MeHow’s Shenzhen GMP Manufacturing Center, in alignment with the cleanliness and sterility requirements for products in the fields of implantation and interventional medicine, has established clean rooms and microbiology laboratories that meet the class 10,000 and class 100,000 GMP standards. MeHow Shenzhen holds the Medical Device Marketing Authorization Holder (MAH) System certificate and is also a contract manufacturer for multiple medical device products registered with the FDA of the U.S.