IEC 62366 Ed. 1.0被替代
Medical devices - Application of usability engineering to medical devices
出版：International Electrotechnical Committee
專家解讀視頻
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.
NF EN 62366:2008 - Identical
EN 62366:2008 - Identical
NEN EN IEC 62366:2008 - Identical
PN EN 62366:2008 - Identical
VDE 0750-241:2008 - Identical
SS EN 62366 Ed. 1 (2008) - Identical
DIN EN 62366 (2008-09) - Identical
OVE/ONORM EN 62366:2008 - Identical
NF EN 62366:2006 - Identical
BS EN 62366:2008 - Identical
