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ISO - DIS 19211

Anaesthetic and respiratory equipment — Fire-activated oxygen shut-off devices for use during oxygen therapy

pending, Most Current
Organization: ISO
Publication Date: 3 March 2023
Status: pending
Page Count: 20
ICS Code (Anaesthetic, respiratory and reanimation equipment): 11.040.10
scope:

This document specifies requirements for fire activated oxygen shut-off devices that stop the flow of oxygen in respiratory therapy tubing when activated by fire.

NOTE 1 Typical arrangements for fire activated oxygen shut-off devices are shown in Annex C.

NOTE 2 Respiratory therapy tubing is covered by ISO 17256.

NOTE 3 Use of fire activated oxygen shut-off devices in medical devices or accessories is not mandated in this document.

The fire activated oxygen shut off devices specified in this document are not suitable for use with oxygen therapy systems with flows in excess of 20 l/min).

Document History

DIS 19211
March 3, 2023
Anaesthetic and respiratory equipment — Fire-activated oxygen shut-off devices for use during oxygen therapy
This document specifies requirements for fire activated oxygen shut-off devices that stop the flow of oxygen in respiratory therapy tubing when activated by fire. NOTE 1 Typical arrangements for...

References

This document references:
EN 13544-2 - Respiratory therapy equipment - Part 2: Tubing and connectors
Published by CEN on October 1, 2002
A description is not available for this item.
This document references:
2001/83/EC - DIRECTIVE OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL on the Community code relating to medicinal products for human use
Published by EU on November 6, 2001
A description is not available for this item.
This document references:
IEC 60601-1-11 - Medical electrical equipment – Part 1-11: General requirements for basic safety and essential performance – Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
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 for use in the HOME HEALTHCARE ENVIRONMENT, as defined...
This document references:
ISO 18190 - Anaesthetic and respiratory equipment - General requirements for airways and related equipment
Published by ISO on November 1, 2016
This International Standard specifies the general requirements common to airways and related equipment and applicable to those device-specific standards that reference it. The requirements of a...
This document references:
ISO 18562-1 - Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 1: Evaluation and testing within a risk management process
Published by ISO on March 1, 2017
This document specifies: — the general principles governing the biological evaluation within a risk management process of the gas pathways of a medical device, its parts or accessories, which are...
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:
DIS 80369-2 - Small-bore connectors for liquids and gases in healthcare applications — Part 2: Connectors for respiratory applications
Published by ISO on May 3, 2021
This document specifies dimensions for two respiratory small-bore connectors. One (R1) for use on medical devices subjected to pressures up to 15 kPa such as a breathing system, the other (R2) for...
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