CORRECT POSTURE
ASSEMBLY THE CUFF
1. Sit beside the table and let the table support your arm as
you take the measurement.
2. Sit upright with your back straight.
3. Make sure that the cuff on the upper arm no cross, and is at
approximately the same level as the heart.
4.Make sure that your feet lie on the ground and no cross.
5.You may lie on your back and take a measurement.Look
at the ceiling, keep calm, and don’t move your neck or body
during the measurement.
1. Insert the edge of the cuff approximately 5 centimeters into
the D-ring as shown in gure.
2.Put the cuff on the left upper arm with the tube pointing
to the direction of palm.lf measurement on your left arm is
difcult, you can use right arm for measurement. In this case,
it is necessary to know that the readings may differ about 5-10
mmHg between left arm and right arm.
3. Wrap cuff around your upper arm with the lower edge of
the cuff approximately 2-3 centimeters above the elbow. The
mark <ARTERY> must be over the artery of the arm.
4. Press the cuff to make sure that it is attached securely. The
cuff should not be too tight or loose is greatly recommended.
Two ngers should be easily put in between cuff and upper
arm.
5. The mark <INDEX> on the cuff must point to
area<NORMAL>Or <LARGE CUFF>.This means the cuff size
is correct, If mark <NDEX> points to the area beyond area
<NORMAL>or <LARGE CUFF>. please consult your dealer
whether you need another size cuff. This device is supplied
with the standard cuff which is t for the arm size 22-32 cm.
6.Sometimes it is difcult to make the cuff regular depending
on the shape of the user’s upper arm. The cone-shape
assembly of cuff is also acceptable.
7.If your clothes restrict the blood circulation of your upper
arm, or you roll your sleeve up so as to result in such
restriction,Please take off your shirt to get an accurate
measurement if necessary.
Caution:
If you experience discomfort during a measurement such
as pain in the upper arm or other complaints, press the
‘START ‘button to release the air immediately from the
cuff. Loosen the cuff and remove it from your arm.
CARRYING OUT A MEASUREMENT
1. Insert the tube plug into the air connector.Before the measurement, take 3~5 times deep
breath and relax yourself. Don’t talk or move your arm;
2. Press button ‘START’,and all symbols will appear on display in 2seconds as Fig.9. Then two
short beep will sound and ‘0 ‘ will appear on the screen, Pump begins to inate with display
showing the reading of pressure. Generally the pressure will reach 190mmHg as Fig.10;
3. The pump stop inating and pressure begins to decrease gradually during which the user’s
blood pressure and pulse will be calculated as Fig.11;
CARE,STORING,REPAIR AND RECYCLING
1. It’s necessary to protect this device against high moisture, direct sunlight,shock, solvent, alcohol
and gasoline.
2. Remove the batteries if the device is being stored for a long time, and keep the batteries far away
from children.
3. Keep the cuff away from sharp objects and don’t extend or twist the cuff.
4. This device is not washable. Never immerse the device in water and do not rinse it under the tap.
Use only soft and dry cloth to clean the device.
5. Do not serve or maintain the cuff and the device when in use with patient.
6. The cuff is sensitive and must be handled with care. You can clean the cuff with damp cloth for
daily maintenance.To avoid cross infection when sharing the cuff, you can sterilize the fabric cover
ofthe cuff with tampons moistened by 3% solution of hydrogen dioxide. After long use there will be
a partial discoloration on the fabric surface of the cuff. Do not laundry the cuff as well as ironing with
a hot atiron.
WARNING: Under no circumstances may you wash the inner bladder!
7. Since neither the device nor batteries are household waste, follow your local recycling rules and
dispose them at an appropriate collection site.
8. Do not open the device, or delicate electrical components as an intricate air unit could be damaged.
lf you can not x the problem using the troubleshooting instruction, please request service from your
dealer.
WARNING: Do not repair the device without manufacturer’s authorization.
Do not carry out maintenance when using the device.
Caution:
Generally, we recommend the device should be inspected every 2 years and utilize the manometer
mode to verify the accuracy of the manometer at least at 50mmHg and 200mmHg after maintenance
and repair. Please contact your dealer for maintenance.
WHO CLASSIFICATION INDICATION
Standards for assessment of high or low blood pressure, regardless of age, have been
established by World Health Organization(WHO) as show in the chart as below
4. There will be along beep following the accomplishment of measurement, The air in the cuff
will deate quickly and the blood pressure reading, pulse reading will show in the display.
Moreover the measuring time will also display together in two screens alternately. At the same
time,the’ ’will ash to remind the user to record the reading as Fig.12;
5. Press button’MEM1’or button’MEM2’to record the reading in corresponding memory, For
example, if button ‘MEM2’is pressed, the display will show as Fig.13. If the user does not
press button, the reading won’t be recorded;
6.Press the button ‘START’ to return to standby mode. Please rest for at least 3 minutes for
another measurement. The device keeps unused for3 minutes, the device will be return to
standby mode automatically.
7. lf irregular heartbeat was detected during the measurement, LCD display the icon’ ’ to
remind users of heartbeat irregularity.
