1, the difference between the first category is a low degree of risk, the implementation of routine management can ensure its safety, effective medical devices. Such as: surgical instruments (knife, scissors, pliers, tweezers, hooks), scraping board, medical X-ray film, surgical gowns, surgical caps, examination gloves, gauze bandages, drainage bags.
2, Class I and Class II, just need to look at the initials of the medical device registration number, 1 for Class I, 2 for Class II. \x0d\\ The difference between Class I and Class II: \x0d\ Article 5 of the state of the medical devices to implement classification management.
3, Class II refers to, on its safety, effectiveness should be controlled medical devices. Generally by the provincial Food and Drug Administration to approve, issue a registration certificate. Class III refers to, implanted in the human body; used to support, maintain life; potentially dangerous to the human body, its safety, effectiveness must be strictly controlled medical devices.
4, the difference between the three classes of medical devices: different security: a class of medical devices through routine management is sufficient to ensure its safety and effectiveness. Class II refers to its safety, effectiveness should be controlled medical devices.