IHealth BPM1 - Clear Manual

IHealth BPM1 - Clear

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Wireless Blood Pressure Monitor (BPM1)

OWNER’S MANUAL

Monitor de tensão arterial sem fios (BPM1)

MANUAL DO PROPRIETÁRIO

MANUELE DEL PROPRIETARIO

dello sfigmomanometro wireless (BPM1)

Vernetztes-Blutdruckmessgerät (BPM1)

BENUTZERHANDBUCH

MANUAL DEL USUARIO

del tensiómetro inalámbrico (BPM1)

Draadloze bloeddrukmeter (BPM1)

GEBRUIKERSHANDLEIDING

Ασύρματο πιεσόμετρο (BPM1)

ΕΓΧΕΙΡΙΔΙΟ ΚΑΤΟΧΟΥ

Tensiomètre connecté (BPM1)

MANUEL D’UTILISATION

INTRODUCTION

PACKAGE CONTENTS

INTENDED USE

BLOOD PRESSURE CLASSIFICATION FOR ADULTS

CONTRAINDICATION

PARTS AND DISPLAY INDICATORS

OPERATING PROCEDURES AND SETUP

OPERATING PROCEDURES

Connecting The Cuff To The Monitor

Apply The Cuff

Body Posture

OPERATION INSTRUCTIONS

SETUP WIRELESS NETWORK

SPECIFICATIONS

GENERAL SAFETY AND PRECAUTIONS

BATTERY HANDLING AND USAGE

TECHNICAL ALARM DESCRIPTION

TROUBLESHOOTING

CARE AND MAINTENANCE

WARRANTY INFORMATION

EXPLANATION OF SYMBOLS

IMPORTANT INFORMATION REQUIRED BY THE FCC

OTHER STANDARDS AND COMPLIANCES

ELECTROMAGNETIC COMPATIBILITY INFORMATION

Table of Contents

Wireless Blood Pressure Monitor (BPM1)

OWNER’S MANUAL

Note: This chart is not intended to provide a basis for any type of emergency condition or diagnosis

based on the color scheme; this chart only depicts different classifications of blood pressure. Consult

your physician for proper interpretation of blood pressure results.

CONTRAINDICATION

It is not recommended for people with serious arrhythmia to use this Blood Pressure Monitor.

Classification of blood pressure for adults

160

180

Systolic

(mmHg)

Diastolic

(mmHg)

140

130

120

80 85 90 100 110

Severe Hypertension

Moderate Hypertension

Mild Hypertension

High-normal BP

Normal BP

BLOOD PRESSURE

CLASSIFICATION SBP

mmHg DBP

mmHg

Optimal <120 <80

Normal 120-129 80-84

High-normal 130-139 85-89

Grade 1 Hypertension 140-159 90-99

Grade 2 Hypertension 160-179 100-109

Grade 3 Hypertension ≥=180 ≥=110

WHO/ISH Denitions and Classication of Blood Pressure Levels

Cuff tube plug

Charge plug

TFT display

User 1 button

User 2 button

OPERATING PROCEDURES AND SETUP

Connecting The Cuff To The Monitor

Insert the cuff tubing connector into the air port on the side of the

monitor. Make sure that the connector is completely inserted to avoid

air leakage during blood pressure measurements.

Avoid compression or restriction of the connection tubing during

measurement which may cause inflation error or harmful injury due to

continuous cuff pressure.

When the monitor is turned off, inserting the cuff tubing connector

will turn the monitor on.

PARTS AND DISPLAY INDICATORS

Cuff tubing connector Cuff

OPERATING PROCEDURES

INTRODUCTION

Thank you for selecting the iHealth Clear. The iHealth Clear is a fully automatic arm cuff blood pressure

monitor that uses the oscillometric principle to measure your blood pressure and pulse rate. The monitor

will transmit your measurements automatically to the iHealth cloud when it is connected to a wireless network.

PACKAGE CONTENTS

• 1 Blood Pressure Monitor

• 1 Quick Start Guide

• 1 Cuff

• 1 Charging Cable

INTENDED USE

The iHealth Clear (Electronic Sphygmomanometer) is intended for use in a professional setting or at

home and is a non-invasive blood pressure measurement system. It is designed to measure the systolic

and diastolic blood pressures and pulse rate of an adult individual by using a technique in which an

inflatable cuff is wrapped around the upper arm. The measurement range of the cuff circumference is

8.6” to 16.5” (22 cm - 42 cm) or 16.5” to 18.9” (42 cm – 48 cm) with the optional cuff.

