Bloo
od pre
essu
ure monito
m
or
with Blueto
tooth and d
data manag
gement in linked
li
app
Opera
ating Instructio
ons
BPM 14
401
ad
deVitaal
Pressurre
Sub
bject to technic
cal changes ass a result of prroduct improve
ements.
Ope
erating Manua
al_BPM1401_E
EN_131210_R
REV001
Thank you for purchasing this Blood Pressure Monitor with app from the adeVital product range.
All the products in the innovative adeVital range – body analyser scales, blood pressure monitor and activity
meter – have Bluetooth functionality to transfer data to the adeVital app. The straightforward interface of the free-todownload app allows you to check your progress easily and clearly and ensures your health data is always available
and up-to-date.
Table of Contents
SAFETY I NFORMATION AND OPERATING INSTRUCTIONS………………………………………….. 3 SAFETY INFORMATION .......................................................................................................................3
INSTRUCTIONS FOR USE ....................................................................................................................4
FEATURES AND COMPONENTS……………………………………………………………………. 4 FEATURES........................................................................................................................................4
THE LCD DISPLAY ............................................................................................................................5
BLOOD PRESSURE MONITOR COMPONENTS .........................................................................................6
CONTENTS OF THE PACKAGE…………………………………………………………………….. 7 FIRST USE…………………………………………………………………………………………7 HOW TO INSTALL THE BATTERIES ........................................................................................................7
EXTERNAL POWER SUPPLY .................................................................................................................8
INSTALLING THE ADEVITAL APP AND CONNECTING ................................................................................8
MONITORING FOR BLUETOOTH MEASUREMENT DEVICES ........................................................................8
BLOOD PRESSURE MONITOR SETTINGS……………………………………………………….… 9 STARTING MEASUREMENT………………………………………………………………………. 11 PUTTING ON THE SLEEVE .................................................................................................................11
STARTING MEASUREMENT ................................................................................................................12
ACCESS SAVED MEASUREMENTS ......................................................................................................12
MEASUREMENT TIPS .......................................................................................................................13
DATA TRANSFER .............................................................................................................................14
ERROR MESSAGES AND TROUBLESHOOTING……………………………………………………. 14 ERROR MESSAGES ..........................................................................................................................14
DURING DATA TRANSFER .................................................................................................................15
DEVICE CARE…………………………………………………………………….………………15 CE DECLARATION OF C ONFORMITY……………………………………………………….……. 16 WARRANTY……………………………………………………………………………………...17 DISPOSAL………………………………………………………………………………………. 17 LEGAL INFORMATION OBLIGATION REGARDING THE DISPOSAL OF BATTERIES ..........................................17
DISPOSAL OF OLD ELECTRICAL DEVICES.............................................................................................17
ABOUT BLOOD PRESSURE………………………………………………………………………. 17 SYSTOLIC/DIASTOLIC BLOOD PRESSURE ............................................................................................17
STANDARD BLOOD PRESSURE CLASSIFICATION ...................................................................................18
IRREGULAR HEARTBEAT ...................................................................................................................18
TECHNICAL DATA……………………………………………………………………………….. 19 2
AVAILABLE ACCESSO
ORIES ............................ .....................................................................................20
0
EMC INF ORMATION……………
…
…………… ……………
……………
…………… ……………
……….. 20
0 SAFETY I NFFORMATION AND OPERATING INSTRRUCTIONS
SAFETY INFFORMATION
The warnin
ng signs and symbols are
e important to
o ensure you use this prod
duct correctlyy and safely and
a to prevent
injuring yourrself or others. The warn
ning signs annd symbols on
o the produ
uct and in thhese operatin
ng instruction
ns
have the following meanings:
Symb
bol for “Read
d the operatinng instructions!”
bol for a Blue
etooth-enableed device
Symb
Symb
bol for “Type BF applied p
part” (medica
al equipment classificationn)
Symb
bol for “Serial Number”
Symb
bol for “Direc
ct Current”
Symb
bol for “Manu
ufacturer”
Only for indoor us
se
F1
T1A//250V Φ 3.6*10CCC
Symb
bol for “Prote
ection Class I I device”
bol for “Meets the require ments of Eurropean Directtives”
Symb
Symb
bol for “Recyycling” – Electtrical products must not be
b disposed of with norm
mal household
d
waste
e. Please rec
cycle the deviice. Please contact your local recyclingg centre or re
etailer for tipss
on re
ecycling.
3
ATTENTION
N!
Please
e read these operating
o
insttructions careefully before using
u
the device.
This device is only intended
i
to be
b used by AD
DULTS AT HOME.
This devic
ce is not dessigned for non-invasive meeasurement and
a monitorin
ng of arterial blood pressure. It is not
designed for use at exttremities othe
er than the up
pper arm or fo
or functions other
o
than meeasuring blood
d pressure.
Do nott confuse selff-monitoring with
w self-diag
gnosis. You ca
an use this de
evice to moniitor your bloo
od pressure.
Start or sttop medical treatment onlyy after consullting your doc
ctor. If you are
e taking med ication, discu
uss with your
doctor wh
hat would be a suitable tim
me to measurre your blood
d pressure. Never change your prescrib
bed medication witho
out your docto
or’s agreement.
This device is not suitable
s
for co
ontinuously m
monitoring bloo
od pressure in medical em
mergencies orr operations.
If the pressure in the sleeve ex
xceeds 40 kP
Pa (300 mmH
Hg), the sleev
ve deflates auutomatically. If the sleeve
does not deflate when
n your blood pressure excceeds 40 kPa
a (300 mmHg
g), remove thee sleeve from
m your upper
arm and p
press the buttton to stop it inflating.
