HoMedics | BPA-3000-EU | Instruction manual | HoMedics BPA-3000-EU blood pressure unit

IB-BPA3000-0912-01:Layout 1 09/01/2013 17:43 Page 1
Deluxe Automatic Arm
Blood Pressure Monitor
Instruction Manual
BPA-3000-EU
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HoMEdics Blood PrEssUrE Monitor
Before use
Before the blood pressure monitor is taken into use, a number of basic steps should be observed. Please read
this manual thoroughly before the blood pressure monitor is used for the first time and keep the manual for
future use.
the blood pressure monitor is intended for home use only. Any measurement is solely for your information
and can under no circumstances replace a visit to the doctor. the blood pressure measurements should
always be assessed by a qualified person (a doctor, nurse or similar) who is familiar with the user’s general
medical condition. By regular use and by keeping a record of the results, this person can be kept well
informed about developments in the user’s blood pressure. Measurements must never be interpreted by the
user with the aim of changing levels in the use of medicine as prescribed by a doctor. the doctor’s
instructions must be followed At All tiMEs.
Use of appropriate cuff size is crucial to correct measurement. Follow the instructions presented in this
manual and printed on the cuff to ensure that the correct cuff size is used.
the blood pressure monitor is not suited for users who suffer from arrhythmia (heart rhythm disturbances)
and errors may occur in the measurement results if the user has suffered a stroke, suffers from cardiovascular
diseases, has a very low blood pressure, or suffers from other symptoms such as circulatory diseases (diabetes,
kidney diseases, arterial sclerosis (deposits in the arteries), or poor peripheral blood circulation (e.g. in hands
and feet).
Electromagnetic disturbances: the device contains sensitive electronic components. Keep it clear of strong
electric or electromagnetic fields in the immediate surroundings (e.g. mobile telephones, microwave ovens)
as these may temporarily reduce measurement accuracy.
Use the blood pressure monitor only for its original purpose.
the device is intended for measurement of blood pressure and pulse with adult persons. do not apply the
monitor to infants nor to persons who cannot express their permission. the device must not be operated by
children.
the blood pressure monitor functions in accordance with the oscillometric measurement principle. these
blood pressure changes are measured in the cuff on the basis of the arm pulse and are converted into a
numerical value of the current blood pressure. simultaneously, the number of pulse beats are registered and
calculated as number of pulse beats per minute.
there are two kinds of discernible blood pressures. Both are expressed in mmHg (millimetres on the mercury
column): the systolic and the diastolic. the systolic (‘the high blood pressure’) states the pressure when the
heart chambers contract to send blood through your body, and the diastolic (‘the low blood pressure’) states
the pressure when the heart is at ease and filling with blood before the next muscle contraction. the
connection between values (mmHg) is expressed as e.g. 130 over 85 which means that the systolic pressure is
130 and the diastolic pressure is 85.
Why is it important to keep an eye on your blood pressure?
GB
Many of today’s most common diseases are connected to hypertension , also referred to as ‘high blood
pressure’. Hypertension is closely connected to cardiovascular diseases, and for people in the danger zone the
blood pressure provides an important tool to keep an eye on the development.
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What are systolic pressure and diastolic
pressure?
When ventricles contract and pump blood out of the heart,
blood pressure reaches its maximum value, the highest
pressure in the cycle is known as systolic pressure. When
the heart relaxes between heartbeats, the lowest blood
pressure is diastolic pressure.
systolic
diastolic
blood discharging
artery
blood entering
vein
press
relax
What is the standard blood pressure
classification?
Below illustrates the blood pressure classification mode by
World Health organization (WHo) and international
society of Hypertension(isa) in 1999.
level
Blood
Pressure
(mmHg)
Optimal
Normal
High-normal
Mild
Moderate
optimal
norm.
norm.
G1
G2
Severe
G3
sYs
<120
120~129
130~139
140~159
160~179
>180
diA
<80
80~84
85~89
90~99
100~109
>110
CautION
only a physician/GP can tell you your normal blood pressure range and the point at which you are at risk.
consult your physician to obtain these values. if the measurements taken with this product fall outside the
range, consult your physician/GP.
GB
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sAFEtY inForMAtion
caution: consult accompanying
documents
type B applied part
cE mark: conforms to essential
requirements of the Medical device
directive 93/42/EEc.
disposal: do not dispose of this product
as unsorted municipal waste. collection
of such waste separately for special
treatment is necessary.
Manufacturer
direct current
specifies serial number
CautION
GB
• this device is intended for adult use only.
