YY 9706.284-2023
Active
Industry standards-Medicine
YY 9706.284-2023 Medical electrical equipment—Part 2-84:Particular requirements for the basic safety and essential performance of ventilators for the emergency medical services environment
YY 9706.284-2023 Medical electrical equipment—Part 2-84:Particular requirements for the basic safety and essential performance of ventilators for the emergency medical services environment
Basic Information
Standard Code:
YY 9706.284-2023
Standard Type:
Industry standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
Surgical room equipment
ICS Name:
-
Publish Date:
2023-03-14
Implement Date:
2026-05-01
Publisher:
国家药品监督管理局
Technical Committee:
全国麻醉和呼吸设备标准化技术委员会(SAC/TC 116)
Pages:
88 pages
Scope
GB 9706的本部分规定了ME设备和ME系统的基本安全和基本性能的通用要求。
本部分适用于医用电气设备和医用电气系统(以下简称ME设备和ME系统)。
如果一章或一条明确指出仅适用于ME设备或ME系统,标题和 章或条的正文会说明。如果不是这种情况,与此相关的章或条同时适用于ME设备和ME系统。
除7.2.13和8.4.1外,本部分范围内的ME设备或ME系统的预期生理效应所导致的危险(源)在本部分中没有具体要求。
本文件规定了与附件组合使用的紧急医疗服务环境用呼吸机(以下简称EMS呼吸机,也称为ME设备)的基本安全和基本性能。
本文件适用于预期在EMS环境中,由专业护理人员操作,给需要不同的人工通气支持水平的患者(包括依赖呼吸机患者)进行有创或无创通气的紧急医疗服务环境用呼吸机。
注1:EMS呼吸机也能用于专业医疗保健机构内的转运。
*除非EMS呼吸机使用患者生理变量调节通气治疗设置,否则不认为EMS呼吸机采用了生理闭环控制系统。
本文件也适用于制造商预期连接到呼吸机呼吸系统或EMS呼吸机的附件,这些附件的特性可能影响EMS呼吸机的基本安全或基本性能。
注2:如果一章或一条明确指出仅适用于ME设备或ME系统,章或条的标题和正文会说明。如果不是这种情况,与此相关的章或条同时适用于ME设备和ME系统。
注3:参见通用标准4.2。
本文件不适用于:
——重症护理呼吸机或附件;
——依赖呼吸机患者使用的家用呼吸机或附件;
——麻醉应用中的呼吸机或附件;
——通气支持设备的呼吸机或附件(预期仅用于增加自主呼吸患者的通气量);
——阻塞性睡眠呼吸暂停症治疗医用电气设备;
——人工复苏器;
——气动急救复苏器;
——持续气道正压(CPAP)医用电气设备
Development Information
Same series standard
YY 9706.230-2023 Medical electrical equipment—Part 2-30:Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers
YY 9706.231-2023 Medical electrical equipment—Part 2-31:Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source
YY 9706.246-2023 Medical electrical equipment—Part 2-46:Particular requirements for the basic safety and essential performance of operating tables
YY 9706.249-2023 Medical electrical equipment—Part 2-49:Particular requirements for the basic safety and essential performance of multifunction patient monitors
YY 9706.256-2023 Medical electrical equipment—Part 2-56:Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement
YY 9706.261-2023 Medical electrical equipment—Part 2-61:Particular requirements for the basic safety and essential performance of pulse oximeter equipment
YY 9706.277-2023 Medical electrical equipment—Part 2-77:Particular requirements for the basic safety and essential performance of robotically assisted surgical equipment
YY 9706.278-2023 Medical electrical equipment—Part 2-78:Particular requirements for basic safety and essential performance of medical robots for rehabilitation,assessment,compensation or alleviation
YY 9706.279-2023 Medical electrical equipment—Part 2-79:Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment
YY 9706.280-2023 Medical electrical equipment—Part 2-80:Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency
Replace the following standards
Referenced Standards
YY 0505-2012 Medical electrical equipment—Part 1-2:General requirements for safety—Collateral standard:Electromagnetic compatibility—Requirements and tests
YY/T 0664-2008 Medical device software—Software life cycle processes
YY 0709-2009 Medical electrical equipment—Part 1-8:General requirements for safety—Collateral standard:General requirements,tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
ISO 2882
ISO 3864-1:2002
ISO 7000:2004
ISO 7010:2011
ISO 9614-1
ISO 80000-1:2009
IEC 60601-1-6
IEC 60730-1:2010
IEC 60851-3:2009
IEC 60851-5:2008
GB/T 31523.1-2015 Safety information identification systems—Part 1:Signs
YY/T 0466.1-2016 Medical devices—Symbols to be used with medical device labels,labelling and information to be supplied—Part 1:General requirements
YY/T 0664-2020 Medical device software—Software life cycle processes
YY 9706.102-2021 Medical electrical equipment—Part 1-2:General requirements for basic safety and essential performance—Collateral standard:Electromagnetic compatibility—Requirements and tests
YY/T 9706.106-2021 Medical electrical equipment—Part 1-6:General requirements for basic safety and essential performance—Collateral Standard:Usability
YY 9706.108-2021 Medical electrical equipment—Part 1-8:General requirements for basic safety and essential performance-Collateral standard:General requirements,tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
ISO 19054
GB/T 2423.56-2006 Environmental testing for electric and electronic products—Part 2:Test methods—Test Fh:Vibration, broad-band random(digital control)and guidance
GB/T 2423.56-2018 Environmental testing—Part 2:Test methods—Test Fh:Vibration, broadband random and guidance
GB/T 2423.56-2023 Environmental testing—Part 2:Test methods—Test Fh:Vibration,broadband random and guidance
GB/T 3767-2016 Acoustics—Determination of sound power levels and sound energy levels of noise sources using sound pressure—Engineering methods for an essentially free field over a reflecting plane
GB 9706.1-2020 Medical electrical equipment—Part 1:General requirements for basic safety and essential performance
GB 9706.212-2020 Medical electrical equipment—Part 2-12:Particular requirements for basic safety and essential performance of critical care ventilators
