What to do if there is an air bubble alarm in my Fresenius Kabi Volumat Agilia?
If the volume of air detected in the line of your Fresenius Kabi Medical Equipment exceeds the limit, remove the air bubbles by rebooting the administration set. Also, check the air bubble size setting, calibrate, or replace the air detector.
What to do if I get an 'Administration set position alarm' on my Fresenius Kabi Volumat Agilia?
If you receive an administration set position alarm on your Fresenius Kabi Medical Equipment, it might be because the pump isn't detecting the safety clamp. Check the position of the administration set and ensure the door is closed. You may also need to check the clamp detection opto and replace it if necessary.
What to do for an Administration set insertion alarm on Fresenius Kabi Volumat Agilia?
If you're getting an administration set insertion alarm on your Fresenius Kabi Medical Equipment, begin by checking the administration set position. Also, check that the magnet is present on the door, calibrate the door sensor, or replace the door sensor.
What to do if my Fresenius Kabi Volumat Agilia shows an OCS test failure alarm?
If your Fresenius Kabi Medical Equipment shows an OCS test failure alarm, it could be because the pumping mechanism hasn't raised the pressure in the line during the test. Try checking the administration set position. Also, verify the pressure sensor calibration, the integrity of the membrane (replacing if needed), and the installation and integrity of the administration set.
What to do if the 'Door opened' alarm appears on my Fresenius Kabi Medical Equipment?
If you receive a 'Door opened' alarm on your Fresenius Kabi Medical Equipment, it might be because the Hall effect sensor detects that the door is open. Start by checking that the magnet is present on the door. Also, calibrate or replace the door sensor.
How to remove air bubble detected at start-up in Fresenius Kabi Volumat Agilia?
To address an air bubble detected at start-up or in stop mode on your Fresenius Kabi Medical Equipment, remove the air bubble by priming the administration set.
General| Brand | Fresenius Kabi |
|---|---|
| Model | Volumat Agilia |
| Category | Medical Equipment |
| Language | English |
Overview of the Volumat Agilia pump and its capabilities within the Agilia range.
Visual representation of the pump's components and internal connections.
Important guidelines for safe and correct usage of the device.
Critical safety measures and considerations during device operation.
Detailed technical data including electrical, mechanical, and material properties.
Specifications related to the device's power supply and electrical components.
Information on the internal electronic boards and their functions.
Physical dimensions and weight of the Volumat Agilia pump.
List of materials used in the construction of various device components.
Details on the device's adherence to relevant medical and safety standards.
Overview of the pump's external structure and main parts.
Details of the device's display board and its connectors.
Information about the central processing unit board and its connectors.
Details of the board managing power distribution and battery charging.
Information on the board connecting to the mains power supply.
Details of the board responsible for detecting air bubbles in the line.
Explanation of how the pump operates, its sub-assemblies, and functions.
How the device checks and maintains the administration set position.
Description of the peristaltic pumping mechanism.
Information on ports for mains power, nurse call, and serial links.
Access to menus for customizing infusion parameters and device settings.
Menu reserved for qualified staff to perform device calibrations.
Menu for performing diagnostic checks and tests on the device.
Menu for entering parameters related to maintenance tasks.
General advice for device care, servicing, and troubleshooting.
Guidelines for routine maintenance and quality control checks.
Specific procedures for maintaining the pump's performance.
Procedures for quality checks performed periodically on the device.
Outlines the different training levels for device maintenance and operation.
Procedures for performing various diagnostic tests on the pump.
Instructions on how to navigate and initiate diagnostic tests.
Procedure for visually inspecting the device's external condition.
Verifies device information including serial number and software versions.
Checks the running time and last maintenance date of the pump.
Displays information related to technical service interventions.
Lists device alarms stamped with date and time.
Measures and displays upstream pressure values and calibration data.
Measures and displays downstream pressure values and calibration data.
Checks the door's Hall Effect sensor values and calibration status.
Displays battery status, running time, cycles, and temperature.
Checks the functionality of indicator lights and the buzzer.
Verifies the correct operation of all keys on the device's keyboard.
Tests the motor block, pumping system, and occlusivity over time.
Assesses the pump's battery life and charge status.
Performs a complete battery discharge test to measure its performance.
Calibrates and tests the air detector board's functionality.
Checks the correct functioning of the clamp motor during displacement.
Verifies the flow rate coefficient and accuracy of the pump.
Displays and allows adjustment of the flow rate corrective coefficient.
Checks the presence, absence, and position of the administration set clamp.
Verifies the operation of the presence limit alarm.
Tests the device's transition between mains and battery power.
Confirms the device meets the required battery operational duration.
Performs electrical safety tests according to relevant standards.
Options for setting maintenance dates and initial device configuration.
Procedure for accessing the device's maintenance and diagnostic modes.
Screen to set the date for the next scheduled maintenance.
Activates initial configuration settings upon next device startup.
Manages and displays logged operational events and alarms.
Table to summarize results obtained from various device tests.
Procedures for measuring and verifying the infusion flow rate accuracy.
Method for checking flow rate using dedicated software and a computer.
Method for checking flow rate using a scale and measurement equipment.
Method for checking flow rate using a test tube and a chronometer.
Guidelines and procedures for cleaning and disinfecting the device.
Recommended conditions and procedures for storing the pump.
Best practices for maximizing the life and performance of the internal battery.
Table listing displayed messages, their meaning, causes, and actions.
List of error codes, their descriptions, and recommended actions.
Steps for safely accessing and replacing the battery or battery door.
Steps for accessing and removing the upper casing of the device.
Steps for accessing and replacing the device's display board.
Steps for accessing and replacing the central processing unit board.
Steps for accessing and replacing the power supply board.
Steps for accessing and replacing components within the device's base.
Steps for accessing and replacing the air detector board.
Steps for accessing and replacing the device's pumping system.
Steps for accessing and replacing the device's motor.
Steps for accessing and replacing the pressure sensors.
Steps for accessing and replacing the OCS clamp motor.
General procedure for accessing and performing device calibrations.
Instructions on how to enter the calibration menu using codes.
Procedure for calibrating the upstream and downstream pressure sensors.
Procedure for calibrating the door's Hall Effect sensor.
Procedure for calibrating the air detector board.
Procedure for calibrating the device's flow rate coefficient.
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