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医用电气设备安全通用要求检测

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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工业诊断 动物实验 植物学检测 环境试验

BS EN 60601-1-6:2004 ..并列标准.可

This Collateral Standard specifies requirements for a PROCESS to analyse, design, verify and validate the USABILITY, as it relates to SAFETY

Medical electrical equipment - General requirements for safety - Collateral standard - Usability

AS/NZS 3200.1.4:1997 试验规格与批准--间接标准:可计的疗系统

Specifies requirements for the process by which a programmable electrical medical system is designed. This Standard is supplementary

Approval and test specification - Medical electrical equipment - General requirements for safety - Collateral Standard: Programmable electrical medical systems

GB 9706.1-2007 第1部分:

本标准适用于医用电气设备(见2.2.15的定义)的安全。虽然本标准主要涉及安全问题,但它也包括一些与安全有关的可靠运行的要求。本标准涉及的设备预期生理效应所导致的安全方面危险未被考虑。除非标准正文中明确指明外,标准中的附录内容不要求强制执行

Medical electrical equipment.Part 1:General requirements for safety

AS/NZS 3200.1.3:1996 试验规格与批准--间接标准:X光诊断的辐射防护

Specifies protective measures to be taken by manufacturers in the design and construction of equipment and its subassemblies. This Standard

Approval and test specification - Medical electrical equipment - General requirements for safety - Collateral Standard: Requirements for radiation protection in diagnostic X-ray equipment

SIS SS-EN 60 601-1-1991 .第1部分:

This Standard applies to the safety of MEDlCAL electrical equipment (as defined in Sub-clause2.2.15). Although this Standard is primarily concerned

Medical electrical equipment — Part 1: General requirements for safety

IEC 60601-1:1988 第1部分:

本标准适用于医用电气设备(见2.2.15的定义)的安全。 虽然本标准主要涉及安全问题, 但它也包括一些与安全有关的可靠运行的要求。 本标准涉及的设备预期生理效应所导致的安全方面危险未被考虑。 除非标准正文中明确指明外, 标准中的附录内容不要求强制执行。 本标准的目的是规定医用电气设备的安全

Medical electrical equipment; part 1: general requirements for safety

IEC 60601-1/AMD2:1995 第1部分: 修改2

Medical electrical equipment - Part 1: General requirements for safety; Amendment 2

IEC 60601-1/AMD1:1991 第1部分: 修改1

Medical electrical equipment; part 1: general requirements for safety; amendment 1

UL 2601-1-1994 . 第1部分:

Medical electrical equipment - Part 1: General requirements for safety

IEC 60601-1/AMD2/COR1:1995 .第1部分:.修改件2

Medical electrical equipment - Part 1: General requirements for safety; Amendment 2

GB 9706.15-2008 .第1-1部分:.并列标准:系统

本部分适用于医用电气系统(见2.201的定义)的安全。本部分规定了为保护患者、操作者及环境所必需提供的安全要求

Medical electrical equipment.Part 1:General requirements for safety.1.Collateral standard:Safety requirements for medical electrical systems

GB 9706.15-1999 第1部分; 1.并列标准: 系统

本标准适用于2.203条定义的医用电气系统的安全,标准规定了为保护患者、操作者和环境所必需的安全要求。 注:相信医用电气系统的组装者或改建者将采取必要措施以保证符合本标准

Medical electrical equipment Part 1: General requiements for safety 1.Collateral standard: Safety requirements for medical electrical systems

HD 395.1 S2/ A1-1993 修改件1 .第1部分:

AMD 1 Medical Electrical Equipment Part 1: General Requirements for Safety

YY/T 0708-2009 .第1-4部分:并列标准:可编程系统

本并列标准适用于带有可编程电子子系统(PESS)的医用电气设备和医用电气系统的安全要求

Medical electrical equipment.Part 1-4:General requirements for safety.Collateral standard:programmable electrical medical systems

DS/EN 60601-1-1:2005 第 1-1 部分: 并列标准:系统

This standard applies to the safety of medical electrical systems, as defined in 2.201. It describes the safety requirements necessary to provide

Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems

BS EN 60601-1-6:2004 ..并列标准.可

This Collateral Standard specifies requirements for a PROCESS to analyse, design, verify and validate the USABILITY, as it relates to SAFETY

Medical electrical equipment - General requirements for safety - Collateral standard - Usability

AS/NZS 3200.1.4:1997 试验规格与批准--间接标准:可计的疗系统

Specifies requirements for the process by which a programmable electrical medical system is designed. This Standard is supplementary

Approval and test specification - Medical electrical equipment - General requirements for safety - Collateral Standard: Programmable electrical medical systems

GB 9706.1-2007 第1部分:

本标准适用于医用电气设备(见2.2.15的定义)的安全。虽然本标准主要涉及安全问题,但它也包括一些与安全有关的可靠运行的要求。本标准涉及的设备预期生理效应所导致的安全方面危险未被考虑。除非标准正文中明确指明外,标准中的附录内容不要求强制执行

Medical electrical equipment.Part 1:General requirements for safety

AS/NZS 3200.1.3:1996 试验规格与批准--间接标准:X光诊断的辐射防护

Specifies protective measures to be taken by manufacturers in the design and construction of equipment and its subassemblies. This Standard

Approval and test specification - Medical electrical equipment - General requirements for safety - Collateral Standard: Requirements for radiation protection in diagnostic X-ray equipment

SIS SS-EN 60 601-1-1991 .第1部分:

This Standard applies to the safety of MEDlCAL electrical equipment (as defined in Sub-clause2.2.15). Although this Standard is primarily concerned

Medical electrical equipment — Part 1: General requirements for safety

IEC 60601-1:1988 第1部分:

本标准适用于医用电气设备(见2.2.15的定义)的安全。 虽然本标准主要涉及安全问题, 但它也包括一些与安全有关的可靠运行的要求。 本标准涉及的设备预期生理效应所导致的安全方面危险未被考虑。 除非标准正文中明确指明外, 标准中的附录内容不要求强制执行。 本标准的目的是规定医用电气设备的安全

Medical electrical equipment; part 1: general requirements for safety

IEC 60601-1/AMD2:1995 第1部分: 修改2

Medical electrical equipment - Part 1: General requirements for safety; Amendment 2

IEC 60601-1/AMD1:1991 第1部分: 修改1

Medical electrical equipment; part 1: general requirements for safety; amendment 1

UL 2601-1-1994 . 第1部分:

Medical electrical equipment - Part 1: General requirements for safety

IEC 60601-1/AMD2/COR1:1995 .第1部分:.修改件2

Medical electrical equipment - Part 1: General requirements for safety; Amendment 2

GB 9706.15-2008 .第1-1部分:.并列标准:系统

本部分适用于医用电气系统(见2.201的定义)的安全。本部分规定了为保护患者、操作者及环境所必需提供的安全要求

Medical electrical equipment.Part 1:General requirements for safety.1.Collateral standard:Safety requirements for medical electrical systems

GB 9706.15-1999 第1部分; 1.并列标准: 系统

本标准适用于2.203条定义的医用电气系统的安全,标准规定了为保护患者、操作者和环境所必需的安全要求。 注:相信医用电气系统的组装者或改建者将采取必要措施以保证符合本标准

Medical electrical equipment Part 1: General requiements for safety 1.Collateral standard: Safety requirements for medical electrical systems

HD 395.1 S2/ A1-1993 修改件1 .第1部分:

AMD 1 Medical Electrical Equipment Part 1: General Requirements for Safety

YY/T 0708-2009 .第1-4部分:并列标准:可编程系统

本并列标准适用于带有可编程电子子系统(PESS)的医用电气设备和医用电气系统的安全要求

Medical electrical equipment.Part 1-4:General requirements for safety.Collateral standard:programmable electrical medical systems

DS/EN 60601-1-1:2005 第 1-1 部分: 并列标准:系统

This standard applies to the safety of medical electrical systems, as defined in 2.201. It describes the safety requirements necessary to provide

Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems

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