Lanaform WBPM-110 User manual

ENGLISH
Presentation
Thank you for choosing the WBPM-110 from Lanaform.
Pleasereadall the instructionsbeforeusing
your product, particularly these basic safe-
ty instructions.
The photographs and other images of the product
in this manual and on the packaging are as accu-
rate as possible, but do not claim to be a perfect
reproduction of the product.
Contents
01 Important information
02 Contents and display indicators
03 Intended use
04 Contraindication
05 Package contents
06 Product description.
07 Specications
08 Notice
09 Setup and operating procedures
10 Maintenance
11 Explanation of symbols on unit
12 Limited warranty
13 Service center
14 Electromagnetic compatibility information
15 Advice regarding the disposal of waste
01. Important information
Normal Blood Pressure Fluctuation
All physical activity, excitement, stress, eating,
drinking, smoking, body posture and many other
activities or factors (including taking a blood pres-
sure measurement) will inuence blood pressure
value. Because of this, it is mostly unusual to ob-
tain identical multiple blood pressure readings.
Blood pressure uctuates continually, day and
night. The highest value usually appears in the
daytime and lowest one usually at midnight. Typi-
cally, the value begins to increase at around 3:00AM,
and reaches to highest level in the daytime while
most people are awake and active.
Considering the above information, it is recom-
mended that you measure your blood pressure at
approximately the same time each day.
Too frequent measurements may cause injury due
to blood ow interference, please always relax a
minimum moment of 1 to 1.5 minutes between meas-
urements to allow the blood circulation in your arm
to recover. It is rare that you obtain identical blood
pressure readings each time.
02. Contents and display indicators
1
2
3
4
6
7
8
5
1313
1111
1010
1212
99
202010LA090207002 · 27/08/20 · 3

4· 202104LA090207003 · 09/02/21
01 Day and time display
02 Systolic
03 Diastolic
04 Pulse rate
05 Irregular heartbeat symbol
06 Low battery indicator
07 The pressure in cu is instable,
or much remnant air in cu
08 Blood pressure level classication indicator
09 Blood pressure level classication indicator
10 MEM button
11 START button
12 LCD
13 Cu
03. Intended Use
FullyAutomaticElectronicSphygmomanometeris
for use by medical professionals or at home and is a
non-invasiveblood pressuremeasurement system
intended tomeasurethediastolicandsystolicblood
pressures and pulse rate of an adult individual by
using a non-invasive technique in which an inat-
able cu is wrapped around the wrist.
04. Contraindication
It is inappropriate for people with serious
arrhythmia to use this Electronic Sphygmo-
manometer.
05. Package contents
01 Manual
02 Wrist blood pressure monitor
03 Battery 2×AAA
06. Product Description
Based on Oscillometric methodology and silicon in-
tegrated pressure sensor, blood pressure and pulse
ratecanbe measuredautomaticallyandnon-inva-
sively. The LCD display will show blood pressure and
pulse rate. The most recent 2×60 measurements can
be stored in the memory with date and time stamp.
The Electronic Sphygmomanometer corresponds to
the below standards: IEC 60601-1Edition 3.1 2012-08/
EN 60601-1:2006/A1:2013(Medical electricalequip-
ment — Part 1: General requirements for basic safety
and essential performance), IEC60601-1-2:2014/
EN60601-1-2:2015 (Medical electrical equipment
— Part 1-2: General requirements for basic safety
and essential performance - Collateral standard:
Electromagneticcompatibility -Requirementsand
tests), IEC80601-2-30:2009+AMD1:2013/EN 80601
2-30:2010/A1:2015(Medicalelectrical equipment –
Part 2-30: Particular requirements for the basic
safety and essential performance of automated
non-invasive sphygmomanometers)EN 1060-1:
1995 + A2: 2009 (Non-invasive sphygmomanom-
eters - Part 1: General requirements), EN 1060-3:
1997 + A2: 2009 (Non-invasive sphygmomanom-
eters - Part 3: Supplementary requirements for
electro mechanical blood pressure measuring
systems);ISO81060-2:2013(Non-Invasive Sphy-
gmomanometers - Part 2: Clinical Validation Of
Automated Measurement Type).
07. Specications
01 Product name: WBPM-110
02 Model: LA090207
03 Classication: Internally powered, Type BF
applied part, IP22, No AP or APG, Continu-
ous operation
04 Machine size: Approx. 83mm × 74mm ×26mm
(3 9/32” ×2 29/32” ×1 1/32”)
05 Cu circumference: 14cm-19.5cm
(5 1/2”-7 11/16”)
06 Weight: Approx. 71g (2 1/2oz.) (exclude bat-
teries and cu)
07 Measuring method: Oscillometric method, au-
tomatic ination and measurement
08 Memory volume: 2×60 times with time and
date stamp

