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ISO 10993-11 FRENCH

Évaluation biologique des dispositifs médicaux - Partie 11: Essais de toxicité systémique

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Organization: ISO
Publication Date: 15 August 2006
Status: inactive
Page Count: 34
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

ISO 10993-11 FRENCH
September 1, 2017
Évaluation biologique des dispositifs médicaux - Partie 11: Essais de toxicité systémique
A description is not available for this item.
ISO 10993-11 FRENCH
August 15, 2006
Évaluation biologique des dispositifs médicaux - Partie 11: Essais de toxicité systémique
A description is not available for this item.

References

This document references:
ASTM F619 - Standard Practice for Extraction of Materials Used in Medical Devices
Published by ASTM on August 1, 2020
This practice covers methods of extraction of medical plastics and may be applicable to other materials. This practice identifies a method for obtaining “extract liquid” for use in determining 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 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 10993-12 - Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
Published by ISO on January 1, 2021
This document specifies requirements and gives guidance on the procedures in the preparation of samples and the selection of reference materials for medical device testing primarily in biological...
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:
JIS T 3250 - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
Published by JSA on March 1, 2013
A description is not available for this item.
This document is referenced by:
JIS T 3248 - Extracorporeal blood circuit
Published by JSA on March 1, 2022
A description is not available for this item.
This document is referenced by:
ISO 29942 - Prophylactic dams — Requirements and test methods
Published by ISO on July 1, 2011
This International Standard specifies the minimum requirements and test methods for prophylactic dams used to assist in the prevention of sexually transmitted infections.
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