IEC 61674:1997

IEC 61674:1997

October 1997
International standard Cancelled

Medical electrical equipment - Dosimeters with ionization chambers and/or semi-conductor detectors as used in X-ray diagnostic imaging

Specifies the performance and some related constructional requirements of diagnostic dosimeters intended for the measurement of air Kerma, air Kerma length or air Kerma rate, in photon radiation fields used in radiography, including mammography, radioscopy and computed tomography (CT), for X-rays with generating potentials not greater than 150 kV.

Main informations

Collections

International IEC standards

Publication date

October 1997

Number of pages

69 p.

Reference

IEC 61674:1997

Print number

1 - 13/06/2005
Sumary
Medical electrical equipment - Dosimeters with ionization chambers and/or semi-conductor detectors as used in X-ray diagnostic imaging

Specifies the performance and some related constructional requirements of diagnostic dosimeters intended for the measurement of air Kerma, air Kerma length or air Kerma rate, in photon radiation fields used in radiography, including mammography, radioscopy and computed tomography (CT), for X-rays with generating potentials not greater than 150 kV.
Standard replaced by (1)
IEC 61674:2012
November 2012
International standard Cancelled
Medical electrical equipment - Dosimeters with ionization chambers and/or semiconductor detectors as used in X-ray diagnostic imaging

IEC 61674:2012 specifies the performance and some related constructional requirements of diagnostic dosimeters intended for the measurement of air kerma, air kerma length product or air kerma rate, in photon radiation fields used in radiography, including mammography, radioscopy and computed tomography, for X-radiation with generating potentials not greater than 150 kV. This International Standard is applicable to the performance of dosimeters with vented ionization chambers and/or semiconductor detectors as used in X-ray diagnostic imaging. The object of this standard is to establish requirements for a satisfactory level of performance for diagnostic dosimeters, and to standardize the methods for the determination of compliance with this level of performance. This standard is not concerned with the safety aspects of dosimeters. The diagnostic dosimeters covered by this standard are not intended for use in the patient environment and, therefore, the requirements for electrical safety applying to them are contained in IEC 61010-1. This second edition cancels and replaces the first edition and constitutes a technical revision.

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