Sale on Manual & Electric Hospital Beds - Starting from 25 September!
Korean certification turns on manufacturing evidence. MediGear partners obtain it from the manufacturer and clear the longest step first.
South Korea has one of the most technically advanced hospital sectors in Asia and a strong domestic manufacturing base, so imported equipment has to justify itself on capability. Approval requires a licensed importer and a documented quality system behind the product.
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 South Korean businesses selling into tertiary university hospitals, general hospitals, private clinics in Seoul and Busan, diagnostic laboratories and dental clinics.
Three program tracks are open to South Korean 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 understand how a tertiary hospital procurement committee assesses new equipment.
Distributors represent MediGear in an agreed country, region or territory and actively develop the local market — the capital region, the provinces, or a single product family nationally. 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 Korean companies holding a business registration 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 retailers 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 aesthetic clinic equipment resellers
Import licence capability is the qualifier. A firm holding an import business licence is worth far more than a larger one that would need to obtain it first.
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.
Medical devices are regulated by the Ministry of Food and Drug Safety under the medical device legislation, with devices sorted into four risk classes. Lower classes are certified by designated bodies and higher classes approved by the ministry itself. Guidance is published by the MFDS.
An importer must hold an import business licence, and quality system certification to the Korean standard is required for most devices. Technical documentation is submitted in Korean, and clinical data expectations depend on the class and on whether the device is already approved in a reference market. Device guidance in English is published in the medical device regulations library.
Import clearance is administered by the Korea Customs Service, which applies tariff and permit controls alongside regulatory checks at entry. MediGear is not the licence 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.
Quality system documentation is the first requirement. Korean certification turns on manufacturing evidence, and a partner able to obtain it from the manufacturer clears the longest step in the process.
Second is coverage. Tertiary hospitals refit in whole departments, and a supplier able to answer one line of the specification is rarely shortlisted.
Aesthetic and dental demand is the third. Korea supports an unusually large private clinic sector in these fields, and it buys on its own authority and its own timetable.
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 South Korean framework and is not legal, regulatory or professional advice. Requirements under the medical device legislation, administered by the Ministry of Food and Drug Safety, including classification, certification or approval, quality system certification and the import business licence, depend on the device and its class. 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 provinces you cover 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 Korean companies holding a business registration number and a genuine route to healthcare buyers: equipment distributors and importers, independent sales agents, online medical supply retailers, biomedical engineering firms, hospital project companies, and dental, laboratory or aesthetic clinic resellers. 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 South Korean 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 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 province, a metropolitan grouping, 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 customs documentation for inbound consignments.
Yes. Devices are sorted into four risk classes, with lower classes certified by designated bodies and higher classes approved by the Ministry of Food and Drug Safety. An importer must hold an import business licence, and quality system certification to the Korean standard is required for most devices. MediGear is not the licence holder for partner products, so confirm your position with the ministry.
Not on its own. Approvals held elsewhere support a Korean submission and can reduce clinical data expectations for some products, but Korean certification or approval, quality system certification and an import business licence remain separate requirements. Confirm the route for each device class before quoting.