IEC 62366:2007

Medical devices — Application of usability engineering to medical devices

Publication date:   Nov 13, 2007

95.99 Withdrawal of Standard   Feb 25, 2015

General information

95.99 Withdrawal of Standard   Feb 25, 2015

IEC

ISO/TC 210 Quality management and corresponding general aspects for medical devices

International Standard

11.040.01   Medical equipment in general

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Scope


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.

Life cycle

NOW

WITHDRAWN
IEC 62366:2007
95.99 Withdrawal of Standard
Feb 25, 2015

CORRIGENDA / AMENDMENTS

WITHDRAWN
IEC 62366:2007/Amd 1:2014

REVISED BY

PUBLISHED
IEC 62366-1:2015