DJO Global ARTROMOT-K1 Modo De Empleo página 50

Warning!
m
Shock hazard –
Strictly observe the following warnings.
Failure to do so endangers the lives of
the patient, the user and other persons
involved.
− Allow ARTROMOT®-K1 to reach
room temperature before use. If the
device has been transported at tem-
peratures below 0 °C/ 30°F), leave it
to dry at room temperature for about
2 hours, until any condensation has
disappeared.
− The ARTROMOT®-K1 device must
only be operated in dry rooms.
− When disconnecting the device from
the power line, remove the plug from
the wall outlet first, before discon-
necting the cable from the device.
− When connecting the device to other
equipment or when creating a medi-
cal system, check that the sum of
leakage currents will not cause any
hazard. Please contact DJO Global,
if you have questions in this matter.
− Do not use multiple portable socket
outlets (MPSO) to connect the device
to the power line. ARTROMOT®-K1
must be connected to a properly in-
stalled wall outlet with a non-fused
earthed wire. Before connecting the
power cord, it must be completely
unrolled and placed such that it will
not get caught by the moving parts
of the device.
− Before cleaning and service interven-
tions, disconnect the device from the
power line by removing the power
cord from the wall outlet.
− Liquids must not be allowed to enter
the CPM device or the programming
unit. If liquids have entered into the
devices, ARTROMOT®-K1 must be
immediately checked by a service
technician, before it can be reused.
ORMBS-12006_Artromot_K1_Comfort_2012_rz.indb 46
Warning!
m
Equipment malfunction –
− Magnetic and electrical fields are
capable of interfering with the proper
performance of the device. For this
reason make sure that all external
devices operated in the vicinity of the
CPM device comply with the relevant
EMC requirements. X-ray equipment,
MRI devices and radio systems are
possible sources of interference as
they may emit higher levels of elec-
tromagnetic radiation. Keep the CPM
device away from these devices and
verify its performance before use.
− Refer repair and maintenance to
authorized persons.
Persons are authorized after training
by a specialist trained and commis-
sioned by the manufacturer.
− Route all cables below the device
frame to either side, ensuring that
they cannot get caught by the mo-
ving parts during operation.
− Inspect ARTROMOT®-K1 for da mage
and loose connections at least once a
year. Damaged and worn parts must
immediately be replaced with original
spare parts by authorized staff.
Caution!
m
Preventing chafing and pressure sores –
When your patient is adipose, very
tall or very short, be sure to prevent
chafing and pressure sores. Place the
leg concerned in a moderate abduction
position, if deemed appropriate.
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