Cigii B02 User Manual
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Cigii B02 User Manual

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CONTACT INFORMATION
Upper Arm Type Blood Pressure Monitor is legal 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. GmbH (Europe)
Contact person: Mr JIN LIANG
Address:
Eiffestrasse 80, 20537 Hamburg, Germany.
Telephone:
+49-40-2513175 / 2513178
FAX:
+49-40-255726
E-mail:
shholding@hotmail.com
Release date: 2021.03.15, Version:A0
1

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  • Page 1 CONTACT INFORMATION Upper Arm Type Blood Pressure Monitor is legal 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:...
  • Page 2 Upper Arm Type Blood Pressure Monitor Model Number: B02 -------------------------------------------------------------------------- USER MANUAL...

  • Page 3: Table Of Contents

    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..................8 5. Measurement Procedure..................... 9 6. Care and Maintenance......................16 7.

  • Page 4: Introduction And Intended Use

    1.Introduction and Intended Use The device is intended to measure systolic and diastolic blood pressure as well as the pulse by wrapping around the upper arm with cuff circumference ranging from 22cm to 40cm . The device is used for adult that age is more than 12 years old ,and the intended populations are the patients with hypertension or need blood pressure monitoring.The device is not used for patients under dialysis therapy or on anticoagulant, antiplatelets, or steroids.
  • Page 5 • Don’t place the cuff over wound part. • Pressurization of the CUFF can temporarily cause loss of function of simultaneously used monitoring ME EQUIPMENT on the same limb. • Apply CUFF and its pressurization to any limb where intravascular access or arteriovenous (A-V) shunts exist, can temporarily interfere with blood flow and may cause injury to the patient.

  • Page 6: Important Information On Blood Pressure And Its Measurement

    Warning: Use of power adapters 1.Adapter: input 100-240V, 50/60hz output DC 5V 1A. 2.Do not to position the device to make it difficult to operate the disconnection device while using adaptor. 3.Do not be prone to water leakage, high temperature, moisture, direct sunlight and more or more corrosive gas environment.
  • Page 7 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.
  • Page 8 • 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.

  • Page 9: Using Your Monitor For The First Time

    13-Heartbeat symbol (Flashes during measurement); 14-Cuff self-checking function 15- Mute symbol 16-WHO Function symbol 3.3. Features of Model B02 1. Talking function 2. Double users: 2 x 120 sets memory 3.Cuff self-checking function 4. Irregular heartbeat checking 5. Average value function 6.

  • Page 10: Measurement Procedure

    Setting the Year: Initial year is 2018, when the year display is flashing, press the memory button, the year will increase by I year each, hold the memory button and it will increase continuously 1 by 1, until 2049, and then rollover to 2018, once the year Setting is OK, press SET button to confirm. Setting Month/Date: Initial Month/Date is 1/01, when the Month display is flashing, press the memory button, the month will increase by 1, press SET button to confirm, and do in the same way to set the date.
  • Page 11 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. • If the arm artery lies considerably lower or higher than the heart, an erroneously high or low blood pressure will be measured! Each 25-30cm difference in height between your heart and the cuff results in a measurement error of 10mmHg! Note: Only use approved cuffs!
  • Page 12 Picture-06 Change the cuff may result in unacceptable risks,the operator should pay attention to the following: • Only use Jamr authorized cuffs, as those not approved for use with the device may provide inaccurate measurements, injury, and/or damage the device. •...
  • Page 13 4. performance of the AUTOMATED SPHYGMOMANOMETER can be affected by extremes of temperature, humidity and altitude 5. To stop the inflation or measurement, push the START/STOP button. The monitor will stop inflating, start deflating, and will turn off. 6. After the monitor has detected your blood pressure and pulse rate, the cuff automatically deflates.
  • Page 14 Sensor abnormal Check if the pump is working or not. If it is working, then the problem is sensor abnormal. Please send it to the local distributor. Monitor could not detect Check if the air releasing is too slow or not. If it pulse wave or cannot is too slow, please check if there is any dust in calculate the blood...
  • Page 15 The following symbols may appear in this manual, on the Digital Upper Arm Type Blood Pressure Monitor B02, or on it's accessories. Some of the symbols represent standards and compliances associated with the Digital Upper Arm Type Blood Pressure Monitor B02 and its use.
  • Page 16 fragile Keep dry Avoid the sun handle gently temperature range 5.9. Memory At the end of a measurement, this monitor automatically stores each result with date and time. Each unit stores 120 sets measurements for 2 users, totally 240 sets（User A and B）. Viewing the stored values With the unit off, press the Memory button.
  • Page 17 Picture-08 Which batteries and which procedure? Use four new, longlife 1.5V AAA batteries. Do not use batteries beyond their expiration date. If the monitor is not going to be used for a prolonged period the batteries should be removed. Using rechargeable batteries You can also operate this instrument using rechargeable batteries.

  • Page 18: Care And Maintenance

    (e.g., by accidental removal of the AC adapter from the outlet) the monitor must be reset by removing the plug from the socket and reinserting the AC adapter connection. 6. Care and Maintenance Wash hands after each time measurement. If one device is used by different patients, wash hands before and after each use. The device,including cuff should be cleaned every week,and the effective repetitive cleaning times is 390 times during the shelf life.

  • Page 19: Technical Specifications

    Electromagnetic compatibility: Device fulfills the stipulations of the International standard IEC60601-1-2 9. Technical Specifications Model: B02 Wight: 290g (batteries and AC adapter is not included) Display: 3.35”x2.28”’ LCD Digital Display Size: 144 (W) x 120 (L) x 67(H) mm Accessories: 1×Main Device, 1×Cuff, 1×Users manual, 1×Warranty card Operating Conditions: Temperature: 5℃...
  • Page 20 * Caution: This unit has been thoroughly tested and inspected to assure proper performance and operation! * Caution: this machine should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is necessary, this machine should be observed to verify normal operation in the configuration in which it will be used Guidance and manufacture’s declaration –...
  • Page 21 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. Electromagnetic environment - Immunity test IEC 60601 test level Compliance level guidance...
  • Page 22 is intended for use in the electromagnetic environment specified below. The customer or the user device of the should assure that it is used in such an environment. device Immunity IEC 60601 test Compliance Electromagnetic environment - guidance test level level Portable and mobile RF communications equipment should be used no closer to any part of the device,...
  • Page 23 additional measures may be necessary, such as re‐orienting or relocating the device. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m. Recommended separation distances between portable and mobile RF communications equipment and the device The device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled.

  • Page 24: Warranty Card

    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. Minimum separation distances for higher IMMUNITY TEST LEVELS shall be calculated using the following equation: Where P is the maximum power in W, d is the minimum separation distance in m, and E is the IMMUNITY TEST LEVEL in V/m.

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