Engineered for minimal insertion force, superior flow dynamics, and strict infection control. We manufacture precision peripheral IV Cannulas (14G–26G) in PTFE, FEP, and Polyurethane for distributors, hospital groups, and OEM brand owners in 52+ countries.
Manufactured strictly according to international standards. Features precision back-cut siliconized Japanese stainless steel needles and radio-opaque catheter stripes.
High-speed injection moulding, catheter tipping, micro-hole punching, and ETO sterilization within Class 10,000 (ISO Class 7) cleanrooms in India.
Supplying 52+ countries with full technical files (STED), Free Sale Certificates (FSC), ISO 13485 QMS, and customized OEM packaging formats.
In global healthcare procurement, selecting the right IV Cannula (Intravenous Catheter) manufacturer is a critical balance of clinical safety, mechanical reliability, regulatory compliance, and cost efficiency. As intravenous therapy represents over 80% of inpatient hospital procedures worldwide, procurement teams and medical device distributors face increasing pressure to eliminate catheter failure rates, vascular trauma, and needle-stick injuries while navigating complex international tenders.
Angiplast Private Limited, established in 1994 in Ahmedabad, India, stands as an industry authority in single-use infusion medical devices. We solve core procurement pain points by engineering peripheral IV Cannulas that integrate ultra-sharp siliconized stainless steel needles, bio-compatible polymers (PTFE, FEP, Polyurethane), and leak-proof flashback chambers. Whether supplying national health ministries or contract-manufacturing for global pharmaceutical brands, our vertical integration guarantees batch-to-batch consistency and full lot traceability from resin to sterile barrier pouch.
ISO 13485 Certified · 30+ Years Excellence Angiplast produces a complete array of peripheral intravenous catheters tailored for distinct clinical settings, patient demographics, and safety mandates. Explore our core configurations engineered for maximum performance.
The global workhorse for general inpatient therapy. Features an integrated injection port with a non-return duckbill valve for needle-free intermittent medication delivery without disrupting primary IV lines. Flexible wings ensure stable skin fixation and minimize mechanical movement.
Send an InquiryDesigned for compact handling, oncology, and emergency medical services (EMS). The sleek, wingless pen-type body offers an intuitive grip for clinicians trained in classic insertion techniques, allowing easy dressing application in tight anatomical sites.
Send an InquiryEngineered for procedures requiring continuous infusion without additional medication ports. The ergonomic wing structure provides maximum contact area for secure taping, reducing catheter displacement and phlebitis risks in pediatric and geriatric wards.
Send an InquiryComplies with OSHA Sharps Injury Prevention regulations and EU Directive 2010/32/EU. Integrates an automated passive safety clip that encapsulates the needle tip instantly upon withdrawal, preventing accidental needle-stick injuries (NSIs) and blood exposure.
Send an InquirySpecially tapered micro-catheters designed for fragile peripheral veins in neonates and infants. Features ultra-fine gauge sizes, minimal dead space, and rapid blood flashback confirmation for high-precision pediatric vascular access.
Send an InquiryAdvanced integrated design featuring pre-attached extension tubing and multi-access ports. Reduces touch contamination, minimizes blood leakage during insertion, and provides a continuous sterile barrier for intensive care environments.
Send an InquiryAll Angiplast IV Cannulas follow ISO 10555-5 international color coding standards. Below is our standard dimensional and clinical application chart:
| Gauge (G) | Color Code | Outer Diameter (mm) | Catheter Length (mm) | Water Flow Rate (mL/min) | Primary Clinical Application |
|---|---|---|---|---|---|
| 14G | Orange | 2.1 mm | 45 mm | 270 mL/min | Trauma, rapid blood transfusion, high-volume fluid resuscitation, surgical procedures. |
| 16G | Grey | 1.7 mm | 45 mm | 180 mL/min | Major surgery, rapid fluid replacement, blood infusion, obstetrics. |
| 18G | Green | 1.3 mm | 32 / 45 mm | 85 mL/min | Routine parenteral nutrition, blood administration, pre-operative IV access. |
| 20G | Pink | 1.1 mm | 32 mm | 55 mL/min | Standard inpatient IV infusions, routine medication administration, adult peripheral veins. |
| 22G | Blue | 0.9 mm | 25 mm | 33 mL/min | General IV therapy in elderly patients, oncology, small adult veins, pediatric infusions. |
| 24G | Yellow | 0.7 mm | 19 mm | 20 mL/min | Pediatric patients, neonates, fragile or micro-veins, low flow-rate infusions. |
| 26G | Violet | 0.6 mm | 19 mm | 10 mL/min | Neonatal intensive care units (NICU), specialized micro-vascular access. |
Class 10,000 Cleanroom Assembly One of the most frequent technical inquiries from biomedical engineers and hospital procurement directors centers on catheter resin selection. Angiplast offers three medical-grade fluorinated and thermoplastic elastomer materials, each tailored to specific clinical dwell time requirements:
1. Fluorinated Ethylene Propylene (FEP): Known for its exceptionally smooth surface finish and chemical inertness. FEP catheters feature rigid wall stability that prevents collapsing under negative pressure during blood sampling, offering ideal performance for short-term peripheral venous placement (<48 hours).
2. Polytetrafluoroethylene (PTFE): Delivers maximum coefficient of friction reduction. PTFE IV cannulas slide smoothly into peripheral veins with minimal insertion drag, making them preferred in high-throughput emergency departments.
