Smiths Medical 21-4485-24 - Port-A-Cath Kit, Includes: Single-Lumen Low Profile Portal, Polysulfone/Titanium, 25x11.5x9.5mm, PolyFlow Polyurethane Catheter, 5.8FR, Straight Needle, Vein Pick, and Point-Lok Device

Smiths Medical 21-4485-24 - Port-A-Cath Kit, Includes: Single-Lumen Low Profile Portal, Polysulfone/Titanium, 25x11.5x9.5mm, PolyFlow Polyurethane Catheter, 5.8FR, Straight Needle, Vein Pick, and Point-Lok Device

The Smiths Medical 21-4485-24 Port-A-Cath Kit is a professional vascular access kit designed for clinicians who require a reliable implantable port system for long-term infusion therapy. The kit includes a single-lumen low profile portal made with polysulfone and titanium, sized at 25 x 11.5 x 9.5 mm, along with a 5.8FR PolyFlow polyurethane catheter and essential placement accessories.

This Port-A-Cath kit is intended to support consistent central venous access for therapies that may require repeated administration, reducing the need for frequent peripheral venipuncture. Its low profile design helps support patient comfort while maintaining dependable clinical performance in appropriate healthcare settings.

Key Benefits

The single-lumen low profile portal supports efficient venous access while helping minimize bulk under the skin. The polysulfone and titanium construction provides strength, durability, and compatibility with long-term implanted access applications.

The included 5.8FR polyurethane catheter is designed for controlled fluid delivery and dependable vascular access. The kit also includes a straight needle, vein pick, and Point-Lok device, helping clinicians manage placement and accessory handling within a comprehensive procedural setup.

By combining the portal, catheter, and key placement components in one kit, the Smiths Medical 21-4485-24 helps streamline procedural preparation and supports standardized inventory management for hospitals, oncology departments, infusion centers, and surgical teams.

Compatibility and Applications

The Smiths Medical 21-4485-24 Port-A-Cath Kit is suitable for use in clinical environments where long-term venous access is required. It may be used in applications involving infusion therapy, chemotherapy, medication delivery, blood sampling, and other physician-directed vascular access procedures where an implantable port is clinically appropriate.

The 5.8FR polyurethane catheter and single-lumen portal configuration are intended for patients who require one access pathway for therapy delivery. The low profile portal size may be especially useful when a smaller implant profile is preferred based on patient anatomy, therapy plan, and clinician judgment.

Usage Guidelines

This product should be used only by qualified healthcare professionals trained in implantable vascular access procedures and in accordance with the facility protocol, product instructions, and applicable clinical standards. Proper patient assessment, sterile technique, imaging guidance when required, and confirmation of catheter placement are essential to safe and effective use.

Before use, inspect the packaging and all kit components to confirm sterility, integrity, and correct product selection. Do not use the kit if packaging is damaged, if components are missing, or if the product appears compromised.

After placement, the port should be accessed, flushed, and maintained according to the manufacturer instructions and institutional policy. Only compatible access needles and approved flushing protocols should be used to support device performance and reduce the risk of complications.

Certifications and Safety Standards

Smiths Medical vascular access products are manufactured for professional medical use and are expected to meet applicable medical device quality, safety, and performance requirements. Healthcare facilities should verify all current regulatory documentation, device labeling, and institutional purchasing requirements before clinical use.

The Port-A-Cath system should be used in accordance with the manufacturer instructions for use, sterile procedure guidelines, infection control policies, and relevant vascular access standards. Final suitability should always be determined by the prescribing clinician and the facilitys clinical governance process.

Comparison with Competitors

Compared with general implantable port kits, the Smiths Medical 21-4485-24 offers a focused configuration with a single-lumen low profile portal, durable polysulfone and titanium materials, and a 5.8FR polyurethane catheter. This combination supports reliable long-term access while helping reduce unnecessary profile size for appropriate patients.

Many competing port systems may require separate accessory selection or may offer a different portal profile, catheter material, or kit configuration. The 21-4485-24 kit provides a streamlined option for clinicians who prefer a ready procedural kit that includes the portal, catheter, straight needle, vein pick, and Point-Lok device in one package.

For healthcare procurement teams, the Smiths Medical brand recognition, standardized kit contents, and clear product configuration can help simplify product selection when compared with less complete or less clearly specified vascular access kits.

Typical User Profile and Application Scenarios

This product is typically used by interventional radiologists, surgeons, vascular access teams, oncology clinicians, infusion specialists, and hospital-based procedural teams. It is appropriate for healthcare facilities that manage patients requiring repeated or long-term venous access.

Common application scenarios may include oncology infusion programs, chronic medication administration, specialty infusion services, and hospital procedures where a dependable implantable venous access port is indicated. The single-lumen design is suitable when one access channel meets the patients therapy requirements.

Best Practices for Use and Maintenance

Follow the manufacturer instructions and facility protocols for implantation, access, flushing, dressing, and ongoing maintenance. Strict aseptic technique should be used during placement and every time the port is accessed to help reduce infection risk.

Use only compatible port access needles and approved accessories. Confirm patency before infusion, monitor for signs of infiltration, infection, occlusion, catheter migration, or patient discomfort, and document all access and maintenance activities according to clinical policy.

Routine inspection, proper flushing technique, and adherence to recommended maintenance intervals are essential for supporting long-term device function. Any concerns regarding device performance should be escalated to the appropriate clinical team immediately.

Regulatory and Safety Information

The Smiths Medical 21-4485-24 Port-A-Cath Kit is intended for professional healthcare use and should not be used outside the scope of its approved labeling. Product selection, implantation, and ongoing management must be performed under the direction of a qualified healthcare provider.

Potential risks associated with implantable venous access devices may include infection, thrombosis, catheter occlusion, device malfunction, vessel injury, migration, and complications related to placement or access. Clinicians should review the complete instructions for use, warnings, contraindications, and precautions before use.

Facilities should confirm current regulatory status, sterility information, expiration date, storage requirements, and compatibility with local policies before purchasing or using this product.

How to Order

Select the Smiths Medical 21-4485-24 Port-A-Cath Kit, Includes: Single-Lumen Low Profile Portal, Polysulfone/Titanium, 25x11.5x9.5mm, PolyFlow Polyurethane Catheter, 5.8FR, Straight Needle, Vein Pick, and Point-Lok Device 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.