Do no
ot use the blo
ood pressure monitor nearr to strong electromagnetic fields (E.G. MOBILE TELEP
PHONE), particular if using the adap
pter.
pter and the patient
p
at the same time.
Do not touch the adap
d pressure monitor
m
is not approved ass a category AP or APG device.
d
It is nnot suitable fo
or use in the
The blood
presence of a flammab
ble anaesthetic mixture witth air (or oxyg
gen and nitrou
us oxide).
PLEASE KEEEP THE DEVIC
CE OUT OF REA
ACH OF CHILDR
REN, AS INHALING OR SWALLOWING SMALLL PARTS MAY CAUSE
C
INJURY
OR EVEN D
DEATH.
Please usse the ACCESS
SORIES and attachments
a
rrecommende
ed and appro
oved by the M
MANUFACTURE
ER. If you do
not, you m
may damage the device an
nd may put thhe user/patien
nt at risk.
PLEASE EN
NSURE THAT THE
T
BLOOD PR
RESSURE MONIITOR IS FUNCT
TIONING CORRE
ECTLY AND IS IN GOOD WOR
RKING CONDITION BEFO
ORE USE.
INSTRUCTIO
ONS FOR U S E
The ADE a
adeVital Preessure BPM1
1401 Blood Pressure Monitor
M
with app
a allows yyou to measu
ure your bloo
od
pressure a
and pulse and to save yo
our measurem
ments autom
matically. The blood pressuure monitor has a life of at
least 3 yea
ars.
The measurements provided by th
he BPM1401 have the sa
ave value as results provvided by a trrained medic
cal
specialist u
using a sleevve and stethoscope.
These ope
erating instru
uctions conta
ain important information about safety
y and how too care for yo
our device an
nd
provide ste
ep-by-step in
nstructions on
n how to usee the product.
Please rea
ad the full ope
erating instructions carefuully before usiing the produ
uct.
FEATURES AND COMPO
ONENTS
FEATURES
User devic
ce memory fo
or 60 x 1 mea
asurements/m
managementt of all measurement resullts is unlimited in the app
Reliable an
nd rapid data
a transfer to the adeVital aapp via Blueto
ooth
Accurate m
measurement of blood pre
essure data ((systolic and diastolic valu
ues) on the up
pper arm
Measurem
ment of pulse frequency
Heartbeat irregularity in
ndicator (arrhyythmia warni ng)
Measurem
ment while infflating
Oscillomettric method, i.e.
i measuring the pulse o
oscillations off the blood flo
ow
Classification of measu
ured values as
s using preseet values from
m the World Health
H
Organnization (WHO
O)*
Date and ttime display
4
Auto switc
choff
Battery levvel indicator
THE LCD D
DISPLAY
SYMBOL
D
DESCRIPTI
ION
EXPLANATTION
Retrieve da
ata/setup buttton
Access saved
s
measu
urements
Setup bu
utton to adjus
st the time
User 1
Start me
easurement fo
or user 1 and
d automatically transfer the
e
results
Program
mming button
User 2
Start me
easurement fo
or user 2 and
d automatically transfer the
e
results
Button to
o connect to the app
Systolic blo
ood pressure
e
Top bloo
od pressure value
v
Diastolic blood pressure
e
Bottom blood
b
pressu
ure value
Pulse
Pulse be
eats/minute
ction
Pulse detec
Shows your
y
heartbea
at when it is d
detected
Data readyy for transfer
Measure
ement data ha
as been saveed on the devvice
Data transffer
Data tran
nsfer in progrress
Average
Average of the last th
hree measureements
minder
Impact rem
a shocks cause
c
inaccuurate measure
ements
Knocks and
Low batterry
The batteries are wea
ak and must be replaced
Unit
o measuremeent
Blood prressure unit of
Current tim
me
Month, day
d (hour, min
nute)
Deflation
The sleeve is deflating
g
eartbeat
Irregular he
ead the furthe
er informationn on page 16
6
Please re
Bluetooth connection
c
Connectts the BPM14
401 to the acctive app
5
BLOOD PRESSURE MONITOR COMPONENTTS
The following componen
nts are parts of
o the devicee or are alread
dy built into th
he device:
Softt sleeve: 22 – 32 cm
BPM
M1401, houssing made fro
om ABS plasttic
Rep
peater
Air ttube
Pum
mp
Valvve
128
8 mm x 50 mm blue LCD display with w
white backgrround light
Con
nnection poin
nt for the mains adapter
Batttery comparttment
S
Sleeve
Aiir tube
Housiing
Displaay last meas--
Connnection point for mains power
User 1 / Programm
ming button
User 2 / Bluetooth
h connection button
Displaay
Batteery compartm
ment
6
CONTENTSS OF THE PACKAGE
BPM
M1401 blood
pressure monitorr
4x AAA
A 1.5 V alkali batteries
Sleeve
(type
e BF applied part)
(AC2
2232-02)
Instrucctions
FIRST USE
Remove all tthe compone
ents from the
e packaging aand remove the
t protective
e film from thee components.
Keep the pa
ackaging for storage
s
and to
t return the product, if ne
ecessary.
Th
his device must
m
not be used
u
by indivviduals (including childre
en) with limitted physical, sensory or
me
ental abilities, or who are
a lacking nnecessary experience
e
and
a
understaanding, unle
ess they are
e
su pervised by another individual respo
onsible for th
heir safety or
o have beenn instructed in the use of
the
e device. It should
s
be en
nsured that cchildren do not
n play with
h the device..
