IEC 60601-1-8:2006
Superseded
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
Amended by
Available format(s)
Hardcopy , PDF
Published date
25-10-2006
Publisher
Superseded date
25-07-2020
€390.75
Excluding VAT
Specifies basic safety and essential performance requirements and tests for alarm systems in medical electrical equipment and medical electrical systems and to provide guidance for their application. This is accomplished by defining alarm categories (priorities) by degree of urgency, consistent alarm signals and consistent control states and their marking for all alarm systems.
| Committee |
TC 62/SC 62A
|
| DevelopmentNote |
NEW CHILD AMD 2 2020 IS ADDED
|
| DocumentType |
Standard
|
| Pages |
389
|
| ProductNote |
NEW CHILD AMD 2 2020 IS ADDED
|
| PublisherName |
International Electrotechnical Committee
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| JIS T 60601-1-8:2023 | Identical |
| NEN-EN-IEC 60601-1-8:2007 | Identical |
| IS 13450 : Part 1 : Sec 8 : 2019 | Identical |
| I.S. EN 60601-1-8:2007 | Identical |
| PN-EN 60601-1-8:2011 | Identical |
| EN 60601-1-8:2007 | Identical |
| PN-EN 60601-1-8:2011/A2:2021-12 | Identical |
| CEI EN 60601-1-8 : 2007 | Identical |
| CEI EN 60601-1-8 : 2009 | Identical |
| JIS T 60601-1-8:2012 | Identical |
| AS/NZS 3200.1.8:2005 | Identical |
| UNE-EN 60601-1-8:2008 | 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) |
| ANSI/AAMI/UL 2800-1:2022 | Standard for Medical Device Interoperability |
| CEI EN IEC 80601-2-30:2019 | Medical electrical equipment Part 2: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers<br> |
| I.S. EN 62366-1:2015/A1:2020 | Medical devices - Part 1: Application of usability engineering to medical devices |
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