Duronic BPM150, Manual

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8
This device is intended for adult use only. 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 atria l fi brillation, the
best result may occur with deviation. Please consult your physician about the result. If the cuff pressure exceeds 40
kPa (300 mmHg), the unit will automatically de fl ate. Should the cuff not de fl ate when pressures exceeds 40 kPa (300
mmHg), detach the cuff from the arm and press the START/STOP button to stop in
fl
ation. The equipment is not AP/
APG equipment and not suitable for use in the presence o
f a fl
ammable 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 the condition of strong electromagneti c fi eld 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 an d fi ngers 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 speci fi ed/ 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 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 Transtek. Don’t
open or repair the device by yourself. Please report to Transtek 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.
Caution