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.
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.
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 qualified
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
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.
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
21
22
23
24
20
19
27
28
29
30
26
25
33
34
35
36
32
31
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 inflation
Apply the cuff correctly
and try again
LCD shows “Er 4”
Pneumatic system leakage or cuff
is too loose during inflation
LCD shows “Er 5”
Cuff pressure above 300mmHg
Measure again after five
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 five
minutes, and then reinstall
all batteries
Guidance and manufacture’s declaration - electromagnetic emissions
The 32777 is intended for use in the electromagnetic environment specified 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 fluctuations/
flicker 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 specified 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 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.
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 specified 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
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 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.
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
d
= 2.3 √
P
800 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
fields, 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
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.
d
= 1.2 √
P
d
= 1.2 √
P
d
= 2.3 √
P
0197
SN
WHO/ISH Definitions and classification 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
