Lanaform ABPM-100 Manuel D'instructions page 9

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Technical alarm – Description
If the (systolic or diastolic) blood pressure taken is
outside the range indicated in the "Technical Fea-
memory, tures" paragraph, the technical alarm displays the
message "Hi" or "Lo" on the screen. In this case,
3 seconds consult a doctor or check that you are using the device
properly. The technical alarm's limit values are values
set by the factory and can neither be changed nor
ERRORS
deactivated. Under the IEC 60601-1-8, these limit
values of the alarm have a lower priority. The tech-
nical alarm is not a locked alarm and does not need to
cuff cor-
try again.
be reset. The signal displayed on the screen switches
off automatically after approximately 8 seconds.
ections
MAINTENANCE AND STORAGE
g to the
sition"
ructions
•
ain.
her
•
ment and
positioning
•
ns and
ns for use.
pressure
•
not
or people
rom
rhythmia
•
displayed
en:
not been
he screen);
tside the
played on
•
3 or ER4 is
•
Hg (ER5 is
ds (ER6 is
•
M-ABPM100-Lot003.indd 9 M-ABPM100-Lot003.indd 9
displayed on the screen);
there is an error on the system or the device
(ER7 or ER8 or ERA is displayed on the screen);
the batteries are nearly flat
(18)
Clean the device and the cuff carefully, using only
a slightly damp cloth.
Do not use detergent or solvent.
Never put either the device or the cuff in water
as this might seep into the device or cuff and
damage them.
Do not put heavy objects on the device or on
the cuff when they are being stored. Remove
the batteries.
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 des-
ignated repairably can be supplied.
It is recommended the performance should be
checked every 2 years or after repair. Please
contact the service center.
The monitor can maintain the safety and perfor-
mance characteristics for a minimum of 10,000
measurements or three years.
The cuff integrity is maintained after 1,000
ABPM-100 EN Instruction manual 202112LA090207003 15/11/2021
open–close cycles of the closure.
• It is recommended the cuff should be disinfect-
ed 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.
• Clean the cuff after the usage of every 200 times
is recommended.
TECHNICAL SPECIFICATIONS
OF THE PRODUCT
Model number LA090206
Measuring
method
Measuring
range
Accuracy of
the indicator
Memory
Dimensions
Weight
Cuff size
Admin. operat-
ing conditions
Permissible
storage and
transport
conditions
Power supply
Battery lifespan Approximately 200 measurements,
Accessories
Ranking
Pressure meas-
uring system
components
Changes could be made to the technical features
without any prior warning for updating purposes.
• The Electronic Sphygmomanometer corre-
sponds to the below standards: IEC 60601-1Edi-
tion 3.1 2012-08/EN 60601-1:2006/A1:2013
EN
FR NL DE SL SV
Measuring blood pressure on the arm,
oscillometric and non-invasive
Pressure in the cuff 0 – 300 mmHg
Systolic pressure 60 – 260 mmHg
Diastolic pressure 40 – 199 mmHg
Pulse 40 – 180 beats/minute
systolic ±3 mmHg
diastolic ±3 mmHg
less than 60:±3bpm, more than 60(incl.):±5%
4 x 30 memory locations
+/- 107 x 80 x 52mm
+/- 287g (without any batteries)
22 - 30cm
+ 10°C a + 40°C, ≤85% relative air
humidity (non-condensing)
-20°C a +50°C, ≤85% relative air humidity,
800 – 1 050 hPa of ambient pressure
4 x 1.5 V AAA batteries
depending on the increased blood
pressure and inflation pressure
Instructions for use, storage box
Internal power supply, IP20, no AP
or APG, continuous use, BF device
Pump,Valve, LCD, Cuff, Sensor
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