• SN EN 61689 : 1996

    Current The latest, up-to-date edition.

    ULTRASONICS - PHYSIOTHERAPY SYSTEMS - PERFORMANCE REQUIREMENTS AND METHODS OF MEASUREMENT IN THE FREQUENCY RANGE 0,5 MHZ TO 5 MHZ

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    Published date:  12-01-2013

    Publisher:  Swiss Standards

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

    INTRODUCTION
    1 Scope
    2 Normative references
    3 Definitions
    4 List of symbols
    5 Requirements for safety and performance declaration
    6 Performance and safety requirements
        6.1 Rated output power
        6.2 Effective intensity
        6.3 Beam non-uniformity ratio
    7 Conditions of measurement and test equipment used
        7.1 Test vessel
        7.2 Hydrophone
        7.3 RMS or peak signal measurement
    8 Type testing reference procedures and measurements
        8.1 Rated output power
        8.2 Hydrophone measurements
        8.3 Effective radiating area
        8.4 Reference type testing parameters
        8.5 Acceptance criteria for reference type testing
    9 Routine measurement procedure
        9.1 Rated output power
        9.2 Beam cross-sectional area at zp
        9.3 Acceptance criteria for routine testing
    10 Sampling and uncertainty determination
        10.1 Reference type testing measurements
        10.2 Routine measurements
        10.3 Uncertainty determination
    Annexes
    A Raster scan measurement and analysis procedures
    B Diametrical or line scan measurement and analysis
        procedures
    C Rationale concerning the beam cross-sectional area
        definition
    D Factor used to convert the beam cross-sectional area
        (ABCS) at the face of the treatment head to the
        effective radiating area (AER)
    E Rationale behind using a limiting value for the beam
        non-uniformity ratio (RBN)
    F Rationale behind using a limiting value for the beam
        non-uniformity ratio (RBN)
    G Determining acoustic power through radiation force
        measurements
    H The validity of low-power measurements of the beam
        cross-sectional area (ABCS)
    J Influence of hydrophone effective diameter
    K Relationship between the effective radiating area (AER)
        and the effective radiating area determined using the
        FDA definition
    L Guidance on uncertainty determination
    M Bibliography
    ZA (normative) Normative references to international
       publications with their corresponding European
       publications

    Abstract - (Show below) - (Hide below)

    Applies to ultrasonic equipment designed for physiotherapy consisting of an ultrasonic transducer generating continuous or quasi-continuous wave ultrasonic energy in the frequency range 0,5 MHz to 5 MHz.

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    Document Type Standard
    Publisher Swiss Standards
    Status Current
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