What to do if Alarm VENTILATOR FAIL !!! on Dräger Medical Equipment?
If the 'VENTILATOR FAIL' alarm appears on your Dräger Medical Equipment, immediately switch to ManSpont ventilation mode. Then, set the APL valve to the 'Man' position and adjust it to the desired pressure. If needed, use the O2 flush key to fill the breathing bag and manually ventilate the patient.
What to do if Dräger Medical Equipment shows alarm messages due to various causes?
Alarm messages can appear on Dräger Medical Equipment due to several reasons. If the upper alarm limit for airway pressure is exceeded, check the breathing hose for kinks. If the alarm limit is set too low, check the breathing system or the alarm limit itself. If breathing or ventilation has stopped, inspect the ventilator. Finally, check the breathing system for any leakage or disconnection.
What to do if there is a power supply failure in Dräger Fabius GS premium Medical Equipment?
If your Dräger Medical Equipment experiences a power supply failure, first ensure that the Fabius is properly connected to the mains power supply by plugging in the mains plug. If the issue persists, there may be a general power failure; in this case, restore the mains power supply to resolve the problem.
How to fix faulty calibration of Dräger Medical Equipment?
Faulty calibration in Dräger Medical Equipment can occur for several reasons. Ensure the O2 sensor is exposed to ambient air during the entire calibration process, without extremely high or low oxygen concentration, or fluctuating oxygen concentration. Expose the O2 sensor to ambient air for 2 minutes, or 15 minutes if it's a new sensor, before calibration. If the maximum period of use has elapsed, replace the O2 sensor and expose the new sensor to ambient air for 15 minutes before calibrating. Also, check and correctly connect the O2 sensor and recalibrate.
What to do if Dräger Fabius GS premium Medical Equipment has battery issues?
If your Dräger Medical Equipment is experiencing battery issues, and the backup power is at 0% of its full charge, replace the fuse. If there's no mains power and the battery is below 20% or 10%, restore the mains power supply.
Why is there a risk of insufficient ventilation with Dräger Fabius GS premium Medical Equipment?
To prevent insufficient ventilation with Dräger Medical Equipment, perform the leakage test before using the device and remedy all leakages.
What causes fresh gas issues in Dräger Fabius GS premium Medical Equipment?
Fresh gas issues in Dräger Medical Equipment can arise from several causes: insufficient fresh-gas supply in all ventilation modes, a blocked or kinked hose, or a leakage/disconnection in the breathing system. To address these, ensure there's a sufficient fresh-gas supply, check the hoses for blockages or kinks, and inspect the breathing system for leaks or disconnections.
What to do if there is a risk due to leakage at the valves of Dräger Fabius GS premium Medical Equipment?
To address the risk of leakage at the valves in Dräger Medical Equipment, perform the leakage test before using the device and check all valves for leakage.
How to correct incorrect patient settings on Dräger Fabius GS premium?
If you encounter incorrect patient settings on Dräger Medical Equipment, after restarting the Fabius, check all settings and adjust them as necessary to suit the patient's needs.
Why leakages can lead to a failure of the system test of Dräger Fabius GS premium?
Leakages can cause the system test to fail on Dräger Medical Equipment. To prevent this, perform the leakage test before using the device and remedy all leakages.
General| Brand | Dräger |
|---|---|
| Model | Fabius GS premium |
| Category | Medical Equipment |
| Language | English |
Explains specific terminology used in the manual.
Details how device screens and illustrations are presented.
Lists registered trademarks used in the document.
Defines the intended users and their required qualifications.
Covers crucial safety guidelines for device operation and user conduct.
Highlights specific hazards and precautions related to the Fabius GS premium.
Specifies the device's intended use and key monitored parameters.
Outlines conditions for use, contraindications, and environmental factors.
Explains data communication protocols for external device integration.
Visual guide to the front panel components of the Fabius GS premium.
Illustrates the top view of the COSY breathing system components.
Details the front and rear views of the COSY heating power supply unit.
Shows the rear panel, pin-index, and screw connections for gas supply.
Describes the interface panel and the function of anesthetic vaporizers.
Details the optional O2 delivery system and the APL valve's functions.
Covers device interfaces and recommended system configurations.
Explains the external fresh-gas outlet and its configurations for gas delivery.
Provides a glossary of terms, symbols, and details on product labels.