3. Medical-Grade Polyurethane (PUR): The premium benchmark for extended dwell times (>72 hours). Polyurethane is rigid at room temperature for crisp dermal insertion, but becomes soft and pliable upon exposure to internal body temperature. This thermo-softening effect allows the catheter to conform naturally to tortuous vascular anatomy, drastically reducing mechanical phlebitis, intima irritation, and extravasation risk.
Search intent analysis and procurement queries from hospital groups reveal significant structural shifts in global IV Cannula sourcing. Importers and distributors must align their supply chains with these five key industry macro-trends:
Regulatory authorities across Europe, North America, and LATAM are enacting strict occupational safety laws mandating passive safety IV Cannulas. Buyers are transitioning away from standard cannulas toward needle-shielded models to reduce hospital liability and healthcare worker sharps injuries.
Hospital infection control boards are prioritizing catheter longevity over initial unit price. Polyurethane IV Cannulas that maintain vessel integrity up to 96 hours reduce catheter replacement frequency, saving nursing time, reducing plastic waste, and lowering overall clinical treatment costs.
Global medical brand owners are actively reducing dependency on single-region supply chains. India, led by integrated manufacturers like Angiplast, has emerged as the premier manufacturing alternative, offering cost efficiencies, robust IP protection, and US FDA / EU MDR compliant quality systems.
Modern IV therapy favors closed peripheral IV catheters integrated with needle-free extensions. This setup eliminates blood leakage during hub attachment, reduces catheter-related bloodstream infections (CRBSIs), and protects healthcare workers from bloodborne pathogens.
Importers face stringent technical documentation requirements under EU MDR. Procurement teams demand suppliers capable of delivering ISO 10993 biocompatibility testing, ISO 11135 ETO residual data, GS1-compliant Unique Device Identification (UDI) barcoding, and complete STED technical dossiers.
Hospitals are evaluating packaging material sustainability. Forward-thinking manufacturers offer lightweight medical-grade paper plastic peel-pouches and recyclable outer master cartons that minimize landed freight volume and lower environmental footprint.
Answers to common technical, regulatory, and supply chain questions asked by medical importers, purchasing officers, and private label partners.
Angiplast manufactures IV Cannula catheters utilizing medical-grade PTFE (Polytetrafluoroethylene), FEP (Fluorinated Ethylene Propylene), and PUR (Polyurethane). FEP and PTFE offer excellent surface smoothness, low friction coefficients, and kink resistance for standard peripheral vascular access. Polyurethane (PUR) softens at body temperature, conforming to vessel architecture to reduce mechanical phlebitis, vascular irritation, and catheter-related complications during extended dwell times.
Every stainless steel lancet tip undergoes high-precision electro-polishing and micro-grinding to form a razor-sharp, double or triple-bevel needle point. Needles are treated with medical-grade silicone lubricant to minimize insertion force and tissue trauma. Automated optical vision inspection systems check 100% of needle points for micro-burrs prior to cleanroom assembly.
We produce full ISO 10555-5 color-coded gauge ranges: 14G (Orange, 270 mL/min), 16G (Grey, 180 mL/min), 18G (Green, 85 mL/min), 20G (Pink, 55 mL/min), 22G (Blue, 33 mL/min), 24G (Yellow, 20 mL/min), and 26G (Violet, 10 mL/min). All gauges include radio-opaque stripes for X-ray visibility under fluoroscopy.
Angiplast provides complete regulatory support for international distributors, including ISO 13485:2016 Quality Management Certification, European CE conformity technical dossiers under EU MDR standards, Free Sale Certificates (FSC), ISO 10993 biocompatibility test reports, ISO 11135 ETO sterilization validation, and lot-release certificates.
Yes. Angiplast is a premier CDMO/OEM partner for global pharmaceutical and medical supply brands. We support customized blister packaging (tyvek or medical paper/plastic), customized color coding, private label brand artwork, multilingual IFUs, GS1 UDI barcoding, and unique kit packaging configurations.
Our Safety IV Cannulas feature an automatic passive safety shield mechanism that encapsulating the sharp stylet needle point immediately upon withdrawal from the catheter hub. This eliminates exposure to bloodborne pathogens and prevents accidental needle-stick injuries (NSIs), complying with OSHA regulations and EU Directive 2010/32/EU.
Angiplast IV Cannulas have a validated shelf life of 5 years when stored in original sealed blister packs. Sterilization is executed in our captive Ethylene Oxide (ETO) plant following ISO 11135 protocols, achieving a Sterility Assurance Level (SAL) of 10^-6 with validated ETO residual limits below ISO 10993-7 requirements.
Standard MOQs start at one complete master carton lot per SKU (typically 10,000 to 50,000 units depending on packaging configuration). Standard shipment lead times range from 3 to 5 weeks post artwork approval, supported by ocean or air freight logistics with full container optimization.
Angiplast Pvt. Ltd. operates a fully integrated, state-of-the-art manufacturing infrastructure in Ahmedabad, Gujarat, India. Unlike trading agents or assemblers who outsource critical components, we maintain total command over every production phase:
Exporting to 52+ Nations Worldwide Connect directly with Angiplast's export engineering team to request sample kits, detailed product dossiers, or custom OEM manufacturing proposals for your market.
