MEDICA 2026 | 16–19 November 2026 | Hall 6, Stall F37 | Düsseldorf, Germany
Thirteen product families covering IV access, infusion therapy, transfusion, respiratory care and injection. Each SKU is validated for sterility, flow rate and biocompatibility before release.
Peripheral intravenous catheters with tri-facet bevelled needle and radio-opaque FEP tubing for smooth venipuncture and stable indwelling therapy.
Sterile single-use venous access with an automatic needle-shielding clip that encapsulates the sharp on withdrawal to protect clinicians during disposal.
Precision flow-direction device for multi-line infusion and pressure monitoring, moulded from high-clarity polycarbonate with a leak-tested rotating handle.
Vented and non-vented gravity infusion sets with calibrated drip chambers, kink-resistant tubing and roller clamps validated for consistent 20 drops/ml delivery.
Two- and three-part disposable syringes with clearly printed graduations, low-friction plunger travel and sharp lubricated stainless-steel needles.
Oxygen therapy and airway management disposables that support controlled inhalation, nebulisation and suction for critical-care and homecare patients.
Examination and procedure gloves offering high tactile sensitivity, tear resistance and dependable barrier protection for daily clinical handling.
An integrated closed-system catheter with pre-attached extension and needle-free connector that limits blood exposure and line manipulation at the bedside.
Burette sets, dial flow regulators and blood transfusion sets for accurate volumetric dosing where precise fluid management is clinically critical.
Our Sonepat (Haryana) facility was designed so that no critical process is outsourced. Mould design, injection moulding, needle grinding, clean-room assembly, ethylene-oxide sterilisation, validation and packing all happen inside the same quality system — which is why our batch-to-batch consistency holds even at high volumes.
We work with importers, hospital groups and tender agents who need documented quality, predictable lead times and one accountable manufacturer instead of a chain of traders.
Since 2005 Lars Medicare has supplied medical disposables into public tenders, private hospital chains and distributor networks across Africa, Latin America, the Middle East, the CIS region and South-East Asia — with repeat business as the main measure of our performance.
Safety shields, blood-control septa and closed-system catheters are developed in-house with our own tooling. When a market needs a different gauge mix, flow rate or connector standard, we prototype and validate it rather than reselling a fixed catalogue.
CE certificates, ISO 13485 scope, EC Declaration of Conformity, Free Sale certificates, ISO 10993 biocompatibility data and EO residue reports are prepared in the format your regulator expects — reducing registration and clearance friction.
Our export managers work with the plant's QA and R&D staff, so questions about sterilisation validation, shelf life, drop factor or packaging integrity get a factual answer — usually within one working day, in your time zone.
A transparent four-stage OEM and bulk-supply workflow that keeps regulatory, artwork and logistics milestones visible from day one.
Share your SKU list, gauge mix, drop factor and regulatory market. We respond with specifications, packing details and the applicable certificates.
Evaluation samples are dispatched with batch documents so your clinical team can test insertion force, flow accuracy and pack integrity before commitment.
Private-label design, multilingual IFUs, barcodes and UDI-ready labelling are proofed and locked; tooling adjustments are completed where required.
Batch manufacturing, EO sterilisation, QC release and container loading — with FOB, CIF or DDP terms and full export documentation.
16–19 November 2026 · Hall 6, Stall No. F37. Review safety IV cannulas, closed IV catheter systems and DEHP-free infusion sets in person, and discuss market-specific OEM programmes with our export and QA team.
Direct access to decision makers keeps quality, pricing and delivery commitments in one place.
Leads manufacturing strategy and quality governance, with two decades of hands-on experience in disposable medical device production and export compliance.
Oversees international business development, distributor partnerships and OEM programme management across EMEA, Asia and Latin America.
Supports customers from our Milton, Ontario office, handling North American supply planning, documentation and after-sales coordination.
Practical answers on certification, OEM, MOQ, lead times and shipping terms — the questions our export desk receives most often.
Every export consignment is supported by a CE certificate, ISO 13485:2016 quality management certification, EC Declaration of Conformity, Certificate of Free Sale, batch-wise Certificate of Analysis, ethylene-oxide sterilisation validation records and residue reports. Technical files are prepared in the format required by your national regulator, which shortens product registration in Africa, Latin America, the CIS region, South-East Asia and the EU.
Yes. We manufacture under your own brand, including artwork design, multilingual instructions for use, custom pouch and carton printing, barcoding, UDI-ready labelling and country-specific pack configurations. Because the tool room, moulding shop and clean-room assembly lines are in-house, colour codes, gauge mixes and pack quantities can be adapted without depending on third-party vendors.
For standard neutral-pack items an order can begin at one mixed pallet. For private-label programmes the MOQ is defined per SKU based on printing and tooling needs. Repeat orders of catalogue items normally ship in 3–4 weeks; first-time OEM programmes need 5–7 weeks to allow artwork approval, sterilisation cycles and pre-shipment inspection.
Yes. IV infusion sets, measured volume burette sets and blood transfusion sets can be produced with DEHP-free, phthalate-free compounds and latex-free components for paediatric, neonatal and oncology use. Material certificates and ISO 10993 biocompatibility test reports are provided on request.
Our safety IV cannula uses a passive needle-shielding mechanism that encapsulates the needle tip automatically on withdrawal, so the sharp is never exposed during disposal. Combined with Blood Control Technology — which stops blood flashback at the catheter hub — it lowers both sharps-injury exposure and blood-borne contamination in high-turnover wards and emergency departments.
We quote FOB, CIF and DDP. Consignments move through Nhava Sheva and Mundra sea ports and Delhi (DEL) air cargo, with consolidated container loading from our Sonepat facility. Documentation includes the commercial invoice, packing list, bill of lading or airway bill, certificate of origin and the applicable free-sale certificate.
Store cartons in a dry, well-ventilated area away from direct sunlight and solvents, within the temperature range printed on the label, and keep pouches sealed until the point of use. Follow the first-expiry-first-out principle, never re-sterilise a single-use device, and inspect each pouch for integrity, expiry date and sterilisation indicator colour before clinical use.
Lars Medicare exports IV cannulas, safety IV cannulas, three-way stopcocks and a complete range of medical consumables for hospital, clinic and homecare use. Send us your SKU list and target market, and our team will respond with technical data sheets, certificates and packing details.
We support distributor appointments, bulk hospital procurement, tender documentation and OEM private-label programmes.
Contact our export teamProcurement notes, market guides and event updates written by our export and quality teams.
Regulatory checkpoints, CE documentation and landed-cost considerations when importing IV consumables into the European market.
Hall 6, Stall F37, 16–19 November 2026 — live demonstrations of safety IV cannulas, closed catheter systems and infusion sets.
How South African distributors evaluate manufacturers on certification, lead time and total cost rather than unit price alone.