Y
yunlong
Hello,
These might seem as a strange question
but I didn't find any clear explanation for a similar situation :
We manufacture medical devices that needs to be associated with other components such as air compressor and tank receivers to operate.
Our final clients in China (Chinese hospitals) only require a CFDA registration certificate"医疗器械注册证? for the full system (= our medical device + these other components) and no individual CFDA registration for our medical device.
If the full system is registered by our distributors (we are ok with this)...do we still need to possess an individual registration of our devices with the CFDA at any point of the process (during control by CIQ at the border ? other stage of the selling process ?) ?
Any help on that matter would be more than welcome!
谢谢!
These might seem as a strange question
We manufacture medical devices that needs to be associated with other components such as air compressor and tank receivers to operate.
Our final clients in China (Chinese hospitals) only require a CFDA registration certificate"医疗器械注册证? for the full system (= our medical device + these other components) and no individual CFDA registration for our medical device.
If the full system is registered by our distributors (we are ok with this)...do we still need to possess an individual registration of our devices with the CFDA at any point of the process (during control by CIQ at the border ? other stage of the selling process ?) ?
Any help on that matter would be more than welcome!
谢谢!