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EVS-EN 60601-2-10:2002

Medical electrical equipment - Part 2-10: Particular requirements for the safety of nerve and muscle stimulators

General information
Withdrawn from 08.06.2015
Base Documents
IEC 60601-2-10:1987+A1:2001; EN 60601-2-10:2000; EN 60601-2-10:2000/A1:2001
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Although the standard’s status is withdrawn, it still has the presumption of conformity in the meaning of regulation 93/42/EEC and conformance with the regulation ’s requirements can be guaranteed by using the withdrawn version of the standard.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
08.06.2015
Main
01.01.2003
Main
Specifies particular requirements for the safety of electrical stimulators of muscles and nerves in the specialized practice of physical medicine. It excludes stimulators used with implanted electrodes, brain stimulation, neurological research, cardiac pacemakers, defibrillators and other surgical procedures.
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