TeleRPM TMB-2092-G Blood Pressure Monitor

Product Guide

Introduction

General Description

Thank you for choosing this TeleRPM Blood Pressure Monitor. Before use, ensure the device packaging is intact and all contents are present. Check for any visible damage to the device or accessories and remove all packaging material. If you have any doubts, do not use the device and contact your retailer or the specified Customer Services address. Please read this manual to use your Blood Pressure Monitor safely and correctly. Keep the manual for future reference.

Key Features:

  • ⚙️ One-Click Operation
  • Antimicrobial material (antibacterial activity rate >99.9%)
  • ? 4G Connectivity (Any time, Anywhere)
  • ? AC Adapter Available (not included)
  • LATEX FREE
  • Measurement Reminder

Indications for Use

This TeleRPM Blood Pressure Monitor TMB-2092-G is a digital monitor intended for measuring blood pressure and heartbeat rate for adults with an arm circumference ranging from 22 cm to 45 cm. It is intended for indoor use only and can detect irregular heartbeat.

Contraindications

  1. Consult a medical professional before using this device if you have an implanted cardiac device, such as a pacemaker or defibrillator.
  2. Consult a medical professional before using this device during pregnancy.

Measurement Principle

This product uses the Oscillometric Measuring method. Before each measurement, the unit establishes a "zero pressure" equivalent to atmospheric pressure. It then inflates the arm cuff and detects pressure oscillations generated by pulsatile blood flow to determine systolic and diastolic pressure, and pulse rate.

Safety Information

The symbols below are used in the manual, labeling, or components and indicate requirements for standard usage:

  • ? Refer to instruction manual/booklet
  • ? Consult instructions for use or consult electronic instructions for use
  • Type BF applied part
  • SN: Serial Number
  • Direct Current
  • Polarity of d.c. power connector
  • Class II Equipment
  • ? For indoor use only
  • LOT: Batch code
  • Date of manufacture
  • Manufacturer
  • ?️ Temperature limit
  • ☁️ Atmospheric pressure limitation
  • ? Humidity limitation
  • ♻️ General symbol for recovery/recyclable
  • ⚠️ MR Unsafe: Identifies items posing unacceptable risks in MR environments.
  • ⚠️ Caution: Indicates necessary operator awareness or action to avoid undesirable consequences.
  • ♻️ Disposal: Indicates the product should not be discarded as unsorted waste but sent for separate collection facilities for recovery and recycling.

CAUTION

  • This device is intended for indoor use and is portable, but not for patient transport or continuous monitoring during medical emergencies.
  • It is for non-invasive measuring of arterial blood pressure on adult arms only. Do not use on neonates, infants, or children unless instructed by a medical professional.
  • Effectiveness is not established for pregnant users, users with implanted electrical devices, users with common arrhythmias, users with peripheral arterial disease, or users undergoing intravascular therapy. Consult a medical professional before use.
  • Do not use for diagnosis or treatment. Consult your physician for any medical problems or before changing medications.
  • If taking medication, consult your physician to determine the proper measurement time.
  • The manufacturer is not liable for incidental, consequential, or special damages caused by misuse or abuse.
  • Report any unexpected operation or events to the manufacturer.
  • Do not apply the cuff on an arm with an intravenous drip or blood transfusion.
  • Warning: Do not kink, fold, stretch, compress, or deform the tube during measurement, as this may prevent blood flow and cause injury.
  • Warning: Frequent blood pressure measurements may disrupt circulation and cause injuries.
  • Warning: Do not apply cuff to areas with delicate or damaged skin. Check cuff site frequently for irritation.
  • Warning: Do not place the cuff on an arm undergoing medical treatment (e.g., intra-vascular access or therapy, AV shunt) as it could disrupt blood circulation.
  • Warning: Do not place the cuff on the arm on the same side as a mastectomy, especially if lymph nodes have been removed. Measure on the unaffected side.
  • Warning: Do not use the cuff on the same arm as another monitoring device.
  • Ensure operation does not result in prolonged impairment of patient blood circulation.
  • Warning: In case of a fault causing the cuff to remain fully inflated, loosen and remove the cuff immediately. Prolonged high pressure may lead to bruising.
  • Warning: Do not use this device with high-frequency surgical equipment simultaneously.