GB 9706.255-2022 Medical electrical equipment—Part 2-55:Particular requirements for the basic safety and essential performance of respiratory gas monitors
GB/T 14574-2000 Acoustics—Declaration and verification of noise emission values of machinery and equipment
GB/T 19000-2000 Quality management systems—Fundamentals and vocabulary
GB/T 19000-2008 Quality management systems—Fundamentals and vocabulary
GB/T 19000-2016 Quality management systems—Fundamentals and vocabulary
GB/T 19000.2-1998 Quality management and quality assurance standards—Part 2:Generic guidelines for the application of GB/T 19001、GB/T 19002 and GB/T 19003
GB/T 19000.3-2001 Quality management and quality assurance standards—Part 3:Guidelines for the application of GB/T 19001-1994 to the development, supply, installation and maintenance of computer software
GB/T 19000.4-1995 Quality management and quality assurance standards—Part 4:Cuide to dependability programme management
GB/T 19974-2005 Sterilization of health care products—General requirement for characterization of a sterilization agent and the development, validation and routine control of a sterilization process for medical devices
GB/T 19974-2018 Sterilization of health care products—General requirement for characterization of a sterilization agent and the development, validation and routine control of a sterilization process for medical devices
GB 50751-2012 Technical code for medical gases engineering
YY 0339-2002 Suction catheter for use in the respiratory tract
YY 0339-2009 Suction catheter for use in the respiratory tract
YY/T 0339-2019 Suction catheters for use in the respiratory tract
YY/T 0339-2024 Suction catheters for use in the respiratory tract
YY/T 0461-2003 Breathing tubes intended for use with aneasthetic apparatus and ventilators
YY/T 0467-2003 Medical devices—Guide to the selection of standards in support of recognized essential principles of safety and performance of medical devices
YY/T 0467-2016 Medical devices—Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices
YY/T 0671-2021 Medical devices—Sleep apnoea breathing therapy—Masks and application accessories
YY 0671.1-2009 Sleep apnoea breathing therapy—Part 1:Sleep apnoea breathing therapy devices
YY 0671.2-2011 Sleep apnoea breathing therapy—Part 2:Masks and application accessories
YY/T 0735.1-2009 Anaesthetic and respiratory equipment—Heat and moisture exchangers(HMEs)for humidifying respired gases in humans—Part 1:HMEs for use with minimum tidal volumes of 250 mL
YY/T 0735.2-2010 Anaesthetic and respiratory equipment—Heat and moisture exchangers(HMEs) for humidifying respired gases in humans—Part 2:HMEs for use with tracheostomized patients having minimum tidal volumes of 250 mL
YY/T 0753.1-2009 Breathing system filters for anaesthetic and respiratory use—Part 1:Salt test method to assess filtration performance
YY/T 0753.2-2009 Breathing system filters for anaesthetic and respiratory use—Part 2:Non-filtration aspects
YY/T 0799-2010 Low-pressure hose assemblies for use with medical gases
YY/T 0802-2010 Sterilization of medical devices—Information to be provided by the manufacturer for the processing of resterilizable medical devices
YY/T 0802-2020 Processing of medical devices—Information to be provided by the medical device manufacturer
YY/T 0802.1-2024 Processing of medical devive—Information to be provided by the medical device manufacturer—Part 1:Critical and semi-critical medical devices
YY/T 0802.2-2024 Processing of medical device—Information to be provided by the medical device manufacturer—Part 2:Non-critical medical devices
YY/T 0916.1-2014 Small-bore connectors for liquids and gases in healthcare applications—Part 1:General requirements
YY/T 0916.1-2021 Small-bore connectors for liquids and gases in healthcare applications—Part 1:General requirements
YY/T 1474-2016 Medical devices—Application of usability engineering to medical devices
YY/T 1778.1-2021 Biocompatibility evaluation of breathing gas pathways in healthcare applications—Part 1:Evaluation and testing within a risk management process
YY/T 9706.110-2021 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
YY 9706.111-2021 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
YY 9706.112-2021 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
YY 9706.274-2022 Medical electrical equipment—Part 2-74:Particular requirements for basic safety and essential performance of respiratory humidifying equipment
YY 1040.1-2003 Anaesthetic and respiratory equipment—Conical connectors—Part 1:Cones and sockets
YY/T 1040.1-2015 Anaesthetic and respiratory equipment—Conical connectors—Part 1:Cones and sockets
ISO 7000(所有部分)
ISO 7396-1
ISO 10524-1
ISO 10524-3
ISO 19223:2019
IEC 62570:2014
Adopt standards
ISO 80601-2-84:2020
Related Standards
DZ/T 0101.12-1994
Active
JJG 204-1980
Active
JJG 204-1980 Meteorological Ventilation Psychrometer
SC 53-1980
Active
SC 53-1980 Transfer blade hydraulic steering gear repair quality standard
DZ 4-1981
Replaced
DZ 4-1981
SC 69-1982
Active
SC 69-1982 ZSS-12 Flash-type seawater desalination production device technical specifications
SC 72-1982
Active