HealthSmart 04-825-001 User manual

Women’s Wrist Digital BlooD
Pressure monitor
Please read this guidebook
completely before operating the unit.
Item # 04–825–001
English • Spanish
instruction manual
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1
limiteD 5-year Warranty
The warrantor guarantees that its Digital Blood Pressure Monitor will be free from
manufacturing defects under normal use for 5 years from the original purchase date. This
warranty covers only normal use, and does not apply for use in any clinical or commercial
applications. This warranty does not cover batteries or other power sources that may be
provided with or used with the Digital Blood Pressure Monitor. The warranty is voided if
the Digital Blood Pressure Monitor product is misused or abused in any manner.
If the Digital Blood Pressure Monitor fails to operate during the first 5 years from the
time originally purchased, please call our Customer Care Help Line at 800-622-4714
and we will try to resolve the issue as soon as possible. If the warrantor determines
the unit failed to operate due to a manufacturing defect, the unit will be replaced at the
option of the warrantor. Replacement is the sole remedy under this limited warranty.
This warranty gives you specific legal rights, which vary from state to state. As a
condition of this warranty, register your product online within 10 days of purchase
date at www.LiveHealthSmart.com.
This warranty constitutes the warrantor’s only responsibility and obligation to replace
materials or components. We make no other express or implied warranties, arising by
operation of law or otherwise, or any warranty of merchantability or fitness for a particular
use or purpose whether or not the use or purpose has been disclosed to the warrantor
in specifications, drawings or otherwise, and whether or not the warrantor’s products
are specifically designed and/or manufactured by the warrantor for the buyer’s use
or purposes, except for the limited warranty stated above. The warrantor will not be
responsible for any indirect, incidental, special, consequential, or punitive damages or
other loss, including, but not limited to, damage to or loss of other property or equipment
and personal injuries, whether to purchaser or others. The warrantor shall in no event be
liable to the purchaser for any amount in excess of the cost of repair and/or replacement
of the unit.
inDeX
Introduction ................................ 2
Product Identification & Caution ...................... 3
General Blood Pressure Information ....................4–6
Important Information Before Use .................... 7–9
World Health Organization (WHO) Indicator ................. 10
Irregular Heartbeat Detection ....................... 11
Battery Installation/Replacement ..................... 12
Setting the Date/Time .......................... 13
Applying Your Blood Pressure Cuff .................. 14–15
Taking Your Blood Pressure Reading.................. 16–17
Recalling Measurements in Memory .................... 18
Description of Symbols ........................ 19–21
Troubleshooting ............................. 22
Care and Maintenance .......................... 23
Product Specifications ........................ 24–31
Sample Blood Pressure Logs ....................... 32
Blood Pressure Log ........................... 33
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2 3
introDuction
Thank you for purchasing a Digital Blood Pressure Monitor. With proper care and use,
your monitor will provide you with many years of reliable readings.
To achieve the maximum benefit from your blood pressure monitor, we recommend
that you first consult with your physician or trained healthcare professional.
The method of measurement that your Monitor uses is called the oscillometric
method. The monitor detects your blood’s movement through the artery in your wrist
and converts the movements into a digital reading. The oscillometric method does not
require a stethoscope, making the monitor easy-to-use. The preformed cuff requires
little effort to apply and is comfortable to wear.
Clinical research has proven a direct relationship between blood pressure in the
wrist and blood pressure in the arm. Because the arteries in the wrist and arm are
connected, changes in wrist blood pressure reflect changes in arm blood pressure.
Frequent wrist blood pressure measurements will provide you and your physician with
an accurate indication of change in your true blood pressure.
People with severe hypertension, severe arteriosclerosis or severe diabetes should
consult their physician about monitoring blood pressure at the wrist.
Blood pressure readings determined with this device are equivalent to measurements
obtained by a trained observer using the cuff/stethoscope auscultation method, within
the limits prescribed by the American National Standard for Electronic or Automated
Sphygmomanometers.
ProDuct iDentification
CAUTION
While taking a measurement, you can stop the inflation or deflation process of the cuff at
any time by pressing the POWER button.
SYS
DIA
mmHg
mmHg
PUL/min
M
Arm Cuff Digital Display
Digital DisplayBattery Compartment
POWER
(on/off)
button
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4 5
development, certain medications or even the time of day can influence blood pressure.
