To prevent illegal import of medical equipment from other countries without publication of free sales, the Ministry of Health has issued certain policies to govern the process of registration for circulation of medical equipment and facilities. According to Circular No:...
Before releasing type A medical equipment, the establishment in charge of selling medical equipment shall send the declaration of applicable standard specified in Article 22 of Decree No. 36/2016/ND-CP to the Department of Health of the area where such establishment...
According to regulations under Decree no. 36/2016 ND-CP, Medical equipment shall be classified into 2 groups which are divided into 4 types depending on the possible levels of risks related to the design and production of such medical equipment, in...