Troubleshooting; Maintenance; Explanation Of Symbols On Unit; Electromagnetic Compatibility Information - Gima JOLLY Gebrauchsanweisung

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. Confirm your selection by
pressing "START" button. The current bank can also be
confirmed automatically after 5 seconds with no operation.
c. If the monitor has stored results, the LCD will momentarily display the most re-
cent 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 inflates the cuff until sufficient 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 c a l -
culated 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. 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 moni-
tor manually.
Note: Please consult a health care professional for interpretation of pressure
measurements.
8. Displaying stored results
Picture 8-1 Picture 8-2 Picture 8-3
Picture 8-4 Picture 8-5 Picture 8-6
a. In Standby Mode, press "MEM" button to display the stored results. The cur-
rent memory bank will blink and the amount of results in this bank will be
displayed. Press "START" button to change over to other bank. Confirm your
selection by pressing "MEM" button. The current bank can also be confirmed
automatically after 5 seconds with no operation. See picture 8-1.
b. After selecting the memory bank, the LCD will display the average values in
this bank. See picture 8-2. If no result stored, LCD will show zeros. See picture
8-5.
c. Press "MEM" button, LCD will display the average value of all the results
which is measured from 5 o'clock to 9 o'clock in last 7 days in the current
user memory zone. See picture 8-3. If no result stored from 5 o'clock to 9
o'clock in last 7 days, LCD will display "0" for blood pressure and pulse rate.
d. Press "MEM" button again, LCD will display the average value of all the results
which is measured from 18 o'clock to 20 o'clock in last 7 days in the current
user memory zone. If no result stored from 18 o'clock to 20 o'clock in last 7
days, LCD will display "0" for blood pressure and pulse rate. See picture 8-4.
e. Then 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. If no result stored,
LCD will show zeros. See picture 8-5.
f. 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 sec-
onds, all results will be deleted. Press the button "MEM" or "START", the monitor
will turn off.
Picture 9-1 Picture 9-2
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
BLOOD PRESSURE
180
CLASSIFICATION
Moderate Hypertension
160
Optimal
Mild Hypertension
Normal
140
High-normal BP
High-Normal
130
Grade 1 Hypertension
Normal BP
120
Grade 2 Hypertension
Grade 3 Hypertension
80 85 90 100 110 WHO/ISH Definitions and classification of blood pressure levels
Diastolic
(mmHg)
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.
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
specified 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.
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12. Troubleshooting (1)

PROBLEM
LCD Display shows
abnormal result
13. Troubleshooting (2)
PROBLEM
LCD Display shows battery
symbol
LCD shows "Er 0"
LCD shows "Er 1"
LCD shows "Er 2"
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PROBLEM
LCD shows "Er 3"
LCD shows "Er 4"
LCD shows "Er 5"
LCD shows "Er 6"
LCD shows "Er 7"
LCD shows "Er 8"
LCD shows "Er A"
No response when you
press button or load battery

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.
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3. If this monitor is stored near freezing, allow it to acclimate to room tempera-
ture before use.
4. Do not attempt to disassemble this monitor.
5. It is recommended the performance should be checked every 2 years or after
repair. Please contact the service center.
6. Clean the monitor with a dry, soft cloth or a soft cloth squeezed well after
moistened with water, diluted disinfectant alcohol, or diluted detergent.
7. No component can be maintained by user in the monitor. The circuit dia-
grams, component part lists, descriptions, calibration instructions, or other
information which will assist the user's appropriately qualified technical per-
sonnel to repair those parts of equipment which are designated repairably
can be supplied.
8. 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.
9. It is recommended the cuff should be disinfected 2 times every week if need-
ed (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.
10. The monitor requires 6 hours to warm from the minimum storage tempera-
ture between uses until the monitor is ready for its INTENDED USE when the
ambient temperature is 20 °C.
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11. The monitor requires 6 hours to cool from the maximum storage tempera-
ture between uses until the monitor is ready for its INTENDED USE when
the ambient temperature is 20°C.
12. Not servicing/maintenance while the monitor is in use.

