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BSI - 20/30423003 DC

Draft BS EN IEC 60601-2-33 Medical electrical equipment. Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis

pending
Organization: BSI
Publication Date: 17 July 2020
Status: pending
Page Count: 138
ICS Code (Diagnostic equipment): 11.040.55

Document History

20/30423003 DC
July 17, 2020
Draft BS EN IEC 60601-2-33 Medical electrical equipment. Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
A description is not available for this item.
BS EN 60601-2-33
November 30, 2010
Medical electrical equipment Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
A description is not available for this item.
BS EN 60601-2-33
November 30, 2010
Medical electrical equipment Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
A description is not available for this item.
BS EN 60601-2-33
November 30, 2010
Medical electrical equipment Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
To be read in conjunction with BS EN 60601-1
BS EN 60601-2-33
November 30, 2010
Medical electrical equipment Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
To be read in conjunction with BS EN 60601-1
BS EN 60601-2-33
November 30, 2010
Medical electrical equipment Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
A description is not available for this item.
BS EN 60601-2-33
November 30, 2010
Medical electrical equipment Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
To be read in conjunction with BS EN 60601-1
BS EN 60601-2-33
November 30, 2010
Medical electrical equipment Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
A description is not available for this item.
BS EN 60601-2-33
October 18, 2002
Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
A description is not available for this item.
BS EN 60601-2-33
October 18, 2002
Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
A description is not available for this item.
BS EN 60601-2-33
October 18, 2002
Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
A description is not available for this item.
BS EN 60601-2-33
June 15, 1996
Medical Electrical Equipment Part 2: Particular Requirements for Safety Section 2.33: Specification for Magnetic Resonance Equipment for Medical Diagnosis
A description is not available for this item.
BS EN 60601-2-33
June 15, 1996
Medical electrical equipment Part 2: Particular requirements for safety Section 2.33 Specification for magnetic resonance equipment for medical diagnosis
A description is not available for this item.
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References

This document references:
IEC 60601-1-2 - Medical electrical equipment – Part 1-2: General requirements for basic safety and essential performance – Collateral Standard: Electromagnetic disturbances – Requirements and tests
Published by IEC on September 1, 2020
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
This document references:
IEC 60601-1-6 - Medical electrical equipment – Part 1-6: General requirements for basic safety and essential performance – Collateral standard: Usability
Published by IEC on July 1, 2020
This International Standard specifies a PROCESS for a MANUFACTURER to analyse, specify, develop and evaluate the USABILITY, as it relates to BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL...
This document references:
IEC 60601-1-8 - 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
Published by IEC on July 1, 2020
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
This document references:
IEEE C95.6 - Standard for Safety Levels with Respect to Human Exposure to Electromagnetic Fields, 0–3 kHz
Published by IEEE on September 12, 2002
In 1960, the American Standards Association approved the initiation of the Radiation Hazards Standards project under the co-sponsorship of the Department of the Navy and the Institute of Electrical...
This document references:
ISO 14117 - Active implantable medical devices — Electromagnetic compatibility — EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices
Published by ISO on September 1, 2019
This document specifies test methodologies for the evaluation of the electromagnetic compatibility (EMC) of active implantable cardiovascular devices that provide one or more therapies for...
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