BD MPX5302-C - Pressure Rated Extension Set with Removable MaxPlus Clear Needleless Connector, Y-Site, 9 Inch, 1.2 mL PV, 50/CS (Continental US Only) (Item on Manufacturer Allocation - Inventory Limited when Available)

BD MPX5302-C - Pressure Rated Extension Set with Removable MaxPlus Clear Needleless Connector, Y-Site, 9 Inch, 1.2 mL PV, 50/CS (Continental US Only) (Item on Manufacturer Allocation - Inventory Limited when Available)

The BD MPX5302-C Pressure Rated Extension Set is a sterile IV extension set designed to support safe, efficient, and controlled infusion therapy in professional healthcare settings. It features a removable MaxPlus Clear needleless connector, pinch clamp, needleless Y-site, male spin luer lock, 9 inch tubing length, and 1.2 mL priming volume.

This extension set is used to extend IV access while providing a secure needle-free access point for compatible fluid administration, medication delivery, flushing, and line management. The pressure-rated construction supports use in compatible infusion applications that require higher pressure tolerance, while the short 9 inch length helps reduce excess tubing near the patient access site.

BD lists the MPX5302-C as a pressure-rated, purple-striped, standard bore MaxPlus extension set with one removable MaxPlus Clear needle-free connector, pinch clamp, spin male luer lock, one NAC-y Y-site, sterile content, 1.2 mL approximate priming volume, and 325 psi pressure rating. :contentReference[oaicite:0]{index=0}

Key Benefits

• Pressure-rated design supports compatible infusion procedures requiring dependable pressure performance.
• Removable MaxPlus Clear needleless connector allows needle-free access and supports flexible connector management.
• Needleless Y-site provides an additional access point for compatible medication or fluid administration.
• Pinch clamp allows quick flow control during priming, setup, connection, and line handling.
• Male spin luer lock helps create a secure connection with compatible IV access devices.
• Standard bore tubing supports efficient fluid pathway management in routine and specialized IV applications.
• Short 9 inch tubing length helps reduce unnecessary line bulk around the patient access site.
• 1.2 mL priming volume supports predictable setup and helps clinicians manage fluid volume accurately.
• Sterile, single-use configuration helps reduce contamination risk when used according to facility protocol.

Compatibility and Applications

The BD MPX5302-C is compatible with standard luer lock IV systems, catheter access devices, compatible infusion pumps, and administration sets that accept a spin male luer lock connection. Its removable MaxPlus Clear connector supports facilities that use BD MaxPlus needle-free access components as part of their IV therapy workflow.

This extension set is suitable for hospitals, outpatient infusion centers, emergency departments, ambulatory surgery centers, oncology clinics, specialty care facilities, and general clinical environments where controlled IV extension access is needed. Common applications include IV line extension, medication administration, fluid delivery, catheter access management, flushing, and access through a needleless Y-site.

McKesson also identifies the MPX5302-C as a sterile MaxPlus Clear pressure-rated IV extension set with standard bore tubing, spin-lock connector, pinch clamp, NAC-y needle-free valve, 9 inch tubing length, and 1.2 mL priming volume. :contentReference[oaicite:1]{index=1}

Usage Guidelines

• Inspect the package before use and do not use the product if the sterile barrier is damaged, opened, or compromised.
• Use aseptic technique when opening, priming, connecting, accessing, or disconnecting the extension set.
• Prime the line completely before patient connection to help remove air from the tubing.
• Verify compatibility with the catheter, administration set, infusion pump, medication, and facility protocol before use.
• Use the pinch clamp to control flow during setup, priming, medication administration, and line changes.
• Disinfect the needleless connector according to institutional policy before each access.
• Do not reuse, reprocess, or resterilize the product.
• Dispose of the extension set after use according to facility medical waste procedures.

Certifications, Safety Standards, and Regulatory Approvals

The BD MPX5302-C is supplied as sterile content and is not made with natural latex according to BDs product specifications. BD also lists the product as registered with Health Canada, manufactured in Mexico, and not CE marked. The product is packaged 50 per case, with GTIN case 50885403237230 and GTIN each 10885403237232. :contentReference[oaicite:2]{index=2}

For procurement teams, these details help support product identification, inventory control, purchasing verification, and clinical supply standardization. Healthcare facilities should confirm current regulatory status, approved indications, instructions for use, and local compliance requirements directly through BD or an authorized distributor before clinical implementation.

Comparison with Competitor Products

The BD MPX5302-C is best compared with other pressure-rated IV extension sets from manufacturers such as B Braun, ICU Medical, Amsino, Codan, and other infusion therapy suppliers. Compared with basic non-pressure-rated extension sets, the MPX5302-C offers the advantage of pressure-rated performance, making it suitable for compatible applications where pressure tolerance is an important purchasing and clinical requirement.

Compared with extension sets that have fixed connectors, the removable MaxPlus Clear needleless connector provides additional flexibility for connector configuration and line management. Compared with extension sets without a Y-site, the BD MPX5302-C provides an added needleless access point, which may help clinicians manage compatible medication delivery or fluid access without adding another separate component.

Compared with longer extension sets, the 9 inch length provides practical access extension while helping reduce excess tubing around the patient. Its 1.2 mL priming volume also supports controlled fluid management, especially in settings where line volume matters during medication administration or catheter access management.

Typical User Profile and Application Scenarios

The typical users of the BD MPX5302-C include registered nurses, infusion nurses, vascular access specialists, emergency department clinicians, anesthesia teams, outpatient infusion staff, oncology nurses, and other trained healthcare professionals responsible for IV therapy and access device management.

This product is especially relevant in clinical workflows that require short IV line extension, needle-free access, a removable connector, a Y-site access point, secure luer connection, and pressure-rated tubing. It is commonly used during fluid administration, medication delivery, catheter connection management, flushing, and compatible infusion procedures across acute care and outpatient environments.

Best Practices for Use and Maintenance

• Store the product in a clean, dry medical supply area according to facility storage procedures.
• Keep the extension set in its original packaging until ready for use.
• Check the product reference number, expiration date, packaging integrity, and configuration before opening.
• Use only with compatible luer lock devices, infusion systems, medications, and pressure settings.
• Trace the IV line before connection, administration, or disconnection to help reduce the risk of misconnections.
• Follow facility policy for connector disinfection, flushing technique, clamping sequence, and replacement intervals.
• Avoid excessive pulling, twisting, kinking, or bending that may compromise tubing or connector integrity.
• Replace the extension set according to institutional protocol, manufacturer instructions, and patient-specific clinical requirements.

Regulatory and Safety Information

The BD MPX5302-C is intended for professional healthcare use by trained personnel. As a sterile, single-use IV extension set, it should not be reused or resterilized. Reuse may increase the risk of contamination, infection, leakage, device failure, or compromised patient safety.

Before use, clinicians should confirm that the device is appropriate for the intended infusion therapy, pressure requirements, medication compatibility, and IV access configuration. Do not use if the package is damaged, if the connector or tubing appears compromised, or if the product does not match the intended clinical application.

How to Order

Select the BD MPX5302-C Pressure Rated Extension Set, Removable MaxPlus Needleless Connector, Pinch Clamp, Needleless Y-Site, Male Spin Lock, 9" Length, 1.2 mL 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.