Jamr Technology B22 User Manual

Jamr Technology B22 User Manual

Upper arm type blood pressure monitor

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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, Shenzhen 518100,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
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Summary of Contents for Jamr Technology B22

  • 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, Shenzhen 518100,PEOPLE'S REPUBLIC OF CHINA Website: www.jiemeirui.com...
  • Page 2 Upper Arm Type Blood Pressure Monitor Model Number: B22 --------------------------------------------------------------------- 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

    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 • Too frequent measurements can cause injury to the PATIENT due to blood flow interference • 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 •...
  • Page 6: Important Information On Blood Pressure And Its Measurement

    pulse rate can be safely used by patient. The routine clean and changing batteries can be performed by the patient. Use of power adapters Warning: 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.
  • 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: Components Of Your Blood Pressure Monitor

    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. Arterial blood vessels in your body are endangered due to constriction caused by deposits in the vessel walls (Arteriosclerosis).
  • Page 9: Using Your Monitor For The First Time

    9. User A 10. User B 12.Battery low symbol 13. WHO symbol 14. Date/Time display 3.3. Features of Model B22: 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

    Record Delete : When you checking the memory data, long press memory to delete existing user measurement data. Note: You can’t delete single measurement record. If you delete the record, you will delete all. Please keep the record in another way, in case you need it some days later. Take the battery out won’t lead to a record missing.
  • Page 11 5.3. Fitting the Cuff Please refer to picture-06 a) The cuff is preformed for easier use. Remove tight or bulky clothing from your upper arm. b) Wrap the cuff around your upper left arm. The rubber tube should be on the inside of your arm extending downward to your hand.
  • Page 12 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.
  • Page 13 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. Information for the doctor on frequent appearance of the Irregular Heartbeat Symbol This instrument is an oscillometric blood pressure monitor device that also analyzes pulse frequency during measurement.
  • Page 14 Monitor could not detect pulse Check if the air releasing is too slow or wave or cannot calculate the not. If it is too slow, please check if blood pressure data there is any dust in the tube plug of the cuff and the cuff port in the device.
  • Page 15 SYMBOL DESCRIPTIONS The following symbols may appear in this manual, on the Digital Blood Pressure Monitor B22, or on it's accessories. Some of the symbols represent standards and compliances associated with the Digital Blood Pressure Monitor B22 and its use.
  • Page 16 fragile Keep dry Avoid the sun handle gently 5.7. 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

    c) Plug the adapter into your electrical outlet. When the AC adapter is connected, no battery current is consumed. Note: No power is taken from the batteries while the AC adapter is connected to the monitor. If electrical power is interrupted, (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.
  • Page 19: Certifications

    Electromagnetic compatibility: Device fulfills the stipulations of the International standard IEC60601-1-2 9. Technical Specifications Model: B22 Wight: 260g (batteries and AC adapter is not included) Display: 3.74”x2.52” 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 * Do not use a mobile phone or other devices that emit electromagnetic fields, near the unit. This may result in incorrect operation of the unit. * 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...
  • Page 21 lines Surge ± 1 kV line(s) to line(s) Not applicable Mains power quality should be that of a typical commercial or IEC 61000-4-5 ± 2 kV line(s) to earth hospital environment. 0 % U ; 0.5 cycle Voltage dips, short Not applicable Mains power quality should be at 0°,45°,90°,...
  • Page 22 Where, P is the maximum output power rating of the 80% AM at 1kHz transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation 80% AM at 1kHz distance. Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, should be less than the compliance level in each frequency range.
  • Page 23 For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
  • 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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