Jamr Technology W02 User manual

Fully Automatic Digital Wrist
Blood Pressure Monitor
Model Number: W02
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USER’S MANUAL
W02说明书:英文成册，材质：封面光面128g铜版纸，内页普通70g书写纸，尺寸： 90×65mm
Shanghai International Holding Corp. GmbH (Europe)
Eiffestrasse 80, 20537 Hamburg, Germany.
[email protected]
Version Number:1.0
Shenzhen Jamr Technology Co., Ltd.
A101-301, D101-201, Jamr Science & Technology Park, No. 2
Guiyuan Road, Guixiang Community, Guanlan Street, Longhua
District, 518100 Shenzhen, PEOPLE'S REPUBLIC OF CHINA.

CONTENTS
1.Introduction and Intended Use......................................................................................1
2.Important Information on Blood Pressure and its Measurement...................................4
3. Components of your blood pressure monitor................................................................6
4. Using your Monitor for the First Time........................................................................... 7
5.Measurement Procedure.............................................................................................10
6.Care and Maintenance................................................................................................20
7. Warranty..................................................................................................................... 21
8. Certifications...............................................................................................................27
9. Technical Specifications..............................................................................................21
10. EMC Declaration.......................................................................................................22

It enables reliable measurement of systolic and diastolic blood pressure as well as pulse
through the oscillometric method.
Before using, please read this instruction manual carefully and then keep it in a safe
place.
• Only a health-care professional is qualified to interpret blood pressure measurements.
• This device is NOT intended to replace regular medical checkups.
• Blood pressure readings obtained by this device should be verified before prescribing or
making adjustments to any medications used to control hypertension. Under no
circumstances should YOU alter the dosages of any drugs prescribed by your physician.
• This monitor is intended for use by adults only. Consult with a physician before using this
instrument on a child.
•In cases of irregular heartbeat , measurements made with this instrument should only be
evaluated after consultation with a physician.
• Host products, including accessories, shall be processed in accordance with local
regulations after reaching the life cycle.
1.Introduction and Intended Use
1.1 Remember…
Warning:
Warning:
Warning:
Warning:
Warning:
Warning:
Warning:
The device contains sensitive electronic components. Avoid strong electrical or
electromagnetic fields in the direct vicinity of the device (e.g. mobile telephones,
microwave ovens).These can lead to temporary impairment of the measuring
accuracy.
The use of other accessories other than those specified or provided by the
equipment manufacturer may cause electromagnetic radiation to increase or
decrease electromagnetic immunity resulting in operational failure.
This system may fail to yield specified measurement accuracy if operated or
stored in temperature or humidity conditions outside the limits stated in the
specifications section of this manual.
Remove the battery if the ME EQUIPMENT is not likely to be used for some time.
The user must check that the equipment functions safely and see that it is in
proper working condition before being used.
No modification of this equipment is allowed.
The device is not suitable for use in the presence of flammable anesthetic
mixtures with air or with oxygen or nitrous oxide.
Warning:
Warning:
This equipment shall not be serviced or maintained while in use with the patient.
The patient is an intended operator, the functions of monitoring blood pressure
and pulse rate can be safely used by patient. The routine clean and changing
batteries can be performed by the patient.
1.2 Warnings and Precautions

2.1. How does high or low blood pressure arise?
Your level of blood pressure is determined in the circulatory center of the brain and
adjusts to a variety of situations through feedback from the nervous system. To adjust
blood pressure, the strength and speed of the heart (Pulse), as well as the width of
circulatory blood vessels is altered.Blood vessel width is controlled by fine muscles in the
blood vessel walls.
Your level of arterial blood pressure changes periodically during heart activity: During the
“blood ejection” (Systole) the value is highest (systolic blood pressure value). At the end
of the heart’s “rest period” (Diastole) pressure is lowest (diastolic blood pressure value).
2.2. Which values are normal?
Please refer to the diagram below(Picture-01)
2.Important Information on Blood Pressure and its Measurement
Caution:
Caution:
Attention:
Attention:
Attention:
Attention:
To avoid damaging the device, keep this unit away from children and pets.
The standard material used for the bladder and tubing is latex-free.
Self-measurement means control, not diagnosis or treatment. Unusual values
must always be discussed with a physician. Under no circumstances should you
alter the dosages of any drugs prescribed by a physician.
The pulse display is not suitable for checking the frequency of heart
pacemakers!
In cases of irregular heartbeat, measurements made with this instrument should
only be evaluated after consultation with a physician.
The temperature of contact parts with the patient is as high as 41.3 ℃, and the
contact time is less than 10 minutes.
Note: To obtain the greatest accuracy from your blood pressure instrument, it is
recommended that the instrument be used within the specified temperature and
the relative humidity, please see the Technical Specifications.
Note: The cuff is treated as the applied part.The user should contact the manufacturer
for assistance, if needed, in setting up, using or maintaining the device.
Note: Do not attempt to service or repair this device yourself. Should a malfunction
occur, refer to local distributor or the manufacturer.

