What this instrument covers
The Private Health Insurance (Medical Devices and Human Tissue Products) Rules (No. 3) 2026 is a rule change made under the Private Health Insurance Act 2007. It sets out which medical devices and human tissue products private health insurers are required to cover. The instrument is administered by the Department of Health, Disability and Ageing.
Status of this version
This version, No. 3 of 2026, applied from 22 June 2026. It has since been repealed as of 31 October 2026, meaning it is no longer in force.
The source text does not specify what changed in this version compared to earlier versions, nor does it detail the specific devices or products listed.
Who this mainly affects
This mainly affects private health insurers rather than everyday small businesses, though health providers who deal with private health insurance claims for medical devices or tissue products may be indirectly affected.
Key actions
- If a business deals with private health insurance claims for medical devices or human tissue products, check the Federal Register of Legislation at https://www.legislation.gov.au/F2026L00773 to see the current version in force, since this one has been repealed
- Confirm with the relevant private health insurer or industry body whether a newer version of these Rules has replaced this one and what it covers
This is a plain-English summary for information only, not legal or compliance advice. Always check the official source or consult a qualified professional.