1
Questions or Concerns? support@etekcity.com • (855) 686-3835
Smart Blood
Pressure Monitor
Model: TMB-1583-BS
User Manual
2
Table of Contents
Package Contents
Specications
Features
Safety Information
Glossary of Symbols
Getting to Know Your Blood
Pressure Monitor
Function Diagram
LCD Display
Power Supply Information
Installing and Replacing the
Batteries
Before First Use
• Setting Date, Time, and
Measurement Unit
• Selecting a User
Pairing the Monitor With the
VeSync App
• VeSync App Setup
Conguration
• Data Transmission
• Transmitter Information
3
3
5
6
13
14
15
16
17
17
18
18
23
24
24
25
28
28
28
28
29
30
30
32
33
34
34
34
35
36
36
40
42
43
44
52
54
Measuring Blood Pressure
• When to Take Blood Pressure
• Before Measurement
Using the Blood Pressure Monitor
• Attaching the Cuff
• Measuring Blood Pressure
• Measurement Tips
Other Functions
• Memory
• Example Readout
• Lock Button
• Maintenance
About Blood Pressure
Troubleshooting Display Readings
Attributions
Federal Communication
Commission Interference
Statement
EMC Guidance
Warranty Information
Customer Support
3
SpecicationsPackage Contents
1 x Smart Blood Pressure Monitor
1 x AC Adapter
1 x Arm Cuff
4 x 1.5V AAA Batteries
1 x User Manual
1 x Quick Start Guide
Power Supply
4 x 1.5V AAA batteries
DC Output: 6V, 1A
AC Adapter
Model: TRANSTEK
BLJ06L060100P-U
Input: AC 100–240V
50/60Hz 0.2A Max
Output: DC 6V, 1A
Note: Please use the AC adapter
authorized by the manufacturer.
Display Mode
Digital LCD, V. A.
3.3 x 2.9 in / 8.4 x 7.3 cm
Measurement
Mode
Oscillographic
Testing Mode
Measurement
Range
Rated Cuff Pressure:
0–299 mmHg / 0–39.9 kPa
Measurement Pressure:
SYS: 60–230 mmHg / 8.0–30.7 kPa
DIA: 40–130 mmHg / 5.3–17.3 kPa
Pulse: 40–199 beats/minute
Accuracy
Pressure:
5°–40°C within ±3 mmHg / 0.4 kPa
Pulse: ±5%
4
Units mmHg / kPa
Operating
Environment
Temperature: 41°–104°F / 5°–40°C
Relative Humidity: 15–90%,
non-condensing, but not requiring
a water vapour partial pressure
greater than 50 hPa
Atmospheric Pressure Range:
700–1060 hPa
Transport
and Storage
Environment
Temperature: -4°–140°F /
-20°–60°C
Relative Humidity: ≤ 93% non-
condensing, at a water vapour
pressure up to 50 hPa
Dimensions
Monitor: 4.2 x 4.1 x 4.6 in /
10.7 x 10.3 x 11.8 cm
Cuff Circumference: 8.6–16.5 in /
22–42 cm
Weight
0.55 lb / 0.25 kg (excluding
batteries and cuff)
Mode of Operation Continuous Operation
Degree of
Protection (Arm
Cuff)
Type BF Applied Part
Water Protection
Level
IP21 (protected from touch by
ngers and objects greater than 12
millimeters and protected from
condensation)
Device
Classication
Battery Powered Mode: Internally
Powered ME Equipment
AC Adapter Powered Mode:
Class II ME Equipment
Software Version A01
Automatic Shutoff
120 seconds
Note: Can be customized in the
VeSync app.
Specications (cont.)
5
• Blood pressure measurement
• Pulse rate measurement
• Result storage
• 90 records per user (unlimited records in the
VeSync app)
• Measurement during ination
• Readings taken by this monitor are equivalent to
those obtained by a trained observer using the
cuff and stethoscope auscultation method
• Smart Bluetooth
®
connection
• Access to smart functions through the free
VeSync app
Features
6
Safety Information
Please read and follow all instructions and safety guidelines in this manual.
READ AND SAVE THESE INSTRUCTIONS
CAUTION
• This monitor should not be used by any person who is or may be pregnant. Besides
providing inaccurate readings, the effects of this device on the fetus are unknown.
• This monitor is not suitable for use on patients with implanted electrical devices, such as
cardiac pacemakers and debrillators.
• Using this monitor on patients undergoing dialysis therapy or on anticoagulants,
antiplatelets, or steroids could cause internal bleeding.
Contraindications:
7
• If the arm cuff causes any discomfort,
immediately press to turn off the
monitor.
• This monitor is intended for adult use in
homes only. Do not use the monitor on
babies or younger children. Consult your
doctor before using this monitor on older
children.
