Andon Health iHealth Track User Manual

Andon Health iHealth Track User Manual

Fully automatic ihealth track connected arm blood pressure monitor

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Fully Automatic iHealth Track Connected
Arm Blood Pressure Monitor
USER MANUAL
1
Note: This is a shortened practical version of the user manual. For the full version of this user manual,
please visit www.ihealthlabs.eu/support

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Summary of Contents for Andon Health iHealth Track

  • Page 1 Fully Automatic iHealth Track Connected Arm Blood Pressure Monitor USER MANUAL Note: This is a shortened practical version of the user manual. For the full version of this user manual, please visit www.ihealthlabs.eu/support...
  • Page 2 MEASURING BLOOD PRESSURE – A FEW BASICS Blood Pressure Monitor that uses the oscillometric principle to measure your blood pressure and pulse rate. Blood pressure fluctuates continually day and night. Any physical activity or excitement will influence your blood pressure. Because of this, it is unusual to obtain identical multiple blood pressure readings. This is why it is recommended that you measure your blood pressure at approximately the same time every day.
  • Page 3 Irregular Heartbeat Symbol Blood Pressure Level Classification Indicator Memory/Sync button Start/Stop button WHY YOU SHOULD CONNECT YOUR DEVICE Taking a measurement is easy. It’s what you do with the measurement that is important. You can use your device as a stand-alone device just to measure your blood pressure, but when you connect it to the free iHealth MyVitals App you will be able to track, store, manage and share your results with your family, doctor or care givers.
  • Page 4: How To Use Your Blood Pressure Monitor

    using the same account as you used with your App. The iHeath Track Blood Pressure Monitor is designed to be used with Bluetooth 4.0 Apple devices and selected Bluetooth 4.0 Android smartphones. Please note that the compatible devices are subject to change.
  • Page 5 b. Sit with your feet flat on the floor without crossing your legs. While seated, place your palm upside in front of you on a flat surface such as a table.Lying Down During Measurement:(You can also lie on your back and place your left arm straight along your side with your hand palm-side up.) Position the air tube in the middle of your arm in line with your middle finger.
  • Page 6: Setting The Date And Time

    Avoid compression or restriction of the connection tubing during measurement,which may cause inflation error, or harmful injury due to continuous cuff pressure. 4. SETTING THE DATE AND TIME Insert the batteries in the device and connect it with the iHealth MyVitals App on your smartphone. The time and date will automatically be updated.
  • Page 7: Blood Pressure Classification

    CLASSIFICATION OF BLOOD PRESSURE AND BACKLIGHT INDICATOR BLOOD PRESSURE Systolic mmHg Diastolic mmHg BACKLIGHT INDICATOR CLASSIFICATION Optimal 91–119 and 61 - 79 Green Normal 120–129 and 80 -84 Green High-normal 130–139 or 85 - 89 Yellow Grade 1 Hypertension 140–159 or 90 - 99 Flashing Yellow Grade 2 Hypertension...
  • Page 8: Troubleshooting

    The monitor will automatically switch off after one minute to save the batteries. Alternatively, you can press the "START/STOP" button to turn off the monitor manually. 7. SYNCHRONIZING WITH THE IHEALTH MYVITALS APP Before you can synchronize all your blood pressure readings, you need to download the iHealth MyVitals App on your smartphone from the Apple Store (for iOS devices) or on GooglePlay Store (for Android).
  • Page 9 Problem Explanation Solution LCD shows low battery Low Battery Change all the batteries symbol Pressure system is unstable before LCD shows “Er 0” measuremente Try again without moving Fail to detect systolic pressure LCD shows “Er 1” LCD shows “Er 2” Fail to detect diastolic pressure Pneumatic system blocked or cuff is too LCD shows “Er 3”...
  • Page 10: General Safety And Precautions

    Please visit the support section of the www.ihealthlabs.eu website to see our comprehensive Frequently Asked Questions on blood pressure. 9. GENERAL SAFETY AND PRECAUTIONS 1. Carefully read the user guide before operating the device. 2. Consult your physician for any of the following situations: a) The application of the cuff over a wound or inflamed area.
  • Page 11: Care And Maintenance

    with preeclampsia. This product might not meet its performance specifications if stored or used outside the specified temperature and humidity ranges. Please do not share the cuff with any infectious person to avoid cross-infection. The monitor, cable, battery and cuff must be disposed of according to local regulations at the end of their usage. 7.
  • Page 12 11. AFTERSALES AND WARRANTEE This device has been developed by iHealth together with a team of medical specialists and engineers. We have taken the utmost care to manufacture a device that is user friendly and clinically accurate. It has been validated against the exacting standard of the ESH (European Society of Hypertension) and as such can be used by a medical professional in clinical practice.
  • Page 13 CE conformity mark iHealthLabs Europe 3 rue Tronchet, 75008, Paris, France support@ihealthlabs.eu www.ihealthlabs.eu ANDON HEALTH CO., LTD Add:No. 3 Jinping Street, YaAn Road, Nankai District, Tianjin 300190, China. Tel: 86-22-60526161 iHealth is a trademark of iHealth Lab Inc. The Bluetooth® word mark and logos are registered trademarks owned by Bluetooth SIG, Inc. and any use of such marks by iHealth Lab Inc.
  • Page 14: Specifications

    13. SPECIFICATIONS Product name: iHeath Track Blood Pressure Monitor Model: KN-550BT Classification: Internally powered, type BF applied part; IPX0, No AP or APG; Continuous operation Machine size: 98 × 98 × 46mm Cuff circumference: 22 - 42cm Weight: 348g (batteries and cuff included) Measuring method: oscillometric method, automatic inflation and measurement Memories: 99 Power source: 4x1.5V...
  • Page 15 This device bears the CE conformity mark. The quality of this wireless device has been verified and conforms to the provisions of the IEC 60601-1:2005 corr.1 (2006) + corr.2 (2007)/EN 60601-1:2006/AC:2010 (Medical electrical equipment – Part 1: General requirements for safety); IEC 60601-1-2:2007 /EN 60601-1-2:2007 /AC:2010 (Medical electrical equipment –...

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