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BSI - BS EN ISO 5367

Anaesthetic and respiratory equipment — Breathing sets and connectors

active, Most Current
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Organization: BSI
Publication Date: 30 November 2014
Status: active
Page Count: 48
ICS Code (Anaesthetic, respiratory and reanimation equipment): 11.040.10

Document History

BS EN ISO 5367
July 31, 2023
Anaesthetic and respiratory equipment — Breathing sets and connectors
A description is not available for this item.
BS EN ISO 5367
November 30, 2014
Anaesthetic and respiratory equipment — Breathing sets and connectors
A description is not available for this item.
BS EN ISO 5367
November 30, 2014
Anaesthetic and respiratory equipment — Breathing sets and connectors
A description is not available for this item.

References

This document references:
4135 - Anaesthetic and respiratory equipment — Vocabulary
Published by ISO on January 1, 2022
This document establishes a vocabulary of terms used for anaesthetic and respiratory equipment and supplies, related devices and supply systems. NOTE 1 To avoid multiple definitions of the same term...
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:
ISO 5356-1 - Anaesthetic and Respiratory Equipment - Conical Connectors - Part 1: Cones and Sockets
Published by ISO on March 15, 2015
This part of ISO 5356 specifies dimensional and gauging requirements for cones and sockets intended for connecting anaesthetic and respiratory equipment, e.g. in breathing systems, anaesthetic gas...
This document references:
EN 1041 - Information supplied by the manufacturer of medical devices
Published by CEN on August 1, 2008
This European Standard specifies requirements for information to be supplied by a manufacturer for medical devices regulated by Council Directive 90/385/EEC relating to active implantable medical...
This document references:
EN 1041 - Information supplied by the manufacturer of medical devices
Published by CEN on August 1, 2008
This European Standard specifies requirements for information to be supplied by a manufacturer for medical devices regulated by Council Directive 90/385/EEC relating to active implantable medical...
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:
ISO 5356-1 - Anaesthetic and Respiratory Equipment - Conical Connectors - Part 1: Cones and Sockets
Published by ISO on March 15, 2015
This part of ISO 5356 specifies dimensional and gauging requirements for cones and sockets intended for connecting anaesthetic and respiratory equipment, e.g. in breathing systems, anaesthetic gas...
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