• I.S. EN 794-2:1997

    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

    LUNG VENTILATORS - PARTICULAR REQUIREMENTS FOR HOME CARE USE

    Available format(s):  Hardcopy, PDF

    Superseded date:  18-08-2004

    Language(s):  English

    Published date:  01-01-1997

    Publisher:  National Standards Authority of Ireland

    For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
    Only cited Standards give presumption of conformance to New Approach Directives/Regulations.

    Dates of withdrawal of national standards are available from NSAI.

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

    Foreword
    Introduction
    Section one General
    1 Scope
    2 Normative references
    3 Terminology and definitions
    4 General requirements and general requirements for test
    5 Classification
    6 Identification, marking and documents
    7 Power input
    Section two Environment conditions
    8 Basic safety categories
    9 Removable protective means
    10 Environmental conditions
    11 Not used
    12 Not used
    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 Separation
    18 Protective earthing, functional 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 ultrasonics)
    36 Electromagnetic compatibility
    Section six Protection against hazards of ignition of
                flammable anaesthetic mixtures
    37 Locations and basic requirements
    38 Marking and accompanying documents
    39 Common requirements for Category AP and Category AGP
        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 temperature
                  and other safety hazards
    42 Excessive temperatures
    43 Fire prevention
    44 Overflow, spillage, leakage, humidity, ingress of
        liquids, cleaning, sterilization, disinfection and
        compatibility
    45 Pressure vessels and parts subject to pressure
    46 Not used
    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
    Annex AA (informative) Rationale
    Annex BB (normative) Legibility and visibility of visual
             indication
    Annex CC (informative) Typical ventilator arrangements
    Annex DD (informative) Special national conditions
    Annex EE (normative) Bibliography
    Annex ZA (informative) Clauses of this European Standard
             addressing essential requirements or other
             provisions of EU Directives

    Abstract - (Show below) - (Hide below)

    Defines requirements for lung ventilators intended largely for home care use for patients, but which can be used in hospital under certain conditions.

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

    Document Type Standard
    Publisher National Standards Authority of Ireland
    Status Superseded
    Superseded By

    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
    EN 738-1:1997/A1:2002 PRESSURE REGULATORS FOR USE WITH MEDICAL GASES - PRESSURE REGULATORS AND PRESSURE REGULATORS WITH FLOW METERING DEVICES
    EN 868-1 : 1997 PACKAGING MATERIALS AND SYSTEMS FOR MEDICAL DEVICES WHICH ARE TO BE STERILIZED - GENERAL REQUIREMENTS AND TEST METHODS
    EN 1281-2 : 1995 ANAESTHETIC AND RESPIRATORY EQUIPMENT - CONICAL CONNECTORS - SCREW-THREADED WEIGHT-BEARING CONNECTORS
    ISO 32:1977 Gas cylinders for medical use — Marking for identification of content
    EN 60601-1-2:2015 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
    EN 552:1994/A2:2000 STERILIZATION OF MEDICAL DEVICES - VALIDATION AND ROUTINE CONTROL OF STERILIZATION BY IRRADIATION
    NFPA 53M : 1990 FIRE HAZARDS IN OXYGEN-ENRICHED ATMOSPHERES
    ISO 9360:1992 Anaesthetic and respiratory equipment — Heat and moisture exchangers for use in humidifying respired gases in humans
    EN 1281-1:1997/A1:1998 ANAESTHETIC AND RESPIRATORY EQUIPMENT - CONICAL CONNECTORS - CONES AND SOCKETS
    ISO 7000:2014 Graphical symbols for use on equipment Registered symbols
    EN 980:2008 Symbols for use in the labelling of medical devices
    EN 554 : 1994 STERILIZATION OF MEDICAL DEVICES - VALIDATION AND ROUTINE CONTROL OF STERILIZATION BY MOIST HEAT
    EN 60801-2 : 1993 ELECTROMAGNETIC COMPATIBILITY FOR INDUSTRIAL-PROCESS MEASUREMENT AND CONTROL EQUIPMENT - PART 2: ELECTROSTATIC DISCHARGE REQUIREMENTS (IEC 801-2:1991)
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