The customer is a French company that mainly produces electrical stimulators, including TENS and EMS technologies.

The rectification audit cycle lasted for a total of 3 rounds. Throughout the entire certification audit and issuance process, our company collaborated with enterprises to complete communication and rectification of issues related to clinical evaluation, product technical characteristics, etc. by auditors one by one, and finally successfully obtained the MDR certificate.

The entire cycle takes about 18 months.