Smiths Medical 21-8052-24 - TRAY PORT-A-CATH DUAL LUMEN 10.2FR 76CM SILICONE TITANIUM/POLYSULFONE PORT STRAIGHT/BLUNT NEEDLE 18GA INTRODUCER NEEDLE J GUIDEWIRE DILATOR/INTRODUCER SYRINGE 90 DEG NEEDLE UNASSEMBLED
The Smiths Medical 21-8052-24 Port-A-Cath Dual Lumen Tray is a specialized vascular access kit designed for clinicians who require a reliable implantable port system for dual-lumen therapy applications. This tray includes a 10.2 Fr, 76 cm silicone catheter with a titanium and polysulfone port construction, supporting long-term venous access where multiple infusion pathways may be clinically required.
Built for controlled placement and procedural efficiency, the tray includes essential components such as a straight and blunt needle, 18 gauge introducer needle, J guidewire, dilator and introducer, syringe, and 90 degree needle. The unassembled configuration allows healthcare professionals to prepare and place the device according to facility protocol and patient-specific needs.
Key Benefits
The Smiths Medical 21-8052-24 Port-A-Cath Dual Lumen Tray provides a complete procedural setup for implantable vascular access placement. Its dual-lumen design supports separate access channels, which may help streamline complex infusion therapy, medication delivery, blood sampling, or treatment regimens requiring distinct pathways.
The silicone catheter is designed for flexibility and patient comfort, while the titanium and polysulfone port materials support durability in long-term clinical use. The 10.2 Fr catheter size and 76 cm length offer practical versatility for vascular access procedures in appropriate clinical settings.
Included placement accessories help support procedural consistency, reduce the need to source separate components, and assist clinicians in maintaining an organized sterile workflow during port placement.
Compatibility and Applications
This Port-A-Cath dual lumen tray is intended for use by trained healthcare professionals in clinical environments where implantable venous access devices are placed and managed. It may be used in hospital, oncology, infusion therapy, interventional radiology, surgical, and specialty care settings where long-term vascular access is required.
The dual-lumen configuration may be suitable for patients who require multiple compatible therapies, frequent medication administration, blood draws, parenteral nutrition, or ongoing infusion protocols, depending on clinical judgment and institutional guidelines.
The tray components are designed to support placement of the Port-A-Cath system and should be used only with compatible clinical supplies, sterile technique, and facility-approved vascular access procedures.
Usage Guidelines
Use of the Smiths Medical 21-8052-24 Port-A-Cath Dual Lumen Tray should be limited to qualified clinicians trained in implantable port placement and vascular access management. Prior to use, inspect the tray packaging, product labeling, catheter, port, and included components to confirm sterility, integrity, expiration status, and correct product selection.
The clinician should follow the manufacturers instructions for use, institutional policy, and applicable clinical standards for patient preparation, sterile field setup, venous access, guidewire handling, catheter positioning, port placement, flushing, and post-placement verification.
All components should be handled using aseptic technique. Do not use the product if the package is damaged, opened, contaminated, or if any component appears defective. Dispose of needles, sharps, and single-use materials according to facility policy and applicable regulations.
Certifications and Safety Standards
The Smiths Medical 21-8052-24 Port-A-Cath Dual Lumen Tray is manufactured for professional medical use and should be handled according to the product labeling, manufacturer instructions, and healthcare facility protocols. As with all implantable vascular access products, proper sterile technique, patient assessment, placement verification, and ongoing maintenance are essential to safe use.
Healthcare providers should confirm all applicable regulatory information, device labeling, and facility requirements before use. Product selection and use should align with clinical standards for implantable ports, infection prevention, sharps safety, and vascular access management.
Comparison with Competitors
Compared with standard single-lumen implantable port systems, the Smiths Medical 21-8052-24 Port-A-Cath Dual Lumen Tray offers two access pathways within one port system, making it a practical choice for patients who may require more complex therapy management. Its included placement components also help simplify procedural preparation compared with sourcing individual items separately.
The combination of silicone catheter material with titanium and polysulfone port construction supports a balance of flexibility, strength, and clinical durability. For facilities that already use Smiths Medical vascular access products, this tray may provide consistency in product familiarity, procedural workflow, and inventory planning.
Typical User Profile and Application Scenarios
This product is typically used by vascular access specialists, surgeons, interventional radiologists, oncologists, infusion therapy teams, and other trained clinicians responsible for implantable port placement or management. It is suited for healthcare environments where dependable long-term venous access is a key part of patient care.
Common application scenarios may include oncology treatment support, long-term infusion therapy, medication administration, blood sampling, nutritional support, or other clinician-directed therapies that require repeated vascular access. The dual-lumen design may be especially useful where therapy separation or simultaneous access capability is clinically preferred.
Best Practices for Use and Maintenance
Before placement, confirm the correct product size, patient suitability, and procedural plan. Maintain sterile technique throughout the procedure and follow manufacturer instructions for catheter preparation, port handling, guidewire use, and device placement.
After implantation, maintain the port according to institutional vascular access protocols. This may include appropriate flushing, locking, dressing care, access needle selection, site assessment, infection prevention practices, and documentation of port function. Only trained healthcare personnel should access or maintain the device.
Regular assessment of the port site and catheter function is important for early identification of complications such as occlusion, infection, infiltration, dislodgement, or mechanical concerns. Any suspected issue should be addressed according to clinical policy and physician direction.
Regulatory and Safety Information
The Smiths Medical 21-8052-24 Port-A-Cath Dual Lumen Tray is intended for professional healthcare use only. It should be used only as directed by the manufacturers instructions for use and only by clinicians qualified to perform or assist with implantable vascular access procedures.
Follow all applicable federal, state, local, and institutional requirements for sterile medical devices, implantable products, sharps handling, patient consent, procedure documentation, and medical waste disposal. This product should not be reused or resterilized unless the manufacturer labeling specifically permits it.
Clinical teams should review all warnings, precautions, contraindications, and compatibility information before use. Final product selection should be based on patient condition, therapy requirements, provider judgment, and facility protocol.
How to Order
Select the Smiths Medical 21-8052-24 TRAY PORT-A-CATH DUAL LUMEN 10.2FR 76CM SILICONE TITANIUM/POLYSULFONE PORT STRAIGHT/BLUNT NEEDLE 18GA INTRODUCER NEEDLE J GUIDEWIRE DILATOR/INTRODUCER SYRINGE 90 DEG 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.
