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AAMI IEC 62366 : 2015

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

MEDICAL DEVICES - APPLICATION OF USABILITY ENGINEERING TO MEDICAL DEVICES
Available format(s)

Hardcopy , PDF

Superseded date

11-01-2017

Language(s)

English

Published date

01-01-2015

Glossary of equivalent standards
Committee representation
Background of AAMI adoption of IEC 62366:2007
FOREWORD
INTRODUCTION
1 Scope
2 Normative references
3 Terms and definitions
4 Principles
5 USABILITY ENGINEERING PROCESS
6 ACCOMPANYING DOCUMENT
7 Training and materials for training
Annex A (informative) - General guidance and rationale
Annex B (informative) - Categories of USER action
Annex C (informative) - Examples of USE ERRORS, ABNORMAL USE
                        and possible causes
Annex D (informative) - Guidance on the USABILITY ENGINEERING
                        PROCESS
ANNEX E (informative) - Questions that can be used to identify
                        MEDICAL DEVICE characteristics
                        associated with USABILITY that could
                        impact on SAFETY
ANNEX F (informative) - Examples of possible USABILITY
                        related HAZARDOUS SITUATIONS
Annex G (informative) - USABILITY goals: Illustrative example
                        for a home parenteral infusion pump
ANNEX H (informative) - Sample USABILITY SPECIFICATION and
                        its inputs
Annex I (informative) - Recommended reading list
Annex J (informative) - Reference to the essential principles
Annex K (normative) - Evaluation of a USER INTERFACE OF
                      UNKNOWN PROVENANCE (UOUP)
Bibliography
Index of defined terms

Specifies a usability engineering process, and provides guidance on how to implement and execute the process to provide safety in medical devices.

Committee
HE
DevelopmentNote
Supersedes AAMI HE74. (11/2010)
DocumentType
Standard
Pages
52
PublisherName
Association for the Advancement of Medical Instrumentation
Status
Superseded
SupersededBy
Supersedes

Standards Relationship
IEC 62366:2007+AMD1:2014 CSV Identical

AAMI TIR61 : 2014 GENERATING REPORTS FOR HUMAN FACTORS DESIGN VALIDATION RESULTS FOR EXTERNAL CARDIAC DEFIBRILLATORS
ANSI/AAMI EQ89:2015 GUIDANCE FOR THE USE OF MEDICAL EQUIPMENT MAINTENANCE STRATEGIES AND PROCEDURES
AAMI TIR50 : 2014 POST-MARKET SURVEILLANCE OF USE ERROR MANAGEMENT
AAMI TIR49 : 2013 DESIGN OF TRAINING AND INSTRUCTIONAL MATERIALS FOR MEDICAL DEVICES USED IN NON-CLINICAL ENVIRONMENTS

ISO 9241-11:1998 Ergonomic requirements for office work with visual display terminals (VDTs) Part 11: Guidance on usability
AAMI HE48 : 1993 HUMAN FACTORS ENGINEERING GUIDELINES AND PREFERRED PRACTICES FOR THE DESIGN OF MEDICAL DEVICES
IEC 60601-1:2005+AMD1:2012 CSV Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
ISO 13485:2016 Medical devices Quality management systems Requirements for regulatory purposes
IEC 60601-1-8:2006+AMD1:2012 CSV Medical electrical equipment - Part 1-8: General requirements forbasic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems inmedical electrical equipment and medical electrical systems
EN 1041:2008+A1:2013 Information supplied by the manufacturer of medical devices
ISO/IEC Guide 51:2014 Safety aspects Guidelines for their inclusion in standards
ISO/TR 16142:2006 Medical devices Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices
ISO 9001:2015 Quality management systems — Requirements
ISO 9000:2015 Quality management systems — Fundamentals and vocabulary
ISO 14971:2007 Medical devices Application of risk management to medical devices
IEC TR 61258:2008 Guidelines for the development and use of medical electrical equipment educational materials

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