Language:
    • Available Formats
    •  
    • Availability
    • Priced From ( in USD )
    • Printed Edition
    • Ships in 1-2 business days
    • $110.00
    • Add to Cart

Customers Who Bought This Also Bought

 

About This Item

 

Full Description

The purpose of this process-oriented standard is to provide ergonomic information and human factors engineering guidance so that optimum user and patient safety, system safety and performance, and operator effectiveness will be reflected in medical device design. This document describes a recommended human factors engineering process for use in fulfilling user interface design requirements in the development of medical devices and systems, including hardware, software, and documentation.
 

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


    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

    👀currently
    viewing


    Human Factors Design Process for Medical Devices

    • Historical Version