• This monitor is not suitable for use on
neonatal patients, pregnant women, patients
with implanted electronic devices, patients
with pre-eclampsia, premature ventricular
beats, atrial brillation, or peripheral arterial
disease, patients undergoing intravascular
therapy or arterio-venous shunt, or patients
who received a mastectomy. Please consult
your doctor prior to using the monitor if you
suffer from any illnesses.
• This monitor is not intended for patient
transport outside a healthcare facility.
• This monitor is not intended for public use.
Household use only.
• This monitor is intended for non-invasive
measuring and monitoring of arterial
blood pressure. It is not intended for use
on extremities other than the arm or for
functions other than obtaining a blood
pressure measurement.
• The monitor is not intended to be a
diagnostic device. The results are for
reference only and cannot substitute for
a doctor’s diagnosis. Only a healthcare
professional is qualied to interpret blood
pressure measurements.
• If you are taking medication, consult your
physician to determine the most appropriate
time to measure your blood pressure.
Never change a prescribed medication
without consulting your physician. Do not
begin or end medical treatment without
asking a physician for treatment advice. Do
not take any therapeutic measures on the
Safety Information (cont.)
8
basis of a self-measurement. Consult your
physician if you have any questions about
your blood pressure.
• When this monitor is used to measure
patients who have common arrhythmias
such as atrial or ventricular premature beats
or atrial brillation, the best results may still
be inaccurate. Please consult your physician
about the results.
• Do not kink the connection tube during
use. This may cause the cuff pressure to
continuously increase, which can prevent
blood ow and result in harmful injury to the
patient.
• When using this monitor, the following
situations may interrupt blood ow and
inuence blood circulation, resulting in
harmful injury to the patient:
- Measuring with a kinked connection tube
too frequently or for multiple consecutive
measurements
- Using the cuff on any arm where
intravascular access or therapy, or an
arterio-venous (A-V) shunt, is present
- Inating the cuff on the side of a
mastectomy
• WARNING: Do not apply the cuff over a
wound, as it can cause further injury.
• If a limb has other monitoring ME equipment
applied to it, do not inate the cuff on that
limb. This could cause the other monitoring
ME equipment to temporarily lose function.
• Rarely, a fault may cause the cuff to remain
fully inated during measurement. In this
case, open the cuff immediately. Prolonged
high pressure (cuff pressure > 300 mmHg or
constant pressure > 15 mmHg for more than
3 minutes) applied to the arm may lead to an
ecchymosis (bruising).
• Always check to make sure that operating
this monitor does not result in prolonged
impairment of patient blood circulation.
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• When measuring, please avoid compression
or restriction of the connection tubing.
• The monitor cannot be used with HF surgical
equipment.
• To verify the calibration of the AUTOMATED
SPHYGMOMANOMETER, please contact the
manufacturer.
• Too frequent and consecutive
measurements could cause disturbances in
blood circulation and injuries.
• This monitor is not suitable for continuous
monitoring of blood pressure during medical
emergencies or operations. The patient’s
arm and ngers will become anaesthetic,
swollen, and even purple due to a lack of
blood.
• When not in use, store the monitor with the
adapter in a dry room and protect it against
extreme moisture, heat, lint, dust, and direct
sunlight. Never place any heavy objects on
the storage case.
• This monitor may be used only for the
purpose described in this booklet. The
manufacturer cannot be held liable for
damage caused by incorrect application.
• This monitor contains sensitive components
and must be treated with caution. Observe
the storage and operating conditions
described in this booklet.
• This monitor is not AP/APG equipment and
is not suitable for use in the presence of a
ammable anesthetic mixture with air or
with oxygen or nitrous oxide.
• WARNING: No servicing/maintenance
while the ME equipment is in use.
• The patient is an intended operator of this
monitor. The patient can measure, transmit
data, and change batteries under normal
circumstances and maintain the monitor
and its accessories according to the user
manual.
• To avoid measurement errors, please
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avoid using in the presence of a strong
electromagnetic eld radiated interference
signal or an electrical fast transient/burst
signal.
• The blood pressure monitor, its adapter,
and the cuff are suitable for use within the
patient environment. If you are allergic to
polyester, nylon or plastic, please don’t use
this monitor or cuff.
• During use, the patient will be in contact
with the cuff. The materials of the cuff
have been tested and found to comply with
requirements of ISO 10993-5:2009 and ISO
10993-10:2010. It will not cause any potential
sensitization or irritation reaction.
• The included adapter is specied as
ME EQUIPMENT.
• If you experience discomfort during a
measurement, such as pain in the arm or
other complaints, press to release the air
immediately from the cuff. Loosen the cuff
and remove it from your arm.
• If the cuff pressure reaches 40 kPa / 300
mmHg, the cuff will automatically deate.
Should the cuff not deate when pressure
reaches 40 kPa / 300 mmHg, detach the
cuff from the arm and press to stop
ination.
• Before use, make sure the monitor and
accessories function safely and are in proper
working condition. Do not use the monitor or
accessories if they are damaged in any way.
The continuous use of a damaged monitor
or damaged accessories may cause injury,
improper results, or serious danger.
