Salter BPA-9301-EU Manual De Usuario página 4

ME EQUIPMENT.
* Before every use, check the device, do not use the
device or an electrode if it is damaged in any way.
The continuous use of a damaged unit may cause
injury, improper results, or serious danger.
* Be careful to strangulation due to cables and
hoses, particularly due to excessive length.
* Keep unit out of the reach of young children / pets
to avoid inhalation or swallowing of small parts. The
cord/tube can cause strangulation.
* At least 30 min required for ME equipment to warm
from the minimum storage temperature between
uses until it is ready for intended use. At least 30
min required for ME equipment to cool from the
maximum storage temperature between uses until it
is ready for intended use.
* When not in use, store the device with the adapter
in a dry room and protect it against extreme
moisture, heat, lint, dust and direct sunlight. Never
place any heavy objects on the storage case.
* Warning: Be careful to regarding the effect of
blood flow interference and resulting harmful injury
to the patient caused by continuous cuff pressure
due to connection tubing.
* When using this device, please pay attention to
the following situation which may interrupt blood
flow and influence blood circulation of the patient,
thus cause harmful injury to the patient: connection
tubing kinking too frequent and consecutive
multiple measurements; the application of the
cuff and its pressurization on any arm where
intravascular access or therapy, or an arterio-
venous (A-V) shunt, is present; inflating the cuff on
the side of a mastectomy.
* Warning: Do not apply the cuff over a
wound;otherwise it can cause further injury.
* Do not inflate the cuff on the samb limb which
other monitoring ME equipment is applied around
simultaneously, because this could cause temporary
loss of function of those simultaneously-used
monitoring ME equipment.
* Please check that operation of the device does
not result in prolonged impairment of patient blood
circulation.
* When measurement, please avoid compression or
restriction of the connection tubing.
* The device cannot be used with HF surgical
equipment at the same time.
* The ACCOMPANYING DOCUMENT shall disclose
that the SPHYGMOMANOMETER was clinically
investigated according to the requirements of ISO
81060-2:2013.
* To verify the calibration of the AUTOMATED
SPHYGMOMANOMETER, please contact the
manufacturer.
* This device may be used only for the purpose
described in this booklet. The manufacturer cannot
be held liable for damage caused by incorrect
application.
* This device comprises sensitive components and
must be treated with caution. Observe the storage
and operating conditions described in this booklet.
* Do not wash the cuff in a washing machine or
dishwasher!
* It is recommended that the performance should
be checked every 2 years and after maintenance
and repair, by retesting at least the requirements
in limits of the error of the cuff pressure indication
and air leakage (testing at least at 50mmHg and
200mmHg).
* There is no luer lock connectors are used in
the construction of tubing, there is a possibility
that they might be inadvertently connected to
intravascular fluid systems, allowing air to be
pumped into a blood vessel.
* This equipment needs to be installed and put into
service in accordance with the information provided
in the ACCOMPANYING DOCUMENTS;
* Wireless communications equipment such as
wireless home network devices, mobile phones,
cordless telephones and their base stations, walkie-
talkies can affect this equipment and should be kept
at least a distance d away from the equipment. The
distance d is calculated by the MANUFACTURER from
the 80 MHz to 5.8 GHz column of Table 4 and Table 9
of IEC 60601-1-2:2014, as appropriate.
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