NOTE: The device will inate to a higher pressure automatically in case the ination pressure
is not sufcient to determine measurement result.
Attention: We recommend contacting your physician if you see the ‘ ’indicator frequently.
The indicator display a segment, based on the current data, corresponding to the WHO classication.
For example, if your blood press is 145mmHg (systolic pressure), 88mmHg(diastolic pressure),
according to the world health organization standard, your blood pressure level is Mild Hypertension.
Note:lf the systolic blood pressure and the diastolic blood pressure fall into different categories, the
higher value should be taken for classication.
MEMORY CLEARANCE
After a measurement is nished or when the device stands by, hold down
button’MEM1’or’MEM2’ for at least 5 seconds,the display will show ‘CLR’
which means the stored reading for’MEM1’or’MEM2’ is removed.
ERROR AND LOW BATTERYINFORMATION
Compliance information for each EMC test
TROUBLESHOOTING
SPECIFICATIONS
NOTE: The EUT is the a.c. mains voltage prior to application of the test level.The following
phenomenon is still fulll the requirement of basic safety and essential performance.
* UT:230V~/50Hz, The pressure of the EUT is deviation the normal value but the value is still
more than 10psi when ow is 4.5l/min.
**UT:230V~/50Hz, The EUT stop working when adding 0% UT, but the EUT can restore its
normal mode automatically.
•
Use of this equipment adjacent to or stacked with other equipment should be avoided
because it could result in improper operation.If such use is necessary this equipment and the
other equipment should be observed to verify that they are operating normally.
•
Portable RF communications equipment(including peripherals such as antenna cables and
external antennas) should be used no closer than 30cm(12 inches to any part of this device,
including cables specied by the manufacturer. Otherwise,degradation of the performance of
this equipment could result.
•
Under the test condition specied in immunity, the product can provide the basic safety and
essential performance.If the essential performance is lost or degraded, additional measures are
necessary,such as reorienting or relocating the device.
INDICATION POSSIBLE REASON CORRECTION METHODS
The cuff is put on wrongly or
the tube plug is inserted too
loosely.
Movement of arm/hand or
talking during measurement.
The cuff is not inated to
necessary pressure.
Make sure that cuff is put on
correctly and the tube plug
is inserted tightly and repeat
the measurement.Repeat the
measurement with following
completely recommendations
of manual.
Repeat the measurement
with pumping cuff to higher
pressure.
The batteries are weak Replace all 4 batteries with
new ones.
Declaration -Electromagnetic Immunity (Home Healthcare Environment)
Immunity test IEC 60601 test level
Compliance level
Conducted RFIEC 61000-4-6 3V 150 kHz to 80 MHZ 6V in
ISM and amateur radio bands
between 0.15 MHz and 80 MHz
3V 150 kHz to 80 MHZ 6V in
ISM and amateur radio bands
between 0.15 MHz and 80 MHz
Radiated RFEC61000-4-3 10 V/m
80 MHz to 2.7GHz also meet
the requirement of table 9 of IEC
60601-1-2:2014.
10 V/m
80 MHz to 2.7GHZ also meet
the requirement of table 9 of lEC
60601-1-2:2014.
Electrostatic discharge (ESD)
EEC 61000-4-2
+8kV contact
+2 kV, +4 kV, ±8 kV, +15 kV air
+8kV contact±2 kV, ±4 kV, ±8 kV,
±15 kV air
Electrical fast transient/burst
IEC 61000-4-4
+2kV for power supply lines +2kV for power supply lines
Surge IEC 61000-4-5 +0.5kV,+ 1 kV line(s) to lines + 0.5kV, ± 1 kV line(s) to lines
Voltage dips,short interruptions
and voltage variations on power
supply input lines IEC 61000-
4-11
0% Ut,0.5 Cycle at 0°, 45°, 90°
135°, 180°225°, 270° and 315°
0% Ut,1 Cycle and 70% Ut
25/30 cycles sigle phase: at 0°
0% Ut, 250/300 cycles
0% Ut,0.5 Cycle at 0°, 45°, 90°
135°, 180°225°, 270° and 315°
0% Ut,1 Cycle and 70% Ut
25 cycles sigle phase: at 0° 0%
Ut, 250 cycles
Power frequency (50/60Hz)
magnetic eld IEC 61000-4-8
30 A/m 30 A/m
MODEL
Warranty Period Two-years from purchasing date
Purchasing date
Purchasing shop Name: Telephone:
Address:
Customer Name: Telephone:
Address:
SYMPTOM CHECK POINT REMEDY
No display when connect the power
The batteries have run down.The
polarity of battery is wrong.The
contact of battery compartment
is polluted.
Replace all the batteries with new
ones.Install the batteries correctly.
Clean the battery terminals with dry
cloth.
Ination stops and reinate later. The automatic ination for ensuring
correct measurement.Did you talk
or move your arm(or hand) during
measurement?
See<AUTOMATICINFLATION>Keep
quiet and silent during the
measurement.
