Smiths Medical 21-4572-24 - KIT PORT-A-CATH SINGLE LUMEN ULTRA LOW PROFILE 1MM ID 1.9MM OD TITANIUM PORT 5.8FR 76CM POLYURETHANE CATHETER STRAIGHT/BLUNT NEEDLE UNASSEMBLED

Smiths Medical 21-4572-24 - KIT PORT-A-CATH SINGLE LUMEN ULTRA LOW PROFILE 1MM ID 1.9MM OD TITANIUM PORT 5.8FR 76CM POLYURETHANE CATHETER STRAIGHT/BLUNT NEEDLE UNASSEMBLED

The Smiths Medical 21-4572-24 Port-A-Cath Single Lumen Ultra Low Profile Titanium Port Kit is designed for reliable long-term vascular access in clinical settings where a compact, durable, and low-profile implanted port system is required. This kit includes an ultra low profile titanium port with a 1mm internal diameter and 1.9mm outer diameter, paired with a 5.8FR, 76cm polyurethane catheter for controlled infusion access.

Built for healthcare professionals who require dependable performance and patient-conscious design, this Port-A-Cath system supports repeated access for therapies such as medication administration, blood sampling, and other prescribed infusion procedures. The titanium port construction provides strength and stability, while the ultra low profile design helps support patient comfort after placement.

Key Benefits

• Ultra low profile port design supports a lower implant profile for improved patient comfort.
• Titanium port construction provides durability and long-term structural reliability.
• Single lumen configuration supports straightforward access for routine infusion therapy and vascular access procedures.
• 5.8FR polyurethane catheter offers flexibility and reliable fluid delivery performance.
• 76cm catheter length allows clinical flexibility during placement and positioning.
• Includes straight and blunt needle components to support procedural setup.
• Unassembled kit format allows clinicians to prepare and configure the system according to facility protocol.
• Designed for professional use in controlled healthcare environments.

Compatibility and Applications

The Smiths Medical 21-4572-24 Port-A-Cath kit is intended for use by trained medical professionals in procedures requiring implanted vascular access. Its single lumen design is suitable for patients who require repeated venous access for prescribed therapies, including infusion treatments, medication delivery, hydration therapy, and blood withdrawal when clinically appropriate.

This product is commonly used in hospitals, oncology departments, infusion centers, interventional radiology suites, outpatient surgical centers, and specialty care environments. The ultra low profile titanium port may be especially useful when a compact port design is preferred due to patient anatomy, placement considerations, or comfort requirements.

Usage Guidelines

The Smiths Medical 21-4572-24 Port-A-Cath system should be used only by qualified healthcare professionals trained in implanted port placement, vascular access, sterile technique, and catheter management. Before use, verify that the product packaging is intact, confirm the product reference number, and review all manufacturer instructions supplied with the device.

Clinical staff should prepare the device in accordance with facility policy and applicable sterile procedures. Placement, flushing, access, maintenance, and removal should follow the prescribing clinicians direction, institutional protocols, and the manufacturers instructions for use. The device should not be used if the packaging is damaged, if sterility is compromised, or if any component appears defective.

Certifications and Safety Standards

Smiths Medical vascular access products are manufactured for use in professional healthcare environments and are expected to comply with applicable medical device quality and safety requirements. Facilities should verify product documentation, labeling, and regulatory status before use, especially when purchasing for institutional protocols, clinical inventory, or procedure-specific applications.

As with all implanted vascular access devices, safe use depends on proper patient selection, correct placement technique, sterile handling, routine maintenance, and adherence to infection prevention standards. Healthcare providers should follow current clinical guidelines and facility policies for implanted port care and catheter access.

Comparison with Competitors

Compared with standard-profile implanted ports, the Smiths Medical 21-4572-24 Port-A-Cath kit offers an ultra low profile titanium design that may support improved patient comfort and a less prominent implanted appearance. The titanium construction provides a strong, dependable port body, while the polyurethane catheter offers flexibility for vascular access applications.

Many competing port systems may offer similar single lumen access, but this model is distinguished by its compact profile, 5.8FR catheter size, 76cm catheter length, and unassembled configuration. For facilities that value procedural flexibility and a durable implanted port platform, this Port-A-Cath kit provides a practical option from a recognized medical device manufacturer.

Typical User Profile and Application Scenarios

This product is intended for use by surgeons, interventional radiologists, oncologists, infusion specialists, vascular access nurses, and other trained clinicians involved in long-term venous access management. It may be selected for patients who require ongoing therapy and benefit from an implanted access device instead of repeated peripheral venipuncture.

Typical application scenarios include long-term infusion treatment, oncology care, recurring medication administration, outpatient infusion therapy, and clinical situations where durable implanted access is preferred. The single lumen design is suitable when one access pathway is clinically appropriate and multi-lumen functionality is not required.

Best Practices for Use and Maintenance

Best practice begins with confirming that the selected port system is appropriate for the patients treatment plan, anatomy, and clinical needs. During preparation and placement, staff should maintain strict sterile technique, inspect all components, and ensure that catheter positioning and port access follow approved procedural standards.

After implantation, routine care should include site assessment, proper flushing protocols, needle access using compatible non-coring port access needles when required, and monitoring for signs of infection, occlusion, catheter migration, leakage, or patient discomfort. Documentation should include product details, placement information, maintenance activity, and any complications or interventions.

Regulatory and Safety Information

The Smiths Medical 21-4572-24 Port-A-Cath Single Lumen Ultra Low Profile Titanium Port Kit is a medical device intended for professional healthcare use. It should be handled, implanted, accessed, and maintained only by trained personnel following manufacturer instructions and institutional clinical protocols.

Potential risks associated with implanted port systems may include infection, thrombosis, catheter occlusion, extravasation, catheter fracture, migration, bleeding, and other procedure-related complications. Patient monitoring, aseptic technique, correct access methods, and timely clinical evaluation are essential for safe and effective use.

Product selection should be based on clinical judgment, physician order, patient condition, and facility policy. Always refer to the official product labeling and instructions for use before clinical application.

How to Order

Select the Smiths Medical 21-4572-24 KIT PORT-A-CATH SINGLE LUMEN ULTRA LOW PROFILE 1MM ID 1.9MM OD TITANIUM PORT 5.8FR 76CM POLYURETHANE CATHETER STRAIGHT/BLUNT NEEDLE UNASSEMBLED and add it to your cart. Complete checkout with your preferred shipping and payment options. For bulk orders, quotes, or further assistance, contact CIA Medical customer service at (312)275-5850 or use the contact form on this page.