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About This Item

 

Full Description

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.
 

Document History

  1. IEC 60601-2-1 Ed. 4.0 b:2020


    Medical electrical equipment - Part 2-1: Particular requirements for the basic safety and essential performance of electron accelerators in the range 1 MeV to 50 MeV

    • Most Recent
  2. IEC 60601-2-1 Ed. 3.1 b:2014


    Medical electrical equipment - Part 2-1: Particular requirements for the basic safety and essential performance of electron accelerators in the range 1 MeV to 50 MeV CONSOLIDATED EDITION

    • Historical Version
  3. IEC 60601-2-1 Ed. 3.0 b:2009


    Medical electrical equipment - Part 2-1: Particular requirements for the basic safety and essential performance of electron accelerators in the range 1 MeV to 50 MeV

    • Historical Version
  4. IEC 60601-2-1 Amd.1 Ed. 2.0 en:2002


    Amendment 1

    • Historical Version
  5. IEC 60601-2-1 Ed. 2.0 b:1998

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    Medical electrical equipment - Part 2-1: Particular requirements for the safety of electron accelerators in the range 1 MeV to 50 MeV

    • Historical Version
 

Amendments, rulings, supplements, and errata

  1. IEC 60601-2-1 Amd.1 Ed. 2.0 en:2002


    Amendment 1