AS IEC 60601.1.6:2017
Current
The latest, up-to-date edition.
Medical electrical equipment General requirements for basic safety and essential performance - Collateral standard: Usability
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English
05-06-2017
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Adopts IEC60601-1-6 to specify a process for a manufacturer to analyse, specify, design, verify and validate usability, as it relates to basic safety and essential performance of medical equipment (ME).
| Committee |
HE-003
|
| DocumentType |
Standard
|
| ISBN |
978 1 76035 806 8
|
| Pages |
20
|
| PublisherName |
Standards Australia
|
| Status |
Current
|
| Supersedes |
This International Standard specifies a PROCESS for a MANUFACTURER to analyse, specify, design, VERIFY and VALIDATE USABILITY, as it relates to BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT, hereafter referred to as ME EQUIPMENT.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.If the USABILITY ENGINEERING PROCESS detailed in this collateral standard has been complied with and the acceptance criteria documented in the USABILITY VALIDATION plan have been met (see 5.9 of IEC 62366:2007), then the RESIDUAL RISKS, as defined in ISO 14971, associated with USABILITY of ME EQUIPMENT are presumed to be acceptable, unless there is OBJECTIVE EVIDENCE to the contrary (see 4.1.2 of IEC 62366:2007).
| Standards | Relationship |
| IEC 60601-1-6:2010+AMD1:2013 CSV | Identical |
First published as AS IEC 60601.1.6:2017.
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