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EVS-EN 60601-2-30:2002

Medical electrical equipment - Part 2-30: Particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment

General information
Withdrawn from 06.01.2014
Base Documents
IEC 60601-2-30:1999; EN 60601-2-30:2000
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Although the standard’s status is withdrawn, it still has the presumption of conformity in the meaning of regulation 93/42/EEC and conformance with the regulation ’s requirements can be guaranteed by using the withdrawn version of the standard.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/

Standard history

Status
Date
Type
Name
04.11.2010
Main
01.01.2003
Main
Main
EVS-EN 60601-2-30:2001
This Standard specifies the particular safety requirements for AUTOMATIC CYCLING INDIRECT BLOOD PRESSURE MONITORING EQUIPMENT as defined in 2.101 and hereinafter also referred to as equipment.
This Particular Standard does not apply to blood pressure measuring equipment which uses finger transducers or to semi-automatic blood pressure measuring equipment (typically in which each determination
needs to be initiated manually).
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