HoMedics CMS50D1A User manual

H ~MED i cs·
PULSE OXIMETER
INSTRUCTIONS FOR USE
INTRODUCTION
M odel CMS50O1A
PIN PX-131COA
In caseofmodifications and software upgrades,the information
contained in this documentissubject tochange without notice.The
Manual describes, in accordancewith the PulseOximeter's features
and requirements,main structure, functions, specifications, correct
methodsfortransportation, installation, usage, operation, repair,
maintenance and storage, etc., aswell as the safetyproceduresto
protect both the userand equipment. Refer to the respective sections
for details.
Please read the Manual very carefully before using this equipment.
These instructions describethe operating proceduresthat must be
followed. Failure tofollowthese instructions can cause measuring
abnormality, equipment damage and personal injury.
The manufacturer is NOTresponsible forthe safety, reliability and per-
formance issues and anymonitoring abnormality, personal injury and
equipmentdamageduetouser's negligence ofthe operation instruc-
tions. The manufacturer's warranty service doesnotcover such faults.
Due to productimprovements, the specific productsyou received may
have slightdifferencestothe description in this User Manual.
This product can beused repeatedly, with a life expectancyof3 years.
WARNING
All uncomfortable or painfulfeeling may appear if usingthe device
ceaselessly, especiallyforthe microcirculation barrier users. It is rec-
ommended thatthe sensorshould notbeappliedtothe samefinger
forover2 hours.
• Use the pulse oximeter only for its intended use. DO NOT use on a
fingerthat has an edemaandtendertissue.
• The light (the infrared is invisible) emitted from the device is
harmfulto the eyes. DO NOTstare intothe light.
• Usercannotuse enamel orothermakeup onthefinger when using.
• User'sfingernail cannot betoo long.
• Please read the relative content abouttheclinical restrictions
and cautions.
• This deviceis not intended fortreatment ordiagnosis.
IMPORTANT PRODUCT NOTICES AND SAFElY INSTRUCTIONS
• Checkthe main unitand all accessories periodicallytomake
sure thatthere is novisible damagethat may affectuser's safetyand
monitoring performance aboutcables and transducers. It is
recommended thatthe device should beinspected once aweekat
least. When there is obviousdamage, stop using the oximeter.
• DO NOT disassemblethis device. If inneed of repair, refertothe
warranty section ofthis manual.
• The oximetercannotbe used togetherwith devices notspecified
inthe User's Manual.
• Useonlythe accessories recommended inthis manual, orinduded
in the box.
• Undernormal usage conditions, this device does not require
calibrationortechnical maintenance otherthan infrequent
replacement ofthe battery.
WARNINGS:
Explosive hazard - DO NOTusethe oximeter in an environmentwith
inflammable gas such assomeignitableanesthetic agents.
A person with allergiestorubbercannot use this device.
Follow local ordinances andrecycling instructions regarding
disposalorrecycling ofthe device and device components,
including batteries.
When using yourpulse oximeter, basic precautions should always
befollowed. Please read andfollow all instructions and warnings
beforeusingthis product. Save these instructions forfuture
reference.
Please don't measurethis devicewith function test paperfor
the device's related information.
DO NOTservice ormaintain this devicewhile inuse.
The useris an intended operator.
The probe ofthe device is theapplied part.
ATTENTION:
• Keepthe oximeterawayfrom dust,vibration, corrosive
substances,explosive materials,high temperatureand
moisture.
• Ifthe oximeter gets wet, please stop operating it.
• When it iscarried from cold environmenttowarm orhumid
environment, please do nouse it immediately.
• DO NOToperate keys on front panel with sharp materials.
• High temperature orhigh pressure steam disinfection ofthe
oximeter is notpermitted.
• Refer tothe "Careand Maintenance" section for instructions
on cleaning and disinfection.
• DO NOTimmersethe unit in water asthiswill result in damageto
the unit.
