Standard

NS-EN ISO 14630:2005

Sept 2005 Withdrawn

Note: This standard has a new edition: NS-EN ISO 14630:2024

Corrigendums and amendments are bought separately.

Language English

Services Read Online (No printing ) kr 772,00 Printed and bound Delivery time: 5-10 days kr 965,00

There are no extended editions available for this standard

There are no available corrigendum or amendments for this standard. Any future corrigendum and amendments will be added automatically for subscribers.

Abstract

This European Standard specifies general requirements for non-active surgical implants. This standard is not applicable to dental implants, dental restorative materials, transendodontic and transradicular implants and intra-ocular lenses. With regard to safety, this standard gives requirements for intended performance, design attributes, materials, design evaluation, manufacture, sterilization, packaging and information supplied by the manufacturer, and tests. Tests required to be used to demonstrate compliance with this standard are contained in other levels.

Document information

Standard from SN
Published: 1 September 2005
Withdrawn: 1 May 2008
Edition: 2005-05
Version: 1
Document type: NAT
ISBN:

ICS 11.040.40
National Committee CEN/TC 285

Legal references

EU law: 93/42/EEC

Product Relations

Replaced by: NS-EN ISO 14630:2008
Replaces: NS-EN ISO 14630:1997
Adopted from: EN ISO 14630:2005 , 0

Product life cycle

Previous product

Withdrawn

NS-EN ISO 14630:1997
Current product

Withdrawn

NS-EN ISO 14630:2005
Replaced by

Withdrawn

NS-EN ISO 14630:2008

NS-EN ISO 14630:2005

Access to standards for the entire organization

Benefits of our business solution:

Contact us today for a non-binding offer

NS-EN ISO 14630:2024

NS-EN ISO 14630:2012

NS-EN ISO 14630:2009

NS-EN ISO 14630:2008