The Prevena Plus 125 Instruction Manual provides essential guidance for safe and effective use of the therapy unit․ It covers setup, application, and operational guidelines, ensuring optimal outcomes for surgical incision management․

1․1 Overview of the Prevena Plus 125 Therapy Unit

The Prevena Plus 125 Therapy Unit is a portable, single-use negative pressure wound therapy (NPWT) system designed for closed surgical incisions․ It is FDA-cleared for use in the United States and intended to manage surgical incisions by promoting wound healing and reducing complications․ The unit operates with a pre-set pressure of -125mmHg, providing continuous or intermittent therapy․ It is compact, lightweight, and designed for patient mobility, making it suitable for both hospital and home use․ The system is compatible with the Prevena Dressing, which is applied directly to the incision site․ The therapy unit is intended for use on closed surgical incisions and should not be used on open or dehisced wounds․ Always refer to the manual for detailed instructions before use․

Indications and Uses of the Prevena Plus 125

The Prevena Plus 125 is FDA-cleared for managing closed surgical incisions, promoting wound healing, and reducing complications through negative pressure therapy in the United States․

2․1 FDA Clearance and Intended Use

The Prevena Plus 125 Therapy Unit is FDA-cleared for use in managing closed surgical incisions․ It is designed to promote wound healing by applying negative pressure therapy to reduce fluid accumulation and enhance recovery․ The system is intended for patients with closed surgical wounds, aiding in the prevention of complications such as seroma or hematoma formation․ It is not approved for open or dehisced wounds․ The therapy unit is specifically engineered for use with Prevena dressings, ensuring a secure and effective application․ Always follow the guidelines outlined in the manual and consult healthcare professionals for proper usage and safety․

2․2 Contraindications and Restrictions

The Prevena Plus 125 Therapy Unit is not intended for use on open or dehisced wounds, or in cases where excessive exudate is present․ Patients with active bleeding, fragile skin, or those requiring antimicrobial therapy should avoid using this device․ It is also contraindicated for individuals with implanted devices that may interfere with negative pressure therapy․ Use is restricted to closed surgical incisions only, and the system should not be applied over exposed organs or non-intact skin․ Always adhere to the contraindications outlined in the manual to ensure safe and effective therapy․ Consult a healthcare professional if unsure about suitability for use․

Setup and Application of the Prevena Plus 125

Setting up and applying the Prevena Plus 125 involves preparing the therapy unit, adhering the dressing to the closed surgical incision, and connecting the system components safely․

3․1 Preparing the Therapy Unit for Use

Before using the Prevena Plus 125, ensure the therapy unit is fully prepared․ Begin by inspecting all components, including the control panel, power button, and connectors, for any damage․ Clean the exterior with a mild disinfectant if necessary․ Charge the unit according to the manufacturer’s instructions to ensure adequate battery life․ Next, review the settings and ensure they are programmed correctly for the intended use․ Finally, perform a quick system check by turning on the unit and verifying that all lights and alarms function properly․ This preparation ensures the therapy unit is ready for safe and effective application․

3․2 Applying the Prevena Dressing

Begin by preparing the surgical site, ensuring it is clean and dry for optimal adhesion․ Peel the backing from the Prevena dressing and carefully place it over the closed incision, aligning it centrally․ Smooth out any wrinkles or air pockets to ensure a secure seal․ Avoid touching the adhesive surface to prevent contamination․

Once applied, inspect the dressing to confirm proper placement and adhesion․ Use the transparent film to check for any gaps or misalignment without disturbing the dressing․ Proper application is critical for effective therapy and to prevent complications․ Ensure the dressing is snug but not overly tight to promote healing․

