GIMA KD-595 Talking Automatic Blood Pressure Monitor User Manual
- June 6, 2024
- GIMA
Table of Contents
KD-595 Talking Automatic Blood Pressure Monitor
PROFESSIONAL MEDICAL PRODUCTS
Gima S.p.A. – Via Marconi, 1 – 20060 Gessate (MI) Italy Italia: tel. 199 400 401 – fax 199 400 403 Export: tel. +39 02 953854209/221/225 – fax +39 02 95380056 gima@gimaitaly.com – export@gimaitaly.com www.gimaitaly.com
SFIGMOMANOMETRO AUTOMATICO VOCALE TALKING AUTOMATIC BLOOD PRESSURE MONITOR DISPOSITIF DE MONITORAGE POUR DÉTECTION AUTOMATIQUE DE LA PRESSION SANGUINE AVEC FONCTION VOCALE MONITOR AUTOMÁTICO CON FUNCIÓN DE VOZ PARA MEDIR LA PRESIÓN SANGUÍNEA MONITOR PARA DETEÇÃO AUTOMÁTICA DA PRESSÃO SANGUÍNEA COM FUNÇÃO DE VOZ SPRECHENDER MONITOR FÜR DIE AUTOMATISCHE ERFASSUNG DES BLUTDRUCKS
Manuale d’uso – User manual – Manuel de l’utilisateur Guía de Uso – Guia para utilização – Gebrauchsanweisung
M-32940-I-GB-F-E-P-D-Rev.0.07.14
ATTENZIONE: Gli operatori devono leggere e capire completamente questo manuale
prima di utilizzare il prodotto. ATTENTION: The operators must carefeully read
and completely understand the present manual before using the product. AVIS:
Les opérateurs doivent lire et bien comprendre ce manuel avant d’utiliser le
produit. ATENCIÓN: Los operadores tienen que leer y entender completamente
este manual antes de utilizar el producto. ATENÇÃO: Os operadores devem ler e
entender completamente este manual antes de usar o produto. ACHTUNG: Die
Bediener müssen vorher dieses Handbuch gelesen und verstanden haben, bevor sie
das Produkt benutzen.
32940 / KD-595
Andon Health Co., Ltd No. 3 JinPing, YaAn Road, Nankai District, Tianjin
300190, China Made in P.R.C.
Lotus Global Co., Ltd. 1 Four Seasons Terrace West Drayton, Middlesex, London,
UB7 9GG, United Kingdom
0197
ENGLISH
20
INDEX
Important InformatIon ……………………………………………………………. 21 ContEntS anD DISpLaY
InDICatorS ………………………………………….. 21 IntEnDED USE……………………………………………………………………………… 22
ContraInDICatIon……………………………………………………………………… 22 proDUCt
DESCrIptIon……………………………………………………………….. 22
SpECIfICatIonS…………………………………………………………………………… 23 notICE
………………………………………………………………………………………… 24 SEtUp anD opEratIng proCEDUrES
…………………………………………. 26 1. battery loading …………………………………………………………………………… 26 2.
Clock and date adjustment ………………………………………………………….. 26 3. Voice setting
………………………………………………………………………………. 27 4. Connecting the cuff to the monitor
……………………………………………….. 27 5. applying the cuff ………………………………………………………………………… 27
6. body posture during measurement……………………………………………….. 28 7. taking your blood
pressure reading ………………………………………………. 28 8. Displaying stored results
……………………………………………………………… 29 9. Deleting measurements from the memory
……………………………………… 29 10. assessing high blood pressure for adults
…………………………………….. 30 11. troubleshooting (1) ……………………………………………………………………. 31 12.
troubleshooting (2) ……………………………………………………………………. 31 maIntEnanCE
……………………………………………………………………………… 32 EXpLanatIon of SYmboLS on UnIt
……………………………………………. 33 ELECtromagnEtIC CompatIbILItY InformatIon ………………………. 34
WarrantY InformatIon ……………………………………………………………. 37
21
ENGLISH
IMPORTANT INFORMATION Normal blood pressure fluctuation
all physical activity, excitement, stress, eating, drinking, smoking, body
posture and many other activities or factors (including taking a blood
pressure measurement) will influence blood pressure value. because of this, it
is mostly unusual to obtain identical multiple blood pressure readings.
blood pressure fluctuates continually —– day and night. the highest value
usually appears in the daytime and lowest one usually at midnight. typically,
the value begins to increase at around 3:00am, and reaches to highest level in
the daytime while most people are awake and active.