HOW TO INS
STALL THE BA
ATTERIES
Open the
e battery com
mpartment co
over on the baack of the
BPM140
01.
Place the
e batteries (4 x 1.5 V AAA
A) into the batttery compartmentt observing th
he polarity markings.
Close the
e battery com
mpartment co
over.
ATTTENTION!
REPLACEE THE BATTER
RIES UNDER THE
T
FOLLOWI NG CIRCUMS
STANCES:
is displayed on the
e LCD displaay.
The LCD display beco
omes weakerr.
The LCD display doess not light up when you sw
witch on the blood
b
pressu
ure monitor.
Used battteries should
d be dispose
ed of as hazzardous wastte. Do NOT dispose of thhem as norm
mal waste.
Please ob
bserve local regulations
r
an
nd recycling information when
w
disposin
ng of used baatteries.
Battery life:
Apprrox. 44 days
Battery capa
acity:
600 mAH. At a ra
ate of three b
ure measurem
ments per daay, 35 s per measuremen
nt,
blood pressu
20 s to display th
he results an d 10 s for da
ata transfer. The power cconsumption is 400 mA fo
or
meassurements, 50
5 mA to dissplay measurrements and
d 50 mA (add
ditionally) for data transfe
er.
The switched
s
off device requirres 35 μA.
Remove the
e batteries if the device will not be used
d for a longerr period of tim
me.
Used batteries may leak..
7
EXTERNAL P
POWER SUPP
PLY
100-240 V~
~, 50-60 Hz, 400 mA (o
only with m
mains adapte
er
UE08WCP-0
060100SPA! / Not provided!)
Disconnect the mains adapter
a
cable
e from the bllood pressure
monitor whe
mains.
en you want to
t disconnec
ct it from the m
Note:
The connec
ction point forr the mains adapter
a
is on the right side
ce. Do not pla
ace anything in the way tto ensure tha
at
of the devic
dapter cable can be disco
onnected eassily.
the mains ad
Mains adapter
INSTALLING THE ADEVITA
AL APP AND CONNECTING
G
Mobile or p
portable devic
ces with Blue
etooth functiionality as pe
er the BLE Technical
T
Sp
pecifications and
a
the Bloo
od
Pressure Prrofile (BLP) protocol from the internatio
onal Bluetoo
oth SIG organ
nisation can receive your personal da
ata
via modern Bluetooth 4.0
0 technologyy.
The adeVital app is available ffrom the App
p Store. You can
c search foor the app in the Store
and install it on yo
our iPhone.
Free ad
deVital app download
Clear p
presentation and
a tracking of all data annd values
MONITORING
G FOR BLUET
TOOTH MEAS
SUREMENT DE
EVICES
Displayys the date fo
or all recorded
d values
Displayys systolic and diastolic re
eading and puulse rate
Pulse frrequency
Create line charts fo
or various tim
me intervals
Graph or table view
w
Easy da
ata delivery via
v the integra
ated email funnction, Faceb
book and Tw
witter
Simply insta
all our specially developed
d app and co
onnect your blood
b
pressu
ure monitor too your mobile
e and portab
ble
devices. You
u will then be
e able to use the extensivee evaluation options
o
in the
e adeVital app
p.
The
e app to con
nnect the blood pressurre monitor iss only availa
able for iPod
d touch (5th generation),
iPh one 4S, iPho
one 5, iPhon
ne 5s, iPad 3
3, iPad Air, iPad mini and
d newer verssions.
mpatibility with
w Bluetooth 4.0 is requuired.
Com
ATTENTION!
BLLUETOOTH MO
ODULE N O.:
NRF8
8001
RAADIO-FREQUEN
NCY RANGE:
2402
2 MHz to 2480 MHz
OU
UTPUT POWER
R RANGE:
0 dBm
m
SU
UPPLY VOLTAG
GE:
3.3 V
TR
RANSMISSION RANGE:
10 m
8
Actiivate Bluetoo
oth and start the
t app.
Makke sure that Bluetooth
B
and
d the adeVitaal app are run
nning
so tthat you can connect the devices.
PREESS AND HOLD
D THE “U SER 2” BUTTON TO
O START THE LINKING
L
PRO
OCESS.
The
symbol and
a
symbol
s
appeaar alternatelyy on the
LCD disp
play and indic
cate that the linking proceess is running.
The
symbol iss displayed on
o the LCD diisplay when the
t connection iss established.
If the con
nnection fails,,
is displayed
d
on tthe LCD disp
play.
BLOOD PR ESSURE MO
ONITOR SETT
TINGS
Please set the time and date before using
u
the blo
ood pressure monitor for the first time, so that all re
ecorded measave a correct timestamp. (defaults: datte: 2012-01-01; time: 00:00; unit of m
measurement: mm Hg)
urements ha
Th e blood presssure monitor switches
s
off aautomatically in setup mode
e 60 secondss after the lastt input.
1. When th
he blood pressure monito
or has switchhed off, presss
and hold
d the “User 1”” button to se
et the time annd date.
9
2. The hourrs and minute
es are shown
n on the disp
play with flash
hing hour digits.
Adjust th
he hour by pressing the
ing) chan
nges to
buttonn,
(morn
n-
a
12 hourss.
(afternoon) after
he SET butto
on to switch
h to minutess and set th
he
3. Press th
minute u
using the
button. Holding dow
wn the
button fa
ast forwards through
t
the minutes.
m
4. Repeat ssteps 2 and 3 to confirm the
t [MONTH AAND DAY].
