Cover IEC 60601-1-6:2010
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IEC 60601-1-6:2010

Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability

Ausgabedatum: 2010-01
Edition: 3.0
Sprache: EN-FR - zweisprachig englisch/französisch
Seitenzahl: 51 VDE-Artnr.: 216976

Inhaltsverzeichnis

IEC 60601-1-6:2010 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. 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). The object of this collateral standard is to specify general requirements that are in addition to those of the general standard and to serve as the basis for particular standards. This document cancels and replaces the second edition of IEC 60601-1-6 which has been technically revised. It was revised to align with the usability engineering process in IEC 62366. To allow for equipment manufacturers and testing organizations to make products and to equip themselves for conducting revised tests in accordance with this third edition, it is recommended by SC 62A that the content of this document not be adopted for mandatory implementation earlier than 3 years from the date of publication for equipment newly designed and not earlier than 5 years from the date of publication for equipment already in production.

Buchempfehlungen zu dieser IEC-Norm

Buchtitel Format
Elektrische Sicherheit in medizinisch genutzten Bereichen
Hofheinz, Wolfgang

Elektrische Sicherheit in medizinisch genutzten Bereichen

Normgerechte Stromversorgung und fachgerechte Überprüfung medizinischer elektrischer Geräte; DIN VDE 0100-100, DIN VDE 0100-410, DIN VDE 0100- 710, DIN IEC/TS 60479-1 (VDE V 0140-479-1), DIN VDE 0701-0702, DIN EN 60601-1 (VDE 0750-1), DIN EN 61140 (VDE 0140-1), DIN EN 61557-8 (VDE 0413-8), DIN EN 61557-9 (VDE 0413-9), DIN EN 62353 (VDE 0751-1)
VDE-Schriftenreihe – Normen verständlich, Band 117

2018, 187 Seiten, Din A5, Broschur

Dieser Buchtitel ist auch als E-Book (PDF) erhältlich
Fachbuch eBook (PDF) Kombi-Fassung - Buch und E-Book
Entwicklung und Herstellung medizinischer Software
Prinz, Thorsten (Hrsg.)

Entwicklung und Herstellung medizinischer Software

Normen in der Medizintechnik
VDE-Schriftenreihe – Normen verständlich, Band 171

2017, 219 Seiten, Din A5, Broschur

Dieser Buchtitel ist auch als E-Book (PDF) erhältlich
Fachbuch eBook (PDF) Kombi-Fassung - Buch und E-Book