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About This Item

 

Full Description

Includes Amendment 1 (2014).

This standard describes a usability engineering process, and provides guidance on how to implement and execute the process to provide safety in medical devices. It is intended to be useful not only for manufacturers of medical devices, but also for technical committees responsible for the preparation of particular medical device standards.
 

Document History

  1. AAMI/IEC 62366-1: 2015/(R2021) +AMD1:2020 (Consolidated Text)


    Medical devices - Part 1: Application of usability engineering to medical devices, including Amendment 1

    • Most Recent
  2. AAMI/IEC 62366-1:2015


    Medical devices - Application of usability engineering to medical devices

    • Historical Version
  3. AAMI/IEC 62366:2007/(R)2013

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    Medical devices - Application of usability engineering to medical devices

    • Historical Version
  4. AAMI/IEC 62366:2007


    Medical devices - Application of usability engineering to medical devices

    • Historical Version
  5. AAMI HE74:2001/(R)2009


    Human Factors Design Process for Medical Devices

    • Historical Version
 

Amendments, rulings, supplements, and errata

  1. AAMI/IEC 62366:2007/(R)2013/A1:2013


    Amendment 1 to ANSI/AAMI/IEC 62366:2007/(R)2013 - Medical devices - Application of usability engineering to medical devices