1.Manufacture of class II and class III Medical Device
体系认证
ISO13485:2016
In order to meet the requirements of cleanliness and sterility of products in the fields of implantation and interventional therapy, MeHow Shenzhen GMP Manufacturing center has established a workshop with class 10K/ Class 100K GMP standards and microbiology laboratory. MeHow ShenZhen is the ownner for Medical Device Marketing Authorization Holder System (MAH) certification and also the medical device manufacturing supplier which asigned by FDA US.