• Do not wash the cuff in a washing machine
or dishwasher.
• The service life of the cuff may vary based
on the frequency of washing, skin condition,
and storage state. The typical service life is
10,000 times used.
• We recommend that the performance of the
monitor and cuff should be checked every
2 years and after maintenance and repair,
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by retesting at least the requirements in
the limits of the error of the cuff pressure
indication and air leakage (testing at least at
50 mmHg and 200 mmHg).
• Please dispose of ACCESSORIES,
detachable parts, and the ME EQUIPMENT
according to the local guidelines.
• The manufacturer will make available on
request circuit diagrams, component part
lists, descriptions, calibration instructions,
etc., to assist service personnel in parts
repair.
• The plug/adapter plug pins insulate the
monitor from the main power supply. Do
not position the monitor in a position where
it is dicult to disconnect from the supply
mains to safely terminate operation of ME
equipment.
• The person operating this device shall not
touch the output of the batteries/adapter
and the patient simultaneously.
• Cleaning: Dust may affect the performance
of the unit. Use a soft cloth to clean every
part of the monitor and cuff before and
after use. Do not use any abrasive or volatile
cleaners.
• The monitor does not need to be calibrated
within two years of reliable service.
• If you have any problems with this monitor,
such as setting up, maintaining, or using,
please contact Customer Support (see
page 54). Don’t open or repair the monitor by
yourself in the event of malfunctions. This
device must only be serviced, repaired, and
opened by individuals at authorized sales/
service centers.
• Please contact Customer Support (page 54)
if any unexpected operation or events occur.
• Keep out of reach of infants, young children,
and pets to avoid inhalation or swallowing of
small parts. This is dangerous or even fatal.
• Be careful to avoid strangulation due
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to cables and hoses, particularly due to
excessive length.
• At least 30 min are required for ME
equipment to warm from the minimum
storage temperature between uses until it is
ready for intended use. At least 30 min are
required for ME equipment to cool from the
maximum storage temperature between
uses until it is ready for intended use.
• Wireless communications equipment
such as wireless home network devices,
mobile phones, cordless telephones and
their base stations, and walkie-talkies
can affect this monitor and should be
kept at least a distance “d” away from the
equipment. Distance “d” is calculated by
the MANUFACTURER from the 80MHz to
5.8GHz column of Table 4 and Table 9 of IEC
60601-1-2:2014, as appropriate.
• Only use ACCESSORIES and detachable
parts specied/authorized by the
MANUFACTURER. Using other parts or
accessories may cause damage to the
monitor or danger to the users/patients.
• There are no luer lock connectors used in
the construction of tubing. If there were,
there is a possibility that they might be
inadvertently connected to intravascular uid
systems, allowing air to be pumped into a
blood vessel.
• Please use the monitor in the environment
which is provided in the user manual.
Otherwise, the performance and lifetime of
the monitor will be impacted and reduced.
• This monitor is not intended for public use.
Household use only.
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Glossary of Symbols
Symbol for “THE OPERATION GUIDE MUST
BE READ”
The degree of protection from water or particulate
matter. Ingress Protection 21: Protected from
touch by ngers and objects greater than 12
millimeters. Protected from condensation.
Symbol for “MANUFACTURER”
Symbol for “TYPE BF APPLIED PARTS”
Symbol for “Class II Equipment”
For indoor use only
MR Unsafe
This device is not intended to operate in Magnetic
Resonance environment. Do not take the device
into MR environments
Indicates the need for the user to consult the
instructions for use for important cautionary
information such as wamings and precautions that
cannot, for a variety of reasons, be presented on
the medical device itself.
Symbol for “ENVIRONMENT PROTECTION” -
Electrical waste products should not be disposed
of with household waste. Please recycle where
facilities exist. Check with your local authority or
retailer for recycling advice.
Symbol for “DIRECT CURRENT”
Symbol for “MANUFACTURE DATE”
Symbol for “Recycle”
T1A/250V Φ3.6*10CCC
The B/N (Batch Number) code combines
the destination country, PO number, date of
manufacture, and serial number.
IP21
B/N
F1
These symbols might be in the user manual,
labelling, or other components.
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Getting to Know Your
Blood Pressure Monitor
The Etekcity Smart Blood Pressure Monitor is a digital
monitor intended for use in measuring blood pressure
and heartbeat rate with an arm circumference of
8.6–16.5 inch / 22–42 cm.
Blood pressure monitors use the oscillometric
method of measuring blood pressure. Before every
measurement, the monitor establishes a “zero
pressure” equivalent to the atmospheric pressure.
It then starts inating the arm cuff while detecting
pressure oscillations generated by beat-to-beat
pulsations, which is used to determine the patient’s
systolic and diastolic blood pressure and pulse rate.
