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Mask export customs clearance guide/recent mask
by：VIPUTRANS
2020-07-28
1. Export requirements for non-medical masks:
1. The name of the manufacturer must be displayed on the product or packaging or certificate (in English, the operator’s registration certificate is required).
2. Each small package/box in the goods must have a certificate (must be stamped), and the product or package or certificate must have: implementation standard, production batch, manufacturer name, manufacturer address, production date, validity period ( Indispensable).
3. Statement of non-medical provision.
4. The goods of ordinary masks: First, the outer packaging cannot have Chinese and English medical words; second, the implemented product standards are non-medical standards; third, the products cannot carry FDA or CE en14683 marks. Those with the above words, standards, and marks are medical masks.
5. Product inspection report
2. Export requirements of medical anti-epidemic materials:
1. The business license of the production enterprise.
2. Medical device registration certificate.
3. Declaration of medical supplies (the form cannot be left blank, and the head of the form should not have the word template, stamped with the official seal of the production and sales unit).
4. The medical device has a production license.
5. The manufacturer's inspection report.
6. The product name and model of the manufacturer and the registration certificate must correspond to the customs declaration information, and the production company needs to be in the customs register (the registration number is valid only if the information of the production company can be found on the Drug Administration website).
7. Each small package/box in the goods must have a certificate (must be stamped), and the product or package or certificate must have: implementation standard, production batch, manufacturer name, manufacturer address, production date, validity period, Medical device registration certificate number, medical device license number (indispensable).
With mask implementation standard (for reference only)
European Executive Standard Classification:
EN-149 civil
EN-143 civil
EN-14683 Medical
Domestic implementation standards:
YY/T 0969-2013 disposable medical
YY 0469-2011 medical
GB 19083-2010 Medical
GB 2626-2006 civil
GB/T32610 civil
Has FDA mark (ASTM F2100:19) medical
The word MEDICAIL appears on the packaging
1. The name of the manufacturer must be displayed on the product or packaging or certificate (in English, the operator’s registration certificate is required).
2. Each small package/box in the goods must have a certificate (must be stamped), and the product or package or certificate must have: implementation standard, production batch, manufacturer name, manufacturer address, production date, validity period ( Indispensable).
3. Statement of non-medical provision.
4. The goods of ordinary masks: First, the outer packaging cannot have Chinese and English medical words; second, the implemented product standards are non-medical standards; third, the products cannot carry FDA or CE en14683 marks. Those with the above words, standards, and marks are medical masks.
5. Product inspection report
2. Export requirements of medical anti-epidemic materials:
1. The business license of the production enterprise.
2. Medical device registration certificate.
3. Declaration of medical supplies (the form cannot be left blank, and the head of the form should not have the word template, stamped with the official seal of the production and sales unit).
4. The medical device has a production license.
5. The manufacturer's inspection report.
6. The product name and model of the manufacturer and the registration certificate must correspond to the customs declaration information, and the production company needs to be in the customs register (the registration number is valid only if the information of the production company can be found on the Drug Administration website).
7. Each small package/box in the goods must have a certificate (must be stamped), and the product or package or certificate must have: implementation standard, production batch, manufacturer name, manufacturer address, production date, validity period, Medical device registration certificate number, medical device license number (indispensable).
With mask implementation standard (for reference only)
European Executive Standard Classification:
EN-149 civil
EN-143 civil
EN-14683 Medical
Domestic implementation standards:
YY/T 0969-2013 disposable medical
YY 0469-2011 medical
GB 19083-2010 Medical
GB 2626-2006 civil
GB/T32610 civil
Has FDA mark (ASTM F2100:19) medical
The word MEDICAIL appears on the packaging
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