体外诊断（IVD）医用设备的专用要求检测

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

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 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

BS EN 61010-2-101:2017 测量、控制和实验室使用的电气设备的安全要求 体外诊断（IVD）医疗设备的特殊要求

Safety requirements for electrical equipment for measurement, control and laboratory use. Particular requirements for in vitro diagnostic (IVD) medical equipment

ONORM EN 375-1993 体外诊断系统．专业用体外诊断剂的标签要求

Diese Norm führt Anforderungen an die Kennzeichnung und Produktinformationen von In-vitro-Diagnostica für den Gebrauch durch Fachpersonal auf

In vitro diagnostic Systems - Requirements for labelling of in vitro diagnostic reagents for professional use

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.)

NF S92-016:1995 体外诊断系统.专用体外诊断仪器使用说明的要求

IN VITRO DIAGNOSTIC SYSTEMS. REQUIRMENTS FOR USER MANUELS FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR PROFESSIONAL USE. (EUROPEAN STANDARD EN 591).

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

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

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

UNE-EN 61010-2-101:2018 测量、控制和实验室用电气设备的安全要求 第2-101部分：体外诊断(IVD)医疗设备的特殊要求

Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for 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

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

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 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

BS EN 61010-2-101:2017 测量、控制和实验室使用的电气设备的安全要求 体外诊断（IVD）医疗设备的特殊要求

Safety requirements for electrical equipment for measurement, control and laboratory use. Particular requirements for in vitro diagnostic (IVD) medical equipment

ONORM EN 375-1993 体外诊断系统．专业用体外诊断剂的标签要求

Diese Norm führt Anforderungen an die Kennzeichnung und Produktinformationen von In-vitro-Diagnostica für den Gebrauch durch Fachpersonal auf

In vitro diagnostic Systems - Requirements for labelling of in vitro diagnostic reagents for professional use

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.)

NF S92-016:1995 体外诊断系统.专用体外诊断仪器使用说明的要求

IN VITRO DIAGNOSTIC SYSTEMS. REQUIRMENTS FOR USER MANUELS FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR PROFESSIONAL USE. (EUROPEAN STANDARD EN 591).

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

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

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

UNE-EN 61010-2-101:2018 测量、控制和实验室用电气设备的安全要求 第2-101部分：体外诊断(IVD)医疗设备的特殊要求

Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for 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