Proposal to list medical devices supplied by InterMed Medical Limited

Hospital devices Consultation Closed

Pharmac is seeking feedback on a proposal to list a range of medical devices in Part III of Section H of the Pharmaceutical Schedule.

What we’re proposing

Pharmac is seeking feedback on a proposal to list a range medical devices supplied by InterMed Medical Limited (“InterMed”) in Part III of Section H of the Pharmaceutical Schedule from 1 December 2023 in the following category

Consultation closes at 4pm Wednesday 25 October 2023 and feedback can be emailed to priscilla.patel@pharmac.govt.nz.

What would the effect be?

From 1 December 2023, InterMed’s range of medical devices in the category above would be listed under a national agreement for all Te Whatu Ora Hospitals to purchase under, subject to consultation and approval by Pharmac’s Board or delegate (“Agreement”).

The Agreement would not be for sole supply, with Te Whatu Ora continuing to be able to purchase other suppliers’ brands of anaesthetic machines, invasive ventilators, neonatal care and critical care patient monitoring devices.

The Agreement would supersede any existing Te Whatu Ora contracts with this supplier for the medical devices listed in Schedule 1 in the Agreement. Any device listed in the Pharmac Agreement and purchased by a Te Whatu Ora Hospital would be at the price, terms and conditions stated in the Agreement, effective from the date of listing on the Pharmaceutical Schedule.

Pricing for the medical devices in the Agreement, subject to any prior termination of the Agreement, would not be increased without prior consultation and approval by Pharmac.

Who we think will be interested

  • DHB clinical staff in a range of different clinical settings including but not limited to:
    • Clinical engineers and maintenance services
    • ICU/HDU/NICU
    • Nurses
    • Patient Monitoring
    • Perioperative staff
    • Procurement and supply chain
    • Radiology
    • Wards and Outpatient Clinics
  • Suppliers and wholesalers

About the medical devices

Critical care

Critical care is the provision of specialised, continuous, multidisciplinary care for patients in a life-threatening, but treatable, condition. The critical care devices can loosely be grouped into three categories:

  • Anaesthetic and invasive ventilation devices
  • Neonatal care devices
  • Critical care patient monitoring

Why we’re proposing this

In 2020 Pharmac released a Requests for Proposals (RFP) for the supply of anaesthetic machines, invasive ventilation devices and critical care patient monitoring devices.

The RFP was for non-exclusive national agreements for listing on the Pharmaceutical Schedule.

Pharmac has been working with suppliers who responded to the RFP and were successful in being progressed to contract negotiation to seek provisional agreements. This proposal is the latest to arise from these processes.

Details about our proposal

Pharmac has entered into a provisional agreement with InterMed for the supply of critical care medical devices.

The proposal would result in Pharmaceutical Schedule listings for:

Category

Manufacturer brands

Line items

Critical care

  • HAMILTON-C6
  • HAMILTON-C3
  • HAMILTON-T1
  • HAMILTON-C1
  • HAMILTON-C1neo
  • HAMILTON-MR1
  • HAMILTON MEDICAL
  • HAMILTON-C1
  • HAMILTON-C1neo

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Further information, including pricing and contractual details, has been provided to Te Whatu Ora Hospital Procurement personnel. Clinicians interested in further detail on what this change means for their Te Whatu Ora Hospitals should engage with their Procurement teams.

To provide feedback

Send us an email: priscilla.patel@pharmac.govt.nz by 4pm 25 October 2023.

All feedback received before the closing date will be considered by PHARMAC’s Board (or its delegate) prior to making a decision on this proposal.

Your feedback may be shared

Feedback we receive is subject to the Official Information Act 1982 (OIA). Please be aware that we may need to share your feedback, including your identity, in response to an OIA request. This applies to anyone providing feedback, whether they are providing feedback themselves or for an organisation, in a personal or professional capacity.

We can only keep feedback confidential as allowed under the OIA and other related laws. If you want any part of your feedback treated as confidential, you need to tell us. Please let us know if you want to keep part of your feedback confidential, and why. Is it commercially sensitive, confidential or proprietary, or personal information? Clearly state this and tell us which parts of your feedback you want to keep confidential for these reasons. We will consider your request under our OIA requirements.