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SRPS EN 1641:2015

Dentistry - Medical devices for dentistry - Materials

Oct 30, 2015
Oct 30, 2015

General information

90.93     May 22, 2024

90.20    Jan 15, 2025

ISS

Z106

European Norm

11.060.10  

Serbian  

From plan 2013/zbog nemogućnosti realizacije planira se za 2014/

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Scope

This European Standard specifies general requirements for materials used in the practice of dentistry for the restoration of the form and function of the dentition and which are medical devices. For the purposes of this standard these materials are defined as restorative materials. Dental implants are specifically excluded and described in EN 1642. This standard also specifies general requirements for materials used in the practice of orthodontics. This standard includes requirements for intended performance, design attributes, components, sterilization, packaging, marking, labelling, and information supplied by the manufacturer.
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

Life cycle

PREVIOUSLY

WITHDRAWN
SRPS EN 1641:2011

NOW

PUBLISHED
SRPS EN 1641:2015
90.93 Standard confirmed
May 22, 2024

Related project

Adopted from EN 1641:2009