| ISO |
ISO 9360-2 |
Anaesthetic and respiratory equipment -- Heat and moisture exchangers (HMEs) for humidifying respired gases in humans -- Part 2: HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml |
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| ISO |
ISO 9360-1 |
Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 1: HMEs for use with minimum tidal volumes of 250 ml |
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| BSI |
BS EN ISO 9360-2 |
Anaesthetic and respiratory equipment. Heat and moisture exchangers (HMEs) for humidifying respired gases in humans. HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml |
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| BSI |
BS EN ISO 9360-1 |
Anaesthetic and respiratory equipment. Heat and moisture exchangers (HMEs) for humidifying respired gases in humans. HMEs for use with minimal tidal volumes of 250 ml |
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| CSA |
CSA Z9360-1:07 (R2022) |
Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 1: HMEs for use with minimum tidal volumes of 250 ml (Adopted ISO 9360-1:2000, first edition, 2000-03-15, with Canadian deviations) |
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| CSA |
CSA C22.2 NO. 60601-2-68:15 (R2020) |
Medical electrical equipment — Part 2-68: Particular requirements for the basic safety and essential performance of X-ray-based image-guided radiotherapy equipment for use with electron accelerators, light ion beam therapy equipment and radionuclide beam therapy equipment (Adopted IEC 60601-2-68:2014, first edition, 2014-09, with Canadian deviations) | Appareils électromédicaux — Partie 2-68 : Exigences particulières pour la sécurité de base et les performances essentielles des appareils de radiothérapie à rayonnement X assistée par imagerie médicale, destinés à être utilisés avec les accélérateurs d’électrons, les appareils de thérapie par faisceau d’ions légers et les appareils de thérapie par faisceau de radionucléides (norme IEC 60601-2-68:2014 adoptée, première édition, 2014-09, avec exigences propres au Canada) |
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| CSA |
CAN/CSA-Z23328-2-03 (R2023) |
Breathing system filters for anaesthetic and respiratory use - Part 2: Non-filtration aspects (Adopted ISO 23328-2:2002, first edition, 2002-10-15) |
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| CSA |
C22.2 NO. 80601-2-74 |
Medical electrical equipment - Part 2-74: Particular requirements for basic safety and essential performance of respiratory humidifying equipment (Adopted ISO 80601-2-74:2021, second edition, 2021-07, with Canadian deviations) |
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| CSA |
CAN/CSA-ISO 5356-2:F18 (C2023) |
Anaesthetic and respiratory equipment — Conical connectors — Part 2: Screw-threaded weight-bearing connectors (Adopted ISO 5356-2:2012, third edition, 2012-11-15) |
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| CSA |
CSA Z5359:F16 (C2020) |
Anaesthetic and respiratory equipment — Low-pressure hose assemblies for use with medical gases, medical vacuum, medical support gases, and anaesthetic gas scavenging systems (Adopted ISO 5359:2014, fourth edition, 2014-10-01, with Canadian deviations) |
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| CSA |
CSA C22.2 NO. 60601-2-64:15 (R2020) |
Medical electrical equipment — Part 2-64: Particular requirements for the basic safety and essential performance of light ion beam medical electrical equipment (Adopted IEC 60601-2-64:2014, first edition, 2014-09, with Canadian deviations) | Appareils électromédicaux — Partie 2-64 : Exigences particulières pour la sécurité de base et les performances essentielles des appareils électromédicaux par faisceau d'ions légers (norme IEC 60601-2-64:2014 adoptée, première édition, 2014-09, avec exigences propres au Canada) |
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| CSA |
CSA C22.2 NO. 60601-2-62:15 (R2020) |
Medical electrical equipment – Part 2-62: Particular requirements for the basic safety and essential performance of high intensity therapeutic ultrasound (HITU) equipment (Adopted IEC 60601-2-62:2013, first edition, 2013-07, with Canadian deviations) | Appareils électromédicaux — Partie 2-62 : Exigences particulières pour la sécurité de base et les performances essentielles des appareils ultrasonores thérapeutiques de haute intensité (HITU) (norme IEC 60601-2-62:2013 adoptée, première édition, 2013-07, avec exigences propres au Canada) |
