Federal Register of Legislation - Australian Government

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SLI 2011 No. 282 Regulations as made
These Regulations amend the Therapeutic Goods (Medical Devices) Regulations 2002 to establish a new statutory committee to be known as the "Advisory Committee on the Safety of Medical Devices".
Administered by: Health
Registered 09 Dec 2011
Tabling HistoryDate
Tabled HR07-Feb-2012
Tabled Senate07-Feb-2012
Date of repeal 19 Mar 2014
Repealed by Health (Spent and Redundant Instruments) Repeal Regulation 2014

Commonwealth Coat of Arms

Therapeutic Goods (Medical Devices) Amendment Regulations 2011 (No. 3)1

Select Legislative Instrument 2011 No. 282

I, QUENTIN BRYCE, Governor-General of the Commonwealth of Australia, acting with the advice of the Federal Executive Council, make the following Regulations under the Therapeutic Goods Act 1989.

Dated 7 December 2011



By Her Excellency’s Command


1              Name of Regulations

                These Regulations are the Therapeutic Goods (Medical Devices) Amendment Regulations 2011 (No. 3).

2              Commencement

                These Regulations commence on the day after they are registered.

3              Amendment of Therapeutic Goods (Medical Devices) Regulations 2002

                Schedule 1 amends the Therapeutic Goods (Medical Devices) Regulations 2002.

Schedule 1        Amendments

(regulation 3)


[1]           Paragraphs 5.3 (1) (c) and (f)


[2]           Subregulation 5.3 (3)


[3]           Regulation 5.4


[4]           Regulation 9.2


on the day when the application that is to be audited is delivered to an office of the Department specified by the Secretary.


28 days after the day that the applicant is notified of the amount of the fee.


1.       All legislative instruments and compilations are registered on the Federal Register of Legislative Instruments kept under the Legislative Instruments Act 2003. See http://www.frli.gov.au.