There are six grids in the display of device. Please refer to the picture-01-01. Different
grids represent different interval scales of WHO.
3.1. Measuring unit
3.2 The symbols on the LCD display
1. User A
3. Bluetooth symbol
5. Irregular heartbeat symbol
7.Average value symbol
9. Heartbeat symbol
11.WHO symbol
13. Diastolic blood pressure
2. User B
4. mute symbol
6. Low battery symbol
8. Date/Time display
10. Pulse display
12. Memory symbol
14.Systolic blood pressure
3. Components of your blood pressure monitor
Picture-01-01
Picture-01
LCD Display
Memory
Sart/Stop
Setting
Batter
Cell Cover
Wrist Cuff

3.3. Features of Model W02
1.Talking function 2. Double users: 2 x 120 sets memory
3.Date/time display 4. Irregular heartbeat checking
5. Average value function 6. Low battery display
7. WHO function 8. Auto power-off
9. Volume adjustment
4.1Activating the pre-installed batteries
Battery Installation
Use only 1.5V “AAA” alkaline batteries with this device.
1. Press the hook on the bottom of the battery cover and lift the cover off in the direction
of the arrow.
2. Install 2 “AAA” size batteries so the + (positive) and - (negative) polarities match the
polarities of the battery compartment, replace the battery cover.Make sure that the
battery cover is securely in position.
Battery replacement
Low Battery Indicator
1.When the Low Battery Indicator appears on the display, turn the monitor off and remove
all the batteries. Replace with 2 new batteries at the same time. Long-life alkaline
batteries are recommended.
2.To prevent the damage of monitor from leaked battery fluid, please take out of battery if
the monitor unused in a long time(generally more than 3 months). If battery fluid should
get in your eyes, immediately rinse with plenty of clean water. Contact a physician
immediately.
3. Dispose of the device, components and optional accessories according to applicable
local regulations. Unlawful disposal may cause environmental pollution.
4.2. System Settings
After you load the battery ,long press the SET button for more than 3s, and then you can
start to set.
Setting the User:
Press the MEM button to select User A or User B. When display A (/B) on the screen,
press the MEM button to switch to user B (/A). Press the SET button to confirm.
4.Using your Monitor for the First Time

5.1. Before measurement:
• Avoid eating and smoking as well as all forms of exertion directly before measurement.
These factors influence the measurement result. Find time to relax by sitting in an
armchair in a quiet atmosphere for about ten minutes before taking a measurement.
• Remove any garment that fits closely to your wrist.
• Always measure on the same wrist (normally left).
5. Measurement Procedure
Setting the Year:
When the year display is flashing, press the MEM button continuously and it will increase
continuously 1 by 1 until 2049, and then return the original year , once the year set is OK,
press SET button to confirm.
Setting Month/Date:
Initial Month/Date is 1/01, when the Month display is flashing, press the MEM button, the
month will increase by 1, press SET button to confirm, and do in the same way to set the
date. Press SET button to confirm.
Setting Time :
When the hour display is flashing, press the MEM button, the hour will increase by 1,
press SET button to confirm, and do in the same way to set the minute. Press SET button
to confirm.
Setting Volume:
When display with SP is flashing, press MEM button to switch ON or OFF. Press SET
button to confirm.
C.Record Delete:
When you checking the memory data, long press MEM button to delete existing user
measurement data.
Note:
You can’t delete all measurement record from the monitor storage at one time, if you
decide to delete the all record, please keep the record in another way, in case you need
it some days later. Take the battery out won’t lead to a record missing.
5.2. Fitting the Cuff
Please refer to picture-04
a) Remove all jewelry and watches. The palm of your hand should be facing you. Apply
the cuff so that the display is facing you.
b) The distance between the cuff and the hand should be 1cm.
c) Secure the cuff with the hook and loop adhesive so that it lies comfortably and not too
tight. It should be comfortable.
d) Lay your arm on a table with your palm upwards. Support your arm with a cushion so
that the cuff rests at about the same height as the heart. Remain still for 2 minutes, sitting
quietly, before beginning a measurement.