CAUTION

  • Warning: This device is not AP/APG equipment. Do not use where flammable anesthetic or oxygen/nitrous oxide mixtures are present.
  • Avoid measurements near strong electromagnetic fields or electrical fast transient/burst signals.
  • Wireless communication equipment (mobile phones, Wi-Fi) may cause interference. Maintain a minimum distance of 1 foot (30 cm) from such devices during measurement.
  • Self-measurement is possible; no third-party operator is required.
  • Use the device within the specified environment to maintain performance and lifetime.
  • The device may require up to 30 minutes to warm up/cool down from storage temperatures before use.
  • Warning: Excessive cuff tube lengths could cause strangulation if not managed properly.
  • Warning: Do not touch the output of batteries/adapter and the user simultaneously.
  • The adapter is specified as part of ME EQUIPMENT.
  • Warning: The power cord is the disconnect device. Ensure the equipment is accessible for disconnection.
  • The monitor, adapter, and cuff are suitable for use within the patient environment.
  • Warning: Do not use if allergic to polyester, nylon, or plastic.
  • Warning: Use only manufacturer-approved accessories to avoid damage or injury.
  • Warning: If you experience discomfort (e.g., pain), press the Power button immediately to release cuff air.
  • No calibration is required within two years of service.
  • Do not attempt self-repair. Repairs must be carried out by authorized service centers.
  • Circuit diagrams, component lists, and calibration procedures are available from the manufacturer/distributor upon request from authorized personnel.
  • Performance checks (after repair, maintenance, and every two years) are recommended for cuff pressure indication and air leakage.
  • Warning: Do not use the device while under maintenance or being serviced.
  • Store the device, cuff, and adapter in a clean, dry place, protected from moisture, heat, lint, dust, and direct sunlight. Do not place heavy objects on it.
  • Ensure the cuff's rubber tube is not squeezed, stretched, or kinked during storage.
  • Warning: Keep device, cuff, and batteries away from children due to choking or strangulation risk.
  • Clean the device and cuff with a soft, dry cloth. Use a dampened cloth with mild detergent if necessary. Avoid alcohol, benzene, or harsh chemicals.
  • Do not wash the cuff in a washing machine or dishwasher.
  • Cuff service life varies; typical life is 10000 times.
  • Dispose of accessories, parts, and the device according to local guidelines.

Before You Start

The Choice of Power Supply

  1. DC 6V, 4 AA size batteries.
  2. AC adapter, 6V 1A. Please use the AC adapter authorized by the manufacturer (not included). Unplug the adapter from utility power when you finish the measurement.

? AC adapter

CAUTION: Use the correct batteries and an authorized power adapter that complies with local safety standards for best effect and to protect your monitor.

Installing and Replacing the Batteries

Please pull the plastic insulating strip before first use. The batteries were installed.

Replace the batteries when:

  • The "Replace batteries" symbol appears on the LCD display.
  • The display dims.
  • The display does not light up.

Steps for replacing batteries:

  1. Slide off the battery cover.
  2. Replace 4 AA size batteries according to the polarity indications inside the battery compartment.
  3. Place back the battery cover.

CAUTION:

  • Do not use new and used batteries together.
  • Do not use different types of batteries together.
  • Do not dispose of batteries in fire; they may explode or leak.
  • Remove batteries if the device is not likely to be used for some time.
  • Worn batteries are harmful to the environment. Do not dispose of them with daily garbage.
  • Dispose of old batteries following your local recycling guidelines.