• this device is intended for non-invasive measuring and monitoring of arterial blood pressure. it is not
intended for use on extremities other than the arm.
• do not confuse self-monitoring with self-diagnosis. this unit allows you to monitor your blood pressure. do
not begin or end medical treatment based solely on the readings from this unit. Always consult your
physician first.
• if you are taking medication,consult your physician to determine the most appropriate time to measure
your blood pressure. never change a prescribed medication without consulting your physician.
• this unit is not suitable for continuous monitoring during medical emergencies or operations.
• if the cuff pressure exceeds 40 kPa (300 mmHg), the unit will automatically deflate. should the cuff not
deflate when pressures exceeds 40 kPa (300 mmHg), detach the cuff from the arm and press the
button
to stop inflation.
• to avoid measurement errors, carefully read this manual before using the product.
• the equipment is not AP/APG equipment and not suitable for use in the presence of a flammable anesthetic
mixture with air of with oxygen or nitrous oxide.
• the operator shall not touch output of Ac adapter and the patient simultaneously.
• to avoid measurement errors, please avoid the condition of strong electromagnetic field radiated
interference signal or electrical fast transient/burst signal when using the Ac adaptor.
• the user must check that the equipment functions safely and see that it is in proper working condition
before being used.
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LCD display signal
Symbol
Description
Explanation
systolic blood pressure
High pressure result
diastolic blood pressure
low pressure result
Pulse
Pulse/minute
deflating
cUFF is deflating
time (hour:minute)
current time
Memory
if “M” shows, the displayed measurement values is
from the memory.
mmHg
Measurement Unit of the blood pressure
(1mmHg = 0.133kPa)
kPa
Measurement Unit of the blood pressure
(1kPa = 7.5mmHg)
low battery
Batteries are low and need to be replaced
Movement error symbol
Movement can result in an inaccurate reading
Average
the average of blood pressure
recalling
recalling records
Arrhythmia
irregular heartbeat
User A
the User A is chosen
User B
the User B is chosen
Grade
the grade of the blood pressure
GB
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Monitor coMPonEnts
cUFF
Air HosE
Air connEctor PlUG
UsEr sElEct sWitcH
MEM
dc PoWEr socKEt
MEM/UP toUcH KEY
stArt/stoP BUtton
lcd disPlAY
sEt/doWn toUcH KEY
BAttErY coMPArtMEnt
Inserting and Changing Batteries
List
1. Blood Pressure Monitor
2. cuff
MEM
3. 4*AAA alkaline batteries
4. User manual
1. slide off the battery cover.
2. install the batteries by matching the
correct polarity, as shown.
3. replace the cover.
Replace the batteries whenever the below happen
• the
shows
• the display dims
• the display does not light up
MEM
CautION
GB
remove batteries if the device is not likely to be used for
some time.
6
Alternatively an Ac adaptor powered mode
is available: 100-240V~, 50-60HZ, 400mA
(You can purchase the Ac adaptor
PP-AdPr2K3K-EU from the HoMedics
website).
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sEttinG dAtE, tiME And MEAsUrEMEnt Unit
it is important to set the clock before using your blood pressure monitor, so that a time stamp can be
assigned to each record that is stored in the memory. (year: 2000—2050, time: 24 H)
1. When the unit if off, hold “sEt” for 3 seconds
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2. Press the “MEM” to change the [YEAr].
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3. When you get the correct year, press “sEt” and it will turn to
the next step automatically.
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4. repeat steps 2 and 3 to set the [MontH] and [dAY].
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5. repeat steps 2 and 3 to set the [HoUr] and [MinUtE].
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6. repeat steps 2 and 3 to set the set the [Unit].
7. once the unit has been set, “done” will show and then the
unit will turn off automatically.
GB
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HoW to UsE tHE Blood PrEssUrE dEVicE
Fitting the cuff
correct cuff size is critical to accurate measurement. this monitor comes with a standard size 22-32cm arm
cuff. A large size cuff 32-42cm is available from the HoMedics website www.homedics.co.uk
1. if the cuff is not assembled at first use, put the end of the cuff which is furthest
away from the tube through the d-ring to form a noose.
2. Apply the tube to the left side of the device.
cm
2~31.2”)
(0.8”~
.–.
.
–
.
.
.
3. remove tight-fitting clothing from your left upper arm and position the cuff at
approximately 2-3 cm above the elbow so that the tube is centred at the middle
of the arm. the tube must face downward towards the hand.
