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Smiths Medical 21-4009-24 - PORT INFUSION SINGLE LUMEN TITANIUM DETACHED SILICONE CATHETER 9FR INTRODUCER

PORT INFUSION SINGLE LUMEN TITANIUM DETACHED SILICONE CATHETER 9FR INTRODUCER
Part Number Smiths Medical 21-4009-24
SKU Number CIA1074119
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List Price $402.54
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Product Description

Smiths Medical 21-4009-24 - PORT INFUSION SINGLE LUMEN TITANIUM DETACHED SILICONE CATHETER 9FR INTRODUCER

The Smiths Medical 21-4009-24 Port Infusion System is a premium implantable vascular access device designed for long-term intravenous therapy. Featuring a durable titanium port body combined with a flexible detached silicone catheter, this single lumen system ensures reliable performance and patient comfort. The 9FR introducer facilitates efficient placement, making it suitable for a wide range of clinical procedures requiring consistent and secure venous access.

Key Benefits

This infusion port system offers exceptional durability due to its titanium construction, providing resistance to corrosion and long-term wear. The detached silicone catheter enhances flexibility and reduces vessel irritation, promoting patient comfort during extended use. Its single lumen design ensures straightforward operation, while the 9FR introducer supports smooth and controlled insertion. The system is engineered for dependable access, minimizing complications and improving clinical efficiency.

Compatibility and Applications

The device is compatible with standard non-coring needles and is suitable for use in oncology, chemotherapy administration, long-term antibiotic therapy, parenteral nutrition, and blood sampling. It integrates seamlessly into hospital and outpatient settings where reliable central venous access is required. The silicone catheter is designed to adapt to vascular anatomy, making it suitable for a variety of patient profiles.

Usage Guidelines

The port infusion system should be implanted by trained healthcare professionals following established sterile techniques. Proper placement using the 9FR introducer is essential to ensure optimal performance and patient safety. Regular flushing protocols and maintenance procedures should be followed to maintain catheter patency. Only compatible access needles should be used to prevent damage to the septum.

Certifications and Safety Standards

This product is manufactured in compliance with recognized medical device quality standards and undergoes rigorous testing to ensure safety and performance. The materials used are biocompatible and designed for long-term implantation. Healthcare providers can rely on consistent quality that aligns with industry regulations for vascular access devices.

Comparison with Competitors

Compared to alternative port systems, this model stands out for its robust titanium housing and high-quality silicone catheter combination. While many competing devices use plastic or composite materials, the titanium design offers superior longevity. The detached catheter configuration also provides greater flexibility during placement compared to fixed systems, giving clinicians more control during procedures.

Typical User Profile and Application Scenarios

This device is ideal for oncologists, interventional radiologists, and vascular surgeons managing patients who require repeated or long-term intravenous access. It is commonly used in hospitals, specialty clinics, and infusion centers where reliability and patient comfort are critical. Patients undergoing chemotherapy or long-term therapies benefit significantly from this system.

Best Practices for Use and Maintenance

To maintain optimal performance, the port should be accessed using appropriate non-coring needles and flushed according to clinical guidelines. Regular inspection for signs of infection or occlusion is essential. Proper training of healthcare staff in handling and maintenance procedures helps extend the life of the device and ensures patient safety.

Regulatory and Safety Information

This implantable port system is intended for use under the supervision of qualified medical professionals. All implantation and maintenance procedures should follow institutional protocols and regulatory requirements. Adverse events should be monitored and reported according to healthcare guidelines. The device is designed for single patient use and should not be reused.

How to Order

To place an order or for additional product information, please contact CIA Medical customer support at (312) 275-5850. Our team is available to assist with product selection, availability, and bulk purchasing options tailored to your clinical needs.

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