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EVS-EN 60580:2003

Medical electrical equipment - Dose area product meters

General information
Withdrawn from 15.04.2020
Base Documents
IEC 60580:2000; EN 60580:2000
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Although the standard’s status is withdrawn, it still has the presumption of conformity in the meaning of regulation 93/42/EEC and conformance with the regulation ’s requirements can be guaranteed by using the withdrawn version of the standard.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
15.04.2020
Main
01.02.2003
Main
This International Standard specifies the performance and testing of DOSE AREA PRODUCT METERS with IONIZATION CHAMBERS intended to measure DOSE AREA PRODUCT and/or DOSE AREA PRODUCT RATE to the PATIENT during MEDICAL RADIOLOGICAL EXAMINATIONS.
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