1
关注
586
浏览

the transducer and surgicalinstruments can be connected into other manufacturesmain engine?

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 22:45

The compatibility of main engine, transducer and surgicalinstruments of ultrasound soft tissue surgical equipment will havegreat influence on the product safety and effectiveness. The designand development of each part needs to be considered as a wholesystem.
Even if there is sufficient verification and validation on thecompatibility with approved product from other manufacturersduring design and development, while still not able to timely graspthe design change and carry out systematic analysis, then it willresult in the introduction of safety and effectiveness risk due to thecompatibility problem.

Therefore if the administrative counterparts have clear cooperativerelationship with the other manufacturers so as to ensure the productdesign changes between each other can be systematic analyzed, it ispossible to apply. If not, the application will not be possible.

关于作者

问题动态

发布时间
2023-09-17 22:44
更新时间
2023-09-17 22:45
关注人数
1 人关注

推荐内容

通过eRPS 系统进行电子申报的事项如何查询 申报进度?
临床评价时对比试剂的线性范围无法覆盖考核试剂,可以倍比稀释后进行比对吗?
对于出数据的定性试剂,阳性判断值/参考区间可否按照参考区间指导原则做,还是必须用ROC曲线的方法?
申报产品名称、型号规格名称发生了改变,原检验报告是否仍可使用?
IVD设备,同一注册单元包含多个机型的,除了电磁兼容性需要全机型送检外,安全和性能部分的测试,是否可以走典型型号覆盖?
体外诊断试剂注册申报资料中,临床试验相关伦理文件的提交应注意哪些事项?
现场审核提供文审资料内容都有哪些,质量手册,程序文件,作业指导书,生产管理规范自查报告,还需要提供什么资料吗?
第二类有源产品的生物相容性试验所用样品必须是同一生产批次吗?
灭菌包装的无源植入器械,产品货架有效期验证应注意哪些内容?
输液管路与高压造影管路在产品结构组成类似、材料相同的情况下,是否可以列入同一注册单元?