Qualification and material requirements:
First of all, is a medical device imported products must have imported medical equipment registration certificate, this certificate each product has a, in the State Drug Administration for.
Importing units for the first and second class of imported units, should provide inspection and quarantine agencies issued by the classification of imported units documents
Additionally you need to determine through the customs code (best to do a pre-categorization to determine the tax number and whether it is a medical device) to determine whether you need to provide the certificate of 3C certification and other certificates.
Documents required by the inspection regulations
The inspection and quarantine agencies to implement on-site inspection of imported medical devices and supervision and inspection may include:
(a) verification of the consistency of the product and the relevant certificates;
(b) the number, specifications and appearance of the inspection;
(c) packaging, labeling and marking of the inspection, such as The use of wooden packaging, the implementation of quarantine;
(d) instructions, verification of random documentation;
(e) mechanical, electrical, electromagnetic compatibility and other safety inspections;
(f) radiation, noise, biochemistry, and other health inspections;
(g) emissions of toxic and hazardous substances, residues, and environmental protection inspections of materials;
(viii) involving diagnosis, treatment of medical devices, performance testing;
(ix) product marking, labeling and verification of Chinese instructions.
Medical equipment import consulting Xin Poster Customs