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医疗器械检验

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IEC60601-1-2:2014+AMD1:2020CSV 医用电气设备.第1-2部分:基本安全和基本性能的一般要求.并列标准:电磁干扰.要求和试验Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests

IEC60601-1-2:2014/AMD1:2020 修改件1.医用电气设备.第1-2部分:基本安全和基本性能的一般要求.附带标准:电磁干扰.要求和试验Amendment 1 - Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests

IEC60601-1-2:2014 医用电气设备第1-2部分:安全通用要求并列标准:电磁兼容要求和试验 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests

IEC60601-1-2:2007 医用电气设备第1-2部分:基本安全和基本性能的通用要求并列标准:电磁兼容要求和试验 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests

IEC60601-1-2:2001/AMD1:2004 医用电气设备第1-2部分:基本安全和基本性能的通用要求并列标准:电磁兼容要求和试验 Medical electrical equipment - Part 1-2: General requirements for safety - Collateral standard: Electromagnetic compatibility - Requirements and tests

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IEC60601-1-2:2001 医用电气设备.第1-2部分:安全的一般要求.并列标准:电磁兼容性.要求和试验Medical electrical equipment - Part 1-2: General requirements for safety - Collateral standard: Electromagnetic compatibility - Requirements and tests

IEC60601-1-12:2014+Amd1:2020 医用电气设备第1-12部分:基本安全和基本性能的通用要求并列标准:预期在紧急医疗服务环境中使用的医用电气设备和医用电气系统的要求 Medical electrical equipment-Part 1-12:General requirements for basic safety and essential performance-Collateral Standard:Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment

IEC60601-1-12:2014 医用电气设备.第1-12部分:基本安全和基本性能的一般要求.附带标准:用于紧急医疗服务环境的医用电气设备和医用电气系统的要求Medical electrical equipment - Part 1-12: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment

IEC60601-1-11:2015+Amd1:2020 医用电气设备第1-11部分:基本安全和基本性能的通用要求并列标准:在家庭护理环境中使用的医用电气设备和医用电气系统的要求 Medical electrical equipment- Part 1-11:General requirements for basic safety and essential performance-Collateral Standard:Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment

IEC60601-1-11:2015 医疗电气设备 - 第1-11部分:基本安全和基本性能的一般要求 - 附带标准:家庭医疗保健环境中使用的医疗电气设备和医疗电气系统的要求Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment

IEC60601-1-10:2007+AMD1:2013+AMD2:2020 医用电气设备第1-10部分:基本安全和基本性能的通用要求并列标准:生理闭环控制器开发要求Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers

IEC60601-1:2012 医用电气设备第1部分:基本安全和基本性能的通用要求 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

IEC60601-1:2005+AMD1:2012CSV 医用电气设备第1部分:基本安全和基本性能的一般要求Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

IEC60601-1:2005+AMD1:2012+AMD2:2020CSV 医用电气设备.第1部分:基本安全和基本性能的一般要求Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

IEC60601-1:2005+Amd1:2012+Amd2:2020 医用电气设备第1部分:基本安全和基��性能的通用要求 Medical electrical equipment - Part 1:General requirements for basic safety and essential performance

IEC60601-1:2005/AMD2:2020 修改件2.医用电气设备.第1部分:基本安全和基本性能的一般要求Amendment 2 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

IEC60601-1:2005/AMD1:2012 修改件1.医用电气设备.第1部分:基本安全和基本性能的一般要求Amendment 1 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

IEC60601-1:2005 医疗电气设备 - 第1部分:基本安全和基本性能的一般要求Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

IEC60118-9:2019 电声学助听器第9部分:骨传导助听器性能特性的测量方法Electroacoustics - Hearing aids - Part 9: Methods of measurement of the performance characteristics of bone conduction hearing aids

IEC60118-7:2005 电声 - 助听器 - 第7部分:用于生产供应和交货质量保证目的的助听器性能特性测量Electroacoustics - Hearing aids - Part 7: Measurement of the performance characteristics of hearing aids for production, supply and delivery quality assurance purposes

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IEC60118-13:2019 电声学助听器第13部分:针对移动数字无线设备的电磁抗扰度要求和测量方法Electroacoustics - Hearing aids - Part 13: Requirements and methods of measurement for electromagnetic immunity to mobile digital wireless devices

IEC60118-0:2022 电声学-助听器第0部分:助听器性能特性的测量Electroacoustics - Hearing aids - Part 0: Measurement of the performance characteristics of hearing aids

ISO9919:2005 医用电气设备.医用脉搏血氧仪设备基本安全和基本性能的特殊要求Medical electrical equipment - Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use

废止，仅限能力项目库范围内现行有效产品标准引用本标准及监督抽检时申请...

ISO9693:2019 牙科学.金属陶瓷和陶瓷系统的兼容性试验Dentistry - Compatibility testing for metal-ceramic and ceramic-ceramic systems

ISO9626:2016 制造医疗器械用不锈钢针管-要求和试验方法 Stainless steel needle tubing for the manufacture of medical devices - Requirements and test methods

ISO9394:2012 眼科光学接触镜和接触镜护理产品兔眼相容性研究试验 Ophthalmic optics - Contact lenses and contact lens care products - Determination of biocompatibility by ocular study with rabbit eyes

ISO8836:2019 吸入导管用于呼吸道Suction catheters for use in the respiratory tract

ISO8836:2014 吸入导管用于呼吸道Suction catheters for use in the respiratory tract

废止，仅限能力项目库范围内现行有效产品标准引用本标准及监督抽检时申请...

ISO8835-3:1997 吸入麻醉系统第3部分:麻醉气体清除系统传输和接收系统Inhalational anaesthesia systems - Part 3: Anaesthetic gas scavenging systems - Transfer and receiving systems

废止，仅限能力项目库范围内现行有效产品标准引用本标准及监督抽检时申请...

ISO8835-2:2007 吸入麻醉系统.第2部分:麻醉呼吸系统Inhalational anaesthesia systems - Part 2: Anaesthetic breathing systems

废止，仅限能力项目库范围内现行有效产品标准引用本标准及监督抽检时申请...

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