Influences such as sleep or relaxation decrease blood pressure, while anxiety or exercise
increase blood pressure.
Why Monitor Your Blood Pressure at Home?
A visit to a physician’s office can be stressful for the patient and anxiety is a known factor
in raising blood pressure. This temporary occurrence of elevated blood pressure at the
physician’s office is commonly referred to as “white coat syndrome.”
Whether or not you experience “white coat syndrome,” home blood pressure monitoring
provides you with the opportunity to supplement measurements taken at your physician’s
office. These home readings, when taken over a period of time, can show an accurate
indication of change. Furthermore, your records can assist your physician in evaluating
your health and in making important decisions in the diagnosis and treatment of your
condition. Because of this, it is important to take consistent daily measurements of your
blood pressure.
The variations in your individual readings should only be interpreted by your physician or
a trained healthcare professional.
general BlooD Pressure information
What is Blood Pressure?
Blood pressure is the pressure that is exerted by blood flowing against the walls of the
blood vessels throughout your body.
Your heart, which is the center of the circulatory system, provides the force for the blood
to flow or circulate. When your heart contracts or “beats,” the blood is forced through the
blood vessels increasing the pressure. This is the highest pressure in the cycle or what is
referred to as SYSTOLIC blood pressure. In-between beats your heart relaxes and your
blood pressure decreases. This is referred to as DIASTOLIC blood pressure.
This complete series of events, which occur in a single heartbeat, is known as the
CARDIAC CYCLE.
Your Digital Blood Pressure Monitor will automatically read your blood pressure and
display both systolic and diastolic readings on the screen. Your systolic reading will be
positioned as the upper number and the diastolic reading will be the lower number.
(systolic)
(diastolic)
120 80
/
Blood pressure is measured in millimeters (mm) of mercury (Hg) and is generally recorded
with the systolic pressure (120) listed first and the diastolic pressure (80) listed second.
The numbers are typically separated by a slash mark (/) as shown.
Both pressure readings, the SYSTOLIC and DIASTOLIC, are necessary for a physician to
evaluate the status of a patient’s blood pressure.
Please contact your physician for specific information regarding your own blood pressure.
What Influences Blood Pressure?
Many factors such as genetics, age, sex, altitude, physical activity, anxiety, muscular
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6 7
WHO Blood Pressure Classifications
Standards for assessment of high or low blood pressure have been established by the
World Health Organization (WHO) as shown on the following chart:
Category Systolic
(mmHg)
Diastolic
(mmHg)
Color
Indicator
Optimal <120 <80 Green
Normal 120–129 80–84 Green
High - Normal 130–139 85-89 Green
Stage 1 - Mild
Borderline Hypertension 140–159 90–99 Yellow
Stage 2 - Moderate
Hypertension 160–179 100-109 Orange
Stage 3 - Severe Hypertension ≥180 ≥110 Red
Isolated Systolic Hypertension ≥140 <90
140–159 <90 Yellow
160–179 <90 Orange
≥180 <90 Red
This chart is only a general guideline. Contact your physician or trained healthcare
professional to determine your NORMAL blood pressure.
Variations in Blood Pressure
Blood pressure is influenced by many factors and can change from moment to moment.
Normally, blood pressure is lowest during sleeping periods and rises during the day.
The graph below represents variations in blood pressure shown over a day with
measurements taken every 5 minutes.
The dotted line represents the
sleep period. The rise in
blood pressure at 1 p.m. (A in
the graph) reflects stressful
occurrence, and at 7 p.m. (B
in the graph), a period of
exercise.
imPortant information Before use
1. Blood pressure measurements should only be interpreted by a physician or a trained
healthcare professional who is familiar with your medical history. Through regular use
of this device and recording of your measurements, you can keep your physician
informed of the changes in your blood pressure.
2. Measure your blood pressure in a quiet place. You should be seated in
a relaxed position.
3. Avoid smoking, eating, taking medication, alcohol consumption or physical activity
30 minutes prior to measuring your blood pressure. If you are exhibiting signs of
stress, avoid measuring your blood pressure until the feeling subsides.
