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Smiths Medical 21-4022-24 - KIT PORT-A-CATH SINGLE LUMEN 1.6MM ID 2.6MM OD TITANIUM PORT 7.8FR 76CM POLYURETHANE CATHETER BLUNT NEEDLE VEIN PICK UNASSEMBLED

KIT PORT-A-CATH SINGLE LUMEN 1.6MM ID 2.6MM OD TITANIUM PORT 7.8FR 76CM POLYURETHANE CATHETER BLUNT NEEDLE VEIN PICK UNASSEMBLED
Part Number Smiths Medical 21-4022-24
SKU Number CIA1074123
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List Price $402.54
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Product Description

Smiths Medical 21-4022-24 - KIT PORT-A-CATH SINGLE LUMEN 1.6MM ID 2.6MM OD TITANIUM PORT 7.8FR 76CM POLYURETHANE CATHETER BLUNT NEEDLE VEIN PICK UNASSEMBLED

The Smiths Medical 21-4022-24 Port-A-Cath Single Lumen Kit is a reliable, implantable vascular access system designed for long-term intravenous therapy. Featuring a durable titanium port and a 76 cm polyurethane catheter, this system supports consistent performance across demanding clinical environments. The unassembled kit includes essential components such as a blunt needle and vein pick, allowing clinicians to customize placement according to procedural needs. Its low-profile design enhances patient comfort while maintaining secure and efficient access.

Key Benefits

This port system is engineered for durability and consistent flow performance, making it suitable for repeated access over extended treatment periods. The titanium port offers exceptional strength and biocompatibility, while the polyurethane catheter ensures flexibility and kink resistance. The single lumen design simplifies infusion management and reduces the risk of complications. The inclusion of essential procedural tools in one kit improves efficiency during implantation.

Compatibility and Applications

The system is compatible with standard non-coring access needles and is widely used in oncology, hematology, and long-term infusion therapies. It is suitable for chemotherapy administration, parenteral nutrition, antibiotic therapy, and routine blood sampling. Its design supports use in both inpatient and outpatient settings where reliable venous access is required.

Usage Guidelines

The device should be implanted by trained healthcare professionals using aseptic technique. Proper catheter placement and port positioning are essential for optimal performance. The port should be accessed using appropriate non-coring needles to maintain septum integrity. Routine flushing protocols should be followed to ensure patency and prevent occlusion.

Certifications and Safety Standards

This product is manufactured in accordance with recognized medical device quality standards and undergoes rigorous testing for safety and performance. Materials used are biocompatible and suitable for long-term implantation. The device meets applicable regulatory requirements for implantable vascular access systems.

Comparison with Competitors

Compared to standard plastic port systems, the titanium construction provides enhanced durability and resistance to wear. The polyurethane catheter offers improved flexibility over silicone alternatives, reducing the likelihood of kinking. The comprehensive kit format, including procedural tools, provides added convenience and value compared to basic port-only offerings.

Typical User Profile and Application Scenarios

This product is ideal for hospitals, oncology centers, infusion clinics, and surgical teams managing patients requiring long-term intravenous access. It is commonly used for patients undergoing chemotherapy, chronic antibiotic therapy, or frequent blood sampling. Surgeons and interventional specialists benefit from its adaptable, unassembled configuration during implantation.

Best Practices for Use and Maintenance

To maintain optimal function, the port should be flushed regularly according to institutional protocols. Only compatible non-coring needles should be used to access the port. Routine inspection for signs of infection or malfunction is recommended. Proper sterile handling during access and maintenance helps extend the lifespan of the device and ensures patient safety.

Regulatory and Safety Information

This device is intended for use by qualified healthcare professionals only. It should be used in accordance with clinical guidelines and manufacturer instructions. Any adverse events or complications should be reported following standard medical reporting procedures. Proper training in implantation and access techniques is essential to minimize risks.

How to Order

To place an order or speak with a product specialist, please contact CIA Medical at (312) 275-5850. Our team is available to assist with product selection, bulk pricing, and delivery options to meet your facilitys needs.

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