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INTRODUCTION

INTRODUCTION

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CAUTION

CAUTION

* This device is intended for adult use in homes only. 

* The device is not suitable for use on neonatal patients, pregnant women,patients with 

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.

* The device is not suitable for measuring the blood pressure of children. Ask your doctor 

before using it on older children.

* The device is not intended for patient transport outside a healthcare facility.

* The device is not intended for public use.

* 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.

* Do not take any therapeutic measures on the basis of a self measurement. Never alter the 

dose of a medicine prescribed by a doctor. Consult your doctor if you have any question 

about your blood pressure.

* 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.

* Don't kink the connection tube during use, otherwise, the cuff pressure may continuously 

increase which can prevent blood flow and result in harmful injury to the PATIENT.

* When using this device, please pay attention to the following situation which may interrupt 

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 

therapy, or an arterio-venous (A-V) shunt, is present; inflating the cuff on the side of a 

mastectomy.

* Warning: Do not apply the cuff over a wound;otherwise it can cause further injury.

*Do not inflate the cuff on the same limb which other monitoring ME equipment is applied 

around simultaneously, because this could cause temporary loss of function of those 

simultaneously-used monitoring ME equipment.

*On the rare occasion of a fault causing the cuff to remain fully inflated during 

measurement, open the cuff immediately. Prolonged high pressure (cuff pressure 

 

300mmHg or constant pressure 

 15mmHg for more than 3 minutes) applied to the arm 

may lead to an ecchymosis.

*Please check that operation of the device does not result in prolonged impairment of 

patient blood circulation.

* When measurement, please avoid compression or restriction of the connection tubing.

* The device cannot be used with HF surgical equipment at the same time.

* The ACCOMPANYING DOCUMENT shall disclose that the SPHYGMOMANOMETER was 

clinically investigated according to the requirements of ISO 81060-2:2013.

* To verify the calibration of the AUTOMATED SPHYGMOMANOMETER, please contact the 

manufacturer.

* 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.

* Too frequent and consecutive measurements could cause disturbances in blood circulation 

and injuries.

* 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.

* When not in use, store the device with the adapter in a dry room and protect it against 

extreme moisture, heat, lint, dust and direct sunlight. Never place any heavy objects on the 

storage case.

* This device may be used only for the purpose described in this booklet. The manufacturer 

cannot be held liable for damage caused by incorrect application.

*This device comprises sensitive components and must be treated with caution. Observe the 

storage and operating conditions described in this booklet.

* 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.

* Warning: No servicing/maintenance while the ME equipment is in use.

* The patient is an intended operator.

* The patient can measure data and change batteries under normal circumstances and 

maintain the device and its accessories according to the user manual.

* To avoid measurement errors, please avoid the condition of strong electromagnetic field 

radiated interference signal or electrical fast transient/burst signal.

* The blood pressure monitor, and the cuff are suitable for use within the patient 

environment. If you are allergic to polyester, nylon or plastic, please don't use this device. 

* 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.

* If you experience discomfort during a measurement, such as pain in the arm or other 

complaints, press the START/STOP button to release the air immediately from the cuff. 

Loosen the cuff and remove it from your arm.

* If the cuff pressure reaches 40 kPa (300 mmHg), the unit will automatically deflate. Should 

the cuff not deflate when pressures reaches 40 kPa (300 mmHg), detach the cuff from the 

arm and press the START/STOP button to stop inflation.

* Before use, make sure the device functions safely and is in proper working condition. 

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.

Summary of Contents for UAM-710

Page 1: ...user manual carefully and thoroughtly so as to ensure the safe usage of this product and keep the manual well for further reference in case you have problems Manufactured for Zewa Inc 12960 Commerce L...

Page 2: ...AGEMENT 15 Recall the Records Delete the Records INFORMATION FOR USER 17 Tips for measurement Maintenances ABOUT BLOOD PRESSURE 19 What are systolic pressure and diastolic pressure What is the standar...

Page 3: ...is intended for adult indoor use only 1 The device is not suitable for use on pregnant women 2 The device is not suitable for use on patients with implanted electrical devices such as cardiac pacemake...

Page 4: ...to an ecchymosis Please check that operation of the device does not result in prolonged impairment of patient blood circulation When measurement please avoid compression or restriction of the connect...

Page 5: ...ed to be calibrated within two years of reliable service If you have any problems with this device such as setting up maintaining or using please contact the SERVICE PERSONNEL of Zewa Don t open or re...

Page 6: ...y 1 Battery powered mode 6VDC 4 AAA batteries 2 AC adaptor powered mode Not included 6V 1A Please only use the recommended AC adaptor model Please unplug the adaptor to depart from the using utility p...

Page 7: ...ing Or when the monitor is off press SET button shortly it will display the time Then hold pressing SET button to enter the mode for year setting 2 Press the MEM to change the YEAR Each press will inc...

Page 8: ...t the cuff is at the same level as your heart Turn your palm upwards Sit upright in a chair and take 5 6 deep breaths Rest for 5 minutes before first measuring Wait at least 3 minutes between measurem...

Page 9: ...st three records If the records are less than three groups it will display the latest record first 2 Press the MEM or SET to get the record you want The most recent record 1 is shown first Each new me...

Page 10: ...a coffee smoking When talking or moving your fingers When you want to discharge urine To delete records follow these steps Delete Records When the monitor is in the memory recall mode hold pressing ME...

Page 11: ...5 or there are four or more pulse intervals the difference between each interval and the average is more than the average value of 15 the irregular heartbeat symbol appears on the display when the mea...

Page 12: ...tion includes a list of error messages and frequently asked questions for problems you may encounter with your blood pressure monitor If the products not operating as you think it should check here be...

Page 13: ...white backlight V A 60mm 40 5mm Approx 110mm 110mm 41mm 4xAAA batteries user manual warranty book A01 About 22cm 42cm Type BF applied part WARNING No modification of this equipment is allowed Power su...

Page 14: ...ogical evaluation of medical devices Part 5 Tests for in vitro cytotoxicity ISO 10993 10 2010 Biological evaluation of medical devices Part 10 Tests for irritation and skin sensitization EN ISO 15223...

Page 15: ...at 1kHz 150 kHz to 80 MHz 3 Vrms 6Vrms in ISM and amateur radio bands 80 Am at 1kHz Electromagnetic environment guidance NOTE 1 At 80 MHz and 800 MHz the higher frequency range applies NOTE 2 These gu...

Page 16: ...r the user of the device should assure that it is used in such an environment NOTE If necessary to achieve the IMMUNITY TEST LEVEL the distance between the transmitting antenna and the ME EQUIPMENT or...

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