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现行 ISO/TR 10993-55:2023
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Biological evaluation of medical devices — Part 55: Interlaboratory study on cytotoxicity 医疗器械的生物学评价.第55部分:细胞毒性的实验室间研究
发布日期: 2023-02-06
本文件描述了2006年进行的一项国际实验室间研究的结果,该研究旨在评估两种不同试验方案在医疗器械生物学评价中细胞毒性效应方面的性能。这些测试的结果用于修订ISO 10993-5。[2]此外,这些测试的结果用于估计这些活细胞测试系统的准确性,以定义被认为是细胞毒性作用的阈值。 笔记?细胞毒性作用的测定在医疗器械生物学评价中具有很高的相关性;根据ISO 10993-1[1],这是建议对每种设备进行的极少数测试之一。

This document describes the results of an international interlaboratory study conducted in 2006 to evaluate the performance of two different test protocols in terms of the cytotoxic effects in the biological evaluation of medical devices. The results of these tests were used for the revision of ISO 10993-5.[2] Furthermore, the results of these tests were used to estimate the accuracy of these test systems with living cells to define a threshold what is considered a cytotoxic effect.

NOTEThe determination of cytotoxic effects has a high relevance in the biological evaluation of medical devices; according to ISO 10993-1[1], it is one of the very few tests which are proposed to be performed for every kind of device.

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发布单位或类别: 国际组织-国际标准化组织
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研制信息
归口单位: ISO/TC 194
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