MEDICA 2026 | 16–19 November 2026 | Hall 6, Stall F37 | Düsseldorf, Germany
Whether you are establishing a new regional distribution channel, procuring bulk medical disposables for hospital systems, or seeking certified OEM private label production, Lars Medicare provides direct technical support and quotation turnaround within 24 hours.
Expand your medical supply portfolio with CE and ISO 13485:2016 certified IV access, infusion therapy, and respiratory devices. We offer complete technical files, regulatory dossiers, free sale certificates, and exclusive country distributor frameworks.
Leverage our integrated tooling, cleanroom moulding, assembly, and validated ethylene-oxide (EO) sterilisation facilities. Custom packaging, multilingual IFUs, UDI barcodes, and specialized product configurations are managed completely in-house.
Ensure reliable clinical quality with batch-tested single-use medical devices. We supply full technical specifications, ISO 10993 biocompatibility compliance data, and competitive FOB, CIF, or DDP container shipment quotes.
Evaluate clinical performance prior to ordering. We supply batch samples accompanied by Certificates of Analysis (CoA), flow-rate test protocols, needle-sharpness testing records, and sterilisation validation reports.
Lars Medicare operates headquarters in India and North America alongside an integrated cleanroom manufacturing facility in Haryana, India, guaranteeing consistent product quality and timely container exports.
Centralizing global tender administration, regulatory compliance dossiers, export logistics, and international distributor partnerships across EMEA, Asia, and Latin America.
Dedicated supply chain management, client relations, customer service, and regional sales execution for healthcare partners in North and South America.
Our state-of-the-art production complex houses an in-house tool room, automated injection moulding, Class 100,000 controlled cleanroom assembly, EO sterilisation chambers, and quality testing laboratories.
At Lars Medicare, we drive continuous innovation in single-use medical device engineering and high-volume sterile manufacturing. We welcome passionate engineers, quality assurance auditors, regulatory experts, and international business managers who share our commitment to clinical safety and excellence.
Explore careers in biomedical design, cleanroom quality management, export compliance, and technical production management at our New Delhi and Sonepat facilities.
Send your resume and professional summary directly to our talent recruitment team for upcoming engineering and export management roles.
Human Resources Desk: [email protected]
Located in New Delhi, India, our corporate office is easily accessible for international procurement visits, regulatory audits, and distributor meetings.