4. Adjustment of elbow angle
5. Adjustment of forearm length
6. Adjustment of headrest
When the optional patient
restraint is used¹
7. Adjustment of headrest and
shoulder restraint¹
− It is not permitted to change the
adjustment of 1 through 7 while a
patient is sitting in the CPM device.
− Movements must not cause any pain
or irritation.
− Patients must be fully conscious
while being instructed in the use of
the CPM device and during therapy.
− The choice of the therapy param-
eters to program and of the therapy
protocols to use is restricted to the
responsible physician or therapist.
It is the physician's or therapist's de-
cision whether or not to use the CPM
device on a specific patient.
− The patient must be familiar with the
functions of the ARTROMOT®-S3
programming unit and the unit must
be within easy reach of the patient,
allowing him or her to stop therapy, if
needed. Patients unable to operate
the programming unit, e.g. paralytic
patients, must never be left unat-
tended during therapy.
− Write the patient's name on the
patient chip card. The card should
only be used for this patient. If the
patient chip card is used for another
patient, be sure to delete the previ-
ous patient's data from the card first
(see sections 4.1 and 5.3, paragraph
"New Patient"). Use original chip
cards only.
− All accessories used with the
ARTROMOT®-S3 device must first be
approved by DJO Global.
− Modifications to the medical device
described in this document without
the manufacturer's written consent is
prohibited.
− Ensure that the medical device is
securely set up on solid ground during
use.
− Do not allow parts of the body or
any objects (such as blankets, cush-
ions or cables) to get caught in the
moving parts of the CPM device.
Warning!
m
− Extreme caution should be taken when
in use around small children and babies!
Sufficient distance to the device is
mandatory for their safety!
− Never leave the device unattended
when it is switched on! Switch the
device off and disconnect the power
cord from the wall outlet!
− After use, store the device in a safe place!
Ensure device stability also during storage!
Do not rest or lean on or push the
assembled device because it might tip
over.
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.
− Before use allow the ARTROMOT®-S3
to reach room temperature. If the
device has been transported at tem-
peratures below 0 °C (32 °F), leave it
to dry at room temperature for about
2 hours, until any condensation has
disappeared.
− The ARTROMOT®-S3 must only be
operated in dry rooms.
− When disconnecting the device from
the power line, remove the plug from
the wall outlet first, before disconnect-
ing the cable from the device.
− When connecting the device to other
equipment or when creating a medical
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®-S3
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 in the moving parts of
the device.
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