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Gunma joins a university hospital and a heavy-ion centre with vehicle plants. MediGear partners cover both sides.
Gunma pairs a university hospital with one of the few heavy-ion treatment centres in the country, so a medical equipment partner here meets advanced clinical buyers alongside a strong manufacturing base. Gunma University Hospital leads from Maebashi, the prefectural cancer centre sits in Ota, and Takasaki carries general volume.
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 businesses in Gunma selling into Gunma University Hospital at Maebashi, the prefectural cancer centre at Ota, the Takasaki general hospitals, municipal hospitals, occupational health services in the Ota industrial belt, clinics and laboratories.
Three program tracks are open to businesses in Gunma. 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. The role suits representatives comfortable with advanced radiotherapy and imaging conversations, and with the occupational clinics attached to the vehicle plants around Ota. Care facilities across the prefecture reorder rehabilitation equipment steadily. Dental practices in Maebashi and Takasaki buy chairside items regularly. Clinics in Ota buy small imaging items on their own account. Plant clinics around Ota keep their own equipment lists.
Distributors represent MediGear in an agreed country, region or territory and actively develop the local market — the Gunma prefecture alone, a wider regional area, 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 Japanese companies holding a corporate number and a genuine 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 stores and e-commerce operators
Biomedical engineering firms adding equipment sales to service contracts
Practice fit-out, day surgery and healthcare project companies
Dental, laboratory and long-term care equipment resellers
Persistence matters more than size. Maebashi evaluates specialist equipment thoroughly and expects application support afterwards. Takasaki buys on volume and service response, while the Ota plants keep their own maintenance schedules. Isesaki and Tatebayashi order in scheduled rounds. Kiryu clinics buy small items steadily. Numata and Annaka order occasionally. Maebashi clinics reorder consumables monthly. The prefectural framework sets the purchasing rounds that municipal hospitals draw against.
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 buyers in Gunma.
Regulatory support. Country-specific import guidance, certification documentation and connections to local regulatory consultants for market entry questions.
Medical devices are regulated under the Pharmaceuticals and Medical Devices Law, with scientific review carried out by the Pharmaceuticals and Medical Devices Agency and approvals issued through the health ministry. Devices are classified into four risk classes with different routes for each, and guidance is published by the PMDA.
A marketing authorisation holder established in Japan is required, holding the appropriate business licence, and lower-class devices are certified by registered certification bodies while higher-class devices are approved centrally. Policy and licensing sit with the Ministry of Health, Labour and Welfare.
Import clearance is handled by Japan Customs, with regulatory status checked alongside tariff treatment at the point of entry. MediGear is not the marketing authorisation holder for partner products 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.
Documentation quality is the first requirement. Japanese reviewers and buyers both expect complete, consistent technical files, and gaps that would pass elsewhere stop a submission here. Licensing is handled from Maebashi, and stock is usually held at Takasaki because it sits on the Shinkansen and expressway junction. Documentation follows the university standard. Inspectors visit the registered premises, and records are held for the statutory period. One Maebashi registration covers Takasaki and Ota without a second filing.
Service depth is the second. Uptime expectations are high, and a partner with trained engineers and spare parts on hand meets a standard that decides repeat business.
Long-horizon supply is the third. Specialist installations here run to long commissioning schedules, and buyers ask about parts availability a decade out. Takasaki is fifty minutes from Tokyo by Shinkansen, which keeps engineers within reach. Maebashi and Takasaki sit twenty minutes apart, which keeps service response short. Stock held at Takasaki covers the whole prefecture within ninety minutes.
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 Japanese framework and is not legal, regulatory or professional advice. Requirements under the Pharmaceuticals and Medical Devices Law, administered by the health ministry with review by the Pharmaceuticals and Medical Devices Agency, depend on the device, its classification, its intended purpose and the marketing authorisation holder appointed in Japan. Partner 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 parts of Gunma 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 Japanese companies holding a corporate number and a genuine route to healthcare buyers: equipment distributors and importers, independent sales agents, online medical supply stores, biomedical engineering firms, hospital project companies, and dental, laboratory or long-term care resellers. Speciality experience carries more weight than company size. Applicants in Gunma with references at the university hospital or the Ota cancer centre are strongly preferred.
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 Japanese 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 handle their own 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 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 one prefecture, a region, or national coverage of a single product group. A territory here is usually taken whole, since the prefecture buys on one schedule.
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 customs documentation for inbound consignments.
Yes. Devices are classified into four risk classes under the Pharmaceuticals and Medical Devices Law, with lower classes certified by registered certification bodies and higher classes approved centrally following review. A marketing authorisation holder established in Japan is required. MediGear is not the marketing authorisation holder for partner products, so confirm your position with the authorities.
Not on its own. Approvals from Europe or the United States support a Japanese submission and are commonly included in the dossier, but Japanese certification or approval and a domestic marketing authorisation holder remain separate requirements. Confirm the route for each device class before quoting.