The registration of a medical device company requires: business license, organization code certificate, tax registration certificate, bank account opening license and medical device business license.
If the production of medical devices, according to the risk of the product and the degree of supervision is divided into I, II, III, if the production of Class I products, you need to go to the local Drug Administration for the record, and then register the product, if the production of Class II, III products, you need to apply for a production license, and then register the product.
Expanded Information
The medical device industry involves a number of industries such as pharmaceuticals, machinery, electronics, plastics, etc. It is a multidisciplinary cross, knowledge-intensive, capital-intensive high-tech industry.
And the basic characteristics of high-tech medical equipment is digital and computerized, is a multidisciplinary, cross-field crystallization of modern high technology, its product technology content is high, high profits, and therefore the various scientific and technological powers, the international large-scale companies competing with each other on the heights of the threshold of intervention is high.
Even in the industry as a whole, lower gross profit margins, input is not high in the sub-industry will continue to have a higher technical content of the product, and from this spawned some of the strong profitability of the enterprise. Therefore, the overall trend of the industry is high input, high yield.
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