4. Rest 15 minutes prior to measuring your blood pressure.
5. Remove any constrictive clothing or jewelry that may interfere with the cuff placement.
6. Apply the cuff to the proper position on the left wrist. The unit should be located
on the inside of your left wrist with the display panel in view.
7. Keep the monitor stable during measurement to achieve an accurate reading.
Remain still; do not talk during the measurement.
8. Record your daily readings on the chart provided.
9. Take your readings at the same time, each day (or as recommended by your
physician) to get an accurate indication of change in your true blood pressure.
10. Wait a minimum of 15 minutes between readings to allow for the blood vessels
to return to normal. The wait time may vary depending on your individual
physiological characteristics.
11. Although such cases are rare, weak or irregular pulse may result in errors that
prevent correct measurement. If abnormal variations are noticed, consult your
physician or trained healthcare professional.
12. This device is intended for adult use.
While taking a measurement, you can stop the inflation or deflation process of the cuff at
any time by pressing the POWER button.
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8 9
imPortant information Before use (continued)
13. It is inappropriate for people with serious arrhythmia to use this Electronic
Sphygmomanometer.
14. Please do not use the cuff other than supplied by the manufacturer, otherwise it
may bring biocompatible hazard and might result in measurement error.
15. Please do not share the cuff with other infectious person to avoid cross-infection.
16. This Electronic Sphygmomanometers should never be used on infants or young
children. Consult your physician or other healthcare professionals before using on
older children.
17. Prolonged over-inflation (cuff pressure exceeds 300 mmHg or maintained above
15 mmHg for longer than 3 minutes) of the cuff bladder may cause ecchymoma
of your arm.
18. The application of the cuff over a wound or inflammation can cause further injury.
19. Avoid application of the cuff on any limb where intravascular access or therapy,
or an arterio-venous (A-V) shunt is present because the temporary interference to
blood flow could result in injury.
20. Consult with your physician before use if any of the following conditions are
present: arrhythmia, inflammatory diseases, intravascular therapy, arteriovenous
shunts or if mastectomy has been performed.
21. Do not use this device with other electronic equipment.
22. Check the blood circulation of the user before measurement.
23. The monitor might not meet its performance specifications or may become a
safety hazard if stored or used outside the specified temperature and humidity
ranges in specifications.
24. For information regarding potential electromagnetic or other interference
between the blood pressure monitor and other devices and for help regarding
advice of such interference please see ELECTROMAGNETIC COMPATIBILITY
INFORMATION section.
25. This equipment has been tested and found to comply with the limits for a Class B
digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to
provide reasonable protection against harmful interference in a residential setting.
imPortant information Before use (continued)
This equipment generates, uses and can radiate radio frequency energy and, if not
installed and used in accordance with the instructions, may cause interference to
radio communications. However, there is no guarantee that interference will not occur
in a particular setting. If this equipment does cause interference to radio or television
reception, which can be determined by turning the equipment off and on, the user is
encouraged to try to correct the interference by one or more of the following measures:
• Reorient or relocate the receiving antenna. Increase the separation between the
equipment and receiver.
• Connect the equipment into an outlet on a circuit different from that to which the
receiver is connected.
• Consult the dealer or an experienced radio/TV technician.
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10 11
WorlD health organization (Who) inDicator
The WHO Indicator, located on the left side of the
Display, will identify your reading within a range in
accordance with the guidelines set by the World Health
Organization. See the chart below for reference.
SYS
DIA
mmHg
mmHg
PUL/min
M
Stage 3 Hypertension
Systolic pressure: ≥180 mmHg
-or-
Diastolic pressure: ≥110 mmHg
Stage 2 Hypertension
Systolic pressure: 160-179 mmHg
-or-
Diastolic pressure: 100-109 mmHg
Stage 1 Hypertension
Systolic pressure: 140-159 mmHg
-or-
Diastolic pressure: 90-99 mmHg
High Normal
Systolic pressure: 130-139 mmHg
-or-
Diastolic pressure: 85-89 mmHg
Normal
Systolic pressure: 120-129 mmHg
-or-
Diastolic pressure: 80-84 mmHg
Optimal
Systolic pressure: <120 mmHg
-and-
Diastolic pressure: <80 mmHg
DIA
SYS
DIA
SYS
DIA
SYS
DIA
SYS
DIA
SYS
DIA
SYS
irregular heartBeat Detection
Your digital blood pressure monitor features
Irregular Heartbeat Detection (IHB). This feature
allows users to accurately monitor blood
pressure even if an irregular heartbeat should
occur.