The readingis extremely low or high. Is the cuff at the same level as
the heart?Is the cuff wrapped
right?Did you strain your arm
during measurement?Did you talk
or move your arm(or hand) during
measurement?
Make sure that your posture is right.
Wrap the cuff correctly.Relax during
measurement.Keep quiet and silent
during the measurement.
Pulse rate is too low or too high. Did you talk or move your arm(or
hand) during measurement?Did
you make measurement right after
exercise?
Keep quiet and silent during the
measurement.Take measurement
again after resting for more than
5minutes.
The batteries are run down soon. Faulty batteries are used. Use alkaline batteries of known
manufacturers.
Date TROUBLE SERVICE MAN
Guarantee Regulation
1. During warranty period the repair could be made at any BPM repair department.
2. The following things not belong to warranty range:
(1) Operating BPM different from procedures or instructions of the manual.
(2) The body is damaged articially.
(3) Self-repairing or modifying the monitor construction in any way.
(4) Breakdown due to corrosion of battery leakage.
(5) Problem which occurs under natural calamity and other force maieures.
Model LD-582
Size 158(L)x120(W)x127(H)mm
Weight Approximately 490g without batteries
Measuring method Oscillometry
Extreme Pressure/ cuff pressure 290mmHg
Measuring range 40 to 180mmHg(DIA,diastolic pressure)
60 to 260mmHg(SYS,systolic pressure)
40 to 160 beats/minute(PUL,pulse rate)
Measuring accuracy ± 3 mmHg for static pressure
± 5% of the reading for the pulse rate
Ination Automatic by the pump
Rapid deation Automatic electronic valve
Batteries Optional component, 4“AA”x1.5V
Adapter Optional component,6V.600mA
Memory 2 Users with 60 sets of memory each
Operation temperature and humidity, air pressure +10°C to+ 40°C,85% and below
800hPa to 1060hPa
Transport and storage temperature and humidity,
air pressure
-20°C to +50°C,85% and below 500hPa to
1060hPa
Upper arm circumference Applicable for arm circumference 22-32 cm
(standard cuff)
Complete kit Main body, storage case, cuff, 4 x AA batteries
(Optional), 1 x CR 2025 button
battery, adapter (Optional), instruction manual
Pollution Degrees Degrees 2
Over voltage category Category ll
High Altitudes(m) ≤2000m
Fuse 1A6V 2.1mm*1.45mm*0.81mm
1. Warranty for this automatic digital blood pressure monitor is 24 months from the date of purchase.
The 24 months warranty excludes the monitor cuff. The cuff is warranted for 12 months.
2. The warranty obligations are prescribed for by warranty certicate for buyer.
3. The addresses of organizations for guarantee maintenance are present in the warranty certicate.
WARNING
Do not modify this equipment without authorization of the manufacturer.
All major maintains on the device must be performed by an authorized service center or distributor. No
use-serviceable parts inside, before servicing to authorized representative or manufacturer!
DECLARATION:
When technical information for user or service personnel requirements is not in the scope of
condentiality of the Company, the Company committed to provide information disclosure in
accordance with procedure, including circuit diagrams and parts lists, and other related type technology
information that do not involve commercial secrets may be disclosed, Access to information channels
and procedures,please contact your dealer or manufacturer.
PERIODIC SAFETY CHECKS
If you use the device with power adapter, preventive inspection and maintenance to be performed
including the frequency of such maintenance.
Every time before use, please check the adapter, once damaged, never to use.
Please clean the plug of adapter plug at least once a year. Too much dust on plug may cause the re.
The manufacturer reserves the right to make technical changes without notice in the interest of
progress.Prior notices will not be given in case of any amendments within this manual. The mentioned
trademarks and names are owned by the corresponding companies.
REQUIRING RECORD
FUNCTION OF MEMORY
MEMORY RECALL
1. LD-582 can store 60 sets of readings each in’ ’and ‘ ‘, and will automatically calculate the
average value of the latest 3 readings for MEM1’and ‘MEM2’ respectively. When the memory is
full (60 sets of readings are stored), the oldest reading will be replaced by new one. Memory will
not clear away even if power supply is removed;
2. After a measurement is nished or when the device stands by,the user can press button
‘MEM1’or button ‘MEM2’ to recall memory.Press button’MEM1’ or ‘MEM2’, the display will
show the average value of the latest 3readings as Fig.14;
3. Press again,the display will show ‘01’, which means the latest reading, then turns to another
screen to show readings and measuring time as Fig.15;
4.Press again, the display will show ‘02’, which means the second to the latest reading...
MANUFACTURER’S DECLARATION
Compliance information for each EMC test
Electromagnetic Emission (Home Healthcare Environment)
Emission test (lEC60601-1-2:2014) Compliance
Conducted and radiated RF emissions CISPR 11 Group1 Class B
Harmonic emissions IEC 61000-3-2 Class A
Voltage uctuations/icker emissions IEC
61000-3-3
Complies
QUALITY GUARANTEE
GIMA WARRANTY TERMS
The Gima 12-month standard B2B warranty applies.
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.
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