ISO 5356-2:2012/Amd 1:2019
(Amendment)Anaesthetic and respiratory equipment - Conical connectors - Part 2: Screw-threaded weight-bearing connectors - Amendment 1
Anaesthetic and respiratory equipment - Conical connectors - Part 2: Screw-threaded weight-bearing connectors - Amendment 1
Matériel d'anesthésie et de réanimation respiratoire — Raccords coniques — Partie 2: Raccords à vis pouvant supporter un certain poids — Amendement 1
General Information
- Status
- Published
- Publication Date
- 28-Jul-2019
- Technical Committee
- ISO/TC 121/SC 1 - Breathing attachments and anaesthetic machines
- Drafting Committee
- ISO/TC 121/SC 1/WG 9 - Anaesthetic systems
- Current Stage
- 6060 - International Standard published
- Start Date
- 29-Jul-2019
- Due Date
- 04-Sep-2020
- Completion Date
- 18-Nov-2019
Relations
- Effective Date
- 18-Dec-2021
Overview
ISO 5356-2:2012/Amd 1:2019 is an important amendment to the international standard focused on anaesthetic and respiratory equipment. Specifically, it addresses conical screw-threaded weight-bearing connectors, which play a crucial role in ensuring safe and reliable connections between heavier or fragile breathing components. The amendment updates the original Part 2 of ISO 5356 to enhance compatibility, safety, and performance of these connectors in medical environments.
This standard is maintained by ISO Technical Committee ISO/TC 121, Subcommittee SC 1, specializing in breathing attachments and anaesthetic machines. The document builds upon the foundations laid out in ISO 5356-1:2015, which specifies requirements for lighter weight cones and sockets.
Key Topics
- Screw-threaded weight-bearing connectors: Designed to support substantial equipment loads during anaesthesia and respiratory procedures.
- Compatibility: Connectors conforming to this standard must remain compatible with cones and sockets defined in ISO 5356-1:2015, enabling flexible and safe component interchange.
- Misconnection prevention: Although the connectors aim to reduce inadvertent misconnection risks, ultimate responsibility for correct assembly lies with the user.
- Measurement and functional testing: Compliance verification requires precise measurement and functional testing to ensure connector performance and safety.
- Standardized dimensions: Key dimensional specifications such as the 22 mm cone and socket sizes are referenced, supporting uniformity and interoperability.
Applications
ISO 5356-2:2012/Amd 1:2019 is primarily used within the healthcare sector, particularly in the design and manufacture of:
- Anaesthetic machines and breathing systems requiring robust, weight-bearing connectors.
- Respiratory equipment where heavier or fragile components demand secure and reliable connections.
- Medical device manufacturing focused on patient safety through standardized connector designs.
- Hospital and clinical settings where compatibility between various breathing apparatus parts is essential.
By adhering to this standard, manufacturers and healthcare providers ensure enhanced safety, reliability, and consistent performance in critical medical equipment interfaces.
Related Standards
- ISO 5356-1:2015 – Anaesthetic and respiratory equipment - Conical connectors - Part 1: Cones and sockets. This is the foundational standard for lightweight connectors compatible with ISO 5356-2 designs.
- ISO 121 (Anaesthetic and respiratory equipment series) – covers broader aspects of anaesthetic and respiratory safety and device interoperability.
- ISO/IEC Directives, Part 1 and 2 – outline procedural and editorial rules governing the drafting and maintenance of ISO international standards.
Conclusion
ISO 5356-2:2012/Amd 1:2019 is a critical amendment enhancing the design and safety requirements for weight-bearing, screw-threaded conical connectors in anaesthetic and respiratory equipment. It ensures interoperability with lighter connectors, promotes resistance to misconnection, and requires thorough testing for compliance. This standard supports manufacturers and healthcare professionals in delivering reliable, high-quality respiratory systems critical to patient care.
For more information or purchasing inquiries, visit ISO's official website.
ISO 5356-2:2012/Amd 1:2019 - Anaesthetic and respiratory equipment — Conical connectors — Part 2: Screw-threaded weight-bearing connectors — Amendment 1 Released:7/29/2019
ISO 5356-2:2012/Amd 1:2019 - Matériel d'anesthésie et de réanimation respiratoire — Raccords coniques — Partie 2: Raccords à vis pouvant supporter un certain poids — Amendement 1 Released:7/29/2019
Frequently Asked Questions
ISO 5356-2:2012/Amd 1:2019 is a standard published by the International Organization for Standardization (ISO). Its full title is "Anaesthetic and respiratory equipment - Conical connectors - Part 2: Screw-threaded weight-bearing connectors - Amendment 1". This standard covers: Anaesthetic and respiratory equipment - Conical connectors - Part 2: Screw-threaded weight-bearing connectors - Amendment 1
Anaesthetic and respiratory equipment - Conical connectors - Part 2: Screw-threaded weight-bearing connectors - Amendment 1
ISO 5356-2:2012/Amd 1:2019 is classified under the following ICS (International Classification for Standards) categories: 11.040.10 - Anaesthetic, respiratory and reanimation equipment. The ICS classification helps identify the subject area and facilitates finding related standards.