5. Press the
e SET button
n to confirm the [Day] annd to switch to
t
year (the
e year with fla
ash).
6. Hold dow
wn the
button until the correcct year is dissplayed. T
The numberss are in a loo
op so that it returns to [1].
Press th
he SET buttton again to
o confirm th e [YEAR] an
nd
switch au
utomatically to
t the UNIT OF
O M EASUREM
MENT .
[ NIT OF MEASUUREMENT].
7. Repeat stteps 2 and 3 too confirm the [U
[mmHg]
[kPaa]
10
STARTING MEASUREMENT
PUTTING ON
N THE SLEEVE
E
1. Connect the air tube
e connector for
f the sleevee to the tube
e
connection point on the left sid
de of the blo
ood pressure
e
monitor.
ound your up
pper arm (seee picture on
n
2. Place the sleeve aro
right).
E
that the sleeve iis 2 to 3 cm
m
3. Fasten tthe sleeve. Ensure
above yo
our elbow.
When th
he sleeve is closed arou
und your upp
per arm, you
u
should o
only be able to
t push one finger betweeen the sleeve
e
and yourr arm.
posture:
4. Correct p
Expose yyour arm or only wear clo
ose-fitting clo
othing for the
e
measure
ement.
Sit comfo
ortably and re
elaxed on a chair.
c
The middle of the sleeve should be at the ssame level ass
your hea
art.
Your legss should be relaxed
r
and your
y
feet poinnt outwards.
Your palm
m should be facing upwards.
11
STARTING M
MEASUREMENT
After correc
ctly positionin
ng the sleeve
e, press the “User 1” (or “User 2”) button to swittch on the blood
b
pressure
monitor. The
e measureme
ent is then pe
erformed auto
omatically.
1. LCD
D display
2. Automatic zeroing
omatic inflatio
on and meas
surement.
3. Auto
ng and savinng results th
hat are trans4. Displayin
ferred au
utomatically tto the adeVital data man
nagementt system. Thee
symbol flashes.
User 1” (or “U
User 2”) to sw
witch off the blood pressu
ure monitor. Otherwise, tthe blood pre
essure monito
or
5. Press “U
switchess off automatiically 1 minutte after the laast action.
A
A. Once the entire meas
surement haas finished, press anoth
her button too start the measuremen
nt
again with the blood pressure
p
monnitor.
B
B. A maximum of 60 reco
orded sets o
of measurem
ment results for user 1 aand user 2 can
c be save
ed
on the devvice and the number is uunlimited in the adeVital app.
ACCESS SA
AVED MEASUR
REMENTS
1. Once the
e blood presssure monitor is switched o
off,
press the
e “Search” bu
utton to open
n saved meassurements. T
The blood pre
essure monito
or displays thhe average of the last three
e measureme
ents.
12
2. Press the
e “Search” bu
utton again to
o browse thee records. Up
p to 60 record
ds are saved for each useer ID.
Measure
ement date an
nd time and shown
s
altern ately.
3. Press the
e “User 1” orr “User 2” buttton to switchh
between users.
NO RECORD FOR USER 2
4. Press “U
User 1” (or “User 2”) to switch off the b lood pressure monitor. Ottherwise, thee blood press
sure monitor
switchess off automatiically 1 minutte after the laast action.
MEASUREM
MENT TIPS
MEASUREMEENTS MAY BE INACCURATE UNDER
U
THE FO
OLLOWING CIR
RCUMSTANCES
S, WHICH SHO
OULD BE AVOID
DED:
Measurements straight aafter tea, cofffee or smok-ing
Within 1 hou
ur of eating and/or
a
drinkin
ng
Within 20 minutes of a ba
ath
er
If you are talking or movinng your finge
In a veryy cold room
If you neeed the toilet
13
health
DATA TRAN
NSFER
01 and your iPhone havee connected successfully, the measure
rement data is transferred
d
If the BPM140
utomatically via
v Bluetooth to your iPho
one when the
e app is open.
au
Th
he
symb
bol is hidden once the datta has been transferred successfully.
s
You can then check your
pe
ersonal health data on your iPhone.
If data transferr fails, the
symbol is nnot hidden. The queued measurement
m
t data is temp
porarily saved
d
on
n the blood pressure
p
mon
nitor and is traansferred to your iPhone after the next
xt measureme
ent.
ATTTENTION!
Interfere
ence is posssible near to devices withh the
with nearby electrica
al devices.
sym
mbol. The blo
ood pressuree monitor ma
ay interfere
This pro
oduct must be
b connected
d to a Bluetoo
oth device at 2.4 GHz to transfer
t
data..
How ca
an I reduce any possible in
nterference?
1. The d
distance betw
ween the bloo
od pressure m
monitor and the
t Bluetooth
h device shouuld be as low
w as possible (between 1 m and 10 m). There
T
should be no obstacles blocking
g the Bluetoooth connectio
on between
e monitor and
d the Bluetoo
oth device.
the blood pressure
2. Otherr electronic devices
d
(partic
cularly devicees with Bluettooth transfe
er/transmitter)) must be ke
ept at least
away from the
e blood press
sure monitor to avoid interference.
1ma
ERROR MEESSAGES AN
ND TROUBLE
ESHOOTING
This section
n contains a list of error messages
m
annd frequently asked questtions for prob
blems that may
m occur with
your blood pressure mo
onitor. If the device
d
is not working as expected, please check tthis list beforre you send in
or repair.
the device fo
ERROR MESSSAGES
Problem
m
No power
Low batteryy
Symptom
Please che
eck
mpty.
