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CAN/CSA-Z5200-17
Cellulose nanomaterials - Blank detail specification
Edition
2017-06-01
CAN/CSA-Z5359A AMD 1
Amendment 1:2019 to CAN/CSA-Z5359:16, Anaesthetic and respiratory equipment - Low-pressure hose assemblies for use with medical gases, medical vacuum, medical support gases, and anaesthetic gas scavenging systems
Edition
2019
CAN/CSA-Z9360-1-07
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
Edition
2007-03-01
CAN/CSA-Z9360-2-07
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
Edition
2007-03-01
CAN/CSA-Z10524-4-12
Pressure regulators for use with medical gases - Part 4: Low-pressure regulators
Edition
2012-10-01
CAN/CSA-Z10651-4-08
Lung Ventilators - Part 4: Particular Requirements for Operator-Powered Resuscitators
Edition
2008-02-01
CAN/CSA-Z10651-5-08
Lung Ventilators for Medical Use - Particular Requirements for Basic Safety and Essential Performance - Part 5: Gas-Powered Emergency Resuscitators
Edition
2008-02-01
CAN/CSA-Z11135
Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (Adopted ISO 11135:2014, second edition, 2014-07-15)
Edition
2015-11-01
CAN/CSA-Z11137-1-07
Sterilization of Health Care Products - Radiation - Part 1: Requirements for Development, Validation and Routine Control of a Sterilization Process for Medical Devices
Edition
2007-03-01
CAN/CSA-Z11137-1-07 AMD 2
Amendment 2:2022 to CAN/CSA-Z11137-1-07, Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (Adopted amendment 2:2018 to ISO 11137-1:2006)
Edition
2022
