|
1. |
Risk management – Guidelines |
ISO 31000:2018 |
2. |
Security and resilience – Business continuity management systems – Requirements |
ISO 22301:2019 |
3. |
Security and resilience – Community resilience – Guidelines for supporting vulnerable persons in an emergency |
ISO 22395:2018 |
4. |
Security and resilience – Emergency management – Guidelines for incident management |
ISO 22320:2018 |
5. |
Security and resilience – Organizational resilience – Principles and attributes |
ISO 22316:2017 |
6. |
Occupational health and safety management – General guidelines for safe working during the COVID-19 pandemic |
ISO/PAS 45005 |
7. |
Protective gloves against dangerous chemicals and micro-organisms – Part 5: Terminology and performance requirements for micro-organisms risks
|
ISO 374-5:2016 |
8. |
Protective clothing – General requirements |
ISO 13688:2013 |
9. |
Respiratory protective devices – Human factors – Part 8: Ergonomic factors |
ISO/TS 16976-8:2013 |
10. |
Clothing for protection against infectious agents – Medical face masks – Test method for resistance against penetration by
synthetic blood (fixed volume, horizontally projected)
|
ISO 22609:2004 |
11. |
Biological evaluation of medical devices – Part 1: Evaluation and testing within a risk management process |
ISO 10993-1:2018 |
12. |
Medical devices – Quality management systems – Requirements for regulatory purposes |
ISO 13485:2016 |
13. |
Medical devices – Sleep apnoea breathing therapy – Masks and application accessories |
ISO 17510:2015 |
14. |
Anaesthetic and respiratory equipment – Dimensions of non-interchangeable screw-threaded (NIST) low-pressure connectors for medical gases
[Including ISO 18082:2014/Amd.1:2017, Amendment 1]
|
ISO 18082:2014
ISO 18082:2014-Amd.1:2017
|
15. |
Anaesthetic and respiratory equipment – Conical connectors – Part 1: Cones and sockets |
ISO 5356-1:2015 |
16. |
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
|
ISO 80601-2-13:2011
ISO 80601-2-13:2011-Amd.1:2015
ISO 80601-2-13:2011-Amd.2:2018
|
17. |
Medical electrical equipment – Part 2-70: Particular requirements for basic safety and essential performance of sleep apnoea breathing therapy equipment
|
ISO 80601-2-70:2015 |
18. |
Medical electrical equipment – Part 2-74: Particular requirements for basic safety and essential performance of respiratory humidifying equipment
|
ISO 80601-2-74:2017 |
19. |
Medical electrical equipment – Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment
|
ISO 80601-2-79:2018 |
20. |
Medical electrical equipment – Part 2-80: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency
|
ISO 80601-2-80:2018 |
21. |
Lung ventilators for medical use – Part 3: Particular requirements for emergency and transport ventilators
|
ISO 10651-3:1997 |
22. |
Lung ventilators – Part 4: Particular requirements for operator-powered resuscitators |
ISO 10651-4:2002 |
23. |
Lung ventilators for medical use – Particular requirements for basic safety and essential performance – Part 5: Gas-powered emergency resuscitators
|
ISO 10651-5:2006 |
24. |
Lung ventilators and related equipment – Vocabulary and semantics |
ISO 19223:2019 |
25. |
Medical electrical equipment – Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators
|
ISO 80601-2-12:2020 |
26. |
Biocompatibility evaluation of breathing gas pathways in healthcare applications – Part 1: Evaluation and testing within a risk management process
|
ISO 18562-1:2017 |
27. |
Biocompatibility evaluation of breathing gas pathways in healthcare applications – Part 2: Tests for emissions of particulate matter
|
ISO 18562-2:2017 |
28. |
Biocompatibility evaluation of breathing gas pathways in healthcare applications – Part 3: Tests for emissions of volatile organic compounds (VOCs)
|
ISO 18562-3:2017 |
29. |
Biocompatibility evaluation of breathing gas pathways in healthcare applications – Part 4: Test for leachables in condensate
|
ISO 18562-4:2017 |
30. |
Biotechnology – Requirements for evaluating the performance of quantification methods for nucleic acid target sequences – qPCR and dPCR
|
ISO 20395:2019 |