Standard: AAMI 62366


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This International Standard specifies a PROCESS for a MANUFACTURER to analyze, 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.

NOTE For the purposes of this standard, USABILITY (see 3.17) is limited to characteristics of the USER INTERFACE.

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 (see 5.9), 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 (see 4.1.2).

This International Standard does not apply to clinical decision-making relating to the use of a MEDICAL DEVICE.

Organization: Association for the Advancement of Medical Instrumentation
Document Number: aami 62366
Publish Date: 2007-01-01
Page Count: 130
Change Type: A1
Available Languages: EN
DOD Adopted: NO
ANSI Approved: YES
Most Recent Revision: YES
Current Version: NO
Status: Inactive

Document History

Document # Change Type Update Date Revision Status
AAMI 62366 Change Type: A1 Revision: 07 Status: INAC
AAMI 62366 Change Type: REAF Update Date: 2007-01-01 Revision: 07 Status: INAC

Standards That Reference This Standard

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