市场监管总局(标准委)推动33项疫情防控国际标准免费公开 市说新语 昨天-88蓝保健品招商网
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市场监管总局(标准委)推动33项疫情防控国际标准免费公开 市说新语 昨天

来源: 市说新语 类别:政策法规 2020年04月25日 12:04:00


为充分发挥标准技术优势,助力应对全球新冠肺炎疫情,有力支持企业复工复产达产,市场监管总局(标准委)积极与国际标准化组织(ISO)、国际电工委员会(IEC)沟通联系,推动疫情防控相关国际标准免费向社会公开。在获得ISO、IEC授权同意后,市场监管总局(标准委)迅速组织在中国标准信息服务网上,免费公开了医用肺呼吸机、防护服、医疗器械生物学评价等33项疫情防控相关国际标准,为战胜疫情贡献标准力量。


中国是ISO、IEC的常任理事国,保护国际标准版权是我们应尽的责任和义务。为此,在公开标准的同时,我们严格遵守ISO、IEC国际标准版权政策要求,切实履行国际标准版权保护的责任和义务。




附:33项疫情防控国际标准清单


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







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