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CAUTION

CAUTION

INTRODUCTION

INTRODUCTION

* 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 Is 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 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 maximum temperature that the applied part can be achieved is 42.8

 while the 

environmental temperature is 40

.

* 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,transmit data and charge 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 sensation or irritation reaction.

* Adaptor is specified as a part of ME EQUIPMENT.

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

complaints, press any 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 pressure reaches 40 kPa (300 mmHg), detach the cuff from the 

arm and press any 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.

* Do not wash the cuff in a washing machine or dishwasher!

Summary of Contents for UAM-820BT

Page 1: ...品型号 材质 尺寸 70g书写纸 100 140 mm 单黑 产品名称 血压计 TMB 995 BS 004 李秋燕 2019 06 12 罗佳钰 2019 06 12 谭文昊 2019 06 12 TMB 995 BS 004 GB 08 PO 2F3502 TMB 995 BS 004 GB 08 说明书 A1 共 17 张 第 1 张 A 1 对应结构图纸 印色 1 1 表面处理 技术要求 1 黏合不可露胶 2 保持印刷面板上的清洁 3 注意套印的准确性 4 表面处理不可爆开 5 结构工艺以结构受控图为准 6 颜色参考 Manufactured for Zewa Inc 12960 Commerce Lakes Drive 29 Fort Myers FL 33913 USA www zewa com Toll Free Customer Service 1 888 993 3592...

Page 2: ... MANAGEMENT 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 standard blood pressure classification Irregular heartbeat detector Why does my blood pressure fluctuate throughout the day Why do I get a different blood pressure at home compared to the hospital Is the...

Page 3: ... use only The Green Dot is the license symbol of a European network of industry funded systems for recycling the packaging materials of consumer goods Symbol for RECYCLE Symbol for THE OPERATION GUIDE MUST BE READ Symbol for MANUFACTURER Symbol for SERIAL NUMBER Symbol for TYPE BF APPLIED PARTS Symbol for DIRECT CURRENT Symbol for ENVIRONMENT PROTECTION Electrical waste products should not be disp...

Page 4: ...pairment 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 pleas...

Page 5: ...e the soft cloth to clean the whole unit before and after use Don t use any abrasive or volatile cleaners The device doesn t need 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 repair the device by yourself in the event of malfunctions The device must ...

Page 6: ...s Replace the batteries whenever the below happens The shows The display dims The display does not light up BEFORE YOU START INTRODUCTION In order to get the best effect and protect your monitor please use the the right batteries and special power adapter which complies with local safety standard CAUTION CAUTION Do not use new and used batteries together Do not use different types of batteries tog...

Page 7: ...TION 1 2 Interference may occur in the vicinity of equipment marked with the following symbol And UAM 820BT may interfering vicinity electrical equipment Sensitive people including pregnant women pre eclamptic and those who implanted medical electronic instruments should avoid using the unit whenever possible Keep the monitor at least 20 centimeters away from the human body especially the head whe...

Page 8: ... on a flat surface Place your elbow on a table so that 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 measurement Wait at least 3 minutes between measurements This allows your blood circulation to recover The patient must relax as much as possible and do not move and talk during the measurement pro...

Page 9: ... measurement The Bluetooth symbol blinks on the LCD indicates data is transmitting 3 If the data is successfully transmitted the Bluetooth symbol will light up and the will disappear then the device will turn off If the data transmission fails the will disappear then the device will turn off 2 Hold and press button again to show the average value of the latest three records If the records are less...

Page 10: ...ath In a very cold environment Immediate measurement after tea coffee smoking When talking or moving your fingers When you want to discharge urine Measurements may be inaccurate if taken in the following circumstances INFORMATION FOR USER The most recent record 1 is shown first Each new measurement is assigned to the first 1 record All other records are pushed back one digit e g 2 becomes 3 and so...

Page 11: ...pertension High Blood Pressure Hypertension Stage 1 High Blood Pressure Hypertension Stage 2 Hypertensive Crisis Consult your doctor immediately Systolic mmHg upper Diastolic mmHg lower less than 120 120 129 130 139 140 or higher Higher than 180 and or or and or less than 80 80 89 90 or higher Higher than 120 This chart reflects blood pressure categories defined by American Heart Association and l...

Page 12: ...lems you may encounter with your blood pressure monitor If the product is not operating as you think it should check here before arranging for servicing PROBLEM SYMPTOM CHECK THIS REMEDY No power Low batteries Error message Display will not light up Batteries are exhausted Replace with new batteries Insert the batteries correctly Replace with new batteries Batteries are inserted incorrectly Batter...

Page 13: ...e 40 199 beat minute IP21 It means the device could protected against solid foreign objects of 12 5mm and greater and protect against vertically falling water drops Device Classification Battery Powered Mode Internally Powered ME Equipment AC Adaptor Powered Mode Class II ME Equipment A temperature range of 5 C to 40 C A relative humidity range of 15 to 90 non condensing but not requiring a water ...

Page 14: ...rt 10 Tests for irritation and skin sensitization EN ISO 15223 1 2016 ISO 15223 1 2016 Medical devices Symbols to be used with medical device labels labelling and information to be supplied Part 1 General requirements IEC 80601 2 30 2009 A1 2013 Medical electrical equipment Part 2 30 Particular requirements for the basic safety and essential performance of automated non invasive sphygmomanometers ...

Page 15: ... domestic purposes Guidance and manufacturer s declaration electromagnetic immunity Immunity test 8 kV contact 15 kV air 8 kV contact 15 kV air 2 kV power supply lines line s to line s 1 kV line s to earth 2 kV 0 UT 0 5 cycle At 0 45 90 135 180 225 270 and 315 0 UT 1 cycle and 70 UT 25 30 cycles Single phase at 0 0 UT 300 cycle 30 A m 50Hz 60Hz NOTE UT is the a c mains voltage prior to application...

Page 16: ...ropriate for the frequency of the transmitter Recommended separation distances d 0 35 d 1 2 10V m 80 Am at 1kHz 80 MHz to 800 MHz d 1 2 800 MHz to 2 7 GHz d 2 3 where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer d is the recommended separation distance in meters m Field strengths from fixed RF transmitters as determined by an electrom...

Page 17: ... TETRA 800 iDEN 820 CDMA 850 LTE Band 5 Pulse modulation b 18Hz 2 0 3 28 1720 1845 1970 1700 1990 GSM 1800 CDMA 1900 GSM 1900 DECT LTE Band 1 3 4 25 UMTS Pulse modulation b 217Hz 2 0 3 28 2 0 3 28 2450 2400 2570 Bluetooth WLAN 802 11 b g n RFID 2450 LTE Band 7 Pulse modulation b 217 Hz 5240 5500 5785 5100 5800 WLAN 802 11 a n Pulse modulation b 217 Hz 0 2 0 3 9 a For some services only the uplink ...

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