Safety instructions
status LEDs and the display during
the self-test.
When fixing the device to a box rail,
Q
do not fix the device near the rail
bracket.
Fully charge the battery before the first
Q
use without an external power supply.
Stacking
4.1.5
Stack a maximum of three devices on
Q
top of one another.
Do not stack in ambulances.
Q
When stacking, ensure that the device
Q
is correctly and safely locked in. You
will hear an audible click sound when
the device is locked in.
WARNING! The use of this device adja-
cent to or stacked with other equip-
ment has to be avoided. Nevertheless,
if adjacent or stacked use is necessary,
the Infusomat compact
other devices have to be observed to
verify normal operation in the con-
figuration in which it will be used.
Note:
A list of equipment with which the
Infusomat compact
in a stacked or adjacent configuration and
with which stacked or adjacent use is per-
mitted can be found in section 20.1.
Operation
4.1.6
Stand in front of the device to operate
Q
it. This ensures that you are able to
reach all control elements and that the
display is clearly visible.
Establish a connection to the patient
Q
only after the infusion line has been
38932401_Infusomat_compactPlusP_EN_IFU_1020_v5.indd 11
plus
P and the
plus
P has been tested
properly inserted and primed. Discon-
nect it from the patient when chang-
ing infusion line in order to prevent
unintended dose administration.
Only use approved infusion lines/
Q
catheters for the intended medical use.
Position the infusion line to the patient
Q
so that it does not have any kinks.
Ensure that installation in rooms
Q
used for medical purposes is done in
accordance with the regulations (e.g.,
VDE 0100, VDE 0107 and/or IEC speci-
fications). Observe all country-specific
regulations and national deviations.
Do not operate the device near inflam-
Q
mable anaesthetics.
Always check the plausibility of the
Q
values shown on the display.
Ensure that there is additional patient
Q
supervision (e.g. monitoring) if life sus-
taining drugs are administered.
When administering highly-effective
Q
drugs, have a second device ready for
the drug.
Avoid mechanical effects on the
Q
device. If the device is moved while in
operation, the set delivery rate may be
exceeded/not be reached.
Irrespective of the soft limit, ensure
Q
that the values set for the patients are
the medically correct values.
When using the device near equipment
Q
that can cause higher interference
emissions (e.g. electrosurgical devices,
magnetic resonance imaging units,
mobile telephones) keep the device
the recommended safe distance away
from such equipment.
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