Irregular Heartbeat Detector - Viatom Wellue B02 Manual Del Usuario

Irregular Heartbeat Detector

This symbol – indicates that certain pulse irregularities were detected
during the measurement.
In this case, the result may deviate from your normal basal blood
pressure – repeat the measurement.
In most cases, this is no cause for concern. However, if the symbol
appears on a regular basis (e.g. several times a week with
measurements taken daily), we advise you to tell your doctor.
Please show your doctor the following explanation:
Information for the doctor on frequent appearance of the Irregular
Heartbeat Symbol.
This instrument is an oscillometric blood pressure monitor device that
also analyzes pulse frequency during measurement. The instrument is
clinically tested.
If pulse irregularities occur during measurement, the irregular heartbeat
symbol is displayed after the measurement. If the symbol appears more
frequently (e.g. several times per week on Measurements performed
daily) or if it suddenly appears more often than usual, we recommend
the patient to seek medical advice. The instrument does not replace a
cardiac examination, but serves to detect pulse irregularities at an early
stage.
Error Indicates
SYMBOL CUASE
No display appears Weak battery or improper placement
Er1 Sensor Abnormal
Er2 Monitor could not defect pulse wave
Er3 Measurement result is abnormal
(SYS<45mmHg or DIA<24mmHg)
Er4 It appears during the process of inflating
Er5 Pipe blocked
Heart rate area display "Hi"
Er6
Heart rate area display "Lo"
Er7
CORRECTION
Replace both batteries with new ones. Check
the battery installation for proper placement of
the battery polarities.
Send it to the local distributor
Make sure the air plug is properly inserted in the
unit
Occasionally – measure for one more
time/Always – Send it to local distributor.
Wrap the cuff properly
Make sure the air flow smooth.
Heart rate is more than 200 beats/Min.
Heart rate is less than 40 beats/Min.
Trouble removal
Authorized Representative in the European Community
CE Mark: conforms to essential requirements of the Medical
Device Directive 93/42/EEC.
Date of manufacture.
Manufacturer
Specifies serial number
Type BF applied part
Direct current
DISPOSAL: Do not dispose this product as unsorted municipal
waste. Collection of such waste separately for special treatment
is necessary.
Follow instructions for use
Put up
Fragile
Keep dry