Smiths Medical 21-4424-24 - KIT, POWER PAC, VEN, TI, PU, 1.9MM, UL 1/EA

Smiths Medical 21-4424-24 - KIT, POWER PAC, VEN, TI, PU, 1.9MM, UL 1/EA

The Smiths Medical 21-4423-24 Kit, Power Pac, Venous, Titanium, Polyurethane, 1.9mm, UL, 1/EA is designed for clinical environments that require a dependable venous access solution with durable component construction and a compact procedural kit format. Built with a titanium port body and polyurethane catheter material, this Power Pac venous access kit supports controlled vascular access for appropriate infusion-related applications under the direction of trained healthcare professionals.

This single-use kit is intended to help streamline preparation, reduce component variability, and support consistent procedural workflow in hospitals, outpatient infusion centers, surgical departments, and specialty care settings. Its 1.9mm configuration offers a practical balance of performance, handling, and patient-focused placement considerations.

Key Benefits

• Titanium construction supports strength, durability, and long-term clinical reliability.
• Polyurethane catheter material provides flexibility and performance for venous access applications.
• 1.9mm size supports efficient use in appropriate vascular access procedures.
• Single-use kit format helps reduce preparation time and supports procedural consistency.
• Designed for professional healthcare use in controlled clinical settings.
• Helps standardize inventory for facilities using Smiths Medical vascular access products.

Compatibility and Applications

The Smiths Medical 21-4423-24 Power Pac Venous Titanium Polyurethane Kit is intended for use in compatible venous access procedures where a titanium port and polyurethane catheter system are clinically appropriate. It may be used in settings that manage infusion therapy, medication administration, oncology care, vascular access placement, and related treatment protocols.

This product should be selected according to facility protocol, clinician judgment, patient anatomy, prescribed therapy, and compatibility with approved access and infusion practices. Healthcare providers should confirm suitability with the applicable instructions for use and institutional standards before placement or use.

Usage Guidelines

Use of the Smiths Medical 21-4423-24 kit should be limited to trained clinicians experienced in venous access procedures. Before use, inspect the packaging and product components to confirm integrity, sterility, correct item number, and expiration status. Do not use the kit if the package is opened, damaged, contaminated, or otherwise compromised.

Prepare the patient and procedural field using aseptic technique in accordance with facility policy. Follow the manufacturer instructions for placement, flushing, access, maintenance, and disposal. After use, dispose of all single-use components according to institutional, local, state, and federal requirements for medical waste and sharps handling.

Certifications and Safety Standards

Smiths Medical vascular access products are manufactured for professional medical use and are designed to meet applicable healthcare quality, safety, and performance expectations. Facilities should review the product labeling, instructions for use, and any applicable regulatory documentation to confirm compliance with internal purchasing, clinical, and safety requirements.

All clinical staff should follow standard precautions, sterile technique, infection prevention procedures, and device-specific instructions when handling or using this product. Proper training and adherence to approved protocols are essential for safe and effective use.

Comparison with Competitors

Compared with general venous access kits, the Smiths Medical 21-4423-24 Power Pac Venous Titanium Polyurethane Kit offers the advantage of a recognized manufacturer, durable titanium construction, and a polyurethane catheter configuration designed for dependable clinical performance. The single-kit format supports efficient workflow and helps reduce the need to source multiple components separately.

For facilities comparing similar vascular access products, this kit may be preferred when standardized Smiths Medical product compatibility, consistent component quality, and established clinical familiarity are important purchasing factors. Its 1.9mm configuration also provides a targeted option for clinicians requiring this specific size profile.

Typical User Profile and Application Scenarios

This product is commonly suited for hospitals, ambulatory surgery centers, oncology departments, infusion centers, interventional radiology teams, and specialty clinics that require reliable venous access products. It is intended for use by physicians, advanced practice providers, vascular access specialists, and other trained healthcare professionals operating within their authorized scope of practice.

Typical scenarios may include planned venous access procedures, infusion therapy support, medication delivery access planning, and patient care situations where a titanium port and polyurethane catheter system are clinically indicated. Selection should always be based on the patients treatment plan and the clinicians assessment.

Best Practices for Use and Maintenance

Store the Smiths Medical 21-4423-24 kit in a clean, dry, temperature-controlled area away from direct sunlight, moisture, and contamination risks. Rotate inventory using first-expiring, first-out practices to help reduce product waste and maintain supply readiness.

Before use, verify product identification, size, package condition, and expiration date. During procedures, maintain strict aseptic technique and follow facility protocols for site preparation, device handling, access, flushing, dressing, documentation, and patient monitoring. Ongoing care should be performed only by qualified personnel following approved maintenance procedures.

Regulatory and Safety Information

The Smiths Medical 21-4423-24 Kit, Power Pac, Venous, Titanium, Polyurethane, 1.9mm, UL, 1/EA is a professional medical product and should be used only in accordance with the manufacturer instructions for use, applicable clinical guidelines, and institutional policies. It is not intended for reuse, reprocessing, or resterilization unless specifically permitted by the manufacturer labeling.

Clinicians should monitor for potential complications associated with venous access devices, including infection, occlusion, thrombosis, infiltration, device migration, or other adverse events. Any suspected device issue should be managed according to facility protocol and applicable reporting requirements.

How to Order

Select the Smiths Medical 21-4424-24 KIT, POWER PAC, VEN, TI, PU, 1.9MM, UL 1/EA 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.