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PRO 03970F Date Released: 14 Aug 2015CPulse System A Heart Assist DeviceInvestigational PlanConfidential Sunshine Heart Inc.This page is intentionally left blank.PRO 03970E Protocol CPulse System
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01
Start by washing your hands thoroughly and ensuring a clean working area.
02
Remove the C-Pulse device from its packaging carefully.
03
Read the user manual to familiarize yourself with the device components and functions.
04
Connect the device to the power supply and ensure it is charged.
05
Position the cuff on the patient's arm according to the instructions.
06
Adjust the settings on the device to match the patient's prescribed treatment.
07
Monitor the device display for proper readings and functionality.
08
Follow any additional instructions provided by the healthcare provider regarding the use of the device.

Who needs sunshine heart c-pulse device?

01
Individuals with moderate to severe heart failure, particularly those who are not candidates for heart transplant.
02
Patients who experience symptoms of heart failure, such as shortness of breath and fatigue.
03
People who are under the care of a cardiologist and have been advised to use mechanical circulatory support.
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The Sunshine Heart C-Pulse device is a type of mechanical circulatory support system designed to assist patients with heart failure by improving blood flow and reducing symptoms.
Healthcare providers or institutions that utilize the Sunshine Heart C-Pulse device for treatment or monitoring of patients are typically required to file related reports.
Filling out the Sunshine Heart C-Pulse device typically involves completing patient data forms, documenting device settings, and reporting clinical outcomes based on the manufacturer's guidelines.
The purpose of the Sunshine Heart C-Pulse device is to enhance the heart's ability to pump blood, thereby relieving symptoms associated with heart failure and improving patient quality of life.
Information that must be reported includes patient identification, device settings, performance metrics, and any complications or adverse events associated with the device's use.
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