Note A: When you pull the plastic insulating strip or replace new batteries, the LCD displays briefly and then turns off after about 5 seconds. The device will then search and pair with the mobile network automatically. If unsuccessful, it enters standby mode.

Note B: This device has a Measurement Reminder function. Contact Customer Support to enable or disable it (maximum 5 reminders). When enabled, the blue LED on the device button lights up as a breathing light to remind the user to measure at the appointment time. The light cancels after startup or 30 minutes of inactivity. If the user does not measure, the reminder icon will not display for the next measurement.

Measurement

Applying the cuff

  1. Remove all jewelry, such as watches and bracelets, from your left arm. Note: If your doctor has diagnosed you with poor circulation in your left arm, use your right arm.
  2. Roll or push up your sleeve to expose the skin. Ensure your sleeve is not too tight.
  3. Hold your arm with your palm facing up. Tie the cuff on your upper arm, aligning the air tube toward the center of your arm.
  4. Ensure the bottom edge of the cuff is 2-3 cm (0.8-1.2 inch) above the inside elbow. Wrap the cuff securely. Note: The cuff should be snug but not too tight; you should be able to insert one finger between the cuff and your arm.
  5. Sit upright in a comfortable chair with your back against the backrest. Keep your feet flat and legs uncrossed. Rest your arm comfortably on a flat table, with the cuff at the same level as your right atrium.
  6. Take 5-6 deep breaths and begin measuring.

Helpful tips to ensure an accurate reading

  • Take the measurement in a silent room.
  • Rest for 5 minutes before a measurement.
  • Remain relaxed, still, and do not talk during measurement.
  • For meaningful comparison, measure under similar conditions (e.g., same time of day, same arm, or as directed by a physician).

A: Using Single Measurement Mode

Start a measurement

When the "TRIPLE MODE" button is set to "1", the monitor is in Single Measurement mode. When the monitor is OFF, press the "START/STOP" button to turn it on. The device will complete the measurement automatically.

Adjust the zero point

The device shows "0" mmHg.

Inflating and measuring

The cuff inflates and the measurement proceeds.

Display the measured result

The LCD displays the systolic pressure, diastolic pressure, and pulse rate.

Data Transmission

After measurement, data transmission begins, indicated by a symbol. If successful, the symbol disappears, and "OK" is displayed. Press "START/STOP" to turn off the device, or it will power off automatically.

If data transmission fails or there is a server connection error, a symbol will appear. Up to 500 measurements can be saved temporarily and sent when cellular internet is available. Refer to page 22 for more information.

If there is no cellular coverage or a cellular connection error, a different symbol will appear. Refer to page 22 for more information.

B: Using Triple Measurement Mode

Start a measurement

When the "TRIPLE MODE" button is set to "3", the monitor is in Triple Measurement mode. When the monitor is OFF, press the "START/STOP" button to turn it on. The device will complete the measurement automatically.

Measurement Process

  1. After the first measurement, readings are not shown. The second measurement starts after 60 seconds.
  2. The device repeats the steps for the third measurement. After three measurements, the LCD displays the average of the 3 readings.
  3. Tip: If a measurement fails during Triple Measurement Mode, an error is reported, and the current measurement repeats. If the error occurs 3 times consecutively, the Triple Measurement mode will automatically quit.
  4. After measurement, data transmission steps as described on page 14 are repeated.
  5. Tip: You can press the "START/STOP" button to stop the measurement at any time.

