Mortara ELI 280, Руководство пользователя

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5
USER SAFETY INFORMATION
Warning: Means there is the possibility of personal injury to you or others.
Caution: Means there is the possibility of damage to the device.
Note: Provides information to further assist in the use of the device.
Warning(s)

This manual gives important information about the use and safety of this device. Deviating from operating
procedures, misuse or misapplication of the device, or ignoring specifications and recommendations could
result in increased risk of harm to users, patients and bystanders, or damage to the device.

Device 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.

Users are expected to be licensed clinical professionals knowledgeable about medical procedures and patient
care, and adequately trained in the use of this device. Before attempting to use this device for clinical
applications, the operator must read and understand the contents of the user manual and other accompanying
documents. Inadequate knowledge or training could result in increased risk of harm to users, patients and
bystanders, or damage to the device. Contact Mortara service for additional training options.

To ensure that electrical safety is maintained during operation from AC (~) power, the device must be plugged
into a hospital-grade outlet.

Only use parts and accessories supplied with the device and/or are available through Burdick/Mortara/Quinton.

Patient acquisition devices intended for use with the device include series resistance (9 Kohm minimum) in
each lead for defibrillation protection. Patient acquisition devices should be checked for cracks or breakage
prior to use.

Conductive parts of the Patient acquisition device, electrodes, and associated connections of type CF applied
parts, including the neutral conductor of the Patient acquisition device and electrodes, should not come into
contact with other conductive parts including earth ground.

ECG electrodes could cause skin irritation; patients should be examined for signs of irritation or inflammation.

To avoid the possibility of serious injury or death during patient defibrillation, do not come into contact with
device or Patient acquisition devices. Additionally, proper placement of defibrillator paddles in relation to the
electrodes is required to minimize harm to the patient.

This device does not automatically switch between direct or wireless Patient acquisition devices. Clinician
must choose Patient acquisition device before ECG acquisition. If your device is equipped with a receiver for a
wireless Patient acquisition device, always make sure that you are receiving data from the expected module.