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Private Health Insurance (Medical Devices and Human Tissue Products) Rules (No. 2) 2023
No longer in force
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Administered by
Department of Health and Aged Care
This item is authorised by the following title:
Private Health Insurance Act 2007
Superseded version
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F2023L01399
18 October 2023
-
10 November 2023
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Volume 1
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Part 1—Preliminary
1 Name
2 Commencement
3 Authority
4 Repeal
5 Definitions
6 Meaning of medical device
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Part 2—Benefit requirements for private health insurance policies that cover hospital treatment and hospital substitute treatment
7 Listing of medical devices and human tissue products
8 Circumstances in which listed items are provided—other than circumstances in which a medicare benefit is payable
9 Conditions to be satisfied in relation to the provision of listed items
10 Benefits for listed items provided as part of hospital treatment
11 Benefits for listed items provided as part of hospital substitute treatment
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Part 3—Listing criteria
12 Purpose
13 General listing criteria
14 Listing criteria for medical devices to be listed in Part A of Schedule 1
15 Listing criteria for human tissue products to be listed in Part B of Schedule 1
16 Listing criteria for medical devices to be listed in Part C of Schedule 1
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Part 4—Cost recovery fees
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Division 1—Cost recovery fees relating to medical devices
17 Cost recovery fees that may be charged
18 Clinical assessment fee
19 Economic assessment fee
20 Full health technology assessment pathway fee
Division 2—Payment of cost recovery fees
21 When cost recovery fee must be paid
22 Person liable to pay cost recovery fee
Division 3—Refunds and waiver of cost recovery fees
23 Refunds
24 Waiver of cost recovery fees
Division 4—Review
25 Reviewable decisions
26 Notice of review rights
27 Internal review of decisions made by delegates
28 Notice of overpayment as a result of a review decision
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Part 5—Miscellaneous
29 Minister may have regard to recommendations and advice
30 Repeal of Part D of Schedule 1
Schedule 1—Listed medical devices and human tissue products
Volume 2