Dr. Trust AFIB Pro User manual

ABOUT US
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Dr Trust
AFIB Pro Blood Pressure Monitor 102
We bring to you a variety of best self medical devices, trusted and used by
Doctors, medical professionals and home users all over the world.
Driven by the passion for innovation, we at Dr Trust endeavour to provide our
customers with the latest medical inventions with an objective to promote good
health and wellness all around the world. All the medical devices and health
monitors provided by Dr Trust are supported by accurate, latest and ground
breaking technologies, innovated at our headquarter in NY, USA. All our
products adhere to the most stringent CE and FDA guidelines and are strongly
recommended by doctors and health practitioners. Our products are designed
in the utmost exemplary ways to ensure that their accuracy and convenience
are unrivalled. The ease of their use and operation makes them even more
suitable for users of all age groups.
Dr Trust strives to enhance the quality of lifestyle by providing with the most
trusted and innovative health care and wellness products. Being a renowned
global leader in health care products, Dr Trust ensures that our technically
efficient team works dynamically and tirelessly to provide the best of the
medical devices to our clients. The products that we have to offer are suitably
designed for use at homes, laboratories and hospitals.
Our ground breaking solutions allow you to monitor your health in the easiest
ways possible. In today's era when all of our lives are too hassled to handle, it
becomes a bit difficult to pay attention to our health. But it has now become
easier with the coming of the monitoring devices which can be conveniently
used at homes and even on the go.
QUICK START GUIDE
Step 1
Check batteries and insert the air tube
from the cuff into the air jack.
Step 2
Before starting the measurement,
select the measuring mode: Standard
Single or AFIB Mode and make
settings for user no, time, and date etc.
Step 3
Slide the blood pressure cuff onto your
upper arm and secure it so that it sits
snugly about one inch above of your
elbow.
Step 4
Simply push the power button and cuff
begins to inflate with controlling
deflation speed automatically.
Step 5
The device is intended for taking 2
measurements in succession in AF
mode. Your result is calculated and
displayed as a single average d
measurement on the display screen
with Atrial Fibrillation detector icon (if
atrial fibrillation is detected).
Step 6
In Standard mode, you will get the
pressure value when the pump stops
af ter reac h i ng to the in f l ation
pressure.
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TABLE OF CONTENTS
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1. INTRODUCTION
1.1. Features of AFIB Pro
1.2. Key Components
1.3. Important Information about Self-Measurement
2. IMPORTANT INFORMATION ON THE SUBJECT OF
BLOOD-PRESSURE AND ITS MEASUREMENT
2.1. How does high/low blood-pressure arise?
2.2. Which values are normal?
3. OPERATION
3.1. Inserting the batteries
3.2. Setting date/time
3.3. User selection
4. CARRYING OUT A MEASUREMENT
4.1. Before the measurement
4.2. Common sources of error
4.3. Fitting the cuff
4.4. Measuring procedure
4.5. Discontinuing a measurement
4.6. Memory – storage and recall of the measurements
4.7. Memory– cancellation of all measurements attention!
5. APPEARANCE OF THE HEART ARRHYTHMIA INDICATOR FOR
EARLY DETECTION
6. ERROR MESSAGES /MALFUNCTIONS
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7. CARE AND MAINTENANCE, RECALIBRATION
8. SAFETY, CARE AND DISPOSAL
9. REFERENCE TO STANDARDS
10. TECHNICAL SPECIFICATIONS
11. MANUFACTURER'S DECLARATION
12. CUSTOMER SUPPORT
13. CONTACT US
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1. INTRODUCTION
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1.1. Features of AFIB Pro
Dr Trust AFIB Pro Blood Pressure Monitor -102 comes with integrated
time/date display. It is a fully automatic, digital blood-pressure measuring
device for use on the arm, which enables very fast and reliable measurement of
the systolic and diastolic blood-pressure as well as the pulse frequency by way
of the oscillometric method of measurement. The device offers very high and
clinical tested measurement accuracy and has been designed to provide
maximum of user-friendliness. The device is intended for self-use in home.
