Smiths Medical 21-6500-51 - PUMP, CADD-LEGACY+, MDL 6500, CE ENGLISH, EACH
The Smiths Medical 21-6500-51 CADD-Legacy+ Model 6500 Ambulatory Infusion Pump is designed for controlled medication delivery in professional healthcare and home infusion settings. Built for dependable ambulatory infusion support, this pump helps clinicians manage prescribed therapies with accuracy, portability, and patient-focused convenience.
This CE English model is supplied as an individual unit and is commonly used where compact infusion technology is required for continuous or intermittent therapy. Its practical design supports clinical workflow, patient mobility, and consistent medication administration under the direction of qualified healthcare professionals.
Key Benefits
The CADD-Legacy+ Model 6500 pump offers a reliable solution for ambulatory infusion therapy, helping healthcare teams deliver medication while allowing patients to remain mobile during treatment. Its compact construction makes it suitable for clinical environments, outpatient care, and home-based infusion programs.
The pump is designed to support controlled delivery of prescribed fluids and medications, helping reduce the need for stationary infusion equipment in appropriate care settings. Its user-focused interface supports efficient programming, monitoring, and operation by trained personnel.
As a recognized infusion pump platform, the CADD-Legacy+ system is valued for its portability, clinical practicality, and compatibility with established infusion workflows. It is a suitable choice for providers looking for a dependable ambulatory pump for regulated infusion therapy.
Compatibility and Applications
The Smiths Medical 21-6500-51 CADD-Legacy+ Model 6500 pump is intended for use with compatible CADD administration sets, accessories, and prescribed infusion protocols. Compatibility should always be confirmed with the facilitys approved device list, manufacturer documentation, and clinical policy before use.
This pump may be used in a range of infusion applications where ambulatory delivery is clinically appropriate. Typical settings include hospitals, outpatient infusion centers, specialty clinics, long-term care environments, and home infusion programs managed by licensed healthcare providers.
Common application areas may include pain management, specialty medication delivery, and other therapies requiring controlled ambulatory infusion. Use should always be based on the prescribers order, the patients clinical condition, and applicable institutional guidelines.
Usage Guidelines
The pump should be prepared, programmed, and operated only by trained healthcare professionals or properly instructed caregivers under clinical supervision. Before use, inspect the pump, confirm the correct medication order, verify compatible administration components, and ensure the device settings match the prescribed therapy.
Clinicians should check the battery condition, cassette or tubing connection, infusion parameters, alarms, and delivery status before starting therapy. The patient or caregiver should be educated on basic handling, alarm awareness, and when to contact the healthcare provider.
Do not use the pump if it appears damaged, fails self-checks, displays unresolved alarms, or does not operate as expected. Always follow the manufacturers instructions for setup, programming, cleaning, storage, and routine checks.
Certifications and Safety Standards
The Smiths Medical 21-6500-51 CADD-Legacy+ Model 6500 is identified as a CE English model, supporting use in markets and clinical environments where CE-marked medical devices are required. Healthcare facilities should confirm regulatory suitability, device status, and documentation before clinical deployment.
Infusion pumps are medical devices that must be used according to manufacturer guidance, institutional policy, and applicable healthcare regulations. Proper training, regular inspection, and adherence to safety procedures are essential for reducing medication delivery risks.
Users should maintain records of device checks, cleaning, service history, and any alarm or performance concerns according to facility protocols. If service or repair is required, the pump should be evaluated by qualified biomedical or authorized service personnel.
Comparison with Competitors
Compared with larger stationary infusion pumps, the CADD-Legacy+ Model 6500 offers a more portable option for therapies where patient mobility is important. Its ambulatory design makes it practical for outpatient and home infusion use while still supporting controlled medication delivery.
Compared with basic gravity-based delivery methods, the pump provides a more structured infusion process with programmable settings and alarm features. This can help clinicians manage therapy more consistently when precise delivery control is required.
For facilities already using CADD infusion systems, this model may also support workflow familiarity, staff training efficiency, and accessory standardization. Final product selection should be based on clinical requirements, therapy type, compatibility, service availability, and procurement policy.
Typical User Profile and Application Scenarios
This product is typically used by hospitals, infusion pharmacies, specialty care providers, outpatient clinics, and home infusion agencies that require reliable ambulatory infusion equipment. It is suited for clinical teams managing patients who need portable infusion support outside a traditional bedside setting.
Example scenarios include a patient receiving prescribed ambulatory therapy at home, an outpatient clinic preparing infusion treatment for continued mobility, or a care team managing therapy that requires controlled delivery over a defined period. The device should always be matched to the treatment plan and patient safety requirements.
Procurement teams may also consider this pump for standardizing ambulatory infusion equipment across clinical programs where CADD-compatible systems are already in use.
Best Practices for Use and Maintenance
Before each use, confirm that the pump is clean, intact, properly powered, and programmed according to the prescribed therapy. Verify the correct medication, dose, route, delivery settings, and administration set before beginning infusion.
Keep the pump protected from impact, excessive moisture, extreme temperatures, and unauthorized handling. Clean the exterior according to manufacturer-approved procedures and avoid using cleaning agents that may damage the device housing or controls.
Routine inspection, preventive maintenance, and calibration checks should be performed according to the manufacturers recommendations and facility policy. Any pump with performance concerns should be removed from use until properly evaluated.
Regulatory and Safety Information
The Smiths Medical 21-6500-51 CADD-Legacy+ Model 6500 should be used only for approved clinical purposes and in accordance with the manufacturers instructions for use. It is intended for medication delivery under the supervision of licensed healthcare professionals.
Users must follow applicable laws, facility policies, prescription requirements, and medication safety procedures. This product should not be used as a substitute for clinical judgment, patient assessment, or required monitoring during infusion therapy.
Always confirm that the pump, accessories, medication, and therapy settings are appropriate for the patient before use. Report device concerns, alarms, or suspected malfunctions according to institutional and regulatory reporting procedures.
How to Order
Select the Smiths Medical 21-6500-51 PUMP, CADD-LEGACY+, MDL 6500, CE ENGLISH, 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.
