BD MPXT1001-C - Pressure Rated T-Connector Extension Set with Removable MaxPlus Clear Needleless Connector, 6 Inch, 1.3 mL PV, 50/CS (Continental US Only)

BD MPXT1001-C - Pressure Rated T-Connector Extension Set with Removable MaxPlus Clear Needleless Connector, 6 Inch, 1.3 mL PV, 50/CS (Continental US Only)

The BD MPXT1001-C Pressure Rated T-Connector Extension Set is a sterile IV extension set designed for controlled infusion access, secure line extension, and needle-free connection in professional healthcare environments. It features a removable MaxPlus Clear needleless connector, pinch clamp, needle-free access T-connector, spin male luer lock, 6 inch approximate length, and 1.3 mL approximate priming volume.

This extension set supports clinicians who need a compact, pressure-rated IV accessory for medication administration, fluid delivery, catheter access management, and line organization. The T-connector configuration provides needle-free access within a short extension set design, while the removable MaxPlus Clear connector allows flexibility in setup and connector management.

BD lists the MPXT1001-C as a pressure-rated MaxPlus extension set with one removable MaxPlus Clear needle-free connector, pinch clamp, needle-free access T-connector, standardbore tubing, spin male luer lock, content sterile status, 325 psi pressure rating, 6 inch approximate length, and 1.3 mL approximate priming volume. :contentReference[oaicite:0]{index=0}

Key Benefits

• Pressure-rated construction supports compatible infusion procedures requiring dependable pressure tolerance.
• Needle-free access T-connector helps reduce unnecessary needle handling during IV therapy.
• Removable MaxPlus Clear needleless connector supports flexible line setup and connector replacement workflows when appropriate.
• Pinch clamp allows fast flow control during priming, connection, disconnection, and line handling.
• Spin male luer lock supports a secure connection with compatible IV access devices and administration systems.
• Short 6 inch configuration helps reduce excess tubing near the patient access site.
• 1.3 mL priming volume supports predictable fluid management during setup and administration.
• Sterile, single-use design helps reduce contamination risk when used according to institutional protocol.
• Not made with natural rubber latex, supporting use in facilities that manage latex-sensitive clinical environments. :contentReference[oaicite:1]{index=1}

Compatibility and Applications

The BD MPXT1001-C is compatible with standard luer lock IV systems, catheter access devices, compatible infusion setups, and administration components that accept a spin male luer lock connection. Its standardbore tubing and MaxPlus Clear needleless connector make it suitable for facilities using BD MaxPlus-compatible infusion components as part of their vascular access and IV therapy workflow.

This extension set is commonly used in hospitals, outpatient infusion centers, emergency departments, ambulatory surgery centers, oncology clinics, specialty care areas, and general clinical environments where short pressure-rated IV extension access is needed. Typical applications include IV line extension, medication administration, fluid delivery, catheter access management, line priming, and needle-free access through a T-connector configuration.

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 removing the extension set from packaging, priming the line, making connections, and accessing the needleless connector.
• Prime the extension set completely before patient connection to help remove air from the line.
• Confirm compatibility with the catheter, administration set, infusion pump, medication, pressure setting, and facility protocol before use.
• Use the pinch clamp to control flow during setup, priming, medication administration, and line handling.
• Disinfect the needleless connector according to institutional policy before each access.
• Do not reuse, reprocess, or resterilize the extension set.
• Dispose of the product after use according to facility medical waste procedures.

Certifications, Safety Standards, and Regulatory Approvals

The BD MPXT1001-C is supplied as sterile content and is not made with natural rubber latex. BD identifies this product as registered with Health Canada, manufactured in Mexico, and not CE marked. The listed packaging quantity is 50 per case, with GTIN case 50885403237322 and GTIN each 10885403237324. :contentReference[oaicite:2]{index=2}

These specifications help procurement teams verify product identity, packaging, and regulatory details before purchase. Healthcare facilities should confirm current regulatory status, approved use, instructions for use, and facility-specific compliance requirements directly through BD or an authorized distributor before clinical implementation.

Comparison with Competitor Products

The BD MPXT1001-C is best compared with other pressure-rated IV extension sets and T-connector 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 MPXT1001-C offers pressure-rated performance up to 325 psi, which can be important for compatible infusion applications where higher pressure tolerance is required.

Compared with longer extension sets, the MPXT1001-C provides a compact 6 inch length that helps reduce tubing clutter around the patient access site. Compared with extension sets that use fixed connectors, its removable MaxPlus Clear connector gives facilities more flexibility in line configuration and connector management. Compared with extension sets without T-connector access, the needle-free T-connector design provides an integrated access point without requiring an additional separate connector.

The B Braun N2150 Spike Adapter is not a direct equivalent to the BD MPXT1001-C because it is a spike adapter rather than a pressure-rated IV T-connector extension set. The BD MPXT1001-C is more appropriate for IV line extension, needle-free access, and catheter connection workflows, while spike adapters are typically used for connecting compatible containers or fluid systems depending on their specific design.

Typical User Profile and Application Scenarios

The typical users of the BD MPXT1001-C include registered nurses, infusion nurses, vascular access specialists, emergency department clinicians, anesthesia teams, outpatient infusion staff, oncology nurses, and trained healthcare professionals responsible for IV therapy and access device management.

This product is most relevant in clinical workflows requiring short line extension, pressure-rated performance, secure luer connection, needle-free access, and controlled flow management. Common scenarios include medication delivery, IV fluid administration, catheter access support, line priming, patient transfer preparation, and infusion setup in acute care or outpatient environments.

Best Practices for Use and Maintenance

• Store the product in a clean, dry medical supply area according to facility storage requirements.
• Keep the extension set in its original packaging until ready for use.
• Check the product reference number, expiration date, packaging integrity, and connector 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 MPXT1001-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 extension set 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 MPXT1001-C Pressure Rated T-Connector Extension Set, Removable MaxPlus Clear Needleless Connector, Pinch Clamp, Male Spin Lock, 6" Length, 1.3 mL PV 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.