Before using, please read this instruction manual carefully keeps it in a safe
place. For further questions on the subject of blood-pressure and its
measurement, please contact your doctor.
a) The LCD Screen of AFIB Pro -102
The LCD screen displays the systolic and diastolic blood pressure
measurements along with AFIB and heart rate. It also displays previously
recorded measurements and the date and time, when the appropriate button
is pressed. 1.3. Important Information about Self-Measurement
·Substitution of a different component might result in measurement error.
·Cuff is replaceable only by an original one.
·Do not use with neonatal patients.
·It will cause harmful injury to the patient or affect the blood pressure due to
connection tubing kinking.
·Too frequent measurements can cause injury to the patient due to blood flow
interference.
·Tying the cuff over a wound can cause further injury.
ATTENTION
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1.2. Key Components
The various components of AFIB Pro -102

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2. IMPORTANT INFORMATION ON THE SUBJECT OF
BLOOD-PRESSURE AND ITS MEASUREMENT
2.1. How does High/Low Blood-Pressure arise?
As your heart beats, it pumps your blood round your body so that your muscles
can get all the energy and oxygen they need. To do this, your heart pushes your
blood through a network of blood vessels called arteries. As the blood travels
through the arteries it pushes against the sides of these blood vessels and the
strength of this pushing is called your blood pressure. As your heart squeezes
and pushes your blood through your arteries, your blood pressure goes up. As
your heart relaxes, your blood pressure goes down. So, with each heartbeat,
your blood pressure will rise to a maximum level and then fall to a minimum
level.
2.2. Which values are normal?
Blood pressure is too high if at rest, the diastolic pressure is above 90 mmHg
and/or the systolic blood-pressure is over 160 mmHg. In this case, please
consult your doctor immediately. Long-term values at this level endanger your
health due to the associated advancing damage to the blood vessels in your
body. Should the systolic blood-pressure values lie between 140 mm Hg and
159 mmHg and/or the diastolic blood-pressure values lie between 90 mmHg
and 99 mmHg, likewise, please consult your doctor. Furthermore, regular self-
checks will be necessary. With blood-pressure values that are too low, i.e.
systolic values under 100 mmHg and/or diastolic values under 60 mmHg,
likewise, please consult your doctor. Even with normal blood-pressure values,
a regular self-check with your blood-pressure monitor is recommended. In
this way you can detect possible changes in your values early and react
appropriately. If you are undergoing medical treatment to control your blood
pressure, please keep a record of the level of your blood pressure by carrying
out regular self-measurements at specific times of the day. Show these values
to your doctor. Never use the results of your measurements to alter
independently the drug doses prescribed by your doctor.
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·The application of the cuff and its pressurization on any limb where
intravascular access or therapy, or an arteriovenous (A-V) shunt, is present
because of temporary interference to blood flow and could result in injury to
the patient.
·Do not let the cuff and its pressurization on the arm on the side of a
mastectomy.
·The need to check that operation of the automated sphygmomanometer does
not result in prolonged impairment of patient blood circulation.
·Not intended to be used together with HF surgical equipment.
·Do not forget: self-measurement means control, not diagnosis or treatment.
Unusual values must always be discussed with your doctor. Under no
circumstances should you alter the dosages of any drugs prescribed by your
doctor.
·The pulse display is not suitable for checking the frequency of heart
pacemakers!
·In cases of cardiac irregularity (Arrhythmia), measurements made with this
instrument should only be evaluated after consultation with the doctor.
Electromagnetic interference
The device contains sensitive electronic components (Microcomputer).
Therefore, avoid strong electrical or electromagnetic fields in the direct vicinity of
the device (e.g. mobile telephones, microwave cookers). These can lead to
temporary impairment of the measuring accuracy.

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2.4. How does AFIB impact you?
One in every six strokes is AFIB-related. While individuals above the age of 65
are more likely to have AFIB, individuals as young as 40 can exhibit AFIB. Early
diagnosis can help reduce the risk of a stroke.
2.5. How does Dr Trust AFIB Pro 102 can help controlling AFIB?
Dr Trust AFIB Pro Blood Pressure Monitor 120 provides a convenient way to
screen for AFIB. Knowing your blood pressure and knowing whether you have
AFIB can help reduce the risk of stroke. AFIB detection provides a convenient
way to screen for AFIB while taking your blood pressure.
