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wounds, ulcers, edemas, by interposing sterile gau-
ze between the accessory and skin;
•
Children or at any rate minors are forbidden to
make direct use of the electro-medical devices, un-
less they are assisted by responsible adults;
•
It is normal that during the first treatments the
patient may perceive a light increase of the pain
sensation, especially if the field emitted goes to
contrast an area where inflammatory processes are
occurring. If the painful sensation is bothersome
and unbearable, we recommend that you tempo-
rarily interrupt the therapy (for 3/5 days), to then
resume it and finish it;
•
It is at any rate a good practice to consult your
doctor and have him advise you on the best use of
the equipment or to clarify any doubts concerning
the treatments;
•
Only use the accessories supplied with device
(cables, charger, etc. indicated in this manual) or
supplied by the manufacturer/assistance: it is for-
bidden (for safety reasons) to use any other type of
accessory; it is likewise forbidden to use the acces-
sories supplied with the device on other equipment.
•
The accessories that are directly applied on the
skin are to be used on one patient only; if otherwise,
they must be washed and cleaned to guarantee
maximum hygiene safety and to prevent possible
infections/contaminations;
•
We recommend that you periodically check the
condition of the accessories, checking, in particu-
lar, that the wires and the parts applied are not da-
maged;
•
The device and its relative accessories must not
be exposed to sources of heat;
•
Use in contact with water is forbidden;
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•
Do not use the Device in the immediate vici-
nity of other equipment (in particular at short
or micro-wave), and do not connect them to the
same power socket (this could compromise their
proper operation);
•
Do not simultaneously use the device with an
HF surgical device connected to the patient;
•
Treatments with Electromagnetotherapy do not
contraindicate, at ay rate, the use of other prescri-
bed therapies (manual, instrumental, or pharma-
ceutical);
•
It is severely forbidden to open the device. This
operation is only allowed to an assistance center
authorized by the manufacturer,; no modification to
the device is allowed;
It is at any rate explicitly forbidden and dange-
•
rous to make any use of the device other than the
one indicated in this manual; the manufacturer
cannot be deemed responsible for any damage cau-
sed by an incorrect, unreasonable improper use of
the device;
•
Recommended environmental operating
conditions:
Room temperature
Relative humidity
Atmospheric pressure
•
Recommended environmental conditions
for storage:
Room temperature
Relative humidity
Atmospheric pressure
•
Recommended environmental conditions
for transport:
Room temperature
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MEDICAL DEVICE LABEL
(The SN and the bar code univocally identify the
device and its date of manufacture)
SERIAL NUMBER (SN):
FN
= Medical Device code
AA
= last 2 digits of the year of manufacture
MM = last 2 digits of the month of manufacture
xxxx = progressive 4-digit number
MEANING OF THE SYMBOLS
15 ÷ 35 °C
a
a
45 ÷ 75%
a
860 ÷ 1060 hPa
012
5 ÷ 50 °C
a
30 ÷ 90%
a
a
860 ÷ 1060 hPa
a
0 ÷ 50 °C
Carefully read the contraindications
and precautions.
Device that emits non-ionizing
radiations.
Device with BF-type parts applied
to the body.
Marking symbol (0123 is the
identification number of the TÜV SÜD
PS Certification Institute).
Device and battery
subjected to separate disposal.
Carefully read the operating
manual.
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