Salter BPA-9301-EU Manual De Usuario página 3

CAUTION
* This device is intended for adult use only. It is not
intended for use with neonatal patients, pregnant or
pre-eclamptic patients.
* The device is not intended for patient transport
outside a healthcare facility.
* The device is not intended for public use.
* This device is intended for no-invasive measuring
and monitoring of arterial blood pressure.
It is not intended for use on extremities other than
the arm or for functions other than obtaining a blood
pressure measurement.
* Do not confuse self-monitoring with self-diagnosis.
This unit allows you to monitor your blood pressure.
Do not begin or end medical treatment without
asking a physician for treatment advice.
* If you are taking medication,consult your physician
to determine the most appropriate time to measure
your blood pressure. Never change a prescribed
medication without consulting your Physician.
* When the device was used to measure patients
who have common arrhythmias such as atrial or
ventricular premature beats or atrial fibrillation, the
best result may occur with deviation. Please consult
your physician about the result.
* If the cuff pressure reaches 40 kPa (300 mmHg),
the unit will automatically deflate. Should the cuff
not deflate when pressure reaches 40 kPa (300
mmHg), detach the cuff from the arm and press the
START/STOP button to stop inflation.
* The equipment is not AP/APG equipment and not
suitable for use in the presence of a flammable
anesthetic mixture with air of with oxygen or nitrous
oxide.
* The operator shall not touch output of batteries /
adapter and the patient simultaneously.
* To avoid measurement errors, please avoid the
condition of strong electromagnetic field radiated
interference signal or electrical fast transient/
burst signal.
* The user must check that the equipment functions
safely and see that it is in proper working condition
before being used.
* This device is contraindicated for any female
who may be suspected of, or is pregnant. Besides
providing inaccurate readings, the effects of this
device on the fetus are unknown.
* Manufacturer will make available on request circuit
diagrams, component parts list etc.
* This unit is not suitable for continuous monitoring
during medical emergencies or operations.
Otherwise, the patient's arm and fingers will become
anaesthetic, swollen and even purple due to a lack
of blood.
* Please use the device under the environment
which was provided in the user manual. Otherwise,
the performance and lifetime of the device will be
impacted and reduced.
* During use, the patient will be in contact with the
cuff. The materials of the cuff have been tested and
found to comply with requirements of ISO 10993-
5:2009 and ISO 10993-10:2010. It will not cause any
potential sensization or irritation reaction.
* Please use ACCESSORIES and detachable partes
specified/ authorised by MANUFACTURE. Otherwise,
it may cause damage to the unit or danger to the
user/patients.
* The device doesn't need to be calibrated within two
years of reliable service.
* Please dispose of ACCESSORIES, detachable parts,
and the ME EQUIPMENT according to the local
guidelines.
* If you have any problems with this device, such as
setting up, maintaining or using, please contact the
SERVICE PERSONNEL of Salter. Don't open or repair
the device by yourself.
* Please report to Salter if any unexpected operation
or events occur.
* Please use the soft cloth to clean the whole unit.
Don't use any abrasive or volatile cleaners.
* Warning: No servicing/maintenance while the ME
equipment is in use.
* The patient is an intended operator. The patient
can measure,transmit data and change battery
under normal circumstances and maintain the
device and its accessories according to the user
manual.
* Adaptor is specified as a part of ME EQUIPMENT.
* The plug/adapter plug pins insulates the device
from the main supply. Do not position the device in
a position where it is difficult to disconnect from
the supply mains to safely terminate operation of
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