BLOOD PRESSURE CLASSIFICATION FOR ADULTS

The World Health Organization (WHO) has created the following guide for assessing high blood pressure

(without regard to age or gender). Please note that other factors (e.g. diabetes, obesity, smoking, etc.)

also need to be considered. Consult with your physician for accurate assessment.

1-2cm（1/2")

Apply The Cuff

a. Pull the cuff end through the metal loop, positioning it outward

(away from your body).

b. Place a bare arm through the cuff and position the cuff 1/2" (1-2 cm)

above the elbow joint.

c. Tighten the cuff and close it by pulling it towards your body, securing

it closed with the Velcro fastener.

d. While seated, place your hand palm-side up in front of you on a flat

surface such as a desk or table. Position the rubber tube in the

middle of your arm aligned with your middle finger.

e. The cuff should fit comfortably, yet snugly around your arm. You should be able to insert one finger

between your arm and the cuff.

Remember to:

1. Make sure that the appropriate cuff size is used; refer to the cuff circumference range in “SPECIFICATIONS”.

2. Measure on the same arm each time.

3. Stay still during measurement. Do not move your arm, body, or the monitor.

4. Stay still and calm for one to one and half minutes before taking a blood pressure measurement.

5. Keep the cuff clean. Cleaning the cuff after every 200 times of usage is recommended.

If the cuff becomes dirty, clean it with a moistened cloth. Do not allow any water to go into the interior

of the cuff, when the cuff is being cleaned. Do not rinse the monitor or cuff with running water.

Body Posture

Sitting Comfortably During Measurement

a. Be seated with your feet flat on the floor without crossing your legs.

Lying Down During Measurement

a. Lie on your back.

b. Place your arm straight along your side with your hand palm-side up.

c. The cuff should be placed at the same level as your heart.

Note: Blood pressure can be affected by the position of the cuff and your physiologic condition.

OPERATION INSTRUCTIONS

a. After applying the cuff and your body is in a comfortable position, press the User 1 or User 2 button to

turn the monitor on. The display will show "While measuring, please relax." The monitor will start to

find the baseline zero pressure. When the cuff is not connected with the monitor, press any key to

display indoor/outdoor temperature (if the wireless network is successfully set), battery level, and time

(if the wireless network is successfully set) for 3 seconds. The monitor will then turn off automatically.

b. The cuff will start to slowly inflate. The blood pressure and pulse will be measured during inflation.

Inflation will stop as soon as the blood pressure and pulse rate have been calculated and displayed

on the screen. The result will automatically be stored in the Memory of the monitor. If memory is

b. Place your hand palm-side up in front of you on a flat surface such as a desk or table.

c. The cuff should be placed at the same level as your heart.

SPECIFICATIONS

1. Product name: iHealth Clear Wireless Blood Pressure Monitor

2. Reference: BPM1

3. Classification: Internally powered, Type BF applied part, IP20, No AP or APG, Continuous operation

4. Machine size: approx. 4.7” x 4.6” x 2.0” (119mm × 118mm × 51mm)

5. Cuff circumference: 8.6’’ - 16.5’’ (22 cm – 42 cm), 16.5’’-18.9’’ (42 cm – 48 cm) (Optional XL size)

6. Weight: approx. 12.3oz (350g) (excluding cuff)

7. Measuring method: Oscillometric method, automatic inflation and measurement

8. Memory volume: 2 × 1000 times with time and date stamp

9. Power: DC:5V 1.0A,

Battery: 1*3.7V Li-ion 2200mAh

stored in the current memory group, the monitor will show the difference between the current

measurement results and the previous measurement. If the monitor is connected to the cloud, the

measurement will be uploaded automatically.

c. After measurement, the monitor will turn off automatically after 1 minute of no operation.

d. During measurement, you can press the any key to turn off the monitor manually.

Important: Please consult a healthcare professional for interpretation of blood pressure measure-

ments

SETUP WIRELESS NETWORK

Download and install the iHealth MyVitals app from the Apple App Store or Google Play Store. Then

press and hold the User 2 button for 10 seconds. Follow the in app steps to finish setting up Wireless-

network.

