Smiths Medical 4000 - Medfusion 4000 Pump, Refurbished, Each

The Smiths Medical 4000 Medfusion 4000 Pump is a refurbished syringe infusion pump designed to support accurate, controlled medication delivery in hospitals, ambulatory care centers, specialty clinics, and other professional healthcare environments. Its programmable infusion capabilities make it suitable for therapies that require precise administration of small medication volumes over a defined period.

The Medfusion 4000 platform is commonly used for neonatal, pediatric, adult, critical care, anesthesia, and specialty infusion applications. The pump accommodates compatible syringe sizes and provides clinicians with configurable delivery options for continuous, intermittent, and dose-based infusion protocols. This refurbished unit is supplied individually and should be inspected, tested, and prepared for use in accordance with the receiving facility's biomedical engineering procedures.

Key Benefits

• Supports precise syringe-based medication and fluid delivery.
• Designed for neonatal, pediatric, and adult infusion applications.
• Offers programmable infusion settings for a variety of clinical protocols.
• Provides clear visual information to help clinicians monitor infusion status.
• Includes audible and visual alarms for conditions requiring clinical attention.
• Compatible with multiple syringe sizes and commonly used syringe brands when properly configured.
• Helps standardize syringe pump workflows across departments and care settings.
• Refurbished configuration may provide a cost-effective alternative to purchasing new infusion equipment.
• Compact design supports use at the bedside, on equipment poles, and during patient transport within healthcare facilities.

Compatibility and Applications

The Smiths Medical Medfusion 4000 Pump is intended for use with compatible syringes that are approved within the pump's configuration and the healthcare facility's medication delivery policies. Syringe compatibility, manufacturer selection, barrel size, and administration set requirements should be confirmed before each infusion.

Typical applications may include:

• Neonatal and pediatric medication administration.
• Critical care and intensive care infusions.
• Anesthesia and perioperative medication delivery.
• Emergency department treatment protocols.
• Cardiovascular and vasoactive medication infusions.
• Pain management and sedative administration.
• Antibiotic, electrolyte, and specialty medication delivery.
• Controlled enteral or fluid administration when clinically appropriate and permitted by facility protocols.

The pump should only be used with approved accessories, mounting hardware, power components, cables, syringes, and administration sets. Compatibility with existing equipment and medication safety systems should be verified by qualified clinical and biomedical personnel before deployment.

Usage Guidelines

1. Inspect the refurbished pump, power supply, housing, display, controls, syringe holder, and mounting components before use.
2. Confirm that preventive maintenance, electrical safety testing, calibration, and functional verification are current.
3. Select a compatible syringe brand and size as required by the facility's approved configuration.
4. Load and secure the syringe according to the manufacturer's operating instructions.
5. Verify the medication name, concentration, patient information, dose, infusion rate, volume, and delivery mode.
6. Prime the administration set and remove air in accordance with clinical policy before connecting it to the patient.
7. Confirm all programmed settings using the facility's independent double-check procedure when required.
8. Begin the infusion and observe the pump for correct operation, appropriate pressure, and secure syringe placement.
9. Respond promptly to occlusion, empty syringe, low battery, displacement, or other alarm conditions.
10. Document infusion details and inspect the patient, vascular access site, tubing, and pump at intervals established by the healthcare facility.

Certifications and Safety Standards

The Smiths Medical Medfusion 4000 Pump was developed for professional clinical use and should be operated in accordance with applicable medical electrical equipment requirements, institutional policies, and manufacturer documentation. Regulatory labeling, software configuration, service history, and available certification may vary according to the age and refurbishment history of the individual unit.

Before placing the refurbished pump into clinical service, the receiving facility should confirm that it has undergone appropriate inspection, calibration, electrical safety testing, alarm verification, battery assessment, and preventive maintenance. Biomedical engineering personnel should also verify that the unit meets applicable federal, state, local, and facility-specific equipment requirements.

Comparison with Competitors

Compared with basic syringe pumps, the Medfusion 4000 provides a broader selection of programmable infusion functions and clinical configuration options. Its interface and alarm system are designed to support complex medication delivery workflows in departments where small-volume accuracy and consistent syringe control are important.

Alternative syringe infusion pumps may offer different drug library functions, networking capabilities, syringe compatibility ranges, battery performance, or user interface designs. The Medfusion 4000 remains a practical choice for facilities that already use Medfusion equipment, maintain compatible accessories, or want to standardize staff training and service procedures around an established syringe pump platform.

A refurbished Medfusion 4000 may also offer a lower acquisition cost than a new syringe pump. Buyers should compare the unit's refurbishment process, software version, battery condition, warranty coverage, service documentation, included accessories, and compatibility with current clinical systems before purchasing.

Typical User Profile and Application Scenarios

The Smiths Medical 4000 Medfusion 4000 Pump is intended for trained healthcare professionals who administer and monitor syringe-based infusions. Typical users include registered nurses, physicians, anesthesiologists, nurse anesthetists, pharmacists, respiratory care professionals, and other authorized clinical personnel.

Common application scenarios include administering carefully controlled medications in a neonatal intensive care unit, managing vasoactive therapy in an adult critical care department, delivering anesthetic agents during perioperative care, or supporting specialty infusions in an emergency department or outpatient treatment center. Biomedical engineering teams may also select this refurbished model when replacing compatible equipment or expanding an existing Medfusion pump inventory.

Best Practices for Use and Maintenance

• Allow only trained and authorized personnel to program and operate the pump.
• Verify the selected syringe manufacturer and size before starting every infusion.
• Use standardized medication concentrations and approved clinical protocols whenever available.
• Perform an independent check for high-alert medications in accordance with facility policy.
• Keep the pump display, controls, syringe mechanism, and alarm openings clean and unobstructed.
• Use only cleaning agents and disinfection methods approved for the device.
• Do not immerse the pump or allow liquids to enter electrical openings.
• Inspect the power cord, battery, mounting clamp, and mechanical components regularly.
• Remove the unit from service if it is damaged, fails a self-test, displays repeated errors, or produces an unresolved alarm.
• Maintain complete records of calibration, battery replacement, software configuration, repair, and preventive maintenance.
• Store the pump in a clean, dry environment within the recommended temperature and humidity ranges.

Regulatory and Safety Information

This syringe infusion pump is intended for professional healthcare use and should not be operated by untrained individuals. Clinicians must review the applicable operating instructions, medication labeling, institutional policies, and patient-specific requirements before initiating therapy.

Incorrect syringe selection, improper loading, inaccurate programming, tubing occlusion, free flow, air in the administration pathway, depleted battery power, or failure to respond to alarms may result in delayed, excessive, or insufficient medication delivery. The pump does not replace direct patient observation or professional clinical judgment.

Because this product is refurbished, purchasers should confirm the refurbishment standard, warranty terms, included components, service records, software version, battery status, and inspection documentation before use. Product availability, physical appearance, accessories, and configuration may vary. Final suitability should be determined by the purchasing facility's clinical, technical, infection control, and biomedical engineering teams.

How to Order

Select the Smiths Medical 4000 Medfusion 4000 Pump, Refurbished, Each 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.