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BSI - 21/30433077 DC

Draft BS EN IEC 60601-2-39 Medical electrical equipment. Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment

pending
Organization: BSI
Publication Date: 1 October 2021
Status: pending
Page Count: 52
ICS Code (Other medical equipment): 11.040.99

Document History

21/30433077 DC
October 1, 2021
Draft BS EN IEC 60601-2-39 Medical electrical equipment. Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment
A description is not available for this item.
BS EN IEC 60601-2-39
August 31, 2019
Medical electrical equipment Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment
A description is not available for this item.
BS EN 60601-2-39
March 31, 2009
Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment
A description is not available for this item.
BS EN 60601-2-39
March 31, 2009
Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment
A description is not available for this item.
BS EN 60601-2-39
December 15, 1999
Medical Electrical Equipment - Part 2-39: Particular Requirements for Safety - Specification for Peritoneal Dialysis Equipment
A description is not available for this item.
BS EN 60601-2-39
December 15, 1999
Medical electrical equipment - Part 2-39: Particular requirements for safety - Specification for peritoneal dialysis equipment
A description is not available for this item.
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References

This document references:
IEC 60601-1-9 - Medical electrical equipment – Part 1-9: General requirements for basic safety and essential performance – Collateral Standard: Requirements for environmentally conscious design
Published by IEC on July 1, 2020
This International Standard applies to the reduction of adverse ENVIRONMENTAL IMPACTS of MEDICAL ELECTRICAL EQUIPMENT, hereafter referred to as ME EQUIPMENT. MEDICAL ELECTRICAL SYSTEMS are excluded...
This document references:
IEC 80001-1 - Application of risk management for IT-networks incorporating medical devices – Part 1: Roles, responsibilities and activities
Published by IEC on October 1, 2010
Recognizing that MEDICAL DEVICES are incorporated into IT-NETWORKS to achieve desirable benefits (for example, INTEROPERABILITY), this international standard defines the roles, responsibilities and...
This document references:
IEC 61672-1 - Electroacoustics - Sound level meters - Part 1: Specifications
Published by IEC on September 1, 2013
This part of IEC 61672 gives electroacoustical performance specifications for three kinds of sound measuring instruments: a time-weighting sound level meter that measures exponential-time-weighted,...
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 60601-1-10 - 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
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....
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