Smiths Medical 21-8066-24 - TRAY PORT-A-CATH DUAL LUMEN 6.6FR POLYURETHANE TITANIUM PORT STRAIGHT/BLUNT NEEDLE VEIN PICK 18GA INTRODUCER NEEDLE J GUIDEWIRE DILATOR SYRINGE 90 DEG NEEDLE TUNNELER

The Smiths Medical 21-8066-24 Port-A-Cath Dual Lumen Tray is a comprehensive implantable vascular access kit designed for clinical teams requiring dependable dual lumen access in long-term infusion therapy. This 6.6FR polyurethane and titanium port system supports controlled medication delivery, blood sampling, parenteral nutrition, chemotherapy, hydration therapy, and other vascular access applications where durable implanted access is clinically appropriate.

The tray includes a dual lumen polyurethane titanium port with supporting placement components, including straight and blunt needles, vein pick, 18GA introducer needle, J guidewire, dilator, syringe, 90 degree needle, and tunneler. Its organized tray configuration helps streamline procedural setup while supporting consistent technique in surgical, interventional radiology, oncology, and hospital infusion environments.

Key Benefits

The Smiths Medical 21-8066-24 Port-A-Cath tray provides a complete procedural solution for dual lumen implanted venous access. The dual lumen design allows separate infusion pathways when clinically indicated, helping support complex therapy plans that may require simultaneous or alternating administration of compatible treatments.

The polyurethane catheter construction is designed for flexibility and vascular compatibility, while the titanium port body offers strength, stability, and long-term implant support. The included tunneler, guidewire, introducer needle, dilator, syringe, and accessory needles help reduce the need to source separate procedural components, improving workflow efficiency and supply standardization.

Its 6.6FR profile is suitable for selected patients requiring reliable implanted access while maintaining a size appropriate for many vascular access procedures. The tray format also supports inventory control by providing essential placement items in one packaged configuration.

Compatibility and Applications

The Smiths Medical 21-8066-24 Port-A-Cath Dual Lumen Tray is intended for use in professional healthcare settings where implantable vascular access devices are placed and managed by qualified clinicians. It may be used in oncology departments, surgical suites, interventional radiology units, infusion centers, hospital vascular access programs, and specialty care facilities.

Common applications include long-term intravenous therapy, chemotherapy administration, medication infusion, blood withdrawal, hydration support, parenteral nutrition, and other treatment plans requiring repeated venous access. The dual lumen configuration may be especially useful when treatment protocols require more than one access pathway, subject to institutional policy, clinician judgment, and product instructions.

This tray should be used only with compatible non-coring access needles and related vascular access supplies as specified by the manufacturer and facility protocol. Clinicians should confirm compatibility with prescribed therapies, flushing protocols, imaging requirements, and institutional vascular access guidelines before use.

Usage Guidelines

The Smiths Medical 21-8066-24 Port-A-Cath tray should be used only by trained healthcare professionals experienced in implantable port placement and vascular access procedures. Prior to use, inspect the package integrity, confirm product size and configuration, and verify that all required components are present and appropriate for the planned procedure.

Placement should follow the manufacturer instructions for use, aseptic technique, facility protocol, and applicable clinical standards. The included introducer needle, J guidewire, dilator, syringe, tunneler, vein pick, and accessory needles should be used according to the procedural approach selected by the clinician.

After implantation, port patency, position, function, and site condition should be assessed according to institutional policy. Ongoing access should be performed with appropriate non-coring needles, and flushing, locking, dressing, and maintenance procedures should follow the prescribing clinicians order and facility vascular access protocol.

Certifications and Safety Standards

The Smiths Medical 21-8066-24 Port-A-Cath Dual Lumen Tray is manufactured for use in regulated healthcare environments and should be handled according to applicable medical device requirements, facility policies, and manufacturer instructions. Healthcare facilities should verify product labeling, sterility status, expiration date, and lot information before use.

As an implantable vascular access product, this device should be used under appropriate clinical supervision and in accordance with infection prevention standards, sterile technique, and accepted vascular access practices. Documentation of product details, implantation information, and patient-specific instructions should be maintained according to facility and regulatory requirements.

Comparison with Competitors

Compared with basic single lumen port kits or component-only vascular access supplies, the Smiths Medical 21-8066-24 tray offers a complete dual lumen solution with key placement accessories included. This can help reduce procedural preparation time and minimize the need to assemble separate items from multiple inventory locations.

Compared with lower-profile or single-access systems, the dual lumen design provides greater flexibility for patients whose therapy plans require more than one access pathway. The polyurethane catheter and titanium port construction also support a balance of flexibility, durability, and long-term implant performance.

For facilities that prioritize standardized trays from established medical device manufacturers, Smiths Medical Port-A-Cath systems are commonly selected for vascular access programs that require dependable product availability, clinical familiarity, and procedural consistency.

Typical User Profile and Application Scenarios

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

Typical clinical scenarios may include oncology treatment, long-term medication infusion, frequent blood draws, nutrition support, and patients with difficult peripheral venous access. The dual lumen configuration may be selected when therapy planning requires independent access channels, provided that the selected application is consistent with clinical judgment and product guidance.

Hospitals, cancer centers, outpatient infusion clinics, and specialty procedural departments may benefit from stocking this tray as part of a standardized vascular access product portfolio.

Best Practices for Use and Maintenance

Best practice begins with confirming the correct product, size, and configuration before the procedure. Clinicians should maintain sterile technique throughout placement, follow the manufacturer instructions for use, and document the device details after implantation.

Port access should be performed only with appropriate non-coring needles to help protect the port septum. The access site should be assessed for signs of infection, swelling, leakage, pain, catheter dysfunction, or other complications. Flushing and locking should be completed according to facility protocol and clinician orders.

Routine maintenance should include careful inspection of the port site, verification of patency when clinically indicated, proper dressing changes, and patient education regarding warning signs that should be reported promptly. Storage should follow package labeling, and products should not be used if the sterile barrier is compromised or the expiration date has passed.

Regulatory and Safety Information

The Smiths Medical 21-8066-24 Port-A-Cath Dual Lumen Tray is intended for professional medical use and should be used only by qualified clinicians in accordance with the manufacturer instructions for use. Proper patient selection, placement technique, sterile handling, and maintenance are essential to support safe and effective use.

Potential risks associated with implantable vascular access devices may include infection, thrombosis, catheter occlusion, bleeding, vessel injury, malposition, extravasation, device damage, and other procedure-related complications. Clinicians should follow institutional policies for prevention, monitoring, documentation, and management of complications.

This content is provided for product identification and procurement support and does not replace the official manufacturer labeling, clinical training, or professional medical judgment. Facilities should review the current instructions for use and applicable regulatory requirements before clinical use.

How to Order

Select the Smiths Medical 21-8066-24 TRAY PORT-A-CATH DUAL LUMEN 6.6FR POLYURETHANE TITANIUM PORT STRAIGHT/BLUNT NEEDLE VEIN PICK 18GA INTRODUCER NEEDLE J GUIDEWIRE DILATOR SYRINGE 90 DEG NEEDLE TUNNELER 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.