Ⅰ Ⅱ Ⅲ class of medical devices how to classify
Class III refers to the implantation of the human body; for the support, to maintain life; the human body is potentially dangerous, its safety, effectiveness must be strictly controlled medical equipment.
Generally by the Municipal Food and Drug Administration to approve, issued to the registration certificate.
Class IIII medical devices are classified according to their safety class I, which refers to medical devices that are routinely managed to ensure their safety and efficacy.
But a medical device is the end of the approval of a few categories to the inside of the class is not life-long, is determined by its security, the National Bureau has the right to change its classification, such as masks in the general period are divided into a class,
Generally approved by the Provincial Food and Drug Administration to issue a registration certificate.
