China proposed Rules for Unique Device Identification System for Medical Device

China Food and Drug Administration proposed rules specify the content of the Unique Device Identification (UDI) system for medical device in China and the requirements of each chapter. It stipulates the responsibilities of the stakeholders, the application requirements of UDI system and the definitions of relevant terms.

Product covered:- Drugs

HS code: 30

Proposed date of adoption: NA

Proposed date of entry into force: NA

Final date for comments: 08-06-2018

If the Proposal/Notification/Regulation will affect your International Business please send us your representation with facts and figures , so that these can be taken up suitably.