1
关注
1079
浏览

the question abaot of non-medical device components?

查看全部 1 个回答

ku13145 二阶会员 用户来自于: 广东省深圳市
2023-09-17 16:45

 For the non-medical device components, they are not allowedto be submitted separately, but can be submitted as components ofmedical devices.
If this component is submitted as part of the medical device, itcan be considered and evaluated as part of the whole device, and itshould be inspected and verified together with the whole device.Ifadministrative counterparts does not submit this component, or doesnot inspect or verify the component with the whole device, then itshall not be included in the product structure composition.For example: Printers, Power supply cord, Fiber optic cablesfor endoscope, Connecting cables of neutral electrode, etc. They allbelong to this situation.


关于作者

问题动态

发布时间
2023-09-17 16:45
更新时间
2023-09-17 16:45
关注人数
1 人关注

推荐内容

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?
设计多项标志物联合检测产品需要考虑的问题有哪些?如何确定多项联检试剂的不同组合形式是否可以作为同一注册单元?
外地注册申请人想委托北京市一家三类医疗器械生产企业进行生产,是否可行?
针对肾功能衰竭患者的血液净化产品生物学评价应如何考虑?
牙科基台种类繁多,在进行产品机械性能(抗扭、紧固、耐疲劳性能)评价时,如何选择试验用典型性样品?
体外诊断试剂临床试验的受试人群有哪些要求?
体外诊断试剂增加适用机型的变更注册中,如在新增机型上试剂或样本的加样量发生变化,是否需要提交临床评价资料?
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?
什么是软件核心算法?如果没有医疗影像和数据的后处理算法,是否可以算作无核心算法?
doesthe original model need to be implemented with the newstandard requirements?