Welcome! This new approach to managing high blood pressure makes it easy to improve your lifestyle choices. It comes with a connected blood pressure monitor and arm cuff, as well as anytime access to expert coaches, personalized insights, reports, and much more. If you have any questions, please call Member Support at (800) 945-4355 or email us at membersupport@teladochealth.com .
Getting Started Depending on your service, open the Teladoc Health or Livongo app and log in. If you don’t have the app yet, download it from the iOS App Store or Google Play Store. Open the app to get started with your connected blood pressure monitor.
Installing the Batteries If this is your first time using the device: 1 . Slide open the battery door on the back of the device. 2 . Install the batteries provided with the device. 3 . Follow the diagram inside the battery compartment for correct polarity —...
Securing the Cuff 1 . Plug the connector on cuff tube into the device. 2 . Expose your left upper arm by removing or adjusting clothing and jewelry. Make sure blood flow is not constricted by a rolled-up sleeve. 3 . Open the cuff and loosen fully. 4 .
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6. Position the cuff’s edge about an inch (2-3 cm) above the elbow. 7. Align the tube with the center of your arm. 8. Tighten the cuff evenly around your arm by 1 inch (2–3 cm) pulling on the end — make sure the tube stays aligned with the center of your arm.
Taking a Measurement 1. Rest for at least 5 minutes, and avoid exercise and caffeine for at least 30 minutes before you take a reading. Lay your arm on a table with your palm facing up. The cuff should be at the same height as your heart. Sit up straight and rest your feet flat on the ground.
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6. The device automatically transmits Notes: measurement results. During this process an · If you wish to abort the measurement while the indicator is shown in the middle of the display. cuff is inflating, press and hold the START/STOP button for 5 seconds. ·...
Contraindications · Consult a medical professional before using this device if you have an implanted cardiac device, such as a pacemaker or defibrillator. · Consult a medical professional before using this device during pregnancy. · Do not use this device on infants. USER GUIDE...
Systolic and Diastolic Blood Pressure When ventricles (the part of the heart that pumps blood) contract and pump blood out of the heart, the blood pressure reaches its maximum value in the cycle, which is called systolic pressure. When the ventricles relax, the blood pressure reaches its minimum value in the cycle, which is called diastolic pressure.
Standard Blood Pressure Classification The chart below is the standard blood pressure classification published by the American Heart Association (AHA). If you have been diagnosed with high blood pressure (hypertension), the AHA recommends keeping your blood pressure below 130/80 mmHg. Blood Pressure Category Systolic mmHg (upper#) Diastolic mmHg (lower#)
Irregular Heartbeat Detector An irregular heartbeat is detected when a heartbeat rhythm varies while the unit is measuring the systolic and diastolic blood pressure. During each measurement, the monitor records all the pulse intervals and calculates the average: If there are two or more pulse intervals, the difference between each interval and the average is more than the average value of ±25%, or there are four or more pulse intervals, the difference between each interval and the average is more than the average value of ±15%, the irregular heartbeat symbol appears on the display...
Precautions · Only use alkaline AA batteries with this device as these offer the longest battery life. Other brands may not be able to provide sufficient power for cellular data transmission. · Only use a cuff that has been approved by the manufacturer for this device model. ·...
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· This device is intended for indoor, home use. This device is not intended for public use. · If in doubt, contact your medical professional before use. · The device may require up to 30 minutes to warm up/cool down from the minimum/maximum storage temperature before it is ready for use.
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· This device is not anesthesia proofed (AP/APG), and it is not suitable for use in the presence of flammable anesthetics. · Do not touch the batteries during measurement. · This device is portable, but should not be operated in transit. ·...
Troubleshooting Problem Possible Reason Resolution Device doesn’t power on Batteries completely drained. Replace all batteries with new ones. when START/STOP button is pressed. Batteries inserted incorrectly. Remove batteries and reinstall them, making sure the + and - polarity symbols Cuff does not inflate. on the batteries match those inside the (display remains off) battery compartment.
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Problem Possible Reason Resolution Readings too high or low. Cuff not positioned correctly. Review instructions on Securing the Cuff, and retry measurement. Readings vary significantly Movement during measurement. Place your arm on a table with your palm between measurements. facing up. The cuff should be at the same level as your heart.
Error Codes Code Description Resolution Er 1 Battery low Replace all batteries with new ones. Er 2 Movement detected Avoid moving or talking while taking a measurement. After securing the cuff and assuming the correct posture, consider waiting for 5 minutes to settle down before starting a measurement.
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Code Description Resolution Er 10 Cellular connectivity suspended Contact Member Support. Er 11 Device is permanently deactivated Contact Member Support. Er 15–19 System error Contact Member Support. Er 20 Cuff did not inflate Confirm the cuff is secured correctly around your arm and the cuff tube is plugged into the monitor.
Storage and Maintenance Do not open the system or attempt any repairs. There are no serviceable parts in this system. There are no parts of the system that are designated as repairable by service personnel. The system uses delicate electrical components and an intricate air unit that could be damaged. If you cannot fix the problem using the Troubleshooting instructions on pages 20–21, contact Member Support.
Symbols Symbol Description Symbol Description Type BF applied part Temperature range The device should not be discarded as unsorted waste Cuff circumference but must be sent to separate collection facilities for recovery and recycling Manufacturer Reference number Complies with FCC regulations Serial number / IMEI The device could be protected against solid foreign IP21...
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Transport/Storage Temperature: -4°F–140°F (-20°C–60°C) Conditions Relative humidity: 0–93% non-condensing Power Supply 4 x 1.5V alkaline AA batteries Cuff Size 8.6–17.7 inches (22–45 cm) arm size Device Weight 274 g (excluding batteries and cuff) Dimensions 102 x 143 x 73 mm International Protection IP21 Applied Part...
Intended Use This digital blood pressure monitor was designed to measure the blood pressure and heartbeat rate of adults with an arm circumference of 8.6–17.7 inches (22–45 cm). The device can be used to detect an irregular heartbeat. This device is intended for adult indoor use only.
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This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications.
EMC Guidance The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare environments. Warning: Don’t use near active HF surgical equipment and the RF shielded room of an ME system for magnetic resonance imaging, where the intensity of EM disturbances is high. Warning: Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation.
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TECHNICAL DESCRIPTION: 1. All necessary instructions for maintaining BASIC SAFETY and ESSENTIAL PERFORMANCE with regard to electromagnetic disturbances for the excepted service life. 2. Guidance and manufacturer’s declaration – electromagnetic emissions and immunity. Guidance and Manufacturer’s Declaration – Electromagnetic Emissions Emissions test Compliance RF emissions...
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Guidance and Manufacturer’s Declaration – Electromagnetic Immunity Immunity Test IEC 60601-1-2 Compliance level Test level Electrostatic discharge (ESD) IEC 61000-4-2 ±8 kV contact ±8 kV contact ±2 kV, ±4 kV, ±8 kV, ±15 kV air ±2 kV, ±4 kV, ±8 kV, ±15 kV air Electrical fast transient/burst IEC 61000-4-4 Not applicable Not applicable...
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Guidance and Manufacturer’s Declaration – Electromagnetic Immunity Test Band Service Modulation Maximum Distance Immunity Radiated RF Frequency (MHz) Power (W) Test Level IEC61000- (MHz) (V/m) 4-3 (Test 380-390 TETRA 400 Pulse modulation b) 1 .8 0 .3 specifications 18Hz for ENCLOSURE PORT IMMUNITY 430-470 GMRS 460, FRS 460...