4. Pull gently at the end of the cuff so that it tightens easily and smoothly around
the arm. the cuff is secured by pulling the Velcro fastener towards the cuff.
5. You should be able to fit two fingers between the cuff and your arm. the cuff
should not be fitted any tighter than this.
6. relax your body and rest your arm on a table with your palm up so that the cuff is
positioned at the same height as the heart. Make sure that the tube does not
bend.
GB
if it is not possible to fit the cuff on the left arm, it can be placed on the
right arm instead. However, it is important that all measurements are
carried out on the same arm. if the measurement is to be taken on the
right arm, the artery symbol on the cuff should be positioned above the
main artery. Press the arm’s arteries with two fingers at approximately 2
cm above the elbow on the inside of the arm to find out where the
pulse is strongest. this is the main artery.
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Worth knowing about blood pressure measurement
• Blood pressure measurements should be performed in quiet and comfortable surroundings as
measurements can be affected by high or low temperatures. the blood pressure should be measured at
normal body temperatures.
• do not move or speak during measurement. Keep your feet flat on the floor.
• do not touch the cuff or the blood pressure device during measurement.
• to obtain the best possible measurement, the blood pressure should be measured at approximately the
same time every day, and on the same arm.
• if you are to perform several successive measurements, please wait 5 minutes between each measurement.
• the measurements are for guidance only. if you have doubts about your blood pressure, consult your
doctor.
• the blood pressure device automatically deflates when the pressure exceeds 300 mmHg.
• the product is not suited for persons suffering from arrhythmia (heart rhythm disturbances).
• Measurement errors may occur if the user suffers from diabetes, poor blood circulation, kidney problems, or
has suffered a stroke.
• the blood pressure changes with every heartbeat and is consequently changing constantly 24 hours a day.
• the measurement of blood pressure can be influenced by the user’s position, condition, or other factors. to
obtain the highest degree of accuracy it is recommended that the measurement is taken 1 hour after
workout, bathing, finishing a meal, consuming alcoholic or caffeine beverages, or after smoking.
• Before measurement it is recommended that you sit still and relax for 15 minutes. the user should not be
physically tired or exhausted when the measurement is taken.
• the user must not talk or move arm or hand during measurement.
How to measure the blood pressure
1. Press the
to turn on the monitor, and it will start and finish the whole measurement automatically.
2. When the measurement is completed, the cuff automatically deflates and the display will show the systolic
pressure, the diastolic pressure, and the pulse. the measurement is simultaneously stored in the monitor’s
memory.
3. the device automatically switches off approximately 1 minute after use but can also be switched off
manually by pressing the
button.
NOtE
if necessary, a measurement can be interrupted by pressing the
button. the cuff will subsequently deflate
immediately.
the cuff will automatically re-inflate if the device determines that the body requires higher pressure to
complete the measurement.
GB
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Recalling the records
1. Please choose user A or B when the blood pressure monitor is
turned off. then press the “MEM” to show the average of the
records you have taken. the sign of "AVG will show in the right
corner.
2. Press the “MEM” or “sEt” to get the record
you want.
UP
DOWN
the order of the record, date, time will
display alternately.
the month and day
the current record
and total number of
records.
the corresponding
time will show and
alternate with date.
CautION
the most recent record (1) is shown first. Each new measurement is assigned to the first (1) record. All other
records are pushed back one digit (e.g., 2 becomes 3, and so on), and the last record (60) is dropped from the
list.
Deleting your records
if you did not get the correct measurement, you can
delete all results using the following steps.
1. Please choose user A or B when the blood
pressure monitor is turned off, press and hold
“MEM” for 3 seconds and the flash display will
show dEl All.
2. Press “sEt” to confirm deleting and the monitor
will turn off automatically.
3. if you don’t want to delete the records, press
to escape.
GB
4. if there is no record the right display will show.
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Error search
this section includes a list of error messages and frequently asked questions for problems you may encounter
with your blood pressure monitor. if irregularities occur during use, please check the following items.
pROBLEM
No power
Low batteries
SyMptOM
CHECk tHIS
REMEDy
Batteries are exhausted.
replace with new batteries
Batteries are inserted
incorrectly
insert the batteries correctly
Batteries are low.
replace with new batteries
E 1 shows
the cuff is not secure.
refasten the cuff and then
measure again
E 2 shows
the cuff is very tight
refasten the cuff and then
measure again
E 3 shows
the pressure of the cuff is
excess.
refasten the cuff and then
measure again
E 10 or E 11 shows
the monitor detected
motion while measuring
Movement can affect the
measurement. relax for a
moment and then measure
again
E 20 or E 21 shows
Measure incorrectly
relax for a moment and then
measure again
A calibration error occurred.
retake the measurement. if
the problem persists, contact
the retailer or our customer
service department for further
assistance. refer to the
warranty for contact
information and return
instructions.
display is dim or will
not light up.
show on the
display
Error Message
Eexx, shows on the
display.
if the device still does not function, please contact the store where the device was purchased. do not attempt
to open the device or adjust any of the inner parts yourself.
