Safety Instructions; Safe Handling; General; Software - B. Braun Infusomat compact plus P Instructions For Use Manual

Safety instructions

4 Safety instructions
Read the safety instructions before
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using the device and observe them.

Safe handling

4.1

General

4.1.1
Make sure that the introductory
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training on the device is given by
a B. Braun sales representative or
another authorised person.
Any serious incident that has occurred
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in relation to this product should be
reported to B. Braun and the compe-
tent authority of the country in which
the product is operated.
If the device is dropped or subjected to
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external forces: stop using the device
and have it tested by an authorised
service workshop.
Protect the device against moisture.
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Keep the device clean.
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Close patient access in standby mode.
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Software

4.1.2
Consult the instructions for use fol-
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lowing each software update to find
out about the most recent changes to
the device and its accessories.
Ensure that the software version on
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the device corresponds to the version
these instructions for use refer to.
Ensure that all devices used in a station
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have the same software version
installed to avoid mistakes when using
differently configured devices.
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Transport and storage

4.1.3
Devices stored at temperatures above
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and below the defined operating
conditions range must be kept at room
temperature for at least one hour
before being powered on.
The risk of transport damage cannot
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be completely eliminated despite care-
ful packaging. Please check on delivery
that all items are present. Do not use
a damaged device. Contact the Service
department. Check that the device is
working correctly before its first use.
This is even a legal requirement in sev-
eral countries. A corresponding form is
available from B. Braun.

Set-up and start-up

4.1.4
For mobile use (patient transport within
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the clinic and outside the clinic), ensure
secure mounting or positioning of the
device. Changes of position and strong
vibrations can cause minor changes
in the delivery characteristics and/or
unintentional bolus administration.
Changing the height during a running
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infusion may lead to flow rate varia-
tions.
Ensure that the device is properly posi-
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tioned and secured, and that it is level.
Do not position the device above the
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patient.
Before switching on the device check
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it, and the air sensor in particular, for
contamination, damage, missing parts
and functionality.
Pay attention to audible and visible
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alarms, the lighting up of the two
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