ISO 5356-2:2012/Amd 1:2019 has the following relationships with other standards: It is inter standard links to ISO 5356-2:2012. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
ISO 5356-2:2012/Amd 1:2019 is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.
Standards Content (Sample)
INTERNATIONAL ISO
STANDARD 5356-2
Third edition
2012-11-15
AMENDMENT 1
2019-08
Anaesthetic and respiratory
equipment — Conical connectors —
Part 2:
Screw-threaded weight-bearing
connectors
AMENDMENT 1
Matériel d'anesthésie et de réanimation respiratoire — Raccords
coniques —
Partie 2: Raccords à vis pouvant supporter un certain poids
AMENDEMENT 1
Reference number
ISO 5356-2:2012/Amd.1:2019(E)
©
ISO 2019
ISO 5356-2:2012/Amd.1:2019(E)
© ISO 2019
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address
below or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Fax: +41 22 749 09 47
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii © ISO 2019 – All rights reserved
ISO 5356-2:2012/Amd.1:2019(E)
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards
bodies (ISO member bodies). The work of preparing International Standards is normally carried out
through ISO technical committees. Each member body interested in a subject for which a technical
committee has been established has the right to be represented on that committee. International
organizations, governmental and non-governmental, in liaison with ISO, also take part in the work.
ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of
electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the
different types of ISO documents should be noted. This document was drafted in accordance with the
editorial rules of the ISO/IEC Directives, Part 2 (see www .iso .org/directives).
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. ISO shall not be held responsible for identifying any or all such patent rights. Details of
any patent rights identified during the development of the document will be in the Introduction and/or
on the IS
...
NORME ISO
INTERNATIONALE 5356-2
Troisième édition
2012-11-15
AMENDEMENT 1
2019-08
Matériel d'anesthésie et de
réanimation respiratoire — Raccords
coniques —
Partie 2:
Raccords à vis pouvant supporter un
certain poids
AMENDEMENT 1
Anaesthetic and respiratory equipment — Conical connectors —
Part 2: Screw-threaded weight-bearing connectors
AMENDMENT 1
Numéro de référence
ISO 5356-2:2012/Amd.1:2019(F)
©
ISO 2019
ISO 5356-2:2012/Amd.1:2019(F)
DOCUMENT PROTÉGÉ PAR COPYRIGHT
© ISO 2019
Tous droits réservés. Sauf prescription différente ou nécessité dans le contexte de sa mise en œuvre, aucune partie de cette
publication ne peut être reproduite ni utilisée sous quelque forme que ce soit et par aucun procédé, électronique ou mécanique,
y compris la photocopie, ou la diffusion sur l’internet ou sur un intranet, sans autorisation écrite préalable. Une autorisation peut
être demandée à l’ISO à l’adresse ci-après ou au comité membre de l’ISO dans le pays du demandeur.
ISO copyright office
Case postale 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Genève
Tél.: +41 22 749 01 11
Fax: +41 22 749 09 47
E-mail: copyright@iso.org
Web: www.iso.org
Publié en Suisse
ii © ISO 2019 – Tous droits réservés
ISO 5356-2:2012/Amd.1:2019(F)
Avant-propos
L'ISO (Organisation internationale de normalisation) est une fédération mondiale d'organismes
nationaux de normalisation (comités membres de l'ISO). L'élaboration des Normes internationales est
en général confiée aux comités techniques de l'ISO. Chaque comité membre intéressé par une étude
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gouvernementales et non gouvernementales, en liaison avec l'ISO participent également aux travaux.
L'ISO collabore étroitement avec la Commission électrotechnique internationale (IEC) en ce qui
concerne la normalisation électrotechnique.
Les procédures utilisées pour élaborer le présent document et celles destinées à sa mise à jour sont
décrites dans les Directives ISO/IEC, Partie 1. Il convient, en particulier, de prendre note des différents
critères d'approbation requis pour les différents types de documents ISO. Le présent document a été
rédigé conformément aux règles de rédaction données dans les Directives ISO/IEC, Partie 2 (voir www
.iso .org/directives).
L'attention est attirée sur le fait que certains des éléments du présent document peuvent faire l'objet de
droits de propriété intellectuelle ou de droits analogues. L'ISO ne saurait être tenue pour responsable
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les références aux droits de propriété intellectuelle ou autres droits analogues identifiés lors de
l'élaboration du document sont indiqués dans l'Introduction et/ou dans la liste des déclarations de
brevets reçues par l'ISO (voir www .iso .org/brevets).
Les appellations commerciales éventuellement mentionnées dans le présent document sont données
pour information, par souci de com
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