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You might be wondering why the rules that apply to various medical devices are different. This is because the rules depend on how your product is classified by the Therapeutic Goods Administration (TGA). For the most part, the classifications are related to the perceived risk of the product type. The Australian regulatory body has defined several different classifications for medical devices. If you have a basic understanding of medical device classifications, it will be easier for you to…
ContinueAdded by Vicki Partridge on May 22, 2020 at 2:18am — 1 Comment
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