EXPLANATION OF SYMBOLS ON UNIT

0197
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SBP DBP Color
mmHg mmHg Indicator
<120 <80 green
120-129 80-84 green
130-139 85-89 green
IP20
140-159 90-99 yellow
160-179 100-109 orange
≥180 ≥110 red
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ELECTROMAGNETIC COMPATIBILITY INFORMATION

Table 1
Emission
Phenomenon
RF emissions
Harmonic distortion
Voltage fluctuations
and flicker
POSSIBLE CAUSE SOLUTION
The cuff position was not correct or it Apply the cuff correctly and try again
was not properly tightened
Body posture was not correct during Review the "BODY POSTURE DUR-
testing ING MEASUREMENT" sections of
the instructions and re-test
Speaking, arm or body movement, an- Re-test when calm and without
gry, excited or nervous during testing speaking or moving during the test
Irregular heartbeat It is inappropriate for people with
(arrhythmia) serious arrhythmia to use this Elec-
tronic Sphygmomanometer
POSSIBLE CAUSE SOLUTION
Low Battery Change the batteries
Pressure system is unstable before
measurement
Don't move and try again
Fail to detect systolic pressure
Fail to detect diastolic pressure
POSSIBLE CAUSE SOLUTION
Pneumatic system blocked or cuff is
Connect the cuff correctly and
too tight during inflation
try again. If the monitor is still
abnormal, please contact the
Pneumatic system leakage or cuff is
local distributor or the factory
too loose during inflation
Cuff pressure above 300mmHg
More than 160 seconds with cuff
Measure again after five
pressure above 15 mmHg
minutes. If the monitor is still
Inner memory error abnormal, please contact the
local distributor or the factory
Device parameter checking error
Pressure sensor parameter error
Incorrect operation or strong Take out batteries for five
electromagnetic interference minutes, and then reinstall
all batteries
Follow instructions for use
Caution: read instructions (warnings) carefully
Type BF applied part
WEEE disposal
Medical Device complies with Directive 93/42/EEC
Manufacturer
Date of manufacture
Authorized representative in the European commu-
nity
Serial number
Covering Protection rate
Keep in a cool, dry place
Keep away from sunlight
Product code
Lot number
Compliance Electromagnetic
environment
CISPR 11 Group 1, Home healthcare
Class B environment
IEC 61000-3-2 Home healthcare
Class A environment
IEC 61000-3-3 Home healthcare
Compliance environment
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Table 2
Enclosure Port
Phenomenon Basic EMC
standard
Electrostatic Discharge IEC 61000-4-2
Radiated RF EM field IEC 61000-4-3
Proximity fields from RF IEC 61000-4-3
wireless communications
equipment
Rated power frequency IEC 61000-4-8
magnetic fields
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Table 3
Proximity fields from RF wireless communications equipment
Test frequency Band (MHz)
(MHz)
385 380-390
450 430-470
710 704-787
745
780
810 800-960
870
930
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1720 1700-1990
1845
1970
2450 2400-2570
5240 5100-5800
5500
5785
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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.
GIMA WARRANTY TERMS
The Gima 12-month standard B2B warranty applies.
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30
IP20
32777 / KD-5920
ANDON HEALTH CO., LTD.
No. 3 JinPing Street, YaAn Road, Nankai District,
Tianjin 300190, China
Made in China
iHealthLabs Europe SAS
36 Rue de Ponthieu,
75008, Paris, France
31
Immunity test levels
Home Healthcare
Environment
±8 kV contact
±2kV, ±4kV, ±8kV, ±15kV air
10V/m
80MHz-2.7GHz
80% AM at 1kHz
Refer to table 3
30A/m
50Hz or 60Hz
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Immunity test levels
Professional healthcare facility
environment
Pulse modulation 18Hz, 27V/m
FM, ±5kHz deviation, 1kHz sine,
28V/m
Pulse modulation 217Hz, 9V/m
Pulse modulation 18Hz, 28V/m
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Pulse modulation 217Hz, 28V/m
Pulse modulation 217Hz, 28V/m
Pulse modulation 217Hz, 9V/m
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35
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0197