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Private Health Insurance (Medical Devices and Human Tissue Products) Rules (No. 1) 2024
No longer in force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Superseded version
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F2024L00770
22 June 2024
-
07 August 2024
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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
17 Listing criteria for medical devices to be listed in Part D 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
18 Cost recovery fees that may be charged
19 Clinical assessment fee
20 Economic assessment fee
21 Full health technology assessment pathway fee
Division 2—Payment of cost recovery fees
22 When cost recovery fee must be paid
23 Person liable to pay cost recovery fee
Division 3—Refunds and waiver of cost recovery fees
24 Refunds
25 Waiver of cost recovery fees
Division 4—Review
26 Reviewable decisions
27 Notice of review rights
28 Internal review of decisions made by delegates
29 Notice of overpayment as a result of a review decision
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Part 5—Miscellaneous
30 Minister may have regard to recommendations and advice
Volume 2
