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Smiths Medical 21-4008-24 - Titanium Contoured Kit, Single-Lumen Portal, 9FR, Silicone, 2.8mm OD x 1.0mm ID x 76cm

Titanium Contoured Kit, Single-Lumen Portal, 9FR, Silicone, 2.8mm OD x 1.0mm ID x 76cm
Part Number Smiths Medical 21-4008-24
SKU Number CIA8069289
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Ships Within Special Order
List Price $620.01
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Product Description

Smiths Medical 21-4008-24 - Titanium Contoured Kit, Single-Lumen Portal, 9FR, Silicone, 2.8mm OD x 1.0mm ID x 76cm

The Smiths Medical 21-4008-24 Titanium Contoured Kit is a high-performance implantable port system designed for long-term vascular access. Featuring a single-lumen portal with a 9FR silicone catheter, this system is engineered for reliability, patient comfort, and consistent clinical performance. The titanium contoured port body enhances durability while maintaining a low-profile design suitable for subcutaneous placement. With a catheter measuring 2.8mm outer diameter, 1.0mm inner diameter, and 76cm in length, it supports efficient infusion therapy across a range of clinical applications.

Key Benefits

This implantable port system offers dependable long-term access for infusion therapies, reducing the need for repeated venipuncture. The titanium construction ensures strength and resistance to corrosion, while the contoured design improves patient comfort and ease of implantation. The silicone catheter provides flexibility and biocompatibility, minimizing irritation and supporting smooth fluid delivery. Its single-lumen configuration ensures straightforward use in standard infusion protocols, making it a reliable choice for clinicians.

Compatibility and Applications

The system is compatible with standard non-coring needles and infusion accessories used in implantable port procedures. It is widely used in oncology, long-term antibiotic therapy, parenteral nutrition, and other treatments requiring repeated vascular access. The device is suitable for use in hospitals, outpatient clinics, and specialty infusion centers where consistent and safe access is essential.

Usage Guidelines

The port should be implanted by trained healthcare professionals using established sterile techniques. Proper placement and secure fixation are critical to ensure optimal performance and patient safety. The catheter should be flushed regularly according to clinical protocols to maintain patency. Only compatible non-coring needles should be used to access the port, and all procedures should follow institutional guidelines for implantable devices.

Certifications and Safety Standards

This product is manufactured in accordance with strict medical device quality standards and complies with applicable regulatory requirements for implantable vascular access systems. The materials used are biocompatible and designed to meet safety expectations for long-term implantation. Each component undergoes rigorous quality control to ensure reliability in clinical use.

Comparison with Competitors

Compared to other implantable port systems, this titanium contoured kit stands out for its balance of durability and patient comfort. The contoured port design offers improved anatomical fit, while the silicone catheter ensures flexibility and reduced risk of vessel irritation. Its consistent performance and trusted manufacturing quality make it a preferred option over standard plastic or less refined port systems.

Typical User Profile and Application Scenarios

This product is ideal for healthcare providers managing patients requiring long-term intravenous therapy. It is commonly used by oncologists, infusion nurses, and surgical teams in both inpatient and outpatient settings. Patients undergoing chemotherapy, extended antibiotic treatment, or nutritional support benefit from the reliable and minimally invasive access this system provides.

Best Practices for Use and Maintenance

To ensure optimal performance, the port should be accessed only with appropriate non-coring needles and maintained through regular flushing protocols. Proper aseptic technique must be followed during each access to reduce infection risk. Routine monitoring for signs of occlusion, infection, or mechanical issues is essential. Adhering to established maintenance schedules helps extend the lifespan of the device and ensures patient safety.

Regulatory and Safety Information

This implantable port system is intended for use by qualified medical professionals and should be handled in accordance with all applicable clinical guidelines. It is designed for single-patient use and should not be reused or reprocessed. Any adverse events or complications should be reported in line with local regulatory requirements. Proper disposal of used components should follow medical waste protocols.

How to Order

To place an order or for more information, please contact our customer care team at (312) 275-5850. Our specialists are available to assist with product selection, availability, and bulk purchasing options tailored to your facility's needs.

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