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CAN/CSA-C22.2 NO. 60601-1:14 + A2:22 (R2022) (CONSOLIDATED) – Medical electrical equipment – Part 1: General requirements for basic safety and essential performance (Adopted IEC 60601-1:2005, edition 3:2005 consolidated with amendment 1:2012 and amendment 2:2020, with Canadian deviations) | Appareils électromédicaux – Partie 1: Exigences générales pour la sécurité de base et les performances essentielles (norme IEC 60601-1:2005 adoptée, édition 3:2005 consolidée par l’amendement 1:2012 et l’amendement 2:2020, avec exigences propres au Canada)

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2387

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CAN/CSA-C22.2 NO. 60601-1:14 (R2022) – Medical electrical equipment – Part 1: General requirements for basic safety and essential performance (Adopted IEC 60601-1:2005, third edition, 2005-12, including amendment 1:2012, with Canadian deviations) | Appareils électromédicaux – Partie 1: Exigences générales pour la sécurité de base et les performances essentielles (norme CEI 60601-1:2005 adoptée, troisième édition, 2005-12, y compris l’amendment 1:2012, avec exigences propres au Canada)

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1448

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CSA C22.2 NO. 60529:16 (R2026) – Degrees of protection provided by enclosures (IP Code) (Adopted IEC 60529:1989, edition 2:1989 consolidated with amendment 1:1999 and amendment 2:2013, with Canadian deviations) | Degrés de protection procurés par les enveloppes (Code IP) (norme IEC 60529:1989 adoptée , édition 2:1989 consolidée par l’amendement 1:1999 et l’amendement 2:2013, avec exigences propres au Canada)

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307

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CSA C22.2 NO. 60601-1-11:15 + A1:20 (CONSOLIDATED) (R2025) – 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 (Adopted IEC 60601-1-11:2015, edition 2:2015 consolidated with amendment 1:2020, with Canadian deviations) | Appareils électromédicaux – Partie 1-11 : Exigences générales pour la sécurité de base et les performances essentielles – Norme collatérale : Exigences pour les appareils électromédicaux et les systèmes électromédicaux utilisés dans l’environnement des soins à domicile (norme IEC 60601-1-11:2015 adoptée, édition 2:2015 consolidée par l’amendement 1:2020, avec exigences propres au Canada)

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748

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CSA C22.2 NO. 60598-2-18:25 – Luminaires — Part 2-18: Particular requirements — Luminaires for swimming pools and similar applications (Adopted IEC 60598-2-18:2022, third edition, 2022-08, with Canadian deviations) | Luminaires — Partie 2-18 : Exigences particulières — Luminaires pour piscines et usages analogues (norme IEC 60598-2-18:2022 adoptée, troisième édition, 2022-08, avec exigences propres au Canada)

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205

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CAN/CSA-C22.2 NO. 60601-1:14/A2:22 (R2022) – Amendment 2:2022 to CAN/CSA-C22.2 NO. 60601-1:14, Medical electrical equipment – Part 1: General requirements for basic safety and essential performance (Adopted amendment 2:2020 to IEC 60601-1:2005, with Canadian deviations) | Modification 2:2022 à CAN/CSA-C22.2 NO. 60601-1:14, Appareils électromédicaux – Partie 1: Exigences générales pour la sécurité de base et les performances essentielles (amendement 2:2020 adoptée à la norme CEI 60601-1:2005, avec exigences propres au Canada)

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608

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CSA C22.2 NO. 60601-1-10:09 (R2025) – Medical electrical equipment – Part 1-10: General requirements for basic safety and essential performance – Collateral Standard: Requirements for the development of physiologic closed-loop controllers (Adopted IEC 60601-1-10:2007, first edition, 2007-11) | Appareils électromédicaux – Partie 1-10: Exigences générales pour la sécurité de base et les performances essentielles – Norme collatérale: Exigences pour le développement des régulateurs physiologiques en boucle fermée (norme IEC 60601-1-10:2007 adoptée, première édition, 2007-11)

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331

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CSA C22.2 NO. 60601-1-10:09 + A1:14 (R2020) + A2:21 (CONSOLIDATED) – Medical electrical equipment — Part 1-10: General requirements for basic safety and essential performance — Collateral Standard: Requirements for the development of physiologic closed-loop controllers (Adopted IEC 60601-1-10:2007, edition 1:2007 consolidated with amendment 1:2013 and amendment 2:2020, with Canadian deviations) | Appareils électromédicaux — Partie 1-10 : Exigences générales pour la sécurité de base et les performances essentielles — Norme collatérale : Exigences pour le développement des régulateurs physiologiques en boucle fermée (norme IEC 60601-1-10:2007 adoptée, édition 1:2007 consolidée par l’amendement 1:2013 et l’amendement 2:2020, avec exigences propres au Canada)

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811

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CSA C22.2 No. 60601-1-10:09/A1:14 (R2025) – Amendment 1:2014 to CSA C22.2 NO. 60601-1-10:09, Medical electrical equipment – Part 1-10: General requirements for basic safety and essential performance – Collateral Standard: Requirements for the development of physiologic closed-loop controllers (Adopted amendment 1:2013 to IEC 60601-1-10:2007) | Modification 1:2014 à CSA C22.2 NO. 60601-1-10:09, Appareils électromédicaux – Partie 1-10: Exigences générales pour la sécurité de base et les performances essentielles – Norme collatérale: Exigences pour le développement des régulateurs physiologiques en boucle fermée (Amendement 1:2013 adoptée de la norme IEC 60601-1-10:2007)

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29

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CSA C22.2 NO. 60601-1-10B:09 – Amendment 2:2021 to CSA C22.2 NO. 60601-1-10:09, Medical electrical equipment – Part 1-10: General requirements for basic safety and essential performance – Collateral Standard: Requirements for the development of physiologic closed-loop controllers (Adopted amendment 2:2020 to IEC 60601-1-10:2007) | Modification 2:2021 à CSA C22.2 NO. 60601-1-10:09, Appareils électromédicaux – Partie 1-10: Exigences générales pour la sécurité de base et les performances essentielles – Norme collatérale: Exigences pour le développement des régulateurs physiologiques en boucle fermée (Amendement 2:2020 adoptée de la norme IEC 60601-1-10:2007)

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84

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ISO 5834:2019

ISO 5834:2019 Implants for surgery – Ultra-high-molecular-weight polyethylene – Part 3: Accelerated ageing methods

CDN $82.00

SKU: 573c42ccc07e Categories: ,

Description

This document specifies a test method for investigating the oxidative stability of ultra-high-molecular-weight polyethylene (UHMWPE) materials as a function of processing and sterilization method. This document describes a laboratory method for accelerated ageing of UHMWPE specimens and components for total joint prostheses. The UHMWPE is aged at elevated temperature and at elevated oxygen pressure, to accelerate oxidation of the material and thereby allow for the evaluation of its potential long-term chemical and mechanical stability.

Edition

2

Published Date

2019-02-12

Status

PUBLISHED

Pages

4

Language Detail Icon

English

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Abstract

This document specifies a test method for investigating the oxidative stability of ultra-high-molecular-weight polyethylene (UHMWPE) materials as a function of processing and sterilization method. This document describes a laboratory method for accelerated ageing of UHMWPE specimens and components for total joint prostheses. The UHMWPE is aged at elevated temperature and at elevated oxygen pressure, to accelerate oxidation of the material and thereby allow for the evaluation of its potential long-term chemical and mechanical stability.

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