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BS EN 14784-1-2005 無損檢驗.用存儲熒光成像板的工業(yè)計算輻射攝影術(shù).系統(tǒng)分類

作者:百檢網(wǎng) 時間:2021-07-15

標準號:BS EN 14784-1-2005
中文標準名稱:無損檢驗.用存儲熒光成像板的工業(yè)計算輻射攝影術(shù).系統(tǒng)分類
英文標準名稱:Non-destructive testing - Industrial computed radiography with storage phosphor imaging plates - Classification of systems
標準類型:H26
發(fā)布日期:2005/9/30 12:00:00
實施日期:2005/9/30 12:00:00
中國標準分類號:H26
國際標準分類號:19.100
適用范圍:This European Standard specifies fundamental parameters of computed radiography systems with the aim of enabling satisfactory and repeatable results to be obtained economically. The techniques are based both on fundamental theory and test measurements. This document specifies the performance of computed radiography (CR) systems and the measurement of the corresponding parameters for the system scanner and storage phosphor imaging plate (IP). It describes the classification of these systems in combination with specified metal screens for industrial radiography. It is intended to ensure that the quality of images - as far as this is influenced by the scanner-IP system - is in conformity with the requirements of Part 2 of this document. The document relates to the requirements of film radiography defined in EN 584-1 and ISO 11699-1. This European Standard defines system tests at different levels. More complicated tests are described, which allow the determination of exact system parameters. They can be used to classify the systems of different suppliers and make them comparable for users. These tests are specified as manufacturer tests. Some of them require special tools, which are usually not available in user laboratories. Therefore, simpler user tests are also described, which are designed for a fast test of the quality of CR systems and long term stability. There are several factors affecting the quality of a CR image including geometrical un-sharpness, signal/noise ratio, scatter and contrast sensitivity. There are several additional factors (e.g. scanning parameters), which affect the accurate reading of images on exposed IPs using an optical scanner. The quality factors can be determined most accurately by the manufacturer tests as described in this document. Individual test targets, which are recommended for practical user tests, are described for quality assurance. These tests can be carried out either separately or by the use of the CR Phantom (Annex B). This CR Phantom incorporates many of the basic quality assessment methods and those associated with the correct functioning of a CR system, including the scanner, for reading exposed plates and in correctly erasing IPs for future use of each plate. The CR System classes in this document do not refer to any particular manufacturers Imaging Plates. A CR system class results from the use of a particular imaging plate together with the exposure conditions -particularly total exposure - the scanner type and the scanning parameters.

相關(guān)標準

《GB/T14233.2-2005》醫(yī)用輸液、輸血、注射器具檢驗方法第二部分:生物實驗方法 GB/T14233.2-2005
《GB/T 16886.1-2011》醫(yī)療器械生物學(xué)評價 第1部分 風(fēng)險管理過程中的評價與試驗 GB/T 16886.1-2011
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《GB/T14233.2-2005》醫(yī)用輸液、輸血、注射器具檢驗方法第二部分:生物實驗方法 GB/T14233.2-2005
《GB/T14233.2-2005》醫(yī)用輸液、輸血、注射器具檢驗方法第二部分:生物實驗方法 GB/T14233.2-2005
《GB/T 16886.1-2011》醫(yī)療器械生物學(xué)評價 第1部分 風(fēng)險管理過程中的評價與試驗 GB/T 16886.1-2011
《GB/T 16886.1-2011》醫(yī)療器械生物學(xué)評價 第1部分 風(fēng)險管理過程中的評價與試驗 GB/T 16886.1-2011
《GB/T14233.2-2005》醫(yī)用輸液、輸血、注射器具檢驗方法第二部分:生物實驗方法 GB/T14233.2-2005
《GB/T 16886.1-2011》醫(yī)療器械生物學(xué)評價 第1部分 風(fēng)險管理過程中的評價與試驗 GB/T 16886.1-2011
《GB/T14233.2-2005》醫(yī)用輸液、輸血、注射器具檢驗方法第二部分:生物實驗方法 GB/T14233.2-2005
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