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作 者:曹碧红[1] 王春晖[1] CAO Bihong;WANG Chunhui(Inspection Center of Huizhou Municipal Central Hospital,Huizhou 516001,China)
机构地区:[1]惠州市中心人民医院检验中心,广东惠州516001
出 处:《标记免疫分析与临床》2022年第4期715-718,共4页Labeled Immunoassays and Clinical Medicine
摘 要:目的对IQ200 Sprint全自动尿液有形成分分析仪进行性能验证分析,评价其性能是否达到质量标准要求。方法在实验室符合ISO 15189实验室管理要求下,从精密度、携带污染率、线性范围、可报告范围、正确度等5个方面分析验证IQ200 Sprint全自动尿液有形成分分析仪的性能。结果IQ200 Sprint全自动尿液有形成分分析仪的精密度、携带污染率、线性范围、可报告范围、正确度验证所得结果均符合厂家及实验室要求。结论IQ 200 Sprint全自动尿液有形成分分析仪性能良好,达到质量标准要求,可用于临床标本检测。Objective To verify the performance of IQ200 Sprint automatic urine formed component analyzer,and to evaluate whether its performance meets the requirements of quality standards.Methods According to ISO 15189 laboratory management requirements,the performance of IQ200 Sprint automatic urine formed component analyzer was evaluated based on five parameters:precision,carryover rate,linear range,reportable range and accuracy verification.Results The results of precision,carryover rate,linear range,reportable range and accuracy verification of IQ200 Sprint were all met the requirements of manufacturers and laboratories.Conclusion IQ200 Sprint automatic urine formed component analyzer shows a good performance and meets the quality standard,which can be used for clinical specimen detections.
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