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Join MediGear as a sales agent, authorised distributor or reseller in Australia. Introduce buyers, represent MediGear in your territory, or resell through the business you already run — with quotations, documentation and fulfilment handled by the MediGear team.
Medical equipment reaches Australian wards, theatres and consulting rooms through a fairly tight network of importers, agents and contracted distributors. Getting in depends on the range you can quote and the paperwork you can produce when a procurement officer asks.
MediGear is a UK-registered medical equipment distributor and B2B marketplace working with verified manufacturers and healthcare buyers in more than 80 countries. Its partner program opens that catalogue to Australian businesses selling into hospitals, clinics, day surgeries, dental rooms and aged care providers.
Three program tracks are open to Australian businesses. Different business models, the same catalogue behind them — the right one depends on how much of the transaction you want to own.
Agents introduce qualified hospitals, clinics, distributors and procurement teams to MediGear. The role focuses on generating opportunities and connecting buyers with the team; MediGear handles quotations, supply, documentation and fulfilment. Earnings are commission-based on confirmed sales; no purchasing or inventory is required, and sales materials and product support are provided. It suits consultants and independent representatives who know how a capital request moves through a state or territory health service.
Distributors represent MediGear in an agreed country, region or territory and actively develop the local market — a single state, a group such as Queensland and the Northern Territory, or national coverage of one product group. Products are purchased at distributor level for onward supply, and territorial rights may be exclusive or non-exclusive. Market development, commercial support, and regulatory and import coordination are included.
Resellers purchase at wholesale and resell independently through an existing medical business, online store, sales network or customer base. Order quantities are flexible, and you sell on your own terms to your own customers. Resellers operate independently without territorial or official distribution rights, so there is no territorial commitment and no market development obligation.
The program is open to registered Australian businesses with an ABN and a clear route to healthcare buyers. Applications commonly come from:
Equipment distributors and importers already supplying public and private hospitals
Independent sales agents with contacts in theatre, imaging, pathology or dental
Online medical supply retailers and e-commerce operators
Biomedical engineering firms adding equipment sales to service contracts
Practice fit-out, day surgery and healthcare project companies
Aged care, NDIS, allied health and veterinary equipment resellers
Experience carries more weight than size. A two-person agency with theatre contacts in Adelaide often fits better than a large firm with no clinical relationships.
Competitive margins. Partner-level commercial terms apply across the catalogue, with performance recognised for partners who hit agreed targets.
Full product catalogue. Certified equipment across diagnostics, surgical and therapeutic, lab and pathology, sterilisation, hospital furniture, dental, ENT and ophthalmic, rehabilitation, orthopaedic, cardiology, gastroenterology, neonatal, dermatology, veterinary and spare parts.
Sourcing and quotation support. Send an enquiry and the team sources the product, negotiates with the manufacturer and returns a documented quotation — including items outside the current catalogue.
Direct partnerships team. Order queries, supplier negotiations, logistics coordination, and after-sales issues go straight to the team by email, so you can focus on selling rather than chasing suppliers.
Marketing support. Co-branded brochures, digital assets, product imagery and joint campaigns you can put in front of Australian buyers.
Regulatory support. Country-specific import guidance, certification documentation and connections to local regulatory consultants for market entry questions.
Anyone selling medical devices here works inside the therapeutic goods framework. As a general rule, a device must be included in the Australian Register of Therapeutic Goods before it can be lawfully supplied, unless an exemption applies, and its classification decides how much evidence sits behind that inclusion. The regulator publishes detailed TGA requirements for medical devices.
Legal responsibility for an ARTG entry rests with the Australian sponsor — the party that imports, exports or manufactures the device, or arranges for someone else to do so — and the TGA sets out the steps an Australian device sponsor must follow. Two points deserve stating plainly: a CE marking, UKCA marking or FDA clearance does not by itself authorise supply here, and "TGA approved" must not be used in advertising without authorisation from the regulator.