3. OPERATION
3.1 Inserting the batteries
·Insert the batteries (4 x size AA 1.5V), thereby observing the indicated polarity.
·The battery warning appears in the display, the batteries remain 20%
power to warn user the batteries will be run out.
·If the battery warning appears in the display, the batteries are empty
and must be replaced by new ones.
ATTENTION
After the battery warning appears, the device is blocked until the batteries
have been replaced.
·Please use «AA» alkaline 1.5V batteries.
·If the blood-pressure monitor is left unused for long periods, please remove
the batteries from the device.
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Table for classifying blood-pressure values (unit: mmHg) according to World
Health Organization:
Range &
broadcasting
Systolic
Blood-pressure
DiastolicBlood-
pressure
Measures
Optimal Self-check
Normal
Slight
hypertension
between 120
and 129
between 140
and 159
between 100
and 120
b e t w e e n 8 0
and 84
b e t w e e n 9 0
and 99
b e t w e e n 6 0
and 80
Self-check
Seek medical
advice
Seek medical
advice
Urgently seek
medical advice!
High to
normal
Medium
hypertension
Stronghypert
ension
between 130
and 139
between 160
and 179
Higher than
180
between 85
and 89
between 100
and 109
Higher than
110
Consult your
doctor
2.3. What is Atrial Fibrillation (AFIB)?
Normally, your heart contracts and relaxes to a regular beat. Certain cells in
your heart produce electrical signals that cause the heart to contract and
pump blood. Atrial fibrillation occurs when rapid, disorganized electrical
signals are present in the heart’s two upper chambers, called the atria; causing
them to contract quickly and irregularly (this is called fibrillation). Atrial
fibrillation is the most common form of heart arrhythmia or irregular heartbeat.
You can live with atrial fibrillation, but it can lead to other rhythm problems,
chronic fatigue, heart failure and - worst of all – a stroke.

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4. CARRYING OUT A MEASUREMENT
4.1. Before the measurement
·Avoid eating, smoking as well as all forms of exertion directly before the
measurement. All these factors influence the measurement result. Try and find
time to relax by sitting in an arm chair in a quite atmosphere for about ten
minutes before the measurement.
·Measure always on the same arm (normally left).
·Attempt to carry out the measurements regularly at the same time of day, since
the blood-pressure changes during the course of the day.
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ŸUnit setting- the unit “ Kpa “ or “ mmH “ flashes on the display : Choose the
desired Unit with “ “ button and confirm with “ “ (ON/OFF) button.
Note: The clock will begin to run from 2016-01-01 01:01, and Unit in mmHg, if no
key is pressed within 20 seconds.
3.3. User selection
Press and hold “ “ memory button for 2 seconds, “ “ flashes on the
display. Press “ “ to choose the desired user.
3.2. Setting date/time
How to enter into the setting mode
ŸAfter batteries are inserted, the device will enter the setting mode
automatically.
ŸPress and hold “ “ (ON/OFF) button for 5 seconds, the setting mode will
appear.
The setting procedure as follows:
It is essential to set date and time. Otherwise, you will not be able to save your
measured value correctly with a date and time.
Use button as adjustment button
If you press and hold button, you can set the values more quickly.
ŸYear setting- the year flashes on the display : Choose the desired year with
“ “ button and confirm with “ “ (ON/OFF) button ,
ŸMonth setting- the month flashes on the display : Choose the desired
month with “ “ button and confirm with “ “ (ON/OFF) button,
ŸDay setting- the day flashes on the display : Choose the desired day with
“ “ button and confirm with “ “ (ON/OFF) button,
ŸHour setting- the hour flashes on the display : Choose the desired hour
with “ “ button and confirm with “ “ (ON/OFF) button,
ŸMinute setting- the minute flashes on the display : Choose the desired
minute with “ “ button and confirm with “ “ (ON/OFF) button,

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4.2. Common sources of error
·All efforts made by the patient to support the arm can increase the blood-
pressure. Make sure you are in a comfortable, relaxed position. Do not activate
any of the muscles during the measurement. Use a cushion for support if
necessary.
