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분야 | TC 62/SC 62A : Common aspects of medical equipment, software, and systems |
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적용범위 | IEC 62366:2007+A1:2014 Specifies a process for a manufacturer to analyse, specify, design, verify and validate usability, as it relates to safety of a medical device. This usability engineering process assesses and mitigates risks caused by usability problems associated with correct use and use errors, i.e. normal use. It can be used to identify but does not assess or mitigate risks associated with abnormal use. If the usability engineering process detailed in this International Standard has been complied with and the acceptance criteria documented in the usability validation plan have been met, then the residual risks, as defined in ISO 14971, associated with usability of a medical device are presumed to be acceptable, unless there is objective evidence to the contrary. This International Standard does not apply to clinical decision-making relating to the use of a medical device. This consolidated version consists of the first edition (2007) and its amendment 1 (2014). Therefore, no need to order amendment in addition to this publication. |
국제분류(ICS)코드 | 11.040.01 : 일반 의료장비 |
페이지수 | 436 |
Edition | 1.1 |
No. | 표준번호 | 표준명 | 발행일 | 상태 |
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1 | IEC 62366:2007/AMD1:2014 | Amendment 1 - Medical devices - Application of usability engineering to medical devices | 2014-01-28 | 폐지(대체) |
2 | IEC 62366:2007+AMD1:2014 CSV | Medical devices - Application of usability engineering to medical devices | 2014-01-28 | 폐지(대체) |
3 | IEC 62366:2007 | Medical devices - Application of usability engineering to medical devices | 2007-10-18 | 폐지(대체) |
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