Considering the above information, it is recommended that you measure your
blood pressure at approximately the same time each day.
please always relax a minimum of 1 to 1.5 minutes between measurements to
allow the blood circulation in your arm to recover. It is rare that you obtain
identical blood pressure readings each time.
CONTENTS AND DISPLAY INDICATORS
ENGLISH
22
INTENDED USE
fully automatic blood pressure monitor is for use by medical professionals or
at home and is a non-invasive blood pressure measurement system intended to
measure the diastolic and systolic blood pressures and pulse rate of an adult
individual by using a non-invasive technique in which an inflatable cuff is
wrapped around the upper arm. the cuff circumference is limited to 22cm-48cm
(approx. 8 21/32″~18 29/32″).
CONTRAINDICATION
It is inappropriate for people with serious arrhythmia to use this electronic
blood pressure monitor.
PRODUCT DESCRIPTION
based on oscillometric methodology and silicon integrated pressure sensor,
blood pressure and pulse rate can be measured automatically and non-
invasively. the LCD display will show blood pressure and pulse rate. the most
recent 60 measurements can be stored in the memory with date and time stamp.
the voice function will ease the operation. the Electronic blood pressure
monitor corresponds to the below standards: IEC 60601-1:2005/En
60601-1:2006/aC:2010 (medical electrical equipment — part 1: general
requirements for basic safety and essential performance), IEC60601-1-2:2007/En
60601-1-2:2007 /aC:2010 (medical electrical equipment — part 1-2: general
requirements for basic safety and essential performance – Collateral standard:
Electromagnetic compatibility requirements and tests), En 1060-1: 1995 + a1:
2002 + a2: 2009 (non-invasive sphygmomanometers – part 1: general
requirements), En 1060-3: 1997 + a1: 2005 + a2: 2009 (non-invasive
sphygmomanometers – part 3: Supplementary requirements for electro-mechanical
blood pressure measuring systems), anSI/aamI Sp-10:2002+a1:2003+a2:2006.
23
ENGLISH
SPECIFICATIONS
1. product name: blood pressure monitor
2. model: KD-595
3. Classification: Internally powered, type bf applied part, IpX0, no ap
or apg,Continuous operation
4. machine size: approx. 135mm x 108mm x 60mm
(6 1/32″ x 4 1/4″ x 2 3/8″)
5. Cuff circumference: 22-30 cm (8 21/32″ -11 13/16″),
30-42cm (11 13/16″-16 17/32″) (optional),
42-48 cm(16 17/32″-18 29/32″) (optional)
6. Weight: approx. 290g (10 7/32 oz.) (exclude batteries)
7. measuring method: oscillometric method, automatic inflation
and measurement
8. memory volume: 60 times with time and date stamp
9. power source: DC 6V 600ma, batteries: 4 ×1.5V
SIzE aa
10. measurement range:
Cuff pressure: 0-300 mmHg
Systolic:
60-260 mmHg
Diastolic:
40-199 mmHg
pulse rate: 40-180 beats/minute
11. accuracy:
pressure:
±3 mmHg
pulse rate: ±5%
12. Environmental temperature for operation: 5°C~40°C (41°f~104°f)
13. Environmental humidity for operation: 90%rH
14. Environmental temperature for storage and transport:
-20°C~55°C (-4°f~131°f)
15. Environmental humidity for storage and transport: 90% rH
16. Environmental pressure: 80kpa-105kpa
17. battery life: approx 180 times
18. a list of all components belonging to the pressure measuring system,
including accessories: pump,Valve, LCD, Cuff, Sensor
Note: these specifications are subject to change without notice.
ENGLISH
24
NOTICE
1. read all of the information in the operation guide and any other
literature in the box before operating the unit.