15
Function Diagram
A. Display
B. Cuff
C. Adapter
D. Air Plug
E. Air Hose
F. Set Button
G. Lock Button
H. Start/Stop Button
I. Memory Button
J. Battery Compartment
K. DC Power Socket
L. Air Connector Plug
C
D
E
A
B
F
15 V AAA
15 V AAA
15 V AAA
15 V AAA
J
H
G
I
K L
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LCD Display
A. User 1 / User 2
B. Memory
C. Average Value
(Last 3 Records)
D. Current Time
E. Bluetooth Icon
F. Bluetooth Connection
G. Low Battery
H. Systolic Blood Pressure
(High Blood Pressure)
I. mmHg Measurement
Unit
J. kPa Measurement Unit
K. Diastolic Blood Pressure
(Low Blood Pressure)
L. Pulse (Beats Per Minute)
M. Irregular Heartbeat
N. Motion Indicator
O. Blood Pressure Level
A
H
J
K
L
O
M N
I
DB C E GF
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Power Supply
Information
Batteries: 4 x 1.5V DC AAA Batteries
AC Adapter: 6V DC 1A
• Please use the AC adapter authorized by the
manufacturer.
• Unplug your adapter to use battery power.
Caution: For best results and to protect your
monitor, use the correct batteries and correct power
adapter which complies with local safety standards.
Installing and Replacing
the Batteries
1. Open the battery compartment cover.
2. Install the batteries by matching the correct
polarity [Figure 1].
3. Close the cover.
Figure 1
15V AAA
15V AAA
15V AAA
15V AAA
Note: Turn the monitor off before replacing the
batteries.
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Before First Use
Installing and Replacing the Batteries (Cont.)
Replace the batteries when:
• + appears on the display.
• The display is dim.
• The display does not light up.
Caution:
• Do not use new and used batteries together.
• Do not use different types of batteries together.
• Do not dispose of the batteries in re. Batteries
may explode or leak.
• Remove batteries if the monitor is not likely to be
used for some time.
• Worn batteries are harmful to the environment.
Do not dispose with daily garbage. Dispose of
the old batteries following your local recycling
guidelines.
Set the clock before using your blood pressure
monitor so that your blood pressure records will have
correct time stamps. The clock will automatically be
set to the correct time when you pair the monitor with
the VeSync App.
Year Setting Range: 2020–2060
Time Format: 24 Hours
Setting Date, Time, and
Measurement Unit
19
Setting Date, Time, and Measurement Unit (Cont.)
1. When the monitor is off, press and hold the
button to change settings.
2. Press the
button to change the year.
20
Setting Date, Time, and Measurement Unit (Cont.)
3. When you have selected the right year, press
to conrm and continue to setting the month
and day.
4. Repeat steps 2 and 3 to set the month and day.
21
5. Repeat steps 2 and 3 to set the hour and minute. 6. Repeat steps 2 and 3 to set the measurement
unit.
Setting Date, Time, and Measurement Unit (Cont.)
22
7. Repeat steps 2 and 3 to choose whether the
monitor will beep.
8. After the beep is set, the display will show
“ ”, then show all the settings you have
selected, and then turn off.
Setting Date, Time, and Measurement Unit (Cont.)
23
Selecting a User
1. When the monitor is off, press once to choose
a user. The User ID will blink.
2. Press again to switch between User 1 and
User 2.
3. After selecting the User ID, press to start
measuring, or press
to display previous
measurement records.
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Pairing the Monitor With
the VeSync App
VeSync App Setup
Note: Due to ongoing updates and improvements,
the VeSync app may appear slightly different than
shown in the manual. In case of any differences,
follow the in-app instructions.
Note: For Android™ users, you must select Allow
to use VeSync.
1. To download the VeSync app, scan the QR code
or search “VeSync” in the Apple App Store
®
or
Google Play Store.
2. Open the VeSync app. If you already have an
account, tap Log In. To create a new account, tap
Sign Up.
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Conguration
Set up your smart blood pressure monitor with the
VeSync app.
1. Open the VeSync app. Make sure Bluetooth is
turned on in your phone settings.
2. When the monitor is off, press and hold to
start pairing your monitor with VeSync. The
monitor display will show and
.
Sign Up
Log In
26
Conguration (Cont.)
3. Follow the in-app instructions to set up your
monitor.
4. If setup is successful, the monitor display will
show
and [ ] . If setup fails, the monitor
display will show
and .
27
Conguration (Cont.)
Caution:
• Interference may occur in the vicinity of
equipment marked with the following symbol:
This monitor may interfere with nearby electrical
equipment.
• Sensitive patients, including pre-eclamptic
pregnant patients and patients with implanted
medical electronic instruments, should avoid
using the monitor whenever possible.
• Keep the monitor at least 8 inches / 20 cm away
from the human body (especially the head)
when the data transmission is occuring after
measurement.
Compatible Devices: Android 4.3 or higher / iOS
®
9.0
or higher
5. The monitor will shut off when the pairing process
is complete.
28
Measuring Blood
Pressure
When to Take Blood Pressure
• The best times to take your blood pressure are
within 1 hour of waking in the morning or 1 hour
before bedtime.
