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8 Hygienic reprocessing
8.1 Intervals
8.2 Preparing hygienic reprocessing
Requirement
232
EN
MEDUCORE Standard
Failure of therapy due to disinfection by immersion,
mechanical reprocessing and sterilization!
If the device, or components or accessories not designed for these
processes are subjected to disinfection by immersion, mechanical
reprocessing or sterilization, they may be damaged.
Never subject the device, or components or accessories not
designed for these processes to disinfection by immersion,
mechanical reprocessing or sterilization.
Part
All parts
* In the event of visible dirt or suspected contamination.
•
The device is switched off
page
119).
•
The device is disconnected from the patient.
•
Battery and SD card are in the device.
•
SD card cover is closed.
1. If the device is connected to line power or to a 12 V on-board
power supply: Disconnect the device from line power
"7.1.2 Disconnecting the device from line power", page
Alternatively:
Disconnect the device from the 12 V on-board power supply
(see "7.1.2 Disconnecting the device from line power",
page
219).
When doing so, please note: The battery remains in the device
for hygienic reprocessing.
2. Disassemble the defibrillation electrodes/paddles and master
cable
(see "7.2 Disassembling defibrillation electrodes/paddles
and master cable", page
2
After every use*
x
(see "6.2 Switching the device off",
221).
At least 1x weekly
x
(see
219).
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