Gima KD-5920 User manual

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.
Avoid compression or restriction of the connection tubing during
measurement, which may cause ination error, or harmful injury due to
continuous cuff pressure.
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 at surface such as a desk or table. Position the air
tube in the middle of your arm in line with your
middle nger.
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 comfortable position, press the
“START” button. A beep is heard and all display characters are shown for
self-test. See Picture 7-1. Please contact the service center if segment is
missing.
Picture 7-1 Picture 7-2 Picture 7-3 Picture 7-4 Picture 7-5
IMPORTANT INFORMATION .............................................................................3
CONTENTS AND DISPLAY INDICATORS .........................................................4
INTENDED USE.................................................................................................5
CONTRAINDICATION........................................................................................5
PRODUCT DESCRIPTION.................................................................................6
SPECIFICATIONS..............................................................................................7
NOTICE .............................................................................................................9
SETUP AND OPERATING PROCEDURES ......................................................12
1. Battery loading ............................................................................................12
2. Clock and date adjustment .........................................................................13
3. Voice setting ................................................................................................14
4. Connecting the cuff to the monitor .............................................................15
5. Applying the cuff .........................................................................................15
6. Body posture during measurement.............................................................16
7. Taking your blood pressure reading ............................................................17
8. Displaying stored results.............................................................................19
9. Deleting measurements from the memory..................................................21
10. Assessing high blood pressure for adults .................................................21
11. Technical alarm description.......................................................................23
12. Troubleshooting (1)....................................................................................24
13. Troubleshooting (2)....................................................................................25
MAINTENANCE...............................................................................................27
EXPLANATION OF SYMBOLS ON UNIT.........................................................28
ELECTROMAGNETIC COMPATIBILITY INFORMATION .................................30
WARRANTY INFORMATION ...........................................................................35
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 inuence blood pressure value. Because of this, it is mostly
unusual to obtain identical multiple blood pressure readings.
Blood pressure uctuates 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.
Too frequent measurements may cause injury due to blood ow interference,
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.
NOTICE
1. Read all of the information in the operation guide and any other literature
in the box before operating the unit.
2. Stay still, 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-ination
(cuff pressure exceed 300 mmHg or maintained above15 mmHg for longer
than 3 minutes) of the bladder may cause ecchymoma of your arm.
7. Consult your physician if you have any doubt about below cases:
1) The application of the cuff over a wound or inammation diseases;
2) The application of the cuff on any limb where intravascular access
or therapy, or an arterio-venous (A-V) shunt, is present;
3) The application of the cuff on the arm on the side of a mastectomy;
4) Simultaneously used with other monitoring medical equipments on the
same limb;
5) Need to check the blood circulation of the user.
8. This Electronic Sphygmomanometers is designed for adults and
should never be used on infants or young children. Consult your phy-
sician or other health care professionals before use on older children.
9. Do not use this unit in a moving vehicle, This may result in erroneous mea-
surement.
10. 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.
11. 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 ELECTROMA-
GNETIC COMPATIBILITY INFORMATION.
12. 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 Sphygmomanometers 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 coefcient of variation (CV) of pulse period >25%.
2) The difference of adjacent pulse period≥0.14s, and the number of such
pulse takes more than 53 percentage of the total number of pulse.
13. Please do not use the cuff other than supplied by the manufacturer,
otherwise it may bring biocompatible hazard and might result in
measurement error.
CONTENTS AND DISPLAY INDICATORS
INTENDED USE
Fully Automatic Electronic Sphygmomanometer 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 inatable cuff is wrapped around the upper arm. The cuff circumference
is limited to 22cm-42cm (approx. 8 21/32”-16 17/32”).
CONTRAINDICATION
It is inappropriate for people with serious arrhythmia to use this
Electronic Sphygmomanometer.
14. The monitor might not meet its performance specications or cause
safety hazard if stored or used outside the specied temperature and
humidity ranges in specications.
15. Please do not share the cuff with other infective person to avoid
cross-infection.
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.
SETUP AND OPERATING PROCEDURES
1. Battery loading
a. Open battery cover at the back of the monitor.
b. Load four “AAA” 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 uid 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.