2. Stay quiet, calm and rest for 5 minutes before blood pressure measurement.
3. the cuff should be placed at the same level as your heart. 4. During
measurement, neither speak nor move your body and arm. 5. measuring on same
arm for each measurement. 6. please always relax at least 1 or 1.5 minutes
between measurements
to allow the blood circulation in your arm to recover. prolonged over-
inflation (cuff pressure exceed 300 mmHg or maintained above 15 mmHg for
longer than 3 minutes) of the bladder may cause ecchymoma of your arm. 7. this
Electronic blood pressure monitor s is designed for adults
and should never be used on infants or young children. Consult your physician
or other health care professionals before use on older children. 8. Do not use
this unit in a moving vehicle, this may result in erroneous measurement. 9.
blood pressure measurements determined by this monitor are equivalent to those
obtained by a trained observer using the cuff/stethoscope auscultation method,
within the limits prescribed by the american national Standard Institute,
Electronic or automated sphygmomanometers. 10. Information regarding potential
electromagnetic or other interference between the blood pressure monitor and
other devices together with advice regarding avoidance of such interference
please see part ELECtromagnEtIC CompatIbILItY InformatIon. 11. If Irregular
Heartbeat (IHb) brought by common arrhythmias is detected in the procedure of
blood pressure measurement, a signal of () will be displayed. Under this
condition, the Electronic blood pressure monitors can keep function, but the
results may not be accurate, it’s suggested that you consult with your
physician for accurate assessment. there are 2 conditions under which the
signal of IHb will be displayed: 1) the coefficient of variation (CV) of pulse
period >25%. 2) the difference of adjacent pulse period0.14s, and the number
of such pulse takes more than 53 percentage of the total number of pulse. 12.
please do not use the cuff other than supplied by the manufacturer, otherwise
it may bring biocompatible hazard and might result in measurement error. 13.
the monitor might not meet its performance specifications or cause safety
hazard if stored or used outside the specified temperature and humidity ranges
in specifications. 14. please do not share the cuff with other infective
person to avoid cross-infection. 15. medical aC adapter which output is DC
6.0V 600ma and complied
25
ENGLISH
with IEC 60601-1/En 60601-1/UL 60601-1 and IEC 60601-1-2/En 60601-1-2/UL
60601-1-2 is suitable for this monitor. please note that the monitor jack
size: hole Ø 5.5mm, center pin Ø 2.0mm. please pay attention to polarity. 16.
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 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 for help. 17. this blood pressure monitor is
verified by auscultatory method. It is recommended that you check annex b of
anSI/aamI Sp-10:2002+a1:2003+a2:2006 for details of verification method if you
need.
ENGLISH
26
SETUP AND OPERATING PROCEDURES
1. Battery loading
a. open battery cover at the back of the monitor.
b. Load four “aa” size batteries. please pay attention to polarity.
c. Close the battery cover. When LCD shows battery symbol
, replace
all batteries with new ones.
rechargeable batteries are not suitable for this monitor.
remove the batteries if the monitor will not be used
for a month or more to avoid relevant damage
of battery leakage.
avoid the battery fluid to get in your eyes. If it should get in your eyes, immediately rinse with plenty of clean water and contact a physician.
the monitor, the batteries and the cuff, must be disposed of according to local regulations at the end of their usage.
2. Clock and date adjustment
a. once you install the battery or turn off the monitor, it will enter Clock
mode, and LCD will display time and date.
b. While the monitor is in Clock mode, press the “Start” and “mEm” button
simultaneously for two seconds, the month will blink at first. press the
button “Start” repeatedly, the day, hour and minute will blink in turn. While
the number is blinking, press the button “mEm” to increase the number. Keep on
pressing the button “mEm”, the number will increase fast.
c. You can turn off the monitor by pressing “Start” button when the minute is
blinking, then the time and date is confirmed.
d. the monitor will turn off automatically after 1 minute of no operation with
the time and date unchanged.
e. once you change the batteries, you should readjust the time and date.
