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SRPS EN ISO 14630:2014

Non-active surgical implants - General requirements (ISO 14630:2012)

Jul 31, 2014
95.99   Withdrawal of Standard   Mar 31, 2025

General information

95.99     Mar 31, 2025

ISS

Z076

European Norm

11.040.40  

English  

za komisiju Medicinska sredstva

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Scope

ISO 14630:2012 specifies general requirements for non-active surgical implants. ISO 14630:2012 is not applicable to dental implants, dental restorative materials, transendodontic and transradicular implants, intra-ocular lenses and implants utilizing viable animal tissue.
With regard to safety, ISO 14630:2012 specifies requirements for intended performance, design attributes, materials, design evaluation, manufacture, sterilization, packaging and information supplied by the manufacturer, and tests to demonstrate compliance with these requirements.

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

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WITHDRAWN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 ISO 14630:2011

NOW

WITHDRAWN
SRPS EN ISO 14630:2014
95.99 Withdrawal of Standard
Mar 31, 2025

REVISED BY

PUBLISHED
SRPS EN ISO 14630:2025

Related project

Adopted from EN ISO 14630:2012

Adopted from ISO 14630:2012 IDENTICAL