3․3 Connecting the Therapy Unit to the Dressing

After applying the Prevena dressing, locate the connector on the dressing and align it with the therapy unit’s port․ Gently insert the tubing into the port until it clicks, ensuring a secure connection․ Turn on the therapy unit and check for indicators, such as lights or sounds, confirming the connection is active․ Avoid over-tightening, as this may misalign the tubing․ Once connected, verify the vacuum is applied evenly by observing the dressing’s conformity to the skin․ Proper connection is essential for effective therapy․ If unsure, refer to the manual for detailed instructions to ensure optimal performance․

Operational Guidelines for the Prevena Plus 125

This section outlines monitoring the therapy unit’s status and troubleshooting common issues, ensuring optimal performance and addressing any malfunctions promptly for effective therapy continuation․

4․1 Monitoring the Therapy and System Status

Regular monitoring of the Prevena Plus 125 system is crucial for optimal therapy performance․ Check the control panel for status indicators, such as pressure levels and battery life․ Ensure the dressing remains securely sealed and free from leaks․ Monitor the therapy unit’s alarms, which signal issues like low battery or blockages․ Maintain the prescribed negative pressure settings and verify proper fluid collection․ If the Visicheck Feature indicates marginal status, assess and address potential concerns promptly․ Keep the therapy unit clean and ensure all connections are secure․ Refer to the manual for guidance on interpreting system status and addressing any anomalies during operation․

4․2 Troubleshooting Common Issues

Common issues with the Prevena Plus 125 may include low battery, blockages, or alarm activations․ If the system status indicates a problem, check the power connection and ensure the dressing is properly sealed․ Verify that tubing is not kinked or obstructed, as this can disrupt therapy․ For persistent alarms, review the control panel indicators to identify the specific issue․ Use the Visicheck Feature to assess dressing integrity and address any leaks or improper connections․ Refer to the manual for detailed troubleshooting steps or contact 3M support for assistance․ Always prioritize resolving issues promptly to maintain therapy effectiveness and patient safety․

Patient Guidelines for Using the Prevena Plus 125 at Home

Patients should follow home use instructions carefully, monitor the system daily, and adhere to safety precautions․ Proper dressing changes and therapy unit management are essential for optimal results;

5․1 Home Use Instructions and Safety Precautions

Patients using the Prevena Plus 125 at home must follow specific instructions to ensure safe and effective therapy․ The system should be operated in a clean, dry environment, away from direct sunlight or extreme temperatures․ Users should monitor the therapy unit daily, checking for proper function and dressing integrity․ In case of alarms, refer to the troubleshooting guide․ Avoid submerging the device in water or exposing it to open flames․ Patients should also maintain personal hygiene and avoid touching the dressing unnecessarily․ Regular follow-ups with healthcare providers are crucial to assess healing progress and address any concerns promptly․

5․2 Managing the Therapy Unit and Dressing

Proper management of the Prevena Plus 125 Therapy Unit and dressing ensures effective therapy and prevents complications․ Patients should perform daily visual inspections of the dressing and tubing for signs of leakage or damage․ The therapy unit should be kept clean and dry, and the dressing should remain securely sealed․ Used dressings and components must be disposed of according to local regulations․ Patients should avoid tampering with the therapy unit or dressing, as this may compromise its function; If the therapy unit indicates low battery or system issues, users should consult the troubleshooting guide or contact their healthcare provider immediately․ Regular dressing changes should only be performed by authorized personnel․

Manufacturer Support and Resources

For assistance, contact 3M customer support at 1-800-275-4524․ Additional resources and troubleshooting guides are available on the official 3M website or through authorized distributors․

6․1 Contact Information for Assistance

For immediate support, contact 3M customer service at 1-800-275-4524․ Additional resources, including troubleshooting guides and FAQs, are available on the official 3M website․ Patients and healthcare providers can also reach out to authorized distributors for further assistance․ The manufacturer ensures comprehensive support to address any inquiries or concerns regarding the Prevena Plus 125 Therapy Unit․ Technical assistance and replacement options are available for defective or malfunctioning units․ For detailed product information or clarification on usage, visit the 3M website or consult the provided patient guide․ Support is available 24/7 to ensure uninterrupted therapy management․