4
G
B
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 based solely on the readings from this unit. Always consult your
physician first.
• 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 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
button
to stop inflation.
• to avoid measurement errors, carefully read this manual before using the product.
• 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.
• 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.
• to avoid measurement errors, please avoid the condition of strong electromagnetic field radiated
interference signal or electrical fast transient/burst signal when using the Ac adaptor.
• the user must check that the equipment functions safely and see that it is in proper working condition
before being used.
• 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 using, the patient will 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 parts 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 the two years of reliable service.
• Please dispose of AccEssoriEs, detachable parts, and the ME EQUiPMEnt according to the local guidelines.
sAFEtY inForMAtion
caution: consult accompanying
documents
caution: these notes must be observed
to prevent any damage to the device
cE mark: conforms to essential
requirements of the Medical device
directive 93/42/EEc.
type BF applied parts
Manufacturer
symbol for “EnVironMEnt
ProtEction - Electrical waste products
should not be disposed of with
household waste. Please recycle where
facilities exist. check with your local
authority or retailer for recycling advice”
serial number
direct current
Manufacture date
0120
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