1
关注
879
浏览

could the software information in the devicecertificate be updated during Registration Renewal?

您还未登录!暂时最多只可查看 1 条回答

登录! 还没有账号?去注册

ku1314520 一阶会员 用户来自于: 广东省深圳市
2023-09-17 22:13

Active medical devices and the cooperated softwareare independent medical devices, each with its own registrationcertificate, and the version of the cooperated software is permissionitems of the registration certificate of medical devices, so it cannot bechanged during the Registration Renewal.
If the medical device is meant to be used with the updatedversion of the software, it shall apply for the Change of PermissionItems, and provide the safety and effectiveness evidence of thecooperation with the new version of the software. If there's noChange of Permission Items submitted, the medical device cannot beused with the new version of software, while still be able to be usedwith the previous version the software.


关于作者

问题动态

发布时间
2023-09-17 22:13
更新时间
2023-09-17 22:13
关注人数
1 人关注

推荐内容

体外诊断试剂临床试验机构间样本如何分配?
生化试剂产品试剂盒中增加校准品或质控品(原试剂盒中未提供配套校准品或质控品)的情况,可以变更注册么?
骨科植入器械力学性能研究应提供哪些资料?
医用电器设备在什么情况下需要进行环境试验?
骨科植入器械进行性能研究试验时应如何选择典型性产品?
IVD类设备软件和网络安全的安全性级别该如何考虑?
《医疗器械网络安全注册技术审查指导原则》适用于哪些医疗器械?网络安全描述文档是否 可以在软件描述文档中提交?
对于产品材料介导致热性,一般应如何评价?
一次性防护服新增大尺寸的型号规格产品,注册检测时可以只检测新增型号的尺寸要求?变更材料中,是否可以提供有效期、包装、运输验证的评价报告,豁免相关实验?
医疗器械工艺验证,例清洗残留验证的检验,一定要委托第三方有资质(CNAS)检验吗,对资质这一块有明确要求吗(法规未查到有这一方面的规定)?