DJO Global ARTROMOT-E2 COMPACT, Operating Instructions Manual

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6.3 Transport
6.3.1 ARTROMOT®-E2
The following operating steps must
be completed before transporting the
ARTROMOT®-E2:
1. Activate the “transport setting” func-
tion in the menu (see also 5.3)
and start the ARTROMOT®-E2.
2. Turn of the ARTROMOT®-E2 power
switch (19).
3. Remove the power cord (18) and dis-
connect the motion element (21) and
the programming unit (32).
4. Open locking screw (4) and pull out the
armrest (14) for the healthy arm.
5. Grasping the motion element at the
bracket (30) for adjustment of the po-
sitioning angle, open the locking screw
(4) and pull out the motion element.
6. set horizontal adduction/abduction to
0° (indexing knob 1).
7. Open the locking screw for adjustment
of the backrest (10), fold the backrest
to the front all the way until lat on the
seat and tighten the screw.
8. Remove the two locking pins (22). Pull
out the legs towards the sides, reverse
and reinsert. Then put the locking pins
back in place.
9. Only use the original shipping box for
transporting the device. Ormed Gmbh
cannot be held liable for transport
damage, if the device was not shipped
in its original shipping box.
10. Place the ARTROMOT®-E2 - legs irst
- on the bottom of the box. The mark-
ings on the bottom of the box indicate
the correct position.
11. Then put the enclosed polystyrene
block on the chair, observing the cut-
outs in the block.
12. Put the programming unit (15) in
the supplied box. Place the motion
element, the armrest and the power
cord in the respective cut-outs in the
polystyrene block of the package.
13. Then close the box.
Reverse the above steps to reassemble
the device after transport.
m
Warning!
shock hazard —
Allow the ARTROMOT®-E2 to reach
room temperature
before use. if the
device has been transported at tempe-
ratures below 0 °C (32°F) , leave it to dry
at room temperature for about 2 hours,
until any condensation has disappeared.
Technical inspections
For safety, the devices require regular
maintenance. To maintain the functional
and operational safety, check all compo-
nents for damage and loose connections at
least once a year.
These checks should be performed by
persons with adequate training and expe-
rience. damaged and worn parts must im-
mediately be replaced with original spare
parts by authorized staf.
m
Warning!
Patient hazard, equipment malfunction
and damage
– Refer repair and maintenance to
authorized persons. Persons are
authorized after training by a special-
ist trained and commissioned by the
manufacturer.
ORMEd Gmbh will make all docu-
ments required for servicing, such as
circuit diagrams, parts lists, descrip-
tions or calibration instructions,
available to authorized experts.
The inspections can be carried out by
djO Global Technical service within the
framework of a service agreement.
The device does not require additional
regular maintenance.
Fuse replacement
m Warning!
Patient hazard, equipment malfunction
and damage —
The replacement of fuses must be
referred to specialists as deined in iEC
60364 or other applicable standards
(e.g. biomedical technicians, electri-
cians, electronics installers).
Fuses used must be T1A H250Vac
fuses.
• before replacing fuses turn of the
ARTROMOT®-E2/-E2 compact and
remove the power cord from the wall
outlet.
• use an appropriate tool to remove the
fuse holder (20/8) situated between the
power switch (19) and the power con-
nector (18) (Fig. 1).
• Replace the fuses and reinsert the fuse
holder (Fig. 2). Check that the fuse
holder locks properly into place.
Fig. 1
Fig. 2