CE certification directives on medical device products to coordinate the management of medical device products in European countries.

If domestic manufacturers want to develop the European market, they must obtain the EU CE certification, which is also a qualification for exporting medical device products to the EU market. The European Union implements the more stringent EN46001 in the quality assurance system of medical device products, which has detailed implementation rules and regulations in the MDD appendix issued by the European Union, and Chinese manufacturers should carefully study and refer to the production of the provisions.

The above is the ETL certification manufacturer's detailed introduction to the CE certification is to open the European market of medical equipment, I hope to help you, if you need to reprint, please indicate the source, Thank you for your cooperation!