5.3. Measure Procedure
Refer to picture-05
The monitor is designed to take measurements and store the measurement values in
memory for two people using User ID A and User ID B.
1. Sit comfortably in a chair with your feet flat on the floor.
2. Select your User ID (A or B).
Stretch your arm forward on the desk and keep relaxing, make sure the palm of hand is
upturned. Make sure wrist is in correct position, to avoid body movement. Sit still and do
not talk or move during the measurement.
After the cuff has been appropriately positioned on the wrist and connected
to the blood pressure monitor, the measurement can begin:
a) Press the START/STOP button. The pump begins to inflate the cuff. In the display, the
increasing cuff pressure is continually displayed.
b) After automatically reaching an individual pressure, the pump stops and the pressure
slowly falls. The cuff pressure is displayed during the measurement.
c) When the device has detected your pulse, the heart symbol in the display begins to blink.
d) When the measurement has been concluded, the measured systolic and diastolic blood
pressure values, as well as the pulse will be displayed.
e) The measurement results are displayed until you switch the device off. If no button is
pressed for 60 seconds, the device switches off automatically.
NOTE:
Patient Position:
1) Comfortably seated
2) Legs uncrossed
3) Feet flat on the floor
4) Back and arm supported
5) Middle of the CUFF at the level of the right atrium of the heart
Recommended Use Methods
1.Recommendation that the PATIENT relax as much as possible and not talk during the
measurement PROCEDURE
2.Recommendation that 5 min should elapse before the first reading is taken
Picture-04

3.Any reading can be affected by the measurement site, the position of the PATIENT,
exercise, or the PATIENT’S physiologic condition
4.Performance of the AUTOMATED SPHYGMOMANOMETER can be affected by
extremes of temperature, humidity and altitude
5.To stop the inflation or measurement, push the START/STOP button. The
monitor will stop inflating, start deflating, and will turn off.
6.After the monitor has detected your blood pressure and pulse rate, the cuff
automatically deflates. Your blood pressure and pulse rate are displayed.
7.The monitor will automatically turn off after one minute.
5.4. Irregular Heartbeat Detector
This symbol - indicates that certain pulse irregularities were detected during the
measurement.
In this case, the result may deviate from your normal basal blood pressure – repeat the
measurement.
Information for the doctor on frequent appearance of the Irregular Heartbeat Symbol.
This instrument is an oscillometric blood pressure monitor device that also analyzes
pulse frequency during measurement. The instrument is clinically tested.
If pulse irregularities occur during measurement, the irregular heartbeat symbol is
displayed after the measurement. If the symbol appears more frequently (e.g. several
times per week on measurements performed daily) or if it suddenly appears more often
than usual, 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.
Picture-05
Keep the machine at the same
height as the heart when measuring

5.6. Error Indicates
SYMBOL CAUSE CORRECTION
No display
appears Weak battery or improper placement
Sensor abnormal
Monitor could not detect pulse wave
or cannot calculate the blood pressure
data
Measurement result is abnormal
(SYS≦45mmHg, DIA≦24mmHg)
Too loose cuff or air leakage
(Cannot inflate to 30mmHg within 15s)
The air tube is crimped
The sensor is sensing great fluctuation
in the pressure
The pressure that the sensor sensing
is over the limit
The demarcation is incorrect or the
device has not been demarcated
Please send back to the local distributor
Please send back to the local distributor
Correct it and make the measurement again
Please keep quiet and don’t move
Tie the cuff correctly and make sure the air plug is properly
inserted in the unit
Check if the air releasing is too slow or not. If it is too slow,
please check if there is any dust in the tube plug of the cuff
and the cuff port in the device. If yes, please clean and
start the measurement again. If no, please send the device
back to the local distributor.
Occasionally-measure for one more time/ Always - send it to
local distributor
The following symbol will appear on the display when measuring abnormal.
Replace both batteries with new ones. Check the battery
installation for proper placement of the battery polarities.
Check if the pump is working or not. If it is working, then
the problem is sensor abnormal. Please send it to the local
distributor.
Trouble removal
Er1
Er2
Er3
Er4
Er5
Er6
Er7
Er8

SYMBOL DESCRIPTIONSt
The following symbols may appear in this manual, on the Digital Blood Pressure Monitor
W02, or on it's accessories. Some of the symbols represent standards and compliances
associated with the Digital Blood Pressure Monitor W02 and its use.
5.6. Memory
At the end of a measurement, this monitor automatically stores each result with date and
time. Each unit stores 120 sets measurements for 2 users, totally 240 sets（User A and
B）.
Viewing the stored values
With the unit off, press the Memory button. The display first shows "A", then shows an
average of all measurements stored in the unit. Please note: Measurements for each
user are averaged and stored separately. Be certain that you are viewing the
Authorized Representative in the European Community
CE Mark: conforms to essential requirements of the Medical Device Directive
93/42/EEC.
Date of manufacture.
Manufacturer
Specifies serial number
Type BF applied part
Direct current
DISPOSAL: Do not dispose this product as unsorted municipal waste. Collection
of such waste separately for special treatment is necessary.
Follow instructions for use
Keep dry
Fragile
Avoid the sun
Handle gently
Temperature range
No Sterilize requirement
Not category AP / APG equipment
Mode of operation: continuous
Put up