Information for User

Tips for Measurement

Measurements may be inaccurate if taken in the following circumstances:

  • Within 1 hour after dinner or drinking
  • Immediate measurement after tea, coffee, smoking
  • Within 20 minutes after taking a bath
  • When moving your fingers or talking
  • In a dry place or exposed to sunshine
  • Touching water; clean with a dry cloth.
  • Avoid intense shaking and collisions
  • In a dusty or unstable temperature environment
  • In a very cold environment
  • When you need to urinate
  • Avoid washing the cuff
  • Using wet cloths to remove dirt

Maintenance

For best performance, follow these instructions:

  • Keep the device in a dry place and avoid direct sunlight.
  • Clean the device and cuff with a soft, dry cloth. If necessary, use a dampened cloth with mild detergent. Do not use alcohol, benzene, or other harsh chemicals.
  • Do not wash the cuff in a washing machine or dishwasher.
  • The service life of the cuff may vary based on washing frequency, skin condition, and storage state. The typical service life is 10000 times.

About Blood Pressure

What are systolic pressure and diastolic pressure?

Systolic pressure is the maximum value reached when the ventricles contract and pump blood out of the heart. Diastolic pressure is the minimum value reached when the ventricles relax.

Diagrams:

  • Systolic: blood discharging artery (press)
  • Diastolic: blood entering vein (relax)

What is the standard blood pressure classification?

The following chart shows the standard blood pressure classification published by the American Heart Association (AHA):

Blood Pressure CategorySystolic mmHg (upper#)Diastolic mmHg (lower#)
Normalless than 120andless than 80
Elevated120-129andless than 80
High Blood Pressure (Hypertension) Stage 1130-139or80-89
High Blood Pressure (Hypertension) Stage 2140 or higheror90 or higher
Hypertensive Crisis (Consult your doctor immediately)Higher than 180and/orHigher than 120

Irregular Heartbeat Detector

An irregular heartbeat is detected when the heartbeat rhythm varies during measurement. The monitor records pulse intervals, calculates the average, and detects significant deviations. If deviations exceed ±25% (or ±15% for four or more intervals), the irregular heartbeat symbol (❤️‍?) appears on the display.

CAUTION: The appearance of the ❤️‍? icon indicates a pulse irregularity consistent with an irregular heartbeat. This is usually not a cause for concern. However, if the symbol appears often, seek medical advice. The device does not replace a cardiac examination but helps detect pulse irregularities early.

Why does my blood pressure fluctuate throughout the day?

  1. Individual blood pressure varies daily and is affected by cuff tying and measurement position. Measure under consistent conditions.
  2. Medication can affect pressure.
  3. Wait at least 3 minutes between measurements.

Why do I get different blood pressure at home compared to the hospital?

Blood pressure varies due to weather, emotion, and exercise. The "white coat" effect can also cause higher readings in clinical settings.

What you need to pay attention to when measuring at home:

  • Ensure the cuff is tied properly.
  • Check cuff tightness (not too tight or too loose).
  • Ensure the cuff is tied on the upper arm.
  • Try to remain calm.
  • Take 2-3 deep breaths before measuring. Relax for 4-5 minutes until calm.

Is the result the same if measuring on the right arm?

It is acceptable to measure on both arms, but results may differ slightly. It is recommended to measure on the same arm each time.

Trouble Shooting

PROBLEMDISPLAYCHECK THISREMEDY
No power / Display can not light up.Batteries are exhausted. Batteries are installed incorrectly or adapter is not plugged in properly.Replace with new batteries. Install the batteries or plug in the adapter properly.
DC Power ErrorThe DC supply voltage is too high or too low.Replace with the authorized adapter.
Low Battery?The battery is too low.Replace with new batteries.
Error messageThe cuff is not wrapped or wrapped too loose. The air connector plug is not properly plugged in or a leak is detected. Excessive body motion (e.g., arm movement) is detected. Pulse is not detected during measuring. Out of measurement range.Wrap and fasten the cuff and measure again. Insert the air connector plug correctly, then measure again. If the issue persists, check the cuff leakage. Relax and then measure again. If the issue persists twice, will display on the LCD; contact customer support. Relax and then measure again. If the issue persists twice, will display on the LCD; contact customer support or your physician.
Data transmission error or Server connection errorMove to another area, preferably closer to a window, try again. Use the device where you get a strong cellular signal. If the issue persists, contact customer support.
No cellular coverage or Cellular connection errorMove to another area, preferably closer to a window, try again. Use the device where you get a strong cellular signal. If the issue persists, contact customer support.
SIM card is not detected or SIM card is abnormal.Check and re-install the SIM card. If the issue persists, contact customer support.
Device failureHardware errorRetake measurement. If the issue persists, contact customer support.

