1Therapeutic Goods Information (Medical Devices) Specification 2017

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Therapeutic Goods Information (Medical Devices) Specification 2017

Therapeutic Goods Act 1989

I, JOHN SKERRITT a delegate of the Minister for Health, make this Specification, under subsection 61(5AB) of the Therapeutic Goods Act 1989.

Dated 29 August 2017

(signed by)

JOHN SKERRITT

Delegate of the Minister for Health

1 Name of Specification

This Specification is the Therapeutic Goods Information (Medical Devices) Specification 2017.

2 Commencement

This Specification commences on the day after it is registered.

3 Definitions

In this Specification:

Act means the Therapeutic Goods Act 1989.

Specified medical device means an implantable medical device or an active implantable medical device

Note: ‘active implantable medical device’ has the same meaning as in the Dictionary to the Therapeutic Goods (Medical Devices) Regulations 2002;

‘implantable medical device’ has the same meaning as in the Dictionary to the Therapeutic Goods (Medical Devices) Regulations 2002;

‘medical device’ has the same meaning as in s 41BD of the Act; and

‘therapeutic goods information’ has the same meaning as in s 61 of the Act. This information is expressly limited to information held by the Department; it does not include information that the Department does not hold, for example, information held only by a manufacturer.

4 Specification

For subsection 61(5AA) of the Act, Schedule 1 specifies the kinds of persons in column 1 to whom the kinds of therapeutic goods information specified in column 2 can be released for the purposes specified in column 3.

Note: The therapeutic goods information specified in Schedule 1 can be released by the Secretary to a person specified in Schedule 1 under subsection 61(5AA) of the Act.

Schedule 1 Specification

(section 4)