Medical device product sales certificate is approved by the Food and Drug Administration, for the medical device export trade enterprises, for this type of documents required for the materials are probably: a copy of the business license, medical device product export sales certificate registration form, a copy of the medical device product registration certificate, a copy of the medical device production license and the material The authenticity of the commitment letter.
If a company develops and operates Class II medical devices, it needs to apply for Class II medical device company business filing, Class III medical devices for medical devices to carry out business licenses, and for the improvement of the production technology enterprise exports, you need to apply for the appropriate medical device registration certificate and production license according to the type of medical devices in China.
Import and export operation right refers to the import and export enterprises to carry out import and export business qualification, apply for import and export operation right of the enterprise only to get the City Bureau of Commerce, Inspection and Quarantine Bureau, the electronic port, the urban customs and other relevant departments of the approval, in the above departments for approval of the approval of various types of certificates, the enterprise is really have the right to import and export rights, can be engaged in import and export business.