• When cleaning thedevice with water,thetemperature should be
lowerthan 140°F (60°C) .
• As tothefingers which are too thin ortoo cold,itwould probably
affectthe normal measure ofthe users' Sp0
2 and pulse
rate , please
clipthethickfinger such as thumb andmiddlefinger deeply enough
intothe probe.
• DO NOTusethe device on infantorneonatal users.
• The product is suitableforadults weighing between 88 lbsto
242.5 lbs (40 kg to 110kg).
• Thedevice may notwork for all users. Ifyou are unabletoachieve
stable readings, discontinueuse.
• The updateperiod ofdata is less than 5 seconds,which will
changeaccording to the user's pulse rate .
• The waveform isnormalized.Please read the measured value
whenthewaveform on screen is equably andsteady1Joing, here
this measured value is optimal value,and the waveform atthe
momentisthe standard one.
• Ifsomeabnormal conditions appear on the screen while using,
pull outthefingerand reinsert to restore normal use.
• The lanyard attached tothe product is madefrom non-allergic
material, if particulargroups are sensitivetothe lanyard, stop
using it. DO NOTwear around the neckto avoid risk ofinjury
tothe neck.
• The instrument does nothave a low-voltage alarm function, it only
showsthe low-voltage, please change the batterywhen the battery
energy is used up.
• The instrument doesnothave an alarm function. Donotusethe
device in situationswherealarms are required.
• Batteries mustberemoved ifthedevice is going tobe stored for
morethan one month, orelse the batteries may leak.
• Aflexible circuit connects the two parts ofthe device. DO NOTtwist
orpull on theconnection.
INDICATION FOR USE:
For usewith sporting and aviation activities, and to monitor heart
rate during exercise.
OVERVIEW
The pulseoxygen saturation is the percentageof Hb0
2 inthetotal Hb
in the blood,so-called the 02 concentration in the blood. Itis an im-
portant bio-parameterforthe respiration. Forthe purposeofmeasuring
the Sp0
2 more easily and accurately,ourcompany developed the
Pulse Oximeter.Atthesame time,the device can measurethe pulse
rate simultaneously.
The Pulse Oximeterfeatures in small volume, lowpowerconsumption,
convenientoperation and being portable. It is only necessaryforuser
toputone ofhisfingers intoafingertip photoelectric sensorfor mea-
surement, andthe displayscreen will directly show measured value of
Hemoglobin Saturation.
FEATURES:
• Operationofthe productis simple and convenient.
• The productis small in volume, light in weightand convenient
tocarry.
• Powerconsumption ofthe product is lowand the2 originally
equippedAAAbatteries can be operated continuouslyfor 20 hours.
• The productwill enter standby modewhen no signal is inthe
productwithin 5 seconds.
• Display direction changes automaticallyforeasy viewing.

MAJOR APPLICATIONS AND SCOPE OF APPLICATION
The Pulse Oximetercan beused in measuring pulseoxygen saturation
and pulse rate through the finger. The productis suitable forfamily use
(It can beused before or afterdoing sports, and itis notrecommended
tousethedevice during the process ofdoing sports).
A The problem ofoverrating would emergewhen the user is
Lil suffering from toxicosis which is caused bycarbon monoxide,
the d6'11ice is not recommended to beusedunderthis circumstance.
ENVIRONMENT REQUIREMENTS
Storage Environment
a. Temperature: -40°F (40°C) -+140"F (+60"C)
b. Relative humidity: s95%
c. Atmospheric pressure: 500 hPa -1060 hPa
Operating Environment
a. Temperature: 50°F (10°C) - 104°F (40°C)
b. Relative Humidity: s75%
c. Atmospheric pressure: 700 hPa -1060 hPa
PRINCIPLE AND CAUTION
Principle of Measurement
Principleofthe Oximeteris asfollows: An experienceformula ofdata
process is establishedtaking use ofLambert Beer Law according to
Spectrum Absorption Characteristics ofReductive Hemoglobin (Hb)
and Oxyhemoglobin (HbO
2)
in glow& near-infrared zones. Operation
principle ofthe instrument is: Photoelectric Oxyhemoglobin Inspection
Technology isadopted in accordancewith Capacity Pulse Scanning
& Recording Technology, sothattwo beams ofdifferentwavelength of
lights can befocused onto human nail tipthrough perspective clamp
finger-type sensor. Then measured signal can beobtained bya pho•
tosensitive element, information acquired through which will beshown
on screen throughtreatment in electronic circuits and microprocessor.
