevent continued operation of the equipment.
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