The Therapeutic Goods Australia (TGA) is responsible for ensuring that therapeutic goods available for supply in Australia are safe and fit for their intended purpose. This includes assessing compliance with a set of internationally agreed essential principles for their quality, safety and performance. Medical devices must be included in the Australian Register of Therapeutic Goods (ARTG), which are then subject to monitoring by the TGA. This monitoring includes a comprehensive adverse event reporting program.
As a registered medical device listed on the ARTG our products are eligible for health care rebates with most Health Funds. This is of course being dependent on your level of cover.
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