ETEKCITY TMB-1583-BS User manual

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Questions or Concerns? [e-mail] • [phone]
Smart Blood
Pressure Monitor
Model: TMB-1583-BS
User Manual

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Table of Contents
Package Contents
Specications
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
Conguration
• Data Transmission
• Transmitter Information
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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
51
55
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

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SpecicationsPackage 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%

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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 (Itmeansthedevicecould
be protected against solid foreign
objects of 12.5mm Ф and greater,
and against vertically falling water
drops.)
Device
Classication
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.
Specications (cont.)

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• Blood pressure measurement
• Pulse rate measurement
• Result storage
• 90 records per user (unlimited records in the
VeSync app)
• Measurement during ination
• 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

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Safety Information
Please read and follow all instructions and safety guidelines in this manual.
READ AND SAVE THESE INSTRUCTIONS
CAUTION
• This device is contraindicated for any person who is connected to a wearable or
implantable electronic device or instrument such as a pacemaker or debrillator.
• This device is not intended to be a diagnostic device. Contract your physician if
hypertensive values are indicated.
Contraindications:
• This Blood Pressure Monitor TMB-1583-BS is a digital monitor intended for use in
measuring blood pressure and heartbeat rate with arm circumference ranging from
22 cm to 42 cm. The device can be used to detect irregular heartbeat.
• It is intended for adult, home use.
Indications for Use:

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• 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 qualied 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.)

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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
inuence 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
- Inating 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 inate 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 inated 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 and ISO
10993-10. It will not cause any potential
sensitization or irritation reaction.
• The included adapter is specied 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 deate.
Should the cuff not deate when pressure
reaches 40 kPa / 300 mmHg, detach the
cuff from the arm and press to stop
ination.
• 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 dicult 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 55). 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 55)
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, as appropriate.
• Only use ACCESSORIES and detachable
parts specied/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”
Itmeansthedevicecould be protected against
solid foreign objects of 12,5mm Ф and greater, and
against vertically falling water drops.
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
Caution
Indicates that caution is necessary when operating
the device or control close to where the symbol is
placed, or that the current situation needs operator
awareness or operator action in order to avoid
undesirable consequences.
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”
Date and Country of manufacture
Symbol for “Recycle”
The B/N (Batch Number) code combines
the destination country, PO number, date of
manufacture, and serial number.
IP21
B/N
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 inating 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.

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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
AB
F
15VAAA
15VAAA
15VAAA
15VAAA
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
LO
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

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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.

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Setting Date, Time, and Measurement Unit (Cont.)
3. When you have selected the right year, press
to conrm and continue to setting the month
and day.
4. Repeat steps 2 and 3 to set the month and day.