Downloads
FOI 4998 – Medical Devices and Human Tissue Products (MDHTP) Rules and billing codes [pack 1]
FOI 4998 – Medical Devices and Human Tissue Products (MDHTP) Rules and billing codes [pack 2]
FOI 4998 – Medical Devices and Human Tissue Products (MDHTP) Rules and billing codes [pack 3]
FOI 4998 – Medical Devices and Human Tissue Products (MDHTP) Rules and billing codes [pack 4]
FOI 4998 – Medical Devices and Human Tissue Products (MDHTP) Rules and billing codes [pack 5]
FOI 4998 – Medical Devices and Human Tissue Products (MDHTP) Rules and billing codes [pack 6]
FOI 4998 – Medical Devices and Human Tissue Products (MDHTP) Rules and billing codes [pack 7]
FOI 4998 – Medical Devices and Human Tissue Products (MDHTP) Rules and billing codes [pack 8]
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The FOI request to PHI 66/23 Private Health Insurance (Medical Devices and Human Tissue Products) Rules (No 2) 2023 and includes:
Copies of notices, emails, recordings, phone records and file notes of calls, digital images, notes, draft documents and working documents, which:
- relate to or are otherwise connected with the drafting and enactment of the PHI 66/23 Private Health Insurance (Medical Devices and Human Tissue Products) Rules (No 2) 2023 (MDHTP Rules); and/or
- which include any reference to, or which otherwise relate to, the condition concerning billing codes for surgical guides and biomodels, including but not limited to:
- documents relating to the Prescribed List post-listing review; and
- documents relating to the discussion conducted in September 2023 by the Medical Devices and Human Tissue Advisory Committee.