Proposal to list infusion devices supplied by Teleflex Medical New Zealand

Hospital devices

Consultation Closed

PHARMAC is seeking feedback on a proposal to list medical devices supplied by Teleflex Medical New Zealand in Part III of Section H of the Pharmaceutical Schedule from 1 December 2020.

What we’re proposing

PHARMAC is seeking feedback on a proposal to list medical devices supplied by Teleflex Medical New Zealand in Part III of Section H of the Pharmaceutical Schedule from 1 December 2020.

We propose to list medical devices in the following categories:

Consultation closes at 4pm Monday 2 November 2020 and feedback can be emailed to tyson.edwards@pharmac.govt.nz.

What would the effect be?

From 1 December 2020, Infusion Devices supplied by Teleflex would be listed under a proposed national agreement for all DHB hospitals to purchase under, subject to consultation and approval by PHARMAC’s Board or delegate (“Agreement”).

The Agreement would not be for sole supply and DHBs could continue to purchase other suppliers’ brands of products in the Infusion Devices category.

The Agreement would supersede any existing DHB contracts with Teleflex for the products included in the Agreement. Any product listed in the Agreement and purchased by a DHB would be in accordance with the terms and conditions, including price, stated in the Agreement effective from the date of listing on the Pharmaceutical Schedule.

Teleflex would provide appropriate educational services that would be tailored to the individual needs of DHBs, in formats and at times as required by DHBs.

Pricing for the devices in this 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 inluding:
    • Procurement officers and supply chain personnel
    • Clinical engineers and maintenance services
    • ICU, emergency, and critical care staff
    • Anaesthetists
    • Perioperative care staff
    • Surgeons
    • Oncologists
    • Nurses (both inpatient and community based)
    • Infection control
    • General medical ward staff
  • Suppliers and wholesalers

About the infusion devices

Infusion devices are medical devices used, or associated with devices used, in the infusion of fluids such as medications, intravenous solutions (such as saline, glucose, and electrolyte solutions), blood, total parenteral nutrition (TPN) solutions into the body. This includes medical devices used in intravenous therapy as well as other infusion therapies.

PHARMAC’s infusion devices category includes:

  • non-dedicated and consumable infusion devices not associated with infusion equipment; and
  • infusion equipment and associated devices.

Why we’re proposing this

In 2018 PHARMAC issued a Request for Proposals for:

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 proposals were progressed to contract negotiation, to seek provisional agreements. This proposal is the latest to arise from this process and we expect to consult on further provisional agreements with suppliers of Infusion Devices throughout 2020 and 2021.

Details about our proposal

PHARMAC has entered into a provisional agreement with Teleflex for the supply of infusion devices. The proposal would result in Pharmaceutical Schedule listings for:

  • 121 non-dedicated & consumable infusion devices supplied by Teleflex under the brand names Arrow, Arrow International, Arrow AutoFuser, Arrow EZ-IO, Arrowg+ard Blue, and Arrowg+ard Blue Plus

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

To provide feedback

Send us an email: tyson.edwards@pharmac.govt.nz by 4pm Monday 2 November 2020.

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.

Feedback we receive is subject to the Official Information Act 1982 (OIA) and we will consider any request to have information withheld in accordance with our obligations under the OIA. Anyone providing feedback, whether on their own account or on behalf of an organisation, and whether in a personal or professional capacity, should be aware that the content of their feedback and their identity may need to be disclosed in response to an OIA request.

We are not able to treat any part of your feedback as confidential unless you specifically request that we do, and then only to the extent permissible under the OIA and other relevant laws and requirements. If you would like us to withhold any commercially sensitive, confidential proprietary, or personal information included in your submission, please clearly state this in your submission and identify the relevant sections of your submission that you would like it withheld. PHARMAC will give due consideration to any such request.