·The performance of the automated sphygmomanometer can be affected by
extremes of temperature, humidity and altitude.
·Avoid compression or restriction of the connection tubing.
·A loose cuff causes false measurement values.
·With repeated measurements, blood accumulates in the respective arm,
which can lead to false results. Correctly executed blood-pressure
measurements should therefore first be repeated after a 5 minute pause or
after the arm has been held up in order to allow the accumulated blood to flow
away(after at least 3 minutes).
4.3. Fitting the cuff
Insert air connector into air outlet (shown
in the pic). Please make sure the fitting of
the air connector is tight and proper to
avoid air leakage.
a) The distance between the edge of cuff
and the elbow should be approx. 2~3cm.
b) Secure the cuff with the Velcro fastener,
so that it lies Comfortably and not too
tight, whereby no space should remain
between the cuff and the arm.
Note: Comparable blood-pressure measurements require the same conditions!
These are always quiet conditions.
c) Lay the arm on a table, with the palm
upwards. Support the arm a little with a
rest (cushion), so that the cuff rests at
about the same height as the heart. Take
care, that the cuff lies free. Remain so for 2
minutes sitting quietly, before beginning
with the measurement.
d) Let legs uncrossed, feet flat on the floor,
back and arm supported
4.4. Measuring procedure
Select the measuring mode:
Standard Single or AF Mode
This device enables you to select
either standard (standard single
mea surem ent) or AF m ode
(automatic twice measurement).
To select standard mode, slide
the AF switch on the side of the
device downwards to position «1»
and to select AF mode, slide this
switch upwards to position «AF».
Cuff OK Symbol
When the cuff is applied correctly, is displayed while taking a
measurement or using the memory function.

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In AF Mode
In AF mode, 2 measurements are automatically taken
in succession and the result is then automatically
analyzed and displayed. Because blood pressure
constantly fluctuates, a result determined in this way
is more reliable than one produced by a single
measurement.
·After pressing the ON/OFF button, the
symbol appears in the display.
·The bottom, left hand section of the display shows
numbers 1, 2 to indicate which of the 2
measurements is currently being taken.
·There is a break of 15 seconds between the
measurements. A countdown indicates the
remaining time.
·The individual results are not displayed. Your
blood pressure will only be displayed after the 2
measurements are taken.
·Do not remove the cuff between measurements.
·If one of the individual measurements was
questionable, a third one is automatically taken.
Measured result
Example 1.
The measured systolic and diastolic blood-pressure
values as well as the pulse are now displayed.
Example (Fig.):
Systole 128, Diastole 70, Pulse 80, arrhythmia
detected.
Example 2.
The measured systolic and diastolic blood-pressure
values as well as the pulse are now displayed.
Example (Fig.):
Systole 128, Diastole 70, Pulse 80, Afib detected.
In Standard Single Mode
a) To slide the AF switch on the side of the device
downwards to position «1». Press the ON/OFF
button, the pump begins to inflate the cuff. In the
display, the increasing cuff-pressure is continually
displayed.
b) After reaching the inflation pressure, the pump
stops and the pressure slowly falls away. The cuff-
pressure is displayed during the measurement.
When the device has detected the pulse, the heart
symbol in the display begins to blink.
c) The measured systolic and diastolic blood-
pressure values as well as the pulse are now
displayed.
In the measuring
After reaching the inflation pressure, the pump stops and the pressure slowly
falls away. The cuff-pressure is displayed during the measurement. When the
device has detected the pulse, the heart symbol in the display begins to blink.
The measurement results are displayed until you switch the device off. If no
button is pressed for 3 minutes, the device switches off automatically.

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Example (Fig.): Systole 128, Diastole 70, Pulse 80
The measurement results are displayed until you
switch the device off. If no button is pressed for 3
minutes, the device switches automatically off.
4.5. Discontinuing a measurement
If it is necessary to interrupt a blood pressure measurement for any reason
(e.g. the patient feels unwell), the “ON/OFF” power button can be pressed at
any time. The device then immediately lowers the cuff-pressure
automatically.