202104LA090207003 · 09/02/21 · 5
09 Power source: batteries: 2×1.5V SIZE AAA
10 Measurement range:
a Cu pressure: 0-300mmHg
b Systolic: 60-260mmHg
c Diastolic: 40-199mmHg
d Pulse rate: 40-180 beats/minute
11 Accuracy:
a Pressure: ±3mmHg
b Pulse rate: ±5%
12 Environmental temperature for operation:
10°C~40°C (50°F~104°F)
13 Environmental humidity for operation: ≤85%RH
14 Environmental temperature for storage and
transport: -20°C~50°C (-4°F~122°F)
15 Environmental humidity for storage andtrans-
port: ≤85%RH
16 Environmental pressure: 80kPa-105kPa
17 Battery life: Approx. 200 times.
18 All components belonging to the pressure meas-
uring system, including accessories: Pump,Valve,
LCD, Cu, Sensor
These specications are sub-
ject to change without notice.
08. Notice
01 Read all of the information in the operation
guide and any other literature in the box be-
fore operating the unit.
02 Stay still, calm and rest for 5 minutes before
blood pressure measurement.
03 The cu should be placed at the same lev -
el as your heart.
04 During measurement, neither speak nor move
your body and arm.
05 Measuringon left wristforeach measurement.
06 Please always relax at least 1 or 1.5 minutes
between measurements to allow the blood
circulation in your arm to recover. Prolonged
over-ination (cu pressure exceed 300 mmHg
or maintained above 15 mmHg for longer than
3 minutes) of the bladder may cause ecchy-
moma of your arm.
07 Consult your physician if you have any doubt
about below cases:
a The application of the cu over a wound or
inammation diseases;
b The application of the cu on any limb where
intravascular access or therapy, or an arter-
io-venous (A-V) shunt, is present;
c The application of the cu on the arm on the
side of a mastectomy;
d Simultaneously used with other monitor-
ing medical equipments on the same limb;
e Need to check the blood circulation of the user.
08 This Electronic Sphygmomanometer is de-
signed for adults and should never be used on
infants or young children. Consult your physi-
cian or other health care professionals before
use on older children.
09 Do not use this unit in a moving vehicle; this may
result in erroneous measurement.
10 Blood pressure measurements determined by
this monitor are equivalent to those obtained
by a trained observer using the cu/stethoscope
auscultationmethod,withinthelimits prescribed
by the American National Standard Institute,
Electronic or automated sphygmomanometers.
11 Information regarding potential electromag-
netic or other interference between the blood
pressure monitor and other devices together
with advice regarding avoidance of such in-
terference please see part ELECTROMAGNETIC
COMPATIBILITY INFORMATION. It is suggested
that the blood pressure monitor be kept 30 cm
away from other wireless devices, such as WLAN
unit, cell phone, microwave oven, etc. It can’t be
used near active HF SURGICAL EQUIPMENT and

6· 202104LA090207003 · 09/02/21
the RF shielded room of an ME SYSTEM for mag-
neticresonance imaging, where the intensity of
EM DISTURBANCES is high.
12 If Irregular Heartbeat (IHB) brought by com-
mon arrhythmias is detected in the procedure
of blood pressure measurement, a sig-
nal will be displayed. Under this condition,
the Electronic Sphygmomanometers can
keep function, but the results may not be ac-
curate, it’s suggested that you consult with
your physician for accurate assessment.
There are 2 conditions under which the signal of
IHB will be displayed:
a The coecient of variation (CV) of pulse
period >25%.
b The dierence of adjacent pulse period≥0.14s,
and the number of such pulse takes more than
53 percentage of the total number of pulse.
13 Please do not use the cu other than supplied
by the manufacturer, otherwise it may bring
biocompatible hazard and might result in meas-
urement error.
14 The monitor might not meet its performance
specications or cause safety hazard if stored
or used outside the specied temperature and
humidity ranges in specications.
15 Please do not share the cu with other infec-
tive person to avoid cross-infection.
16 This equipment has been tested and found to
comply with the limits for a Class B digital de-
vice, pursuant to part 15 of the FCC Rules. These
limits aredesignedtoprovide reasonable protec-
tionagainstharmfulinterference inaresidential
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 harmfulinterference toradioor television
reception, which can be determined by turning
the equipment o and on, the user is encouraged
to try to correct the interference by one or more
of the following measures:
a Reorient or relocate the receiving antenna.
b Increase the separation between the equip-
ment and receiver.
c Connect the equipment into an outlet on a
circuit dierent from that to which the re-
ceiver is connected.
d Consult the dealer or an experienced radio/
TV technician for help.
17 Measurementsare notpossibleinpatients with
a high frequency of arrhythmias.
18 The device is not intended for use on neonates,
children or pregnant women. (Clinical testing
has not been conducted on neonates, children
or pregnant women.)
19 Motion, trembling, shivering may aect the
measurement reading.
20 The device would not apply to the patients with
poorperipheralcirculation,noticeablylowblood
pressure, or low body temperature (there will be
low blood ow to the measurement position).
21 The device would not apply to the patients who use
an articial heart and lung (there will be no pulse)
22 Consult your physician before using the device for
any of the following conditions: common arrhyth-
mias such as atrial or ventricular premature beats
or atrial brillation, arterial sclerosis, poor per-
fusion,diabetes, pre-eclampsia,renaldiseases.
23 The patient can be an intended operator.
24 This device complies with part 15 of the FCC
Rules. Operation is subject to the following two
conditions: (1) This device may not cause harm-
ful interference, and (2) this device must accept
anyinterference received, includinginterference
that may cause undesired operation.

