1
关注
1165
浏览

How to determine the productcategory and classification code?

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

ku13145 二阶会员 用户来自于: 广东省深圳市
2023-09-17 16:49

There are many cases of combination products in activemedical devices.One product contains two independent functionalmodules, and each module belongs to a different classificationcategory and code.In this case, the classification level should bemanaged according to the higher one of the two categories.For the classification codes,if there is already clearly classifiedannouncement,it shall prevail. If not,administrative counterpartsmay justify which module of the product is the major one and use thecategory and code of this module. If manufacture cannot justify, theneither one can be used when submitting and no separate classificationrequest is not needed.

For instance of the Integrated Surgical Equipment of Ultrasoundand High Frequency, the category code of Ultrasound SurgicalEquipment is 01-01-01 and the High Frequency Surgical Equipmentis 01-03-01, both of which are class [l device under 01 categoryso the whole device is also class Il.If the main function is theultrasound surgical, then the application category code should be 01-01-01.


关于作者

问题动态

发布时间
2023-09-17 16:48
更新时间
2023-09-17 16:49
关注人数
1 人关注

推荐内容

动物源性医疗器械的研发,有个关于原材料采购的问题?
Is it necessary to associate EMC test report withelectrical safety test report?
软件测试记录及报告中常见问题有哪些?
血管内支架疲劳试验研究应注意哪些内容?
有源医疗器械主机包含一款外购的成熟工业模块(含软件),模块供应商不能提供完整的软件资料,该产品申报注册时应如何提交软件研究资料?
口腔材料生物学评价中,哪些生物学试验需要采用两种浸提介质?亚慢性毒性试验对样品要求量较大,是否只考虑一种浸提介质即可?
注册申请人住所以及医疗器械生产许可证的地址为某大厦的二层、三层、四层。其中二层生产无菌器械,三层生产有源器械,四层为行政办公室。申报注册二类有源器械,生产地址可否写二层、三层、四层?
骨科植入器械产品疲劳极限应如何获得?
口腔修复用陶瓷材料需考虑哪些性能研究?
注册申请人通过自检方式提交产品检验报告的,应当提交哪些申报资料?