Homedics BPW-O200 User Manual

INSTRUCTION MANUAL

BPW-O200

IMPORTANT PRODUCT NOTICES AND
SAFETY INSTRUCTIONS

When using your blood pressure monitor, basic precautions should always be
followed. Please read and follow all instructions and warnings before using this
product. Save these instructions for future reference.

• Please note that this is a home healthcare product only and it is not intended
to serve as a substitute for the advice of a physician or medical professional.

• This device uses oscillemetric method to measure systolic and diastolic blood
pressure, as well as heart rate.

• Do not use this device for diagnosis or treatment of any health problem or
disease. Measurement results are for reference only. Consult a healthcare
professional for interpretation of pressure measurements. Contact your
physician if you have or suspect any medical problem. Do not change your
medications without the advice of your physician or healthcare professional.

• This product is not suitable for people with arrhythmias. This device may have
diculty determining the proper blood pressure for pregnant women, and
for users with irregular heartbeat, diabetes, poor circulation of blood, kidney
problems, or for users who have suered a stroke.

• Not suitable for those undergoing intravenous injection on any limb or women
with pre-eclampsia.

• For those who have undergone mastectomy or lymph nodectomy surgery, it is
recommended to take a measurement on the unaected side.

• Excessive use may result in blood flow interference, which is likely to cause
uncomfortable sensations, such as partial subcutaneous hemorrhage, or
temporary numbness to your wrist. In general, these symptoms should not last
long. However, if you do not recover in time, please seek advice from a medical
professional.

• The pulse display is not suitable for checking the frequency of heart
pacemakers.

• Electromagnetic interference: 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 may
lead to temporary impairment of measurement accuracy.

• When used among medical electronic equipment on the same limb,
pressurization of the cu may cause the other devices to temporarily
malfunction.

• Please use this device indoors only, in a home healthcare environment.

• Use blood pressure monitor only for its intended use.

• Do not wrap the cu around body parts other than your wrist.

• Not for use by or on persons under the age of 18.

• Do not use this device on infants, children, or those who cannot express their
own intention.

• Please use only the 1.5V AAA alkaline batteries for power supply.

Blood pressure measurements determined with this device are equivalent to
those obtained by a trained observer using the cu/stethoscope auscultatory
method within the accuracy limits prescribed by the American National Standard
for manual, electronic, or automated sphygmomanometers.

ABOUT BLOOD PRESSURE

What is blood pressure?

Blood pressure is the pressure exerted on the artery walls while blood flows
through the arteries. The pressure measured when the heart contracts and
sends blood out of the heart is systolic (highest) blood pressure. The pressure
measured when the heart dilates with blood flowing back into the heart is called
diastolic (lowest) blood pressure.

Why measure your blood pressure?

Among today’s various health problems, those associated with high blood
pressure are very common. High blood pressure dangerously correlates with
cardiovascular diseases. Therefore, blood pressure monitoring is important for
identifying those at risk.

Why do my readings vary?

Blood pressure is a body parameter that is subject to normal variations
throughout the day. A single reading that is dierent from your and your doctor’s
readings are not necessarily inaccurate. The average of several readings, taken
under similar conditions, using the same arm, is preferred for accurate blood
pressure readings.

Why are my readings dierent than those taken at my
doctor’s oce?

Many experience a phenomenon called “White Coat Hypertension” when
measured by a doctor. White Coat Hypertension refers to blood pressure that
rises above its usual level when measured in a clinical setting, such as a doctor’s
oce.

BLOOD PRESSURE STANDARD

The table below contains defined levels of hypertension that are publicly
available from the American Heart Association® (AHA 2017) (www.heart.org/
HEARTORG/Conditions/HighBloodPressure/KnowYourNumbers/Understanding­Blood-Pressure-Readings_UCM_301764_Article.jsp#.WusfWogvy71). Users
can compare their own blood pressure readings against these defined levels to
determine if they may be potentially at increased risk.

This table is applicable to most adults age 18 and older.