NOTE: If the product still does not work, contact Customer Service. Do not disassemble or attempt to repair the unit yourself.

Specifications

ParameterValue
Product NameTeleRPM Blood Pressure Monitor
External dimensionsApprox. 148.3 mm × 100.5 mm × 52 mm
Display modeDigital LCD V.A. 79 mm × 93 mm
WeightApprox. 325 g (Excluding batteries and cuff)
Measurement modeOscillographic testing mode
Mode of operationContinuous operation
Measurement rangeRated cuff pressure: 0 mmHg ~ 299 mmHg; Measurement pressure: SYS: 60 mmHg ~ 230 mmHg; DIA: 40 mmHg ~ 130 mmHg; Pulse value: (40-199) beat/minute
AccuracyPressure: ±3 mmHg; Pulse value: ±5%
Normal working conditionTemperature: +41°F to +104°F; Relative humidity: 15% to 90% non-condensing (water vapour partial pressure < 50 hPa); Atmospheric pressure: 700 hPa to 1060 hPa
Storage condition & transportation conditionTemperature: -4°F to +140°F; Relative humidity: ≤93% non-condensing (water vapour pressure ≤ 50 hPa); Atmospheric pressure: 500 hPa to 1060 hPa
Measurement perimeter of the upper armAbout 22-45 cm (8.6-17.7 inch)
Degree of protectionType BF applied part
Device ClassificationBattery Powered Mode: Internally Powered ME Equipment; AC Adaptor Powered Mode: Class II ME Equipment
Protection against ingress of waterIP21 (protected against solid foreign objects ≥ 12.5 mm and vertically falling water drops)
Expected Lifetime5 years or 10000 measurements (may vary based on usage conditions)

WARNING: No modification of this equipment is allowed.

Authorized Component

Please use the authorized adapter (Not included).

  • Adapter: Type: BLJ06L060100P-U; Input: 100-240V, 50-60Hz, 0.2A max; Output: 6V 1000 mA

EMC Guidance

The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare environments.

Warning: Do not use near active HF surgical equipment or RF shielded rooms for magnetic resonance imaging where EM disturbances are high.

Warning: Avoid using adjacent to or stacked with other equipment to prevent improper operation. If necessary, observe both units to ensure normal operation.

Warning: Use only specified accessories, transducers, and cables provided by the manufacturer to avoid increased electromagnetic emissions or decreased immunity.

Warning: Portable RF communications equipment (including peripherals) should be used no closer than 30 cm (12 inches) to any part of the equipment TMB-2092-G. Otherwise, performance degradation may occur.

Technical description:

  1. Instructions for maintaining BASIC SAFETY and ESSENTIAL PERFORMANCE regarding electromagnetic disturbances for the expected service life.
  2. Guidance and manufacturer's declaration – electromagnetic emissions and Immunity.

Table 1: Guidance and manufacturer's declaration – electromagnetic emissions

Emissions testCompliance
RF emissions CISPR 11Group 1
RF emissions CISPR 11Class B
Harmonic emissions IEC 61000-3-2Class A
Voltage fluctuations/flicker emissions IEC 61000-3-3Comply