GB
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GB
Specifications
power supply
Battery powered mode: 6Vdc 4*AAA alkaline batteries
Ac adaptor powered mode: 100-240V~, 50-60HZ, 400mA
(You can purchase the Ac adaptor PP-AdPr2K3K-EU from the
HoMedics website).
Display mode
digital lcd V.A.128*50mm
Measurement mode
oscillographic testing mode
Measurement range
Pressure: 0~40kpa (0~300mmHg)
pulse value: (40~199) times/minute
accuracy
Pressure:
15~25ºc within ± 0.4kpa (3mmHg)
10ºc~40ºc (out of 15ºc~25ºc)
within ± 0.8kpa (6mmHg)
pulse value: ±5%
Normal working condition
temperature: 10ºc~40ºc relative humidity ≤80%
Storage & transportation condition
temperature: -20ºc~60ºc
relative humidity: 10%~93%
Measurement perimeter of the
upper arm
About 22cm~32cm
Weight
Approx. 300g (Excluding the batteries)
External dimensions
Approx. 180*100*39mm
attachment
4*AAA alkaline batteries, manual, cuff
Mode of operation
continuous operation
Degree of protection
type B applied part
protection against ingress of water
iPX-0
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Cleaning and maintenance
the blood pressure monitor and the cuff can be wiped with a soft cloth moistened with a mild detergent and
wiped dry with a soft, dry cloth or paper towel. never use strong, caustic detergents as these may cause
damage to the synthetic parts. Also, never use diluents, alcohol or kerosene to clean the device.
Safety and electrical devices
• When the device is not used, store it in a safe place.
• only use the device on the upper arm, not on other body parts.
• When the device is not used for extended periods of time, it is recommended that you remove the batteries
to avoid leakage which may cause damage to the device.
• if the device has been stored at very low temperatures near the freezing point, please allow it to obtain
room temperature before using it again.
• neither device nor cuff must be dissembled as this may cause serious damage to the device. if repair is
necessary, the device must be returned to the store where it was purchased. do not attempt to open the
device or adjust the inner parts yourself.
• do not submerge the device in water or other liquids as this will cause damage to the device.
• do not expose the device nor the cuff to extreme temperatures, moisture or direct sunlight. Protect the
device against dust.
• the cuff and the tube should not be folded up tightly. the device must not be activated if it is not
appropriately fitted to the upper arm.
• Avoid dropping the device and do not subject it to heavy pressure.
• the device must not be exposed to extreme shocks such as being dropped on the floor.
• the device is intended for use in private households only and is only suited for use with adults (over 18
years of age).
• if the highly unlikely incident should occur that the cuff continues to inflate and does not stop, immediately
remove the cuff from the upper arm.
Battery Directive
this symbol indicates that batteries must not be disposed of in the domestic waste as they contain
substances which can be damaging to the environment and health. Please dispose of batteries in
designated collection points.
WEEE explanation
this marking indicates that this product should not be disposed with other household wastes
throughout the EU. to prevent possible harm to the environment or human health from uncontrolled
waste disposal, recycle it responsibly to promote the sustainable reuse of material resources. to return
your used device, please use the return and collection systems or contact the retailer where the
product was purchased. they can take this product for environmental safe recycling.
GB
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table 1 Guidance and manufacture’s declaration – electromagnetic emissions for all EQUiPMEnt
and sYstEMs
Guidance and manufacture’s declaration – electromagnetic emission
GB
the BPA-3000-EU is intended for use in the electromagnetic environment specified below. the customer of
the user of the BPA-3000-EU should assure that it is used in such and environment.
Emission test
Compliance
Electromagnetic environment – guidance
rF emissions
cisPr 11
Group 1
the BPA-3000-EU 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 emission
cisPr 11
class B
Harmonic emissions
iEc 61000-3-2
not applicable
Voltage fluctuations/
flicker emissions iEc
61000-3-3
not applicable
the BPA-3000-EU 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.