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| CSA |
C22.2 NO. 80601-2-90 |
Medical electrical equipment - Part 2-90: Particular requirements for basic safety and essential performance of respiratory high-flow therapy equipment (Adopted ISO 80601-2-90:2021, first edition, 2021-08, with Canadian deviations) |
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| CSA |
CAN/CSA-ISO 5366:F18 (C2023) |
Anaesthetic and respiratory equipment — Tracheostomy tubes and connectors (Adopted ISO 5366:2016, first edition, 2016-10-01) |
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| CSA |
CSA C22.2 NO. 60601-2-65:15 (R2020) |
Medical electrical equipment – Part 2-65: Particular requirements for the basic safety and essential performance of dental intra-oral x-ray equipment (Adopted IEC 60601-2-65:2012, first edition, 2012-09, with Canadian deviations) | Appareils électromédicaux – Partie 2-65 : Exigences particulières pour la sécurité de base et les performances essentielles des appareils à rayonnement x dentaires intra-oraux (norme IEC 60601-2-65:2012 adoptée, première édition, 2012-09, avec exigences propres au Canada) |
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| CSA |
CSA C22.2 NO. 60601-2-63:15 (R2020) |
Medical electrical equipment — Part 2-63: Particular requirements for the basic safety and essential performance of dental extra-oral X-ray equipment (Adopted IEC 60601-2-63:2012, first edition, 2012-09, with Canadian deviations) | Appareils électromédicaux – Partie 2-63 : Exigences particulières pour la sécurité de base et les performances essentielles des appareils à rayonnement X dentaires extra-oraux( norme IEC 60601-2-63:2012 adoptée, première édition, 2012-09, avec exigences propres au Canada) |
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| CSA |
CSA ISO 10079-2:24 |
Medical suction equipment - Part 2: Manually powered suction equipment (Adopted ISO 10079-2:2022, fourth edition, 2022-03) |
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| CSA |
CAN/CSA-Z434-F14 (C2024) |
Industrial robots and robot systems (Adopted ISO 10218-1:2011, second edition, 2011-07-01, with Canadian deviations and ISO 10218-2:2011, first edition, 2011-07-01, with Canadian deviations) |
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| CSA |
CSA ISO 16628:F24 |
Anaesthetic and respiratory equipment — Tracheobronchial tubes (Adopted ISO 16628:2022, second edition, 2022-06) |
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| CSA |
CSA ISO 5364:F16 (C2021) |
Anaesthetic and respiratory equipment - Oropharyngeal airways (Adopted ISO 5364:2016, fifth edition, 2016-09-01) |
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| CSA |
C22.2 NO. 60601-2-68 |
Medical electrical equipment - Part 2-68: Particular requirements for the basic safety and essential performance of X-ray-based image-guided radiotherapy equipment for use with electron accelerators, light ion beam therapy equipment and radionuclide beam therapy equipment (Adopted IEC 60601-2-68:2014, first edition, 2014-09, with Canadian deviations) | Appareils électromédicaux - Partie 2-68 : Exigences particulières pour la sécurité de base et les performances essentielles des appareils de radiothérapie à rayonnement X assistée par imagerie médicale, destinés à être utilisés avec les accélérateurs d’électrons, les appareils de thérapie par faisceau d’ions légers et les appareils de thérapie par faisceau de radionucléides (norme IEC 60601-2-68:2014 adoptée, première édition, 2014-09, avec exigences propres au Canada) |
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| CSA |
CSA ISO 5356-1:15 (R2020) |
Anaesthetic and respiratory equipment — Conical connectors — Part 1: Cones and sockets (Adopted ISO 5356-1:2015, fourth edition, 2015-03-15) |
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| CSA |
CSA Z10524-4:12 (R2022) |
Pressure regulators for use with medical gases - Part 4: Low-pressure regulators (Adopted ISO 10524-4:2008, first edition, 2008-06-01, with Canadian deviations) |
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