DIN EN 60601-2-33:2017
Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis(IEC 60601-2-33:2010 + COR1:2012 + A1:2013 + A2:2015 + COR2:2016); German version EN 6060

Standard No.

DIN EN 60601-2-33:2017

Release Date

2017

Published By

German Institute for Standardization

Latest

DIN EN 60601-2-33:2017

Replace

DIN EN 60601-2-33:2011 DIN EN 60601-2-33/A1:2012 DIN EN 60601-2-33/A2:2016

Scope

This International Standard addresses technical aspects of the medical diagnostic MR-SYSTEM and the MR-EQUIPMENT therein related to the safety of PATIENTS examined with this system, the safety of the MR-WORKER involved with its operation and the safety of the MR-WORKER involved with the development, manufacturing, installation, and servicing of the MR-SYSTEM.

DIN EN 60601-2-33:2017 Referenced Document

• DIN EN 45502-2-1:2004 Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers); German version EN 45502-2-1:2003
• DIN EN 60601-1-10:2016 Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers (IEC 60601-1-10:2007 + A1:2013); German version EN ...
• DIN EN 60601-1-11:2016 Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment (IEC 6060
• DIN EN 60601-1-12:2016 Medical electrical equipment - Part 1-12: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical service
• DIN EN 60601-1-1:2002 Medical electrical equipment - Part 1-1: General requirements for safety; Collateral standard: Safety requirements for medical electrical systems (IEC 60601-1-1:2000); German version EN 60601-1-1:2001
• DIN EN 60601-1-2:2016 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic disturbances - Requirements and tests (IEC 60601-1-2:2014); German version EN 60601-1-2:2015
• DIN EN 60601-1-3:2014 Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment (IEC 60601-1-3:2008 + A1:2013); German version EN 60601-1-3:2008 + Cor.:2010
• DIN EN 60601-1-4:2001 Medical electrical equipment - Part 1-4: General requirements for safety; Collateral standard: Programmable electrical medical systems (IEC 60601-1-4:1996 + A1:1999); German version EN 60601-1-4:1996 + A1:1999
• DIN EN 60601-1-6:2016 Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability (IEC 60601-1-6:2010 + A1:2013); German version EN 60601-1-6:2010 + A1:2015
• DIN EN 60601-1-8:2014 Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems (IEC
• DIN EN 60601-1-9:2014 Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design (IEC 60601-1-9:2007 + A1:2013); German version EN 60601-1-9:2008 + A1:2013
• DIN EN 60601-1:2013 Medical electrical equipment.Part 1: General requirements for basic safety and essential performance (IEC 60601-1:2005 + Cor. :2006 + Cor. :2007 + A1:2012); German version EN 60601-1:2006 + Cor. :2010 + A1:2013
• DIN EN 60601-2-1:2016 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 (IEC 60601-2-1:2009 + A1:2014); German version EN 60601-2-1:2015
• DIN EN 60601-2-2:2010 Medical electrical equipment - Part 2-2: Particular requirements for basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories (IEC 60601-2-2:2009); German version EN 60601-2-2:2009
• DIN EN 60601-2-3:2017 Medical electrical equipment - Part 2-3: Particular requirements for the basic safety and essential performance of short-wave therapy equipment (IEC 60601-2-3:2012 + A1:2016); German version EN 60601-2-3:2015 + A1:2016
• DIN EN 60601-2-4:2012 Medical electrical equipment - Part 2-4: Particular requirements for the basic safety and essential performance of cardiac defibrillators (IEC 60601-2-4:2010); German version EN 60601-2-4:2011
• DIN EN 60601-2-5:2016 Medical electrical equipment - Part 2-5: Particular requirements for the basic safety and essential performance of ultrasonic physiotherapy equipment (IEC 60601-2-5:2009); German version EN 60601-2-5:2015
• DIN EN 60601-2-6:2017 Medical electrical equipment - Part 2-6: Particular requirements for the basic safety and essential performance of microwave therapy equipment (IEC 60601-2-6:2012 + A1:2016); German version EN 60601-2-6:2015 + A1:2016
• DIN EN 60601-2-8:2016 Medical electrical equipment - Part 2-8: Particular requirements for the basic safety and essential performance of therapeutic X-ray equipment operating in the range 10 kV to 1 MV (IEC 60601-2-8:2010 + A1:2015); German version EN 60601-2-8:2015 + A1:2016

DIN EN 60601-2-33:2017 history

• 2017 DIN EN 60601-2-33:2017 Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis(IEC 60601-2-33:2010 + COR1:2012 + A1:2013 + A2:2015 + COR2:2016); German version EN 6060
• 2011 DIN EN 60601-2-33:2011 Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis (IEC 60601-2-33:2010); German version EN 60601-2-33:2010 + Cor. :2010
• 2008 DIN EN 60601-2-33:2008 Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis (IEC 60601-2-33:2002 + A1:2005 + A2:2007); German version EN 60601-2-33:2002 + A1:2005 + A2:2008