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ISO 10993-17 FRENCH

Évaluation biologique des dispositifs médicaux - Partie 17: Établissement des limites admissibles des substances relargables

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Organization: ISO
Publication Date: 1 December 2002
Status: active
Page Count: 34
ICS Code (Laboratory medicine): 11.100

Document History

ISO 10993-17 FRENCH
December 1, 2002
Évaluation biologique des dispositifs médicaux - Partie 17: Établissement des limites admissibles des substances relargables
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References

This document is referenced by:
ASTM F2027 - Standard Guide for Characterization and Testing of Raw or Starting Materials for Tissue-Engineered Medical Products
Published by ASTM on October 1, 2016
This document provides guidance on writing a materials specification for raw or starting materials intended for use in tissue engineering scaffolds for growth, support, or delivery of cells and/or...
This document is referenced by:
ISO 18340 - Endoscopes — Trocar pins, trocar sleeves and endotherapy devices for use with trocar sleeves
Published by ISO on July 1, 2020
This document specifies the design, testing and labelling of trocar sleeves and trocar pins that are universally interchangeable and reusable. It also specifies the design, testing and labelling of...
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