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 4x30 measurements can be stored in the memory with date
and time stamp. The voice function will ease the operation. The Electronic
Sphygmomanometers corresponds to the below standards: IEC 60601-1:2005
+A1:2012(E)/EN 60601-1:2006/A11: 2011 (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), IEC80601-2-30:2009+AMD1:2013/EN 80601-
2-30:2010/A1:2015(Medical electrical equipment – Part 2-30: Particular
requirements for the basic safety and essential performance of automated
non-invasive sphygmomanometers)EN 1060-1: 1995 + A2: 2009 (Non-invasive
sphygmomanometers - Part 1: General requirements), EN 1060-3: 1997 +
A2: 2009 (Non-invasive sphygmomanometers - Part 3: Supplementary
requirements for electro-mechanical blood pressure measuring systems).
14. Environmental temperature for storage and transport: -20°C~50°C
(-4°F~122°F)
15. Environmental humidity for storage and transport: ≤85%RH
16. Environmental pressure: 80kPa-105kPa
17. Battery life: Approx 100 times.
18. All components belonging to the pressure measuring system, including:
Pump,Valve, LCD, Cuff, Sensor
Note: These specications are subject to change without notice.
d. The cuff should t comfortably, yet snugly around your arm. You should be
able to insert one nger between your arm and the cuff.
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. Body posture during measurement
Sitting Comfortably Measurement
a. Be seated with your feet at on the oor, and don’t
cross your legs.
b. Place palm upside in front of you on a at surface
such as a desk or table.
b. Then the current memory bank (U1, U2, U3 or U4) is shown. See picture
7-2. Press “MEM” button to change over to other bank. Conrm your
selection by pressing “START” button. The current bank can also be
conrmed automatically after 5 seconds with no operation.
c. 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.
See Picture 7-3.
d. If the voice function is switched on, the monitor will speak out measurement
tips.
e. Then the monitor starts to seek zero pressure. See picture 7-4.
f. Then the monitor inates the cuff until sufcient pressure has built up for a
measurement. 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
classication 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. See Picture 7-5.
g. 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.
h. During measurement, you can press the “START” button to turn off the
monitor manually.
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 display the corresponding
language code.
Picture 3-1 Picture 3-2
b. Voice volume setting: Once you have selected a language, keeping on
pressing the button “MEM” again. A column of bar will appear on the left
side of the LCD. The higher the bars, the louder the volume. Release button
“MEM” at your desirable volume for conrmation.
SPECIFICATIONS
1. Product name: Arm Blood Pressure Monitor
2. Model: 32777 / KD-5920
3. Classication: Internally powered, Type BF applied part, IP20, No AP
or APG, Continuous operation
4. Machine size: Approx.150 mm × 95 mm × 41 mm (5 29/32” x 3 3/4” x 1 5/8”)
5. Cuff circumference: 22-30 cm (8-11”), 30-42 cm (11-16”) optional,
42-48 cm (16-18.2”) optional
6. Weight: Approx. 235 g (8 9/32 oz.) (exclude batteries)
7. Measuring method: Oscillometric method, automatic ination and
measurement
8. Memory volume: 4×30 times with time and date stamp
9. Power source: batteries: 4×1.5 V SIZE AAA
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: 10°C~40°C (50°F~104°F)
13. Environmental humidity for operation: ≤85% RH
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 rst. 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.
Picture 2-1 Picture 2-2 Picture 2-3 Picture 2-4 Picture 2-5 Picture 2-6
c. You can turn off the monitor by pressing “START” button when the minute is
blinking, then the time and date is conrmed.
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.
JOLLY DIGITAL BLOOD PRESSURE MONITOR
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ATTENTION:
The operators must carefully read
and completely understand the present manual
before using the product.
PROFESSIONAL MEDICAL PRODUCTS
Operation Guide
Rubber tube
Pulse
Deate the remnant air
Low battery
Irregular heartbeat symbol
START/STOP button
Cuff tubing
connector
Gima S.p.A.
Via Marconi, 1 - 20060 Gessate (MI) Italy
[e-mail] - [email protected]
www.gimaitaly.com

b. Alternatively, press “MEM” button in Clock Mode to display the stored
results. The current memory bank will blink and the amount of results in this
bank will be displayed. Press “START” button to change over to other bank.
Conrm your selection by pressing “MEM” button. The current bank can
also be conrmed automatically after 5 seconds with no operation.
