- 11 - 05/2020
Copyright © 2020, F
4. An A6 , which means that the month (1 – 12)
needs to be set.
5. Repeatedly press the M A4 button until the required month appears on the display
A6.
6. Once the month is set, press the ST A5 button to save the month in the
memory of the blood pressure monitor
7. AA6 , which means that the day needs to be set.
8. Repeatedly press the M A4 button until the required day (1 - 30/31) appears on the
display
9. Once the daST A5 button to sa
memory of the blood pressure monitor
10. The numerical hour value will starA6 .
11. Repeatedly press the M A4 button until the required hour (1 – 24) appears on the
display
12. ST A5 button to save the hour in the
memory of the blood pressure monitor
13. The numerical minutes value will starA6 .
14. M A4 button un
on the display
15. Once the minutes are set, press the ST A5 button to sa
the memory of the blood pressure monitor
16. The displa
The display A6 will turn off.
BEFORE ST
Basic instructions for achieving the most accurate measuring results
Always take measurements at the same time of da
and in the evening under the same conditions or according to the r
of your doctor
Do not perform measurement sooner than 30 –45
tea or smoking acigarette.
Wait at least 20 minutes after taking ahot shower or bath.
During measurement, sit calmly
which the cuff is attached.
Do not eat or drink approximately 1 hour prior to measurement
Do not perform measurements in an excessively cold envir
Do not perform measurements when you need to go to the toilet.
Wait appro– 5minutes before measuring again.
Attaching and securing the cuff
Remove all tight clothing from the arm before a
Attach the cuff 2- 3cm abov
is located above the brachial artery, as illustrated on the cuff label
The cuff must not be too loose or too tight.
inserting one finger between the cuff and the arm.
Place the forearm on an even table surface
Note:
Blood pressure can be measured both on the left and the right arm.
However
may differ
measurements always on the same arm.
MEASURING BL
While the display A6 is turned off, prST A5 button and the display
A6 will be lit and all the icons will appear temporarily
The device will automatically pressurise the cuff
the pulse rate is being detected. It is indicated by the flashing symbol on the
LCD displa
Then the pressure in the cuff is continuously r
(SYS) and diastolic (DIA) pressur
TST A5 button. If you
device, it will turn itself off automatically within 1minute of the last measurement.
Remove the cuff from your arm after completing the measurement
Note:
If the symbol appears on the display, the device has detected
cardiac arrhythmia.
VIEWING V
While the device is turned off, prM A4 button. The a
three measurements will be shown on the display A6 . In the event tha
three measurements were performed, the results of the last measur
shown.
Press the M A4 button again and the last measured values will be sho
and time will intermittently be shown on the display
DELETING V
If you did not get correct measurement results or if the measurement was
unsuccessful or conditions were poor
results.
Hold down the M A4 button for appro
appears on the display A6 .
Hold down the ST button t
memory. A6 .
Then the display A6 will turn off.
When button M A4 is pressed, no values will be shown on the displaA6 .
Note:
If you need to exit from the delete menu, press the ST A5
button.
CLEANING AND MAINTENANCE
Keep the device clean. W
Do not wash device or the cuff under running water or submerge it in water
Do not use abrasive cleaning products or petrol for cleaning. Otherwise the device
may be damaged.
Storage
If you will not be using the device for an extended period of time, remov
batteries.
Protect the device against impacts and falls.
Store the device in aclean, dry place that is out of reach of children. Do not expose
the device to direct sunlight or extreme temperature changes
CALIBRA
Recommendation:
is calibrated after two years of operation. All costs associat
borne by the customer
ELECTROMAGNETIC INTERFERENCE
T
not use this device in the vicinity of mobile telephones or microwave o
COMPLIANCE WITH NORMS
This device complies with European norms:
-
Application of risk management to medical devices.
-
to be used with medical device labels, labelling and information to be supplied –
Part 1: General requirements.
-
medical devices
-
equipment – Part 1: General basic safety and necessary performance
requirements
1-11: General basic safety and necessary performance requirements – Group
norm: Requirements for medical electrical equipment and medical electrical
systems used in the home healthcare environmen
-
electrical equipment- Part 1-2: General basic safety and necessary performance
requirements – Group norm: Electromagnetic interference – Requir
tests
- Performance requirements:
and test methods for non-automated measuremen
requirements for electromechanical systems f
pressure
requirements for the basic saf
non-invasive sphy
- Clinical examination:
for determining the overall accur
monitor systems.
investigation of automated measur
- Applications
equipment- Part 1-6: Particular basic safety and necessary performance
requirements - Group norm: Applications
medical devices.
-
A1:2015 Medical device software - Software life-
- Biological compatibility
and testing within arisk management process
vitro cytotoxicity
irritation and skin sensitization
