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ISO 10993-6 FRENCH

Évaluation biologique des dispositifs médicaux - Partie 6: Essais concernant les effets locaux après implantation

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Organization: ISO
Publication Date: 15 April 2007
Status: inactive
Page Count: 30
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

ISO 10993-6 FRENCH
December 1, 2016
Évaluation biologique des dispositifs médicaux - Partie 6: Essais concernant les effets locaux après implantation
A description is not available for this item.
ISO 10993-6 FRENCH
April 15, 2007
Évaluation biologique des dispositifs médicaux - Partie 6: Essais concernant les effets locaux après implantation
A description is not available for this item.

References

This document references:
ISO 10993-1 - Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
Published by ISO on August 1, 2018
This document specifies: — the general principles governing the biological evaluation of medical devices within a risk management process; — the general categorization of medical devices based on the...
This document references:
ISO 10993-2 - Biological evaluation of medical devices Part 2: Animal welfare requirements
Published by ISO on July 15, 2006
This part of ISO 10993 is aimed at those who commission, design and perform tests or evaluate data from animal tests undertaken to assess the biocompatibility of materials intended for use in medical...
This document references:
ISO 5832-1 - Implants for surgery - Metallic materials - Part 1: Wrought stainless steel
Published by ISO on July 15, 2016
This part of ISO 5832 specifies the characteristics of, and corresponding test methods for, wrought stainless steel for use in the manufacture of surgical implants. NOTE 1 The mechanical properties...
This document references:
ISO 5832-2 - Implants for surgery - Metallic materials - Part 2: Unalloyed titanium
Published by ISO on March 1, 2018
This document specifies the characteristics of, and corresponding test methods for, unalloyed titanium for use in the manufacture of surgical implants. Six grades of titanium based on tensile...
This document is referenced by:
BS EN ISO 10993-12 - Biological evaluation of medical devices Part 12: Sample preparation and reference materials
Published by BSI on October 31, 2012
A description is not available for this item.
This document is referenced by:
EN ISO 25539-1 - Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses
Published by CEN on March 1, 2017
This document specifies requirements for the evaluation of endovascular systems (prostheses and delivery systems) and requirements with respect to nomenclature, design attributes and information...
This document is referenced by:
EN ISO 25539-2 - Cardiovascular implants - Endovascular devices - Part 2: Vascular stents
Published by CEN on September 1, 2020
This document specifies requirements for the evaluation of stent systems (vascular stents and delivery systems) and requirements with respect to nomenclature, design attributes and information...
This document is referenced by:
BS EN ISO 10993-10 - Biological evaluation of medical devices Part 10: Tests for skin sensitization
Published by BSI on February 28, 2023
A description is not available for this item.
This document is referenced by:
SN EN ISO 15798 - Ophthalmic implants - Ophthalmic viscosurgical devices
Published by SNV on February 1, 2022
This document is applicable to ophthalmic viscosurgical devices (OVDs), a class of surgical invasive medical devices with viscous and/or viscoelastic properties, intended for use during surgery in...
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