4.6. Memory – storage and recall of the measurements
The blood-pressure monitors automatically stores each of 120 measurement
values.
By pressing “ ” MEMORY button, to review an average value of the
last 3 measurements and all of the records of 120 measurements (MR1, MR3,
...,Mr120) can be displayed.
(MR1: Values of the oldest measurement)
4.7. Memory – cancellation of all measurements
Before you delete all readings stored in the memory, make sure you need not
refer the readings at a later date. Keeping a written record is prudent and may
provide additional information for your doctor’s visit. In order to delete all
stored readings, depress the MEMORY button for at least 7 seconds, the
display will show the symbol «CL» and then release the button. To
permanently clear the memory, press the MEMORY button while «CL» is
flashing.
This symbol indicates detection of pulse irregularities during the measurement.
In this case, the result may deviate from your normal blood pressure. In most cases,
this is no cause for concern. However, if the symbol appears on a regular basis (e.g.
several times a week with measurements taken daily) we advise you to consult your
doctor.
5. APPEARANCE OF THE HEART ARRHYTHMIA
INDICATOR FOR EARLY DETECTION
Information for the doctor on frequent appearance of the Arrhythmia indicator
This instrument is an oscillometric blood pressure monitor that also analyses
pulse frequency during measurement. The instrument is clinically tested. The
arrhythmia symbol is displayed after the measurement, if pulse irregularities
occur during measurement. If the symbol appears more frequently (e.g. several
times per week on measurements performed daily) we recommend the patient to
seek medical advice. The instrument does not replace a cardiac examination, but
serves to detect pulse irregularities at an early stage.
Arm Movement Indicator
The Arm Movement Error indicator is displayed, if you move your arm/body
during the measurement. Please remove the arm cuff, and wait 2-3 minutes. Take
another measurement, remain still during cuff inflation.

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Measuring range
Pressure: 30 to 280 mmHg (in 1 mmHg
increment)
Pulse: 40 to 199 beat/minute
Measuring resolution 1mmHg
Inflation Automatic inflation by internal pump
Memory function 2 x 120 memories for 2 users (SYS, DIA, Pulse)
Decompression Constant exhaust valve system
Power Source 4- size “AA” alkaline Batteries
Operation Temperature 5~40°C/41~104°F
Operation Humidity 15%~85%RH maximum
Storage Temperature -10~55°C/14~131°F
Storage Humidity 10%~95%RH maximum
Dimensions 135×112×71±1.0 mm
Static accuracy Pressure: ±3mmHg / Pulse: ±5% of reading
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If an error occurs during a measurement, the measurement
is discontinued and a corresponding error code is displayed
(Example: Error No. 2).
Other possible malfunctions and their elimination
If problems occur when using the device, the following points should be checked
and if necessary, the corresponding measures are to be taken:
6. ERROR MESSAGES/MALFUNCTIONS
Error No.
Malfunction
Possible cause(s)
Remedy
ERR 1
ERR 2
ERR 3
No pulse has been detected.
Unnatural pressure impulses influence the measurement
result. Reason: The arm was moved during the Measurement
(Artefact).
The inflation of the cuff takes too long. The cuff is not
correctly seated.
ERR 5 The measured readings indicated an unacceptable difference
between systolic and diastolic pressures. Take other reading
following directions carefully. Contact you doctor if you
continue to get unusual readings.
Err8 Pressure in cuff is over 290 mmHg.
The display remains empty when
the instrument is switched on
although the batteries are in place.
1. Check batteries for correct polarity and
if necessary insert correctly.
2. If the display is unusual, re-insert
batteries or exchange them.
The device frequently fails to
measure the blood pressure values,
or the values measured are too low
(too high).
Every measurement produces a
di f ferent va l u e alt h ough t he
instrument functions normally and
the values displayed are normal.
Blood pressure measured differs
from those values measured by the
doctor.
1. Check the positioning of the cuff.
2. Measure the blood-pressure again in
peace and quiet under observance of the
details made under point 5.
1. Please read the following information
and the points listed under «Common
s o u r c e s o f e r r o r » . R e p e a t t h e
measurement.
Please note: Blood pressure fluctuates
continually so successive measurements
will show some variability.
