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6. Storage and shipment
Caution!
In case of storage in the cold conditions the instrument has be kept indoor at tem-
pe18 +25 °С during at least 4 hours prior to switching it on.
The instrument should be stored indoor with natural ventilation at the temperature range from
+ 5°C to + 40°С and relative air humidity to 80% at 31°С. In case of long-term storage, when
it is not used, the instrument should be kept in the manufacturer’s package.
A room, where the instrument is stored or operated, should be free of dust, acid and alkali va-
pors, corrosive gases and other harmful substances that may cause corrosion of the metal parts
and electric insulation breakdown.
During transportation, the instrument should be protected from dust and precipitation.
It is
forbidden to tilt and turn over the instrument!
Prior to the shipment, the instrument should
be secured to ensure its stable position and exclude any displacement and shocks.
Instrument can be shipped by any kinds of transport and it has to be carried in the manufac-
turer’s transport package and treated with accordance to manipulation signs applied on the
outer surface of transport package. Acceptable environmental conditions for transportation are
the following: temperature from - 50°C to + 50°C and relative air humidity up to 80 % at +
6°C.
Note!
The instrument contains precision mechanical parts. To avoid their damage during han-
dling and shipping, the requirements of manipulation signs applied on package should be
strictly followed.
Attention!
The instrument has to be shipped with the closed thermal block only.
7. Recycling
Recycling of medical devices has to be carried out in accordance with the classification,
rules for the collection, use, disinfection, storage, transportation, accounting and disposal of
medical waste established by the authorized federal executive authority.
Recycling of the instrument has to be carried out by special companies, which have the
appropriate license, using specially equipped places in accordance with the requirements stip-
ulated by existing Federal laws and in compliance with the mandatory requirements for envi-
ronmental protection in accordance with the local regulations.
8.
EMS declaration
The instrument complies with the immunity and electromagnetic emission requirements of
EN 61326-2-6: 2013.
The instrument is intended for use in the electromagnetic environment described below:
-
The device was designed and tested in accordance with the requirements of
CISPR 11 and it is suitable for use in all rooms, including ones, which are di-
rectly connected to the public low-voltage mains network.
-
The quality of the electricity supply has to comply with typical conditions of use
in commercial institutions or hospitals.
-
Power frequency of magnetic fields has to be at a level corresponded with typi-
cal conditions of use in commercial institutions or hospitals.