MEDICA 2026 | 16–19 November 2026 | Hall 6, Stall F37 | Düsseldorf, Germany
Explore our certified OEM/ODM intravenous cannula configurations. Manufactured under cleanroom conditions with automated assembly, bio-compatible polymers, and rigorous zero-defect quality control.
Universal peripheral IV catheter series featuring standard ISO color-coded hubs, siliconized stainless steel needles, and multi-faceted bevel geometry for painless venipuncture.
Clinical-grade medical disposables designed for high-turnover outpatient departments and surgical suites, offering secure luer-lock attachment and smooth flashback confirmation.
Specialized butterfly-winged catheter system engineered for veterinary medicine, providing flexible fixation on animal limbs and resistance to vein collapse during movement.
Premium medical intravenous device featuring an integrated non-return injection port valve for needle-free bolus medication administration without compromising sterile barriers.
Ultra-fine gauge peripheral vascular catheters tailored for feline, canine, and exotic animal care, ensuring gentle insertion into delicate subcutaneous veins.
High-volume wholesale supply option featuring transparent ergonomic flashback chambers for instantaneous venous entry visual notification in emergency wards.
Advanced safety-engineered veterinary IV catheter incorporating self-activating needle-shielding mechanisms to eliminate accidental needle-sticks for veterinary staff.
Full spectrum safety cannula series designed for comprehensive veterinary hospital usage, ranging from large livestock emergency access (14G) to avian care (26G).
An authoritative analysis on material innovations, needle-stick safety legislation, regulatory compliance frameworks, and contract manufacturing strategies for medical supply importers.
Healthcare authorities globally—including the European OSHA directives, US Needlestick Safety and Prevention Act, and WHO guidelines—are mandating the transition from standard IV cannulas to passive safety catheters. OEM contracts increasingly mandate automatic needle-shielding clips that encapsulate the sharp needle tip immediately upon withdrawal, neutralizing needle-stick injuries (NSIs) and bloodborne pathogen exposures for hospital staff.
Modern catheter manufacturing centers around polymer selection. While Fluorinated Ethylene Propylene (FEP) and Polytetrafluoroethylene (PTFE) offer low friction coefficients and rigid insertion dynamics, Polyurethane (PUR) is rapidly becoming the industry gold standard. Thermosensitive PUR softens inside the patient's vein at body temperature, significantly reducing mechanical phlebitis, catheter kinks, and dwell-time complications.
| Gauge Size | Color Code | Outer Diameter (mm) | Catheter Length (mm) | Water Flow Rate (mL/min) | Primary Clinical Applications |
|---|---|---|---|---|---|
| 14G | Orange | 2.1 mm | 45 / 50 mm | 270 – 290 mL/min | Trauma, Rapid Blood Transfusion, High-Volume Resuscitation |
| 16G | Grey | 1.7 mm | 45 / 50 mm | 180 – 200 mL/min | Major Surgery, Emergency Infusion, Viscous Fluid Transfer |
| 18G | Green | 1.3 mm | 32 / 45 mm | 85 – 105 mL/min | Routine Blood Transfusion, Parenteral Nutrition, Surgical Wards |
| 20G | Pink | 1.1 mm | 32 mm | 55 – 65 mL/min | Core Clinical Standard, IV Medication Administration, Adult Wards |
| 22G | Blue | 0.9 mm | 25 mm | 31 – 36 mL/min | Geriatric Patients, Small Veins, Oncology Infusion Therapy |
| 24G | Yellow | 0.7 mm | 19 mm | 18 – 22 mL/min | Pediatrics, Neonatal Care, Small Animal Veterinary Infusion |
| 26G | Violet | 0.6 mm | 19 mm | 10 – 13 mL/min | Extreme Premature Infant Access, Avian & Exotic Pet Care |
Unlike trading agencies or fragmented contract assemblers, Lars Medicare operates an integrated, single-site manufacturing ecosystem in Sonepat, Haryana, supported by global sales headquarters in New Delhi and North American logistics in Milton, Canada.
Our dedicated tool room designs and builds high-precision injection molds for catheter hubs, flashback chambers, injection caps, and wings. This eliminates dependency on third-party component vendors and ensures tight dimensional tolerances for leak-free Luer connections compliant with ISO 80369-7.
All catheter tip-forming, needle silicone coating, hub tipping, and pouch packaging operations occur inside ISO Class 8 (Class 100,000) cleanrooms. Air purity, temperature, micro-particle counts, and bioburden controls are continuously logged to comply with strict international regulatory standards.
Our fully automated Ethylene Oxide (ETO) sterilizers operate under strict physical parameter validation (temperature, humidity, gas concentration, and exposure time). Each sterilizer cycle undergoes biological indicator (Bacillus atrophaeus) challenge testing and residual ETO testing per ISO 11135.