• When measuring in the morning, measure after
urinating and before eating breakfast.
• Always measure your blood pressure before
taking blood pressure medication.
• If you need to measure your blood pressure at
another time of day, make sure you are calm and
stable before measuring.
• Measure your blood pressure at the same time
every day. Blood pressure changes during the
course of the day by as much as 20–40 mmHg.
• Follow any directions given by your physician
regarding how and when to measure your blood
pressure.
Data Transmission
• To enable the data transmission function, this
product should be paired with the VeSync app.
• To decrease possible interference:
• Your monitor and your phone should be
reasonably close, within 3–32 ft / 1–10 m.
• Ensure no obstacles are between your
monitor and your phone to allow for quality
connection and to lower the RF output range.
• To avoid interference, other electronic devices
(particularly those with wireless transmission)
should be kept at least 3 ft / 1 m away from the
monitor.
Transmitter Information
• Bluetooth Module No.: LS51802
• RF Frequency Range: 2402–2480MHz
• Output Power Range: ≤ 4dBm
• Supply Voltage: 2–3.6V
• Transmitting Distance: 33 ft / 10 m
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Before Measurement
• If the monitor is being used by multiple people,
wash hands before each measurement.
• Remove any clothing that ts closely to your
upper arm.
• Your blood pressure should be measured sitting
down. Take note if your blood pressure is taken
in a different position.
• Take measurements on the same arm (normally
left) every time unless necessary.
• Avoid any electromagnetic interference when
taking measurements.
• If the arm artery lies considerably lower or
higher than the heart, the measurement may be
incorrect.
• Only use the included cuff.
• A loose or improperly tted cuff will result in
incorrect measurements.
Caution:
• Do not measure blood pressure until at least 30
minutes after physical activity. Do not smoke or
drink stimulating beverages, such as coffee or
alcohol, before measurement.
• Blood pressure should be measured at intervals
of no less than 3 minutes, depending on your
physical condition.
• People with arrhythmia and/or arteriosclerosis
should be measured by medical staff for a
professional diagnosis.
• Avoid pressing the cuff to your body while taking
measurements.
30
Using the Blood Pressure
Monitor
1. Rest in a comfortable position for at least 5
minutes before measuring to ensure the best
results.
2. Plug the air plug into the air port. Make sure the air
plug is completely inserted to avoid air leaking.
3. Place the cuff on your upper left arm with the
“Artery” symbol directly on top of your artery, and
make sure the air hose is on the inside of your
arm. The band should not be wrapped too tightly
(leave space to insert about 2 ngers), and the
lower edge of the cuff should be about 0.8–1.2
inches / 2–3 cm away from your elbow.
[Figure 2.1]
4. Select a user (see page 23).
5. Place your arms on a surface and sit with your
feet at on the oor so that the cuff is at the same
level as your heart. Your arms should be in a
relaxed, natural position. [Figure 2.2]
Note: Your upper arm should be bare or wearing
only thin material.
Attaching the Cuff
Figure 2.1
0.8–1.2 in / 2–3 cm
31
Note:
• Avoid exing arm muscles or trying to
support yourself on your arm, as this can
increase blood pressure. Use a cushion for
support if necessary.
• For patients with hypertension, the middle
of the cuff should be at the level of the right
atrium of the heart.
Figure 2.2
Using the Blood Pressure Monitor (Cont.)
32
Using the Blood Pressure Monitor (Cont.)
Note: If data transmission fails, the display
will show “!”. This will disappear when data
transmission succeeds.
Note:
• Press at any time to stop measuring.
• If the cuff causes any increased discomfort,
immediately press to turn off the
monitor.
• After taking a measurement and seeing the
reading, press to turn off the monitor. If
you do not, it will turn off automatically after
2 minutes of inactivity. You can change this
time setting in the VeSync app.
• Do not pull on the air hose to disconnect from
the air port. Only use the air plug to connect
or disconnect the arm cuff.
Measuring Blood Pressure
1. When the monitor is off, press . This will turn
on the monitor and it will automatically begin
measuring.
2. Relax and avoid moving or talking while
measuring. When the measuring is nished,
the results will display.
3. The monitor will automatically transmit your
results to the VeSync app. The Bluetooth symbol
will show on the display while this is happening.
4. Wait 3 minutes before taking a second
measurement, if necessary. This allows your
blood circulation to recover.
33
Measurements may be inaccurate if taken in the
following circumstances:
• Within 1 hour after eating or drinking
• Immediately after tea, coffee, or smoking
• Within 20 minutes of taking a bath
• When talking or moving your ngers
• In a very cold environment
• When you need to urinate
Measurement Tips
Using the Blood Pressure Monitor (Cont.)
34
Other Functions
Results are automatically saved after each
measurement. The monitor can save up to 90 results
for each user. The VeSync app can store unlimited
results.