When an irregular heartbeat is detected, the IHB
icon will appear on the display, Fig. 1.
NOTE: Please consult your physician or trained
healthcare professional for further information
regarding an irregular heartbeat if this symbol
appears frequently at the end of a reading.
If Irregular Heartbeat caused by common arrhythmias is detected in the process of
blood pressure measurement, a signal will be displayed. Under this condition, the
Electronic Sphygmomanometers will function, but the results may not be accurate
and it’s suggested that you consult your physician for accurate assessment.
Fig. 1
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12 13
Battery installation/rePlacement
Replace the batteries when the Low Battery symbol appears
on the display, Fig. 1, or when the display remains blank when
the POWER Button is pressed.
To change the batteries:
1. Open the battery cover, Fig. 2.
2. Making sure the battery polarity is correct, install 2 AAA alkaline
batteries, Fig. 3.
3. Close the battery cover, Fig. 4. The monitor, the batteries and the cuff,
must be disposed of according to local regulations at the end of their usage.
The monitor, the batteries and the cuff, must be disposed of according
to local regulations at the end of their usage.
NOTE: It is recommended to remove the batteries if the unit will not be used for an
extended period of time. Rechargeable batteries are not suitable for this monitor.
Fig. 1
Fig. 2 Fig. 3 Fig. 4
setting the Date/time
NOTE: When the unit is off, the date and time will still appear at
the top of the screen.
1. When the unit is off, press both the POWER and
MEMORY button at the same time for 2 seconds. The
month will begin to flash, Fig. 1.
2. Press and hold the MEMORY button until the desired
number appears.
3. Press the POWER button to set the entry.
4. The date, Fig. 2, followed by the hour and minutes will
flash. Repeat Steps 2 and 3 to adjust the date/time
setting.
5. After setting the minutes, the unit will automatically exit
out of the date/time setting mode, Fig. 3.
NOTE: The time is expressed in 24-hour military time. The chart
below shows the time conversion.
Fig. 1
Fig. 3
Regular Time
(12 hours)
Military Time
(24 hours)
Regular Time
(12 hours)
Military Time
(24 hours)
12 am
Midnight 012 pm Noon 12
1 am 11 pm 13
2 am 22 pm 14
3 am 33 pm 15
4 am 44 pm 16
5 am 55 pm 17
6 am 66 pm 18
7 am 77 pm 19
8 am 88 pm 20
9 am 99 pm 21
10 am 10 10 pm 22
11 am 11 11 pm 23
Fig. 2
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aPPlying your BlooD Pressure cuff
Cuff Dimensions 3¼" x 2¾" x 1¹/8" (8.26 cm x 7 cm x 2.9 cm)
Wrist Circumference Range Suitable for 5½" – 7
5
/8" (14 cm – 19.5 cm)
Avoid smoking, eating, taking medication, alcohol
consumption or physical activity 30 minutes prior to
measuring your blood pressure. If you are exhibiting signs
of stress, avoid measuring your blood pressure until the
feeling subsides. Rest 15 minutes prior to taking your blood
pressure reading.
1. Remove any constrictive clothing or jewelry that may
interfere with the cuff placement.
2. You should be seated with your feet flat on the floor.
3. Hold your left arm in front of you with your
palm facing upward.
4. Apply the preformed cuff to your left wrist. The digital
display panel should be positioned on the inside area
of your wrist facing you, Fig. 1.
5. Adjust the cuff as shown in Fig. 2 and make sure that
the wrist cuff does not cover the protruding part of the
wrist bone (ulna) on the outside of the wrist.
SYS
DIA
mmHg mmHg
PUL/min
HealthSmart
TM
SYS
DIA
mmHg mmHg
PUL/min
HealthSmart
TM
Fig. 1
Fig. 2
Fig. 3
aPPlying your BlooD Pressure cuff (continued)
6. Wrap and fasten the cuff securely, yet comfortably
around your wrist, Fig. 3.
NOTE: The left wrist should be used unless you are unable
to or should not use your left arm or wrist. Consult your
physician to modify these instructions for use on your right
wrist.