Details the main elements and functions of the device's control panel.
Explains softkey functions and the main screen layout.
Guides users on how to select and adjust device settings and ventilation parameters.
Explains the fresh-gas delivery system, total flow tube, and flow monitoring settings.
Details the meaning of LED indicators and color coding conventions.
Covers initial steps like battery activation and mains power connection.
Guides on connecting gas supply, cylinders, and mounting vaporizers.
Details steps for preparing and assembling the ventilator and breathing system.
Covers installation and replacement of CO2 absorbers and COSY heating.
Guides on connecting the compact breathing system and its components.
Covers connection of suction systems and breathing hoses, including filters.
Guides on connecting various sensors, measurement lines, and hoses.
Details attaching a resuscitator and mounting accessories safely.
Outlines the essential daily and pre-use checks for device readiness.
Details the steps and system tests involved in switching the device on.
Explains how to interpret system test results for operational readiness.
Describes the initial standby screen, fresh gas settings, and S-ORC function.
Explains how to set the concentration of anesthetic gases using the vaporizer.
Details O2 flush function, low-flow anesthesia, and nitrogen rinsing.
Provides instructions for replacing the soda lime absorber.
Details ManSpont, Volume Control, Pressure Control, Pressure Support, and SIMV/PS modes.
Guides on adopting settings when switching between ventilation modes.
Covers ventilator safety features and device behavior under specific conditions.
Outlines steps for managing patient changes, including resetting defaults.
Explains using the external fresh-gas outlet for different configurations.
Details the procedure for safely ending device operation.
Provides instructions for preparing the device for storage or transportation.
Explains how alarms are signaled optically and acoustically, and displayed.
Details the priority levels assigned to different alarm messages.
Covers methods for suppressing alarm tones and adjusting alarm limits.
Describes the data displayed on the main operational screen.
Covers O2 monitoring, parameter display, alarm settings, and calibration.
Details monitoring of breathing volumes, alarms, and their settings.
Explains airway pressure monitoring, parameter display, and alarm limit configuration.
Covers standby mode settings including calibrations, tests, and defaults.
Details how to adjust default settings and restore factory defaults.
Explains how to perform configuration tasks while the device is operating.
Covers enabling/disabling volume alarms and setting the pressure threshold.
Details O2 sensor calibration and desflurane compensation settings.
Covers accessing the alarm logbook and adjusting the alarm volume.
Provides methods for identifying and fixing leaks in the system.
Addresses problems related to power supply failures and battery operation.
Details how to handle ventilator failures and bypass the unit.
Covers troubleshooting steps for O2 sensor failures and calibration errors.
Explains alarm hierarchy, priorities, and provides specific troubleshooting steps.
Provides step-by-step instructions for disassembling device components.
Details reprocessing classifications, procedures, testing, and sterilization methods.
Provides tables and guidelines for reprocessing various device components.
Covers final steps before using the device on patients again.
Provides an overview of maintenance requirements and defines key terms.
Outlines regular inspection schedules and mandatory safety checks.
Details scheduled preventive maintenance tasks and repair recommendations.
Guides on the proper disposal of the medical device and its accessories.
Provides instructions for the safe disposal of non-rechargeable batteries.
Provides general specifications and operating environmental conditions.
Details device data, power specifications, fuses, and electrical safety compliance.
Lists applicable national and international safety standards for anesthesia systems.
Specifies the control ranges and accuracy for the ventilator functions.
Details technical data for the gas supply module and vaporizer interface.
Lists technical specifications for the breathing system, including compliance.
Details alarm limits, tone sequences, and acoustic signal characteristics.
Explains S-ORC, device outlets, and essential performance features.
Covers EMC compliance and electromagnetic immunity standards.
Details safety clearance distances for portable and mobile communication equipment.
Discusses device compatibility and IT network connectivity requirements.
Provides visual illustrations and a gas flow diagram of the breathing system.
Provides a form for recording daily and pre-use checkout procedures.
Covers checks for battery charge and gas supply connections/pressures.
Details checks for gas cylinders and the O2 flush function.
Covers fresh gas delivery checks, sensor calibration, and gas type verification.
Details checks for vaporizers and soda lime condition.
Covers checks for airway pressure, leaks, valves, ventilator function, and alarms.
Final checks before connecting to the patient.
Explains the configuration password for software and its management.
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