Bedienungsanleitung Rossmax AC1000f (Seite 7 von 19) (Englisch)

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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.

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