SYS
DIA
mmHg mmHg
PUL/min
HealthSmart
TM
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16 17
taking your BlooD Pressure reaDing
Proceed only after reading the previous sections of this manual.
1. Rest your elbow on a solid surface with your palm facing
upward. Elevate your hand so that the cuff is at the
same level as your heart, Fig. 1. Relax your left hand. Sit
comfortably and don’t cross your legs. The middle of the cuff
should be at the level of the right atrium of the heart.
2. The unit will beep and run a self-test, Fig. 2, and show the
last measured reading, Fig. 3, or if there is no previous
measurement, “0” as shown in Fig. 4.
3. When the display appears as shown, Fig. 5, the monitor is
ready. The cuff will automatically begin to inflate.
4. The display will show the increasing pressure in the cuff,
along with the measurement progress on the left side
of the screen.
5. The cuff will automatically inflate to approximately 190 mmHg
or 40 mmHg higher than the last systolic pressure stored
in memory.
6. Once the cuff inflates to the appropriate pressure level, the
measurement will begin.
7. The unit will begin to automatically deflate and the numbers
appearing on the display will decrease.
Measurement value
becomes lower.
Measurement value
becomes higher.
Correct measurement
position (at same
height as heart).
Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
taking your BlooD Pressure reaDing (continued)
8. When all the air is deflated, the measurement is complete.
The unit will display your blood pressure (systolic and
diastolic) measurements and pulse rate, Fig. 6.
9. Record your readings on a chart.
10. At this point, your measurements will be automatically saved
in memory.
11. To conserve the batteries, press the POWER button to turn the power off.
Otherwise, the unit will automatically shut off after approximately 1 minute.
Fig. 6
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18 19
recalling measurements in memory
You can recall up to 60 measurements in the memory. These
measurements can be shared with your physician or trained
healthcare professional.
1. Press and release the MEMORY button. It will show how
many measurements are stored within the memory bank,
followed by the last result, Fig. 1.
2. Press the MEMORY button again to scroll through the
saved measurements. After you’ve scrolled through all the
readings, the unit will automatically turn off.
NOTE: When the number of readings exceeds 60, the oldest
data will be replaced with the new record.
To erase all stored measurements:
1. Press and release the MEMORY button. The unit will display how many
measurements are stored within the memory bank.
2. Press and hold down the MEMORY button until two horizontal
lines flash. This indicates that all measurements within the
memory bank have been erased, Fig. 2.
Fig. 1
Fig. 2
DescriPtion of DisPlay symBols
Indicates a measurement within
Stage 3 Hypertension.
Indicates a measurement within
Stage 2 Hypertension.
Indicates a measurement within
Stage 1 Hypertension.
Appears when batteries should be replaced.
SYS
SYS
SYS
DIA
DIA
DIA
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20 21
DescriPtion of DisPlay symBols (continued) DescriPtion of DisPlay symBols (continued)
SN
Symbol for “THE OPERATION GUIDE MUST BE READ” (The sign back-
ground color: blue. The sign graphical symbol: white)
Symbol for “WARNING”
Symbol for “TYPE BF APPLIED PARTS” (The cuff is type BF applied part).
Symbol for “SERIAL NUMBER”
Symbol for “ENVIRONMENT PROTECTION” – Waste electrical 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 “KEEP DRY”
Shows the pulse rate per minute.
Occurs when an error was made during measurement.
Appears when there is an irregular heartbeat detected
during measurement.
Appears when the cuff is unstable or it has too much air left
in it. Once the arrow stops flashing, the unit is ready to take a
measurement.
Appears when a measurement error has occurred. Restart the
measurement.
Appears when recalling a measurement from memory.
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22 23
trouBleshooting
If any abnormality occurs during use, please check and correct the following:
Condition Correction
Display is blank when power is on Check and correct the polarity of the
installed batteries. Reinstall or replace
batteries.
Measurement incomplete or abnormally
low or high values displayed
Review and follow “Applying your Blood
Pressure Cuff” and “Taking Your Blood
Pressure Reading” sections. Replace
the batteries.
Measurements are different from those
typically measured by physician or
every measurement reading is different.
Remember, blood pressure readings
are influenced by physical and mental
conditions and/or even the time of day.