See picture 8-1.
c. After selecting the memory bank, the LCD will display the average values in
this bank. See picture 8-2&8-3&8-4. If no result stored, LCD will show zeros.
See picture 8-5. Press “MEM” button to switch to next scene.
d. When the average is displayed, press the “MEM” button, the most recent
result will be displayed. See picture 8-6. Followed by, the blood pressure
and pulse rate will be shown separately. Irregular heartbeat symbol (if any)
will blink. Press “MEM” button again to review the next result. In this way,
repeatedly pressing the “MEM” button displays the respective results
measured previously.
e. When displaying the stored results, the monitor will turn off automatically
after 1 minute 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. Press the button “MEM” or “START”,
the monitor will turn off.
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
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.
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 qualied
technical personnel to repair those parts of equipment which are
designated repairably can be supplied.
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 open–close cycles of the closure.
11. Technical alarm description
The monitor will show ‘HI’ or ‘Lo’ as technical alarm on LCD with no delay if
the determined blood pressure (systolic or diastolic) is outside the rated range
specied in part SPECIFICACIONS. In this case, you should consult a physician
or check if your operation violated the instructions.
The technical alarm condition (outside the rated range) is preset in the factory
and cannot be adjusted or inactivated. This alarm condition is assigned as low
priority according to IEC 60601-1-8.
The technical alarm is non-latching and need no reset. The signal displayed on
LCD will disappear automatically after about 8 seconds.
13. Troubleshooting (2)
ELECTROMAGNETIC COMPATIBILITY INFORMATION
Table 1
For all ME EQUIPMENT and ME SYSTEMS
Symbol for “COMPILES WITH MDD93/42/EEC
REQUIREMENTS”
Symbol for “DATE OF MANUFACTURE”
Symbol for “EUROPEAN REPRESENTATION”
Symbol for “SERIAL NUMBER”
Symbol for “KEEP DRY”
Symbol for “KEEP AWAY FROM SUNLIGHT”
Symbol for “PRODUCT CODE”
Symbol for “LOT NUMBER”
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.
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”
Note: Please consult a health care professional for interpretation of pressure
measurements.
8. Displaying stored results
a. After the measurement, you can review the measurements in the current
memory bank by pressing button “MEM”. Now the LCD displays the
amount of the results in the current bank.
Picture 8-1 Picture 8-2 Picture 8-3
Picture 8-4 Picture 8-5 Picture 8-6
M-32777-GB-Rev.0.11.17
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32777 / KD-5920 0197
ANDON HEALTH CO., LTD.
No. 3 JinPing Street, Ya An Road, Nankai District,
Tianjin 300190, China
Made in China
Lotus Global Co., Ltd.
1 Four Seasons Terrace, West Drayton,
Middlesex, London, UB7 9GG, United Kingdom
PROBLEM POSSIBLE CAUSE SOLUTION
LCD Display shows
battery symbol
Low Battery Change the batteries
LCD shows “Er 0” Pressure system is unstable before
measurement
Don’t move and try again
LCD shows “Er 1” Fail to detect systolic pressure
LCD shows “Er 2” Fail to detect diastolic pressure
LCD shows “Er 3” Pneumatic system blocked or cuff
is too tight during ination Apply the cuff correctly
and try again
LCD shows “Er 4” Pneumatic system leakage or cuff
is too loose during ination
LCD shows “Er 5” Cuff pressure above 300mmHg
Measure again after ve
minutes. If the monitor is still
abnormal, please contact the
local distributor or the factory
LCD shows “Er 6” More than 160 seconds with cuff
pressure above 15 mmHg
LCD shows “Er 7” Inner memory error
LCD shows “Er 8” Device parameter checking error
LCD shows “Er A” Pressure sensor parameter error
No response when you
press button or load
battery
Incorrect operation or strong
electromagnetic interference
Take out batteries for ve
minutes, and then reinstall
all batteries
Guidance and manufacture’s declaration - electromagnetic emissions
The 32777 is intended for use in the electromagnetic environment specied below.
The customer or the user of the 32777 should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1 The 32777 uses RF energy only for its internal
function. Therefore, its RF emissions are very
low and are not likely to cause any interference
in nearby electronic equipment.