Blood Pressure Category

Normal <120 and <80 Green

Elevated 120-129 and <80 Yellow

High Blood Pressure (hypertension) Stage 1 130-139 or 80-89

Hypertension Crisis (consult your doctor immediately) >180 and/or >120

Systolic mm Hg
(upper number)

Diastolic mm Hg

(lower number)

LED Indicator

Color

RedHigh Blood Pressure (hypertension) Stage 2 140-180 or 90-120

Blood pressure tends to go up and down, even in people who normally don’t have
high readings. If your numbers stay above the “normal” range most of the time,
you may be at increased risk and should consult your physician.

Although one can easily find where their own blood pressure readings fall
on this table, this monitor comes equipped with a Risk Category Index that
automatically compares each reading to the defined levels and provides a helpful
cue if your reading falls into one of the stages that could potentially indicate an
increased risk.

Please note that cues provided by this monitor are only intended to assist you
in using this table. The table and cues are only provided for convenience to help
you understand your non-invasive blood pressure reading as it relates to the AHA
2017 information. They are not a substitute for a medical examination by your
physician. It is important for you to consult with your physician regularly. Your
physician will tell you your normal blood pressure range as well as the point at
which you may actually be considered to be at risk.

NAME/FUNCTION OF EACH PART

LCD Display

Storage
Case

Date/Time
Set Button

Set
Button

Risk Category Indicator

Start/Stop Button

Memory Button

Wrist Cu

BATTERY INSTALLATION

1. Slide the battery cover to open.

2. Install or replace 2 AAA alkaline batteries in the battery compartment. Make
sure the polarities “+” and “-” ends coincide with similar markings inside the
compartment.

3. Close the battery cover by sliding back into place.

Replace the batteries if:

• The low battery symbol appears on the display.

• Nothing appears on the display when the

power is switched on.

NOTE:

• Date and time must be reset if batteries are

removed or replaced.

• Replace all batteries at one time (as

simultaneous set). Use only 1.5V AAA alkaline
batteries.

• When the batteries are removed, the measurement values stored in memory

are retained.

• Clean contacts on battery and in battery compartment with a soft, dry cloth

each time you install batteries.

• Batteries are hazardous waste. Do not dispose of them together with

household garbage.

DATE AND TIME SET

Press the DATE/TIME SET button and the YEAR will flash on the screen. Press
USER/

+ button to increase to desired YEAR; press DATE/TIME SET button to

confirm. Repeat steps for MONTH, DAY, HOUR, and MINUTE.

DISPLAY EXPLANATIONS

Hour : Minute

Average of Last 3 Measurements

Memory Record Number

Irregular Heartbeat Symbol

EE

Month/Date

Blood Pressure Unit
Low Battery Symbol

Pulse Symbol

Heart Rate

Low Battery Symbol: Appears when batteries should be replaced.

Pulse Symbol: Shows the heart rate per minute.

Risk Category Indicator: See Blood Pressure Standard section for more

information.

Irregular Heartbeat Detector: See below for more information.

Memory Average: Displays average of last 3 readings.

Measurement Error: Adjust the cu and keep wrist steady during
measurement.

Systolic Rate

Risk Category Indicator Bar

Diastolic Rate

IRREGULAR HEARTBEAT DETECTOR

The appearance of the icon indicates that
a pulse irregularity consistent with an irregular
heartbeat was detected during measurement.
Usually, this is not a cause for concern. However,
if the symbol appears often, we recommend you
seek medical advice. Please note that
the device does not replace a cardiac
examination, but serves to detect pulse
irregularities at an early stage.

Movement, shaking, or talking during the measurement can result in pulse
irregularities that may cause the appearance of this icon. Therefore, it is of great
importance to not move or talk during measurement.

To determine the presence of an irregular heartbeat, the average of the
heartbeat intervals is calculated with the first 3 normal eective heartbeat
values. It is important to note that the average is not a strict mathematical
averaging of all recorded intervals. At least 3 beats with 25% or greater
dierence from the average heartbeat interval will generate the
the screen.

Irregular
Heartbeat
Detector

icon on

USING THE WRIST CUFF

1. Wrap the cu snugly around the left wrist with palm
facing up and the monitor facing you. Do not make
too tight.

2. Fold the remaining part of the wrist cu back out of
the way.

0.4 inch (10 mm)

3. Make sure that you leave approximately 1/4” to
1/2” from the palm and that there is not extra space
between the cu and wrist.

