BD 2652210 - PowerLoc PAK Safety Infusion Set, 22G x 1", Without Y-Injection Site", 5/CS (Temp Sensitive; Non-Returnable) (Continental US Only)

BD 2652210 - PowerLoc PAK Safety Infusion Set, 22G x 1", Without Y-Injection Site", 5/CS (Temp Sensitive; Non-Returnable) (Continental US Only)

The BD 2652210 PowerLoc PAK Safety Infusion Set is a professional port-access solution designed for accessing compatible surgically implanted vascular ports. The set features a 22-gauge non-coring needle with a 1-inch length and is configured without a Y-injection site, providing a streamlined direct fluid pathway for compatible infusion and vascular-access procedures.

The PowerLoc system is designed to support the administration of compatible fluids and medications, blood specimen collection, implanted port flushing, and power injection through appropriately rated vascular access systems. The 22-gauge configuration provides a smaller needle profile for applications where moderate flow capability is appropriate.

The 1-inch needle length accommodates implanted ports positioned at a moderate depth beneath the skin. Proper needle-length selection helps support complete septum access, secure positioning, effective dressing application, and appropriate access-site management.

Because BD 2652210 is configured without a Y-injection site, it provides a direct infusion pathway without an integrated secondary medication or fluid-access point. This design may be suitable for clinical workflows where a single primary connection is preferred.

The PowerLoc safety mechanism is designed to help reduce accidental needlestick exposure during port deaccessing. As the needle is removed from the implanted port and enters the base, a protective shield covers the needle point and the needle locks into place. Tactile feel, an audible click, and visual confirmation help verify safety activation.

The PowerLoc platform also features a small footprint, low-profile construction, lightweight design, site visibility, ergonomic wings, and adaptability for appropriate dual-lumen implanted ports. The PAK presentation provides an organized, all-in-one approach intended to simplify the multi-step sterile port-access preparation process. BD 2652210 is supplied five sets per case.

Key Benefits

• 22-gauge non-coring needle supports access to compatible surgically implanted vascular ports.
• One-inch needle length accommodates ports positioned at a moderate depth beneath the skin.
• Smaller 22-gauge profile is suitable for applications where moderate flow capability meets clinical requirements.
• Power-injectable design supports compatible contrast-enhanced diagnostic imaging procedures.
• 22-gauge PowerLoc configurations support power-injection flow rates up to 2 mL per second when the complete vascular-access system is appropriately rated.
• Configuration without a Y-injection site provides a streamlined direct fluid pathway.
• Non-coring needle design supports repeated access to compatible implanted port septa.
• Integrated safety mechanism covers and locks the needle point following deaccessing.
• Tactile, audible, and visual confirmation help verify safety lockout.
• Low-profile design supports appropriate dressing application.
• Small footprint helps maintain access-site visibility.
• Lightweight construction helps minimize unnecessary bulk at the port site.
• Downward-angled tubing helps support dressing integrity.
• Ergonomic wing design supports controlled access and site visibility.
• Adaptable for appropriate dual-lumen implanted port applications.
• Suitable for compatible medication administration, blood sampling, port maintenance, and power-injection workflows.
• PAK configuration helps organize supplies used during sterile port-access preparation.
• Five-per-case packaging supports efficient clinical inventory management.

Compatibility and Applications

The BD 2652210 PowerLoc PAK Safety Infusion Set is intended for use with compatible surgically implanted vascular access ports designed to accept non-coring port-access needles.

Potential clinical applications include medication administration, antibiotic therapy, hydration, selected chemotherapy treatments, parenteral nutrition, blood specimen collection, implanted port flushing, long-term infusion therapy, and compatible contrast-media injection during diagnostic imaging procedures.

The 22-gauge configuration may be selected when a smaller needle profile and moderate flow capability meet the requirements of the prescribed therapy. Selection should consider medication or solution characteristics, required flow rate, implanted port specifications, infusion equipment, imaging requirements, and professional clinical judgment.

The 1-inch needle length may be appropriate when a 0.75-inch access needle does not provide sufficient depth but a 1.5-inch configuration would provide unnecessary additional length. Tissue depth and implanted port position should be assessed before needle selection.

Because the set does not include a Y-injection site, it provides a direct fluid pathway without an integrated secondary access point. This configuration may be appropriate when the planned treatment uses a single primary connection and does not require intermittent medication or fluid administration through a Y-site.

For power injection, the implanted port, PowerLoc needle, tubing, connectors, extension components, and every other device within the complete fluid pathway must be appropriately rated for the intended procedure. The lowest-rated component determines the maximum allowable operating pressure and flow rate.

Compatibility should be confirmed with the exact implanted port model, septum design, tissue depth, prescribed therapy, infusion pump, power injector, connector system, dressing materials, and institutional vascular-access procedures.