Wash hands after each time measurement.
If one device is used by different patients, wash hands before and after each use.
a) Do not expose the device to either extreme temperatures, humidity, dust or direct
sunlight.
b) The cuff contains a sensitive air-tight bubble. Handle this cuff carefully and avoid all
types of stress through twisting or buckling.
c) Clean the device with a soft, dry cloth. Do not use gas, thinners or similar solvents.
Spots on the cuff can be removed carefully with a damp cloth and soapsuds. The cuff with
bladder must not be washed in a dishwasher, clothes washer, or submerged in water.
d) Handle the tube carefully. Do not pull on it. Do not allow the tubing to kink and keep it
away from sharp edges.
e) Do not drop the monitor or treat it roughly in any way. Avoid strong vibrations.
f) Never open the monitor! This invalidates the manufacturer’s warranty.
g) Batteries and electronic instruments must be disposed of in accordance with the locally
applicable regulations, not with domestic waste.
6.1. Accuracy test
Sensitive measuring devices must be checked for accuracy from time to time. We
recommend a periodical inspection of your unit by an authorized dealer every 1 year.
Please turn to local distributor or the manufacturer.
6. Care and Maintenance
measurements for the correct user. Pressing the Memory button again displays the
previous value. To view a particular stored memory, press and hold the Memory button to
scroll to that stored reading.
5.7. Discontinuing a Measurement
If it is necessary to interrupt a blood pressure measurement for any reason (e.g the
patient feels unwell), the Start/Stop button can be pressed at any time. The device then
immediately lowers the cuff pressure automatically.
5.8. Battery Change Indicator
Batteries discharged– replacements required
When the batteries are discharged, the battery symbol will flash as soon as the
instrument is switched on. You cannot take any further measurements and must replace
the batteries.
The battery compartment is located on the back side of the unit.
a) Remove cover from the bottom plate, as illustrated below picture-06
b) Insert the batteries (2 x size AA A). Always use AAA long life batteries or alkaline 1.5v
batteries.
c) The memory retains all values although date
and time must be reset - the year number
therefore flashes automatically after the
batteries are replaced.
d) To set date and time, follow the procedure
described in Section 4.2. Picture-06
Battery
Push back

Your blood pressure monitor is guaranteed for 1 year against manufacturers’ defects for
the original purchaser only, from date of purchase. The warranty does not apply to
damage caused by improper handling, accidents, professional use, not following the
operating instructions or alterations made to the instrument by third parties.
Warranty only applies to the main device and its cuff. All other accessories are not
covered by warranty.
There are no user serviceable parts inside. Batteries or damage from old batteries is not
covered by the warranty.
Note: According to international standards, your monitor should be checked for accuracy
every year.
7. Warranty
8. Certifications
Model: W02
Weight: 101g (Batteries are not included)
Display: 41.5*49.5mm 【1.63"x1.95"】LCD Digital Display
Size: 68 (W) x 68 (L) x 30 (H) mm【2.68"(W)x2.68"(L)x1.18"(H)】
Accessories: 1×Main Device, 1×Cuff, 1×Users manual,
Operating Conditions: Temperature: 5℃to 40℃;Humidity: 15% to 93% RH;
Storage And Shipping Conditions:Temperature: -25℃to 70℃; Humidity: ≤93%RH
Atmospheric pressure range：70kPa~106kPa
Measuring method: Oscillometric
Pressure sensor: Resistive
Measuring range: DIA: 40-130mmHg; SYS: 60-230mmHg
Pulse: 40 to 199 per minute
Cuff pressure display range:<300mmHg
Memory: Automatically stores the last 120 measurements for 2 users (total 240)
Measuring resolution: 1 mmHg
Accuracy: Pressure within ± 3 mmHg / pulse ± 5 % of the reading
Power source: 2*AAA batteries, 1.5 V
Cuff : 4.92”-8.64” (12.5-21.5cm)
Automatically power off : 60 seconds
Users: Adult
Expected service life of the device and accessories: 5 years
Technical alterations reserved!
9. Technical Specifications
Device standard:
This device is manufactured to meet the European blood pressure monitors:
IEC 80601-2-30 / IEC60601-1-11 / IEC60601-1
Electromagnetic compatibility:
Device fulfills the stipulations of the International standard
IEC60601-1-2