5.3 ~ 7.7 inch

(135 ~ 195 mm)

MEASUREMENT PROCEDURE

IMPORTANT:

It is extremely important that the cu be at the same
height as the heart. Having the cu higher or lower may
cause inaccurate results.

BEFORE MEASUREMENT

• Wait 1 hour after exercising, bathing, eating, drinking
alcoholic or caeinated beverages, or smoking before
taking a measurement.

• Sit quietly and rest for 15 minutes; for any
subsequent measurements, it is recommended to
wait a minimum of 5 minutes.

• Take your blood pressure at normal body
temperature.

DURING MEASUREMENT

• Do not talk or move your arm or hand muscles.

• Do not cross your legs. Sit with feet flat on the floor.

• Do not touch cu or monitor during measurement.

• Position the blood pressure monitor on your wrist.

• Place your elbow on the table and rest the back of your hand on the device
storage case or other object.

• Rest your wrist on the armrest until it’s at the same height as your heart.

• Relax your hand and turn your palm upward.

• Do not use this device if your wrist has any wound or injury.

• Once the measurement has started, keep your wrist steady until the
measurement is complete.

1. Press START/STOP button to turn the monitor ON.

2. Press USER/

3. With the cu wrapped around your wrist, press the START/STOP button. Do

not inflate the cu unless it is wrapped around your wrist. All digits will light
up to check the display function. The checking procedure will be completed
after about 1.5 seconds.

4. After all symbols disappear, the display will show “00”. The monitor is “Ready

to Measure” and will automatically inflate the cu to begin measurement.

5. When the measurement is completed, the cu will deflate entirely. Systolic

pressure, diastolic pressure, and pulse will be shown simultaneously on the
LCD screen. The measurement is then automatically stored into memory.

NOTE:

• This monitor automatically turns o approximately 1 minute after last
operation. You may also press the START/STOP button to turn the unit o.

• To interrupt the measurement, you may press the START/STOP button. The
cu will deflate immediately after a button is pressed.

+ button to choose User 1 or 2.

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RECALLING VALUES FROM MEMORY

This monitor can be used by 2 individuals. Each user can store up to 30
measurements.

1. Press USER/

+ button to select User 1 or 2.

2. Press MEM button to access the Memory.

3. If there is no data stored in memory, nothing (except for month, date, and
time) will appear on the display. If there is data, the first reading will be the
average of the last 3 measurements.

4. Every new press of the MEM button will recall a previous reading. The latest
reading will be recalled first.

5. To stop recalling readings from memory, press the START/STOP button.

CLEARING VALUES FROM MEMORY

1. Press USER/+ button to select User 1 or 2.

2. Press MEM button to access the Memory.

3. Press and hold the DATE/TIME SET buttons (

USER/+) at the same time

while in memory recall mode, and the data for the selected user will be
erased automatically.

Note: Once deleted, your readings cannot be restored.

CARE, MAINTENANCE, AND CLEANING

• Clean the blood pressure monitor body and cu carefully with a slightly damp,

soft cloth. Do not press. Do not wash cu or use chemical cleaner on it. Never
use thinner, alcohol, or petrol (gasoline) as cleaner.

• Leaky batteries can damage the unit. Remove the batteries when the unit will

not be used for a long time.

• Follow local ordinances and recycling instructions regarding disposal or

recycling of the device and device components, including batteries.

• If the unit is stored near freezing, allow it to acclimate to room temperature

before use.

• This blood pressure monitor is not field-serviceable. You should not use any

tool to open the device nor should you attempt to adjust anything inside the
device. If you have any problems with this device, please contact HoMedics
Consumer Relations (contact information can be found on the Warranty page).

• Do not immerse the unit in water as this will result in damage to the unit.

• Do not subject the monitor or cu to extreme temperatures, humidity,

moisture, or direct sunlight. Protect from dust.

• Do not fold the cu and tubing tightly.

• Do not disassemble the monitor or cu. If in need of repair, refer to the

Warranty section of this manual.

• Do not subject the monitor to extreme shocks (do not drop on floor).

• Do not inflate the cu unless wrapped around wrist.

• Do not wrap the cu around body parts other than your wrist.

