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Mastech is authorized to draft an official document about restrictive standards in the medical device industry   According to SFDA document No: 359(2004) about <<Notice regarding modification to restrictive standards in the medical device industry>>, Mastech is authorized to draft an official document about this project. Mastech and JiNan Medical Device Quality Examination Center are responsible to draft restrictive standards in the medical device industry about sterile disposable syringe. Technical commission belongs to the State Medical Syringe Standards Technology Commission. It marks that sterile disposable syringes produced by Mastech have reached the leading level in our country and have been approved by the State privileged department in design, production and quality supervision control procedure.