IEC 60580 Ed. 3.0 b:2019

Current Revision
Medical electrical equipment - Dose area product meters

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Medical electrical equipment - Dose area product meters

PUBLISH DATE 2019
PAGES 74

Medical electrical equipment - Dose area product meters

IEC 60580:2019 is available as IEC 60580:2019 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.

IEC 60580:2019 specifies the performance and testing of Dose Area Product Meters intended to measure Dose Area Product and/or Dose Area Product Rate to which the Patient is exposed during Medical Radiological Examinations.

This document is applicable to the following types of Dose Area Product Meters:

  • a) Field-Class Dose Area Product Meters normally used for the measurement of Dose Area Products during Medical Radiological Examinations;
  • b) Reference-Class Dose Area Product Meters normally used for the Calibration of Field-Class Dosimeters.

NOTE: Reference-Class Dose Area Product Meters can be used as Field-Class Dose Area Product Meters.

The object of this document is

  • 1) to establish requirements for a satisfactory level of performance for Dose Area Product Meters, and
  • 2) to standardize the methods for the determination of compliance with this level of performance.

Two levels of performance are specified:

  • – a lower level of performance applying to Field-Class Dose Area Product Meters;
  • – a higher level of performance applying to Reference-Class Dose Area Product Meters.

IEC 60580:2019 cancels and replaces the second edition published 2000, and constitutes a technical revision.

This edition includes the following significant technical changes with respect to the previous edition:

  • a) a second class of devices is introduced with tighter uncertainty tolerances;
  • b) this document has been expanded to include detectors other than ionization chambers;
  • c) radiation qualities have been updated to the new definitions according to IEC 61267;
  • d) a requirement on the linearity of the dose area product rate measurement was added;
  • e) changed chamber light transmission requirement from 70 % to 60 %.
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