Help, medical device manufacturers of some of the relevant issues, newcomers do not understand.

Application for product registration certificate is required on-site system assessment, health and environmental aspects of the words to go to the local environmental department to issue an environmental report;

Products sent to the registered type inspection, the inspection report and product technical requirements of the pre-evaluation of the opinion form, the certificate of registration is sent to the inspection you pass the registration through the declaration of pass to be obtained;

Sales of the company's production has been obtained Registration certificate of the product is not required to apply for a business license, but you need to contact the dealer sales qualifications;

If you have now been licensed by the medical device manufacturer, then you declare the product registration process of the system assessment is to come to the site, the requirements of your production environment is in full compliance with the conditions of production, that is to say, to meet the standards of all aspects.

If there is anything unclear, you can leave your QQ, I add you to discuss.