All employees of Maizhuo warmly welcome the visit of the EU CE team
The “CE” mark in the EU market is a compulsory certification mark，
Whether it is a product produced by an enterprise within the EU or a product produced by another country, in order to be freely circulated in the EU market, a “CE” mark must be affixed， to indicate that the product meets the basic requirements of the EU Directive on Medical Device Directives. This is a mandatory requirement for products in EU law.
The visit of CE team, will conduct an audit of the EN ISO 13485 upgrade, which is a good opportunity for the Maizhuo team to learn and improve.