Glow and Infrared-ray -
Emission Tube
l
Glow and Infrared-ray -
Receipt Tube
Figure 1. Operating Principle
Caution
1. The fingershould be placed properly (referto Figure 7), or else it
maycause inaccurate measurement.
2. The Sp0
2 sensorand photoelectric
receiving tubeshould be arranged
in awaywiththe subject's arteriole in aposition there between.
3. The Sp0
2 sensorshould not be usedata location orlimbtied
with
arterialcanal orblood pressurecufforreceiving intravenousinjection.
4. Make surethe optical path isfree from any optical obstacles like
rubberized fabric.
5. Excessive ambientlight may affectthe measuring result. Itincludes
fluorescent lamp, dual rubylight, infrared heater, directsunlight, etc.
6. Strenuous action ofthe subject or extreme electrosurgical
interference mayalso affectthe accuracy.
7. Usercannot use enamel orothermakeup on the finger when using.
CLINICAL RESTRICTIONS
1. k. the measure is taken on the ba5is of arteriole pulse, substantial
pulsating bloodflow of subject is required. For a subject with weak pulse
duetoshock, low ambienVbody temperature, major bleeding, or use of
vascular contracting drug, the Sp0
2
waveform (Pl.ETH) will decrease. In
this case, the measurement will be more sensitiveto interference.
2. Forthose with asubstantial amount ofstaining dilution drug (such as
methylene blue, indigo green and acid indigo blue), or carbon
monoxidehemoglobin (COHb), ormethionine (Me+Hb) orthiosalcylic
hemoglobin, and some with icterus problem, the Sp0
2 determination
bythis monitormaybe inaccurate.
3. Thedrugs like dopamine, procaine, prilocaine, lidocaineand butacaine
may also bea majorfactor blamed forseriouserrorof Sp0
2
measure.
4. k. the SpO2 value servesas a reference value for judgementof
anemic anoxiaand toxic anoxia, some users with serious anemia
mayalso reportgoodSpO2 measurement.
TECHNICAL SPECIFICATIONS
1. Display Format: LCD Display;
SpO2 Measuring Range: O"/o - 100%;
Pulse Rate Measuring Range: 30 bpm -250 bpm;
Pulse Wave Display: bar--graph display and thewaveform display.
2. PowerRequirements: 2 x 1.5VAAAalkaline battery (or use
rechargeable batteries), adaptable range: 2.6V - 3.6 V.
3. PowerConsumption: Less than30 mA.
4. Resolution: 1%forSpO2 and 1bpmfor Pulse Rate.
5. MeasurementAccuracy: ±2% in stageof 70% - 100"/o Sp0
2, and
meaninglesswhen stage being smallerthan 70%. ±2 bpm or ±2%
(select larger) for Pulse Rate. Clinical Trial: Sp0
2 regression plotand
Bland-Altman plot, Refer to Figure 2 & Figure3.
6. MeasurementPerformance in Weak Filling Condition: Sp0
2 and
pulse rate can beshown correctlywhen pulse-filling ratio is 0.4%.
SpO2 error is ±4%,pulse rate erroris ±2 bpm or ±2% (select larger).
7. Resistance tosurrounding light: The deviation between thevalue
measured inthe condition ofman-made light, indoor natural light
and darkroom is lessthan ::t1 %.
