What to do if there is an air bubble alarm in my Fresenius Kabi Volumat MC 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 Medical Equipment?
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 MC Agilia Medical Equipment?
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 MC Agilia Medical Equipment 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 Volumat MC Agilia?
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 Medical Equipment?
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| Type | Infusion Pump |
|---|---|
| Manufacturer | Fresenius Kabi |
| Model | Volumat MC Agilia |
| Flow Rate Accuracy | ± 5% |
| Power Supply | 100-240 V AC, 50/60 Hz or rechargeable battery |
| Volume to be Infused (VTBI) | 1 ml to 9999 ml |
| Infusion Modes | Intermittent |
| Alarm System | Occlusion, Air-in-line, Low Battery, End of infusion |
| Occlusion Pressure | Adjustable |
| Bolus Rate | Adjustable |
| Battery Life | Approximately 8 hours at 5 ml/h |
| Display | LCD |
Explains the three distinct modes for programming the pump.
Details the various authorised infusion modes available for the pump.
Specifies intended use and essential safety precautions for device operation.
Labels and identifies the main external parts of the infusion pump.
Overview of the pump's front panel controls and screen elements.
Illustrates various methods for positioning the infusion pump unit.
Explains the procedure for using the pump's fixing clamp for secure mounting.
Steps for installing the device, preparing the set, and purging.
Detailed steps for correctly installing the tubing set into the pump.
Explanation of the pump's monitoring screen elements and their functions.
Operating without a drug name in ml/h flow rate mode.
Details alternative infusion modes in ml/h rate.
Explains Time/Rate, Simple rate, and Drops/minute modes.
Instructions for using the Ramp infusion mode.
Details programming and using the Sequential mode.
Describes the use of the Secondary infusion mode.
Operating in dose rate mode without a drug name.
Inputting patient data and selecting volume in dose rate mode.
Selecting flow rate and administering a loading dose.
Details alternative infusion modes in dose rate mode.
Explains Time/Rate, Simple rate, and Drug Labelling modes.
Using the Vigilant® Drug'Lib mode for safe drug administration.
Instructions for programming and administering boluses.
Initiating and managing programmed bolus infusions.
Procedure for administering a manual bolus.
Steps for priming the set and checking for air bubbles.
Managing infusion stop, switch-off, and pause functions.
Adjusting VTBI, managing pressure, and using DPS.
How to access and view infusion history data.
Viewing pressure, occlusion, and flow rate history.
Procedures for changing sets and pre-programming infusions.
Using the warning function and the optional drop sensor.
Symbols shown continuously on the pump's screen.
Explanation of the pump's indicator lights.
Symbols that assist the user in programming the pump.
Symbols for alarms, key functions, and menu access.
Menu options and symbols for specific flow rate expressions.
Alarms related to the infusion set and OCS.
Alarms and warnings related to infusion status.
Alarms and warnings related to pressure changes.
Alarms for battery and mains power status.
Alarms for drop sensor, drug library, and technical errors.
Details functions available in the permanent menu.
Details menu functions accessible in option mode.
Further menu functions like Primary/Secondary and Patient info.
Customisation settings for screen display.
User-configurable settings for menu, language, and KVO.
Settings for beep sound, sound level, and initial parameters.
Authorising functions, units, modes, and drop sensor.
Configuring pre-alarm, drops/min, and rate modification.
A protocol for a quick check of pump functionality.
Specifies available ranges for infusion and bolus rates and VTBI.
Details dose range settings and infusion time limits.
Accuracy specifications and pressure management features.
Explains calculation rules for V, T, R parameters in different modes.
Lists dilution units, dose rate units, and conversion rules.
Details power supply, battery, and communication port specs.
Lists compliance standards for safety and EMC.
Provides physical dimensions and weight of the pump.
Explains how to interpret trumpet curves for accuracy assessment.
Graphs illustrating flow rate performance in Ramp and Sequential modes.
Declaration on the device's electromagnetic emissions.
Declaration on the device's electromagnetic immunity.
Details electromagnetic immunity test levels and guidance.
Recommended separation distances from RF communication equipment.
Instructions for cleaning and disinfecting the pump.
Specifies storage and use conditions for the device.
Guidelines for handling and maintaining the Li-ion battery.
General recommendations for safe and optimal pump operation.
Specific advice for using Volumat Lines with the pump.
Details on product guarantee, quality control, and preventive maintenance.
Information on device servicing and return procedures.
Lists compatible accessories and maintenance tools.
Details on data management cables and software.
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