Unique identification for the 1st batch of medical devices

According to the Rules for the Unique Identification System of Medical Devices promulgated by the National Medical Product-NMPA Administration in August, on October 14, NMPA issued Notices for the Unique Identification for the First Batch of Medical Devices, which clearly stipulated the scope, schedule and work requirements. According to the circular, some high-risk class III medical devices such as active implants and passive implants are identified as the only implementation varieties of the first batch of medical devices. Nine categories and 64 varieties of pacemaker, hip prosthesis and plastic injection filler were listed in the first batch of products withRead More →

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