I.S. EN 60601-1-6:2010/A1:2015
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability
Hardcopy , PDF
08-05-2021
English - French
06-09-2015
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FOREWORD
INTRODUCTION
1 Scope, object and related standards
2 Normative references
3 Terms and definitions
4 General requirements
5 * Replacement of requirements given in IEC 62366
Annex A (informative) General guidance and rationale
Annex B (informative) Mapping between the elements of IEC 60601-1-6:2006 and the related elements in IEC 62366:2007
Annex C (informative) References to items of USABILITY provided in IEC 62366:2007 and their use in other standards
Bibliography
Index of defined terms used with this collateral standard
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.
| Committee |
TC 62
|
| DocumentType |
Standard
|
| ISBN |
978-2-8322-1132-8
|
| Pages |
84
|
| ProductNote |
THIS STANDARD ALSO REFERS TO CEI 60601-1:2005, CEI 60601-1:2005 Amendement 1:2012, CEI 60601-1-8:2006, CEI 60601-1-8:2006 Amendement 1:2012, CEI 62366:2007, CEI 62366:2007 Amendement 1, ANSI/AAMI HE 74:2001. The date of any NSAI previous adoption may not match the date of its original CEN/CENELEC document.
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| IEC 60601-1-6:2010/AMD1:2013 | Identical |
| EN 60601-1-6:2010/A1:2015 | Identical |
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