The Covidien Kendall SCD 700 Series Manual is a comprehensive guide detailing operation, safety, and maintenance protocols for the sequential compression system, essential for healthcare professionals.
1.1 Overview of the Kendall SCD 700 Series
The Kendall SCD 700 Series is a sequential compression system designed to apply intermittent pneumatic compression, enhancing venous blood flow to prevent deep vein thrombosis and pulmonary embolism. It features a controller, tubing set, and compression sleeves or foot cuffs. The system is intended for use in healthcare settings and is customizable to individual patient needs, with a compliance meter to monitor therapy effectiveness. It is a critical tool for patients at risk of venous thromboembolism, offering safe and effective therapy.
1.2 Importance of the Manual for Users
The Covidien Kendall SCD 700 Series Manual is essential for safe and effective use of the system. It provides detailed instructions for setup, operation, and troubleshooting, ensuring optimal performance. The manual highlights safety precautions, maintenance requirements, and compliance standards, helping users adhere to regulatory guidelines. By following the manual, healthcare professionals can deliver proper therapy, minimize risks, and maintain device longevity. It serves as a critical resource for understanding system functionality and ensuring patient safety.
Indications and Contraindications
The Kendall SCD 700 Series is indicated for preventing deep vein thrombosis and pulmonary embolism in at-risk patients. Contraindications include severe leg injuries or active bleeding.
2.1 Approved Uses of the Kendall SCD 700 Series
The Kendall SCD 700 Series is designed for intermittent pneumatic compression therapy to enhance venous blood flow, primarily used for preventing deep vein thrombosis (DVT) and pulmonary embolism (PE) in at-risk patients. It is also indicated for circulation improvement, edema management, and post-operative recovery. The system is suitable for patients requiring prophylaxis or therapy in clinical or home care settings. Its design ensures safe and effective application of compression to legs or feet, tailored to individual patient needs, with a focus on improving blood flow and reducing venous stasis.
2.2 Contraindications for Use
The Kendall SCD 700 Series should not be used in cases of active deep vein thrombosis, severe peripheral artery disease, or presence of pacemakers/internal electronic devices. It is also contraindicated for patients with severe edema, fragile skin, recent surgery at the compression site, or conditions where increased venous return is harmful, such as severe heart failure. Additionally, patients with allergies to the device materials or inability to use the device correctly due to cognitive impairment should avoid using it.
System Components and Accessories
The Kendall SCD 700 Series includes a controller, tubing set, compression sleeves, cuffs, and a compliance meter. These components ensure safe and effective therapy delivery.
3.1 Controller and Tubing Set
The Kendall SCD 700 Series features a user-friendly controller that manages the sequential compression therapy. It includes a digital interface for setting therapy parameters and monitoring operation. The tubing set connects the controller to the compression sleeves or cuffs, ensuring proper airflow and pressure delivery. The controller also incorporates a compliance meter to track therapy effectiveness. Regular inspection and maintenance of the tubing set are crucial to ensure optimal performance and patient safety, as outlined in the manual. Proper storage and handling are also emphasized to prevent damage.
3.2 Compression Sleeves and Cuffs
The Kendall SCD 700 Series includes compression sleeves and cuffs designed for intermittent pneumatic compression therapy. The sleeves are used for leg compression to enhance venous blood flow, while the cuffs are for foot compression, aiding circulation and edema reduction. Proper sizing and fitting are crucial for effective therapy and patient comfort. The manual emphasizes cleaning and storing the sleeves and cuffs according to guidelines to maintain hygiene and longevity. Regular inspection ensures optimal functionality and safety during use.
3.3 Compliance Meter and Additional Features
The Kendall SCD 700 Series features a Compliance Meter to monitor and record therapy duration, ensuring adherence to treatment regimens. Additional features include adjustable pressure settings and customizable therapy modes. The system incorporates Covidien’s patented Vascular Refill Detection technology, which adapts compression to individual patient needs. These features enhance therapy effectiveness, improve patient comfort, and provide healthcare providers with valuable insights. The manual details how to utilize these tools for optimal performance and patient outcomes.
Operation and Service Manual Details
The manual provides detailed guidance for operating and servicing the Kendall SCD 700 Series, ensuring proper functionality and maintenance for healthcare professionals and technicians.
4.1 Quick Start Guide for Initial Setup
The Quick Start Guide simplifies initial setup of the Kendall SCD 700 Series. Begin by unpacking the controller from its polybag and inflatable packaging. Ensure all components, including the tubing set and compression sleeves, are included. Connect the tubing to the controller and compression sleeves, following the manual’s diagrams. Power on the device and perform a self-test to ensure proper function. Set the desired therapy parameters using the control panel. Refer to the manual for detailed instructions on initializing therapy and troubleshooting common issues during setup.
4.2 Step-by-Step Operating Instructions
Power on the Kendall SCD 700 controller and perform a self-test to ensure all functions are operational. Connect the tubing set to the controller and compression sleeves, ensuring secure attachments. Select the appropriate therapy mode and adjust pressure settings according to patient needs. Use the control panel to set therapy duration and cycle times. Monitor the Compliance Meter to track therapy effectiveness. Adjust settings as needed for patient comfort and therapeutic efficacy. Refer to the manual for guidance on pausing, resuming, or terminating therapy. Follow troubleshooting steps if errors occur during operation.