RF emissions
CISPR 11
Class B
The 32777 is suitable for use in all establishments
other than domestic and those directly connected
to the public low-voltage power supply network
that supplies buildings used for domestic purposes.
Harmonic emissions
IEC 61000-3-2
Not applicable
Voltage uctuations/
icker emissions
IEC 61000-3-3
Not applicable
Table 2
For all ME EQUIPMENT and ME SYSTEMS
Table 3
For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING
Table 4
For ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING
Guidance and manufacturer’s declaration - electromagnetic immunity
The 32777 is intended for use in the electromagnetic environment specied below.
The customer or the user of the 32777 should assure that it is used in such an environment.
IMMUNITY TEST IEC 60601test
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 oors
are covered with synthetic
material, the relative humidity
should be at least 30%.
Power frequency
(50/60 Hz)
magnetic eld
IEC 61000-4-8
3 A/m 3 A/m Power frequency magnetic
elds should be at levels
characteristic of a typical
location in a typical commercial
or hospital environment.
12. Troubleshooting (1)
PROBLEM POSSIBLE CAUSE SOLUTION
LCD Display shows
abnormal result
The cuff position was not
correct or it was not properly
tightened
Apply the cuff correctly
and try again
Body posture was not correct
during testing
Review the “BODY POSTURE
DURING MEASUREMENT”
sections of the instructions
and re-test
Speaking, arm or body
movement, angry, excited or
nervous during testing
Re-test when calm and
without speaking or moving
during the test
Irregular heartbeat
(arrhythmia)
It is inappropriate for people
with serious arrhythmia
to use this Electronic
Sphygmomanometer
Guidance and manufacturer’s declaration - electromagnetic immunity
The 32777 is intended for use in the electromagnetic environment specied below.
The customer or the user of the 32777 should assure that it is used in such an environment.
IMMUNITY TEST IEC 60601
test level
Compliance
level
Electromagnetic environment - guidance
Radiated RF
IEC 61000-4-3
3 V/m
80 MHz
to 2.5 GHz
3 V/m Portable and mobile RF communications
equipment should be used no closer to any
part of the 32777, including cables, than
the recommended separation distance
calculated from the equation applicable to
the frequency of the transmitter.
Recommended separation distance
Where Pis 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 xed RF transmitters,
as determined by an electromagnetic site
survey,ashould 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 reection from structures, objects and people.
aField strengths from xed 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 xed RF transmitters, an electromagnetic site survey should be considered. If the measured eld
strength in the location in which the 32777 is used exceeds the applicable RF compliance level
above, the 32777 should be observed to verify normal operation. If abnormal performance
is observed, additional measures may be necessary, such as re-orienting or relocating the 32777.
bOver the frequency range 150 kHz to 80 MHz, eld strengths should be less than 3 V/m.
d = 2.3 √ P800 MHz to 2,5 GHz
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
devices or 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.
Recommended separation distances between portable and mobile RF communications
equipment and the 32777
The 32777 is intended for use in an electromagnetic environment in which radiated RF disturbances
are controlled. The customer or the user of the 32777 can help prevent electromagnetic interference
by maintaining a minimum distance between portable and mobile RF communications equipment
(transmitters) and the 32777 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 80 MHz to 800 MHz 800 MHz to 2,5 GHz
0,01 0,12 0,12 0,23
0,1 0,38 0,38 0,73
1 1,2 1,2 2,3
10 3,8 3,8 7,3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation
distance din meters (m) can be determined using the equation applicable to the frequency of the
transmitter, where Pis 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 reection from structures, objects and people.
d = 1.2 √ P d = 1.2 √ P d = 2.3 √ P
0197
SN
WHO/ISH Denitions and classication of blood pressure levels
80 85 90 100 110
120
130
140
150
160
Severe Hypertension
Moderate Hypertension
Mild Hypertension
High-normal BP
Normal BP
Diastolic
(mmHg)
Sistolic
(mmHg)
BLOOD PRESSURE
CLASSIFICATION
SBP
mmHg
DBP
mmHg
Color
Indicator
Optimal <120 <80 green
Normal 120-129 80-84 green
High-Normal 130-139 85-89 green
Grade 1 Hypertension 140-159 90-99 yellow
Grade 2 Hypertension 160-179 100-109 orange
Grade 3 Hypertension ≥180 ≥110 red