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ISO/IEC TR 10000-1:1998
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Information technology Framework and taxonomy of International Standardized Profiles Part 1: General principles and documentation framework
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ISO 10241:1992
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International terminology standards Preparation and layout
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CSA C22.2 No. 25 : 1966
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ENCLOSURES FOR USE IN CLASS 2, DIVISION 1, GROUPS E, F, AND G HAZARDOUS LOCATIONS
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ISO 690:2010
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Information and documentation Guidelines for bibliographic references and citations to information resources
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ISO 11135:2014
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Sterilization of health-care products Ethylene oxide Requirements for the development, validation and routine control of a sterilization process for medical devices
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IEC 60601-1:2005+AMD1:2012 CSV
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Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
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CSA ISO 11137 : 1998
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STERILIZATION OF HEALTH CARE PRODUCTS - REQUIREMENTS FOR VALIDATION AND ROUTINE CONTROL - RADIATION STERILIZATION
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ISO 5356-1:2015
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Anaesthetic and respiratory equipment Conical connectors Part 1: Cones and sockets
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ISO 14937:2009
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Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
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CSA ISO 11134 : 0
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STERILIZATION OF HEALTH CARE PRODUCTS - REQUIREMENTS FOR VALIDATION AND ROUTINE CONTROL - INDUSTRIAL MOIST HEAT STERILIZATION
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CSA Z10651.3 : 0
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LUNG VENTILATORS FOR MEDICAL USE - PART 3: PARTICULAR REQUIREMENTS FOR EMERGENCY AND TRANSPORT VENTILATORS
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ISO 5356-2:2012
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Anaesthetic and respiratory equipment — Conical connectors — Part 2: Screw-threaded weight-bearing connectors
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ISO 32:1977
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Gas cylinders for medical use — Marking for identification of content
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ISO 5367:2014
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Anaesthetic and respiratory equipment — Breathing sets and connectors
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CSA ISO 11135 : 1998:R2003
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MEDICAL DEVICES - VALIDATION AND ROUTINE CONTROL OF ETHYLENE OXIDE STERILIZATION
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ISO 690-2:1997
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Information and documentation Bibliographic references Part 2: Electronic documents or parts thereof
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ISO 10297:2014
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Gas cylinders — Cylinder valves — Specification and type testing
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ISO 5359:2014
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Anaesthetic and respiratory equipment Low-pressure hose assemblies for use with medical gases
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ISO 10524-3:2005
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Pressure regulators for use with medical gases Part 3: Pressure regulators integrated with cylinder valves
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CSA Z180.1 : 2013
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COMPRESSED BREATHING AIR AND SYSTEMS
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CSA C22.2 No. 60529 : 2016
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DEGREES OF PROTECTION PROVIDED BY ENCLOSURES (IP CODE)
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ISO 23328-2:2002
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Breathing system filters for anaesthetic and respiratory use — Part 2: Non-filtration aspects
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IEC 60027-3:2002
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Letter symbols to be used in electrical technology - Part 3: Logarithmic and related quantities, and their units
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IEC 60529:1989+AMD1:1999+AMD2:2013 CSV
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Degrees of protection provided by enclosures (IP Code)
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ISO 11607:2003
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Packaging for terminally sterilized medical devices
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ISO 23328-1:2003
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Breathing system filters for anaesthetic and respiratory use — Part 1: Salt test method to assess filtration performance
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CSA Z5359 : 2016
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ANAESTHETIC AND RESPIRATORY EQUIPMENT - LOW-PRESSURE HOSE ASSEMBLIES FOR USE WITH MEDICAL GASES, MEDICAL VACUUM, MEDICAL SUPPORT GASES, AND ANAESTHETIC GAS SCAVENGING SYSTEMS
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IEC 60027-2:2005
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Letter symbols to be used in electrical technology - Part 2: Telecommunications and electronics
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ISO 9170-1:2017
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Terminal units for medical gas pipeline systems — Part 1: Terminal units for use with compressed medical gases and vacuum
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ISO 11134:1994
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Sterilization of health care products — Requirements for validation and routine control — Industrial moist heat sterilization
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IEC 60027-4:2006
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Letter symbols to be used in electrical technology - Part 4: Rotating electric machines
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ISO 14971:2007
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Medical devices Application of risk management to medical devices
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ISO 4135:2001
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Anaesthetic and respiratory equipment Vocabulary
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ISO 10524-1:2006
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Pressure regulators for use with medical gases Part 1: Pressure regulators and pressure regulators with flow-metering devices
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ISO 11137:1995
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Sterilization of health care products Requirements for validation and routine control Radiation sterilization
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CSA C22.2 No. 60601.1 : 2014
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MEDICAL ELECTRICAL EQUIPMENT - PART 1: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE
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EN 980:2008
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Symbols for use in the labelling of medical devices
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ISO 17664:2017
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Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices
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CAN/CSA-Z23328-2-03 (R2018)
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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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ISO 15223:2000
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Medical devices Symbols to be used with medical device labels, labelling and information to be supplied
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