Cautions - Duronic BPM120 Manual De Instrucciones

Cautions

This device is intended for adult use only. This device is intended for non-invasive measuring
and monitoring of arterial blood pressure. It is not intended for use on any extremities other
than the arm or for any functions other than obtaining a blood pressure measurement. Do not
confuse self-monitoring with self-diagnosis. This machine allows you to monitor your blood
pressure. Do not begin or end medical treatment without asking a doctor for treatment advice.
If you are taking medication, consult your doctor to determine the most appropriate time of day
to measure your blood pressure. Never change a prescribed medication without consulting
your doctor. When the device is 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 doctor about the result.
If the cuff pressure exceeds 40 kPa (300 mmHg), the unit will automatically deflate. Should the
cuff not deflate when pressure exceeds 40 kPa (300mmHg), detach the cuff from the arm and
press the START /STOP button to stop inflation.
The equipment is not AP/APG equipment and is 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 and the patient simultaneously. To avoid measurement errors, please
avoid exposing the machine to 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 numb, 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 the accessories and detachable parts specified/authorised by Duronic. Otherwise,
it may cause damage to the unit or danger to the user/patients.
The device should not need to be calibrated within the two years of reliable service. When
disposing of the accessories, detachable parts, or any of the medical equipment, do so
according to the local refuse/ recycling guidelines.
If you have any problems with this device, such as setting up, maintaining or using it, please
contact the Customer Care Team at Duronic. Do not open or repair the device by yourself.
When cleaning, use the soft cloth to clean the whole unit. Don't use any abrasive or volatile
cleaners.
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