• During defibrillation, keep a sufficient distance from the patient and metal objects
connected to the patient to avoid electric shocks.
1.2.2 Warnings
• The equipment, connection lines and accessories must be checked for proper operation
before use. Do not use this device in case of failure is discovered.
• The user should confirm that the synchronous input device is suitable for the
Defibrillator Monitor and that the input signal is valid.
• This device can only be used for a single patient at one time.
• This device is not suitable for use in a magnetic resonance imaging (MRI) environment.
• This device uses only disposable batteries provided by our company.
• Do not disassemble the Defibrillator Monitor to prevent electric shocks.
• The pad should be adhered strongly to the patient's skin without leaving any gap, and
the patient's chest hair should be removed if necessary.
• If you want to use the device with any equipment not mentioned in this Manual, please
consult the manufacturer.
• During operation, keep the device away from sources of electromagnetic interference
(e.g. electric motors, generators, X-ray devices, radio transmitters, cell phones, nuclear
magnetic resonance and other such devices) as they may interfere with the signals being
collected and analyzed. See Chapter 23 "EMC" for details.
• Do not operate the device in standing water, do not immerse any part of the device in
water, or drop any liquid on it. If the equipment gets wet, please dry it thoroughly.
• Do not store or use the device in a damp environment. If the device gets wet, wipe its
surface with a dry towel, and place the device in a dry, environment with a temperature of
20℃ for a period of time, until the equipment is completely dry before use.
• Always prepare a fully charged and properly maintained spare battery. Replace the
battery when the device displays a low battery warning, otherwise, the device may shut
down.
• Disconnect all other devices without defibrillation protection from the patient during
defibrillation.
• The alarm volume and alarm limit should be set according to the patient's actual
condition. Do not rely solely on an audible alarm system for patient monitoring. Low alarm
volume setting may result in patients being in danger.
• When the device is attached to the patient, no functional examination should be
performed to avoid accidental electric shock to the patient.
• When using this device for treatment, attention should always be paid to the actual
condition of the patient. If there is a delay in delivering a shock, there may be a situation
where a heart rate that has been analyzed as shockable changes to a non-shockable heart
rate, resulting in electric shocks being delivered incorrectly.
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