Last week, the General Administration of Customs of the People's Republic of China issued an announcement: In accordance with the "Law of the People's Republic of China on Import and Export Commodity Inspection" and its implementing regulations, the General Administration of Customs decided to implement export commodity inspection on medical supplies under customs commodity numbers such as " 6307900010 " (see the attachment for details) from the date of this announcement.
However, less than forty-eight hours after the General Administration of Customs issued Announcement No. 53, that is, at 14:28 p.m. (April 11) , the Customs issued an emergency notice, providing an authoritative explanation of the specific operations of Announcement No. 53! For the 11 categories of exported legally inspected medical supplies listed in Announcement No. 53, enterprises declare and file customs declarations through a single window. Unlike other exported legally inspected goods, the newly added legally inspected exported medical supplies adopt a verification management method, without the need for origin inspection and no export electronic ledger is required for customs declaration. The content is as follows: In accordance with the requirements of Document No. 72, for the 11 categories (19 commodity codes) of exported medical supplies subject to legal inspection as stipulated in Announcement No. 53, a verification management method is adopted, which means that there is no need for commodity quality inspection or export electronic ledger, and enterprises can declare customs declarations normally. Document submission requirements: For the five categories of medical supplies listed in the "Announcement No. 5" issued by the three ministries, submit the medical device product registration certificate and the company's commitment statement; for medical supplies outside the "Announcement No. 5" issued by the three ministries, the company submits the registration certificate and quality and safety commitment letter, and non-medical supplies are not required to submit registration certificates and quality and safety commitment letters. Source: Cross-border Black Technology |
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