Baatteries are em
The display
d
is weak
w
or
Baatteries are no
ot
does not light up.
insstalled correc
ctly.
n the
on
diisplay
Thhe batteries are
a
weeak.
14
S
Solution
Insta
all new batterries.
Insta
all batteries ccorrectly.
all new batterries.
Insta
Problem
m
Symptom
Please chec
ck
Soolution
E 1 is displayed
d
Thhe sleeve is not
tig
ght enough.
Refastten the sleevee and repeat the
measu
urement.
E 2 is displayed
d
Thhe sleeve is to
oo
tig
ght.
Refastten the sleevee and repeat the
measu
urement.
Relax for a momennt and then re
epeat the
measu
urement.
E 3 is displayed
d
Movem
ment can affeect the measurement.
Relax for a momennt and then re
epeat the
measu
urement.
E 10 or
Error messa
age E 11 iss displayed
E 20 or
E 21 iss displayed
Relax for a momennt
hen repeat thee measureme
ent.
and th
Eexx iss displayed
Please
e repeat the m
measurement. If the
proble
em persists, p
please contac
ct your
dealer or our custoomer service. Contact
information and insstructions for returning
your product
p
are p
provided in the Warranty
section.
A ccalibration errror
haas occurred.
DURING DAT
ATA TRANSFER
Erro
or
Data Transffer
failed.
Description
Soluution
B
Bluetooth
is OFF.
O
Turn Bluetoo
oth ON via “S
Settings >> Ge
eneral >>
Bluetooth”.
T app is OFF
The
O (not runniing).
Tap the app
p symbol to sta
tart the app.
Outside the maximum
O
m
Bluuetooth
r
range.
Place your iPhone closeer to the deviice.
DEVICE CAARE
Please follow
w these instru
uctions to ca
are for your deevice:
Put the device in a dry place and avo
oid direct sun light
erge the devicce in water
Do not subme
15
Avvoid exposing the device to dusty envvironments
an
nd variations in temperatuure
Avoid shakin
ng or knockin
ng the device
e
h the sleeve
Do not wash
Remove dirt with a lightly dampened cloth
Cleaning:
C
Before use
T
Take the entirre device ou t of its stora
age bag. Use
e a soft clothh to remove dirt from the
e
b
blood
pressurre monitor. C lean the sleeve with some
e alcohol befoore attaching
g it.
After use
W
Wipe off the device
d
with a soft cloth. Disinfect the
e sleeve with some alcoh
hol. Place the
e
entire device in the storagee bag.
PLEAASE ALWAYS DISINFECT
D
THE
E SLEEVE BEFO
ORE YOU USE IT FOR A DIFFERENT PATIEN
NT .
Plea
ase note that ONLY THE MA
ANUFACTURER
R’ S SERVICE TECHNICIANS are
a permittedd to replace parts.
p
Old sensors may resultt in inaccuratte measurem
ments. Loose electrodes may
m prevent tthe blood pre
essure monito
or
switching o
on.
Proper carre has a majo
or influence on
o the life of yyour blood prressure monitor.
Do not usse aggressive
e detergent, abrasives o
or other chem
micals to wip
pe dirt off thhe device. Th
his can causse
discoloura
ation, malfunc
ction and dam
mage to the d
device.
Do not disa
assemble or modify the de
evice. In the eevent of problems with the
e device, pleaase contact se
ervice partnerr.
CE DECLAARATION OF C ONFORMITTY
T
This productt is manufacttured accord
ding to harm
monised European standaards. It comp
plies with the
e
p
provisions of the following
g EC Directivees:
E
EMC Directivve 2004/108//EC
R
R&TTE Directive 99/5/EC
M
MDD Directivve 93/42/EEC
C
16
WARRANTYY
ADE agreess to rectify an
ny material orr manufacturiing defects by
b offering fre
ee repair or reeplacement, for a period of
3 years from
m the purcha
ase date (exc
cluding wearinng parts and
d batteries). At
A the time oof purchase, please get th
he
retailer to fill in and stamp the guaran
ntee card. In ccase of a wa
arranty claim, please returnn the blood pressure
p
mon
nitor to your re
etailer including guarantee
e card and sttating the rea
ason for the claim.
c
ADE
E GmbH & Co.
C
Ham
mmer Steinda
amm 27 – 29, 22089 Ham
mburg, Germa
any
DISPOSAL
LEGAL INFO
ORMATION OB
BLIGATION REGARDING T
THE DISPOSA
AL OF BATTER
RIES
Do not disp
pose of batteries in domes
stic waste. A
As a consumer, you are le
egally requireed to return used
u
batterie
es.
You may retturn your use
ed batteries to
t public colllection pointss in your com
mmunity or too any retailer that sells ba
atteries of the same type.
Note:
ollowing symbols are used
d on batteries:
The fo
Li = Battery co
ontains lithium
m
Al =
Battery co
ontains alkali
Mn =
Battery co
ontains mang
ganese
CR (Li); AA ((Al, Mn); AAA
A (Al, Mn)
DISPOSAL O
OF OLD ELEC
CTRICAL DEV
VICES
T
The symbol on
o the product or its packkaging indica
ates that this product musst not be disp
posed of with
h
rregular household waste; instead, it m
must be disp
posed of at a collection point for the
e recycling of
e
electrical and
d electronic equipment.
F
For further details about recycling, co
ontact your lo
ocal council, municipal reecycling comp
panies or the
e
sshop where you
y bought th
he product.
B
Best regards,
A
ADE GmbH & Co.
