BD Nexiva™ Closed IV Catheter System with Single Port, 24GA, 0.56" Yellow, 383510

BD Nexiva™ Closed IV Catheter System with Single Port, 24GA, 0.56" Yellow, 383510

The BD Nexiva™ Closed IV Catheter System, item 383510, is a yellow, 24-gauge single-port configuration with a catheter length of 0.56 inches. It features Vialon™ biomaterial and is listed as latex-free, with a listed flow rate of 960 mL/hr. Available packaging includes 20 systems per box or 4 boxes per case, totaling 80 systems.

Product Features:

• Single-port configuration: Identifies the port arrangement for matching the required Nexiva™ system.
• 24-gauge size and 0.56-inch length: Specify the catheter dimensions for selecting item 383510.
• Vialon™ biomaterial: Identifies the catheter material listed for this configuration.
• Yellow colour: Provides a colour identifier for checking stock and ordering records.
• Latex-free: Reflects the listed latex-content specification.
• Listed flow rate: 960 mL/hr; consult the manufacturer's labeling for test conditions and applicable limitations.
• Box and case options: Choose 20 systems per box or 4 boxes per case, totaling 80 systems.

Product Specifications:

• Brand: BD
• Product line: Nexiva™
• Product type: Closed IV catheter system
• Port configuration: Single port
• Gauge: 24G
• Catheter length: 0.56 inches
• Colour: Yellow
• Material: Vialon™ biomaterial
• Latex content: Latex-free
• Listed flow rate: 960 mL/hr
• Item code: 383510
• Packaging: 20 systems per box; 4 boxes per case, 80 systems total

Product Selection and Ordering:

Match the BD Nexiva™ product line, single-port configuration, 24-gauge size, 0.56-inch catheter length, yellow colour, Vialon™ biomaterial and item code 383510 when reordering. Select the required box or case quantity. Other IV catheter systems may differ in port configuration, dimensions, materials or components and should not be assumed interchangeable based on colour or product-family name alone.

Professional Use and Handling:

For professional healthcare use. Consult the manufacturer's labeling and instructions and applicable clinical protocols for patient suitability, component compatibility, preparation, insertion, port use, flow-rate conditions, handling and disposal.