Mortara Instrument ELI 25O, Руководство пользователя

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USER SAFETY INFORMATION
Means there is the possibility of personal injury to you or others.
Means there is the possibility of damage to the equipment.
Provides information to further assist in the use of the device.
Federal law restricts this device for sale to or on the order of a physician.
• Device (electrocardiograph, Class I) captures and presents data reflecting a patient’s physiological condition
that when reviewed by a trained physician or clinician can be useful in determining a diagnosis. However,
the data should not be used as a sole means for determining a patient’s diagnosis.
• To ensure that electrical safety is maintained during operation from AC (~) power, the device must be
plugged into a Hospital Grade outlet.
• To maintain designed operator and patient safety, peripheral equipment and accessories used that can come
in direct patient contact, must be in compliance with UL 2601-1, IEC 601-1 and IEC 601-2-25.
• Patient cables intended for use with the ELI 250 include series resistance (10 Kohm minimum) in each lead
for defibrillation protection. Patient cables should be checked for cracks or breakage prior to use.
• Conductive parts of the patient cable, electrodes and associated connections of Type CF applied parts,
including the neutral conductor of the patient cable and electrode should not come into contact with
other conductive parts, including earth ground.
• To maintain designed operator and patient safety, only use parts and accessories supplied with the device
and available through Mortara Instrument, Inc.
• ECG electrodes could cause skin irritation and should be examined for signs of irritation or inflammation.
• To prevent possible infection, single use components (e.g., electrodes) should be limited to one-time use only.
• To avoid the possibility of serious injury or death during patient defibrillation, do not come into contact with
device or patient cables. Additionally, proper placement of defibrillator paddles in relation to the electrodes
is required to minimize harm to the patient.
• To ensure the safety of both the patient and the device, 1.5 meters (5 feet) of open area should surround
the patient.
• A possible explosion hazard exists; do not use the device in the presence of flammable anesthetics.
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Warning
Warning(s)
Caution
Note