27
ENGLISH
3. Voice setting
a. Voice language setting: In clock mode, you can select
the voice language by keeping on press the button “mEm”.
now LCD blink “L0”, “L1”, “L2” … “Ln” (n means the number
of language) circularly. “L0” represents closing voice function,
“L1” represents language 1, “L2” represents language 2, …,
“Ln” represents language n, and so on. You can select the wanted language by releasing button “mEm” when
displa
y
the corresponding language code.
b. If the number of language is only one, LCD will twinkle “on”
and “–” circularly. Here “on” represents opening the voice
function and “–” represents closing the voice function.
c. Voice volume setting: once you have selected a language,
keeping on will appear
opnretshseinlegftthseidbeuottfotnhe”mLCEmD.”tahgeahinig.
ahecrothluembnaorsf,ba
r
the louder the volume. release button “mEm” at your desirable
volume for confirmation.
4. Connecting the cuff to the monitor
Insert the cuff tubing connector into the socket in the left
side of the monitor. make certain that the connector is
completely inserted to avoid air leakage during blood
pressure measurements.
5. Applying the cuff
a. pulling the cuff end through the medal loop (the cuff is packaged like this already), turn it outward (away from your body) and tighten it
and close the Velcro fastener.
b. place the cuff around a bare arm 1-2cm above
the elbow joint.
c. While seated, place palm upside in front of you
on a flat surface such as a desk or table.
position the air tube in the middle of your arm in line
with your middle finger.
d. the cuff should fit comfortably, yet snugly around
your arm. You should be able to insert one finger
between your arm and the cuff.
ENGLISH
28
Note: 1. please refer to the cuff circumference range in “SpECIfICatIonS”
to make sure that the appropriate cuff is used. 2. measuring on same arm each
time. 3. Do not move your arm, body, or the monitor and do not move the rubber
tube during measurement. 4. Stay quiet, calm for 5 minutes before blood
pressure measurement. 5. 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. Clean the cuff
after the usage of every 200 times is recommended. 6. Do not place the cuff
around your arm if the arm has any inflammation, acute diseases, infections
skin wounds.
6. Body posture during measurement
Sitting Comfortably Measurement
a. be seated with your feet flat on the floor,
and don’t cross your legs.
b. place palm upside in front of you on a flat surface
such as a desk or table
c. the middle of the cuff should be at the level
of the right atrium of the heart.
Lying Down Measurement a. Lie on your back. b. place your arm straight along
your side with your
palm upside. c. the cuff should be placed at the same level
as your heart.
7. Taking your blood pressure reading
a. after applying the cuff and your body is in a comfo
rtable position, press the “Start” button. a beep is heard and all display
characters are shown for self-test. You can check the LCD display according to
the right picture. please contact the service center if segment is missing.
b. If the monitor has stored results, the LCD will momentarily display the
most recent one. If no result has been stored, zero will appear on LCD.
c. If the voice function is switched on, the monitor will speak out
measurement tips.
d. then the monitor inflates the cuff until sufficient pressure has built up
for a measurement.
29
ENGLISH
then the monitor slowly releases air from the cuff and carries out the
measurement. finally the blood pressure and pulse rate will be calculated and
displayed on the LCD screen. the blood pressure classification indicator and
Irregular heartbeat symbol (if any) will blink on the screen. If the voice
function is on, it will announce the measurement result. the result will be
automatically stored in the monitor. e. after measurement, the monitor will
turn off automatically after 1 minute of no operation. alternatively, you can
press the “Start” button to turn off the monitor manually. f. During
measurement, you can press the “Start” button to turn off the monitor
manually.
Note: please consult a health care professional for interpretation of pressure
measurements.
8. Displaying stored results
a. In Clock mode, press “mEm” button, the last result
will be displayed with date and time. Irregular
heartbeat symbol (if any) and the indicator of blood
pressure classification will blink at the same time.
press “mEm” button repeatedly to review the
results measured previously.
b. If the voice function is on, the monitor will
announce each result in the memory.
c. When displaying the stored results, the monitor will turn off automatically
after 2 minutes of no operation. You can also press the button “Start”
to turn off the monitor manually.