Table 2: Guidance and manufacturer's declaration – electromagnetic Immunity

Immunity TestIEC 60601-1-2 Test levelCompliance level
Electrostatic discharge (ESD) IEC 61000-4-2±8 kV contact; ±2 kV, ±4 kV, ±8 kV, ±15 kV air±8 kV contact; ±2 kV, ±4 kV, ±8 kV, ±15 kV air
Electrical fast transient/burst IEC 61000-4-4±2 kV for power supply lines; ±1 kV signal input/output; 100 kHz repetition frequency±2 kV for power supply lines; NA; 100 kHz repetition frequency
Surge IEC61000-4-5±0.5 kV, ±1 kV differential mode; ±0.5 kV, ±1 kV, ±2 kV common mode±0.5 kV, ±1 kV differential mode; N/A
Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-110% UT; 0.5 cycle at 0°, 45°, 90°, 135°, 180°, 225°, 270°, 315°; 0% UT; 1 cycle and 70% UT; 25/30 cycles; Single phase at 0°; 0% UT; 250/300 cycle0% UT; 0.5 cycle at 0°, 45°, 90°, 135°, 180°, 225°, 270°, 315°; 0% UT; 1 cycle and 70% UT; 25/30 cycles; Single phase at 0°; 0% UT; 250/300 cycle
Power frequency magnetic field IEC 61000-4-830 A/m; 50 Hz / 60 Hz30 A/m; 50 Hz / 60 Hz
Conducted RF IEC61000-4-63 V; 0.15 MHz - 80 MHz; 6 V in ISM and amateur radio bands (0.15 MHz - 80 MHz); 80% AM at 1 kHz3 V; 0.15 MHz - 80 MHz; 6 V in ISM and amateur radio bands (0.15 MHz - 80 MHz); 80% AM at 1 kHz
Radiated RF IEC61000-4-310 V/m; 80 MHz - 2.7 GHz; 80% AM at 1 kHz10 V/m; 80 MHz - 2.7 GHz; 80% AM at 1 kHz

NOTE: UT is the a.c. mains voltage prior to application of the test level.

Table 3: Guidance and manufacturer's declaration – electromagnetic Immunity

Immunity TestTest Frequency (MHz)Band (MHz)ServiceMaximum ModulationPower (W)Distance (m)IEC 60601-1-2 Test Level (V/m)Compliance level (V/m)
Radiated RF IEC61000-4-3 (Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless communications equipment)385380-390TETRA 400Pulse modulation 18 Hz1.80.32727
450430-470GMRS 460, FRS 460FM ± 5k Hz deviation; 1 kHz sine20.32828
710-745704-787LTE Band 13, 17Pulse modulation 217 Hz0.20.399
810-930800-960GSM 800/900, TETRA 800, iDEN 820, CDMA 850, LTE Band 5Pulse modulation 18 Hz20.32828
1720-19701700-1990GSM 1800; CDMA 1900; GSM 1900; DECT; LTE Band 1, 3, 4, 25; UMTSPulse modulation 217 Hz20.32828
2400-2570Bluetooth, WLAN, 802.11 b/g/n, RFID 2450, LTE Band 7Pulse modulation 217 Hz20.32828
5100-5800WLAN 802.11 a/nPulse modulation 217 Hz0.20.399

FCC Statement

FCC ID: OU9TMB2092-G

This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.

Caution: The user is cautioned that changes or modifications not expressly approved by the party responsible for compliance could void the user's authority to operate the equipment.

NOTE: 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. However, there is no guarantee that interference will not occur in a particular installation.

If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:

  • Reorient or relocate the receiving antenna.
  • Increase the separation between the equipment and receiver.
  • Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.
  • Consult the dealer or an experienced radio/TV technician for help.

FCC Radiation Exposure Statement: This equipment complies with FCC radiation exposure limits set forth for an uncontrolled environment. This equipment should be installed and operated with a minimum distance of 20cm between the radiator and your body. This transmitter must not be co-located or operating in conjunction with any other antenna or transmitter.

Models: TMB-2092-G TeleRPM Blood Pressure Monitor, TMB-2092-G, TeleRPM Blood Pressure Monitor, Blood Pressure Monitor, Pressure Monitor

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References

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