Back

EVS-EN 12182:2012

Assistive products for persons with disability - General requirements and test methods

General information
Valid from 05.06.2012
Base Documents
EN 12182:2012
Directives or regulations
None
Standard history
Status
Date
Type
Name
Main
prEN ISO 21856
05.06.2012
Main
This European Standard specifies general requirements and test methods for assistive products for persons with a disability, which are medical devices according to the definition laid down in the EU Directive 93/42/EEC. This European Standard does not apply to assistive products which achieve their intended purpose by administering pharmaceutical substances to the user. Where other European Standards exist for particular types of assistive products then those standards apply. However, some of the requirements of this standard may still apply and may be considered in addition to those in other European standards. NOTE Not all the items listed in EN ISO 9999 are medical devices. Contracting parties may wish to consider if this standard or parts of this standard can be used for assistive products which are not medical devices as defined in the EU Directive 93/42/EEC.
*
*
*
PDF
22.86 € incl tax
Paper
22.86 € incl tax
Price: 2.40 € incl tax
Standard monitoring
Customers who bought this item also bought
Main + amendment

EVS-EN 16307-1:2013+A1:2015

Industrial trucks - Safety requirements and verification - Part 1: Supplementary requirements for self-propelled industrial trucks, other than driverless trucks, variable-reach trucks and burden-carrier trucks
Withdrawn from 15.09.2020
Amendment

EVS-EN 55016-1-3:2007/A1:2016

Specification for radio disturbance and immunity measuring apparatus and methods - Part 1-3: Radio disturbance and immunity measuring apparatus - Ancillary equipment - Disturbance power
Newest version Valid from 01.06.2016
Main + amendment

EVS-EN 1041:2008+A1:2013

Information supplied by the manufacturer of medical devices
Withdrawn from 17.05.2021
Main

EVS-EN ISO 14971:2012

Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
Withdrawn from 02.01.2020