9. Deleting measurements from the memory
When any result is displaying, keeping on pressing button “mEm” for three
seconds, all results will be deleted after three “beep”. press the button
“mEm” or “Start”, the monitor will turn off.
ENGLISH
30
10. Assessing high blood pressure for adults
the following guidelines for assessing high blood pressure (without regard to
age or gender) have been established by the World Health organization (WHo).
please note that other factors (e.g. diabetes, obesity, smoking, etc.) need to
be taken into consideration. Consult with your physician for accurate
assessment, and never change your treatment by yourself.
Classification of blood pressure for adults
Sistolic (mmHg)
Severe Hypertension 160
moderate Hypertension
150 mild Hypertension
140 High-normal bp
130
normal bp 120
BLOOD PRESSURE CLASSIFICATION optimal normal High-normal grade 1 Hypertension grade 2 Hypertension grade 3 Hypertension
SBP mmHg <120 120-129 130-139 140-159 160-179 180
DBP COLOR mmHg INDICATOR
<80
green
80-84
green
85-89
green
90-99
yellow
100-109 orange
110
red
80 85 90 100 110 Diastolic (mmHg)
WHo/ISH Definitions and classification of blood pressure levels
Note: It is not intended to provide a basis of any type of rush toward emergency conditions/diagnosis based on the color scheme and that the color scheme is meant only to discriminate between the different levels of blood pressure.
31
ENGLISH
11. Troubleshooting (1)
PROBLEM
LCD Display shows battery symbol
POSSIBLE CAUSE
Low battery
SOLUTION
Change all the batteries
arm or blood pressure monitor was moved during testing
re-test taking care to not move your arm or the blood pressure monitor
LCD Display shows “EE”
the cuff does not inflate properly or pressure falls quickly during testing
make certain the rubber tube is fully inserted into the blood pressure monitor
Irregular heartbeat (arrhythmia)
It is inappropriate for people with serious arrhythmia to use this blood pressure monitor
12. Troubleshooting (2)
PROBLEM
LCD Display shows “EE”
POSSIBLE CAUSE
the cuff was not properly applied or the rubber tube was bent or pressed
SOLUTION
review the cuff applying and testing sections of the instructions and re-test
LCD Display shows abnormal result
the cuff position was not correct or it was not properly tightened
body posture was not correct during testing
Speaking, arm or body movement, angry, excited or nervous during testing
apply the cuff correctly and try again
review the body posture and testing sections of the instructions and re-test
re-test when calm and without speaking or moving during the test
no response when you press Incorrect operation, or strong
button or load battery
electromagnetic interference
take out batteries for five minutes, and then reinstall all batteries
ENGLISH
32
MAINTENANCE
1. Do not drop this monitor or subject it to strong impact. 2. avoid high
temperature and solarization. Do not immerse the monitor
in water as this will result in damage to the monitor. 3. If this monitor is
stored near freezing, allow it to acclimate to room
temperature before use. 4. Do not attempt to disassemble this monitor. 5. If
you do not use the monitor for a long time, please remove
the batteries. 6. It is recommended the performance should be checked every 2
years
or after repair. please contact the service center. 7. Clean the monitor with
a dry, soft cloth or a soft cloth squeezed well after
moistened with water, diluted disinfectant alcohol, or diluted detergent. 8.
no component can be maintained by user in the monitor. the circuit
diagrams, component part lists, descriptions, calibration instructions, or
other information which will assist the user’s appropriately qualified
technical personnel to repair those parts of equipment which are designated
repairably can be supplied by us. 9. the monitor can maintain the safety and
performance characteristics for a minimum of 10,000 measurements or three
years, and the cuff integrity is maintained after 1,000 openclose cycles of
the closure. 10. It is recommended the cuff should be disinfected 2 times
every week if needed (for example, in hospital or in clinique). Wipe the inner
side (the side contacts skin) of the cuff by a soft cloth squeezed after
moistened with Ethyl alcohol (75-90%), then dry the cuff by airing.
