INTRODUCTION
INTRODUCTION
CAUTION
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implanted, electronical devices, patients with pre-eclampsia, premature ventricular beats,
atrial fibrillation, peripheral, arterial disease and patients undergoing intravascular therapy
or arterio-venous shunt or people who received a mastectomy. Please consult your doctor
prior to using the unit if you suffer from illnesses.
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before using it on older children.
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pressure.It is not intended for use on extremities other than the arm or for functions other
than obtaining a blood pressure measurement.
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blood pressure.Do not begin or end medical treatment without asking a physician for
treatment advice.
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to measure your blood pressure. Never change a prescribed medication without consulting
your physician.
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dose of a medicine prescribed by a doctor. Consult your doctor if you have any question
about your blood pressure.
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atrial or ventricular premature beats or atrial fibrillation, the best result may occur with
deviation. Please consult your physician about the result.
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increase which can prevent blood flow and result in harmful injury to the PATIENT.
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blood flow and influence blood circulation of the patient, thus cause harmful injury to the
patient: connection tubing kinking too frequent and consecutive multiple measurements; the
application of the cuff and its pressurization on any arm where intravascular access or
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mastectomy.
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around simultaneously, because this could cause temporary loss of function of those
simultaneously-used monitoring ME equipment.
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ment, open the cuff immediately. Prolonged high pressure (cuff pressure
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300mmHg or
constant pressure
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ecchymosis.
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patient blood circulation.
CAUTION
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was clinically investigated according to the requirements of ISO 81060-2:2018.
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the manufacturer.
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Besides providing inaccurate readings, the effects of this device on the fetus are unknown.
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circulation and injuries.
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operations.Otherwise, the patient’s arm and fingers will become anaesthetic, swollen and
even purple due to a lack of blood.
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extreme moisture, heat, lint, dust and direct sunlight. Never place any heavy objects on
the storage case.
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manufacturer cannot be held liable for damage caused by incorrect application.
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the storage and operating conditions described in this booklet.
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flammable anesthetic mixture with air of with oxygen or nitrous oxide.
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can measure ,transmit data and change batteries under normal circumstanc-
es and maintain the device and its accessories according to the user manual.
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radiated interference signal or electrical fast transient/burst signal.
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device.
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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.
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complaints, press the START/STOP button to release the air immediately from the cuff.
Loosen the cuff and remove it from your arm.
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from the arm and press the START/STOP button to stop inflation.
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Check the device, do not use the device if it is damaged in any way. The continuous use
of a damaged unit may cause injury, improper results, or serious danger.
