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EVS-EN 60601-2-22:2001

Medical electrical equipment - Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment

General information
Withdrawn from 05.02.2013
Base Documents
IEC 601-2-22:1995; EN 60601-2-22:1996
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Although the standard’s status is withdrawn, it still has the presumption of conformity in the meaning of regulation 93/42/EEC and conformance with the regulation ’s requirements can be guaranteed by using the withdrawn version of the standard.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/

Standard history
Status
Date
Type
Name
Applies to laser equipment for medical applications, classified as a class 3B or class 4 laser product according to the classification in IEC 825-1.
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