8. It is equipped with a switchfunction: The productwill enter standby
modewhen nosignal is in the productwithin 5 seconds.
9. Optical Sensor: Red light(wavelength is 660 nm, 6.65 mW), infrared
(wavelength is 905 nm, 6.75 mW).
PRODUCT SET UP
Low~battery indication
Pulse rate bar graph
ACCESSORIES
• 1lanyard
• 2AAAbatteries
• 1User Manual
• 1 Storage bag
Figure 2. Sp0
2 regression plot
Figure3. Bland-Altman plot
Sp(n display Pulse rate display
Button
PUL SE XI ME T ER
Pulse rate waveform
Figure 4. FrontView
\~
Figure 5. Attachingthelanyard
ATTACHING THE LANYARD
1. Puttheend ofthe lanyardthroughthe hole.
2. Putanother end of the lanyardthroughthe firstone and then
tighten it
BATTERY INSTALLATION
1. Refer to Figure 6. and insertthe2 AAA size batteries properly in
therightdirection.
2. Putback the cover.

A Pleasetake care when you insertthebatteriesforthe
~ improperinsertion maydamagethe device.
• Replace all batteriesat one time (as simultaneous set) . Use only
1.5V AAA alkaline batteries. Use onlythe size and type ofbatteries
specified.
• When installing batteries,observe proper +/- polarities.Incorrect
installation ofbatteries may cause damagetothe unit.
• Clean contacts on batteryand in battery compartment with a soft ,
drycloth each time you install batteries.
• Batteries are hazardous waste . DO NOT disposeofthem together
with household garbage.
• DO NOT dispose of batteries in fire. Batteries may explode or leak.
• Recycle ordispose ofproperty in accordance with local, state,
province, and country regulations.
Figure6. Battery Installation
OPERATING GUIDE
([W\
Figure 7. Finger Position
1. Wrth the batteries inthe devicepress
the back of thedeviceto open the clip.
2. Place thefinger between therubber cushions of theclip asshown
inFigure7 (make sure thefinger is inthe right position), and then
clipthe finger.
3. Press the powerbutton to startmeasurement.
4. DONOTmovethefinger or body during measurement.
5. The measurementinformation will be shown directlyonthe display.
6. Longpressthebuttontoadjustbrightness preference. Choose from
5 levels ofbrightness. When in Standby mode, ashortpress of the
buttonwill exit it.
7. Displayviewing angle will change automatically accordingtothe
direction of the hand.
A\ Fingernails and the luminescenttube
~ should beon the sameside.
CARE AND MAINTENANCE
• Replace the batteriesifthelowbattery symbol appearsonthedisplay,
or when any buttonis pressed andnothing isdisplayed on the screen.
• Pleaseclean the surface of thedevice before using. Wipe the device
with rubbing alcoholfirst, letitair dry, or clean itusingasoft, dry
pieceofdean fabric.
• Use rubbing alcohol to disinfectthe productafteruse to prevent
spreading infection between uses.
• Remove batteries when unitisnotin use for extended periodsof time.
• The packed device can betransported byordinaryconveyance or
according totransportcontract. The devicecannot betransported
mixed with toxic, harmful, corrosive material.
• Storageenvironmentof the deviceis -40"F (- 40°C) to + 140°F (60°C),
<95%RH.
A\ High-pressuresterilization cannot be used onthedevice.
~ DO NOT immerse the device in liquid.
It is recommended that the device should be kept in a dry
environment.
Htmidily may reduce the useful life of the device, or even damage it.
TROUBLESHOOTING
PROBLEM CAUSE SOLUTION
The Sp0
2 and pulse rate
1. Thefinger is notproper-1. Placethefingerproperty
are notdisplayed normally ly positioned. andtryagain.
2.The user's S~ istoo 2. Try a~ain.Go to a hos-
low to bedet ed.
pita! ora diagnosis ~
youare sure thedevice
works all right.