1. Record the daily development of the
values and consult your doctor. Please
note: Individuals visiting their doctor
frequently experience anxiety which can
result in a higher reading at the doctor
than obtained at home under resting
conditions.
Further Information
The level of blood-pressure is subject to fluctuations even with healthy people.
Important thereby is, that comparable measurements always require the same
conditions (Quiet conditions)!
If, in spite of observing all these factors, the fluctuations are larger than 15mmHg,
and/or you hear irregular pulse tones on several occasions, please consult your
doctor.
For licensing, the device has been subjected to strict clinical tests, by which the
computer program used to measure the blood-pressure values was tested by
experienced specialist doctors in Germany. The same computer program is used
in every individual device, and has thus also been clinically tested.

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The manufacture of the devices takes place according to the terms of the
European standard for blood-pressure measuring devices (see technical data)
You must consult your specialist dealer or chemist if there are technical
problems with the blood-pressure instrument. Never attempt to repair the
instrument yourself!
a) Do not expose the device to extreme temperatures, humidity, dust, or direct
sunlight.
b) The cuff contains a sensitive air-tight bubble. Handle it carefully and avoid all
types of straining through twisting or buckling.
c) Clean the device with a soft and a dry cloth. Do not use petrol, thinners, or similar
other solvents. Spots on the cuff can be removed carefully with damp cloth and
soapsuds. The cuff must not be washed!
d) Do not drop the instrument or treat it roughly in any way.
e) Never open the device! Otherwise, the manufacturer calibration becomes
invalid!
Periodical recalibration
Sensitive measuring devices must be checked for accuracy time to time. We
therefore recommend a periodical inspection of the static pressure display every 2
years. Your specialist dealer would be pleased to provide more extensive
information about this.
7. CARE AND MAINTENANCE, RE-CALIBRATION
Safety and protection
·This instrument may be used only for the purpose described in this booklet. The
manufacturer cannot be held responsible for the damage caused by incorrect
application.
·This instrument comprises sensitive components therefore must be treated
with caution. Observe the storage and operating conditions described in the
“Technical specifications” section!
·Protect it from water and moisture, extreme temperatures, impact and
dropping, contamination and dust, direct sunlight, heat and cold, etc.
·The cuff is sensitive and must be handled with care.
·Only pump up the cuff once fitted.
·Do not use the instrument close to strong electromagnetic fields such as
cellphones or radio installations.
·Do not use the instrument if you think it is damaged or notice anything unusual.
·If the instrument is not going to be used for a prolonged period, the batteries
should be removed. Read the additional safety instructions in the individual
sections of this booklet.
·Ensure that children do not use the instrument unsupervised: some parts are
small enough to be swallowed.
·Must use the recognized accessories, detachable parts and materials, if the
useofotherpartsormaterialscandegrademinimumsafety.
·A warning to remove primary batteries if the instruments is not likely to be used
for some time.
8. SAFETY, CARE AND DISPOSAL
Instrument care
Clean the instrument only with a soft and dry cloth.
Disposal
Batteries and electronic instruments must be disposed off in accordance with
the locally applicable regulations, not with domestics waste.

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10. TECHNICAL SPECIFICATIONS
9. REFERENCE TO STANDARDS
Device Standard: Device corresponds to the requirements of the European
standard for
Standard
IEC60601-1-6:2010+A1:2013/ EN60601-1-6:2010+A1:2015
IEC60601-1:2005+A1:2012/EN60601-1:2006+A11:2011+A1:2013+A12:2014
IEC60601-1-2:2014/ EN60601-1-2:2015
IEC/EN60601-1-11:2015
IEC80601-2-30:2009+A1:2013/EN80601-2-30:2010+A1:2015
The stipulations of the EU-Guidelines 93/42/EEC for Medical Products Class IIa
have been fulfilled.
