IEC 60601-2-33/AMD1:2006
Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis; Amendment 1

Standard No.
IEC 60601-2-33/AMD1:2006
Release Date
2006
Published By
International Electrotechnical Commission (IEC)
Status
Replace By
IEC 60601-2-33:2002/AMD2:2007
Latest
IEC 60601-2-33:2022/ISH1:2023
Replace
IEC 62B/573/FDIS:2005 IEC 60601-2-33 AMD 1:2005
Scope
Establishes requirements for the safety of magnetic resonance equipment to provide protection for the patient. Establishes requirements to provide information to the operator, staff associated with magnetic resonance equipment and the general public. Pro

IEC 60601-2-33/AMD1:2006 history

  • 2023 IEC 60601-2-33:2022/ISH1:2023 Interpretation Sheet 1 — Medical electrical equipment — Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
  • 2022 IEC 60601-2-33:2022 Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
  • 2016 IEC 60601-2-33:2010/COR2:2016 Medical electrical equipment – Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis (Edition 3.0)
  • 2015 IEC 60601-2-33:2010/AMD2:2015 Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis; Amendment 2
  • 2015 IEC 60601-2-33:2015 Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
  • 2013 IEC 60601-2-33/AMD3:2013 Medical electrical equipment.Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
  • 2013 IEC 60601-2-33:2010/AMD1:2013 Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
  • 2013 IEC 60601-2-33:2013 Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
  • 2012 IEC 60601-2-33:2010/COR1:2012 Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis; Corrigendum 1
  • 2010 IEC 60601-2-33:2010 Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
  • 2008 IEC 60601-2-33:2008 Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
  • 1970 IEC 60601-2-33:2002/AMD2:2007 Amendment 2 - Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
  • 2006 IEC 60601-2-33/AMD1:2006 Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis; Amendment 1
  • 2006 IEC 60601-2-33:2006 Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
  • 1970 IEC 60601-2-33:2002/AMD1:2005 Amendment 1 - Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
  • 2002 IEC 60601-2-33:2002 Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
  • 1995 IEC 60601-2-33:1995 Medical electrical equipment - Part 2: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis



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