ZOLL R Series Monitor Defibrillator Rev K Operators Guide - Manual (Page 144)

C HAPTER 13 M AINTENANCE
13–2 www.zoll.com 9650-0904-01 Rev. K
Routine Procedures
Daily Visual Inspection
Equipment
Ensure that the unit is clean (with no fluid spills) and free of visible damage.
Inspect all cables, cords, and connectors for good condition (no cuts, fraying or bent pins).
Check that the paddle surfaces are clean and free of electrolyte gel and other contaminants.
Supplies and accessories
Verify the presence, proper condition and quantity of all disposable supplies (such as ECG
monitoring electrodes, electrode gel, stripchart paper, alcohol swabs, razors, and
antiperspirant).
Ensure that two sets of ZOLL therapy pads are available in sealed packages. Check the
expiration date on all ZOLL therapy pad packages.
Batteries
Check that a fully charged battery pack is installed in the unit.
Check that a fully charged spare battery pack accompanies the unit.
Code Readiness status
Look at the /x Code Readiness indicator on the R Series defibrillator. If the Code Readiness
indicator displays a red “X” the unit is not ready for therapeutic use.
Should the automatic Code Readiness test fail, the R Series unit sets its Code Readiness
indicator to a red “X”. If the failed unit is connected to AC power, it will also display a Code
Readiness status report highlighting the defibrillator functions or accessories that are
compromised. If the failed unit is not connected to AC power, only the red “X” will display.
Connect the unit to AC power. Turn the unit ON, press the Manual Mode softkey and then the
Confirm softkey to enter the Manual mode of operation. Press the Report softkey, then the
Test Log softkey to determine the problem. Readiness test reports can be displayed and printed
as described in “Code Readiness Log” on page 13-7.
Take corrective actions (for example, replace electrodes), or remove the unit from service, and
consult “Troubleshooting” on page 14-1.
While a red “X” indicates the unit is not ready for therapeutic use, the device will not prevent a
user from attempting to deliver therapy. An example of a condition in which therapy delivery
may still be possible is when expired electrodes are connected to the device.