Importing is separate again. Consignments must clear the Australian Border Force, and permit and labelling requirements differ by product; the government publishes Australian importing requirements for commercial importers. MediGear is not a sponsor and does not give regulatory advice.
Apply online. Complete the partner application form and tell us about your market, your experience and which track interests you.
Discovery call. The partnerships team reviews your application and arranges a call to discuss goals, coverage and fit.
Agreement and onboarding. Sign the partner agreement and complete onboarding, including commercial terms, product training and marketing assets.
Start earning. Begin selling, distributing, or referring while MediGear coordinates manufacturing, documentation, and freight.
Distance comes first. Australia sits a long way from most manufacturing centres, and running relationships with a dozen overseas factories is slow and hard to police for quality. MediGear consolidates that into one vetted manufacturer base.
Breadth comes second. A partner who can quote across imaging, monitoring, theatre and furniture in one response is more useful to a facility manager fitting out a day surgery than one selling a single line.
Timing comes third. Many Australian health services finalise capital purchases before 30 June, when a quickly turned-around, documented quote wins the work.
This page is published for general business and information purposes and is not an offer of partnership. MediGear reviews all applications, and approval is not guaranteed. Any partnership that proceeds is governed by the written terms agreed between MediGear and the partner. Product availability, category coverage, territory arrangements, commercial terms and any commission or margin structure vary by application and may change. The regulatory information here is general information about the Australian framework and is not legal, regulatory or professional advice. Requirements administered by the Therapeutic Goods Administration, including inclusion in the Australian Register of Therapeutic Goods, depend on the device, its classification, its intended purpose, the sponsor and the supply arrangement involved. Australian businesses remain responsible for confirming what applies to their own products, and should obtain qualified regulatory, customs or legal advice where required.
Apply with your business details, the states or territories you cover and the track that interests you. The MediGear partnerships team reviews every application and will come back to you to discuss it.
The program is open to registered Australian businesses with an ABN and a genuine route to healthcare buyers: equipment distributors and importers, independent sales agents, online medical supply retailers, biomedical engineering firms, practice fit-out companies, aged care and allied health resellers, and veterinary equipment specialists. Speciality experience carries more weight than company size.
Three. Sales agents introduce hospitals, clinics, distributors and procurement teams and earn commission on confirmed sales without holding stock. Authorised distributors represent MediGear in an agreed territory, purchase at distributor level and develop the local market. Resellers buy at wholesale and resell independently through a business they already run, without territorial rights or commitments.
No. Joining is free for Australian businesses. There are no registration charges, subscriptions or upfront payments required to become an agent, distributor or reseller. Distributors and resellers purchase the products they sell, and partners cover their own trading costs, such as local delivery, storage, and any marketing they run beyond the assets MediGear provides.
Agents earn commission on confirmed sales rather than a retainer. The rate depends on the product category, the order value and the volume you bring, and is confirmed in writing before you begin introducing buyers. Because agents hold no stock and carry no inventory risk, earnings simply follow completed orders.
Exclusive territorial rights are available to qualified distributors who can demonstrate market reach, financial capability and alignment with MediGear's standards, and are assessed case by case. Non-exclusive distribution is also offered and is more common for partners entering a new product category. A territory may be a single state, a group of them, or national coverage of one product group.
Partners receive onboarding, product knowledge materials, regulatory guidance for their market, sales tools and co-branded marketing assets. The partnerships team handles order queries, supplier negotiations, and logistics coordination, including certification and import documentation for shipments arriving at Australian ports.
As a general rule, yes. Medical devices must be included in the Australian Register of Therapeutic Goods before they can be lawfully supplied here, unless an exemption applies; the required evidence depends on the device classification. Legal responsibility for an ARTG entry sits with the Australian sponsor. MediGear is not a sponsor, so confirm your position with the TGA.
Not on its own. Certification held in Europe, the United Kingdom or the United States does not automatically authorise supply in Australia. Assessments from comparable overseas regulators can, in some circumstances, support an Australian application, but Australian requirements still apply. Partners should also avoid describing products as "TGA approved" in advertising without regulator authorisation.