11.
ture between uses until the monitor is r
the ambient temperature is 20°C.
12.
EXPLANA
7. 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 r
rent memory bank will blink and the amount of results in this bank will be
displayed. Press “ST
selection by pressing “MEM” button. The current bank can also be conrmed
automatically after 5 seconds with no operation. See picture 8-1.
b.
this bank. See picture 8-2. If no result stor
8-5.
c.
which is measured from 5 o’clock to 9 o’clock in last 7 days in the curr
user memory zone. See picture 8-3. If no r
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 r
which is measured from 18 o’clock to 20 o’clock in last 7 days in the curr
user memory zone. If no result stor
days, LCD will display “0” for blood pressure and pulse rate. See pictur
e. Then press the “MEM” button, the most recent result will be displayed. See
picture 8-6. Followed by
separately
again to review the next result. In this way
button displays the respective results measur
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. Y
the monitor manually
8. Deleting measurements from the memory
When any result is displaying, keeping on pressing button “MEM” for thrsec-
onds, all results will be deleted. Press the button “MEM” or “ST
will turn off.
Picture 9-1 Picture 9-2
9. Assessing high blood pressure for adults
The following guidelines for assessing high blood pressure (without r
age or gender) have been established by the W
Please note that other factors (e.g. diabetes, obesity
taken into consideration. Consult with your physician for accurate assessment,
and never change your treatment by yourself.
12. T
Classication of blood pressure for adults
Note: It is not intended to provide a basis of any type of rush toward emer
conditions/diagnosis based on the color scheme and that the color scheme is
meant only to discriminate between the different levels of blood pr
ELECTROMAGNETIC COMP
T
Emission
3. If this monitor is stored near fr
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
6. Clean the monitor with a dry
moistened with water
7. No component can be maintained by user in the monitor
grams, component part lists, descriptions, calibration instructions, or other
information which will assist the user’
sonnel to repair those parts of equipment which are designated r
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 cuf
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 fr
ture between uses until the monitor is ready for its INTENDED USE when the
ambient temperature is 20 °C.
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. Conrm your selection by
pressing “ST
conrmed automatically after 5 seconds with no operation.
c.
If the monitor has stored results, the LCD will momentarily display the most r
cent one. If no result has been stored, zer
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 pictur
f. Then the monitor inates the cuff until suf
measurement. Then the monitor slowly releases air fr
out the measurement. Finally the blood pressur a l -
culated and displayed on the LCD screen. The blood pressur
indicator and Irregular heartbeat symbol (if any) will blink on the screen. The
result will be automatically stored in the monitor
g.
no operation. Alternatively
monitor manually
h. During measurement, you can press the “ST
tor manually
Note: Please consult a health care professional for interpr
measurements.
M32777-GB-Rev
21
22
23
24
20
19
27
28
29
30
26
25
33
34
35
36
32
31
32777 / KD-5920
PROBLEM POSSIBLE CAUSE SOLUTION
LCD Display shows battery
symbol
Low Battery Change the batteries
LCD shows “Er 0” Pressure system is unstable befor
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
PROBLEM POSSIBLE CAUSE SOLUTION
LCD shows “Er 3” Pneumatic system blocked or cuff is
too tight during ination Connect the cuff correctly and
try again. If the monitor is still
abnormal, please contact the
local distributor or the factory
LCD shows “Er 4” Pneumatic system leakage or cuff is
too loose during ination
LCD shows “Er 5” Cuff pressur
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 err
No response when you
press button or load battery
Incorrect operation or strong
electromagnetic interference
T
minutes, and then reinstall
all batteries
T
Enclosure Port
T
Proximity elds from RF wir
10. T
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
specied 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.
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 DUR-
ING MEASUREMENT” sections of
the instructions and re-test
Speaking, arm or body movement, an-
gry
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 Elec-
tronic Sphygmomanometer
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 specic
recycling point for electric and electronic equipment.
GIMA WARRANTY TERMS
The Gima 12-month standard B2B warranty applies.
WHO/ISH Denitions and classication of blood pressure levels
80 85 90 100 110
120
130
140
160
180
Severe Hypertension
Moderate Hypertension
Mild Hypertension
High-normal BP
Normal BP
Diastolic
(mmHg)
Sistolic
(mmHg)
BLOOD PRESSURE
CLASSIFICA
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
ANDON HEAL
No. 3 JinPing Street, Y
Tianjin 300190, China
Made in China
iHealthLabs Europe SAS
36 Rue de Ponthieu,
75008, Paris, France
11. T
MAINTENANCE
1. Do not drop this monitor or subject it to str
2. Avoid high temperatur
in water as this will result in damage to the monitor
Follow instructions for use
Caution: read instructions (warnings) carefully
T
WEEE disposal
0197
Medical Device complies with Directive 93/42/EEC
Manufacturer
Date of manufacture
Authorized representative in the Eur
nity
Serial number
IP20 Covering Protection rate
Keep in a cool, dry place
Keep away from sunlight
Product code
Lot number
Phenomenon Compliance Electromagnetic
environment
RF emissions CISPR 11 Group 1,
Class B
Home healthcare
environment
Harmonic distortion IEC 61000-3-2
Class A
Home healthcare
environment
V
and icker
IEC 61000-3-3
Compliance
Home healthcare
environment
Phenomenon Basic EMC
standard
Immunity test levels
Home Healthcare
Environment
Electrostatic Dischar IEC 61000-4-2 ±8 kV contact
±2kV
Radiated RF EM eld IEC 61000-4-3 10V/m
80MHz-2.7GHz
80% AM at 1kHz
Proximity elds from RF
wireless communications
equipment
IEC 61000-4-3 Refer to table 3
Rated power frequency
magnetic elds
IEC 61000-4-8 30A/m
50Hz or 60Hz
T
(MHz)
Band (MHz) Immunity test levels
Professional healthcare facility
environment
385 380-390 Pulse modulation 18Hz, 27V/m
450 430-470 FM, ±5kHz deviation, 1kHz sine,
28V/m
710 704-787 Pulse modulation 217Hz, 9V/m
745
780
810 800-960 Pulse modulation 18Hz, 28V/m
870
930
1720 1700-1990 Pulse modulation 217Hz, 28V/m
1845
1970
2450 2400-2570 Pulse modulation 217Hz, 28V/m
5240 5100-5800 Pulse modulation 217Hz, 9V/m
5500
5785
01
IP20