Measurement Procedure
Oscillometric , corresponding to
Korotkoff method: Phase I :
systolic , Phase V : diastolic
Display Digital display
Measuring range Pressure: 30 to 280 mmHg (in 1 mmHg
increment)
Pulse: 40 to 199 beat/minute
Measuring resolution 1mmHg
Inflation Automatic inflation by internal pump
Memory function 2 x 120 memories for 2 users (SYS, DIA, Pulse)
Decompression Constant exhaust valve system
Power Source 4- size “AA” alkaline Batteries
Operation Temperature 5~40°C/41~104°F
Operation Humidity 15%~85%RH maximum
Storage Temperature -20~+55°C/~4~+131°F
Storage Humidity 10%~95%RH maximum
Dimensions 113×90×56±1.0 mm
Static accuracy Pressure: ±3mmHg / Pulse: ±5% of reading

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Weight 518 g±5g (including batteries and cuff)
Cuff pressure display range 0~290mmHg/0~38.7kPa
Electrical shock protection: Internal power unit
Safety classifications: Type BF equipment
Mode of operation: Continuous operation
Protection against ingress of
water:
IP22
Accessories: M-L size Cuff , 4 “AA” batteries, string
bag, instruction manual, adapter
Notice: - Adapter must comply with EN60601-1, EN60601-1-2
,
11. MANUFACTURER S DECLARATION
Dr Trust AFIB Pro Blood Pressure Monitor 102 is intended for use in the
electromagnetic environment specified below. The customer or the user of Afib
Pro should assure that it is used in such an environment. Electromagnetic
Emissions: (IEC60601-1-2).
Electromagnetic Emissions: (IEC60601-1-2)
Electrostatic
discharge
(ESD) IEC
61000-4-2
±6 kV contact
±8 kV air
±6 kV contact
±8 kV air
Immunity test IEC60601-1-2
test level
Compliance
level
Electromagnetic
environment -guidance
Electromagnetic Immunity: (IEC60601-1-2)
Floors should be wood,
concrete, or ceramic tile.
If floors are covered with
synthetic material, the
relative humidity should
be at least 30 %.
Emission Test Compliance Electromagnetic Environment
RF emission
CISPR 11
Dr Trust AFIB Pro Blood Pressure Monitor
102 uses RF energy only for internal
functions. Therefore, this RF emission is
extremely weak and there is little chance of
it creating any kind of interference
whatsoever with nearby electronic
equipment.
Group 1
RF emissions
CISPR 11
Class B
Harmonic
emissions IEC
61000-3-2
Not applicable
Voltage
fluctuations/flicker
IEC 61000-3-3 Not applicable
Dr Trust Afib Pro Blood Pressure Monitor
102 is suitable for use in all establishments,
including domestic establishments and
those directly connected to the public low
voltage power supply network that supplies
buildings used for domestic purposes.

Surge IEC
61000-4-5
±1 kV differential
mode
±2 kV common
mode
Not applicable Mains power quality
should be that of a
typical commercial or
hospital environment.
Electric fast
transient/ burst
IEC 61000-4-4
±2 kV for power
supply lines
±1 kV for
input/output
lines
Not applicable Mains power quality
should be that of a
typical commercial or
hospital environment.
Voltage dips,
short
interruptions,
and voltage
variations on
power supply
input lines IEC
61000-4-11
<5 % UT（95%
dip inUT. ） for
0.5 cycle
40 % UT（60%
dip in UT ）for 5
cycles
70 % UT (30% dip
inUT) for 25
cycles
<5 % UT（95%
dip inUT）for 5
sec.
Not applicable Mains power quality should
be that of a typical
commercial or hospital
environment. If the user of
the upper arm style
requires continued
operation during power
mains interruptions, it is
recommended that Dr
Trust AFIB Pro Blood
Pressure Monitor 102 with
MDI be powered from an
uninterruptible power
supply or a battery.
Power
frequency (50/
60 Hz)
magnetic field
IEC 61000-4-8
3 A/m Not applicable Not applicable
Note: UT is the a.c. mains voltage prior to application of the test level.
Immunity test IEC60601-1-2
test level
IEC60601-1-
2 test level
Electromagnetic
environment - guidance
Conducted RF
IEC 61000-4-6
3 Vrms 150 kHz
to 80 MHz 80%
AM (2Hz)
3 Vrms
P o r t a b l e a n d m o b i l e R F
communications equipment
should be used no closer to any
part of Dr Trust AFIB Pro Blood
Pressure Monitor 102, including
cables, than the recommended
separation distance calculated
from the equation applicable to
the frequency of the transmitter.
