IEC 60601-1-6:2006
Superseded
View Superseded by
Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability
Hardcopy , PDF
English - French, English, French, Spanish, Castilian
12-08-2006
12-31-2021
Specifies requirements for a process to analyse, design, verify and validate the usability, as it relates to basic safety and essential performance of medical electrical equipment. This collateral standard addresses normal use and use errors but excludes abnormal use.The object of this collateral standard is to specify general requirements that are in addition to those of the general standard IEC 60601-1 and to serve as the basis for particular standards.
| Committee |
TC 62/SC 62A
|
| DocumentType |
Standard
|
| Pages |
145
|
| PublisherName |
International Electrotechnical Committee
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| CEI EN 60601-1-6 : 2008 | Identical |
| BS EN 61241-10:2004 | Identical |
| CAN/CSA-C22.2 NO. 60601-1-6:11 (R2021) | Identical |
| BS EN 60601-1-6:2007 | Identical |
| BS EN 61249-2-44:2016 | Identical |
| UNE-EN 60601-1-6:2008 | Identical |
| CSA IEC 62366-1:15 (R2020) | Medical devices — Part 1: Application of usability engineering to medical devices (Adopted IEC 62366-1:2015, first edition, 2015-02) | Dispositifs médicaux — Partie 1 : Application de l’ingénierie de l’aptitude à l’utilisation aux dispositifs médicaux (norme IEC 62366-1:2015 adoptée, première édition, 2015-02) |
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