The registration of medical devices is so important throughout the world that an error found in the built-in process of it can put a person’s life at stake. For every nation, its citizens are essential. They have prime importance. Government bodies cannot compromise the safety of there people. In 2002, Australia also standardized its rules towards “Registration of medical devices.” It has constructed a platform chiefly, a “regulatory body” for the assessment and classification of medical devices. That Regulatory body is called the “Australian Register of Therapeutic Goods (ARTG).” All the medical devices that are up to the mark following the prescribed rules described by ARTG are eligible for the commencement of their businesses in the medical device field in Australia. Inside ARTG, all the related companies have to register themselves. Its rules are to the point, and any loose-hand by a company can ban its product supply in the country. ARTG has some exclusions as well, which are related to low-risk consumer products.