R e c o m m e n d s e p a r a t i o n
distance is
3V
1/2
d = 1.2×p 80Mhz to 800 MHz
1/2
d = 2.3×p MHz to 2.5 GHz
Where P is the maximum output
power rating of the transmitter
in watts (W) according to the
transmitter manufacturer and d
is the recommended separation
distance in meters (m).
Field strengths from fixed RF
transmitters as determined by
a
an electromagnetic site survey ,
s h o u l d b e l e s s t h a n t h e
c o m p l i a n c e l e v e l i n e a c h
b
frequency range . Interference
may occur in the vicinity of
equipment marked with the
following symbol:
Radiated RF
IEC 61000-4-3
3 Vrms 80 MHz
to 2.5 GHz 80%
AM (2Hz)
3 V/m
26 27
102

Note1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note2: These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures,
objects, and people.
aField strengths from fixed transmitters, such as base stations for radio
(cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM
radio broadcast and TV broadcast cannot be predicted theoretically with
accuracy. To assess the electromagnetic environment due to fixed RF
transmitters, an electromagnetic site survey should be considered. If the
measured field strength in the location in which the Dr Trust AFIB Pro Blood
Pressure Monitor 102 is used exceeds the applicable RF compliance level above,
Dr Trust AFIB Pro Blood Pressure Monitor 102 should be observed to verify
normal operation. If abnormal performance is observed, additional measures
may be necessary, such as reorienting or relocating Dr Trust AFIB Pro Blood
Pressure Monitor 102.
bOver the frequency range 150 kHz to 80MHz, field strengths should be less than 3
V/m.
Recommended Separation Distances:
Recommended separation distance between portable and mobile RF
communications equipment and Dr Trust AFIB Pro Blood Pressure Monitor 102.
Dr Trust AFIB Pro Blood Pressure Monitor 102 is intended for use in an
electromagnetic environment in which radiated RF disturbances are controlled.
The customer or the user of Dr Trust AFIB Pro Blood Pressure Monitor 102 can
help prevent electromagnetic interference by maintaining a minimum distance
between portable and mobile RF communications equipment (transmitters) and
Dr Trust AFIB Pro Blood Pressure Monitor 102 as recommended below, according
to the maximum output power of the communications equipment.
Rated maximum
output power of
transmitter (W)
Separation distance according to frequency of transmitter m
150 kHz to 80
MHz
1/2
d = 1.2×p
80 MHz to 800
MHz
1/2
d = 1.2×p
800 MHz to 2.5 GHz
1/2
d = 2.3×p
0.01 0.12 0.12 0.23
0.1
1
10
100
0.38
1.2
3.8
12
0.38
1.2
3.8
12
0.73
2.3
7.3
23
29 30
102

31 32
For transmitters rated at a maximum output power not listed above, the
recommended separation distance d in meters (m) can be determined using the
equation applicable to the frequency of the transmitter, where P is the maximum
output power rating of the transmitter in watts (W) according to the transmitter
manufacturer.
Note1: At 80MHz and 800MHz, the separation distance for the higher frequency
range applies
Note2: These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures, objects and
people.
CUSTOMER SUPPORT
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Product Demo Video
www.drtrustusa.com/102
CONTACT ADDRESS
USA
Nureca INC.USA
276 5th Avenue, Suite 704-397,
New York (NY) - 10001, USA
INDIA
Corporate Office (Mumbai)
Nureca Limited
128 Gala Number Udyog Bhavan,
1st Floor Sonawala Lane, Goregaon East
Mumbai City Maharashtra 400063
Contact us
India: [phone] /[phone]
Website: www.drtrust.in
Corp Website: www.nureca.com
Customer Care Executive Email: [e-mail]
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Remark
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abandon and disposal at will
Manufacturer’s name and address
Attention consult accompanying documents
Reading Instruction Book before use
Inapplicable baby
IP 22
ingress of water
Type BF equipment
Cuff Connector
TUV NO.
AC/DC Adapter