Australian Market Approval
The Therapeutic Goods Administration regulates medical devices supplied in Australia. The RX1 is included on the Australian Register of Therapeutic Goods (ARTG), confirming it meets the safety, performance, and quality requirements of the Therapeutic Goods Act 1989.
- Included on the Australian Register of Therapeutic Goods
- Compliant with Therapeutic Goods (Medical Devices) Regulations 2002
- Australian Sponsor on file with TGA
Full documentation available on request. Contact support@revogenlab.com.