GENERAL SAFETY AND PRECAUTIONS

1. Read all of the information in the Owner’s Manual and other provided instructions before operating the unit.

2. Stay still, calm and rest for 5 minutes before blood pressure measurement.

3. The cuff should be placed at the same level as your heart.

10. Measurement range:

Cuff pressure: 0-300 mmHg

Systolic: 60-260 mmHg

Diastolic: 40-199 mmHg

Pulse rate: 40-180 beats/minute

11. Accuracy:

Pressure: ±3 mmHg

Pulse rate: ±5%

12. Wireless communication:

IEEE 802.11b/g/n

13. Environmental temperature for operation: 10℃～40℃ (50℉～104℉)

14. Environmental humidity for operation: ≤85%RH

15. Environmental temperature for storage and transport: -20℃～50℃ (-4℉～122℉)

16. Environmental humidity for storage and transport: ≤85%RH

17. Environmental pressure: 80kPa-105kPa

18. Battery life: more than 180 measurements on a full charge

19. The blood pressure measurement system includes accessories, pump, valve, cuff, and sensor.

Note: These specifications are subject to change without notice.

4. During measurement, neither speak nor move your body and arm.

5. Measuring on same arm for each measurement.

6. Please always relax at least 1 or 1.5 minutes between measurements to allow the blood circulation in

your arm to recover. Prolonged over-inflation (cuff pressure exceed 300 mmHg or maintained above

15 mmHg for longer than 3 minutes) of the bladder may cause ecchymoma of your arm.

7. Consult your physician for any of the following situations:

a) The application of the cuff over a wound or inflamed area

b) The application of the cuff on any limb with intravascular access or therapy, or an arterio-venous (A-V) shunt

c) The application of the cuff on the arm on the side of a mastectomy

d) Simultaneous use with other medical monitoring equipment on the same limb

e) The blood circulation of the user needs to be checked

8. This Blood Pressure Monitor is designed for adults and should never be used on infants, young

children, pregnant or pre-eclamptic patients. Consult your physician before use on children.

9. Do not use this product in a moving vehicle as this may result in inaccurate measurements.

10. Blood pressure measurements determined by this product are equivalent to those obtained by

professional healthcare practitioners using the cuff/stethoscope auscultation method within the limits

prescribed by the American National Standard, Electronic or Automated Sphygmomanometer.

11. Information regarding potential electromagnetic or other interference between the blood pressure

monitor and other devices together with advice regarding avoidance of such interference, please see

ELECTRO MAGNETIC COMPATIBILITY INFORMATION. It is suggested that the blood pressure

monitor be kept 10 meters away from other wireless devices, such as WLAN unit, cell phone,

microwave oven, etc.

12. Please do not use any other cuff other than that supplied by the manufacturer as this may result in

measurement errors and a biocompatible hazard.

13. This product might not meet its performance specifications if stored or used outside the specified

temperature and humidity ranges.

14. Please do not share the cuff with any infectious person to avoid cross-infection.

15. This product should not be used as a USB device.

16. If the determined blood pressure (systolic or diastolic) is outside the rated range specified in part

SPECIFICATIONS, the app will immediately display a technical alarm on screen. In this case, consult

a physician or ensure that proper measurement procedures are followed. The technical alarm is

preset in the factory and cannot be adjusted or inactivated. This technical alarm is assigned as low

priority according to IEC 60601-1-8.The technical alarm is non-latching and does not need to be

reset.

17. A medical AC adapter with an output of DC 5.0V and complies with IEC 60601-1/UL 60601-1 and

IEC 60601-1-2/EN 60601-1-2 is suitable for this monitor. Please note that the monitor jack size is

USB micro-B.

18. Use of Charging Cable other than those specified or provided by the manufacturer of this equipment

could result in increased electromagnetic emissions or decreased electromagnetic immunity of this

equipment and result in improper operation.

19. Measurements are not possible in patients with a high frequency of arrhythmias.

20. The device is not intended for use on neonates, children or pregnant women. (Clinical testing has

not been conducted on neonates, children or pregnant women.)

21. Motion, trembling, shivering may affect the measurement reading.

22. The device would not apply to the patients with poor peripheral circulation, noticeably low blood

pressure, or low body temperature (there will be low blood flow to the measurement position).

