YY 0648-2008 测量、控制和试验室用电气设备的安全要求.第2-101部分:体外诊断(IVD)医用设备的专用要求
除下述内容外，GB 4793.1中的该章适用。 替换： 本标准适用于预期用作体外诊断（IVD）医用目的，包括自测体外诊断医用目的的设备。 体外诊断医用设备，论单独或组合使用，是制造商预期用于体外样品检查，这些样品包括来自人体的血和组织样本，其单独或主要目的是为下面一个或几个方面提供信息
Safety requirments for electrical equipment for measurement,control and laboratory use.Part 2-101:Particular requirments for in vitro diagnostic(IVD）medical equipment
DIN EN 61326-2-6:2013 测量, 控制和实验室用电气设备. 电磁兼容性 (EMC) 要求. 第2-6部分:特殊要求. 体外诊断 (IVD) 医用设备 (IEC 61326-2-6-2012); 德文版本EN 61326-2-6-2013
Electrical equipment for measurement, control and laboratory use - EMC requirements.Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (IEC 61326-2-6:2012); German version EN 61326-2-6:2013
MEDDEV 2.14/3-2007 医疗设备指导方针.有关体外诊断设备的指导方针:使用说明书(IFU)和其他体外诊断(IVD)医疗设备信息的提供.适用于制造商和公告机构的指导方针.修订件1
GUIDELINES ON MEDICAL DEVICES IVD GUIDANCES: Supply of Instructions For Use (IFU) and other information for In-vitro Diagnostic (IVD) Medical Devices A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES
BS EN IEC 61326-2-6:2021 测量、控制和实验室用电气设备 EMC要求 特殊要求 体外诊断（IVD）医疗设备
Electrical equipment for measurement, control and laboratory use. EMC requirements. Particular requirements. In vitro diagnostic (IVD) medical equipment
BS EN ISO 23640:2015 跟踪更改 体外诊断医疗设备 体外诊断试剂稳定性评价
Tracked Changes. In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
BS EN IEC 61010-2-101:2022+A11:2022 测量、控制和实验室用电气设备的安全要求 体外诊断（IVD）医疗设备的安全要求
1 Scope and object This clause of Part 1 is applicable except as follows: 1.1.1 General Replacement
Safety requirements for electrical equipment for measurement, control, and laboratory use - Safety requirements for in vitro diagnostic (IVD) medical equipment
UNE-EN 61326-2-6:2013 测量、控制和实验室用电气设备 EMC 要求 第2-6部分：特殊要求 体外诊断(IVD)医疗设备
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (Endorsed by AENOR in June of 2013.)
DS/EN IEC 61326-2-6:2021 测量、控制和实验室用电气设备《EMC 要求》第 2-6 部分：特殊要求《体外诊断（IVD）医疗设备》
Electrical equipment for measurement, control and laboratory use – EMC requirements – Part 2-6: Particular requirements – In vitro diagnostic (IVD) medical equipment
NF C46-050-2-6*NF EN IEC 61326-2-6:2021 测量、控制和实验室用电气设备 EMC 要求 第 2-6 部分：特殊要求 体外诊断（IVD）医疗设备
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6 : particular requirements - In vitro diagnostic (IVD) medical equipment
EN IEC 61326-2-6:2021 测量、控制和实验室用电气设备 EMC 要求 第 2-6 部分：特殊要求 体外诊断（IVD）医疗设备
IEC 61326-2-6:2020 is available as IEC 61326-2-6:2020 RLV which contains the International Standard and its Redline version, showing all changes
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
JIS C 61326-2-6:2023 测量、控制和实验室用电气设备 EMC 要求 第 2-6 部分：特殊要求 体外诊断 (IVD) 医疗设备
Electrical equipment for measurement, control and laboratory use -- EMC requirements -- Part 2-6: Particular requirements -- In vitro diagnostic (IVD) medical equipment
GB/T 18268.26-2010 测量、控制和实验室用的电设备 电磁兼容性要求 第26部分：特殊要求 体外诊断(IVD)医疗设备
GB/T 18268.1的范围适用于本部分。此外，GB/T 18268的本部分根据体外诊断(IVD)医疗设备的特性及其电磁环境，规定了其电磁兼容性的抗扰度和发射的基本要求
Electrical equipment for measurement,control and laboratory use.EMC requirements.Part 26:Particular requirements.In vitro diagnostic(IVD) medical equipment
IEC 61326-2-6:2020 电气设备用于测量 控制和实验室使用 - Emc要求 - 第2-6部分:特殊要求 - 体外诊断（ivd）医疗设备
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
BS EN 61326-2-6:2013 测量、控制和实验室用电气设备.电磁兼容性(EMC)的要求.详细要求.体外诊断(IVD)医疗设备
Electrical equipment for measurement, control and laboratory use. EMC requirements. Particular requirements. In vitro diagnostic (IVD) medical equipment
NF C46-050-2-6*NF EN 61326-2-6:2013 测量, 控制和实验室使用电气设备. EMC要求. 第2-6部分: 详细要求. 体外诊断(IVD)医疗设备
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6 : particular requirements - In vitro diagnostic (IVD) medical equipment
