BD 2865B - Alaris Medsystem III Infusion Pump Refurbished, EACH
The BD 2865B Alaris Medsystem III Infusion Pump Refurbished is a reliable large-volume infusion pump designed to deliver precise, controlled IV fluid and medication therapy across a wide range of clinical settings. Manufactured by Becton, Dickinson and Company, the Alaris Medsystem III platform is widely recognized for its durability, accuracy, and ease of use in demanding healthcare environments.
This refurbished unit has been professionally inspected, tested, and restored to meet functional performance standards, offering a cost-effective solution for facilities seeking dependable infusion technology without the expense of new capital equipment.
Product Overview
The Alaris Medsystem III pump is engineered to support continuous and intermittent infusion therapies with consistent flow accuracy. Its intuitive interface allows clinicians to program infusion parameters efficiently, helping reduce setup time and user error.
Designed for compatibility with dedicated Alaris administration sets, the system supports standardized infusion practices while maintaining dependable performance in high-utilization environments.
Key Benefits
The refurbished BD 2865B infusion pump provides reliable infusion accuracy while significantly reducing acquisition costs. Its proven design supports consistent medication and fluid delivery, helping clinicians maintain therapeutic precision.
The robust construction is suited for repeated clinical use, and the intuitive controls support efficient staff training and daily operation. Refurbishment extends the service life of the device while supporting sustainable equipment utilization.
Compatibility and Applications
The BD Alaris Medsystem III pump is designed for use with compatible Alaris IV administration sets. It integrates seamlessly into existing infusion workflows and IV therapy protocols.
Typical applications include IV fluid delivery, medication infusions, hydration therapy, and maintenance fluids in hospitals, outpatient clinics, infusion centers, emergency departments, and long-term care facilities.
Usage Guidelines
The pump should be set up and programmed by trained clinical staff following institutional infusion protocols. Only compatible administration sets should be used to ensure proper flow performance and alarm functionality.
Routine operational checks should be performed prior to use, and infusion parameters should be verified before initiating therapy. Cleaning and handling should follow facility biomedical equipment policies.
Certifications, Safety Standards, and Regulatory Approvals
The BD Alaris Medsystem III infusion pump is manufactured in accordance with FDA medical device regulations and internationally recognized quality standards. Refurbished units are inspected and tested to confirm functional performance and safety.
Regulatory compliance supports use in regulated healthcare environments and reinforces confidence in infusion accuracy and device reliability.
Comparison with Competitor Products
Compared with newer infusion platforms, the Alaris Medsystem III offers a proven, straightforward design without unnecessary complexity. While some competitor pumps include advanced connectivity features, the Medsystem III is often preferred for its simplicity, durability, and lower total cost of ownership.
Healthcare facilities frequently choose refurbished Alaris pumps to expand or replace infusion capacity while maintaining consistency across their equipment fleet.
Typical User Profile and Application Scenarios
Typical users include nurses, infusion specialists, biomedical technicians, and trained healthcare professionals responsible for IV therapy administration.
The pump is particularly effective in hospitals, outpatient infusion centers, emergency departments, surgical recovery areas, and long-term care environments where dependable infusion delivery is essential.
Best Practices for Use and Maintenance
Best practice includes routine inspection of the pump before use, verification of infusion settings, and adherence to facility cleaning protocols between patients. Scheduled biomedical evaluations help ensure continued performance and safety.
Using approved administration sets and following manufacturer and institutional guidelines supports optimal infusion accuracy and device longevity.
Regulatory and Safety Information
The BD 2865B Alaris Medsystem III Infusion Pump is classified as a regulated medical device and complies with applicable FDA requirements. Its design supports adherence to institutional IV therapy safety standards and equipment management policies.
Proper training, programming, and routine maintenance are essential to ensure safe, compliant operation.
How to Order
The BD 2865B Alaris Medsystem III Infusion Pump Refurbished is available through the CIA Medical website. Add the product to your cart and proceed through the secure checkout process.
For availability confirmation, bulk equipment inquiries, or additional assistance, contact CIA Medical customer service at 312 275 5850 or use the contact form available on this page for prompt support.