23. The device would not apply to the patients who use an artificial heart and lung (there will be no pulse).

BATTERY HANDLING AND USAGE

Do not replace the battery. If the battery can no longer be charged, please contact Customer Service.

• When charging is needed, please connect the monitor to a power source.

• When the cuff is not connected with the monitor, press any key to display indoor/outdoor temperature (if

wireless network is successfully set), battery level, and time (if wireless network is successfully set) for 3

seconds. If the battery level is less than 20% (the battery indicator will only display a battery symbol),

please charge the battery. The monitor will not work until the battery is sufficiently charged.

• When you charge the monitor, the monitor will display with different indicator indicating the charging

status. See the table below for details.

• It is suggested that you charge the battery when the battery is less than 25%.

Overcharging the battery may reduce its lifetime.

Lithium battery replacement by inadequately trained personnel could result in a hazard such as a fire

or explosion.

Do not plug or unplug the power cord into the electrical outlet with wet hands.

If the AC adapter is abnormal, please change the adapter.

Do not use the monitor while charging.

Do not use any other type of AC adapter as it may harm the monitor.

24. Consult your physician before using the device for any of the following conditions: common

arrhythmias such as atrial or ventricular premature beats or atrial fibrillation, arterial sclerosis, poor

perfusion, diabetes, pre-eclampsia, enal diseases.

25. The patient can be an intended operator.

26. Please contact the service center if the character or number displayed is incomplete.

The monitor, cable, battery and cuff must be disposed of according to local regulations at the end

their usage.

Note：The battery has limited charge cycles and may eventually need to replaced by an iHealth service

provider. Battery life and charge cycles vary by use and settings.

Monitor Status

Charging

Fully charged

Status Indicator

Dynamical battery symbol

Charging battery symbol

Empty battery symbol and reminder: "Low battery, unable to perform

measurement, please recharge""

Low battery

TECHNICAL ALARM DESCRIPTION

The monitor will show SYS or DIA beyond measurement range, or SYS or DIA below measurement range as

technical alarm on screen with no delay if the determined blood pressure (systolic or diastolic) is outside the

rated range specified in part SPECIFICATIONS. In this case, you should consult a physician or check if your

operation violated the instructions.

The technical alarm condition (outside the rated range) is preset in the factory and cannot be adjusted or

deactivated. This alarm condition is assigned as low priority according to IEC 60601-1-8.

The technical alarm is non-latching and needs no reset. The signal displayed on screen will disappear

automatically after about 8 seconds.

TROUBLESHOOTING

PROBLEM POSSIBLE CAUSE SOLUTION

Low Battery Battery is less than 20% Charge the battery

The cuff position was not correct or

it was not properly tightened

Body posture was not correct

during testing

Speaking, moving arm or body,

being angry, excited or nervous

during test

Incorrect operation or strong

electromagnetic interference

Review the cuff supplication instructions

and retest

Review body posture instructions and

retest

Retest when calm; avoid speaking

or movement during the test

Press the User 2 button for 10 seconds

to reset the device and try again.

No response

Display reads an

abnormal result

CARE AND MAINTENANCE

1. Do not drop this monitor or subject it to strong impact.

2. Avoid high temperature and direct sunlight. Do not immerse the monitor in water as this will result

in damage to the monitor.

3. If this monitor is stored near freezing temperatures, allow it to acclimate to room temperature before

use.

4. Do not attempt to disassemble this monitor.

5. If the monitor is not used for a long time, please be sure to fully charge it every month.

6. It is recommended that product performance be checked every 2 years or after each repair. Please

contact the service center.

7. No monitor component needs to be maintained by the user. The circuit diagrams, component part

lists,descriptions, calibration instructions, or other information which will assist the user’s appropri-

ately qualified technical personnel to repair those parts of the equipment which are designated for

repair can be supplied.

8. Clean the monitor with a dry, soft cloth or a moistened and well wrung soft cloth using water, diluted

disinfectant alcohol, or diluted detergent

9. The monitor can maintain the safety and performance characteristics for a minimum of 10,000

measurements or three years of usage, and the cuff integrity is maintained after 1,000 open–close

cycles of the closure.

10. The battery can maintain the performance characteristics for a minimum of 300 charge cycles.

Battery replacement should only be performed by a qualified iHealth technician. To do otherwise will

void your warranty and possibly damage your unit.

