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Pulse Arrhythmia Detection (ARR)
Once the occurrence of pulse arrhythmia has been detected in the
course of your blood pressure measurement, the icon ARR is displayed.
In the case, that the found pulse arrhythmia can be specied by the
PARR technology, the ARR icon is accompanied by the specically de-
tected type of arrhythmia, e.g. PC, AF(AFib), TACH or BRAD. Once the
kind of found pulse arrhythmia cannot be safely determined by PARR,
the device is displaying ARR without any additional pulse arrhythmia
type icon.
Note: It is strongly recommended, that you consult your physician, if ei-
ther the ARR icon occurs newly for several times, or, if your ARR is
known to your doctor, but the incidence of ARR readings changes
over time. This is independent whether the ARR icon is specied
by another pulse arrhythmia icon or not. Your doctor will then be
able to provide all required medical test and possible therapeutic
procedures.
The PARR technology is able to detect and display combined pulse ar-
rhythmia ndings.
Display Results
- Normal nding
ARR Pulse Arrhythmia without type-specic detection
ARR PC
Pulse Arrhythmia-Premature ventricular, atrial or nodal
beat detection
ARR AF(AFib) Pulse Arrhythmia-Atrial brillation detection
ARR TACH Tachycardia detection
ARR BRAD Bradycardia detection
ARR PC BRAD
Combined Pulse Arrhythmia: Premature beats &
Bradycardia detection
ARR PC TACH
Combined Pulse Arrhythmia: Premature beats &
Tachycardia detection
ARR AF(AFib) TACH
Combined Pulse Arrhythmia: Atrial brillation &
Tachycardia detection
ARR AF(AFib) PC
Combined Pulse Arrhythmia: Atrial brillation & Premature
beats detection
ARR AF(AFib) PC TACH
Combined Pulse Arrhythmia: Detection of Atrial Fibrillation,
Premature Beats and Tachycardia.
Real Fuzzy Measuring Technology
This unit uses the oscillometric method to detect your blood pressure.
Before the cuff starts inating, the device will establish a baseline cuff
pressure equivalent to the air pressure. This unit will automatically de-
termine the appropriate ination level based on pressure oscillations,
followed by cuff deation.
During the deation, the device will detect the amplitude and slope of
the pressure oscillations and thereby determine your actual the systolic
blood pressure, diastolic blood pressure, and pulse rate.
Preliminary Remarks
This Blood Pressure Monitor complies with the European regulations and
bears the CE mark “CE 0120”. The quality of the device has been veri-
ed and conforms to the provisions of the EC council directive 93/42/
EEC (Medical Device Directive), Annex I essential requirements and ap-
plied harmonized standards.
EN 1060-1: 1995/A2: 2009 Non-invasive sphygmomanometers - Part
1 - General requirements
EN 1060-3: 1997/A2: 2009 Non -invasive sphygmomanometers - Part
3 - Supplementary requirements for electro-mechanical blood pressure
measuring systems
EN 1060-4: 2004 Non-invasive sphygmomanometers - Part 4: Test Pro-
cedures to determine the overall system accuracy of automated non-in-
vasive sphygmomanometers. This blood pressure monitor was designed
for long service periods. In order to ensure continued accuracy, it’s rec-
ommended that all digital blood pressure monitors require re-calibra-
tion. This monitor (under normal usage with approx. 3 measurements
a day) does not require re-calibration for 2 years. Once the unit should
be re-calibrated the device will display
. The unit should
also be re-calibrated if the monitor sustains damage due
to blunt force (such as dropping) or exposure to uids and
/ or extreme hot or cold temperature / humidity changes.
When appears, simply return your device to your nearest
dealer for re-calibration service.
7


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