2.782.465.02(HME)ESS/l.l 1.4.01.35.391 2021.08
The Sp0
2
and pulse rate
1.The finger is notplaced 1. Place thefinger property
are notdisplayed S1ably
insidedeep enou\Jh . and try again.
2. The finger is shaking or 2. Keep the usercalm.
the userismoving.
The devicecannot be 1.The batteries are 1. Change batteries.
turned on drained oralmost 2. Reinstall batteries.
drained. 3. Please contact
2.The batteries are not Consumer Relations.
inserted properly.
3.The device is
malfunctioning.
The display is offsuddenly 1.The product will enter
1. Normal.
standbymode when no 2. Change batteries.
signal is detected within
5 seconds.
2.The batteries are almost
drained.
SYMBOLS
SYMBOL DESCRIPTION SYMBOL DESCRIPTION
00
Type BF
::a
WEEE (2002/96/EC)
-
(t
Refer to instruction
manual/booklet IP22 Ingress
of liquidsrank
%SpO, The pulse
o~gen
saturation(%
...
Manufacturer
PRbpm Pulse rate (bpm)
rl
ManufactureDate
~
Alarm Inhibit
...-c
t •60'C
¥J::;~i~a~r~ 1~t!C~~
Thebatteryvoltage
.. ¢ '
CJ
indication 1s deficient
~~~i8ll/17~l!f;~~
0
r1
(changethe battery in
time avoiding the inexact
measure)
1: ~~ ~~~t~~~r:iinal
-Storage and Transport
--
ft
Atmospheric pressure
inadequacy limltallon
+
~~r:Wesit i ve
11
This side UP
-Batterynegative
electrode ! Fragile, handle with care
···••-CJ
I. Exit standby mode
-1
Keep dry
2. Changebrightness of
the screen
SN Serial number
.:- ..
Recyclable
SPECIFICATIONS
DISPLAY INFORMATION DISPLAY
MODE
ThePulse OxygenSaturation(SpO,) LCD
Pulse Rate(PR) LCD
Pulse lntensitv (bar-araph) LCD
bar graph display
Pulse wave LCD
Sp0
2 Parameter Specification
Measurina ranae 0% -100% (the resolution
is 1%).
Accuracy 70% -100%: ±2% , below70%
unspecified.
Optical Sensor Red light (wavelength is 660 nm)
Infrared (wavelength is 905 nm)
Pulse Parameter Specification
Measuring range 30 bpm -250 bpm (the resolution
is 1 bpm)
Accuracv ±2 born or ±2% select laraer
Pulse Intensity
Range Continuous bar-graph display, the
higherdisplay indicate the stronger
pulse.
Battery Requirement
1.5V (AAA size) alkaline batteries x 2 or rechargeable battery
Battery Life
Up to 20 hours
Dimensions and Weight
Dimensions 2.36'(L) X 1.42'
(W) X 1.26"(H)
60(L) X36(W) X 32(H) mm
Weiaht About0.002 lbs (57g) w~h the batteries
APPENDIX
Guidanceand manufacture's declaratio~lectromagneticemission
forall EQUIPMENT and SYSTEMS
GUIDANCE AND MANUFACTURE'S DECLARATION-
ELECTROMAGNETIC EMISSION

The PX-131CO Pulse Oximeter is intended for use in the electromagnetic
environment specified below. The customer or the user of the PX-131 CO Pulse
Oximeter should assure that it is used in such an environment.
Emission test
Comoliance Electromaanetlc environment-auidance
RF emissions Group 1 The PX -131 CO PulseOximeter uses RF
CISPRII energrc only for their internal function .
There ore, its RF emissions are ve~ low
and are not likely to cause any inte erence
in nearbv electronic equioment.