11. It is recommended that if the cuff is used, for example, in a hospital or a clinic, it be disinfected

1413 15 16

WARRANTY INFORMATION

The Blood Pressure Monitor is warranted to be free from defects in materials and workmanship within

one year from the date of purchase when used in accordance with the provided instructions. The

warranty extends only to the end user. We will, at our option, repair or replace without charge the Blood

Pressure Monitor covered by the warranty. Repair or replacement is our only responsibility and your only

remedy under the warranty.

EXPLANATION OF SYMBOLS

Symbol for ”THE OPERATION GUIDE MUST BE READ”

The sign background color: blue. The sign graphical symbol: white.

Symbol for “WARNING”

Symbol for “TYPE BF APPLIED PARTS” (The cuff is type BF applied part)

Symbol for “MANUFACTURER”

Symbol for “COMPILES WITH MDD93/42/EEC REQUIREMENTS”

Symbol for“ DATE OF MANUFACTURE”

Symbol for “SERIAL NUMBER”

Symbol for “EUROPEAN REPRESENTATIVE”

Symbol for “KEEP DRY”

iHealth is a trademark of iHealth Labs, Inc.

Manufactured for iHealth Labs, Inc.

120 San Lucar Ct.,Sunnyvale, CA 94086, USA

1-855-816-7705

www.ihealthlabs.com

iHealthLabs Europe SARL

3 rue Tronchet, 75008, Paris, France

ANDON HEALTH CO., LTD.

No. 3 Jinping Street, Ya An Road, Nankai District, Tianjin 300190, China

Tel: 86-22-60526161

twice a week. Wipe the inner side (the side that contacts skin) of the cuff with a soft cloth lightly

moistened with Ethyl alcohol (75-90%). Then air dry the cuff.

support@ihealthlabs.eu www.ihealthlabs.eu

Symbol for “DO NOT TOUCH THE CONNECTOR WITH ESD

WARNING SYMBOL DURING MEASUREMENT”

IMPORTANT INFORMATION REQUIRED BY THE FCC

This device complies with Part 15 of the FCC Rules. Its 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.

Changes or modifications not expressly approved by iHealth Labs, Inc. would void the user’s authority

to operate the product.

NOTE: This product 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 product 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 product 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.

The SAR limit of USA (FCC) is 1.6 W/kg averaged over one gram of tissue. Device has also been tested

against this SAR limit.

This product complies with Industry Canada. IC: RSS-210

IC NOTICE

This device complies with Industry Canada licence-exempt RSS standard(s). Operation is subject to the

following two conditions:

OTHER STANDARDS AND COMPLIANCES

The Blood Pressure Monitor corresponds to the following standards: IEC 60601-1:2005

+A1:2012(E)/EN 60601-1：2006/A11: 2011 (Medical electrical equipment -- Part 1: General require-

ments for basic safety and essential performance), IEC 60601-1-2:2014(Medical electrical equipment --

Part 1-2: General requirements for basic safety and essential performance - Collateral standard:

Electromagnetic compatibility - Requirements and tests), IEC80601-2-30:2009+AMD1：2013/EN

80601-2-30:2010/A1：2015(Medical electrical equipment –Part 2-30: Particular requirements for the

basic safety and essential performance of automated non-invasive sphygmomanometers)EN 1060-1:

1995 + A2: 2009 (Non-invasive sphygmomanometers - Part 1: General requirements), EN 1060-3: 1997

+ A2: 2009 (Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-me-

chanical blood pressure measuring systems).

ELECTROMAGNETIC COMPATIBILITY INFORMATION

This product is applicable to the equipment and system requirements for the purpose of receiving radio

frequency energy for the purpose of the work,Wireless network receive bandwidth 22M. This product

can also be used to include RF transmitter equipment and system requirements and emission frequency

of 2.4GHz ISM band, Wireless network modulation types: DBPSK/DQPSK/CCK (DSSS)

BPSK/QPSK/16QAM/64QAM (OFDM) , effective radiated power: < 20dBm .

(1) this device may not cause interference, and

(2) this device must accept any interference, including interference that may cause undesired operation

of the device.

This product is approved in accordance to R&TTE directive transmitter.