33
ENGLISH
EXPLANATION OF SYMBOLS ON UNIT
Symbol for “tHE opEratIon gUIDE mUSt bE rEaD” (the sign background colour:
blue.the sign graphical symbol: white)
Symbol for “WarnIng”
Symbol for “tYpE bf appLIED partS” (the cuff is type bf applied part)
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 “manUfaCtUrEr”
0197 Symbol for “CompILES WItH mDD93/42/EEC rEQUIrEmEntS”
Symbol for “DatE of manUfaCtUrE”
Symbol for “EUropEan rEprESEntatIon”
Sn Symbol for “SErIaL nUmbEr”
Symbol for “KEEp DrY”
ENGLISH
34
ELECTROMAGNETIC COMPATIBILITY INFORMATION
Table 1 For all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacture’s declaration – electromagnetic emissions
the KD-595 is intended for use in the electromagnetic environment specified
below. the customer or the user of the KD-595 should assure that it is used in
such an environment.
Emissions test
Compliance
Electromagnetic environment – guidance
rf emissions CISpr 11
group 1
the KD-595 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
Harmonic emissions IEC 61000-3-2
Voltage fluctuations/ flicker emissions IEC 61000-3-3
Class b not applicable not applicable
the KD-595 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
Table 2 For all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacturer’s declaration – electromagnetic immunity
the KD-595 is intended for use in the electromagnetic environment specified below. the customer or the user of the KD-595 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
35
ENGLISH
Table 3 For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING
Guidance and manufacturer’s declaration – electromagnetic immunity
the KD-595 is intended for use in the electromagnetic environment specified below. the customer or the user of the KD-595 should assure that it is used in such an environment.
IMMUNITY test
IEC 60601 test level
Compliance Electromagnetic environment –
level
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 KD-595, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.
Recommended separation distance:
d = 1.2 P 80 mHz to 800 mHz d = 2.3 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 meters (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.b 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.
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 KD-595 is used exceeds
the applicable rf compliance level above, the KD-595 should be observed to
verify normal operation. If abnormal performance is observed, additional
measures may be necessary, such as re-orienting or relocating the KD-595. b
over the frequency range 150 kHz to 80 mHz, field strengths should be less
than 3 V/m.
ENGLISH
36
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 KD-595
the KD-595 is intended for use in an electromagnetic environment in which
radiated rf disturbances are controlled. the customer or the user of the
KD-595 can help prevent electromagnetic interference by maintaining a minimum
distance between portable and mobile rf communications equipment
(transmitters) and the KD-595 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
80 MHz to 800 MHz 800 MHz to 2,5 GHz
d = 1.2 P
d = 1.2 P
d = 2.3 P
0,01
0,12
0,1
0,38
1
1,2
10
3,8
100
12
0,12
0,23
0,38
0,73
1,2
2,3
3,8
7,3
12
23
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.
37
ENGLISH
Disposal: The product must not be disposed of along with other domestic waste.
The users must dispose of this equipment by bringing it to a specific
recycling point for electric and electronic equipment. For further information
on recycling points contact the local authorities, the local recycling center
or the shop where the product was purchased. If the equipment is not disposed
of correctly, fines or penalties may be applied in accordance with the
national legislation and regulations.
GIMA WARRANTY CONDITIONS
Congratulations for purchasing a gIma product.this product meets high
qualitative standards both as regards the material and the production. the
warranty is valid for 12 months from the date of supply of gIma. During the
period of validity of the warranty, gIma will repair and/or replace free of
charge all the defected parts due to production reasons. Labor costs and
personnel traveling expenses and packaging not included. all components
subject to wear are not included in the warranty. the repair or replacement
performed during the warranty period shall not extend the warranty. the
warranty is void in the following cases: repairs performed by unauthorized
personnel or with non-original spare parts, defects caused by negligence or
incorrect use. gIma cannot be held responsible for malfunctioning on
electronic devicesor software due to outside agents such as: voltage changes,
electro-magnetic elds, radio interferences, etc. the warranty is void if the
above regulations are not observed and if the serial code (if available) has
been removed, cancelled or changed. the defected products must be returned
only to the dealer the product was purchased from. products sent to gIma will
be rejected.
Read User Manual Online (PDF format)
Read User Manual Online (PDF format) >>