We provide full OEM brand enablement: custom artwork design, multi-lingual Instructions for Use (IFU), unique device identification (UDI) barcoding, specialized blister strip packing, and custom outer carton loading configured specifically for your market's regulatory framework.
Define gauge configuration, polymer choice (PUR/FEP), wing type, and injection port requirements.
Receive complete technical dossiers (CE, ISO 13485, CoA, Free Sale Certificates) for local registration.
Clinical sample evaluations for insertion force, penetration smoothness, and flashback visualization.
Cleanroom production, automated packaging, ETO sterilization, and port dispatch via Nhava Sheva or DEL cargo.
Making informed sourcing decisions requires understanding the risks associated with unverified medical device brokers versus certified contract manufacturers.
| Evaluation Parameter | Direct Certified Factory (e.g., Lars Medicare) | Third-Party Medical Trading Agent |
|---|---|---|
| Quality System Audits | Direct access to ISO 13485:2016 cleanroom audits, batch device history records (DHR), and raw resin certificates. | Limited visibility into sub-tier suppliers; reliance on re-issued or shared certificates. |
| Regulatory Technical Files | Comprehensive technical documentation, ISO 10993 biocompatibility testing, and ETO residue validation. | Fragmented paperwork often missing country-specific regulatory approvals (e.g., ANVISA, SFDA). |
| Custom Tooling & Modifications | In-house tool room can modify catheter hub dimensions, needle bevel geometry, and gauge color matrices. | Fixed catalogue offerings; unable to adjust component molds or customized flow specs. |
| Batch Consistency & Traceability | 100% automated optical inspection (AOI) for needle tip burrs and tip-hub concentricity. | Variable quality between shipments due to sourcing from multiple unaligned factories. |
| Supply Chain & Landed Cost | Transparent direct FOB/CIF/DDP pricing without middleman markup or agent commissions. | Hidden markups, fluctuating lead times, and lack of direct control over production schedules. |
Find authoritative answers to critical inquiries regarding regulatory support, OEM private labelling, sterilization standards, and minimum order quantities for international distributors.
Every export consignment shipped from our manufacturing facility is accompanied by a full regulatory compliance dossier. This includes our CE Certificate under European directives, ISO 13485:2016 Quality Management Certification, EC Declaration of Conformity, Certificate of Free Sale (CFS), and batch-specific Certificates of Analysis (CoA). Additionally, we provide biological indicator incubation results, physical testing logs (tensile strength, flow rate, and pressure leakage), and Ethylene Oxide (ETO) residual analysis reports compliant with ISO 10993-7.
Standard peripheral IV cannulas require clinicians to manually shield or dispose of the exposed stainless steel needle post-catheter placement, presenting a risk of accidental needle-stick injuries. Safety IV catheters incorporate an integrated passive needle safety clip mechanism. As the introducer needle is withdrawn from the catheter hub, the spring-loaded metallic clip automatically engages and permanently encapsulates the needle tip. This passive activation requires no extra steps by the healthcare provider, fully protecting clinical personnel from blood-borne cross-contamination.
Yes. We specialize in OEM and private-label contract manufacturing for medical device distributors, hospital supply chains, and government tender awardees. Our in-house graphics design and technical team handles custom packaging artwork, multi-language Instructions for Use (IFU), customized blister film printing, inner carton design, and master shipping box configuration. All private label packaging is prepared with Unique Device Identification (UDI) matrix codes and GS1-compliant barcodes tailored to your destination country's labeling regulations.
We manufacture catheters utilizing bio-compatible medical polymers, offering Fluorinated Ethylene Propylene (FEP), Polytetrafluoroethylene (PTFE), and Polyurethane (PUR). All our catheter tubings and molded hubs are 100% DEHP-free, phthalate-free, and latex-free, minimizing the risk of toxic leaching or allergic reactions during extended intravascular therapy. Material compliance reports and ISO 10993 cytotoxicity, sensitization, and systemic toxicity testing data are available upon request.
For standard neutral-brand products in stock catalog configurations, minimum order quantities can start at one consolidated pallet. For customized OEM private-label projects, the MOQ generally ranges between 50,000 to 100,000 units per gauge SKU depending on printing tooling setup. Repeat production orders typically complete within 3 to 4 weeks, while initial OEM orders requiring artwork approval and customized mold validation ship within 5 to 7 weeks.
We quote under all major Incoterms 2020 including EXW, FOB (Nhava Sheva / Mundra / Delhi), CIF, CFR, and DDP. Consolidated sea freight shipments are dispatched directly from our manufacturing hub in Haryana through Nhava Sheva or Mundra ports, while urgent air freight orders move via Indira Gandhi International Airport (DEL), Delhi. Our logistics team handles complete export documentation, consular legalization, and Certificate of Origin (COO) issuance.
Partner directly with a certified IV catheter manufacturer. Request factory-direct quotation pricing, technical dossiers, and evaluation samples today.