RF emissions Class B The PX-131
CO PulseOximeter is suitable
CISPRII for use in all establishments.including
Harmonic Not
domestic establishments and those
emissions IEC applicable
directlyconnected to the publiclow-voltage
61000-3-2
power supply network that supplies
Not
buildings used for domestic purposes.
Voltage
fluctuations/flicker
applicable
emission
IEC 61000-3-3
Guidanceand manufacture's declaration-electromagnetic immunity
forall EQUIPMENT and SYSTEMS
GUIDANCE AND MANUFACTURE'S DECLARATION -
ELECTROMAGNETIC IMMUNITY
The PX-131CO Pulse Oximeter is intended for use in the electromagnetic
environment specified below. The user of PX-131 CO Pulse Oximeter should
assure that it is used in such an environment.
Immunity test IEC60601 Compliance Electromagnetic
test level level environment-guidance
Electrostatic ±6KV ± 6KV con tact Floors should be wood,
discharge (EDS) contact
±8KVai r concrete or ceramic tile. If
IEC 61000-4-2 ±8KVai r
floors are covered with
synthetic material, the
relative humidity should be
at least 30%.
Power frequency 3Nm 3Nm Power frequency of
(50Hz) magnetic magnetic
fields should be
field at levelscharacteristic of a
IEC 61000-4-8 typical location in a
typical
comme rcial or hospital
environment.
Guidance and manufacture 's declaration-electromagnetic immunity
for EQUIPMENT and SYSTEMS that are not LIFE SUPPORTING
GUIDANCE AND MANUFACTURE'$ DECLARATION-
ELECTROMAGNETIC IMMUNITY
The PX-131 CO Pulse Oximeter is intended for use in the electromainetic
environment specified below . The customer or the user of PX-131C Pulse
Oximeter should assure that it is used in such an environment.
Immunity test IEC60601 Compliance Electromagnetic
test level level environment-auidance
Portable and mobile RF
communication equircment
should be used no c oser to
any part of the PX-131 CO
PulseOximeter, including
cables, than the
recommended separation
distance calculated from the
equation applicable to the
frequency of the transmitter.
Recommended separation
distance
d = [ T, ]Jp 80MHz to 800MHz
Radiated 3V/m
d = [ i: ]Jp 800MHz to 2.5GHz
RF 80MHz
3V/m
ICE to
WhereP is the maximum
61000-4-3 2.5G Hz
output power rating of the
transmitter inwatts 0N)
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
survey, • should be lessthan
the compliance level in each
frequencyrange '·
Interference may occur in the
vicinfy of equipment marked
with the following
svmbol:¢'i'i
NOTE 1: At 80MHz and 800MHz, the higher frequency ran~e applies.
NOTE 2: These iuidelines may not apply in all situations. lectromagnetic
propagation is a ected by absorption and refle ctio n from structures, objects
and people.
a. Field strengthsfrom fixed transmitters, such as base stationsfor radio (cellular/
cordless) telephones and land mobileradios, amateurradio, AM and FM radio
broadcastand TV broadcastcannot be predicted theoretically with accuracy.
To assess theelectromagnetic environment due to fixed RF transmitters,
an electromagneticsite survey should be considered. If the measuredfield
strength in the location in whichThePX- 131 CO PulseOximeteris used
exceeds the applicable RF compliancelev el abcve, the PX-131 CO Pulse Oxim-
eter should be observed to verify normaloperation. tt abnormalperformance
isobserved, additional measures may be necessary, such as reorienting or
relocatini the PX-131CO PulseOximeter.
b. Over the equency range 150KHz to 80 MHz,field strengths should be less
than 3V/m.
