The attached documents and documents required for import and export declaration | Baitong Logistics
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The attached documents and documents required for import and export declaration

Jan 04,2022

To support to return to work and production enterprise, to help enterprises to apply for link related policies, with the foot with good accurate declaration, customs clearance, according to "about further promote the reform of customs clearance work paperless work related matters of announcement (the General Administration of Customs 2014 no. 25), and other related requirements, small make up to comb the import and export declaration for the attached documents required information below.


Declaration of import

Processing trade and bonded customs declaration forms

When an enterprise declares imports to the customs, it may not submit to the customs documents such as the contract, packing list and cargo manifest (manifest) attached to the declaration form of processing trade and bonded trade.


Non-processing trade and bonded customs declaration forms

When the enterprise declares the import to the customs, it is the declaration form of non-processing trade and bonded trade. The packing list, cargo manifest (manifest) and other documents attached to it may not be submitted to the customs.

Note: the above documents will be submitted again if necessary for customs examination.

Declared export goods

When an enterprise declares to the customs for export (including all kinds of customs declaration forms), it may not submit to the customs documents such as contract, packing list, cargo manifest (manifest) and other attached documents.

Note: the above documents will be submitted again if necessary for customs examination.

Special cargo
The picture
Declaration for export of anti-epidemic materials
With the rapid growth of the export volume of epidemic prevention materials, the state has introduced a series of policies to strengthen supervision:

△ Announcement of the Ministry of Commerce, the General Administration of Customs and the National Medical Products Administration No. 5, 2020, hereinafter referred to as "Announcement No. 5")

△ Implementation of Export Commodity Inspection on Medical Goods (Announcement of the General Administration of Customs [2020] No.53, hereinafter referred to as "Announcement No.53")

△ Announcement on Further Strengthening the Quality Supervision over the Export of Anti-Epidemic Materials (Announcement No.12, 2020 of the Ministry of Commerce, the General Administration of Customs and the State Administration for Market Regulation, hereinafter referred to as "Announcement No.12")

When an enterprise declares that the export goods belong to epidemic prevention materials, it shall, according to the different circumstances of the declaration, provide relevant attached documents as required.

A situation

For Novel Coronavirus detection reagents, medical masks, medical protective clothing, respirators and infrared thermometers that meet China's quality standards, please submit the "Registration Certificate of Medical Device Products" (which can be checked through the website of the "State Food and Drug Administration" at www.nmpa.gov.cn) and the "Declaration of Medical Supplies for Export" (either written or electronic statement) according to the requirements of "Announement No. 5".
The medical device product registration certificate shall be the original or the scanned copy of the original.


Case 2

Not given drug regulatory approval in China for medical equipment product registration certificate, but for foreign standards certification or registration will be coronavirus detection reagent, surgical masks, medical protective clothing, breathing machine, infrared thermometer, in accordance with requirements of the "12 announcement", submit "declaration by export medical supplies", commitment to product conform to the requirements of the importing countries (regions) quality standards and safety.


Scenario 3

When exporting the newly added medical materials in Announcement No. 53, enterprises should indicate whether they are medical or not when declaring to the customs. According to the management category of Classification Catalogue of Medical Devices, it is suggested to provide the registration/filing certificate of medical devices and the statement of quality and safety respectively according to the requirements of Announcement No. 5.
Registration certificate/filing certificate of medical device products should be the original or the scanned copy of the original.

Scenario 4

When exporting non-medical masks, enterprises should submit the "Joint Statement of Exporting and Importing Parties" as the attached documents according to the requirements of Announcement No. 12, to confirm that the products meet the quality standards of China or foreign countries, and that the importer accepts the quality standards of the products purchased and is not for medical purposes.

Special instructions
01

The declaration in the above four cases is issued by the "domestic consignor" on the customs declaration form;
If the "production and sales entity" on the customs declaration form entrust the domestic consignor to export, the production and sales entity shall issue a statement of commitment on quality and safety and provide a power of attorney.
The customs will not accept the declaration issued by the declaration unit.

02

If the aforesaid epidemic prevention materials are exported in the form of foreign aid materials, the enterprises implementing foreign aid projects under the charge of the Ministry of Commerce shall submit the Foreign Aid Project Task Notice issued by the Ministry of Commerce, the Leading Group of the Inter-ministerial Working Mechanism of Emergency Aid or the project management agency when applying for export.

03

If the aforesaid epidemic prevention materials are exported in the form of donated materials, the enterprises shall submit relevant certificates of donation when declaring for export.

04

For epidemic prevention materials imported and re-exported, the enterprises shall submit the import medical registration certificate issued by the drug administration department and the enterprise quality standard commitment statement when applying.

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