ABOUT BLO
OOD PRESS URE
SYSTOLIC/D
DIASTOLIC BLOOD PRESS
SURE
Systo
olic
Your blood pressure is at
a its maximu
um in the cyccle when
ers of the hea
art contract and pump b
blood out
the chambe
of the heart. This value is referred to as the systo
olic pressure. Your b
blood pressu
ure is at its minimum
m
in tthe cycle
when the c
chambers of the heart expand.
e
This value is
referred to a
as the diastolic pressure.
17
Blood goes into the
artery
y
Contrac
ction
Diasttolic
Blood comes
c
from the vein
Expan
nsion
STANDARD BLOOD PRES
SSURE CLAS
SSIFICATION
ATTEENTION!
Only a do
octor can tell you what your
y
normal rrange of
blood pre
essure would
d be. Please
e consult a d
doctor if
your bloo
od pressure iss outside tha
at range. Pleaase note
that only a doctor can tell you whether youur blood
s level.
pressure has reached a dangerous
Blood pressure gra
rade 3 (severe)
Diastolic blood pressure (mmHg)
The blood pressure cla
assification published
p
byy the World
Health Orga
anization (WH
HO) and the Internationaal Society of
Hypertensio
on (ISH) in 199
99 is as follow
ws:
Blood pressure grrade 2 (moderate)
Blood pressure level 1 (mild)
Bo
orderline
High normal blood pressuree
Normal blood pressure
Optimal
blood
pressure
Systolic bblood pressure (mm
mHg)
Valu
ue
Blood
pressure
(mmHg)
Optimal
Normal
High normal
Mild
M
M
Moderate
Severe
SYS
S
<120
120-129
130-13
39
140
0-159
1160-179
•180
DIA
A
<80
80-84
85-89
9
90
0-99
1100-109
•110
IRREGULAR
R HEARTBEAT
T
This blood p
pressure mon
nitor comes with an intellligent irregula
ar heartbeat detector (IHB
B). The IHB records
r
the in
ntervals betw
ween heartbe
eats during every measure
rement and determines
d
th
he standard deviation. If the calculate
ed
deviation is greater or eq
qual to 15, the
e IHB symbo
ol is shown on
n the display with the resuult.
ATTENTION!
The IHB ssymbol indicates that a pulse
p
irregulaarity in conjun
nction with an
n irregular heeartbeat has been identified durin
ng the measu
urement. This is normallyy NOT a cau
use for conce
ern. Howeverr, if the symbol appears
frequentlyy, we recom
mmend that you
y
seek meedical advice
e. Please notte that the d
device does not replace
proper testing of your cardiovascular system, b
but can detec
ct pulse irregu
ularities at ann early stage.
VARIATIONS IN BLOOD PREESSURE OVER THE COURSE
1.Your blood pressure varies
v
during
g the
day. This d
depends in part
p on how tightly you atta
ach your slee
eve and the posip
tion you a
adopt for me
easurement. You
should the
erefore try to
o measure under
the same c
conditions.
2.Variations in blood pres
ssure are gre
eater
if you are ttaking medica
ation.
3.Wait at le
east 4-5 min
nutes before the
next meassurement.
OF A DAY
IF
THE HOSPITA
AL / FROM THE DOCTOR AND
D AT
YOU MEASUR
RE YOUR BLOO
OOD PRESSUREE AT HOME ON
N YOUR OWN,
PL
PLEASE NOTE THE
T
FOLLOWIN
NG :
HOME
The sleeve must
m
be place
ed correctly.
DIFFERENT
B
BLOOD PRESS
SURE RESULT
T AT
od pressure varies during
g the
Your bloo
day. Reason
ns can includ
de the weathe
er,
emotions, m
movement etc
c. and, in particular, the ‘whitte coat’ effec
ct in the hosp
pital or
at the docto
or’s, which ca
an cause high
her
blood pressure results th
han at home.
m
not be to
oo tight or tooo loose.
The sleeve must
m
not be attached
a
at thhe wrist.
The sleeve must
n be worrie
ed when the ssleeve inflates
s.
You should not
mes before measurement
m
t
You should breathe in deeply 2-3 tim
starts.
Tip : Leave 4-5
5 minutes be
efore the meaasurement to calm down.
18
DIFFERENT
B
BLOOD PRESS
SURE RESULT
TS ON
EACH ARM
Blood prressure can be
b measured on
both arms, b
but the resultts are differen
nt on
each arm. Y
You should th
herefore alwayys
measure you
ur blood presssure on the same
arm.
TECHNICALL DATA
Power sup
pply:
B
Battery opera
ated:
ali batteries)
6 V (4 x AAA alka
M
Mains operatted:
0-240 V~, 50--60 Hz,400 mA
m (on100
with mains ada
apter UE08W
WCP-060100S
SPA!)
