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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: 1 December 2016
Status: active
Page Count: 38
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 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 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:
5832-3 - Implants for surgery — Metallic materials — Part 3: Wrought titanium 6-aluminium 4-vanadium alloy
Published by ISO on November 1, 2021
This document specifies the characteristics of, and corresponding test methods for, the wrought titanium alloy known as titanium 6-aluminium 4-vanadium alloy (Ti-6Al-4V alloy) for use in the...
This document references:
5832-5 - Implants for surgery — Metallic materials — Part 5: Wrought cobalt-chromium-tungsten-nickel
Published by ISO on March 1, 2022
This document specifies the characteristics of, and corresponding test methods for, wrought cobalt-chromium- tungsten-nickel alloy for use in the manufacture of surgical implants. NOTE The 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:
BS EN ISO 7405 - Dentistry - Evaluation of biocompatibility of medical devices used in dentistry
Published by BSI on November 30, 2018
A description is not available for this item.
This document is referenced by:
BS EN ISO 11979-5 - Ophthalmic implants — Intraocular lenses Part 5: Biocompatibility
Published by BSI on October 31, 2020
A description is not available for this item.
This document is referenced by:
SN EN ISO 25539-2 - Cardiovascular implants - Endovascular devices - Part 2: Vascular stents
Published by SNV on January 1, 2021
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...
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