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EVS-EN 60601-2-25:2001

Medical electrical equipment - Part 2: Particular requirements for the safety of electrocardiographs

General information
Withdrawn from 04.11.2015
Base Documents
IEC 601-2-25:1993+A1:1999; EN 60601-2-25:1995; EN 60601-2-25:1995/A1:1999
Directives or regulations
93/42/EEC Medical devices (MDD)

Although the standard’s status is withdrawn, it still has the presumption of conformity in the meaning of regulation 93/42/EEC and conformance with the regulation ’s requirements can be guaranteed by using the withdrawn version of the standard. The presumption of conformity is valid until a corresponding amendment is published in the Official Journal of the European Union.
 
To view the latest lists of harmonised standards published in the Official Journal of the European Union, visit: 
http://ec.europa.eu/growth/single-market/european-standards/harmonised-standards/

Directive 93/42/EEC (Medical devices) Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.

Standard history

Status
Date
Type
Name
04.11.2015
Main
01.12.2001
Main
This Particular International Standard specifies the particular safety requirements for ELECTROCARDIOGRAPHS as defined in 2.102, intended for the production of detachable ELECTROCARDIOGRAMS for diagnostic purposes. It also applies to vector-cardigraphs and EQUIPMENT for stress testing. This particular standard covers minimum safety requirements.
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