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AUTOMATIC ARM BLOOD PRESSURE MONITOR
The Blood Pressure Monitor JOYCARE detects the Systolic, Diastolic, and the Pulse rate using the oscillometric method. All values are displayed on
the large LCD screen. Please read carefully this entire instruction manual before use and keep it. For further questions about blood pressure and its
measurement, please contact your doctor.
IMPORTANT INFORMATION BEFORE MEASURING
Blood pressure changes during the day and is also influenced by many factors such as smoking, drinking alcohol, taking drugs and physical activity.
The blood pressure measurement should be performed by a doctor or a healthcare assistant who knows your medical history thoroughly. The regular
use of the JOYCARE'S blood pressure meter will allow you to keep your doctor abreast of the continuing trend of your blood pressure, and therefore
provide a useful tool for your health diagnosis. Ensure you wear the cuff correctly, paying particular attention to its position relative to your heart, since
a position above or below it could affect the measurement. Do not move the device, body or arm and do not talk during the measurement, otherwise
the readings will not be reliable. Perform the measurement while in a comfortable position, sitting, resting quietly and at ease. Never wrap the cuff
around the sleeve of your jacket or shirt, otherwise the readings are not reliable. Please allow at least 3-5min between measurements to restore normal
circulation. Measure the pressure always in the same arm, preferably the left one, as the pressure between arms may differ. Certain factors may affect
the measurement, cause variations, and unreliable readings, including bathing, talking during the measurement, alcohol, exercise or agitated
movement, large meals, sudden temperature changes, nervous tension, stress, etc...
CAUTION
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 based
solely 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 artrial fibrillation, the
best result may occure 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 armand 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 provided inaccurate readings, the affects 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 been
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 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 in 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 with Authorized Service Center.
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