Microlife WatchB Home T. Bedienungsanleitung

Accu

mea

with

Instru

rate home

surements

the WatchB

tion Manual

lood pressu

P Home T.

Federal Communications Commission (FCC) Statement

changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to

operate theequipment.

This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions:

(1) this device may not cause harmful interference, and

(2) this device must accept any interference received, including interference that may cause undesired operation.

Note: This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to Part 15 of the

FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation.

This equipment generates, uses, and can radiate radio frequency energy, and if not installed and used in accordance with the

instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not

occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be

determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the

following measures:

–

Reorient or relocate the receiving antenna.

–

Increase the separation between the equipment and receiver.

–

Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.

Consult the dealer or an experienced radio/TV technician for help.

This device complies with FCC radiationexposure limits set forth for an uncontrolled environment. End users must follow the

specific operating instructions for satisfying RF exposure compliance.)

3 EN

Microlife WatchBP Home T is the world’s first digital blood pressure measurement device that strictly follows European Society of

Hypertension (ESH)1, 2 and American Heart Association (AHA) recommendations for home blood pressure measurement. Using the

WatchBP Home T device helps you collect accurate home blood pressure measurements your doctor can trust. This WatchBP Home T

device has been clinically validated according to the ESH protocol 3.

Indications For Use

The Microlife Upper Arm Automatic Digital Blood Pressure Monitor, M o d el W a t chB P H o m e T ( B P 3MX 1- 3T ) i s a d e vi ce i nt e nd ed t o

measure the systolic and diastolic blood pressure and pulse rate of an adult individual with arm cuff circumference sizes ranging

from 22 -42 cm by using a non-invasive oscillometric technique in one inflatable cuff being wrapped around the upper arm.

The memory data can be transferred to the PC (personal computer) running the WatchBP Analyzer Home software by connecting the

monitor via cable. The device can also be used in connection with smart mobile devices running the APP and via Bluetooth.

The device detects the appearance of atrial fibrillation during measurement and gives a warning signal with the reading once

atrial fibrillation is detected. It is intended for use in individuals previously diagnosed with AFib. The feature has not been tested

for and is not intended for use in people under 22 years of age.

Table ofContents

Before using WatchBP Home T for the first time

Product description.......................................................5–6

Activating the device........................................................7

Selecting thecorrect cuff..................................................8

Taking measurements using WatchBP Home T

«DIAG.» Mode .............................................................9–10

«USUAL» Mode .............................................................. 12

Eight steps for measure blood pressure properly

Blood pressuremeasurement procedures ..............13–14

Special Function

Atrial Fibrillation Detection ........................................... 17

About Atrial Fibrillation ................................................. 18

Atrial Fibrillation Detector ............................................. 19

Atrial fibrillationdetection instructions ........................ 20

Information forthe doctor ............................................. 20

Viewing, deleting, and transferring measurements

Viewing measurements .......................................... 21–22

Deleting measurements.......................................... 23–24

Installation of the software program ............................ 25

Bluetooth connectivity .............................................26-27

Batteries andpower adaptor................................... 29–30

Safety, care, accuracy test and disposal .................. 31–32

Error messages......................................................... 33–34

Important facts......................................................... 35–36

Technical specifications ................................................. 37

Appendix....................................................................... 38

5 EN

USUAL

DIAG.

NOCTURNAL

Bluetooth symbol

SYS

mmHg

DIA

mmHg

PUL

/min

Serial Port

Mode Switch Power Socket

Display ON/OFF Button

M Button (Memory)

Battery Compartment

Cuff Socket

Atrial

Outsid

Mode Indicatio

Doctor Symb

ibrillation Detecti

Measurement Ti

Rel

Battery Displ

Delete Memory Da

Stored Val

Morning Data

Evening Data

Date/Time

Systolic Value

Diastolic Valu

Pulse Indicato

Pulse Rate

Number of St

red Data

Before u

Activating

Pull out the pro

compartment.

Set the year

installing ne

the display. U

the ON/OFF

sing

Watch

he Device

ective strip from the

– Upon removing the

batteries, the Year

se the M Button to s

utton to confirm yo

P Home T

battery

protective strip or

umber flashes in

lect the Year. Press

r selection.

or the first

Set the month

Press the ON/

Set the day

– Pr

Press the ON/O

time

Press M But

Press ON/

– Press the M Button

FF Button to confirm.

ess the M Button to s

F Button to confirm.

7EN

n to make selectio

F Button to confir

to set the Month.

t the Day.

Set the time

–

Minutes and p

time are set, a

If you want to

battery from t

put it back. Th

process as des

–

Once you have set

essed the ON/OFF B

d the current time is

hange the date and

e battery compart

Year number will fla

ribed above.

the Hour and

tton, the date and

displayed.

ime, take out one

ent briefly and

h. Complete the

Selecting the

The WatchBP Ho

cuff sizes. If the cu

unsuitable size , p

please use only

M (Me

22 - 32

M is the

L (Larg

32 - 42

correct cuff

e T device is availa

ff provided with the

lease consult your d

icrolif

cuffs!

iumsize)

cm (8.7

- 12.6 inch

correct size for most

size)

cm (12.6

- 16.5 inch

le with different

evice is an

ctor.

opl

es)

Taking

Prior to each m

right side of th

mode. The two

«DIAG.» (Diag

DIAG.

easureme

asurement, use the

device to select the

options include:

ostic) or «USUAL» (

ts using

Mode Switch on the

roper measuremen

sual) mode.

USUAL

tchBP Ho

«DIAG.» Mod

The «DIAG.» mod

by your doctor w

accordance with t

European Society

e T

e should be selected

en blood pressure i

he measurement gui

of Hypertension (ES

AG.

9 EN

as requested

measured in

delines of the

No measureme

In «DIAG.» mode

taken on 7 cons

week days). No r

«non-working»

in thismode!

JanJ

ts on non-work d

, blood pressure mea

cutive working d

eadings should be t

days (or particularly

surements are

(or normal

aken on

relaxing days)

orking

Two sets of meas

ESH guidelines rec

taken in the morni

the evening betwe

measurements b

unless otherwise

rements per day

mmend one doubl

g between 06:00 - 0

n 18:00 - 21:00. Al

fore taking your

irected by your do

SH Guidelines

06:00 -09:00

18:00 -21:00

measurement

:00 and one in

ays perform

edication,

tor.

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