Recommended separation distances between portableand mobile
RF communications equipmentandthe EQUIPMENT or SYSTEM
for EQUIPMENT or SYSTEM that not LIFE-SUPPORTING
RECOMMENDED SEPARATION DISTANCES BETWEEN
PORTABLE AND MOBILE RF COMMUNICATIONS EQUIPMENT
AND THE PX-131CO PULSE OXIMETER
The PX- 131 CO PulseOximeteris intended for use in the electromagnetic
environ ment in which radia ted RF disturbances are controlled The customer
or the user of th e PX-131 CO PulseOximeter can help preventelectromagnetic
interfere nce by maintaining a minim um distance between portable and mobile
RF communications equipment (transmitters) and the PX-131 CO Pulse
Oximeter as re commended below, according to the maximum output power
of the communications eauioment.
Separation distance according to frequency
of transmitter 1ml
Rated maximum
150 KHz to 80 80 MHz to 800 MHz to
output power of
MHz 800 MHz 2.5 GHz
transmitter
d=[~J/p
d=[~1/p
d =U,]Jp
(W)
O.Q1 0 .1 2 0.12 0.23
0.1 0.37 0.37 0.74
1 1.17 1.17 2.33
10 3.69
3.69 7.38
100 11.67 11 .67 23.33
For transmitters rated at a maximum output power not listedabcve, the
recom mended separationdistanced in mete rs (m) can be estimated using the
equation applicable to the frequency of the transmitter, whereP is the maximum
output power rating of the transmitter inwatts 0N) according to the transmitter
manufacturer.
NOTE 1: At 80MHz and 800MHz, the separation distance for the higher
frequency rangeapplies.
NOTE 2: These iuideiines may not apply in all situations. Electromagnetic
propagation isa ected by absorption and reflection from structures, objects
and oeople.
2-YEAR LIMITED WARRANTY
HoMedics sells its products with the intent that they are free of defects in
manufacture and workmanship for a period of 2 years from the date of original
purchase, except as noted below. HoMed ics warrants that its products wilr be
free of defects ,n material and workmanship under normal use and service.
This warranty ex1ends only to Consumers and does not ex1end to Retailers.
To obtain warranty ser vice on your HoMedics product, contact a consumer
relations representative for assistance. Please make sure to have the model
numbe r of the product available.
HoMedics does not authorize anyone , incl uding , but not limited to, Retailers,
the subsequen t Consumer purchaser of the product from a Retailer or rem ote
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; im proper
use of electrical/power supply; loss of power ; dropped product; malfunction
or damage of an operating part from failure to provide manufacturer's
recomme nded 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 effective 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 INC LUDING 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. HOM EDI CS
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
WHICH 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, HOMED ICS
RESERVES THE RIGHT TO MAKE PRODUCT SUBSTITUTIONS IN LIEU OF
REPAIR OR REPLACEMENT.
This warranty does not ex1end to the purchase of opened, used, repaired,
repackaged and /o r resealed products, including but not limited to the sale
of such products on internet auction sites and/or sa les of such products
by su rp lus or bulk resellers. Any and all warranties or guarantees shall
immediately cease and terminate as to any products or pa rts thereof which are
repaired, replaced, altered , or modified, without the prior express and written
consent of HoMedics.
This warranty provides you with specific legal rights. You mar have
additional riljhts which may vary from state to state. Because o ind ividual
state regulations, some of the above limitations and exclusions may not apply
to you.
For more in formati on rega rding our product line in the USA, please vis~:
www . homedics . com .
For service or repair, do not return lhis
unit to the retailer. Contact HoMedics
Consumer Relations:
Email: [email protected]
Phone: [phone]
Business Hours: 8:30am-7pm EST,
Monday-Friday
HoMedics" is a registered trademark of
HoMedics, LLC.
©2020 HoMedics, LLC. All rights
reserved.
IB-PX131 COB
Doc: L-00752, Rev.4
In USA Distributed by:
HoMedics USA, LLC
3000 N Pontiac Trail
Commerce Township , Ml 48390
Printed in China
In Canada Manufactured for:
HoMedics Group Canada
A Division of HoMedics USA , LLC
6460 Kennedy Road , Unit C.
Mississauga, ON LST 2X4
Toll Free: 1-888-225-7378
Made in China