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Luvion Doppler de luxe 80 Manual

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Attention:
This user manual is written and compiled in accordance with the council
directive MDD93/42/EEC for medical devices and harmonized standards.
In case of modications and software upgrades, the information contained
in this document is subject to change without notice. This user manual
includes special documents, which under protection of copyright law. All
rights reserved. Without written announcement from our company, the user
manual should not be transferred, copied or translated into other language.
Our company assumes no responsibility for incidental or consequential
damage in connection with the furnishings, performance or use of this
material. The information contained in this document is subject to change
without notice.
MANUFACTURER’S RESPONSIBILITY
Our company only consider itself responsible for any eects on safety,
reliability and performance of the equipment if:
Assembly operations, extensions, readjustments, modications or repairs
are carried out by persons authorized by Our company, and the electrical
installation of the relevant room compiles with national standard, and the
document is used in accordance the instruction for use.
WARRANTY
The unit can not be repaired by users themselves. All services must be done
by the engineers approved by manufacturer. We warrant that each product
we sell you is free from defects in labor and materials and shall conform to its
product specications as dened in the user documentation. If the product
doesn’t function as warranted during the warranty period, we will repair
or replace it without charge. Misuse, improper maintenance may void the
warranty.
Warning: This device is not intended for treatment. The intended use is
for clinical use.If the FHR result is distrustful, please use other methods
such as stethoscope to verify immediately.
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