202104LA090207003 · 09/02/21 · 7
25 Attention that changes or modication not ex-
pressly approved by the party responsible for
compliance could void the user’s authority to
operate the equipment.
26 Swallowing batteries and/or battery uid can
be extremely dangerous. Keep the batteries
and the unit out of the reach of children and
disabled persons.
27 Ifyouareallergictoplastic/rubber,pleasedon’t
use this device.
09. Setup And Operating Procedures
01 Battery Loading
a Open battery cover at the back of the monitor.
b Load two AAA size batteries. Please pay at-
tention to polarity.
c Close the battery cover.
When LCD shows battery symbol , re-
place all batteries with new ones.
Rechargeable batteries are not suit-
able for this monitor.
Remove the batteries if the monitor will not
be used for a month or more to avoid rel-
evant damage of battery leakage.
Avoid the battery uid to get in your eyes. If it
should get in your eyes, immediately rinse with plen-
ty of clean water and contact a physician.
The monitor, the batteries and the cu, must
be disposed of according to local regulations
at the end of their usage.
02 Clock And Date Adjustment
a Once you install the battery or turn o the
monitor, it will enter Clock Mode, and LCD will
display time and date. See picture 2.
b While the monitor is in Clock Mode, press
the START and MEM button simulta-
neously for two seconds, then release the
buttons, the monitor will be in Clock and
Date Adjustment Mode.
c In Clock and Date Adjustment Mode, the time
format will blink at rst. See picture2-1.
While time format is blinking, press the
button MEM to change the time format.
The default time format is 24h.
d Pressthebutton START repeatedly,theyear
(range is 2018~2099), month, day, hour and
minute will blink in turn. See picture2- 2&2-3
& 2-4 & 2-5 & 2-6. While the number is blink-
ing, press the button MEM toincrease the
number, keep on pressing the button MEM ,
the number will increase faster.
e During adjusting clock and date, the monitor
will go back to Clock Mode automatically when
no button will be pressed within 60 seconds.
f You can turn off the monitor by press-
ing START button when the minute is
blinking, then the time and date is conrmed.

8· 202104LA090207003 · 09/02/21
Note
01 The clock format could be set by user.
02 Table 2-1 instructs the conversion relations
between 24hour format and 12hour format.
Table 2-1
24 HOUR
FORMAT
12 HOUR
FORMAT
24 HOUR
FORMAT
12 HOUR
FORMAT
0:00 12:00 AM 12:00 12:00 PM
1:00 1:00 AM 13:00 1:00PM
2:00 2:00 AM 14:00 2:00 PM
3:00 3:00 AM 15:00 3:00 PM
4:00 4:00 AM 16:00 4:00 PM
5:00 5:00 AM 17:00 5:00 PM
6:00 6:00 AM 18:00 6:00 PM
7:00 7:00 AM 19:00 7:00 PM
8:00
8:00 AM
20:00
8:00 PM
9:00
9:00 AM
21:00
9:00 PM
10:00
10:00 AM
22:00
10:00 PM
11:00
11:00 AM
23:00
11:00 PM
03 Connecting The Cu To The Monitor
The cu is attached to the monitor when it is pack-
aged. Should the cu become unattached, align the
two plugs and four brackets of the cu with the
plug sockets and bracket sockets of the monitor
and press the cu to the monitor until the plugs
and brackets are securely attached.
04 Applying The Cu
a Place the cu around a bare wrist 1-2cm above
the wrist joint on the palm side of the wrist.
b While seated, place the arm with the cued
wrist in front of your body on a desk or table
with the palm up. If the cu is correctly placed,
you can read the LCD display.
c The cu must be neither too tight nor too loose.
Note
d Please refer to the cu circumference range
in “SPECIFICATIONS” to make sure that the
appropriate cu is used.
e Measuring on left arm each time.
f Do not move your arm, body, or the moni-
tor and do not move the rubber tube during
measurement.
g Stay quiet, calm for 5 minutes before blood
pressure measurement.
h Please keep the cu clean. Clean the cu
by wet soft cloth and mild detergent if the
cu becomes dirty. Do not remove the cu
from the monitor. Clean the cu after the
usage of every 200 times is recommended.

