Smiths Medical 21-4152-24 - KIT PORT-A-CATH SINGLE LUMEN 1MM ID 1.9MM OD PLASTIC PORT 5.8FR 76CM POLYURETHANE CATHETER STRAIGHT/BLUNT NEEDLE VEIN PICK UNASSEMBLED

Smiths Medical 21-4152-24 - KIT PORT-A-CATH SINGLE LUMEN 1MM ID 1.9MM OD PLASTIC PORT 5.8FR 76CM POLYURETHANE CATHETER STRAIGHT/BLUNT NEEDLE VEIN PICK UNASSEMBLED

Smiths Medical 21-4152-24 is a single lumen Port-A-Cath kit designed for reliable long-term vascular access in clinical environments where consistent performance, patient comfort, and procedural efficiency matter. This kit features a plastic port paired with a 5.8FR, 76 cm straight polyurethane catheter with a 1 mm inner diameter and 1.9 mm outer diameter. It also includes a blunt needle, vein pick, and unassembled components that support controlled placement and clinician flexibility during implantation.

Built for facilities that require dependable implanted access systems for repeated infusions, blood sampling, and ongoing therapeutic protocols, this Port-A-Cath configuration supports streamlined vascular access management while helping clinicians maintain a secure and professional standard of care. The single lumen design is particularly suitable for patients who need durable central venous access without the added complexity of multi-lumen systems.

Key Benefits

The Smiths Medical 21-4152-24 kit supports long-term central venous access with a practical and well-balanced design that helps clinicians manage repeated therapy sessions more efficiently. Its single lumen construction offers straightforward handling for routine infusion and access needs, while the 76 cm catheter length provides appropriate reach for many implanted port procedures.

The polyurethane catheter offers a combination of strength and flexibility, which is important for maintaining catheter integrity while supporting patient comfort over time. The plastic port design provides a lightweight option that can be attractive in applications where dependable access is required with a simplified implantable system. Because the kit is supplied with key procedural components, including a blunt needle and vein pick, it also helps reduce sourcing complexity and supports procedural readiness in hospital and specialty care settings.

For providers, another important benefit is consistency. A well-specified implanted port kit can improve standardization across vascular access procedures, promote familiarity among clinical staff, and support better inventory management for recurring patient care needs.

Compatibility and Applications

This Port-A-Cath kit is suitable for a range of long-term vascular access applications in acute care, oncology, infusion therapy, and specialty treatment settings. It is commonly used when patients require repeated administration of medications, fluids, nutritional support, or blood product delivery through an implanted central venous access device.

The single lumen configuration makes it a strong fit for patients whose treatment plans do not require multiple simultaneous infusion channels. It may be considered in care pathways involving chemotherapy, long-term antibiotic therapy, intermittent blood draws, and other recurring intravenous treatment regimens where implanted access can improve convenience and reduce the frequency of peripheral venipuncture.

Because the kit includes an unassembled configuration, it offers clinicians procedural flexibility during preparation and placement. It is intended for use by trained healthcare professionals in accordance with institutional protocols, port implantation guidelines, and patient-specific vascular access requirements.

Usage Guidelines

This product should be used only by qualified healthcare professionals trained in implanted port placement and central venous access techniques. Prior to use, the full kit should be inspected to confirm package integrity, product consistency, and readiness for sterile procedural use. All components should be handled in accordance with aseptic technique and the facility's vascular access protocols.

During implantation, clinicians should assess patient anatomy, therapy requirements, and intended access duration before selecting the device and implantation site. The catheter and port components should be prepared according to the manufacturers instructions for use and the clinical teams standard procedural workflow. After placement, the device should be properly accessed, flushed, and maintained according to accepted port care standards.

Routine post-placement care should include monitoring for proper function, patency, and signs of complication. Access procedures should be completed using appropriate non-coring needles and established sterile technique. Ongoing maintenance protocols should align with institutional policy and the needs of the individual patient.

Certifications and Safety Standards

Smiths Medical products are widely recognized in the clinical market for being developed to meet applicable healthcare manufacturing and quality expectations. For this implanted port kit, healthcare purchasers typically evaluate the product based on the manufacturers published specifications, packaging details, sterility information, and compliance documentation available at the time of procurement.