Usage Guidelines

The BD 2652210 should be used only by healthcare professionals trained and authorized to access implanted vascular ports. Current manufacturer instructions, aseptic technique, institutional procedures, and the implanted port manufacturer's directions should be followed throughout the procedure.

• Confirm the patient's identity, prescribed therapy, implanted port type, and power-injection status when applicable.
• Assess the location and depth of the implanted port before selecting the 1-inch needle.
• Verify that the 22-gauge configuration provides appropriate flow capability for the intended therapy or imaging procedure.
• Confirm that a configuration without a Y-injection site is appropriate for the planned workflow.
• Inspect the package for damage, punctures, contamination, moisture, or compromised integrity before use.
• Prepare the implanted port site according to institutional skin-antisepsis and sterile-access procedures.
• Prime the complete fluid pathway with an approved solution using aseptic technique.
• Remove air from the fluid pathway before accessing the implanted port.
• Stabilize the implanted port and insert the non-coring needle perpendicular to the septum using an approved technique.
• Advance the needle carefully until appropriate access to the implanted port reservoir is achieved.
• Verify correct needle placement according to institutional policy, including aspiration for blood return when clinically appropriate.
• Flush the implanted port according to current manufacturer instructions and facility protocol.
• Position and secure the tubing to minimize pulling, twisting, pressure, and dressing disruption.
• Apply an approved dressing while maintaining appropriate access-site visibility.
• Monitor the site for pain, swelling, redness, leakage, displacement, or other abnormalities throughout therapy.
• Confirm power-injection eligibility before connecting the system to a power injector.
• Do not exceed 2 mL per second or the lower operating limit of any component within the complete vascular-access system.
• After therapy, flush and lock the implanted port according to the prescribed protocol.
• Stabilize the port while withdrawing the needle and allowing the safety mechanism to engage.
• Confirm safety lockout through tactile feel, the audible click, and visual verification.
• Dispose of the used device immediately in an approved sharps container.

Stop the procedure and assess the vascular-access system if unexpected resistance occurs during flushing, appropriate blood return cannot be obtained when expected, the patient experiences unusual discomfort, or swelling, leakage, displacement, or another abnormality develops at the port site.

Certifications and Safety Standards

The BD 2652210 PowerLoc PAK Safety Infusion Set is designed for professional medical use within established vascular-access, infusion-therapy, diagnostic imaging, infection-prevention, and occupational safety programs.

The device should be incorporated into facility procedures addressing implanted port assessment, sterile preparation, skin antisepsis, port access, infusion administration, dressing management, power injection, deaccessing, and sharps disposal.

The integrated safety mechanism is designed to help reduce the risk of needle-related injury during deaccessing. As the needle is withdrawn into the base, a safety shield rotates over the needle point and the needle locks into place.

Tactile feedback, an audible click, and visual confirmation help clinicians verify that the safety lockout has engaged before transportation and disposal.

The safety mechanism supports needlestick-prevention practices but does not replace appropriate clinician training, personal protective equipment, safe sharps handling, exposure-control procedures, or immediate disposal in an approved sharps container.

The non-coring needle should be selected according to patient anatomy, implanted port depth, prescribed therapy, required flow characteristics, and the current instructions supplied with the implanted port and access device.

Healthcare organizations should review current manufacturer documentation for applicable regulatory status, UDI information, sterilization details, material composition, natural rubber latex information, DEHP information, shelf life, pressure limitations, warnings, precautions, contraindications, and other product-specific requirements.

Comparison with Competitors

Compared with conventional implanted port needles without integrated safety technology, the BD PowerLoc system incorporates a mechanism that covers and locks the needle point during deaccessing. This design can support safer handling between needle removal and final sharps disposal.

Compared with PowerLoc configurations containing a Y-injection site, BD 2652210 provides a direct fluid pathway without an integrated secondary access point. This may simplify the tubing configuration when secondary medication or fluid administration through a Y-site is not required.

Compared with non-power-injectable port-access devices, the PowerLoc platform supports compatible power-injection procedures when used with an appropriately rated implanted port and complete vascular-access system.

Compared with 19-gauge and 20-gauge PowerLoc configurations, the 22-gauge needle provides a smaller external profile but lower maximum power-injection flow capability. The 22-gauge platform supports up to 2 mL per second, while larger-gauge PowerLoc options may be selected when higher flow capability is required.

Compared with a 0.75-inch needle, the 1-inch configuration accommodates ports positioned at a greater tissue depth. Compared with a 1.5-inch needle, it may provide a lower access profile when additional needle length is unnecessary.

Compared with loose individual port-access supplies, the PAK presentation provides an organized solution for the multi-step sterile preparation process. This can help streamline preparation and support consistent port-access workflows across clinical teams.

