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Smiths Medical 21-4063-24 - TRAY PORT-A-CATH SINGLE LUMEN POPYSULFONE/TITANIUM PORT 6FR 76CM POLYURETHANE CATHETER STRAIGHT/BLUNT NEEDLE VEIN PICK 18GA INTRODUCER NEEDLE J GUIDEWIRE VESSEL DILATOR 90 DEG NEEDLE GRIPPER NEEDLE SYRINGEX2 TUNNELER PREASSEMBLED

TRAY PORT-A-CATH SINGLE LUMEN POPYSULFONE/TITANIUM PORT 6FR 76CM POLYURETHANE CATHETER STRAIGHT/BLUNT NEEDLE VEIN PICK 18GA INTRODUCER NEEDLE J GUIDEWIRE VESSEL DILATOR 90 DEG NEEDLE GRIPPER NEEDLE SYRINGEX2 TUNNELER PREASSEMBLED
Part Number Smiths Medical 21-4063-24
SKU Number CIA1074154
Sell Unit EACH
Ships Within Call for Availability
List Price $402.54
Product Description

Smiths Medical 21-4063-24 - TRAY PORT-A-CATH SINGLE LUMEN POPYSULFONE/TITANIUM PORT 6FR 76CM POLYURETHANE CATHETER STRAIGHT/BLUNT NEEDLE VEIN PICK 18GA INTRODUCER NEEDLE J GUIDEWIRE VESSEL DILATOR 90 DEG NEEDLE GRIPPER NEEDLE SYRINGEX2 TUNNELER PREASSEMBLED

The Smiths Medical 21-4063-24 Port-A-Cath Tray is a comprehensive, single lumen implantable vascular access system designed to support long-term intravenous therapies. Built with a durable polysulfone and titanium port, this system ensures reliable performance and patient comfort over extended use. The included 6FR, 76 cm polyurethane catheter offers flexibility and strength, supporting consistent flow rates and minimizing complications during insertion and therapy.

This all-in-one sterile tray includes essential components required for efficient and controlled implantation, such as a straight blunt needle, vein pick, 18GA introducer needle, J guidewire, vessel dilator, tunneler, preassembled needle gripper, and syringes. Designed for clinical precision and procedural efficiency, this tray simplifies workflow in operating rooms and interventional settings while maintaining high safety standards.

Key Benefits

The system delivers dependable long-term venous access, reducing the need for repeated needle sticks and improving patient experience. Its titanium port construction enhances durability while resisting corrosion, making it suitable for extended implantation.

The polyurethane catheter balances flexibility and strength, reducing the risk of kinking while maintaining consistent fluid delivery. The complete tray design eliminates the need for additional sourcing, improving procedural efficiency and saving valuable clinical time.

The inclusion of a preassembled tunneler and needle system supports smooth placement and minimizes procedural complexity. Each component is designed for compatibility and ease of use, ensuring predictable outcomes across a wide range of clinical applications.

Compatibility and Applications

This Port-A-Cath system is widely used in oncology, hematology, and long-term infusion therapy settings. It is ideal for administering chemotherapy, parenteral nutrition, antibiotics, and other intravenous medications requiring repeated or continuous access.

The system is compatible with standard infusion devices and access needles used in hospital and outpatient settings. Its single lumen design is suitable for therapies requiring a dedicated access channel while minimizing complexity.

Usage Guidelines

The device is intended for implantation by trained healthcare professionals in a sterile surgical environment. Proper anatomical placement and secure tunneling are essential to ensure optimal device performance and reduce complications.

Clinicians should follow established protocols for venous access, catheter placement, and port positioning. Post-implantation care includes routine flushing, proper needle access technique, and monitoring for signs of infection or occlusion.

Only compatible non-coring needles should be used to access the port to maintain septum integrity and extend device lifespan.

Certifications and Safety Standards

The Smiths Medical Port-A-Cath system is manufactured in compliance with stringent medical device quality standards. Each component undergoes rigorous testing to ensure sterility, durability, and performance consistency.

The materials used, including titanium and medical-grade polymers, are biocompatible and designed to meet regulatory safety requirements. The sterile packaging ensures readiness for immediate use in clinical environments.

Comparison with Competitors

Compared to alternative implantable port systems, this product offers a well-balanced combination of durability, ease of use, and procedural efficiency. The inclusion of a complete tray distinguishes it from competitors that require separate component sourcing.

The titanium and polysulfone port construction provides enhanced longevity compared to plastic-only designs. Additionally, the polyurethane catheter offers improved flexibility over more rigid materials, reducing patient discomfort and complication risks.

The preassembled components streamline the implantation process, making it a preferred choice for facilities prioritizing efficiency and consistency.

Typical User Profile and Application Scenarios

This product is designed for use by surgeons, interventional radiologists, and trained clinical staff involved in vascular access procedures. It is commonly utilized in hospitals, cancer treatment centers, infusion clinics, and specialized care facilities.

Patients requiring long-term intravenous therapy, particularly those undergoing chemotherapy or chronic treatment regimens, benefit significantly from this system. It is also suitable for patients with poor peripheral venous access.

Best Practices for Use and Maintenance

Proper aseptic technique should always be followed during implantation and access. Routine flushing with appropriate solutions helps maintain catheter patency and prevents clot formation.

Regular inspection of the access site is essential to detect early signs of infection or complications. Clinicians should ensure that only approved needles and accessories are used to maintain device integrity.

Documentation of access frequency and maintenance procedures supports long-term device performance and patient safety.

Regulatory and Safety Information

This device is intended for use by qualified healthcare professionals only. It must be handled and implanted in accordance with clinical guidelines and manufacturer instructions.

Potential risks include infection, thrombosis, catheter occlusion, and mechanical complications. Proper training, patient monitoring, and adherence to established protocols significantly reduce these risks.

The device should not be used if packaging is compromised or if sterility is in question. All components are single-use and must not be reused or re-sterilized.

How to Order

To place an order for the Smiths Medical 21-4063-24 Port-A-Cath Tray, please contact CIA Medical customer support at (312) 275-5850. Our team is available to assist with product details, bulk pricing, and shipping arrangements to meet your facilitys needs.

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