• CSA C22.2 No. 60601.2.12 : 2003

    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

    MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR THE SAFETY OF LUNG VENTILATORS - CRITICAL CARE VENTILATORS

    Available format(s):  Hardcopy, PDF

    Superseded date:  01-11-2012

    Language(s):  English

    Published date:  01-01-2003

    Publisher:  Canadian Standards Association

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    Table of Contents - (Show below) - (Hide below)

    Foreword
    Introduction
    Section One - General
    1 Scope And Object
    2 Terminology And Definitions
    3 General Requirements
    4 General Requirements For Tests
    5 Classification
    6 Identification, Marking And Documents
    7 Power Input
    Section Two - Environmental Conditions
    8 Basic Safety Requirements
    9 Removable Protective Means
    10 Environmental Conditions
    Section Three - Protection Against Electric Shock
                    Hazards
    13 General
    14 Requirements Related To Classification
    15 Limitation Of Voltage And/Or Energy
    16 Enclosures And Protective Covers
    17 Insulation And Protective Impedances
    18 Earthing And Potential Equalization
    19 Continuous Leakage Currents And Patient Auxiliary
       Currents
    20 Dielectric Strength
    Section Four - Protection Against Mechanical Hazards
    21 Mechanical Strength
    22 Moving Parts
    23 Surfaces, Corners And Edges
    24 Stability In Normal Use
    25 Expelled Parts
    26 Vibration And Noise
    27 Pneumatic And Hydraulic Power
    28 Suspended Masses
    Section Five - Protection Against Hazards From Unwanted
                   Or Excessive Radiation
    29 X-Radiation
    30 Alpha, Beta, Gamma, Neutron Radiation And Other
       Particle Radiation
    31 Microwave Radiation
    32 Light Radiation (Including Lasers)
    33 Infra-Red Radiation
    34 Ultra-Violet Radiation
    35 Acoustical Energy (Including Ultrasonic)
    36 Electromagnetic Compatibility
    Section Six - Protection Against Hazards Of Ignition
                  Of Flammable Anesthetic Mixtures
    37 Locations And Basic Requirements
    38 Marking, Accompanying Documents
    39 Common Requirements For Category Ap And Category Apg
       Equipment
    40 Requirements And Tests For Category Ap Equipment,
       Parts And Components Thereof
    41 Requirements And Tests For Category Apg Equipment,
       Parts And Components Thereof
    Section Seven - Protection Against Excessive Temperatures
                    And Other Safety Hazards
    42 Excessive Temperatures
    43 Fire Prevention
    44 Overflow, Spillage, Leakage, Humidity, Ingress Of
       Liquids, Cleaning, Sterilization And Disinfection
    45 Pressure Vessels And Parts Subject To Pressure
    46 Human Errors
    47 Electrostatic Charges
    48 Biocompatibility
    49 Interruption Of The Power Supply
    Section Eight - Accuracy Of Operating Data And
                    Protection Against Hazardous Output
    50 Accuracy Of Operating Data
    51 Protection Against Hazardous Output
    Section Nine - Abnormal Operation And Fault Conditions;
                   Environmental Tests
    52 Abnormal Operation And Fault Conditions
    53 Environmental Tests
    Section Ten - Constructional Requirements
    54 General
    55 Enclosures And Covers
    56 Components And General Assembly
    57 Mains Parts, Components And Layout
    58 Protective Earthing - Terminals And Connections
    59 Construction And Layout
    Appendix L - References - Publications mentioned in this
                 standard
    Annex AA (informative) - Rationale
    Annex BB (normative) - Legibility and visibility of visual
                             indications
    Annex CC (informative) - Intelligent alarm systems
    Bibliography
    Terminology - Index of defined terms

    Abstract - (Show below) - (Hide below)

    Specifies safety requirements for lung ventilators that incorporate electrical devices, where the equipment is designed for medical use.

    General Product Information - (Show below) - (Hide below)

    Document Type Standard
    Publisher Canadian Standards Association
    Status Superseded
    Superseded By

    Standards Referenced By This Book - (Show below) - (Hide below)

    CSA Z8185 : 2008 RESPIRATORY TRACT HUMIDIFIERS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR RESPIRATORY HUMIDIFICATION SYSTEMS
    CSA Z8185 : 2008(R2013) RESPIRATORY TRACT HUMIDIFIERS FOR MEDICAL USE - PARTICULAR REQUIREMENTS FOR RESPIRATORY HUMIDIFICATION SYSTEMS

    Standards Referencing This Book - (Show below) - (Hide below)

    EN 556:1994 + A1:1998 STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR TERMINALLY-STERILIZED MEDICAL DEVICES TO BE LABELLED "STERILE"
    EN 550 : 1994 STERILIZATION OF MEDICAL DEVICES - VALIDATION AND ROUTINE CONTROL OF ETHYLENE OXIDE STERILIZATION
    IEC 60416:1988 General principles for the formulation of graphical symbols
    ISO 10651-2:2004 Lung ventilators for medical use Particular requirements for basic safety and essential performance Part 2: Home care ventilators for ventilator-dependent patients
    NFPA 53 : 2016 MATERIALS, EQUIPMENT, AND SYSTEMS USED IN OXYGEN-ENRICHED ATMOSPHERES
    IEC 60601-1-2:2014 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
    EN 1041:2008+A1:2013 Information supplied by the manufacturer of medical devices
    ISO 10651-3:1997 Lung ventilators for medical use Part 3: Particular requirements for emergency and transport ventilators
    IEC 60601-2-13:2003+AMD1:2006 CSV Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems
    IEC TR 60878:2015 Graphical symbols for electrical equipment in medical practice
    EN 552:1994/A2:2000 STERILIZATION OF MEDICAL DEVICES - VALIDATION AND ROUTINE CONTROL OF STERILIZATION BY IRRADIATION
    ISO 11195:1995 Gas mixers for medical use Stand-alone gas mixers
    IEC 60601-1-1:2000 Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems
    ISO 594-1:1986 Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment Part 1: General requirements
    IEC 60601-1-4:1996+AMD1:1999 CSV Medical electrical equipment - Part 1-4: General requirements for safety - Collateral Standard: Programmable electrical medical systems
    EN 554 : 1994 STERILIZATION OF MEDICAL DEVICES - VALIDATION AND ROUTINE CONTROL OF STERILIZATION BY MOIST HEAT
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