Federal Register of Legislation - Australian Government

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Specifications as made
This Specification sets out those purposes (excluded purposes) for which a kind of in-vitro diagnostic medical device for self-testing may not be used. In-vitro diagnostic medical devices to be used for purposes that are excluded can not be included in the Australian Register of Therapeutic Goods.
Administered by: Health
Registered 30 Jun 2010
Tabling HistoryDate
Tabled HR28-Sep-2010
Tabled Senate28-Sep-2010
Date of repeal 01 Oct 2020
Repealed by Therapeutic Goods (Medical Devices—Excluded Purposes) Specification 2020
Enabled by
Authoritative version Therapeutic Goods Act 1989
C2004A03952No. 21, 1990