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Latest certification requirements of CCPIT for information d


EDIT TIMES:2020-06-12 17:34
1、 Certification requirements of CCPIT for masks and non epidemic prevention materials:

1. Non masks:

A. Documents issued by competent government departments and third-party testing institutions:
Requirements: one certificate and one trial(official website or telephone confirmation);
Attestation testimony: A. original - Certified seal is true; B. photocopy - Certified photocopy is consistent with the original;

B. Documents, contracts, statements and free sales certificates issued by the enterprise itself:
Requirements: the expression is used for non-medical use
Materials required:
a. Business license b. Product test report;
c. Letter of guarantee d. Joint declaration of exporter and importer;
e. Customs declaration.

2. Masks:

The certification requirements and required information are the same as those for non masks.

1. Export according to foreign standards: the Ministry of Commerce's white list and not the blacklist of the market supervision and Administration Bureau in Document No. 12;
1 2. Export according to domestic standards: as long as the enterprises are not on the blacklist.



2、 Certification requirements of CCPIT for epidemic prevention materials documents:

1. Documents issued by competent government departments and third-party testing institutions:
Requirements: one certificate and one trial(official website or telephone confirmation)
Br - certified copy of the original certificate
2. Documents, contracts, statements and free sales certificates issued by the enterprise itself:
Requirements: for the enterprises in the No.5 document of the drug administration website, the product name should be consistent with the document No.5;
the Information required:
a. Business license(business scope includes medical device related);
b. Record certificate or production license of medical device products c. Production record certificate or production license of medical device;
d. Business record certificate or production license of medical devices e. Product test report;
f. Letter of guarantee(see No. 115 document of the General Assembly)
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