1 |
ISO 374-5:2016 |
Protective gloves against dangerous chemicals and micro-organisms - Part 5: Terminology and performance requirements for micro-organisms risks
危险化学品和微生物防护手套——第5部分:微生物风险的术语和性能要求 |
2 |
ISO 10993-1:2018 |
Biological evaluation of medical devices – Part 1: Evaluation and testing within a risk management process
医疗器械生物学评价——第1部分:风险管理过程中的评价与试验 |
3 |
ISO 13688:2013 |
Protective clothing – General requirements
防护服——一般要求 |
4 |
ISO 22301:2019 |
Security and resilience – Business continuity management systems –Requirements
安全性及恢复能力——商业连续性管理系统——要求 |
5 |
ISO 22395:2018 |
Security and resilience – Community resilience – Guidelines for supporting vulnerable persons in an emergency
安全性及恢复能力——社区恢复能力——紧急情况下支持弱势人群的准则 |
6 |
ISO 22320:2018 |
Security and resilience – Emergency management – Guidelines for incident management
安全性及恢复能力——应急管理——事故管理指南 |
7 |
ISO 22316:2017 |
Security and resilience – Organizational resilience – Principles and attributes
安全性及恢复能力——组织机构恢复能力——原则和属性 |
8 |
ISO 31000:2018 |
Risk management – Guidelines
风险管理——指南 |
9 |
ISO 10651-3:1997 |
Lung ventilators for medical use — Part 3: Particular requirements for emergency and transport ventilators
医用肺呼吸机——第3部分:急救和运送用呼吸机的特殊要求 |
10 |
ISO 10651-4:2002 |
Lung ventilators — Part 4: Particular requirements for operatorpowered resuscitators
肺呼吸机——第4部分:操作员控制用人工呼吸机的特殊要求 |
11 |
ISO 10651-5:2006 |
Lung ventilators for medical use — Particular requirements for basic safety and essential performance — Part 5: Gas-powered emergency resuscitators
医用肺呼吸机——基本安全和基本性能的特殊要求——第5部分:气动急救人工呼吸器 |
12 |
ISO 13485:2016 |
Medical devices — Quality management systems - Requirements for regulatory purposes
医疗器械——质量管理体系——监管要求 |
13 |
ISO 17510:2015 |
Medical devices — Sleep apnoea breathing therapy — Masks and application accessories
医疗器械——睡眠窒息呼吸治疗——面罩和应用附件 |
14 |
ISO 18082:2014 |
Anaesthetic and respiratory equipment — Dimensions of noninterchangeable screw-threaded (NIST) low-pressure connectors for medical gases [Including ISO 18082:2014/Amd.1:2017, AMENDMENT 1]
麻醉剂和呼吸设备——医疗气体用非交替式螺栓.螺纹(NIST)低压力连接器尺寸 [包括ISO 18082:2014/Amd.1:2017, 修订 1] |
15 |
ISO 18562-1:2017 |
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 1: Evaluation and testing within a risk management process
医疗保健应用中呼吸气体通道的生物相容性评估——第1部分: 风险管理过程中的评估和试验 |
16 |
ISO 18562-2:2017 |
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 2: Tests for emissions of particulate matter
医疗保健应用中呼吸气体通道的生物相容性评估——第2部分: 颗粒物排放试验 |
17 |
ISO 18562-3:2017 |
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 3: Tests for emissions of volatile organic compounds (VOCs)
医疗保健应用中呼吸气体通道的生物相容性评估——第3部分: 挥发性有机化合物(VOC)排放试验 |
18 |
ISO 18562-4:2017 |
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 4: Tests for leachables in condensate
医疗保健应用中呼吸气体通道的生物相容性评估——第4部分: 冷凝物中的析出物试验 |
19 |
ISO 19223:2019 |
Lung ventilators and related equipment — Vocabulary and semantics
呼吸机及相关设备——词汇和语义 |
20 |
ISO 20395:2019 |
Biotechnology — Requirements for evaluating the performance of quantification methods for nucleic acid target sequences — qPCR and dPCR
生物技术——核酸目标序列量化方法性能评估要求——qPCR和dPCR(实时荧光定量聚合酶链式反应和数字聚合酶链式反应) |
21 |
ISO 5356-1:2015 |
Anaesthetic and respiratory equipment — Conical connectors — Part 1: Cones and sockets
麻醉剂和呼吸设备——锥形连接器——第1部分:锥体和插孔 |
22 |
ISO 80601-2-12:2020 |
Medical electrical equipment — Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators
医用电气设备——第2-12部分:重症监护呼吸机基本安全和基本性能的特殊要求 |
23 |
ISO 80601-2-13:2011 |
Medical electrical equipment — Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation [Including: ISO 80601-2-13:2011/Amd.1:2015, AMENDMENT 1 and ISO 80601-2-13:2011/Amd.2:2018, AMENDMENT 2]
医疗电气设备——第2-13部分: 麻醉工作站的基本安全和基本性能的特殊要求[包括 ISO 80601-2-13:2011/Amd.1:2015, 修订 1 和 ISO 80601-2-13:2011/Amd.2:2018, 修订 2] |
24 |
ISO 80601-2-70:2015 |
Medical electrical equipment — Part 2-70: Particular requirements for basic safety and essential performance of sleep apnoea breathing therapy equipment
医疗电气设备——第2-70部分:睡眠窒息呼吸治疗设备的基本安全和基本性能的特殊要求 |
25 |
ISO 80601-2-74:2017 |
Medical electrical equipment — Part 2-74: Particular requirements for basic safety and essential performance of respiratory humidifying equipment
医疗电气设备——第2-74部分: 呼吸加湿器基本安全和基本性能的特殊要求 |
26 |
ISO 80601-2-79:2018 |
Medical electrical equipment — Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment
医疗电气设备——第2-79部分:呼吸受损的呼吸支持设备基本安全和基本性能的特殊要求 |
27 |
ISO 80601-2-80:2018 |
Medical electrical equipment — Part 2-80: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency
医疗电气设备——第2-80部分:呼吸功能不全的呼吸支持设备基本安全和基本性能的特殊要求 |
28 |
ISO/TS 16976-8:2013 |
Respiratory protective devices — Human factors — Part 8: Ergonomic factors
呼吸保护装置——人为因素——第8部分:人体工学因素 |
29 |
IEC 60601-1:2005+AMD1:2012 CSV |
Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
医用电气设备——第1部分:基本安全和基本性能 |
30 |
IEC 60601-1-2:2014 |
Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic disturbances - Requirements and tests
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——汇编标准:电磁干扰-要求和测试 |
31 |
IEC 60601-1-6:2010 |
Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability
医用电气设备——第1-6部分:基本安全性和必要性能的通用要求——汇编标准:可用性 |
32 |
IEC 60601-1-8:2006 |
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
医用电气设备——第1-8部分:基本安全和基本性能的通用要求——汇编标准:医疗电气设备和医疗电气系统报警系统的通用要求、试验和指南 |
33 |
IEC 60601-1-11:2015 |
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
医疗电气设备——第1-11部分:基本安全和基本性能的通用要求——汇编标准:家庭保健用医疗电气设备和医疗电气系统的要求 |