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BSI - BS EN ISO 80601-2-79

Medical electrical equipment Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment

inactive
Organization: BSI
Publication Date: 31 August 2019
Status: inactive
Page Count: 86
ICS Code (Anaesthetic, respiratory and reanimation equipment): 11.040.10

Document History

23/30441461 DC
May 16, 2023
Draft BS EN ISO 80601-2-79 Medical electrical equipment Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment
A description is not available for this item.
BS EN ISO 80601-2-79
August 31, 2019
Medical electrical equipment Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment
A description is not available for this item.
BS EN ISO 80601-2-79
August 31, 2019
Medical electrical equipment Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment
A description is not available for this item.
BS ISO 80601-2-79
August 31, 2018
Medical electrical equipment Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment
A description is not available for this item.
BS EN ISO 80601-2-79
August 31, 2018
Medical electrical equipment Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment
A description is not available for this item.

References

This document references:
BS EN ISO 80601-2-80 - Medical electrical equipment Part 2-80: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency
Published by BSI on August 31, 2018
A description is not available for this item.
This document references:
EN 15986 - Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalates
Published by CEN on March 1, 2011
This European Standard specifies requirements for the labelling of a medical device or parts of a medical device to indicate the presence of phthalates, when required by Annex I of Directive...
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 60601-1-3 - Medical electrical equipment – Part 1-3: General requirements for basic safety and essential performance – Collateral Standard: Radiation protection in diagnostic X-ray equipment
Published by IEC on January 1, 2021
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...
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