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USER SAFETY INFORMATION
8
Caution(s)
To prevent possible damage to the touchscreen, do not use sharp objects to touch the screen icons, only use
fingertips.
Do not attempt to clean the device or patient acquisition device by submersing into a liquid, autoclaving, or
steam cleaning as this may damage equipment or reduce its usable life. Wipe the exterior surfaces with a warm
water and mild detergent solution and then dry with a clean cloth. Use of unspecified cleaning/disinfecting
agents, failure to follow recommended procedures, or contact with unspecified materials could result in
increased risk of harm to users, patients and bystanders, or damage to the device.
No user-serviceable parts inside. Screw removal by qualified service personnel only. Damaged or suspected
inoperative equipment must be immediately removed from use and must be checked/repaired by qualified
service personnel prior to continued use.
The rechargeable internal battery is a sealed lead-acid type and it is totally maintenance free. If the battery
appears to become defective, refer to Mortara Instrument Service Department.
Do not pull or stretch patient acquisition device as this could result in mechanical and/or electrical failures.
Patient cables should be stored after forming them into a loose loop.
Calibration of the display is required before initial operation of the unit. No special equipment is needed for the
proper operation or maintenance of the device.
When necessary, dispose of the device, its components and accessories (e.g., batteries, cables, electrodes),
and/or packing materials in accordance with local regulations.
Proper functioning backup items such as a spare patient cable, front-end device, display monitor, and other
equipment are recommended on hand to prevent delayed treatment due to an inoperable device.
Note(s)
Patient movement may generate excessive noise that may affect the quality of the ECG traces and the proper
analysis performed by the device.
Proper patient preparation is important to proper application of ECG electrodes and operation of the device.
The algorithm detecting electrode misplacements is based on normal physiology and ECG lead order, and tries
to identify the most likely switch; however, it is advisable to check the other electrode positions in the same
group (limb or chest).
There is no known safety hazard if other equipment, such as pacemakers or other stimulators, is used
simultaneously with the device; however, disturbance to the signal may occur.
The display of a thick baseline while using the WAM wireless acquisition module (square waves on rhythm
printout) could be due to the WAM being turned off or having no battery, or the WAM being out of range or
experiencing a calibration error. Review the LED indicator on the WAM to ensure the unit is turned on and has
proper battery level. Ensure the WAM is paired correctly and is within recommended proximity of the
electrocardiograph, and/or power cycle the WAM to re-calibrate. Review the WAM user manual for details.
Содержание ELI 280
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