10. EMC Declaration Technical description
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
Table 1
The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare environments and so on.
Warning: Don’t near 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 specified or provided by the
manufacturer of this equipment could result in increased electromagnetic emissions or decreased
electromagnetic immunity of this equipment and result in improper operation.”
Warning: Portable RF communications equipment (including peripherals such as antenna cables
and external antennas) should be used no closer than 30 cm (12 inches) to any part of the Blood
Pressure Monitor (model: W02), including cables specified by the manufacturer. Otherwise,
degradation of the performance of this equipment could result.
If any: a list of all cables and maximum lengths of cables (if applicable), transducers and other
ACCESSORIES that are replaceable by the RESPONSIBLE ORGANIZATION and that are likely to
affect compliance of the ME EQUIPMENT or ME SYSTEM with the requirements of Clause
7 (EMISSIONS) and Clause 8 (IMMUNITY). ACCESSORIES may be specified either
generically (e.g. shielded cable, load impedance) or specifically (e.g. by MANUFACTURER and
EQUIPMENT OR TYPE REFERENCE).
If any：the performance of the ME EQUIPMENT or ME SYSTEM that was determined to be
ESSENTIAL PERFORMANCE and a description of what the OPERATOR can expect if the
ESSENTIAL PERFORMANCE is lost or degraded due to EM DISTURBANCES (the defined
term “ESSENTIAL PERFORMANCE” need not be used).
Guidance and manufacturer’s declaration - electromagnetic emissions
Emissions test
RF emissions
CISPR 11
Group 1
Class B
Not applicable
Not applicable
RF emissions
CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Compliance

Guidance and manufacturer’s declaration - electromagnetic Immunity
Immunity Test
Electrostatic discharge (ESD)
IEC 61000-4-2
Power supply lines：±2 kV
input/output lines：±1 kV
±8 kV contact
±2 kV, ±4 kV, ±8 kV, ±15 kV air
±8 kV contact
±2 kV, ±4 kV, ±8 kV, ±15 kV air
Not application
line(s) to line(s)：±1 kV.
line(s) to earth：±2 kV.
100 kHz repetition frequency
0% 0.5 cycle At 0º, 45 º, 90 º, 135 º,
180 º, 225 º, 270 º and 315 º
0% 1 cycle And 70% 25/30 cycles
Single phase: at 0
0% 300 cycle
Not application
Not application
Electrical fast transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips, short interruptions
and voltage variations on power
supply input lines
IEC 61000-4-11
Power frequency magnetic field
IEC 61000-4-8
Conduced RF
IEC61000-4-6
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
150KHz to 80MHz：3Vrms
6Vrms (in ISM and amateur radio bands)
80% Am at 1kHz
Not application
30 A/m
50Hz/60Hz
30 A/m
50Hz/60Hz
IEC 60601-1-2 Test level Compliance level
WLAN 802.11
a/n
Pulse
Modulation
217 Hz
5100-5800
0.2 0.3 9
5240
5240
5785
Guidance and manufacturer’s declaration - electromagnetic Immunity
Test
Frequency
(MHz)
385
450
710
745
780
810
870
930
704-787
800-960
2450
2400-2570
Bluetooth,
WLAN
802.11 b/g/n,
RFID 2450,
LTE Band 7
Pulse
Modulation
217 Hz
GSM 1800;
CDMA 1900;
GSM 1900;
DECT;
LTE Band 1,3
4,25;UMTS
Pulse
Modulation
217 Hz
1700-1990
GSM 800/900,
TETRA 800,
iDEN 820,
CDMA 850,
LTE Band 5
Pulse
modulation
18 Hz
LTE Band 13,17 Pulse Modulation
217 Hz
GMRS 460,
FRS 460
FM ±5 kHz deviation
1 kHz sine
380-390
380-390
TETRA 400 Pulse Modulation 18 Hz 1.8 0.3 27
2 0.3 28
2 0.3 28
2 0.3 28
2 0.3 28
0.2 0.3 9
Band
(MHz) Service MoModulation Modulation (W)
Distance
(m)
IMMUNITY
TEST LEVEL
(V/m)
1720
1845
1970
NOTE UT is the a.c. mians voltage prior to application of the test level.
Radiated RF
IEC61000-4-3
(Test specifications
for ENCLOSURE
PORT IMMUNITY
to RF wireless
communications
equipment)
Table 3
Table 2