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Repealed by Therapeutic Goods (Medical Devices—Excluded Purposes) Specification 2020
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Legislative Instrument
 
F2010L01889 : Authoritative PDF Document : 0.2MB Primary Document Icon F2010L01889 : ZIP Document : 26KB
2 pages
 

Explanatory Statement
 
F2010L01889ES : PDF Document : 13KB Primary Document Icon F2010L01889ES : ZIP Document : 11KB
2 pages