Daily measurement recordings should
be interpreted by your physician.
EE Symbol Displays Do not talk or move during the
measurement. Review “Applying Your
Blood Pressure Cuff” section.
care anD maintenance
1. Use only a soft, dry cloth to clean your blood pressure monitor.
2. Avoid using any types of liquids on the monitor or cuff.
3. Store your monitor in the provided storage case when not in use.
4. Do not store the unit where it will be exposed to direct sunlight, dust or humidity.
Avoid extreme temperatures.
5. Never disassemble the monitor or cuff.
6. Dropping or subjecting your blood pressure monitor to strong shocks should
be avoided.
7. Remove batteries prior to storing.
8. It is recommended to disinfect the cuff twice a week if needed (for example, in
hospital or in clinic). Wipe the inner side (the side that contacts skin) of the cuff
with a soft cloth squeezed after moistened with Ethyl alcohol (75-90%), then
dry the cuff by airing.
9. No component of the monitor should be serviced by the user. The circuit diagrams,
component part lists, descriptions, calibration instructions, or other information will
assist the user’s appropriately qualified technical personnel in repair. Those parts of
equipment that are designated repairable, can be supplied.
10. It is recommended for the performance to be checked every 2 years.
11. Please keep the cuff clean. If the cuff becomes dirty, remove it from the monitor
and clear it by hand in a mild detergent, then rinse it thoroughly in cold water. Never
dry the cuff in clothes dryer or iron it. Cleaning the cuff after the usage of every 200
times is recommended.
12. The monitor can maintain the safety and performance characteristics for a minimum
of 10,000 measurements or 5 years.
13. The cuff’s integrity is maintained after 1,000 open–close cycles of the closure.
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24 25
ProDuct sPecifications
Name and Item Number Women’s Wrist Blood Pressure Monitor, 04-825-001
Display System Digital display/LCD
Measuring Method Oscillometric Method
Automatic Air Inflation and Measurement
Power Source 2 X 1.5V Size AAA batteries
Measuring Range Pressure: 0 to 300 mmHg
Pulse: 40-180 beats/minute
Accuracy Pressure: ±3 mmHg; Pulse: ±5% of reading
Diastolic Range 40-199 mmHg
Systolic Range 60-260 mmHg
Pressurization Automatic pressurization by pump
Deflation Automatic pressure-release valve
Memory Built-in memory enabling display of up
to 60 measurements
Automatic Power-Off Approximately 1 minute after last button operation
Battery Life Approximately 120 times
Operation Environment Temperature 41°F – 104°F (5°C – 40°C)
Humidity ≤90% RH max
Storage Environment Temperature -4°F – 131°F (-20°C – 55°C)
Humidity ≤90% RH max
Weight 4.3-oz. (without batteries)
Dimensions 3⅝" x 2⅞" x 1⅛"
Wrist Circumference Range Suitable for 5½" – 7⅝" (14 cm – 19.5 cm)
Accessories Storage case, Instruction Guidebook, 2
AAA alkaline batteries, Quick Start Guide
Specifications are subject
to change without notice.
This device complies with Part 15 of the FCC Rules. Operation is subject to the following
two conditions: (1) This device may not cause harmful interference, and (2) this device
must accept any interference received, including interference that may cause
undesired operation.
ELECTROMAGNETIC COMPATIBILITY INFORMATION
Table 1
For all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacture’s declaration - electromagnetic emission
The 04-825-001 is intended for use in the electromagnetic environment specified
below. The customer or the user of the 04-825-001 should assure that it is used in
such an environment
Emissions test Compliance Electromagnetic
environment guidance
RF emissions
CISPR 11 Group 1
The 04-825-001 uses RF
energy only for its internal
function. Therefore, its RF
emissions are very low
and are not likely to cause
any interference in nearby
electronic equipment.
RF emissions
CISPR 11 Class B The 04-825-001 is suitable for use in all
establishments other
than domestic and those
directly connected to
the public low-voltage
power supply network that
supplies buildings used for
domestic purposes.
