EN 61689:2013

FOREWORD
INTRODUCTION
1 Scope
2 Normative references
3 Terms and definitions
4 List of symbols
5 Ultrasonic field specifications
6 Conditions of measurement and test equipment
  used
7 Type testing reference procedures and measurements
8 Routine measurement procedure
9 Sampling and uncertainty determination
Annex A (informative) - Guidance for performance
        and safety
Annex B (normative) - Raster scan measurement and
        analysis procedures
Annex C (normative) - Diametrical or line scan
        measurement and analysis procedures
Annex D (informative) - Rationale concerning the beam
        cross-sectional area definition
Annex E (informative) - Factor used to convert the
        beam cross-sectional area (A[BCS]) at the face
        of the treatment head to the effective
        radiating area (A[ER])
Annex F (informative) - Determining acoustic power
        through radiation force measurements
Annex G (informative) - Validity of low-power measurements
        of the beam cross-sectional area (A[BCS])
Annex H (informative) - Influence of hydrophone effective
        diameter
Annex I (informative) - Effective radiating area measurement
        using a radiation force balance and absorbing
        apertures
Annex J (informative) - Guidance on uncertainty determination
Bibliography
Annex ZA (normative) - Normative references to international
         publications with their corresponding European
         publications

IEC 61689:2013 is applicable to ultrasonic equipment designed for physiotherapy containing an ultrasonic transducer generating continuous or quasi-continuous wave ultrasound in the frequency range 0,5 MHz to 5 MHz. This standard only relates to ultrasonic physiotherapy equipment employing a single plane non-focusing circular transducer per treatment head, producing static beams perpendicular to the face of the treatment head. This standard specifies: - methods of measurement and characterization of the output of ultrasonic physiotherapy equipment based on reference testing methods; - characteristics to be specified by manufacturers of ultrasonic physiotherapy equipment based on reference testing methods; - guidelines for safety of the ultrasonic field generated by ultrasonic physiotherapy equipment; - methods of measurement and characterization of the output of ultrasonic physiotherapy equipment based on routine testing methods; - and acceptance criteria for aspects of the output of ultrasonic physiotherapy equipment based on routine testing methods. Therapeutic value and methods of use of ultrasonic physiotherapy equipment are not covered by the scope of this standard. This third edition cancels and replaces the second edition published in 2007. It constitutes a technical revision which includes the following significant technical changes with respect to the previous edition: - restriction introduced of 0,2 W/cm² effective intensity during hydrophone measurements for treatment heads with ka≤20, to limit the likelihood of cavitation; - change in the factor F_ac, to determine the effective radiating area, from 1,354 to 1,333; - and change to SI units for terms and definitions.