Facilities should confirm the most current product documentation, labeling, and regulatory details through their internal purchasing process before clinical use. Standard evaluation may include verification of sterility status, product traceability, lot control, and adherence to applicable medical device quality standards used within the healthcare supply chain.

As with any implantable vascular access device, safe use depends not only on the product itself but also on professional placement, proper maintenance, and compliance with institutional infection prevention and patient safety protocols.

Comparison with Competitors

Compared with many alternative implanted port systems, Smiths Medical 21-4152-24 offers a practical balance of catheter size, lumen simplicity, and included accessory support. The 5.8FR polyurethane catheter provides a durable option for long-term access, while the single lumen format keeps the system straightforward for treatment plans that do not require multiple channels.

Some competing port kits may focus on titanium construction, lower-profile body designs, or assembled configurations. In contrast, this model offers a plastic port and unassembled format, which may appeal to clinicians and facilities seeking a specific procedural workflow or a lightweight implanted port option. The inclusion of a blunt needle and vein pick also adds procedural convenience, helping the kit stand out in settings where complete, ready-to-stage components are valued.

For buyers comparing long-term access devices, this product can be a strong option when the priority is reliable single lumen functionality, a recognized manufacturer, and a kit format suited to standard port implantation practice.

Typical User Profile and Application Scenarios

This product is commonly selected by hospitals, outpatient infusion centers, oncology clinics, surgical teams, and vascular access specialists managing patients who need stable, repeated central venous access over an extended period. It is especially relevant in treatment environments where patient comfort, reduced peripheral access attempts, and reliable long-term infusion support are important priorities.

Typical patient scenarios may include individuals undergoing scheduled infusion therapy, cancer treatment, long-term medication administration, or repeated laboratory access needs. Clinical teams may choose this single lumen system when one dependable access channel is sufficient and when an implanted device is preferred over repeated peripheral cannulation or temporary external access solutions.

From an operational perspective, supply chain teams and purchasing departments may also favor this kit in facilities aiming to standardize a specific class of implanted access devices while maintaining consistent clinical inventory for scheduled procedures.

Best Practices for Use and Maintenance

Best results with implanted port systems depend on careful placement, correct access technique, and disciplined maintenance protocols. Clinicians should follow sterile handling procedures throughout implantation and every subsequent access event. Device patency should be maintained using established flushing and locking procedures consistent with the manufacturers instructions and the facilitys vascular access guidelines.

Ongoing assessment is important. Staff should monitor for changes in flow, resistance, site condition, and patient comfort during access and infusion. Documentation should be maintained for implantation details, access frequency, maintenance intervals, and any observed issues requiring follow-up.

Training also plays a major role in performance. Facilities that ensure consistent staff competency in port access, maintenance, and complication awareness are better positioned to extend device usability and support patient safety. Care should always be tailored to patient condition, treatment frequency, and clinical indication.

Regulatory and Safety Information

This implanted port kit is intended for professional medical use and should be stored, handled, and used in accordance with the manufacturers instructions and all applicable facility policies. As an implantable vascular access device, it must be used under appropriate clinical oversight with careful attention to aseptic technique, implantation standards, and ongoing monitoring.

Healthcare providers should review the product labeling and instructions for use before implantation. Any decision regarding device suitability should be based on clinical judgment, patient anatomy, intended therapy, and institutional protocol. The device should not be used if packaging is damaged, sterility is compromised, or components appear altered in any way.

As with other central venous access devices, clinicians should remain alert to potential complications associated with implantation, access, and long-term maintenance. Product selection and use should always be guided by trained medical professionals and supported by current procedural standards.

How to Order

Smiths Medical 21-4152-24 Port-A-Cath Single Lumen Plastic Port Kit is a strong choice for healthcare providers seeking dependable long-term vascular access performance with procedural flexibility and trusted clinical utility. It supports the needs of hospitals, specialty clinics, and infusion teams looking for a practical implanted port solution from a recognized medical manufacturer.

To place an order, confirm pricing, check availability, or speak with a product specialist about compatibility and purchasing requirements, contact CIA Medical at (312) 275-5850.