Manual Rossmax R43 Blood Pressure Monitor

Manual

3

2

Systolic

(SYS.)

Diastolic

(DIA.)

< 120

and

< 80

120 – 139

or

80 – 89

140 – 159

or

90 – 99

≥ 160

or

≥ 100

Normal Prehypertension Stage 1

Hypertension

Stage 2

Hypertension

Normal Prähypertonie Hypertenesion

Bluthochdruck,

Stufe 1

Hypertenesion

Bluthochdruck,

Stufe 2

Normale Préhypertension Hypertension

stade 1

Hypertension

stade 2

Normal Prehipertensión Fase 1

Hipertensión

Fase 2

Hipertensión

Normal Pré-hipertensão Hipertensão de

estágio 1

Hipertensão de

estágio 2

Ciśnienie

normalne

Ciśnienie podwyższone Nadciśnienie

pierwszego stopnia

Nadciśnienie

drugiego stopnia

Normal Pre-ipertensione Stadio 1

Ipertensione

Stadio 2

Ipertensione

Normaal Prehypertensie Fase 1

Hypertensie

Fase 2

Hypertensie

Normal Prehipertansiyon 1. Evre

Hipertansiyon

2. Evre

Hipertansiyon

ﺔﻠﺣﺮﻤﻟا

ﺔﻴﻌﻴﺒﻄﻟا

مﺪﻟا ﻂﻐﺿ ةدﺎیز ﻞﺒﻗ ﺎﻡ ﻦﻡ ﺔﻴﻧﺎﺜﻟا ﺔﻠﺣﺮﻤﻟا

مﺪﻟا ﻂﻐﺿ ةدﺎیز

ﻦﻡ ﻰﻟوﻷا ﺔﻠﺣﺮﻤﻟا

مﺪﻟا ﻂﻐﺿ ةدﺎیز

Норма Предгипертоническое

состояние

1 стадия

гипертонии

2 стадия

гипертонии

Γલ іᐆ܉ೈ ஑ʙೈіᐆ ஑ʠೈіᐆ

Introduction

Blood pressure measurements determined with R43 are equivalent to those

obtained by a trained observer using cuff/stethoscope auscultation method,

within the limits prescribed by the American National Standard, Electronic

or Automated Sphygmomanometers.

R43 is protected against manufacturing defects by an established

International Warranty Program. For warranty information, you can contact

the manufacturer, Rossmax International Ltd. or your local distributors.

Attention: Consult the accompanying documents.

Please read this manual carefully before use. For specific information

on your ownblood pressure, contact your physician. Please be sure to

keep this manual.

Preliminary Remarks

This Blood Pressure Monitor complies with the European regulations underlying

the German Law governing medical products (MPG) and bears the CE mark "CE

0366". The quality of the device has been verified and conforms to the provisions

of the EC council directive 93/42/EEC dated 14 June 1993 concerning medical

devices, as well as the EMC directive 89/336/EEC;EN 1060-1 (Dec. 1995)

Non-invasive blood pressure measuring equipment General requirements and EN

1060-3 (Feb. 1997) Noninvasive blood pressure measuring equipment

Supplementary requirements for electromechanical blood pressure measuring

systems.

To ensure accurate measurements, it is recommended that calibration will be

completed every two years.

How “R43” Works

R43 uses oscillometric method to detect your blood pressure. Before the cuff

starts inflating, the device will establish a baseline cuff pressure, which is

equivalent to the air pressure. The measurement of your blood pressure is

based on this baseline pressure. After the cuff inflates to block your blood in the

artery, the deflation process starts. During the deflation of the wrist cuff, R43 is

detecting the pressure oscillations generated by the beat-to-beat pulsatile. Any

muscle movement during this period of time will cause measurement error. After

detecting the amplitude and the slope of the pressure oscillations during the

deflation process, R43 will determine the systolic and diastolic pressures for you,

and your pulse rate is detected at the same time.

For reliable monitoring and reference of blood pressure, keeping long-

term records is recommended. Please download the blood pressure

log(chart for recording and tracking crucial info : date, time, blood pressure,

pulse rate and body condition) at www.rossmax.com.tw

Rating

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