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Smiths Medical 21-8068-24 - TRAY PORT-A-CATH DUAL LUMEN 9.6FR POLYURETHANE TITANIUM PORT STRAIGHT/BLUNT NEEDLE VEIN PICK 18GA INTRODUCER NEEDLE J GUIDEWIRE DILATOR SYRINGE 90 DEG NEEDLE TUNNELER
The Smiths Medical 21-8067-24 Port-A-Cath Dual Lumen Tray is a comprehensive vascular access tray designed for procedures requiring a 9.6 Fr dual lumen polyurethane catheter with a titanium port. This tray supports implantable port placement by providing essential procedural components, including a straight/blunt needle, vein pick, 18 gauge introducer needle, J guidewire, dilator, syringe, 90 degree needle, and tunneler.
Built for clinical efficiency and procedural consistency, this Port-A-Cath tray helps healthcare teams maintain an organized setup during implantable venous access procedures. Its dual lumen configuration is intended for situations where separate access channels may be clinically useful, supporting infusion, medication administration, blood sampling, and long-term vascular access needs when used according to facility protocols and clinician judgment.
Key Benefits
The Smiths Medical 21-8067-24 tray is designed to support accurate placement, dependable access, and streamlined preparation in clinical environments. The 9.6 Fr polyurethane catheter offers flexibility for vascular access applications, while the titanium port provides a durable implantable access platform suitable for long-term use.
The dual lumen design allows clinicians to manage compatible therapies through separate lumens when clinically appropriate. The included introducer needle, J guidewire, dilator, syringe, tunneler, vein pick, and needle components help reduce the need to gather multiple separate items before the procedure. This can support workflow efficiency, inventory control, and standardization across vascular access teams.
Compatibility and Applications
The Smiths Medical 21-8067-24 Port-A-Cath Dual Lumen Tray is commonly used in hospital, outpatient, interventional radiology, oncology, infusion therapy, and surgical settings where implantable venous access is required. It is suitable for clinical applications involving long-term vascular access, repeated infusion therapy, medication administration, blood draws, and compatible treatment protocols requiring an implanted port system.
The 9.6 Fr dual lumen polyurethane catheter and titanium port configuration should be used only by trained healthcare professionals familiar with implantable port placement, vascular access technique, sterile field management, and institutional policies. Compatibility with medications, infusion systems, access needles, and treatment protocols should always be confirmed by the clinician, facility guidelines, and the product documentation supplied with the device.
Usage Guidelines
Use of the Smiths Medical 21-8067-24 tray should follow the manufacturers instructions for use, institutional vascular access protocols, and applicable sterile technique requirements. Before opening the tray, verify the product reference number, package integrity, expiration date, and all required components for the planned procedure.
The device should be handled in a sterile environment by qualified healthcare personnel. Clinicians should assess patient anatomy, vascular access needs, therapy requirements, and contraindications before placement. After implantation, port access, flushing, dressing care, and maintenance should be performed according to facility policy and accepted clinical standards.
Certifications and Safety Standards
The Smiths Medical 21-8067-24 Port-A-Cath tray is intended for professional medical use and should be handled in accordance with applicable healthcare regulations, sterile processing expectations, and facility safety procedures. As with all implantable vascular access products, clinicians should consult the product labeling and manufacturer documentation for specific indications, contraindications, warnings, precautions, and storage requirements.
Healthcare facilities should ensure that staff using this product are trained in central venous access, implantable port placement, infection prevention, sharps handling, and post-placement care. Safety protocols should include sterile technique, proper patient identification, procedural timeout, documentation, and monitoring for potential complications.
Comparison with Competitors
Compared with general vascular access kits or trays requiring separately sourced components, the Smiths Medical 21-8067-24 offers a procedure-focused configuration that includes the port, catheter, introducer components, guidewire, dilator, syringe, needle options, vein pick, and tunneler in one organized tray. This can help reduce preparation time and support a more consistent procedural setup.
The titanium port construction, dual lumen design, and 9.6 Fr polyurethane catheter make this tray a strong option for facilities that need a dependable implantable access solution from a recognized medical device manufacturer. While competing products may offer different catheter materials, lumen configurations, or tray contents, this model is well suited for clinicians seeking a comprehensive dual lumen Port-A-Cath tray with essential placement accessories included.
Typical User Profile and Application Scenarios
This product is typically used by surgeons, interventional radiologists, vascular access specialists, oncology teams, infusion therapy clinicians, and trained procedural nurses working under appropriate supervision. It is commonly selected for patients who require reliable long-term vascular access for repeated therapies or clinical monitoring.
Typical application scenarios may include oncology infusion programs, long-term medication administration, complex infusion therapy, and other clinical settings where repeated peripheral access may be difficult or inappropriate. The dual lumen format may be considered when separate access pathways are needed for compatible therapies, subject to clinician assessment and facility protocol.
Best Practices for Use and Maintenance
Best practice begins with careful patient assessment, appropriate product selection, and confirmation that the tray configuration matches the planned procedure. Maintain strict sterile technique throughout setup and placement. Inspect all components before use and do not use the product if packaging is damaged, opened, or compromised.
After placement, follow facility protocols for port access, flushing, locking, dressing care, needle changes, and routine assessment. Monitor for signs of infection, occlusion, infiltration, catheter migration, thrombosis, or other complications. Proper documentation should include product details, placement site, patient tolerance, procedural findings, and post-procedure care instructions.
Regulatory and Safety Information
The Smiths Medical 21-8067-24 Port-A-Cath Dual Lumen Tray is a medical device intended for use by qualified healthcare professionals. It should not be used without appropriate clinical training, patient evaluation, and adherence to the manufacturers instructions for use. The device should be stored, handled, and disposed of according to applicable regulations and facility policies.
Because this product includes sharps and implantable vascular access components, users should follow all infection control, sharps safety, biohazard disposal, and procedural safety requirements. Patient-specific risks, contraindications, and therapy compatibility should be reviewed before use. This product description is for purchasing and product identification purposes and does not replace clinical training, prescribing judgment, or official product labeling.
How to Order
Select the Smiths Medical 21-8067-24 TRAY PORT-A-CATH DUAL LUMEN 9.6FR 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.
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