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Standard [WITHDRAWN]

DIN EN 80601-2-30:2016-02

VDE 0750-2-30:2016-02

Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers (IEC 80601-2-30:2009 + Corrigendum Jan. 2010 + A1:2013); German version EN 80601-2-30:2010 + A1:2015

German title
Medizinische elektrische Geräte - Teil 2-30: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von automatisierten nicht-invasiven Blutdruckmessgeräten (IEC 80601-2-30:2009 + Corrigendum Jan. 2010 + A1:2013); Deutsche Fassung EN 80601-2-30:2010 + A1:2015
Publication date
2016-02
Original language
German
Pages
69
Note
The publisher recommends this document in lieu of the withdrawn document DIN EN 1060-3:2010-03 , for which no replacement is available.

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Publication date
2016-02
Original language
German
Pages
69
Note
The publisher recommends this document in lieu of the withdrawn document DIN EN 1060-3:2010-03 , for which no replacement is available.

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Overview

This standard contains amendments to DIN EN 80601-2-30 (VDE 0750-2-30):2011-05. These are primarily editorial corrections and clarifications. In addition, they clarify the requirements for operation in the event of failure of the supply network and reference new and updated collateral standards. This standard has been published with a simplified Annex ZZ in order to make the European version available. A listing of this standard in the European Official Journal of the EU under the Medical Devices Directive has not yet been made. The committee responsible is Subcommittee UK 812.1 "Diagnostik" ("Diagnostics") of the DKE (German Commission for Electrical, Electronic and Information Technologies) at DIN and VDE.

Replacement amendments

This document replaces DIN EN 80601-2-30:2011-05; VDE 0750-2-30:2011-05 .

This document has been replaced by: DIN EN IEC 80601-2-30:2020-03; VDE 0750-2-30:2020-03 .

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