IEC 62220-2-1:2023
Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 2-1: Determination of dual-energy subtraction efficiency - Detectors used for dual-energy radiographic imaging
IEC 62220-2-1:2023 describes the performance metrics associated with DUAL-ENERGY IMAGING capable DIGITAL X-RAY IMAGING DEVICES meant for medical applications and specifies the methods for their determination. These metrics can be used to analyse TISSUE-SUBTRACTED IMAGES and to evaluate dose performance, noise characteristics, and tissue-subtraction efficacy of DIGITAL X-RAY IMAGING DEVICES. The described methods indicate the procedures to obtain MULTI-SPECTRAL PRIMARY DATA and to compute their derived TISSUE-SUBTRACTED IMAGES.The intended users of this document are MANUFACTURERS and well-equipped test laboratories. This document is restricted to DIGITAL X-RAY IMAGING DEVICES that are used for single or multiple exposure dual-energy radiographic imaging based on, for example, CR systems, direct and indirect flat panel-detector based systems.This document excludes and is not applicable to:? DIGITAL X-RAY IMAGING DEVICES intended to be used in mammography or in dental RADIOGRAPHY;? slot scanning DIGITAL X-RAY IMAGING DEVICES;? COMPUTED TOMOGRAPHY or CONE-BEAM COMPUTED TOMOGRAPHY;? photon-energy discriminating devices such as photon counting X-RAY IMAGING DEVICES;? devices for dynamic imaging (where series of images are acquired, as in fluoroscopy or cardiac imaging).? DIGITAL X-RAY IMAGING DEVICES intended to be used with RADIOTHERAPY beams.
IEC 62220-2-1:2023 describes the performance metrics associated with DUAL-ENERGY IMAGING capable DIGITAL X-RAY IMAGING DEVICES meant for medical applications and specifies the methods for their determination. These metrics can be used to analyse TISSUE-SUBTRACTED IMAGES and to evaluate dose performance, noise characteristics, and tissue-subtraction efficacy of DIGITAL X-RAY IMAGING DEVICES. The described methods indicate the procedures to obtain MULTI-SPECTRAL PRIMARY DATA and to compute their derived TISSUE-SUBTRACTED IMAGES.
The intended users of this document are MANUFACTURERS and well-equipped test laboratories. This document is restricted to DIGITAL X-RAY IMAGING DEVICES that are used for single or multiple exposure dual-energy radiographic imaging based on, for example, CR systems, direct and indirect flat panel-detector based systems.
This document excludes and is not applicable to:
? DIGITAL X-RAY IMAGING DEVICES intended to be used in mammography or in dental RADIOGRAPHY;
? slot scanning DIGITAL X-RAY IMAGING DEVICES;
? COMPUTED TOMOGRAPHY or CONE-BEAM COMPUTED TOMOGRAPHY;
? photon-energy discriminating devices such as photon counting X-RAY IMAGING DEVICES;
? devices for dynamic imaging (where series of images are acquired, as in fluoroscopy or cardiac imaging).
? DIGITAL X-RAY IMAGING DEVICES intended to be used with RADIOTHERAPY beams.
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