To view saved results:
1. While the monitor is off, press
to display
the average of the last 3 results. Press
again to view each result, beginning with the
most recent measurement.
2. Press
or repeatedly to cycle through
results.
Memory
To delete a saved result:
1. While the monitor is off, press
to display
the average of the last 3 results. Press
again to view each result, beginning with the
most recent measurement.
2. When the result you want to delete is selected,
press and hold
. The display will show “
”.
Example Readout
Note: The most recent result (01) is shown rst.
Each new measurement is assigned to the rst (01)
result. All other results are pushed back one digit
(02 becomes 03, and so on), and the last result (90)
is dropped from the list.
Result
Number
Result
Date
Result
Time
35
Accidentally touching the buttons will make the
monitor turn on and waste electricity. To avoid this,
use the button to lock the keys.
To delete all saved results:
1. When the monitor is off, press .
The display will show “ ”. The other buttons
( , , and
) will be locked.
2. Press again to unlock all buttons. The
display will show “ ”.
1. While the monitor is off, press
to display
the average of the last 3 results. Press
again to view each result, beginning with the
most recent measurement.
2. Press and hold
. The display will show
“ ”.
3. Press
again to switch to deleting all
results. The display will show “
”.
4. Press to conrm deletion.
3. Press to conrm deletion.
Lock Button
Note: To cancel deletion, press instead.
Note: To cancel deletion, press instead.
36
About Blood Pressure
When ventricles 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.
This chart shows the standard blood pressure
classication published by American Heart
Association (AHA).
What are systolic pressure and diastolic
pressure?
What is the standard blood pressure
classication?
• Put in a dry place and avoid sunshine.
• Avoid exposing to water. Clean with a dry cloth.
• Use a damp cloth to clean if necessary.
• Avoid intense shaking or collisions, or dropping
the monitor.
• Avoid dusty environments, and avoid
environments with unstable temperatures.
• Do not clean the cuff or monitor with water. Never
immerse the cuff or monitor in water.
Maintenance
37
Blood Pressure Category
Systolic mmHg
(upper #)
Diastolic mmHg
(lower #)
Normal Less than 120 and Less than 80
Elevated 120–129 and Less than 80
High Blood Pressure (Hypertension)
Stage 1
130–139 or 80–89
High Blood Pressure (Hypertension)
Stage 2
140 or higher or 90 or higher
Hypertensive Crisis (Consult your
doctor immediately)
Higher than 180 and / or Higher than 120
Caution:
• Please consult a physician if your measuring result falls outside the range.
• Please note that only a physician can tell whether your blood pressure value has reached
a dangerous point.
Using the Blood Pressure Monitor (Cont.)
38
Irregular Heartbeat Detector
Why does my blood pressure uctuate
throughout the day?
An irregular heartbeat is detected when a heartbeat
rhythm varies while the monitor is measuring
systolic pressure and diastolic pressure. During
each measurement, the monitor will keep a record
of all the pulse intervals and calculate their average
value. If there are two or more pulse intervals and the
difference between each interval and the average is
more than ±25%, or if there are four or more pulse
intervals and the difference between each interval
and the average is more than ±15%, then the irregular
heartbeat symbol will appear on the display with the
measurement result.
• Individual blood pressure varies throughout the
day. It is also affected by the way you tie your cuff
and your measurement position, so please take
measurements under the same conditions each
time.
• If you take medicine, your blood pressure will vary
more.
• Wait at least 3 minutes between measurements.
Caution:
• The appearance of the irregular heartbeat icon
( ) indicates that a pulse irregularity consistent
with an irregular heartbeat was detected during
measurement. Usually this is not a cause for
concern. However, if the symbol appears often,
we recommend you seek medical advice.
Please note that this monitor does not replace a
cardiac examination, but serves to detect pulse
irregularities at an early stage.
Using the Blood Pressure Monitor (Cont.)
39
Using the Blood Pressure Monitor (Cont.)
Why do I get a different blood pressure at
home compared to the hospital?
Is the result the same if measuring on the
right arm?
What you need to pay attention to when you
measure your blood pressure at home:
Your blood pressure is different throughout the day
due to weather, emotion, exercise, etc. Also, you may
have a different blood pressure in a hospital due to
the “white coat” effect, which means blood pressure
usually increases in clinical settings.
Measuring on either arm is acceptable. However,
results may differ for some people. We recommend
measuring on the same arm each time.
If your problem is not listed, please contact
Customer Support (see page 54).
• If the cuff is tied properly
• If the cuff is too tight or too loose
• If the cuff is tied on the upper arm
• If you feel anxious
• Taking 2–3 deep breaths before beginning will be
better for measuring
• Relax for 4–5 minutes to help your calmness
40
Troubleshooting Display Readings
Symbol Solution
Display will not turn on Replace batteries. Make sure the batteries and AC adapter are inserted correctly.
Display is dim or shows
“ + ”
Replace batteries.
The cuff is too tight or too loose. Refasten the cuff, then measure again.
