Standard

NS-EN ISO 10993-16:2010

May 2010 Withdrawn

Note: This standard has a new edition: NS-EN ISO 10993-16:2017

Corrigendums and amendments are bought separately.

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Abstract

This part of ISO 10993 gives principles on how toxicokinetic studies relevant to medical devices should be designed and performed. Annex A describes the considerations for inclusion of toxicokinetic studies in the biological evaluation of medical devices.

Document information

Standard from SN
Published: 1 May 2010
Withdrawn: 1 March 2018
Edition: 1
Version: 1
Document type: NAT
ISBN:

ICS 11.100.20
National Committee SN/K 115

Legal references

EU law: 2007/47/EC, 90/385/EEC, 93/42/EEC

Product Relations

Replaced by: NS-EN ISO 10993-16:2017
Referred by: NS-EN ISO 10993-6:2016
Replaces: NS-EN ISO 10993-16:2009
Replaced by: NS-EN ISO 10993-16:2009
Adopted from: EN ISO 10993-16:2010 , 0

Product life cycle

Previous product

Withdrawn

NS-EN ISO 10993-16:2009
Current product

Withdrawn

NS-EN ISO 10993-16:2010
Replaced by

Withdrawn

NS-EN ISO 10993-16:2009

Published

NS-EN ISO 10993-16:2017

NS-EN ISO 10993-16:2010

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NS-EN ISO 10993-16:2017