Joytech Arm Type Fully Autimatic Blood Presssure Monitor

Precautions to Ensure Safe, Reliable Operation Do not drop the unit. Protect it from sudden jars or shocks. Do not insert foreign objects into any openings. Do not attempt to disassemble the unit. Do not crush the pressure cuff. If the unit has been stored at temperatures below 0 ℃, leave it in a warm place for about 15 minutes before using it. Otherwise, the cuff may not inflate properly. If the unit has been stored at temperatures above 40 ℃, leave it in a cool place for about 15 minutes before using it. Otherwise, the cuff may not inflate properly. Do not store the unit in direct sunlight, high humidity or dust. To avoid any possibility of accidental strangulation, keep this unit away from children and do not drape tubing around your neck. Ensure that children do not use the instrument unsupervised; some parts are small enough to be swallowed. Some may get a skin irritation from the cuff taking frequent readings over the course of the day, but this irritation typically goes away on its own after the monitor is removed. Important Instructions Before Use Do not confuse self-monitoring with self-diagnosis. Blood pressure measurements should only be interpreted by a health professional who is familiar with your medical history. Contact your physician if test results regularly indicate abnormal readings. If you are taking medication, consult with your physician to determine the most appropriate time to measure your blood pressure. NEVER change a prescribed medication without first consulting with your physician. Individuals with serious circulation problems may experience discomfort. Consult your physician prior to use. For persons with irregular or unstable circulation resulting from diabetes, liver disease, arteriosclerosis or other medical conditions, there may be variations in blood pressure values measured at the wrist versus at the upper arm. Monitoring the trends in your blood pressure taken at either the arm or the wrist is nevertheless useful and important. People suffering from vascular constriction, liver disorders or diabetes, people with cardiac pacemakers or a weak pulse, and women who are pregnant should consult their physician before measuring their blood pressure themselves. Different values may be obtained due to their condition. People suffering from arrhythmias such as atrial or ventricular premature beats or atrial fibrillation only use this blood pressure monitor in consultation with your doctor. In certain cases oscillometric measurement method can produce incorrect readings. Too frequent measurements can cause injury to the patient due to blood flow interference. The cuff should not be applied over a wound as this can cause further injury. DO NOT attach the cuff to a limb being used for IV infusions or any other intravascular access, therapy or an arterio-venous (A-V) shunt. The cuff inflation can temporarily block blood flow, potentially causing harm to the patient. The cuff should not be placed on the arm on the side of a mastectomy. In the case of a double mastectomy use the side of the least dominant arm. Pressurization of the cuff can temporarily cause loss of function of simultaneously used monitoring equipment on the same limb. A compressed or kinked connection hose may cause continuous cuff pressure resulting in blood flow interference and potentially harmful injury to the patient. Check that operation of the unit does not result in prolonged impairment of the circulation of the patient. Product is designed for its intended use only. Do not misuse in any way. Product is not intended for infants or individuals who cannot express their intentions. Prolonged over-inflation of the bladder may cause ecchymoma of your arm. Do not disassemble the unit or arm cuff. Do not attempt to repair. Use only the approved arm cuff for this unit. Use of other arm cuffs may result in incorrect measurement results. The system might produce incorrect readings if stored or used outside the manufacturer’s specified temperature and humidity ranges. Make sure to store the blood pressure monitor, children, pets and pests are outside of accessible range. Do not use the device near strong electrical or electromagnetic fields generated by cell phones or other devices, they may cause incorrect readings and interference or become interference source to the device. Do not mix new and old batteries simultaneously. Replace batteries when Low Battery Indicator“JOYTECH-DBP-6286B-Arm-Type-Fully-Automatic-Digital-Blood-Pressure-Monitor-01 ”appears on screen. Replace both batteries at the same time. Do not mix battery types. Long-life alkaline batteries are recommended. Remove batteries from device when not in operation for more than 3 months. Dispose batteries properly; observe local laws and regulations. Only use a recommended class II AC Medical approved adaptor which comply with 2MOPP, and pass IEC 60601-1, IEC 60601-1-2(or FCC) standard . An unauthorized adapter may cause fire and electric shock. Advising operator that Instruction manual/ Booklet must be consulted. Do not use the device during transport vehicles for influencing measurement accuracy such as patient transport in an ambulance or helicopter. Contains small parts that may cause a chocking hazard if swallowed by infants. Please align the polarities of each battery with the +ve and -ve signs imprinted on the battery housing when you replace the batteries . Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally. Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the unit, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result. the blood pressure monitors equipped with bluetooth(BT) module is only transmit historical blood pressure (BP) from the subject device to a user-supplied digital device, and is not intended for active patient monitoring.