Why does the GS corpuls3 defibrillator take so long to charge?
The battery state of charge might be low. Connect the defibrillator to an external power supply if possible, or connect the defibrillator with the other modules to be able to access their energy reserve.
Why are ECG curves not displayed on the GS corpuls3?
Poor contact between the ECG electrodes and the patient’s skin can cause this issue. Ensure the electrodes are firmly attached, especially the green and black ones on the 4-pole ECG monitoring cable. Remove any excessive hair and clean the skin with an alcohol-based substance before applying new ECG electrodes. Also, check the connection of the clip to the ECG electrodes, particularly the green and black ones. Electrical interference in the environment can also cause this issue, remove or switch off any sources of electrical interference if possible. Incorrect ECG or mains filter settings can also cause this, check the ECG filter setting for monitoring and diagnostic and check the mains filter settings.
Why is the ECG recording quality poor on GS corpuls3 Medical Equipment?
The ECG electrodes used may have passed their expiry date. Only use ECG electrodes whose expiry date printed on the packaging has not passed. Also, using ECG electrodes from different manufacturers can cause this. Only use ECG electrodes from the same manufacturer. The ECG electrodes may also be dried out. Do not use ECG electrodes stored outside the packaging for a prolonged period or with the packaging open. Do not use ECG electrodes exposed to the sun or excessive ambient temperatures for a prolonged period. Please read and follow the instructions for storage on the electrode packaging.
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.
What to do if the GS Medical Equipment monitoring unit won't switch on?
This may be caused by a malfunction in the network connection, or because the On/Off key on the monitoring unit was last pressed for more than 8 seconds. Disconnect the monitoring unit from the defibrillator/pacer and the patient box. Check if the defibrillator/pacer and patient box are switched on. Then, switch on the monitoring unit again by pressing the On/Off key.
Why is the acoustic signal transmitter on the GS Medical Equipment too faint?
The acoustic signal transmitter volume may be set too low. Set the volume to a readily audible value. Also, the opening of the acoustic signal transmitter may be dirty. Clean the opening of the acoustic signal transmitter.
How to fix faint loudspeaker volume on GS corpuls3?
The loudspeaker volume may be set too low. Adjust the volume to a readily audible level. Also, the opening of the loudspeaker may be dirty. Clean the opening of the loudspeaker.
What causes LT-ECG to be unavailable on GS corpuls3 Medical Equipment?
This issue may be because no CompactFlash® card is inserted. Insert CompactFlash® card correctly. It may also be that a non-original CompactFlash® card is inserted. Only use original corpuls3- CompactFlash® cards. If the CompactFlash® card is full, delete the data on the CompactFlash® card and re-insert.
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 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.
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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