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EVS-EN 60601-2-24:2001

Medical electrical equipment - Part 2-24: Particular requirements for the safety of infusion pumps and controllers

General information

Withdrawn from 08.06.2015
Base Documents
IEC 60601-2-24:1998; EN 60601-2-24:1998
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Although the standard’s status is withdrawn, it still has the presumption of conformity in the meaning of regulation 93/42/EEC and conformance with the regulation ’s requirements can be guaranteed by using the withdrawn version of the standard.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
01.07.2001
Main
This Particular Standard specifies the requirement for infusion pumps, infusion controllers, syringe pumps and pumps for ambulatory use, as defined in 2.101 to 2.110. These devices are intended for use by medical staff and home patients as prescribed and medically indicated.

Required fields are indicated with *

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