This part of ISO 11737 specifies the general criteria for tests of sterility on medical devices that have been exposed to a treatment with the sterilizing agent reduced relative to that anticipated to be used in routine sterilization processing. These tests are intended to be performed when defining, validating or maintaining a sterilization process.
DIN EN ISO 12625-12-2010由德国标准化学会 DE-DIN 发布于 2010-05。
DIN EN ISO 12625-12-2010 在中国标准分类中归属于: Y33 纸制品。
* 在 DIN EN ISO 12625-12-2010 发布之后有更新,请注意新发布标准的变化。
非常抱歉,我们暂时无法提供预览,您可以试试: 免费下载 DIN EN ISO 12625-12-2010 前三页,或者稍后再访问。
点击下载后,生成下载文件时间比较长,请耐心等待......
Copyright ©2007-2022 ANTPEDIA, All Rights Reserved
京ICP备07018254号 京公网安备1101085018 电信与信息服务业务经营许可证:京ICP证110310号