Why is the QRS tone inaudible on GS corpuls3 Medical Equipment?
Acoustic reproduction of the QRS tone may not be enabled. Press the left softkey [QRS] in monitoring mode. Also, the loudspeaker of the monitoring unit may not be enabled. Activate the loudspeaker of the monitoring unit.
What to do if D-ECG, LT-ECG, and NIBP functions are unavailable on the GS corpuls3 Medical Equipment?
This issue may occur due to an internal error. Try switching off the GS Medical Equipment and restarting it. Also, ensure that the patient box and/or defibrillator/pacer are switched on, as they might be switched off.
How to fix 'No connection to Defibrillator Unit' error on GS Medical Equipment?
This error message can appear if the defibrillator/pacer is outside the radio range. Ensure the defibrillator module is switched on and reduce the distance between the module or connect the modules mechanically. Also, check for any foreign bodies in front of the infrared interface of the individual modules and remove them. If necessary, clean the infrared interfaces.
Why is the oximetry value not displayed on my GS corpuls3 Medical Equipment?
This problem can arise if the oximetry sensor is not correctly placed on the patient’s body. Reposition the oximetry sensor according to the sensor manufacturer's instructions. Ensure that you are using an oximetry sensor suitable for the patient’s age and weight. Clean the oximetry sensor. Also, ensure that the oximetry intermediate cable is connected to the 'oximetry' socket on the patient box and that the oximetry sensor is connected to the oximetry intermediate cable. If the connection with the patient box is cut off, reduce the distance between the monitoring unit and the patient box. The measurement site on the patient may be dirty or disturbed by other influences, rotate the finger sensor by 90°, clean the measurement site and choose another measurement site.
How to extend radio connection range for GS Medical Equipment?
The radio unit in the patient box may be shadowed by metallic or metallised objects, or by people or body parts of the patient. If possible, choose a position that allows an unimpeded view to the other modules. Put the patient box in an upright position or use an appropriate bracket. Remove any metallic or metallised objects.
Why can't I trigger a shock via corPatch clip electrodes on GS Medical Equipment?
The corPatch clip electrodes may not be properly connected. Check the cable and plug interfaces.
How to correct the date on GS corpuls3?
The date is not correctly set. Correctly set the date.
Why did configuration export fail on GS corpuls3?
The configuration was not saved. The configuration has to be saved before exporting.
What to do if no shock is triggered on GS corpuls3?
The shock buttons may have been pressed too briefly. Release the shock again and hold the shock buttons down for at least 1 second in manual defibrillation mode. The shock paddles may also be faulty. Replace the shock paddles and use corPatch electrodes in the meantime.
How to resolve connection issues between modules on GS corpuls3?
This issue might be caused by foreign bodies in front of the infrared interfaces on individual modules. Remove any foreign objects and clean the infrared interfaces if necessary. Also, the connection authorisation (Pairing) may not be taking place. Check if all modules are switched on and repeat pairing.
General information on operating the corpuls3 device safely.
Qualifications and training required for operating staff using the corpuls3.
Limitations on using defibrillation, cardioversion, and pacing functions.
Procedures and authorization for maintaining the corpuls3 device.
Explains various labels and symbols found on the corpuls3 device.
Defines warning symbols and their meanings used in the manual.
Details specific risks associated with electric shock and EMC during operation.
Describes the intended purpose and use of the corpuls3 device.
Lists optional monitoring functions like oximetry, capnometry, etc.
Lists situations and operations for which the corpuls3 is not intended.
Overview of the corpuls3 device components and their functions.
Details the different design configurations of the corpuls3 system: compact, semi-modular, modular.
Explains the procedures for pairing and ad-hoc connection between corpuls3 modules.
Description of the monitoring unit, its operating elements, LEDs, and interfaces.
Description of the patient box, its display, and the accessory bag for storage.
Description of the defibrillator/pacer unit, including its components and features like equipotential bonding.
Lists various available brackets for the device and their power supply options.
Overview of the operating elements and LEDs on the monitoring unit.
Instructions for switching the corpuls3 device on and off in different configurations.
Explains how to navigate menus using the jog dial, softkeys, and function keys.
Procedures for safely connecting and disconnecting the corpuls3 modules.
Instructions for fitting and packing the accessory bag for the patient box.
Details the types of therapy electrodes and how to connect them for defibrillation and pacing.
Steps to prepare the patient before performing defibrillation, cardioversion, or pacer therapy.
Information and procedures for using the defibrillator in AED mode.
Detailed instructions for performing manual defibrillation and cardioversion.
Information and instructions for using the external pacer function of the corpuls3.
Information on the CPR feedback system for monitoring compression quality.
Details the routine monitoring of heart rhythm and heart rate using ECG, including required cables.
Explains the diagnostic ECG function, HES® Light, and therapy suggestions.
Describes the longterm ECG function for monitoring and evaluating cardiac dysrhythmias.
Explains oximetry for measuring SpO2, SpMet, SpCO, SpHb, and pulse rate.
Explains CO2 monitoring for ventilation, haemodynamics, and metabolism in intubated/non-intubated patients.
Describes NIBP monitoring using the oscillometry method for systolic, diastolic, and mean blood pressure.
Explains IBP function for measuring arterial, venous, and intracranial pressures.
Describes temperature monitoring for body core and surface temperatures.
Details system settings including language, display, and master data.
Configuration options for monitoring functions like ECG, Oximetry, CO2, NIBP, IBP, and CPR.
How to configure alarm settings, limits, and suspension parameters.
Advanced configurations requiring higher authorization, including user management and system settings.
Process of automatically creating a new data record or patient file upon switching on the device.
Instructions for inserting and managing the CompactFlash® card for data storage.
Configuration and saving of master data such as transport type, radio ID, and EMS location.
Details about telemetry options, abbreviations, and data transmission methods.
Information about the Bluetooth® data interface for wireless data transfer and system connection.
Importance of regular maintenance and testing for device readiness and a summary of checks.
User-performed checks to ensure device functionality and readiness, supplementing automatic self-tests.
Description of the automatic system check performed upon device startup.
Guidelines for regular maintenance tasks, including safety and metrological checks.
Procedures for cleaning, disinfecting, and sterilizing device modules and accessories.
List of approved accessories, spare parts, and consumables for the corpuls3 device.
Lists device alarms, their priority, explanation, and recommended measures for elimination.
Provides solutions for common malfunctions and corrective actions.
Explains notifications shown on the message line and recorded in the protocol.
Explains various symbols used in the manual and on the device interface.
Details the default factory configuration settings for system, display, and alarms.
Provides detailed technical specifications for device components and modules.
General safety guidelines and precautions for using the corpuls3 and its accessories.
Describes the ECG analysis process in AED mode, including shock recommendations and timing.
Information on the manufacturer's limited warranty against material and manufacturing defects.
Adherence to data protection directives for saving and transferring personalized data during operation.
General| Brand | GS |
|---|---|
| Model | corpuls3 |
| Category | Medical Equipment |
| Language | English |
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