AAMI TIR50:2014(R2017)
Superseded
View Superseded by
Post-market surveillance of use error management
English
12-06-2017
01-17-2026
This document addresses the issue of use error detection for medical devices from clinical, manufacturer, and regulatory perspective regarding human factors assessment.
| DocumentType |
Standard
|
| ISBN |
978-1-57020-514-9
|
| Pages |
46
|
| PublisherName |
Association for the Advancement of Medical Instrumentation
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| AAMI TIR105:2020 | Risk management guidance for combination products |
| AAMI HE75 : 2009 | HUMAN FACTORS ENGINEERING - DESIGN OF MEDICAL DEVICES |
| AAMI ES60601-1 : 2005 : R2012 | MEDICAL ELECTRICAL EQUIPMENT - PART 1: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE (IEC 60601-1:2005, MOD) |
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