Alternative safety infusion sets may vary in gauge, needle length, power-injection capability, safety activation method, tubing configuration, Y-site availability, kit contents, and package quantity. BD 2652210 combines a 22-gauge, 1-inch non-coring needle with a direct no-Y-site configuration, integrated safety technology, power-injection capability, and organized PAK presentation.

Typical User Profile and Application Scenarios

The BD 2652210 PowerLoc PAK Safety Infusion Set is intended for trained healthcare professionals responsible for accessing and managing implanted vascular ports. Typical users include infusion nurses, oncology nurses, radiology nurses, vascular-access specialists, physicians, advanced practice clinicians, and other qualified healthcare personnel.

Common use environments include hospitals, oncology centers, outpatient infusion clinics, diagnostic imaging departments, ambulatory treatment centers, emergency departments, specialty practices, and other healthcare facilities where surgically implanted vascular ports are routinely accessed.

The product may be selected for patients whose implanted port requires a 1-inch access needle and whose prescribed treatment or diagnostic procedure is compatible with a 22-gauge device.

Typical application scenarios include medication infusion, antibiotic therapy, hydration, selected chemotherapy treatments, parenteral nutrition, blood specimen collection, routine implanted port maintenance, and compatible contrast-media injection procedures.

The configuration without a Y-injection site is particularly relevant for clinical workflows using a direct primary connection that do not require an integrated secondary medication or fluid-access point within the tubing.

Best Practices for Use and Maintenance

The BD 2652210 is intended as a single-use medical device. Best practices focus on appropriate storage, accurate product selection, sterile preparation, implanted port access, site monitoring, power-injection verification, safety activation, and disposal.

• Store unopened sets according to current manufacturer-recommended environmental conditions.
• Protect packages from moisture, excessive temperatures, crushing, punctures, and contamination.
• Rotate inventory according to expiration dates and facility stock-control procedures.
• Verify the BD 2652210 catalog number before opening the package.
• Confirm the 22-gauge size, 1-inch needle length, and configuration without a Y-injection site.
• Assess the patient's tissue depth and implanted port position before selecting the needle length.
• Confirm that the prescribed therapy and required flow characteristics are appropriate for a 22-gauge access device.
• Use strict aseptic technique during preparation, priming, insertion, connection, and dressing application.
• Prime the complete fluid pathway before accessing the implanted vascular port.
• Stabilize the implanted port during both needle insertion and removal.
• Position the tubing to minimize pulling, twisting, or pressure at the access site.
• Monitor the implanted port site and tubing connections throughout therapy.
• Verify that the entire vascular-access system is appropriately rated before any power-injection procedure.
• Do not exceed 2 mL per second or the lowest flow or pressure limit of any component within the complete system.
• Do not bend, cut, modify, repair, or otherwise alter the infusion set.
• Do not reuse or reprocess a device intended for single use.
• Confirm complete safety lockout immediately after needle withdrawal.
• Place the protected device directly into an approved sharps container.

Regulatory and Safety Information

The BD 2652210 PowerLoc PAK Safety Infusion Set should be used only by appropriately trained healthcare professionals and only for applications consistent with current manufacturer labeling, implanted port instructions, professional clinical judgment, and institutional policy.

Before use, verify the product identity, 22-gauge size, 1-inch needle length, no-Y-site configuration, package integrity, expiration date, and compatibility with the implanted vascular port. Do not use a device that is expired, damaged, contaminated, or supplied in compromised packaging.

The set should not be used for power injection unless the implanted port and every component within the complete fluid pathway are specifically rated for the intended procedure. Permitted pressure, flow rate, contrast-media characteristics, and other operating conditions must be confirmed before use.

Compatible 22-gauge PowerLoc configurations support power injection up to 2 mL per second under applicable manufacturer-specified conditions. The lowest-rated component within the complete vascular-access system determines the maximum allowable operating limit.

Incorrect needle-length selection, incomplete septum access, excessive pressure, needle displacement, or improper securement may contribute to infiltration, extravasation, leakage, tissue injury, implanted port damage, interrupted therapy, or other complications.

Because BD 2652210 does not include a Y-injection site, it does not provide an integrated secondary access point within the tubing. Clinical teams should confirm that a direct fluid pathway meets the requirements of the planned therapy before use.

The integrated safety mechanism should be activated according to current manufacturer instructions. The device remains a contaminated sharp following deaccessing and should be discarded immediately in an approved sharps container.

BD 2652210 is supplied five sets per case with a minimum order quantity of one case according to the manufacturer listing. Purchasing personnel should confirm current availability, shipping eligibility, storage requirements, order quantity, and applicable return conditions before purchasing.

How to Order

Select the BD 2652210 - PowerLoc PAK Safety Infusion Set without Y-Injection Site, 22G x 1" 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.