DeRoyal Prospera PRO Series, Руководство пользователя, Страница: 19 / 44

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3 Operation
CAUTION!
Hazard of persons due to improper handling.
•
Use the device for its intended purpose only.
•
Read chapter 3.1 and 3.2.
ATTENTION!
Malfunction due to wound exudate overflow.
•
Ensure that the disposable exudate canister of the PRO-II
®
and
PRO-III ® device is replaced on a regular basis. If the disposable
exudate canister is full, the integrated overflow protection system
will be triggered. This disrupts the aspiration process.
• Switch the device off when replacing the disposable exudate
canister.
•
If the internal filter of the PRO-II ® or the PRO-III ® device is
blocked, the device must be serviced by DeRoyal. or by an
authorized service partner of DeRoyal.
WARNING!
Hazard of persons due to inadequate monitoring of patient.
Adequate monitoring of patients is mandatory in cases of highly exuding
wounds, wounds with viscous or strongly deposited exudate and strong
bleeding. Particular attention must be paid to exudate retention in the
wound dressing and the proper sealing of the dressing.
The establishment of monitoring intervals must be dependent on the
wound situation, the health of the patient and the settings of the alarm
sensitivities.
WARNING!
Hazard of persons due to decreasing the alarm sensitivities.
When greatly decreasing alarm sensitivities, it is possible that a blockage
or leakage in the wound and tube system may not be detected and thus
no alarm will be triggered.
The PRO-II ® and PRO-III ® devices are designed to build up a vacuum in
the wound drainage system and to extract the exudate. The devices are
not designed to detect strong bleeding of the wound. For this reason,
you must not rely solely on the alarm system of the PRO-II
®
and PRO-
III ® devices.
The regular monitoring of the patient and the wound dressing can reduce
a severe deterioration of health of the patient dramatically.
WARNING!
Hazard of persons during operation in a domestic environment.
Due to the increasing mobility of patients in a domestic environment,
there is an increasing risk of forming leaks or blockages in the wound
dressing or tube system.
For this reason, detailed training and instruction for patients as well as
performing regular monitoring of the wound dressing and negative
pressure wound therapy system by trained personnel is mandatory.
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3.1 Setup and Startup
3.1.1 Startup
It is important to follow the safety instruction in chapter 1.6 prior to initial startup.
Always have one backup disposable exudate canister for the PRO-II ® and one backup
disposable canister and tubing for the PRO-III
®
device ready since it is absolutely necessary
for safe operation.
• Please read the entire instruction for use before operating the PRO-II ® or PRO-III ®
device for the first time.
•
Remove the device and the accessories from the packaging.
•
Always place the device on a sturdy and flat surface. Take care to correctly position
the device.
• Inspect all tubing as well as the power supply unit for damage prior to each startup
of the PRO-II
®
and PRO-III
®
device. It is important to avoid kinking when connecting
the tubing. Ensure prior to switching on the unit that the disposable exudate
canister and all tubing are properly connected.
• Fully charge the battery prior to initial startup.
•
Perform a function test (Please refer to chapter 5.1).
3.1.2 Connecting the PRO-II ® and PRO-III ® Devices
Use the socket for power supply unit of the PRO-II ® device (chapter 2.1.1, fig.1 (G)) or the
socket for power supply unit of the PRO-III ® device (chapter 2.1.3, fig.2 (G)) to connect the
device to the main power supply via the supplied power supply unit for charging or operation
as required.
Use the supplied power supply unit only. First connect the power supply unit to the socket
for power supply unit of the PRO-II ® or PRO-III ® device and then to the main power supply.
Fig. 3 Connecting the PRO-II ® and PRO-III ® devices to the patient and accessories