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 6.6FR Polyurethane Titanium Port Tray is a comprehensive implantable vascular access tray designed for clinicians who require a reliable dual lumen port system for long-term infusion therapy, medication administration, blood sampling, and other vascular access procedures. This tray includes a 6.6FR polyurethane catheter with a titanium port, along with essential procedural components such as a straight and blunt needle, vein pick, 18GA introducer needle, J guidewire, dilator, syringe, 90 degree needle, and tunneler.

Built for procedural efficiency and consistent clinical performance, this Port-A-Cath tray supports sterile technique and organized workflow during port placement. The dual lumen configuration allows separate access channels, making it suitable for patients who may require multiple compatible therapies or frequent vascular access under qualified medical supervision.

Key Benefits

The Smiths Medical 21-8066-24 Port-A-Cath tray offers a complete procedural setup for implantable vascular access placement, helping reduce the need to source multiple components separately. The dual lumen design supports flexible therapy management where separate infusion pathways may be clinically required.

The 6.6FR polyurethane catheter is designed to balance flexibility and performance for vascular access applications, while the titanium port construction provides durability for long-term implanted use. The included J guidewire, introducer needle, dilator, tunneler, and accessory needles help support a controlled and efficient placement process.

Key advantages include:

• Dual lumen implantable port design for multi-channel vascular access needs
• 6.6FR polyurethane catheter for clinical vascular access applications
• Titanium port construction for long-term durability
• Comprehensive tray format with placement accessories included
• Useful for oncology, infusion therapy, parenteral nutrition, and medication delivery settings
• Designed to support sterile procedural workflow and clinical efficiency

Compatibility and Applications

The Smiths Medical 21-8066-24 Port-A-Cath Dual Lumen 6.6FR Tray is intended for use in healthcare environments where implantable vascular access devices are placed and managed by trained medical professionals. It may be used in hospitals, outpatient surgery centers, interventional radiology departments, oncology infusion centers, and specialty care facilities.

Common clinical applications may include long-term medication administration, chemotherapy access, compatible infusion therapy, blood draws, parenteral nutrition, and other vascular access needs determined by the treating clinician. The dual lumen configuration can help support patients who require separate access pathways for compatible therapies, depending on institutional protocol and patient-specific clinical requirements.

This tray should be used only with compatible vascular access techniques, accessories, flushing protocols, and maintenance procedures approved by the facility and the product instructions for use.

Usage Guidelines

The Smiths Medical 21-8066-24 Port-A-Cath tray should be used only by qualified healthcare professionals trained in implantable port placement and vascular access management. Before use, clinicians should review the product packaging, verify tray contents, confirm sterility, and inspect all components for damage or expiration.

Placement should be performed using appropriate sterile technique and in accordance with institutional policy, physician preference, and the manufacturers instructions for use. The included introducer needle, J guidewire, dilator, syringe, 90 degree needle, tunneler, vein pick, and related components should be used only as clinically indicated for the procedure.

After placement, port function should be confirmed according to facility protocol. Ongoing care should include proper access technique, flushing, dressing management, infection prevention practices, and routine monitoring for complications such as occlusion, infection, catheter migration, infiltration, or thrombosis.

Certifications and Safety Standards

The Smiths Medical 21-8066-24 Port-A-Cath Dual Lumen 6.6FR Tray is a medical device intended for professional healthcare use. It should be handled in accordance with applicable medical device regulations, sterile procedure standards, hospital policies, and the manufacturers instructions for use.

Clinicians should confirm the products labeling, packaging integrity, sterility status, lot information, and expiration date before use. Any damaged, opened, expired, or compromised packaging should not be used. Facilities should follow applicable standards for implantable vascular access devices, sharps handling, infection prevention, and post-procedure documentation.

Comparison with Competitors

Compared with basic single-lumen port options, the Smiths Medical 21-8066-24 Port-A-Cath Dual Lumen Tray provides two access pathways, which can be beneficial in selected patients who require more flexible long-term vascular access. The complete tray configuration also offers procedural convenience by including key placement components in one organized package.

Compared with trays that require additional separately sourced accessories, this Smiths Medical Port-A-Cath tray may help streamline preparation, reduce setup complexity, and support consistency across procedures. The titanium port and polyurethane catheter combination is designed for durable implanted access while maintaining compatibility with standard clinical workflows for long-term infusion management.

Typical User Profile and Application Scenarios

This product is typically used by physicians, surgeons, interventional radiologists, vascular access specialists, oncology clinicians, and trained procedural teams responsible for implantable port placement and management. It is suitable for healthcare facilities that provide long-term infusion therapy, oncology treatment, specialty medication administration, and recurring vascular access services.

Typical scenarios may include patients requiring repeated infusions, long-term medication therapy, oncology care, parenteral nutrition, or frequent blood sampling. The dual lumen design may be preferred when clinical care plans require separate access channels, subject to therapy compatibility and provider assessment.

Best Practices for Use and Maintenance

Best practices for using the Smiths Medical 21-8066-24 Port-A-Cath tray include careful pre-procedure planning, confirmation of patient suitability, strict sterile technique, proper component inspection, and adherence to institutional vascular access protocols. All procedural staff should be familiar with the tray contents and the correct use of each component before beginning the procedure.

For maintenance, healthcare teams should follow approved port access, flushing, locking, dressing, and needle-change protocols. Proper aseptic technique should be used whenever the port is accessed. Documentation should include device details, placement information, lot number when required, site assessment, patient response, and any complications or follow-up instructions.

Facilities should also maintain staff training on implantable port care, infection prevention, occlusion management, and safe sharps disposal. Routine monitoring helps support long-term device performance and patient safety.

Regulatory and Safety Information

The Smiths Medical 21-8066-24 Port-A-Cath Dual Lumen 6.6FR Polyurethane Titanium Port Tray is intended for use by licensed healthcare professionals in appropriate clinical settings. It should not be used by untrained personnel or outside approved medical procedures.

All users should follow the manufacturers instructions for use, facility policies, and applicable regulatory requirements. The product should be stored according to labeled conditions and used before the expiration date. Any adverse events, suspected device malfunctions, or product quality concerns should be reported according to institutional policy and applicable reporting requirements.

As with all implantable vascular access devices, potential risks may include infection, bleeding, thrombosis, embolism, catheter occlusion, catheter fracture, vessel injury, port rotation, migration, and other procedure-related complications. Patient selection, placement technique, and ongoing maintenance should be guided by qualified clinical judgment.

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.