Version Number: 1.0 Issue date:2020.04.10 CONTACT INFORMATION Digital Blood Pressure Monitor is manufactured by: Company name: Shenzhen Jamr Technology Co., Ltd Address: A101-301,D101-201, Jamr Science & Technology Park, No. 2 Guiyuan Road, Guixiang Community,Guanlan Street, Longhua District, 518100 Shenzhen ,PEOPLE'S REPUBLIC OF CHINA Website: www.jiemeirui.com Telephone: 0086 755 85292057 Authorized European Representative: Company Name: Shanghai International Holding Corp.
Version Number: 1.0 Issue date:2020.04.
Version Number: 1.0 Issue date:2020.04.10 CONTENTS 1. Introduction and Intended Use..............................................................................................3 2. Important Information on Blood Pressure and its Measurement...........................................5 3. Components of your blood pressure monitor.........................................................................7 4. Using your Monitor for the First Time.................................................................
Version Number: 1.0 Issue date:2020.04.10 1.Introduction and Intended Use This manual is for F1701T models. It is a fully automatic digital blood pressure measuring device for use by adults on the upper arm at home or in your doctor’s/nurse’s office. It enables very fast and reliable measurement of systolic and diastolic blood pressure as well as pulse through the oscillometric method. This device offers clinically proven accuracy and has been designed to be user friendly.
Version Number: 1.0 Issue date:2020.04.10 Contraindication Use of this instrument on patients under dialysis therapy or on anticoagulant, antiplatelets, or steroids could cause internal bleeding. 1.2 Warnings and Precautions Warning: Do not use cuffs, AC adapters or batteries other than those included with this product or replacement parts supplied by the manufacturer. Warning: Do not use the batteries and the AC adapter to provide power at the same time.
Version Number: 1.0 Issue date:2020.04.10 Note: The cuff is treated as the applied part.The user should contact the manufacturer for assistance, if needed, in setting up, using or maintaining the device. 1.3 FCC Compliance statement • This device complies with Part 15 of the FCC Rules.
Version Number: 1.0 Issue date:2020.04.10 Picture-01 There are six grids in the display of device. Please refer to the picture-01-01. Different grids represent different interval scales of WHO. Picture-01-01 Blood pressure is very high if your diastolic pressure is above 90 mmHg and/or your systolic blood pressure is over 160 mmHg, while at rest. In this case, please consult your physician immediately.
Version Number: 1.0 Issue date:2020.04.10 conditions of physical or psychological stress, it is possible that you are suffering from so-called “labile hypertension.” Consult your doctor. • Correctly measured diastolic blood pressure values above 120mmHg require immediate medical treatment. 2.3. What can be done if regular high or low values are obtained? 1) Consult your doctor. 2) Increased blood pressure values (various forms of hypertension) are associated with considerable health risks over time.
Version Number: 1.0 Bluetooth Issue date:2020.04.10 User ID Memory Picture-04 Picture-05 3.
Version Number: 1.0 Issue date:2020.04.10 A. Setting the Users Press the Setting button and then you can set the A/B user by shifting the A/B user button B. Setting the Year/Month&Date/Time/Volume Long press the Setting button for more than 3s, and then you can start to set.
Version Number: 1.0 Issue date:2020.04.10 5.2. Common sources of error: Note: Comparable blood pressure measurements always require the same conditions! •Conditions should always be quiet. •All efforts by the user to support the arm can increase blood pressure. Make sure you are in a comfortable, relaxed position and do not flex any of the muscles in the measurement arm during the measurement. Use a cushion for support if necessary.
Version Number: 1.0 Issue date:2020.04.10 Picture-06 5.4. Measure Procedure Refer to picture 07 The monitor is designed to take measurements and store the measurement values in memory for two people using User ID A and User ID B. 1. Sit comfortably in a chair with your feet flat on the floor. 2. Select your User ID (A or B). Stretch your arm forward on the desk and keep relaxing, make sure the palm of hand is upturned. Make sure arm is in correct position, to avoid body movement.
Version Number: 1.0 Issue date:2020.04.10 then select Bluetooth Device button. A moment later, the device will be connected as picture App 05 and App 06. App04 App05 App 06 d) Start the measurement Once the Bluetooth is connected, click the “START” button on the App to start the testing as picture App 06. When measuring is done, the assessment will be voiced out and a interface about checking the result will show up as picture App 07 and App 08.