ly w
Display mo
ode:
w
backgro
ound lighting
Bluee LCD with white
Disp
play area: 128
8 mm (L) x 50
0 mm (W)
Measurem
ment mode:
Osccillographic te
est method
Measurem
ment range:
Bloo
od pressure: 0-40 kpa (0~
~300 mmHg)
Pulsse:
(40-19
99) pulse bea
ats/minute
Precision:
Blood prressure: At
At
(or
at
°
5 °C – 40 °C
0 °C – 45 °C
°
5 °C – 40 °C)
°
withhin
withhin
± 0.4 kP
Pa (3 mm Hg)
± 0.7 kP
Pa (5 mm Hg); pulse: ±5 %
Operating conditions:
Tempe
erature: 5 °C
C – 40 °C
Relative humidity: •85 %
Air pre
essure: 86 – 106 kPa
onditions:
Storage & transport co
Tempe
erature: - 20 °C – 60 °C
Relative humidity: 10 % - 93 %
Air pre
essure: 50 – 106 kPa
ence of uppe
er arm that can
c
Circumfere
be measurred:
App
prox. 22 – 32 cm
Weight:
App
prox. 385 g (w
without batteries)
External diimensions:
App
prox. 120 x 16
60 x 69 mm
Accessorie
es:
4xA
AAA alkali ba
atteries, user instructions
Operating mode:
Conntinuous operration
Protection class:
Typee BF applied part
Device cla ssification:
Batttery operated
d: Medical equipment (ME
E) device with
h internal
pow
wer supply via
a mains adap
pter: Class II M
ME device
IP class:
IP22
2
Software vversion:
V01
19
AVAILABLE A
ACCESSORIE
ES
Storag
ge bag
Mains adap
pter
ADAPTER:
Type:
A
UE08WCP--060100SPA
Input:
100-240 V, 50-60 Hz, 400
4 mA
Output:
6V
1A
(expected liife: 50,000 h))
EMC INFO
ORMATION
MANUFACTU RER' S DECLARATION – ELEECTROMAGNETTIC EMISSIONS (IEC 60601
1-1-2)
The BPM14
401 blood pre
essure monito
or is intended
d to be opera
ated in the ele
ectromagnetiic environment specified
below. The c
customer or the user of th
he BPM1401 blood presssure monitor should ensurre that it is op
perated in
such an envvironment.
Rad
diated emission test
Co
ompliance
Electrom
magnetic envvironment (EM
ME) –
guidanc
ce
The BPM
M1401 blood
d pressure monitor uses
radio-fre
equency enerrgy for internal function
only. Therefore, its raadio-frequenc
cy emissionss
are very
y low and aree not likely to cause any
interfere
ence in nearb
by electronic equipment.
e
Radio-frequency emissio
ons in accord
dance with C
CISPR 11
Group 1
Radio-frequency emissio
ons in accord
dance with C
CISPR 11
Class B
Harmonic cu
urrent emissions in accord
dance with IE
EC 61000-3-2
2
Not app
plicable
Voltage flucttuations/flicke
er emissions in
accordance with IEC 610
000-3-3
Not app
plicable
The BPM
M1401 blood
d pressure monitor is suit-able for use in all esttablishments,, including
domestic establishm
ments and tho
ose directly
connectted to the puublic low-volta
age power
supply network
n
that supplies buildings used
for domestic purposees.
MANUFACTU RER' S DECLARATION – ELEECTROMAGNETTIC IMMUNITY (IEC 60601--1-2)
The BPM14
401 blood pre
essure monito
or is intended
d to be opera
ated in the ele
ectromagnetiic environment specified
below. The c
customer or the user of th
he BPM1401 blood presssure monitor should ensurre that it is op
perated in
such an envvironment.
Immunity tesst
IEC
C 60601 testt level
Co
ompliance levvel
Electro
omagnetic ennvironment (E
EME) –
guidan
nce
±6
Electrostatic
c dis6 kV contact discharge (ESD
D) in
ch
harge
accordance with IEC ±8
8 kV air discharge
61000-4-2
Floor should
±6
6 kV contact disd
s
be woood, concrete
e, or ceramic
chaarge
tile. If floors
f
are covvered with syn
nthetic mate±8
8 kV air discharge rial, the
e relative hum
midity should be at least 30
0
%.
Electrical fasst transi- ±2
2 kV for mains
s
ent/burst in accordance with IE
EC
61000-4-4
±2
2 kV for mainss
The qu
uality of the ssupply voltage should be
to the standard of a typical business or hos-pital environment.
Surges in ac
ccordance with IE
EC
±1 kV normal mode
volltage
The qu
uality of the ssupply voltage should be
to the standard of a typical business or hos--
or±1 kV conducto
co
onductor
20
61000-4-5
Voltage dipss, short
interruptionss and
voltage varia
ations on
power supp
ply in
accordance with IEC
61000-4-11
pital environment.
5% UT
<5
(>9
95% dip in UT) for
1/2
2 period
40
0% UT
(60
0% dip in UT ) for
5 cycles
c
70
0% UT
(30
0% dip in UT ) for
25
5 cycles
<5
The qu
5% UT
uality of the ssupply voltage should be
(>9
95% dip in UT) for to the standard of a typical business or hos-pital environment. IIf the user of the
1/2
2 period
BPM1401 blood prressure monitor requires
0% UT
40
continued operatioon during pow
wer mains
(60
0% dip in UT ) for
interruptions, it is reecommended that the
5 ccycles
BPM1401 blood prressure monitor is powwer supply or
o
ered frrom an uninteerruptible pow
0% UT
70
ery.
(30
0% dip in UT ) for a batte
25
5 cycles
<5
5% UT
5% UT
<5
(>9
95% dip in UT) for 5 s (>9
95% dip in UT) for
5s
Power frequ
uency
A
3 A/m
(50/60 Hz) m
magnetic
field in acco
ordance
with IEC 610
000-4-8
3A
A/m
Powerr frequency m
magnetic fields
s should be at
a
levels characteristic
c
c of a typical location in a
typical commercial or hospital en
nvironment.
NOTES: UT iss the AC mains voltage prrior to applicaation of the te
est level.
MANUFACTU RER' S DECLARATION – ELEECTROMAGNETTIC IMMUNITY (IEC 60601--1-2)
The BPM14
401 blood pre
essure monito
or is intended
d to be opera
ated in the ele
ectromagnetiic environment specified
below.