YY 0648-2008 测量、控制和试验室用电气设备的安全要求.第2-101部分:体外诊断(IVD)医用设备的专用要求
除下述内容外，GB 4793.1中的该章适用。 替换： 本标准适用于预期用作体外诊断（IVD）医用目的，包括自测体外诊断医用目的的设备。 体外诊断医用设备，论单独或组合使用，是制造商预期用于体外样品检查，这些样品包括来自人体的血和组织样本，其单独或主要目的是为下面一个或几个方面提供信息
Safety requirments for electrical equipment for measurement,control and laboratory use.Part 2-101:Particular requirments for in vitro diagnostic(IVD）medical equipment
DIN EN 61326-2-6:2013 测量, 控制和实验室用电气设备. 电磁兼容性 (EMC) 要求. 第2-6部分:特殊要求. 体外诊断 (IVD) 医用设备 (IEC 61326-2-6-2012); 德文版本EN 61326-2-6-2013
Electrical equipment for measurement, control and laboratory use - EMC requirements.Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (IEC 61326-2-6:2012); German version EN 61326-2-6:2013
MEDDEV 2.14/3-2007 医疗设备指导方针.有关体外诊断设备的指导方针:使用说明书(IFU)和其他体外诊断(IVD)医疗设备信息的提供.适用于制造商和公告机构的指导方针.修订件1
GUIDELINES ON MEDICAL DEVICES IVD GUIDANCES: Supply of Instructions For Use (IFU) and other information for In-vitro Diagnostic (IVD) Medical Devices A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES
BS EN IEC 61326-2-6:2021 测量、控制和实验室用电气设备 EMC要求 特殊要求 体外诊断（IVD）医疗设备
Electrical equipment for measurement, control and laboratory use. EMC requirements. Particular requirements. In vitro diagnostic (IVD) medical equipment
BS EN ISO 23640:2015 跟踪更改 体外诊断医疗设备 体外诊断试剂稳定性评价
Tracked Changes. In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
BS EN IEC 61010-2-101:2022+A11:2022 测量、控制和实验室用电气设备的安全要求 体外诊断（IVD）医疗设备的安全要求
1 Scope and object This clause of Part 1 is applicable except as follows: 1.1.1 General Replacement
Safety requirements for electrical equipment for measurement, control, and laboratory use - Safety requirements for in vitro diagnostic (IVD) medical equipment
UNE-EN 61326-2-6:2013 测量、控制和实验室用电气设备 EMC 要求 第2-6部分：特殊要求 体外诊断(IVD)医疗设备
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (Endorsed by AENOR in June of 2013.)
DS/EN IEC 61326-2-6:2021 测量、控制和实验室用电气设备《EMC 要求》第 2-6 部分：特殊要求《体外诊断（IVD）医疗设备》
Electrical equipment for measurement, control and laboratory use – EMC requirements – Part 2-6: Particular requirements – In vitro diagnostic (IVD) medical equipment
NF C46-050-2-6*NF EN IEC 61326-2-6:2021 测量、控制和实验室用电气设备 EMC 要求 第 2-6 部分：特殊要求 体外诊断（IVD）医疗设备
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6 : particular requirements - In vitro diagnostic (IVD) medical equipment
EN IEC 61326-2-6:2021 测量、控制和实验室用电气设备 EMC 要求 第 2-6 部分：特殊要求 体外诊断（IVD）医疗设备
IEC 61326-2-6:2020 is available as IEC 61326-2-6:2020 RLV which contains the International Standard and its Redline version, showing all changes
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
JIS C 61326-2-6:2023 测量、控制和实验室用电气设备 EMC 要求 第 2-6 部分：特殊要求 体外诊断 (IVD) 医疗设备
Electrical equipment for measurement, control and laboratory use -- EMC requirements -- Part 2-6: Particular requirements -- In vitro diagnostic (IVD) medical equipment
GB/T 18268.26-2010 测量、控制和实验室用的电设备 电磁兼容性要求 第26部分：特殊要求 体外诊断(IVD)医疗设备
GB/T 18268.1的范围适用于本部分。此外，GB/T 18268的本部分根据体外诊断(IVD)医疗设备的特性及其电磁环境，规定了其电磁兼容性的抗扰度和发射的基本要求
Electrical equipment for measurement,control and laboratory use.EMC requirements.Part 26:Particular requirements.In vitro diagnostic(IVD) medical equipment
IEC 61326-2-6:2020 电气设备用于测量 控制和实验室使用 - Emc要求 - 第2-6部分:特殊要求 - 体外诊断（ivd）医疗设备
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
BS EN 61326-2-6:2013 测量、控制和实验室用电气设备.电磁兼容性(EMC)的要求.详细要求.体外诊断(IVD)医疗设备
Electrical equipment for measurement, control and laboratory use. EMC requirements. Particular requirements. In vitro diagnostic (IVD) medical equipment
NF C46-050-2-6*NF EN 61326-2-6:2013 测量, 控制和实验室使用电气设备. EMC要求. 第2-6部分: 详细要求. 体外诊断(IVD)医疗设备
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6 : particular requirements - In vitro diagnostic (IVD) medical equipment
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