• SN EN 60580 : 2000

    Current The latest, up-to-date edition.

    MEDICAL ELECTRICAL EQUIPMENT - DOSE AREA PRODUCT METERS

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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 and object
    2 Normative references
    3 Terminology and definitions
    4 General requirements
          4.1 Performance requirements
          4.2 Minimum EFFECTIVE RANGES of DOSE AREA PRODUCT
                 and DOSE AREA PRODUCT RATE
          4.3 Plane of measurement
          4.4 REFERENCE VALUES and STANDARD TEST CONDITIONS
          4.5 General test conditions
                 4.5.1 STANDARD TEST CONDITIONS
                 4.5.2 Test of components
                 4.5.3 STABILIZATION TIME
                 4.5.4 Adjustments during test
                 4.5.5 Uniformity of radiation field
          4.6 Statistical fluctuations
          4.7 Uncertainty of measurement
          4.8 Constructional requirements as related to
                 performance
                 4.8.1 Display
                 4.8.2 Indication of polarizing voltage
                          failure
                 4.8.3 Over-ranging
                 4.8.4 Indication of reset or other inactive
                          condition
                 4.8.5 IONIZATION CHAMBER
          4.9 STABILITY CHECK DEVICEth their corresponding
                 European publications
          4.10 Adjustment
          4.11 Electrical safety
    5 Limits of PERFORMANCE CHARACTERISTICS under STANDARD
          TEST CONDITIONS
          5.1 RELATIVE INTRINSIC ERROR
          5.2 Warning function
          5.3 Repeatability
          5.4 RESOLUTION of reading
          5.5 STABILIZATION TIME
          5.6 Reset on DOSE AREA PRODUCT ranges
          5.7 Drift of INDICATED VALUES
          5.8 Long term stability
          5.9 RESPONSE TIME
          5.10 Spatial uniformity of RESPONSE
    6 LIMITS OF VARIATION for effects of INFLUENCE QUANTITIES
          6.1 Energy dependence of RESPONSE
          6.2 DOSE AREA PRODUCT RATE dependence of DOSE AREA
                 PRODUCT measurements
                 6.2.1 MEASURING ASSEMBLY
                 6.2.2 IRONIZATION CHAMBER - Recombination
                          losses
          6.3 IRRADIATION TIME
          6.4 Field size
          6.5 Operating voltage
          6.6 Air pressure
          6.7 Temperature and humidity
          6.8 Air density fluctuation in the IONIZATION
                 CHAMBER
          6.9 Electromagnetic compatibility
                 6.9.1 General
                 6.9.2 Electrostatic discharge
                 6.9.3 Radiated electromagnetic fields
                 6.9.4 Conducted disturbances induced by
                          bursts and high frequencies
                 6.9.5 Surges
                 6.9.6 Voltage dips, short interruptions and
                          voltage VARIATIONS
          6.10 COMBINED STANDARD UNCERTAINTY
    7 Marking
          7.1 MEASURING ASSEMBLY
          7.2 IONIZATION CHAMBER
    8 ACCOMPANYING DOCUMENTS
    Table 1 - Minimum EFFECTIVE RANGES
    Table 2 - REFERENCE VALUES and STANDARD TEST CONDITIONS
    Table 3 - Number of readings required to detect true
              differences (95 percent confidence level) between
              two sets of instrument readings
    Table 4 - RELATIVE INTRINSIC ERROR, I
    Table 5 - Maximum values for the COEFFICIENT OF VARIATION,
              Vmax
    Table 6 - LIMITS OF VARIATION for the effects of INFLUENCE
              QUANTITIES
    Table 7 - Example for assessment of the COMBINED STANDARD
              UNCERTAINTY
    Bibliography
    Index of defined terms
    Annex ZA (normative) Normative references to international
                         publications with their corresponding
                         European publications

    Abstract - (Show below) - (Hide below)

    Defines performance and testing of DOSE AREA PRODUCT METERS with IONIZATION CHAMBERS for measurement of DOSE AREA PRODUCT and/or DOSE AREA PRODUCT RATE to which the PATIENT is exposed during MEDICAL RADIOLOGICAL EXAMINATIONS. Objectives are to: establish criteria for a satisfactory performance level for DOSE AREA PRODUCT METERS, and standardize the methods for determining compliance with this level of performance.

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    Document Type Standard
    Publisher Swiss Standards
    Status Current
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