Harmonic emissions
Not Applicable
IEC 61000-3-2
Voltage fluctuations/ flicker
emissions IEC 61000-3-3
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26 27
Table 2
For all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacture’s declaration - electromagnetic immunity
The 04-825-001 is intended for use in the electromagnetic environment specified
below. The customer or the user of the 04-825-001 should assure that it is used in
such an environment
IMMUNITY test IEC 60601
test level Compliance level
Electromagnetic
environment
guidance.
Electrostatic
discharge (ESD)
IEC 61000-4-2
± 6 kV contact
± 8 kV air
± 6 kV contact
± 8 kV air
Floors should be
wood, concrete
or ceramic tile. If
floors are covered
with synthetic
material, the
relative humidity
should be at least
30 %.
Power frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
3 A/m 3 A/m
Power frequency
magnetic fields
should be at levels
characteristic of a
typical location in a
typical commercial
or hospital
environment.
NOTE: UT is the a.c. mains voltage prior to application of the test level.
Table 3
For all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacture’s declaration - electromagnetic immunity
The 04-825-001 is intended for use in the electromagnetic environment specified
below. The customer or the user of the 04-825-001 should assure that it is used in
such an environment.
IMMUNITY test IEC 60601test Compliance level Electromagnetic
environment guidance.
Radiated RF
IEC
61000-4-3
3 V/m 80 MHz
to 2.5 GHz 3 V/m
Portable and mobile
RF communications
equipment should be
used no closer to any
part of the 04-825-001,
including cables, than the
recommended separation
distance calculated from
the equation applicable
to the frequency of the
transmitter.
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28 29
Table 3 - Continued
For all ME EQUIPMENT and ME SYSTEMS
Radiated RF
IEC 61000-
4-3
3 V/m 80
MHz
to 2.5 GHz
3 V/m
Recommended separation distance:
d=1.2 P80 MHz to 800 MHz
d=1.3 P800 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 an
electromagnetic site surveya, should
be less than the compliance levelbin
each frequency range. Interference
may occur in the vicinity of equipment
marked with the following symbol:
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation
is affected by absorption and reflection from structures, objects and people.
Table 3 - Continued
For all ME EQUIPMENT and ME SYSTEMS
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 04-825-001 is used exceeds the applicable RF compliance level
above, the 04-825-001 should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as re-orienting
or relocating the 04-825-001.
bOver the frequency range 150 kHz to 80 MHz, field strengths should be less
than 3 V/m.
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30 31
Table 4
For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING
Recommended separation distances between portable and mobile RF
communications equipment and the 04-825-001.
The 04-825-001 is intended for use in an electromagnetic environment in which
radiated RF disturbances are controlled. The customer or the user of the 04-825-001
can help prevent electromagnetic interference by maintaining a minimum distance
between portable and mobile RF communications equipment (transmitters) and the
04-825-001 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.
150 kHz to 80 MHz
d=1.2 P
80 MHz to 800
MHz
d=1.2 P
800 MHz to 2.5
GHz
d=1.2 P
0,01 0.12 0.12 0.23
0,1 0.38 0.38 0.73
11.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
Table 4 - Continued
For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING
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.
NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency
range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation
is affected by absorption and reflection from structures, objects and people
and animals.
Manufactured for:
HealthSmart®International
1931 Norman Drive
Waukegan, IL 60085
Register this product at LiveHealthSmart.com
#91-000-825 02/15
©2015 HealthSmart®International
Satisfaction
Guaranteed
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32 33
samPle BlooD Pressure log BlooD Pressure log
04-825-001 IM_13Feb2015.indd 32-33 2/13/15 5:18 PM

35
manual De instrucciones
monitor Digital De Presión
arterial Para la muñeca - mujer
Sírvase leer toda esta guía
antes de operar la unidad.
Artículo n.º 04-825-001
Inglés • Español
garantía limitaDa Por 5 años
El garante garantiza que su Monitor Digital de Presión Arterial estará libre de defectos
de fabricación bajo condiciones de uso normal durante 5 años a partir de la fecha de
compra original. Esta garantía cubre solo el uso normal, y no aplica para uso en ningún
entorno clínico o comercial. Esta garantía no cubre las baterías ni otras fuentes de
energía que se puedan proveer con o usar con el Monitor Digital de Presión Arterial. Esta
garantía no tendrá validez si el producto Monitor Digital de Presión Arterial no se usa
correctamente o se maltrata de cualquier manera.
