DIN EN ISO 10993-1-2010 医疗器械的生物学评价.第1部分:在风险管理系统内的评价与试验

标准号：DIN EN ISO 10993-1-2010
中文标准名称：医疗器械的生物学评价.第1部分:在风险管理系统内的评价与试验
英文标准名称：Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO 10993-1:2009); German version EN ISO 10993-1:2009
标准类型：C30
发布日期：1999/12/31 12:00:00
实施日期：1999/12/31 12:00:00
中国标准分类号：C30
国际标准分类号：11.100.20
引用标准：ISO 10993-2;ISO 10993-3;ISO 10993-4;ISO 10993-6;ISO 10993-5;ISO 10993-9;ISO 10993-7;ISO 10993-10;ISO 10993-11;ISO 10993-12;ISO 10993-13;ISO 10993-14;ISO 10993-15;ISO 10993-16;ISO 10993-17;ISO 10993-18;ISO 10993-19;ISO 10993-20;ISO 14971
适用范围：The role of this part of ISO 10993 is to serve as a framework in which to plan a biological evaluation which, as scientific knowledge advances our understanding of the basic mechanisms of tissue responses, minimizes the number and exposure of test animals by giving preference to chemical constituent testing and in vitro models, in situations where these methods yield equally relevant information to that obtained from in vivo models. It is not intended that this international standard will provide a rigid set of test methods, including pass/fail criteria, as this might result in either an unnecessary constraint on the development and use of novel medical devices, or a false sense of security in the general use of medical devices. Where a particular application warrants it, experts in the product or in the area of application concerned can choose to establish specific tests and criteria, described in a product-specific vertical standard. This part of ISO 10993 is intended for use by professionals, appropriately qualified by training and experience, who are able to interpret its requirements and judge the outcomes of the evaluation for each medical device, taking into consideration all the factors relevant to the device, its intended use and the current knowledge of the medical device provided by review of the scientific literature and previous clinical experience.