With the increase in the export volume of epidemic prevention products such as masks and protective clothing, market regulatory authorities have found that some individuals and organizations, with the purpose of making profits, use information such as "handling CE certification" to induce enterprises to entrust them to represent so-called "CE certification certificates" that are actually invalid or unnecessary, and charge high fees based on this. This not only causes economic losses to enterprises, but also seriously disrupts the order of the certification market.

The information of the notified body can be obtained from the certificate to check whether the notified body issuing the certificate has the corresponding qualifications of the EU medical device directive MDD 93/42/EEC, the MDR medical device regulation (EU) 2017/745 or the (EU) 2016/425 personal protective equipment regulation.