Smiths Medical 21-4024-24 - KIT PORT-A-CATH SINGLE LUMEN 1MM ID 1.9MM OD TITANIUM PORT 5.8FR 76CM POLYURETHANE CATHETER STRAIGHT/BLUNT NEEDLE VEIN PICK UNASSEMBLED

Smiths Medical 21-4024-24 - KIT PORT-A-CATH SINGLE LUMEN 1MM ID 1.9MM OD TITANIUM PORT 5.8FR 76CM POLYURETHANE CATHETER STRAIGHT/BLUNT NEEDLE VEIN PICK UNASSEMBLED

The Smiths Medical 21-4024-24 Port-A-Cath Single Lumen Kit is a comprehensive, implantable vascular access solution designed for long-term intravenous therapies. Engineered with precision and durability in mind, this system features a titanium port combined with a flexible polyurethane catheter measuring 76 cm in length with a 5.8 French size. The catheter offers a 1 mm internal diameter and 1.9 mm outer diameter, enabling consistent and reliable fluid delivery.

This unassembled kit is supplied with a straight, blunt needle vein pick, providing clinicians with the flexibility to assemble and customize placement based on patient-specific anatomical and procedural needs. The Port-A-Cath system is widely trusted in oncology, chronic illness management, and extended infusion therapies, where repeated vascular access is required over an extended period.

Key Benefits

The titanium port construction offers exceptional strength, biocompatibility, and resistance to corrosion, ensuring long-term reliability within the body. The polyurethane catheter is designed for optimal flexibility and durability, minimizing the risk of kinking or occlusion during use. The single lumen configuration allows for straightforward infusion management, reducing complexity during treatment.

The inclusion of a straight, blunt needle vein pick enhances safety during insertion, helping to reduce the risk of vessel trauma. The unassembled format gives clinicians greater procedural control, allowing precise configuration and placement tailored to each patients needs. This system supports consistent flow rates, helping to ensure efficient delivery of medications, fluids, or nutrition.

Compatibility and Applications

This Port-A-Cath system is compatible with standard non-coring needles and infusion systems used in clinical settings. It is suitable for a wide range of long-term therapies, including chemotherapy, parenteral nutrition, antibiotic administration, and repeated blood sampling.

Its design makes it ideal for patients requiring frequent or continuous vascular access, reducing the need for repeated peripheral needle insertions. The system is commonly used in hospitals, oncology centers, outpatient infusion clinics, and specialized care facilities.

Usage Guidelines

The device should be implanted by trained healthcare professionals using sterile surgical techniques. Proper placement typically involves subcutaneous implantation of the titanium port, with the catheter inserted into a central vein. Clinicians should ensure that all components are assembled correctly prior to insertion, following established procedural protocols.

Routine maintenance includes flushing the system with appropriate solutions to maintain patency and prevent clot formation. Access should always be performed using compatible non-coring needles to preserve the integrity of the port septum. Regular inspection and monitoring are recommended to ensure proper function and to detect any signs of complications.

Certifications and Safety Standards

The Smiths Medical Port-A-Cath system is manufactured in compliance with stringent medical device quality standards. It is designed to meet applicable regulatory requirements for safety, performance, and biocompatibility. Each component undergoes rigorous testing to ensure reliability in clinical use.

The materials used, including titanium and medical-grade polyurethane, are selected for their proven compatibility with human tissue and long-term implantation. The product is supplied sterile and intended for single-patient use to maintain infection control standards.

Comparison with Competitors

Compared to alternative implantable port systems, this Smiths Medical kit offers a balanced combination of durability, flexibility, and procedural adaptability. The titanium port provides enhanced longevity compared to plastic alternatives, while the polyurethane catheter offers superior flexibility compared to more rigid materials.

The inclusion of a vein pick and unassembled configuration sets it apart from pre-assembled kits, giving clinicians greater control during implantation. Its precise dimensions and consistent flow characteristics make it a reliable choice for demanding clinical environments.

Typical User Profile and Application Scenarios

This product is intended for use by surgeons, interventional radiologists, and trained healthcare professionals specializing in vascular access procedures. It is particularly suited for patients undergoing long-term treatments such as cancer therapy, chronic disease management, or extended intravenous medication regimens.

Common scenarios include oncology treatment plans requiring repeated chemotherapy sessions, patients receiving long-term antibiotics for infection control, and individuals requiring parenteral nutrition due to gastrointestinal conditions. The system supports improved patient comfort by reducing the need for repeated venipuncture.

Best Practices for Use and Maintenance

To ensure optimal performance, clinicians should follow established protocols for implantation, access, and maintenance. Regular flushing with appropriate anticoagulant or saline solutions is essential to maintain catheter patency. Proper needle selection and insertion technique help preserve the integrity of the port septum.

Healthcare providers should monitor the site for signs of infection, occlusion, or mechanical issues. Routine care and adherence to sterile techniques during access significantly reduce the risk of complications. Proper training and adherence to institutional guidelines are key to maximizing the lifespan and effectiveness of the device.

Regulatory and Safety Information

This device is intended for use under the supervision of qualified medical professionals. It should be used in accordance with clinical guidelines and manufacturer instructions. The product is supplied sterile and must not be reused or re-sterilized.

Any adverse events or device malfunctions should be reported in accordance with local regulatory requirements. Proper disposal of used components should follow established medical waste protocols. The device is designed to support safe and effective long-term vascular access when used as intended.

How to Order

To place an order for the Smiths Medical 21-4024-24 Port-A-Cath Single Lumen Kit, please contact our customer care team at (312) 275-5850. Our representatives are available to assist with product details, availability, and bulk purchasing options to support your clinical needs.