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BD 20019E - Pressure Rated Smallbore Bifuse Extension Set with 2 SmartSite Needle-Free Connectors, 9.5 Inch Length, 0.4 mL Priming Volume

BD  # 20019E - Pressure Rated Smallbore Bifuse Extension Set with 2 SmartSite Needle-Free Connectors, 9.5 Inch Length, 0.4 mL Priming Volume
Part Number BD 20019E
SKU Number CIA8042239
Sell Unit CASE
Ships Within Special Order
List Price Call for Pricing
Product Description

BD 20019E - Pressure Rated Smallbore Bifuse Extension Set with 2 SmartSite Needle-Free Connectors, 9.5 Inch Length, 0.4 mL Priming Volume

The BD 20019E Pressure Rated Smallbore Bifuse Extension Set is a sterile IV extension set designed for vascular access management, medication administration, and compatible contrast media delivery in professional healthcare settings. This configuration features smallbore bifuse tubing, two SmartSite needle-free connectors, two slide clamps, a Spin Male Luer Lock connector, a 9.5-inch tubing length, and an ultra-low 0.4 mL priming volume. The extension set is not made with DEHP and is labeled for use with compatible low-pressure power injectors up to 325 psi at the manufacturer's specified maximum flow rate.

The dual-access bifuse design provides greater flexibility for IV therapy while maintaining a compact fluid pathway that helps minimize medication and contrast media waste. The pressure-rated construction supports compatible imaging and infusion procedures, while the SmartSite needle-free connectors promote safe, efficient vascular access.

ManufacturerApplicationSterility
20019EIV Extension SetSterile

Key Benefits

The pressure-rated design is labeled for use with compatible low-pressure power injectors up to 325 psi and the manufacturer's specified maximum flow rate.

The two SmartSite needle-free connectors provide dual access points for medication administration, flushing, and vascular access maintenance while helping reduce sharps exposure risks.

The bifuse configuration supports simultaneous access and efficient multi-line management without requiring additional extension components.

The two slide clamps provide independent flow control during setup, priming, transport, and infusion management.

The ultra-low 0.4 mL priming volume helps minimize residual medication and contrast media within the extension set.

The DEHP-free construction supports healthcare facilities seeking infusion products manufactured without DEHP-containing materials.

Compatibility and Applications

The BD 20019E Extension Set is compatible with standard Luer Lock IV systems, compatible vascular access devices, infusion pumps, administration sets, syringes, SmartSite-compatible needle-free systems, and low-pressure power injectors operating within the manufacturer's specified limits.

Typical applications include IV medication administration, saline flushing, vascular access maintenance, compatible contrast media delivery, diagnostic imaging procedures, emergency medicine, critical care treatment, specialty infusion therapy, and outpatient infusion services.

This extension set is commonly used in hospitals, CT imaging suites, radiology departments, emergency departments, infusion centers, intensive care units, and outpatient treatment facilities.

Usage Guidelines

Use the BD 20019E only by trained healthcare professionals following manufacturer instructions, institutional protocols, and accepted infusion therapy standards. Before use, inspect the packaging to verify sterility, integrity, expiration date, and compatibility with the intended procedure.

Prime the extension set according to facility procedures and remove all air from the fluid pathway before patient connection. Verify secure attachment of the Spin Male Luer Lock connector, confirm proper operation of both slide clamps, and disinfect each SmartSite needle-free connector before every access.

When using a compatible low-pressure power injector, do not exceed the labeled operating limit of 325 psi or the manufacturer's specified maximum flow rate. Always follow the instructions for both the extension set and the injector system.

Certifications and Safety Standards

The BD 20019E Extension Set is manufactured under established medical device quality management systems and is intended to support safe infusion and vascular access practices in healthcare environments.

The sterile fluid pathway, pressure-rated construction, SmartSite needle-free connector technology, bifuse configuration, and DEHP-free materials support healthcare facility initiatives related to medication safety, infection prevention, and imaging workflow efficiency.

Comparison with Competitor Products

Compared with standard extension sets that are not pressure rated, the BD 20019E is designed for compatible low-pressure power injector applications up to 325 psi.

Compared with single-access extension sets, the bifuse configuration with two SmartSite needle-free connectors provides greater flexibility for medication administration and vascular access management.

The combination of pressure-rated performance, ultra-low priming volume, dual slide clamps, and DEHP-free construction makes this extension set well suited for demanding infusion and diagnostic imaging workflows.

Typical User Profile and Application Scenarios

The BD 20019E is commonly used by radiology technologists, infusion nurses, vascular access specialists, emergency clinicians, critical care professionals, anesthesiologists, oncology nurses, and outpatient infusion teams.

Typical applications include compatible contrast-enhanced imaging procedures, dual-access IV therapy, medication administration, saline flushing, vascular access maintenance, emergency treatment, specialty infusion therapy, and multi-line infusion management.

Best Practices for Use and Maintenance

Store the BD 20019E in a clean, dry environment according to manufacturer recommendations. Keep the extension set in its original sterile packaging until ready for use.

Use aseptic technique during setup and connection. Properly prime the tubing, disinfect both SmartSite needle-free connectors before each use, verify slide clamp operation, and ensure all Luer Lock connections remain secure throughout therapy or imaging procedures.

This extension set is intended for single-patient use only and should not be reused, reprocessed, or resterilized. Replace the set according to institutional protocols and manufacturer recommendations.

Regulatory and Safety Information

The BD 20019E Extension Set is intended for professional healthcare use only. It should be used according to manufacturer instructions, facility policies, vascular access guidelines, pressure-rated system requirements, and applicable healthcare regulations.

Healthcare personnel should verify compatibility with the intended infusion or imaging equipment before initiating pressure-assisted procedures and always remain within the manufacturer's specified operating limits.

Dispose of the used extension set according to facility policies and applicable biomedical waste regulations.

How to Order

Select the BD 20019E Pressure Rated Smallbore Bifuse Extension Set with Two SmartSite Needle-Free Connectors, Two Slide Clamps, Spin Male Luer Lock, Not Made with DEHP, 9.5 Inch Length, 0.4 mL Priming Volume, Sterile Fluid Path, and Labeling for Use with Compatible Low-Pressure Power Injectors up to 325 psi at the Manufacturer's Specified Maximum Flow Rate and add it to your cart. Complete checkout with your preferred shipping and payment options. For bulk orders, quotes, product availability, or further assistance, contact CIA Medical customer service at (312)275-5850 or use the contact form on this page.