Version Number: 1.0 Issue date:2020.04.10 App 09 App 10 App 11 2 ) Operate on the device a) Press the Stop/Start button. The pump begins to inflate the cuff. In the display, the increasing cuff pressure is continually displayed. b) After automatically reaching an individual pressure, the pump stops and the pressure slowly falls. The cuff pressure is displayed during the measurement. c) When the device has detected your pulse, the heart symbol in the display begins to blink.
Version Number: 1.0 6. Issue date:2020.04.10 After the monitor has detected your blood pressure and pulse rate, the cuff automatically deflates. Your blood pressure and pulse rate are displayed. 7. The monitor will automatically turn off after one minute. Picture-07 5.5. Irregular Heartbeat Detector This symbol - indicates that certain pulse irregularities were detected during the measurement. In this case, the result may deviate from your normal basal blood pressure – repeat the measurement.
Version Number: 1.0 Issue date:2020.04.10 Er2 Monitor could not detect pulse wave or cannot calculate the blood pressure data Check if the air releasing is too slow or not. If it is too slow, please check if there is any dust in the tube plug of the cuff and the cuff port in the device. If yes, please clean and start the measurement again. If no, please send the device back to the local distributor.
Version Number: 1.0 Issue date:2020.04.10 SYMBOL DESCRIPTIONS The following symbols may appear in this manual, on the Digital Blood Pressure Monitor F1701T, or on it's accessories. Some of the symbols represent standards and compliance associated with the Digital Blood Pressure Monitor F1701T and its use. Authorized Representative in the European Community CE Mark: conforms to essential requirements of the Medical Device Directive 93/42/EEC. Date of manufacture.
Version Number: 1.0 Issue date:2020.04.10 Viewing the stored values With the unit off, press the Memory button. The display first shows "A", then shows an average of all measurements stored in the unit. Please note: Measurements for each user are averaged and stored separately. Be certain that you are viewing the measurements for the correct user. Pressing the Memory button again displays the previous value.
Version Number: 1.0 Issue date:2020.04.10 • Recharge these batteries using an external charger and follow manufacturer’s instructions Carefully. 5.10. Using the AC Adapter You may also operate this monitor using the AC adapter (output 5V DC/1A with Micro USB plug). Use only the approved AC adapter to avoid damaging the unit（class II). a) Ensure that the AC adapter and cable are not damaged. b) Plug the adapter cable into the AC adapter port on the right side of the blood pressure monitor.
Version Number: 1.0 Issue date:2020.04.10 original purchaser only, from date of purchase. The warranty does not apply to damage caused by improper handling, accidents, professional use, not following the operating instructions or alterations made to the instrument by third parties. Warranty only applies to the instrument. All accessories including the cuff are guaranteed for one year, USB charging cable is not included. There are no user serviceable parts inside.
Version Number: 1.0 Issue date:2020.04.10 Users: Adult Expected service life of the device and accessories: 5 years Technical alterations reserved! 9.1. EMC Declaration * This product needs special precautions regarding EMC and needs to be installed and 1) put into service according to the EMC information provided, and this unit can be affected by portable and mobile RF communications equipment. * Do not use a mobile phone or other devices that emit electromagnetic fields, near the 2) unit.
Version Number: 1.0 RF emission CISPR 11 Harmonic emissions IEC 61000-3-2 Issue date:2020.04.10 Class B The device is suitable for use in all establishments, including domestic establishments other than domestic and those directly connected to the public low-voltage Not applicable power supply network that supplies buildings used for domestic purposes.
Version Number: 1.0 Issue date:2020.04.10 Guidance and manufacture’s declaration – electromagnetic immunity The device is intended for use in the electromagnetic environment specified below. The customer or the user of device should assure that it is used in such an environment.
Version Number: 1.0 Issue date:2020.04.10 Guidance and manufacture’s declaration – electromagnetic immunity The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that it is used in such an environment.
Version Number: 1.0 Issue date:2020.04.10 survey should be considered. If the measured field strength in the location in which the device is used exceeds the applicable RF compliance level above, the device should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re‐orienting or relocating the device. b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
Version Number: 1.0 Issue date:2020.04.10 Guidance and manufacturer’s declaration - electromagnetic immunity The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device, should assure that it is used in such an environment. The MANUFACTURER should consider reducing the minimum separation distance, based on RISK MANAGEMENT, and using higher IMMUNITY TEST LEVELS that are appropriate for the reduced minimum separation distance.
Version Number: 1.0 Issue date:2020.04.10 10.