The customer or the use
er of the BPM
M1401 blood pressure mo
onitor should ensure that itt is operated in such an
environmentt.
Immunity tesst
IEC
C 60601 test level
Comp
pliance level
Electroma
agnetic enviroonment (EME
E) – guidance
e
Portable and
a mobile R
RF communic
cations
equipmen
nt should be uused no clos
ser to any parrt
of the BPM1401 blood
d pressure monitor,
m
inables, than thhe recommen
nded separa-cluding ca
tion distan
nce calculateed from the equation appropriate to the frequeency of the transmitter.
Recommended sepaaration distan
nce:
Immunity to conducted distu
urbances
induced by radiofrequency fie
elds in
accordance with
IEC 61000-4
4-6
V
150 kHzz to
3 Vrms
80 MHz
3 Vrm
ms
Radiated, ra
adiofrequency, e
electromagnetic
c field
immunity in accordance with IEC
61000-4-3
3 V/m
V 80 MHz to
t
2.5 GHz
3 V/m
m
d = 1.167
7
d = 1.167
7
for 80 MHz to 800 MHz
d = 2.333
3
for 8000 MHz to 2.5
5 GHz
where P is
s the maximum
m output pow
wer rating of
the transm
mitter in watts (W) according to the
transmitter manufactureer and d is the
e recommended separation
s
dist
stance in metrres (m).
Field stren
ngths from fixxed RF transmitters as
determine
ed by an elecctromagnetic site surveya
should be
e less than thhe compliance
e level in
each frequency range..b
Interference may occuur in the
vicinity of equipment m
marked with
the follow
wing symbol:
21
NOTE 1
At 80 MHz and 80
00 MHz, the hhigher freque
ency range ap
pplies.
NOTE 2
This guidance
g
mayy not apply inn all situationss. Electromag
gnetic propaggation is affected by absorption and reflec
ction from strructures, obje
ects, and peo
ople.
a
b
Field stre
engths from fixed
f
transmittters, such ass base station
ns for radio (c
cellular/ cord
dless) telepho
ones and land
d
mobile ra
adio, AM and
d FM radio brroadcast, and
d TV broadca
ast cannot be
e predicted thheoretically with
w accuracyy.
To assesss the electro
omagnetic environment duue to fixed RF
F transmitters
s, an electrom
magnetic site
e survey
should b
be considered
d. If the meas
sured field strrength in the location in which
w
the BPM
M1401 blood
d pressure
monitor iis used excee
eds the applicable RF com
mpliance leve
el above, the BPM1401 b
blood pressurre monitor
should b
be observed to
t verify norm
mal operation.. If abnormal performance
e is observedd, additional measures
m
may be n
necessary, su
uch as reorienting or reloccating the BP
PM1401 blood pressure m
monitor.
V/m.
Over the frequency ra
ange 150 kHzz to 80 MHz,, field strengths should be
e less than 3 V
mended sepa
aration distan
nce between portable and
d mobile RF communicatio
c
ons equipme
ent and the
Recomm
ME d
device or ME system – forr ME devices or ME system that are no
ot life-sustainning – are as follows:
f
RECOMMEND
DED SEPARATIION DISTANCE
E BETWEEN PO
ORTABLE AND MOBILE RF COMMUNICATIO
ONS EQUIPMENT AND THE
BPM1401 B
BLOOD PRESSURE MONITOR
R.
The BPM14
401 blood pre
essure monito
or is intended
d for use in an electromag
gnetic environnment in whic
ch radiated
RF disturban
nces are con
ntrolled. The customers
c
orr the users off the BPM140
01 blood presssure monito
or can help
prevent elec
ctromagnetic interference by maintaininng a minimum
m distance between portaable and mob
bile RF communicationss equipment (transmitters)
(
and the BPM
M1401 blood
d pressure mo
onitor as recoommended below,
b
according to th
he maximum output powe
er of the com
mmunicationss equipment.
Output pow
wer of transm
mitter in
W
Watts (W)
Sep
paration distaance according to frequen
ncy of the traansmitter in metres
m
(m)
150 kHz to 8
80 MHz
80 MHz to 800 MHz
d = 1.167
7
d = 1.167
800 MHzz to 2.5 GHz
d = 2.3
333
0.01
0.167
7
0.16
67
0..233
0.1
0.369
9
0.36
69
0..738
1
1.167
7
1.16
67
2..333
10
3.690
0
3.69
90
7..338
100
11.67
7
11.6
67
23
3.33
For transmittters rated at a maximum output poweer not listed above,
a
the rec
commended separation distance
d
d in
metres (m) c
can be estima
ated using th
he equation aapplicable to the
t frequency
y of the transsmitter, where P is the
maximum output power rating of the transmitter inn watts (W) according
a
to the
t transmitteer manufactu
urer.
NOTE 1
0 MHz, the hhigher frequen
ncy range applies.
At 80 MHz and 800
NOTE 2
uidance mayy not apply in all situationss. Electromag
gnetic propaggation is affec
cted by abThis gu
sorptio
on and reflecttion from struuctures, objects, and people.
22
Guarantee ca
ard – 3 years on the blood pressure mo
onitor (except wearing
w
parts and batteries)
• Sender
• Reason ffor claim
• Date of purch
hase _________________
urchase to your retaile
er.
Please return this seection and proof of pu
Operating
g Manual_BA1400_E
EN_131217_REV001
23
Record, m
manage an
nd analyse
e health daata simply and clearly
ly with thee new adeV
Vital product rangee with Blueetooth func
ctionality aand the inte
telligent ad
deVital appp.
This is tod
day's heallth monitorring techno
nology!
24
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