Hereby, [iHealth Labs, Inc.],declares that this BPM1 is in compliance with the essential requirements and

other relevant provisions of Directive 1999/5/EC. Directive 1999/5/EC declaration of conformity can be

downloaded on the following link: https://www.ihealthlabs.eu/support/certifications

Table 1 - Emission

Phenomenon

RF emissions

Harmonic distortion

Voltage fluctuations and flicker

CISPR 11 Group 1, Class B

IEC 61000-3-2 Class A

IEC 61000-3-3 Compliance

Electromagnetic environment

Home healthcare environment

Compliance

Table 2 - Enclosure Port

Phenomenon

Electrostatic Discharge

Radiated RF EM field

Proximity fields from RF

wireless communications

equipment

Rated power frequency

magnetic fields

Basic EMC standard

IEC 61000-4-2

IEC 61000-4-3

IEC 61000-4-8

±8 kV contact ±2kV, ±4kV, ±8kV, ±15kV air

10V/m 80MHz-2.7GHz 80% AM at 1kHz

Refer to table 3

30A/m 50Hz or 60Hz

Immunity test levels

Home Healthcare Environment

Table 3 – Proximity fields from RF wireless communications equipment

Test frequency (MHz)

385

450

710

745

780

810

870

930

1720

1845

1970

2450

5240

5500

5785

Band (MHz)

380-390

430-470

704-787

800-960

1700-1990

2400-2570

5100-5800

Immunity test levels

Professional healthcare facility environment

Pulse modulation 18Hz, 27V/m

FM, ±5kHz deviation, 1kHz sine, 28V/m

Pulse modulation 217Hz, 9V/m

Pulse modulation 18Hz, 28V/m

Pulse modulation 217Hz, 28V/m

Pulse modulation 217Hz, 9V/m

19 20

Table 4 – Input a.c. power Port

Phenomenon

Electrical fast

transients/burst

Surges

Line-to-line

Surges

Line-to-ground

Conducted

disturbances

induced by RF fields

Voltage dips

Voltage interruptions

Basic EMC standard

IEC 61000-4-4

IEC 61000-4-5

IEC 61000-4-6

IEC 61000-4-11

Immunity test levels

Home Healthcare Environment

±2 kV 100kHz repetition frequency

±0.5 kV, ±1 kV

±0.5 kV, ±1 kV, ±2 kV

3V, 0.15MHz-80MHz

6V in ISM and amateur radio bands between

0.15MHz and 80MHz

80%AM at 1kHz

0% UT; 0.5 cycle

At 0º, 45º, 90º, 135º, 180º, 225º, 270º and 315º

0% UT; 1 cycle and 70% UT; 25/30 cycles

Single phase: at 0º

0% UT; 250/300 cycles

Symbol for “ENVIRONMENT PROTECTION – Waste electrical products should not be disposed

of with household waste. Please recycle where facilities exist. Check with your local authority or

retailer for recycling advice”.

LCD shows

“Error Code 000”

LCD shows

“Error Code 001”

LCD shows

“Error Code 002”

LCD shows

“Error Code 003”

LCD shows

“Error Code 004”

LCD shows

“Error Code 005”

LCD shows

“Error Code 006”

LCD shows

“Error Code 007”

LCD shows

“Error Code 010”

LCD shows

“Error Code 011”

Pressure system is unstable before

measurement

Fail to detect systolic pressure

Fail to detect diastolic pressure

Pneumatic system blocked or cuff is

too tight during inflation

Pneumatic system leakage or cuff is

too loose during inflation

Cuff pressure above 300mmHg

More than 160 seconds with cuff

pressure above 15 mmHg

Memory abnormality or temperature

chip error

Pressure sensor parameter error

When uploading data not connected

to the cloud

Don’t move and try again.

Apply the cuff correctly and try again

Measure again after five minutes.

If the monitor is still abnormal,

please contact the local distributor

or the factory.

LCD shows

“Error Code 012”

LCD shows

“Error Code 013”

LCD shows

“Error Code 015”

LCD shows

“Wireless network

password is wrong”

Wireless network

module initialization failed

Network not found

Failed to get IP

Wireless network password is wrong

Re-set Wireless network and make

sure the connected network is in good

condition. Measure again after five

minutes. If the monitor is still abnormal,

please contact the local distributor or

the factory.

Check the Wireless network password

and re-set Wireless network

Produkt Specifikationer

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Model:	BPM1 - Clear

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