Safety Precautions and Warnings
The manual emphasizes electromagnetic compatibility guidelines to prevent interference with other medical devices. It also outlines error types and troubleshooting steps to ensure safe operation and resolve issues promptly.
5.1 Electromagnetic Compatibility Guidelines
The Covidien Kendall SCD 700 Series Manual provides specific electromagnetic compatibility guidelines to ensure safe operation in healthcare environments. The device is designed to function in controlled electromagnetic conditions, minimizing potential interference with other medical equipment. Users are advised to adhere to these guidelines to prevent malfunctions. Proper placement and operation in the specified electromagnetic environment are crucial. Failure to comply may result in device errors or inconsistent performance. Always consult the manual for detailed specifications and precautions.
5.2 Error Types and Troubleshooting
The Covidien Kendall SCD 700 Series Manual outlines three error types: User Resettable, Manual Reset Required, and Service Required. Each error type is defined with specific solutions. User Resettable errors can be resolved by the operator, while Manual Reset Required errors need manual intervention. Service Required errors demand professional assistance. The manual provides detailed troubleshooting steps to address common issues, ensuring optimal device performance and patient safety. Regular review of these guidelines helps users identify and resolve errors efficiently.
Maintenance and Service Requirements
Regular cleaning, disinfection, and replacement of wearable parts are crucial for optimal performance. Service technicians must follow detailed procedures to ensure proper device functionality and safety.
6.1 Cleaning and Disinfection Procedures
Proper cleaning and disinfection are essential for maintaining the Covidien Kendall SCD 700 Series. The controller and tubing sets should be cleaned with mild detergents, ensuring no residue remains. Visible extraneous markings or materials on returned tubing sets must be removed during cleaning; if not, the set should be discarded. Follow the manual’s guidelines for disinfection to ensure patient safety and device longevity. Regular cleaning prevents contamination and maintains optimal system performance.
6.2 Replacement of Wearable Parts
Replacement of wearable parts in the Covidien Kendall SCD 700 Series is crucial for maintaining system performance and patient safety. Tubing sets and compression sleeves should be replaced if damaged or soiled. The controller and compression cuffs must be inspected regularly, with worn or defective components replaced immediately. Use only Covidien-authorized parts to ensure compatibility and safety. Refer to the manual for specific part numbers and replacement procedures to guarantee optimal functionality and compliance with manufacturer guidelines.
Compliance and Regulatory Information
The Covidien Kendall SCD 700 Series complies with FDA clearance, international standards, and electromagnetic compatibility guidelines, ensuring regulatory adherence and safe operation as declared by the manufacturer.
7.1 FDA Clearance and Standards
The Covidien Kendall SCD 700 Series has received FDA clearance, ensuring compliance with strict regulatory standards for medical devices; It adheres to guidelines set by the U.S. Food and Drug Administration, confirming its safety and effectiveness in preventing deep vein thrombosis and pulmonary embolism; The system is designed to meet international standards for electromagnetic compatibility and performance, guaranteeing reliable operation in healthcare settings. This clearance underscores the manufacturer’s commitment to delivering high-quality, compliant solutions for patient care.
7.2 Manufacturer’s Declarations
Covidien declares the Kendall SCD 700 Series is designed to meet FDA standards and international regulations. The system is intended for use in healthcare settings to prevent deep vein thrombosis and pulmonary embolism. It complies with electromagnetic compatibility guidelines, ensuring safe operation in medical environments. The manufacturer emphasizes adherence to the manual for proper use, maintenance, and safety protocols. This ensures optimal performance and patient outcomes, aligning with Covidien’s commitment to quality and regulatory compliance.
The Covidien Kendall SCD 700 Series Manual effectively guides users on safe and optimal system operation, ensuring enhanced patient care and prevention of venous thromboembolism.
8.1 Summary of Key Features and Benefits
The Covidien Kendall SCD 700 Series offers a sequential compression system designed to enhance venous blood flow, preventing deep vein thrombosis and pulmonary embolism. Key features include intermittent pneumatic compression, a Compliance Meter for therapy tracking, and customizable settings. The system is user-friendly, with clear operating instructions and safety guidelines. It also incorporates Vascular Refill Detection Technology for personalized therapy. The device is versatile, supporting both leg and foot compression, making it suitable for various patient needs. Its compact design and portability enhance clinical utility, ensuring effective and reliable operation in healthcare settings. The manual provides detailed maintenance and troubleshooting tips, ensuring longevity and optimal performance.
8.2 Final Recommendations for Use
Adhere to the Covidien Kendall SCD 700 Series Manual for optimal performance and safety. Regularly inspect and maintain the system to ensure functionality. Train healthcare staff thoroughly on operation and troubleshooting. Monitor patient response closely and adjust settings as needed. Follow contraindications to avoid complications. Use genuine Covidien accessories to maintain device integrity. Clean and disinfect according to guidelines to prevent infection risks. Leverage the Compliance Meter for accurate therapy tracking. Always update to the latest software version for enhanced features. Ensure proper storage and transport to prolong device lifespan.