202104LA090207003 · 09/02/21 · 9
Do not place the cu around your arm if the
arm has any inammation, acute diseases,
infections skin wounds.
05 Body Posture During Measurement
Sitting Comfortably Measurement
a Be seated with your feet at on the oor,
and don’t cross your legs.
b Place palm upside in front of you on a at
surface such as a desk or table, with your
elbow resting on a chair or table
c The middle of the cu should be at the lev-
el of the right atrium of the heart.
06 Taking Your Blood Pressure Reading
a After applying the cu and your body is in a com-
fortable position, press the START button.
All display characters are shown for self-test.
You can check the LCD display according to the
picture.Pleasecontact the service centerifseg -
ment is missing. See picture 6-1.
b Then the current memory bank is blink. See
picture 6-2. Press MEM buttontochange
over to other bank. Conrm your selection by
pressing START button. The current bank
can also be conrmed automatically after 5
seconds with no operation.
c If the monitor has stored results, the LCD
will momentarily display the most recent one.
See picture 6-3. If no result has been stored,
zero will appear on LCD. See picture 6-4.
d Then the monitor starts to seek zero pres-
sure. See picture 6-5.
e Then the monitor inates the cu until su-
cient pressure has built up for a measurement.
Then the monitor slowly releases air from
the cu and carries out the measurement.
Finally the blood pressure and pulse rate
will be calculated and displayed on the LCD
screen. The blood pressure classication
indicator and Irregular heartbeat symbol
(if any) will blink on the screen. See pic-
ture 6-6. The result will be automatically
stored in the monitor.
f After measurement, the monitor will turn o
automaticallyafter 1minute ofno operation.
Alternatively, you can press the START but-
ton to turn o the monitor manually.
g During measurement, you can press
the START button to turn o the mon-
itor manually.
Please consult a health care professional for in-
terpretation of pressure measurements.

10 · 202104LA090207003 · 09/02/21
07 Displaying Stored Results
a In Clock Mode, press MEM button, the
monitor will display sign of current group.
The amount of results in current user mem-
ory zone will be displayed. See picture 7-1.
Press START button to switch group,
press MEM to conrm current group. The
current bank can also be conrmed auto-
matically after 5 seconds with no operation.
b Then LCD will display the average value of all
results in the current bank. See picture 7-2. If
no result stored in the current user memory
zone, LCD will display “0” for blood pressure
and pulse rate. See picture 7-3.
c Press MEM button, the LCD will display the
average value of the last three results in the
current user memory zone. See picture 7-4. If
no result stored in the current user memory
zone, LCD will display “0” for blood pressure
and pulse rate. See picture 7-5.
d Press MEM but ton again, the memory num-
ber in the current user memory zone will be
displayed. See picture 7-6. If the monitor has
no result stored in the current user memory
zone, the LCD will display “0”. See picture 7-7.
e Then the most recent result will be displayed
with date and time stamp. See picture 7-8. Ir-
regular heartbeat symbol (if any) and blood
pressure classication indicator will blink
at the same time. Press MEM button re-
peatedly to review the results measured
previously. If the monitor has no result stored
in the current user memor y zone, the LCD will
display “0” for blood pressure and pulse rate.
See picture 7-9.
f When displaying the stored results, the moni-
tor will turn o automatically after 1 minutes
of no operation. You can also press the but-
ton START to turn o the monitor manually.
08 Deleting Measurements From The Memory
When any result is displaying (exclude average value
displaying), keeping on pressing button MEM for
three seconds, all results in the current bank will be
deleted. See picture 8. Press the button START ,
the monitor will be turned o.
09 Assessing High Blood Pressure For Adults
The following guidelines for assessing high blood
pressure (without regard to age or gender) have
been established by the World Health Organiza-
tion (WHO). Please note that other factors (e.g.
diabetes, obesity, smoking, etc.) need to be tak-
en into consideration. Consult with your physician
for accurate assessment, and never change your
treatment by yourself.