• Do not drop or insert any object into any opening or hose.

• Always store the unit in the storage case between uses.

• This monitor may not meet its performance specifications if stored outside

these temperature and humidity ranges:

Storage/Transportation Environment Operating Environment

Temperature: -13°F ~ 158°F (-25°C ~ 70°C)
Humidity: less than 93% RH

Temperature: 41°F ~ 104°F (5°C ~ 40°C)
Humidity: 15% ~ 93% RH

TROUBLESHOOTING

If any abnormality arises during use, please check the following points.

SYMPTOMS POSSIBLE CAUSES CORRECTION

Unit does not turn on
when the START/STOP
button is pushed.

EE measurement error
symbol shown on
display or the blood
pressure value is
displayed excessively
low (or high).

E1 error symbol shown
on display.

E2 error symbol shown on
display.

E3 error symbol shown on
display.

EP error symbol shown on
display.

Batteries have run down. Replace them with 2 new

Battery polarities (+/ -) have
been positioned incorrectly.

The wrist cu has been
positioned on the arm
incorrectly.

Did you talk or move during
measurement?

Shaking of the arm with the
cu on.

Air circuit abnormality. Cu
tube may not be plugged
into monitor correctly.

Inflation pressure exceeding
300 mmHg.

Error determining
measurement data.

System error. Remove batteries. After 1

AAA alkaline batteries.
Re-insert the batteries in the

correct positions.
Re-wrap the cu properly so

that it is positioned correctly.
Take new measurement.

Keep arm steady during
measurement. Measure
again. Refer to “Measurement
Procedure” instructions.

Check cu connection. Take
new measurement. See “Using
the Wrist Cu” section.

Switch the unit o and then
turn back on. Take new
measurement.

Re-wrap the cu properly so
that it is positioned correctly.
Take new measurement.

minute, re-insert the batteries.
Take new measurement.

Note: If the unit still does not work, contact HoMedics Consumer Relations.
Under no circumstance should you disassemble or attempt to repair the unit by
yourself. Contact information for HoMedics Consumer Relations can be found on
the Warranty page.

SPECIFICATIONS

Measurement Method:
Rated Range of Cu Pressure:
Measurement Range:

Rated Range of Determination:
Accuracy:

Pressure Sensor:
Inflation:
Deflation:
Display:
Memory:
Unit Dimensions:

Unit Weight:

Cu Size:
Storage/Transportation

Environment:
Operation Environment:

Atmospheric pressure:
Power Supply:
Battery Life:
Product Life:
Sleeping Mode:

Accessories:

Note: These specifications are subject to change without notice.

POTENTIAL FOR ELECTROMAGNETIC INTERFERENCE

To avoid inaccurate results caused by electromagnetic interference between
electrical and electronic equipment, do not use the device near a cell phone
or microwave oven. For most wireless communication
devices, it is recommended to maintain a distance of 10.8
feet (3.3m) in order to avoid electromagnetic interference.

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.

Oscillometric
0-300 mmHg
Pressure: 40~280 millimeters Mercury (mmHg)

Pulse: 40~199 beats/minute
40-280 mmHg
Pressure: ±3 mmHg

Pulse: +5% Max.
Semi-conductor
Automatic inflation (air pump)
Automatic air release control valve
Liquid Crystal Display
60 memory total for 2 users
75 x 75 x 26 mm (L x W x H)

2.95 x 2.95 x 1.02 inch (L x W x H)

79.5 g + 5 g (2.80 oz + 0.18 oz)
(without cu and batteries)

135 ~ 195 mm (approx. 5.3 ~ 7.7 inch)
Temperature: -25°C ~ 70°C (-13°F ~ 158°F)

Humidity: < 93% RH
Temperature: 5°C ~ 40°C (41°F~104°F)

Humidity: 15% ~ 93% RH
700 hPa ~ 1060 hPa
DC 3 V, AAA “LR03” (1.5 V) alkaline battery x 2
Approx. 250 measurements
5 years (4 times a day)
Without any operation for 1 minute, device

automatically shuts o
Instruction manual, storage case, 2 AAA (LR03)

alkaline batteries
Internally powered equipment

Type BF equipment
IP22-degrees of protection provided by
enclosures
Not suitable for use in presence of flammable
anesthetic mixture with air, oxygen, or nitrous
oxide.
Continuous operation with short-time loading.

