RB/T 039-2020
检测实验室仪器设备计量溯源结果确认指南
Guidance for metrological traceability results confirmation of instruments and equipments in testing laboratory
2020-08-26
ASME B89.7.5-2006
Metrological Traceability of Dimensional Measurements to the SI Unit of Length (An ASME Technical Report)
尺寸测量到国际单位制长度的计量溯源性（ASME技术报告）
2006-07-17
CNAS GL013-2018
量值溯源要求在医学测量领域的实施指南
2018-03-01
KS P ISO 17511(2016 Confirm)
체외진단 의료기기－생물 유래 시료의 정량 측정－보정 및 대조물질에 부여된 값의 측정학적 소급성
体外诊断医疗器械生物样品数量的测量校准品和对照品数值的计量溯源性
2010-12-17
GB/T 21415-2008
体外诊断医疗器械 生物样品中量的测量 校准品和控制物质赋值的计量学溯源性
In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials
2008-01-22
CNAS GL18-2008
量值溯源要求尖医学测量领域的实施指南
2008-10-08
BS EN ISO 17511-2021
In vitro diagnostic medical devices. Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
体外诊断医疗设备 建立校准器、真实性控制材料和人体样本所分配值的计量可追溯性的要求
2021-06-07
BS ISO 21151-2020
In vitro diagnostic medical devices. Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samples
体外诊断医疗设备 建立校准器和人体样本值计量溯源性的国际协调协议要求
2020-05-27
GB/T 44672-2024
体外诊断医疗器械 建立校准品和人体样品赋值计量溯源性的国际一致化方案的要求
In vitro diagnostic medical devices—Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samples
2024-09-29
KS P ISO 21151
체외 진단 의료기기 — 교정 물질과 인체 시료에 부여된 값의 측정학적 소급성 수립을 위한 국제 조화 프로토콜에 대한 요구사항
体外诊断医疗器械——建立校准品和人体样品计量可追溯性的国际协调协议的要求
2023-12-28
KS P ISO 17511
체외 진단 의료기기 — 교정 물질, 진도 관리 물질 및 인체 시료에 부여된 값의 측정학적 소급성 수립에 관한 요구사항
体外诊断医疗器械.校准品、真实性控制材料和人体样本赋值的计量溯源性建立要求
2021-12-28
GOST R ISO 21151-2021
Медицинские изделия для диагностики in vitro. Требования к международным протоколам гармонизации установления метрологической прослеживаемости значений, приписываемых калибраторам и образцам биологического материала человека
体外诊断医疗器械 国际协调协议的要求 建立分配给校准器和人体样品的值的计量可追溯性
ISO 21151-2020
In vitro diagnostic medical devices — Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samples
体外诊断医疗设备 - 生物来源样本中的数量测量 - 旨在建立分配给产品（最终用户）校准器和患者的值的计量可追溯性的国际协调协议要求
样品
2020-05-25
ISO 17511-2020
In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
体外诊断医疗器械.校准品 真实性控制材料和人体样品值的计量溯源性要求
2020-04-24
UNE-EN ISO 17511-2004
In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials (ISO 17511:2003)
体外诊断医疗器械.生物样品中数量的测量.校准品和控制材料赋值的计量溯源性（ISO 17511-2003）
2004-04-07
KS P ISO 18153(2016 Confirm)
체외진단 의료기기－생물 유래 시료의 정량 측정－보정 및 대조물질에 부여된 효소 촉매 농도 값의 측정학적 소급성
体外诊断医疗器械生物样品量的测量校准品和对照品酶催化浓度值的计量溯源性
2010-12-17
DIN EN ISO 17511
In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials (ISO 17511:2003)
体外诊断医疗器械.生物样品中数量的测量.校准器和控制材料赋值的计量溯源性（ISO 17511-2003）；德文版EN ISO 17511:2003
2003-11-01
BS EN ISO 18153-2003
In vitro diagnostic medical devices. Measurement of quantities in biological samples. Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials
体外诊断医疗设备 生物样品中数量的测量 校准品和控制材料酶催化浓度值的计量溯源性
2003-08-19
YY/T 0638-2008
体外诊断医疗器械 生物样品中量的测量 校准品和控制物质中酶催化浓度赋值的计量学溯源性
In vitro diagnostic medical devices -Measurement of quantities in biological samples - Metrological traceability of assigned values for catalytic concentration of enzymes in calibrators and control materials
2008-04-25
KS P ISO 18153(2021 Confirm)
체외진단 의료기기－생물 유래 시료의 정량 측정－보정 및 대조물질에 부여된 효소 촉매 농도 값의 측정학적 소급성
体外诊断医疗器械——生物样品数量的测量——校准品和对照品酶催化浓度值的计量溯源性
2010-12-17