The monitor detected motion or talking, or the pulse is too poor while
measuring. Relax for a moment, then measure again.
The monitor does not detect the pulse signal. Loosen the clothing on the arm,
then measure again.
The measurement failed. Relax for a moment, then measure again.
EEx
A calibration error occurred. Retake the measurement. If the problem continues,
contact Customer Support (see page 54).
Bluetooth pairing with the VeSync app has failed. Make sure the phone’s
Bluetooth is on and within range of the monitor, then try again.
41
Symbol Solution
Remove the arm cuff and wait 2–3 minutes before taking another measurement.
If this error continues to appear, contact your physician.
“OUT”
This error message means “Out of measurement range”. Remove the arm
cuff. Relax for a moment, refasten the cuff, then measure again. If this error
continues to appear, contact your physician.
“LOC”
The , , and
buttons are locked. Press to unlock these buttons.
“ UNL”
The , , and
buttons have been unlocked. Press to lock these
buttons.
If your problem is not listed, please contact Customer Support (see page 54).
42
iOS is a registered trademark of Cisco Systems, Inc.
and/or its aliates in the United States and certain
other countries.
Apple App Store is a trademark of Apple Inc.
Android, Google Home, and Google Play are
trademarks of Google LLC.
Amazon, Echo, and all related logos are trademarks of
Amazon.com, Inc. or its aliates.
The Bluetooth
®
word mark and logos are registered
trademarks owned by Bluetooth SIG, Inc. and any
use of such marks by Etekcity Corporation is under
license. Other trademarks and trade names are those
of their respective owners.
Attributions
43
Federal Communication Commission
Interference Statement
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.
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 Caution: Any changes or modications not expressly approved by
the party responsible for compliance could void the user’s authority to
operate this equipment.
FCC ID: OU9TMB1583BS
FCC Radiation Exposure
Statement
This equipment complies with FCC radiation exposure limits set forth
for an uncontrolled environment. End users must follow the specic
operating instructions for satisfying RF exposure compliance. To
maintain compliance with FCC RF exposure compliance requirements,
please follow operation instructions as documented in this manual.
This transmitter must not be co-located or operating in conjunction
with any other antenna or transmitter. This equipment should be
installed and operated with a minimum distance of 20cm between
the radiator and your body. The availability of some specic channels
and/or operational frequency bands are country dependent and
are rmware programmed at the factory to match the intended
destination. The rmware setting is not accessible by the end user.
44
EMC Guidance
This ME EQUIPMENT or ME SYSTEM is suitable for
home healthcare environments.
Technical Description:
Warning: Don’t be near the 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. If
such use is necessary, this equipment and the other
equipment should be observed to verify that they are
operating normally.
Warning: Use of accessories, transducers and
cables other than those specied 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.
Warning: Portable RF communications equipment
(including peripherals such as antenna cables and
external antennas) should be used no closer than 12
inch / 30 cm to any part of this equipment, including
cables specied by the manufacturer. Otherwise,
degradation of the performance of this equipment
could result.
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.
45
Guidance and Manufacturer’s Declaration – Electromagnetic Emission
Emissions Test Compliance
RF emissions
CISPR 11
Group 1
RF emissions
CISPR 11
Class [ B ]
Harmonic emissions
IEC 61000-3-2
Class A
Voltage uctuations/
icker emissions
IEC 61000-3-3
Comply
Table 1
46
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
Immunity Test IEC 60601-1-2 Test level Compliance Level
Electrostatic
discharge (ESD)
IEC 61000-4-2
±8 kV contact
±2 kV, ±4kV, ±8 kV, ±15 kV air
±8 kV contact
±2 kV, ±4kV, ±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
Not Applicable
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
Not Applicable
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
0 % UT; 0,5 cycle. At 0°, 45°, 90°, 135°, 180°,
225°, 270° and 315°.
0 % UT; 1 cycle and 70 % UT; 25/30 cycles;
Single phase: at 0°.0 % UT; 250/300 cycle
0 % UT; 0,5 cycle. At 0°, 45°, 90°, 135°,
180°, 225°, 270° and 315°. 0 % UT;
1 cycle and 70 % UT; 25/30 cycles;
Single phase: at 0°.
