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SRPS EN 1640:2011

Dentistry - Medical devices for dentistry - Equipment

Aug 29, 2011
95.99   Withdrawal of Standard   Nov 30, 2015

General information

95.99     Nov 30, 2015

ISS

Z106

European Norm

11.060.20  

English  

From plan 2011

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Scope

This European Standard specifies general requirements for dental equipment used in the practice of dentistry and which are medical devices. It includes requirements for intended performance, design attributes, components, packaging, marking, labelling, and information supplied by the manufacturer.
This European Standard does not apply to dental X-ray equipment.
This European Standard does not apply to any dental instruments connected to an item of dental equipment. These instruments are covered by EN 1639.
Tests for demonstrating compliance with this standard are contained in the level 3 standards, if appropriate.

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

93/42/EEC

Medical devices

Harmonized
2007/47/EC

Directive 2007/47/EC of the European Parliament and of the council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market

Life cycle

PREVIOUSLY

WITHDRAWN
SRPS EN 1640:2009

NOW

WITHDRAWN
SRPS EN 1640:2011
95.99 Withdrawal of Standard
Nov 30, 2015

REVISED BY

PUBLISHED
SRPS EN 1640:2015

Related project

Adopted from EN 1640:2009