标准号 | 标准名称 |
| 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 |
| 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 |
| Protective clothing – General requirements 防护服 - 一般要求 |
| 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 |
| 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 |
| 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 |
| 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 |
ISO 31000:2018 | Risk management – Guidelines 风险管理 - 指南 |
| 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 |
| 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 |
| 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 |
| Medical devices — Quality management systems - Requirements for regulatory purposes 医疗器械 - 质量管理体系 - 用于法规的要求 |
| 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 |
| 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] |
| 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 |
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 |
| 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 |
| 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 |
| Lung ventilators and related equipment —Vocabulary and semantics 呼吸机及相关设备 - 词汇和语义 |
| 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 |
| 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 |
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 |
| 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] |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
|手机版|蒲公英|ouryao|蒲公英
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发表于 2020-4-11 08:31:24
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