0 % UT; 250/300 cycle
Table 2
47
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
Immunity Test IEC 60601-1-2 Test level Compliance Level
Power frequency
magnetic eld
IEC 61000-4-8
30 A/m
50 Hz / 60 Hz
30 A/m
50 Hz / 60 Hz
Conduced RF
IEC61000-4-6
3 V
0,15 MHz – 80 MHz
6 V in ISM and amateur radio bands
between 0,15 MHz and 80 MHz
80 % AM at 1 kHz
3 V
0,15 MHz – 80 MHz
6 V in ISM and amateur radio bands
between 0,15 MHz and
80 MHz
80 % AM at 1 kHz
Radiated RF
IEC61000-4-3
10 V/m
80 MHz – 2,7 GHz
80 % AM at 1 kHz
10 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 2
48
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
Radiated RF
IEC610004-3
(Test specications for
ENCLOSURE PORT
IMMUNITY to RF wireless
communications
equipment)
Test Frequency (MHz) Band (MHz) Service
385 380-390 TETRA 400
450 430-470 GMRS 460, FRS 460
710
704-787 LTE Band 13, 17745
780
810
800-960
GSM 800/900,
TETRA 800, iDEN 820,
CDMA 850, LTE Band 5
870
930
Table 3
49
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
Modulation Maximum Power (W) Distance (m)
IEC 60601-1-2 Test Level
(V/m)
Compliance Level
(V/m)
Pulse modulation
18 Hz
1.8 0.3 27 27
FM ± 5k Hz
deviation
1 kHz sine
2 0.3 28 28
Pulse
modulation
217 Hz
0.2 0.3 9 9
Pulse
modulation
18 Hz
2 0.3 28 28
Table 3
50
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
Radiated RF
IEC610004-3
(Test specications for
ENCLOSURE PORT
IMMUNITY to RF wireless
communications
equipment)
Test Frequency (MHz) Band (MHz) Service
1720
1700-1990
GSM 1800; CDMA 1900;
GSM 1900; DECT;
LTE Band 1, 3,
4,25; UMTS
1845
1970
2450 2400-2570
Bluetooth, WLAN,
802.11 b/g/n, RFID
2450, LTE
Band 7
5240
5100-5800
WLAN
802.11
a/n
5500
5785
Table 3
51
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
Modulation Maximum Power (W) Distance (m)
IEC 60601-1-2 Test Level
(V/m)
Compliance Level
(V/m)
Pulse
modulation
217 Hz
2 0.3 28 28
Pulse
modulation
217 Hz
2 0.3 28 28
Pulse
modulation
217 Hz
0.2 0.3 9 9
Table 3
52
Warranty Information
Product Name Smart Blood Pressure Monitor
Model TMB-1583-BS
For your own reference, we strongly recommend that you
record your order ID and date of purchase.
Order ID
Date of Purchase
• If the product has been modied from its original
condition;
• If the product has not been used in accordance with
directions and instructions in the user manual;
• To damages or defects caused by accident, abuse,
misuse or improper or inadequate maintenance;
• To damages or defects caused by service or repair of the
product performed by an unauthorized service provider
or by anyone other than Etekcity;
• To damages or defects occurring during commercial
use, rental use, or any use for which the product is not
intended;
• To damages or defects exceeding the cost of the
product.
Etekcity will not be liable for indirect, incidental, or
consequential damages in connection with the use of the
product covered by this warranty.
This warranty extends only to the original consumer purchaser
of the product and is not transferable to any subsequent
owner of the product regardless of whether the product is
transferred during the specied term of the warranty.
This warranty does not extend to products purchased from
unauthorized sellers. Etekcity’s warranty extends only to
products purchased from authorized sellers that are subject to
Etekcity’s quality controls and have agreed to follow its quality
controls.
Terms & Policy
Etekcity Corporation (“Etekcity”) warrants this product to the
original purchaser to be free from defects in material and
workmanship, under normal use and conditions, for a period of
2 years from the date of original purchase.
Etekcity agrees, at our option during the warranty period,
to repair any defect in material or workmanship or furnish
an equal product in exchange without charge, subject to
verication of the defect or malfunction and proof of the date
of purchase.
There is no other express warranty. This warranty does
not apply:
53
ALL IMPLIED WARRANTIES ARE LIMITED TO THE
PERIOD OF THIS LIMITED WARRANTY.
This warranty gives you specic legal rights and you may
also have other rights which vary from state to state. Some
states do not allow the exclusion or limitation of incidental or
consequential damages, so the above limitation or exclusion
may not apply to you.
If you discover that your product is defective within the
specied warranty period, please contact Customer Support
via support@etekcity.com. DO NOT dispose of your product
before contacting us. Once our Customer Support Team has
approved your request, please return the product with a copy
of the invoice and order ID.
Every Etekcity product automatically includes a 2-year
warranty. To make the customer support process quick and
easy, register your product online at www.etekcity.com/
warranty.
This warranty is made by:
Etekcity Corporation
1202 N. Miller St., Suite A
Anaheim, CA 92806
54
Customer Support
If you have any questions or concerns about your new
product, please contact our helpful Customer Support
Team.
Distributed by Etekcity Corporation
1202 N. Miller St., Suite A
Anaheim, CA 92806
Email: support@etekcity.com
Toll-Free: (855) 686-3835
Guangdong Transtek Medical Electronics Co., Ltd.
Zone B, No.105 , Dongli Road, Torch Development District, Zhongshan, 528437,
Guangdong, China
Support Hours
Monday—Friday
9:00 am —5:00 pm PST/PDT
*Please have your order invoice and order ID ready before contacting Customer Support.
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