Duronic BPM080 Manual De Instrucciones página 9

Caution
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 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 is used to measure patients who have common arrhythmias such as atrial or
ventricular premature beats or atrial fibrillation, the results may contains deviations. Please consult
your physician about the results.
If the cuff pressure exceeds 40 kPa (300 mmHg), the unit will automatically deflate. Should the cuff
not deflate when pressures exceeds 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 is not suitable for use in the presence of a flammable
anesthetic mixture with air of with oxygen or nitrous oxide.
The operator should not touch the batteries 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, or is pregnant. Besides providing inaccurate
readings, the effects of this device on the fetus are unknown. Circuit diagrams, component parts
list etc. are available from the manufacturer upon request. This unit is not suitable for continuous
monitoring during medical emergencies or operations. This could cause the patients arm to become
red and swollen as the blood supply is cut off.
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. The use
of unouthorised parts may cause damage to the unit or danger to the user/patients.
The device does not need to be calibrated within the 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 SHINEMART. Don't open or repair the device by yourself.
Please report to SHINEMART if any unexpected operation or events occur.
Please use the soft cloth to clean the whole unit. Do not use any abrasive or volatile cleaners.
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