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Built for Innovation

Kirsion Medical exists to put proven vascular technology into the hands of the clinicians who use it — supported properly, and understood properly.

EU MDR 2017/745 CE 0344 · DEKRA Class IIb IEC 60601-1 / 60601-2-2 Reg. 2026/275588/07

Why a narrow catalogue

Most device distributors grow by breadth: another line, another specialty, another territory. Kirsion Medical was set up the other way round — one field, understood properly, with the depth to answer a clinical question rather than forward it to a manufacturer in another time zone.

Venous disease is a good field for that. The technique is exacting and the learning curve is real, but the equipment list is short and the outcomes are measurable. A supplier who understands tumescent technique, tip position and why a segment failed to reach temperature is worth more than a catalogue.

Founded from practice

The company was founded and is led from clinical practice rather than from sales. That shapes what gets supplied and how: proctored first cases and theatre set-up are part of supply, not an added service line.

Company

  • Registered nameKirsion Medical (Pty) Ltd
  • Registration no.2026/275588/07
  • Entity typePrivate company
  • Incorporated8 April 2026
  • Registered officeThe Workspace, Units S8 & S9
    Cnr De Beers Avenue & Broadway Boulevard (R44)
    Somerset West, Western Cape, 7130
  • Financial year endDecember
  • TerritorySouth Africa

Regulatory and supply chain

Where we stand

Stated plainly, because anyone buying a Class IIb device should be able to check it.

Regulatory status

  • Device conformityCE marked, Class IIb, EU MDR 2017/745, certified by DEKRA (notified body 0344)
  • SAHPRAEstablishment licence application submitted — pending
  • ManufacturerZhejiang CuraWay Medical Technology Co., Ltd — SRN CN-MF-000025983
  • EU representativeProlinx GmbH, Düsseldorf

Warehousing and distribution

Stock is held in South Africa by RTT, our logistics partner, so a list is not waiting on a shipment.

  • ISO 13485 compliant
  • SAHPRA-compliant warehousing
  • Good Distribution Practice compliant fleet
  • National delivery to hospitals, day theatres and practices

Service and maintenance

Servicing is handled in South Africa by Surgi-Clin, our repairs and maintenance partner.

  • SAHPRA registered, ISO compliant
  • Qualified biomedical engineers nationwide
  • Output verification and electrical safety testing
  • Calibration certificates accepted at facility inspection
  • Loan units where a repair runs long
  • Scheduled preventative maintenance contracts

How we work

Four commitments

These are the things a customer should be able to hold us to, and the things we would want to be judged on.

Med-tech focus

A narrow catalogue in one field rather than a broad one across many. Depth in venous disease is the point.

Engineering-driven

Selection built on specification and conformity — power control, temperature accuracy, sterility, service life.

Clinical excellence

Proctored first cases and theatre set-up as part of supply. We attend your opening list in person.

Global scalability

Built on manufacturing certified to EU MDR, so the model extends beyond a single market.

Support

What comes with the system

Proctored first cases

Access, tumescence, tip position and pull-back reviewed case by case until the workflow is yours.

Theatre set-up

Console siting, sheath and guidewire pairing, tumescent recipe, and the consumables list your scrub team needs on the trolley.

Ongoing service

Fault triage, output verification and maintenance through Surgi-Clin, our South African service partner — not an overseas desk.

Arrange a demonstration at your rooms or theatre

Contact us