MEDICA 2026 | 16–19 November 2026 | Hall 6, Stall F37 | Düsseldorf, Germany
Lars Medicare Private Limited is a trusted CE and ISO 13485:2016 certified manufacturer specializing in precision-moulded, single-use medical components. Engineered to rigorous international standards (ISO 80369-7 and ISO 7864), our medical parts ensure seamless integration, zero-leakage reliability, and optimal clinical performance for global healthcare device assemblers, pharmaceutical companies, and bulk importers.
Manufactured in automated ISO Class 8 cleanroom facilities, each component undergoes stringent quality testing for dimensional accuracy, biocompatibility, and structural durability.
Ultra-sharp stainless steel needles engineered with siliconized tri-bevel tips for smooth insertion and reduced tissue trauma. Suitable for standard syringes, blood collection devices, and specialized injection sets.
Dual-function, dual-ended protective closure caps designed to seal male and female Luer connections securely. Provides an effective contamination barrier for IV lines, stopcocks, and catheters during clinical transport and set preparation.
Closed-system needleless access site engineered to protect healthcare professionals from needlestick injuries and prevent microbial contamination during multi-dose IV therapy and fluid administration.
Tight-fitting rubber diaphragm closure cap designed for intermittent injections and flushing of IV cannulas, catheter hubs, and central lines without fluid leakage.
At Lars Medicare, every component is manufactured under complete quality control at our state-of-the-art facility in Sonepat, India. Our integrated tool room and high-precision injection moulding equipment guarantee strict tolerance limits for every single batch.
We provide full technical documentation and regulatory dossiers to streamline product registration and international market entry for our B2B clients.
Certified under ISO 13485:2016 and CE directives, ensuring complete traceability from raw material resin to finished component shipment.
Luer connectors and hub dimensions adhere strictly to ISO 80369-7 specifications for 100% leak-proof compatibility across standard healthcare devices.
Available in bulk non-sterile packaging for device assembly plants or individual sterile blister packs for distribution under FOB, CIF, or DDP terms.
Every shipment is backed by Certificates of Analysis (CoA), material batch compliance certificates, and ethylene oxide validation records.
Answers to standard queries from medical device original equipment manufacturers (OEMs) and importers.
We offer both options. Components can be supplied in bulk non-sterile packaging inside double PE bags for medical device manufacturers with their own cleanroom and sterilisation facilities, or individually EO-sterilised in medical-grade blister/pouch packaging ready for immediate market distribution.
Yes. Lars Medicare operates an in-house tool room and R&D engineering department. We design custom moulds, modify dimensional specifications, and tailor plastic polymer formulations (e.g., DEHP-free, lipid-resistant, latex-free) according to customer engineering drawings.
We provide full Technical Files including ISO 13485 certificate, CE mark certificate, Certificate of Analysis (CoA) per batch, ISO 10993 biocompatibility test reports, and Free Sale Certificates to support regulatory submission in target export markets.
MOQs depend on whether the product is a standard stock component or requires custom tooling/color coding. For standard items, minimum orders start at a single carton or mixed pallet level. For custom OEM moulding, MOQs are aligned with production cycle efficiency.
Contact our technical export team today to receive detailed product specifications, samples, and a competitive FOB/CIF quotation within 24 hours.
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