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BSI - BS EN ISO 5364

Anaesthetic and respiratory equipment - Oropharyngeal airways

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Organization: BSI
Publication Date: 31 August 2011
Status: inactive
Page Count: 22
ICS Code (Anaesthetic, respiratory and reanimation equipment): 11.040.10

Document History

BS EN ISO 5364
October 31, 2016
Anaesthetic and respiratory equipment - Oropharyngeal airways
A description is not available for this item.
BS EN ISO 5364
August 31, 2011
Anaesthetic and respiratory equipment - Oropharyngeal airways
A description is not available for this item.

References

This document references:
BS EN ISO 10993-1 - Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
Published by BSI on December 31, 2020
A description is not available for this item.
This document references:
7000 DATABASE SNAPSHOT - Graphical symbols for use on equipment - Registered symbols
Published by ISO on June 3, 2020
A description is not available for this item.
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:
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:
11607-1 AMD 1 - Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems AMENDMENT 1: Application of risk management
Published by ISO on September 1, 2023
A description is not available for this item.
This document references:
EN 556-1 - Sterilization of Medical Devices - Requirements for Medical Devices to Be Designated "Sterile" - Part 1: Requirements for Terminally Sterilized Medical Devices
Published by CEN on October 1, 2001
This European Standard specifies the requirements for a terminally-sterilized medical device to be designated "STERILE". Part 2 of this European Standard specifies the requirements for an aseptically...
This document references:
ISO TR 11991 - Guidance on Airway Management During Laser Surgery of Upper Airway First Edition
Published by ISO on January 1, 1995
A description is not available for this item.
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