Medical devices supplied in Australia must be included on the Australian Register of Therapeutic Goods (ARTG) unless a valid exemption applies. The iLivTouch device family supplied by Elastography Australia is TGA approved and ARTG listed, enabling lawful supply and clinical use in Australian healthcare settings.
What TGA approval means for your practice
ARTG listing confirms the device meets Australian therapeutic goods requirements for safety, quality, and performance. Practices can procure and deploy iLivTouch for liver stiffness and steatosis assessment with confidence in regulatory compliance. Confirm the exact ARTG identifier, sponsor details, and cleared intended purpose on the TGA ARTG database or by contacting Elastography Australia.
Related pages
See the broader regulatory overview and clinical evidence hub. For purchasing conversations, request a demo.