发布时间:2024-05-27 17:49:26 - 更新时间:2024年06月29日 15:22
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Electrical equipment for measurement, control and laboratory use. EMC requirements. Particular requirements. In vitro diagnostic (IVD) medical equipment
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
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
Electrical equipment for measurement, control and laboratory use -- EMC requirements -- Part 2-6: Particular requirements -- In vitro diagnostic (IVD) medical equipment
Electrical equipment for measurement, control and laboratory use -- EMC requirements -- Part 2-6: Particular requirements -- In vitro diagnostic (IVD) medical equipment
In addition to the scope of International Standard IEC 61326-1, this part specifies minimum requirements for immunity and emissions regarding
Electrical equipment for measurement, control and laboratory use - EMC requirements - Particular requirements - In vitro diagnostic (IVD) medical equipment
This standard is about Electrical equipment for measurement, control and laboratory use, control and laboratory use - EMC requirements - Part 2-6
Electrical equipment for measurement, control and laboratory use, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In-vitro diagnostic (IVD) medical equipment; Corrigendum 1
本标准适用于大型医疗设备或系统的电磁兼容性现场测试。 注1:测试过程中有可能使被测设备造成损坏或其他装置受到不适当的影响,检测人员应向用户和制造商提示相关风险,经双方同意后再进行测试。 注2:其现场环境条件下得到的评估结果只对各个独立的大型医疗设备或系统在其特定安装场所的实际测量有效
Electromagnetic compatibility(EMC)-Determination of limits for industrial, scientific and medical equipment
Medical electrical equipment. Part 2. Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
Medical electrical equipment - Part 2-33 : particular requirements for the safety of magnetic resonance equipment for medical diagnosis.
Electromagnetic compatibility(EMC)-Determination of limits for industrial, scientific and medical equipment
本专用标准适用于由2.2.101定义的磁共振设备和由2.2.102定义的磁共振系统。 本标准不涵盖磁共振设备预期用途之外的应用
Medical Electrical Equipment.Part 2-33:Particular Requirements for the Safety of Magnetic Reconance Equipment for Medical Diagnosis
本标准适用于2.2.101定义的磁共振设备。 本标准不包括用于医学研究的磁共振设备
Medical electrical equipment.Part 2:Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
本标准规定了一般船舶(包括海洋平台)和特种船舶(如调查船、海洋考察船、试验船等)安装的电气和电子设备以及船舶总体电磁兼容的要求。 本标准适用于导线间电压不大于500V(直流或交流)或导线与地之间电压不大于250V(直流)或220V(交流有效值)的电气和电子设备。不适用于频率超过
Electromagnetic compatibility of electrical and electronic installations in ships
Electrical equipment for measurement, control and laboratory use. EMC requirements. Particular requirements. In vitro diagnostic (IVD) medical equipment
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
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
Electrical equipment for measurement, control and laboratory use -- EMC requirements -- Part 2-6: Particular requirements -- In vitro diagnostic (IVD) medical equipment
Electrical equipment for measurement, control and laboratory use -- EMC requirements -- Part 2-6: Particular requirements -- In vitro diagnostic (IVD) medical equipment
In addition to the scope of International Standard IEC 61326-1, this part specifies minimum requirements for immunity and emissions regarding
Electrical equipment for measurement, control and laboratory use - EMC requirements - Particular requirements - In vitro diagnostic (IVD) medical equipment
This standard is about Electrical equipment for measurement, control and laboratory use, control and laboratory use - EMC requirements - Part 2-6
Electrical equipment for measurement, control and laboratory use, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In-vitro diagnostic (IVD) medical equipment; Corrigendum 1
本标准适用于大型医疗设备或系统的电磁兼容性现场测试。 注1:测试过程中有可能使被测设备造成损坏或其他装置受到不适当的影响,检测人员应向用户和制造商提示相关风险,经双方同意后再进行测试。 注2:其现场环境条件下得到的评估结果只对各个独立的大型医疗设备或系统在其特定安装场所的实际测量有效
Electromagnetic compatibility(EMC)-Determination of limits for industrial, scientific and medical equipment
Medical electrical equipment. Part 2. Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
Medical electrical equipment - Part 2-33 : particular requirements for the safety of magnetic resonance equipment for medical diagnosis.
Electromagnetic compatibility(EMC)-Determination of limits for industrial, scientific and medical equipment
本专用标准适用于由2.2.101定义的磁共振设备和由2.2.102定义的磁共振系统。 本标准不涵盖磁共振设备预期用途之外的应用
Medical Electrical Equipment.Part 2-33:Particular Requirements for the Safety of Magnetic Reconance Equipment for Medical Diagnosis
本标准适用于2.2.101定义的磁共振设备。 本标准不包括用于医学研究的磁共振设备
Medical electrical equipment.Part 2:Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
本标准规定了一般船舶(包括海洋平台)和特种船舶(如调查船、海洋考察船、试验船等)安装的电气和电子设备以及船舶总体电磁兼容的要求。 本标准适用于导线间电压不大于500V(直流或交流)或导线与地之间电压不大于250V(直流)或220V(交流有效值)的电气和电子设备。不适用于频率超过
Electromagnetic compatibility of electrical and electronic installations in ships