Si el Monitor Digital de Presión Arterial presenta fallas de operación durante los
primeros 5 años a partir del momento original de compra, llame a nuestra Línea de
Ayuda de Atención al Cliente al 800-622-4714 y trataremos de resolver su problema
tan pronto como sea posible. Si el garante determina que la unidad presentó fallas de
operación debido a un defecto de fabricación, la unidad se reemplazará a discreción
del garante. El reemplazo es el único recurso de reparación cubierto por esta garantía
limitada. Esta garantía le brinda derechos legales específicos, que varían según el
estado. Como condición de esta garantía, debe registrar su producto en línea en un
plazo de 10 días a partir de la fecha de compra en www.livehealthsmart.com.
Esta garantía constituye la única responsabilidad y obligación del garante respecto
del reemplazo de materiales y componentes. No prometemos ninguna otra garantía,
expresa o implícita, que surja de la intervención legal u otra, ni ninguna garantía de
comerciabilidad o ajuste para un uso u objetivo en particular, independientemente
de que se haya revelado el uso o el objetivo al garante en especificaciones, planos u
otro, e independientemente de que los productos del garante estén específicamente
diseñados y/o fabricados por el garante para el uso u objetivo del comprador,
excepto por la garantía limitada mencionada más arriba. El garante no será
responsable de ningún daño indirecto, incidental, especial, consecuencial o punitivo
u otra pérdida, que incluye, pero no se limita a, daño o pérdida de otra propiedad o
equipo y lesiones personales, ya sea que afecten al comprador o a otros. El garante
no será, en ningún caso, responsable ante el comprador por ninguna suma que
supere el costo de reparación y/o reemplazo de la unidad.
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36 37
ínDice
Introducción ............................... 37
Identificación del Producto y Precaución ................. 38
Información General Acerca de la Presión Arterial ............39-41
Información Importante Previo al Uso ..................42-44
Indicador de la WHO (Organización Mundial de la Salud) .......... 45
Detección de Latidos del Corazón Irregulares................ 46
Colocación/Cambio de Baterías ..................... 47
Cómo Fijar la Fecha/Hora......................... 48
Cómo Colocar el Brazalete de Presión Arterial ............. 49–51
Cómo Tomar la Lectura de la Presión Arterial ............... 52
Cómo Llamar Las Mediciones de la Memoria................ 53
Descripción de los Símbolos ......................54-56
Análisis de Fallas............................. 57
Cuidado y Mantenimiento ........................ 58
Especificaciones del Producto .................... 59–66
Ejemplo de Registro de la Presión Arterial ................67-68
introDucción
Gracias por comprar el Monitor digital de presión sanguínea. Con el cuidado y uso
adecuados, su monitor le brindará muchos años de lecturas confiables.
Para obtener el máximo beneficio del monitor de presión arterial, se recomienda consultar
primero con el médico o profesional capacitado del área de salud.
El método de medición que usa su Monitor se llama método oscilométrico. El monitor
detecta el movimiento de la sangre por la arteria de la muñeca y lo convierte en lectura
digital. El método oscilométrico no requiere del uso de un estetoscopio; por lo que
el monitor resulta fácil de usar. El brazalete preconformado se coloca con muy poco
esfuerzo y es cómodo.
Las investigaciones clínicas han demostrado que existe una relación directa entre la
presión arterial en la muñeca y la presión arterial en el brazo. Debido a que las arterias de
la muñeca y del brazo están conectadas, los cambios en la presión arterial de la muñeca
reflejan cambios en la presión arterial del brazo. Las mediciones frecuentes de la presión
arterial de la muñeca le servirán a usted y a su médico como indicador exacto del cambio
de su presión arterial real.
Las personas que padacen de hipertensión severa, arterioesclerosis severa o
diabetes severa, deben consultar con su médico para determinar si pueden
monitorear la presión en la muñeca.
Las lecturas de presión arterial determinadas con este dispositivo equivalen a las
obtenidas por un observador capacitado que emplee el método de auscultación con
brazalete/estetoscopio, dentro de los límites prescritos por la American National Standard
for Electronic or Automated Sphygmomanometers (Norma Nacional Estadounidense de
Esfigmomanómetros Electrónicos o Automatizados).
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