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Ensure precise, safe intravenous therapy delivery with this premium IV pump administration set featuring advanced GVS Speedflow filtration technology, extended 105-inch DEHP-free tubing, and comprehensive sterile fluid path design. Engineered for compatibility with major infusion pump systems, this professional-grade IV set is ideal for hospitals, surgical centers, infusion clinics, ambulatory care facilities, and long-term care settings requiring reliable, filtered IV solution delivery with enhanced patient safety features and clinical versatility.
The integrated GVS Speedflow filter incorporates precision 0.22 micron filtration technology that effectively removes particulate matter, bacteria, air emboli, and potential contaminants from IV solutions before they reach the patient's bloodstream. This advanced filtration capability provides an essential safety barrier that protects patients from particulate-related complications, reduces the risk of phlebitis and catheter occlusion, and ensures the purity of administered medications and fluids. The 0.22 micron pore size represents the gold standard for IV filtration, capable of removing virtually all bacteria and fungi while maintaining optimal flow rates for clinical efficiency. The Speedflow design minimizes flow resistance despite the fine filtration, enabling consistent infusion rates without compromising pump performance or extending treatment times.
Manufactured using non-pyrogenic materials and processes, this IV pump set eliminates the risk of fever-inducing pyrogen contamination that can cause adverse patient reactions during infusion therapy. The non-pyrogenic designation ensures that all fluid-contact surfaces are free from endotoxins and pyrogenic substances that could trigger inflammatory responses, fever, chills, or other systemic reactions in patients receiving IV therapy. This critical safety feature is particularly important for immunocompromised patients, pediatric populations, and individuals receiving long-term or high-volume infusion therapy where pyrogen exposure could lead to serious complications or treatment interruptions.
The generous 105-inch tubing length provides exceptional flexibility in patient positioning and equipment arrangement, accommodating diverse clinical scenarios from bedside infusion therapy to ambulatory treatments where patient mobility is desired. This extended length eliminates the need for extension sets in most applications, reducing connection points that could introduce contamination risks or create potential failure points in the fluid pathway. The DEHP-free tubing construction addresses health concerns associated with di(2-ethylhexyl) phthalate exposure, making this set suitable for use with all patient populations including neonates, pregnant women, and individuals requiring long-term infusion therapy. The DEHP-free formulation maintains excellent flexibility, durability, and chemical compatibility with a wide range of IV medications and solutions without the potential health risks associated with phthalate plasticizers.
The complete sterile fluid path design ensures that all solution-contact surfaces from spike to patient connection maintain sterility until the moment of use, providing comprehensive protection against healthcare-associated infections and contamination-related complications. This sterile pathway includes the vented/non-vented spike, drip chamber, filter housing, tubing, ports, and connectors, creating an unbroken chain of sterility that safeguards patient safety throughout the infusion process. The sterile fluid path supports rigorous infection control protocols and aligns with evidence-based practices for preventing catheter-related bloodstream infections (CRBSIs) and other infusion-related complications.
The integrated two-port system features advanced needle-free Clave Y-port technology that enables safe, convenient medication administration and secondary infusion connections without the risks associated with traditional needle access. These needle-free ports significantly reduce needlestick injury hazards for healthcare workers while maintaining closed-system integrity that minimizes contamination risks during medication administration. The Y-port configuration provides strategic access points along the tubing for administering IV push medications, connecting secondary medication infusions, or drawing blood samples when appropriate, all while maintaining the sterile fluid pathway and supporting efficient clinical workflows.
The dual flow control mechanism incorporates both roller clamp and slide clamp technologies, providing healthcare professionals with precise, reliable flow rate adjustment capabilities and secure shut-off functionality. The roller clamp enables fine-tuned flow rate adjustments for gravity infusions or manual flow control scenarios, while the slide clamp provides quick, positive shut-off for line clamping during tubing changes, medication administration, or emergency situations. This redundant clamping system enhances safety by providing backup flow control options and supports diverse clinical protocols across different care settings and infusion scenarios.
The integrated back check valve prevents retrograde fluid flow and air entry into the IV line, protecting patients from potential air embolism complications and ensuring unidirectional solution delivery. This critical safety feature is particularly important during secondary medication infusions, preventing primary solution from flowing back into secondary containers and ensuring accurate medication delivery. The back check valve also facilitates efficient sequential medication administration and supports complex multi-medication infusion protocols without requiring additional components or complicated setup procedures.
The versatile spike design accommodates both vented and non-vented IV solution containers, providing compatibility with diverse solution packaging formats and eliminating the need to stock multiple administration set types. The precision-engineered drip chamber features a 10 drops per milliliter drip rate calibration, enabling accurate visual flow rate monitoring and manual flow calculations when needed. The clear drip chamber design allows healthcare professionals to easily visualize solution flow, detect air bubbles, and monitor infusion status at a glance, supporting vigilant patient monitoring and early detection of potential infusion complications.
The terminal male Luer lock connector provides secure, leak-resistant attachment to IV catheters, extension sets, and vascular access devices. The threaded Luer lock design creates a positive mechanical connection that resists accidental disconnection during patient movement, bed transfers, or routine care activities, significantly reducing the risk of line separation incidents that could lead to blood loss, air embolism, or medication delivery interruptions. The universal Luer lock standard ensures broad compatibility with virtually all IV access devices and connection systems used in modern healthcare settings.
Specifically designed for use with major infusion pump platforms including compatible models from leading manufacturers, this IV set ensures reliable performance with electronic infusion devices that provide precise flow rate control, dose calculation, and safety alarm features. The tubing dimensions, material properties, and construction specifications are optimized for pump compatibility, ensuring accurate occlusion detection, consistent flow delivery, and reliable pump operation throughout the infusion duration.
The economical 50-unit box packaging provides healthcare facilities with cost-effective bulk purchasing options while maintaining manageable inventory quantities. This packaging format supports efficient supply chain management, reduces per-unit costs, and ensures adequate stock levels for busy clinical units without requiring excessive storage space or capital investment in large case quantities.
This IV pump administration set with integrated filtration represents an essential component of infusion therapy supply inventories for healthcare facilities committed to patient safety, infection prevention, and clinical excellence. The combination of advanced 0.22 micron filtration, extended DEHP-free tubing, sterile fluid path integrity, needle-free port access, and comprehensive safety features makes this administration set a trusted choice for healthcare professionals delivering critical IV therapy across diverse patient populations and clinical scenarios.
We provide shipping worldwide and most of our orders are delivered within 7-15 days.
We have a 30-day return policy, which means you have 30 days after receiving your item to request a return.
To be eligible for a return, your item must be in the same condition that you received it, unworn or unused, with tags, and in its original packaging. You’ll also need the receipt or proof of purchase.
To start a return, you can contact us at cetabo.contact@gmail.com. Please note that returns will need to be sent to the following address: 2236 W Holcombe Blvd, Houston Texas 77030, United States