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table 2 Guidance and manufacture’s declaration – electromagnetic immunity – for all
ME EQUiPMEnt and ME sYstEMs
Guidance and manufacture’s declaration – electromagnetic immunity
the BPA-3000-EU is intended for use in the electromagnetic environment specified below. the customer of
the user of the BPA-3000-EU should assure that it is used in such an environment.
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 floor are covered with synthetic
material, the relative humidity should be at
least 30%.
Electrical fast
transient/burst
iEc 61000-4-4
±2 kV for power
supply lines
±2kV for power
supply lines
Mains power quality should be that of a
typical commercial or hospital environment
surge iEc
61000-4-5
±1 kV line(s) to
line(s)
±1 kV differential
mode
Mains power quality should be that of a
typical commercial or hospital environment.
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines iEc
61000-4-11
<5% Ut
(>95% dip in Ut )
for 0.5 cycle
<5% Ut
(>95% dip in Ut )
for 0.5 cycle
40% Ut
(60% dip in Ut )
for 5 cycles
40% Ut )
(60% dip in Ut )
for 5 cycles
Mains power quality should be that of a
typical commercial or hospital environment.
if the user of the BPA-3000-EU requires
continued operation during power mains
interruptions, it is recommended that the
BPA-3000-EU be powered from an
uninterruptible power supply or a battery.
70% Ut
(30% dip in Ut )
for 25 cycles
70% Ut
(30% dip in Ut )
for 25 cycles
<5% Ut
(>95% dip in Ut )
for 5 sec
<5% Ut
(>95% dip in Ut )
for 5 sec
3A/m
3A/m
Immunity test
Power frequency
(50Hz) magnetic
field iEc
61000-4-8
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.
GB
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table 3 Guidance and manufacture’s declaration – electromagnetic immunity – for ME
EQUiPMEnt and ME sYstEMs that are not liFE-sUPPortinG
Guidance and manufacture’s declaration – electromagnetic immunity
the BPA-3000-EU is intended for use in the electromagnetic environment specified below. the customer or
the user should assure that it is used in such an environment.
Immunity test
IEC 60601 test
level
Compliance level
conducted rF
iEc 61000-4-6
3 Vrms
3 Vrms
150 kHz to 80 MHz
radiated rF
iEc 61000-4-3
3 V/m 80 MHz
to 2.5 GHz
Electromagnetic environment - guidance
Portable and mobile rF communications
equipment should be used no closer to any
part of the Ys-6100, including cables, than
the recommended separation distance
calculated from the equation applicable to
the frequency of the transmitter.
Recommended separation distance
—
d = 1.167 √ P
—
d = 1.167 √ P 80 MHz to 800 MHz
—
d = 2.333 √ P 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).
3 V/m
Field strengths from fixed rF transmitters, as
determined by an electromagnetic site
survey, a should be less than the compliance
level in 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.
GB
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.
a 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 ElE007839V1 is used
exceeds the applicable rF compliance level above, the ElE007839V1 should be observed to verify normal
operation. if abnormal performance is observed, additional measures may be necessary, such as
reorienting or relocating the ElE007839V1.
b over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
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table 4 recommended separation distances between portable and mobile rF communications
equipment and the EQUiPMEnt or sYstEM – for ME EQUiPMEnt or ME sYstEM that are not
liFE-sUPPortinG
recommended separation distances between portable and mobile rF communications equipment and the
ElE007839V1 Fitness Equipment.
the BPA-3000-EU is intended for use in an electromagnetic environment in which radiated rF disturbances
are controlled. the customer or the user of the BPA-3000-EU can help prevent electromagnetic interference
by maintaining a minimum distance between portable and mobile rF communications equipment
(transmitters) and the BPA-3000-EU 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
m
150 kHz to 80 MHz
—
d = 1.167 √ P
80 MHz to 800 MHz
—
d = 1.167 √ P
800 MHz to 2,5 GHz
—
d = 2.333 √ P
0,01
0.167
0.167
0.233
0,1
0.369
0.369
0.738
1
1.167
1.167
2.333
10
3.690
3.690
7.338
100
11.67
11.67
23.330
For transmitters rated at a maximum output power not listed above, the recommended separation distance
d in meters (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 is affected by
absorption and reflection from structures, objects and people.
GB
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HoMedics Group ltd, HoMedics House
somerhill Business Park, Five oak Green road
tonbridge, Kent tn11 0GP, UK
0120
register your product today at:
http://www.homedicsgroup.com/register
iB-BPA-3000EU-0912-01
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