Follow instructions for use.

FEDERAL COMMUNICATIONS COMMISSION COMPLIANCE
STATEMENT

Changes or modifications to this equipment not expressly approved by the
manufacturer could void the user’s authority to operate the equipment. 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
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 harmful interference to radio or
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:

• Reorient or relocate the receiving antenna.

• Increase the separation between the equipment and receiver.

• Connect the equipment into an outlet on a circuit dierent from that to which
the receiver is connected.

• Consult the dealer or an experienced radio/TV technician for help.

ELECTROMAGNETIC COMPATIBILITY (EMC)

Guidance and manufacturer’s declaration – electromagnetic emissions

The device is intended for use in the electromagnetic environments listed below,
and should only be used in such environments:

Emissions test Compliance Electromagnetic environment - guidance

RF emissions CISPR 11 Group 1 RF energy is used only to maintain device‘s
RF emissions CISPR 11 Class B

Harmonic emissions IEC
61000-3-2

Voltage fluctuations/flicker
emissions IEC 61000-3-3

Not
Applicable

Not
Applicable

Guidance and manufacturer’s declaration – electromagnetic immunity

The device is intended for use in the electromagnetic environments listed below,
and should only be used in such environments:

Immunity
test

Electrostatic
discharge
(ESD)
IEC 61000­4-2

Power
frequency
magnetic
field
IEC 61000­4-8

IEC 60601
test level

± 8 kV contact
discharge

± 15 kV air
discharge

30 A/m
50 or 60 Hz

Compliance
level

± 8 kV contact
discharge

±15 kV air
discharge

30 A/m
50 or 60 Hz

Recommended separation distances between portable and mobile RF
communication equipment and the device.

The device is intended for use in an electromagnetic environment where radiated
RF disturbances are under control. User can help prevent electromagnetic
interference by keeping the device at a minimum distance from portable and
mobile RF communications equipment (transmitters). Below table details the
maximum output power of transmitter :

Rated maximum
output power of

transmitter W

0.01

0.1

1

10

100

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be
estimated 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 ls aected by absorption and reflection from
structures, objects, and people.

150 kHz to 80 MHz

Not applicable

N/A 0.12 0.23

N/A 0.38 0.73

N/A 1.2 2.3

N/A 3.8 7.3

N/A 12 23

operation.
Therefore, its RF emissions are so low that
it’s not likely to cause any interference in
nearby electronic equipment.

The device 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.

Electromagnetic environment-guidance

The relative humidity should be at least
5%

Power frequency magnetic fields should
be at levels characteristic of a typical
location in a typical commercial or
hospital environment. Recommended
separation distance
I
r = ---------(m)
188
where I is the current in amperes in a
power bus or an appliance wire and r is
the recommended separation distance
between your device and the power bus
or application wire, in meters (m).

Separation distance according to frequency of transmitter m

80 MHz to 800 MHz

d = 1.2

800 MHz to 2.5 GHz

d = 2.3

Guidance and manufacturer’s declaration – electromagnetic immunity

The device is intended for use in the electromagnetic environments listed below,
and should only be used in such environments:

Immunity test IEC 60601

Conducted
RF
IEC 61000-4-6

Radiated RF
IEC
61000-4-3

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 aected by absorption and reflection from
structures, objects, and people.

a Field 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 device is used exceeds the applicable RF compliance level above, the device should
be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as
reorienting or relocating the device.

test level

3Vrms
At 0.15-80MHz

6Vrms
At ISM & Radio
Amateur Freq.

3 V/mat 80 -2700
MHz (10V/m
Home Healthcare)

AM Modulation
And 9-28V/mat
385-6000MHz,
Pulse Mode and
other Modulation

Compliance

level

Not Applicable

3 V/mat 80 -2700
MHz (10V/m
Home Healthcare)

AM Modulation
And 9-28V/mat
385-6000MHz,
Pulse Mode and
other Modulation

Electromagnetic environment- guidance

Portable and mobile RF communications equipment should be
used no closer to any part of the device, including cables,
than the recommended separation distance calculated from the
equation applicable to the frequency of the transmitter.

Recommended separation distance

8O MHz to 800 MHz

d = 1.2
d = 2.3 800 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 metres (m).
Field strengths from fixed RF transmitters, as determined
by an electromagnetic site surveya, should be less than the
compliance level in each frequency range.
Interference may occur in the vicinity of equipment marked
with the following symbol:

WARRANTY

HoMedics sells its products with the intent that they are free of defects in
manufacture and workmanship for a period of 5 years from the date of original
purchase, except as noted below. HoMedics warrants that its products will be free
of defects in material and workmanship under normal use and service. This blood
pressure monitor meets the simulated measurement cycles test requirement per
EN1060-3, part 8.10. This warranty extends only to consumers and does not extend
to Retailers.

To obtain warranty service on your HoMedics product, contact a Consumer Relations
representative by telephone at 1-800-466-3342 for assistance. Please make sure to
have the model number of the product available.

HoMedics does not authorize anyone, including but not limited to Retailers,
the subsequent consumer purchaser of the product from a Retailer, or remote
purchasers, to obligate HoMedics in any way beyond the terms set forth herein.
This warranty does not cover damage caused by misuse or abuse; accident; the
attachment of any unauthorized accessory; alteration to the product; improper
installation; unauthorized repairs or modifications; improper use of electrical/power
supply; loss of power; dropped product; malfunction or damage of an operating part
from failure to provide manufacturers recommended maintenance; transportation
damage; theft; neglect; vandalism; or environmental conditions; loss of use during the
period the product is at a repair facility or otherwise awaiting parts or repair; or any
other conditions whatsoever that are beyond the control of HoMedics.

This warranty is eective only if the product is purchased and operated in the
country in which the product is purchased. A product that requires modifications or
adoption to enable it to operate in any other country than the country for which it was
designed, manufactured, approved, and/or authorized, or repair of products damaged
by these modifications is not covered under this warranty.

THE WARRANTY PROVIDED HEREIN SHALL BE THE SOLE AND EXCLUSIVE
WARRANTY. THERE SHALL BE NO OTHER WARRANTIES EXPRESS OR IMPLIED,
INCLUDING ANY IMPLIED WARRANTY OF MERCHANTABILITY OR FITNESS OR ANY
OTHER OBLIGATION ON THE PART OF THE COMPANY WITH RESPECT TO PRODUCTS
COVERED BY THIS WARRANTY. HOMEDICS SHALL HAVE NO LIABILITY FOR ANY
INCIDENTAL, CONSEQUENTIAL, OR SPECIAL DAMAGES. IN NO EVENT SHALL THIS
WARRANTY REQUIRE MORE THAN THE REPAIR OR REPLACEMENT OF ANY PART OR
PARTS THAT ARE FOUND TO BE DEFECTIVE WITHIN THE EFFECTIVE PERIOD OF THE
WARRANTY. NO REFUNDS WILL BE GIVEN. IF REPLACEMENT PARTS FOR DEFECTIVE
MATERIALS ARE NOT AVAILABLE, HOMEDICS RESERVES THE RIGHT TO MAKE
PRODUCT SUBSTITUTIONS IN LIEU OF REPAIR OR REPLACEMENT.

This warranty does not extend to the purchase of opened, used, repaired,
repackaged, and/or resealed products, including but not limited to sale of such
products on internet auction sites and/or sales of such products by surplus or bulk
resellers. Any and all warranties or guarantees shall immediately cease and terminate
as to any products or parts thereof that are repaired, replaced, altered, or modified,
without the prior express and written consent of HoMedics.

This warranty provides you with specific legal rights. You may have additional rights
that may vary from state to state. Because of individual state regulations, some of the
above limitations and exclusions may not apply to you.

©2018 HoMedics, LLC. All rights reserved. HoMedics is a registered trademark of HoMedics, LLC.

LIMITED 5-YEAR WARRANTY

Distributed by Homedics, LLC, 3000 N Pontiac Trail, Commerce Township, MI 48390

IB-BPWO200

P/N: 323103143 VER: 001

Printed in China

IB-BPW-O200--04.indd 2 2018/7/9 上午10:38