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Bluetooth®
Blood Pressure Monitor
Bluetooth®
Blood Pressure Monitor
Bluetooth®
Blood Pressure Monitor
User
Manual
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User-friendly
Manual
Bluetooth®
Blood Pressure Monitor
Bluetooth®
Blood Pressure Monitor
Dok./Rev.-Nr. 92785_20141202
QR codes take you where you want to go
quickly and easily
Whether you require product information, spare parts or accesso-
ries, details on warranties or aftersales services, or if you want to
watch a product demonstration video, our QR codes will take you
there in no time at all.
What is a QR code?
A QR code (QR = Quick Response) is a type of matrix that can be read
with a smartphone camera and that contains a link to a website or
contact details, for example.
Advantage: You do not need to manually enter a website address or
contact details.
This is how it works
To scan the QR code, all you need is a smartphone with QR code rea-
der software and an internet connection*. This type of software can
be downloaded for free from your app store.
Try it out now
Just scan the QR code with your smartphone and
find out more about the Aldi product you have
purchased.*
Your Aldi Service Portal
All details mentioned above can also be found in
the Aldi Service Portal at www.aldi.co.uk.
* Depending on your tarif plan you may be charged for the
connection.
Overview .................................4
Use ............................................5
Scope of delivery/
device parts .............................6
General information ...............7
Reading and storing the
instruction manual ...............7
Explanation of symbols ......8
Safety ..................................... 10
Proper use ............................10
Safety notes .........................12
Checking the product contents
16
Crane Connect app .................17
Compatibility .......................18
Description of the device ...... 18
Control elements ................19
Display .................................20
LED indicator ....................... 22
Device modes ..................... 22
Start-up .................................25
Inserting batteries ............. 25
Setting the measurement
computer ............................. 26
Installing the app ............... 27
Creating a user account .... 27
Configuring users ..............28
Handling ................................30
Performing a
measurement ..................... 30
Preparing
a measurement .................. 33
Manual data transfer ......... 37
Viewing the measurements
on the measurement
computer ............................. 38
Erasing measurements ....39
Evaluating the
measurements ......................40
Cardiac arrhythmia ...........40
WHO classifications .............41
Cleaning and maintenance ..44
Changing the batteries.....45
Storage ................................45
Troubleshooting ...................46
Technical data ....................... 51
Full display reference ........ 54
Manufacturer information ...55
Declaration of conformity ....55
Disposal .................................56
Disposing of the packaging .
56
Disposing of old devices ... 56
Electromagnetic
compatibility .........................58
Electromagnetic
emissions .............................58
Electromagnetic
immunity ............................. 59
Recommended separation
distances .............................62
Trademark protection
notices ...................................64
Warranty ................................65
Contents
A
B
2
3
5
13
14
15
17
19
20
16
18
21
22
23
12
1
4
7 6
8
9
10
11
4
Overview
GB IRE
C
D
F
E
5
Use
GB IRE
6 Scope of delivery/device parts
Product contentsdevice parts
GB IRE
1
Measurement
computer
2
Cuff
3
Cuff hose
4
Batteries (AAA), 4x
5
Bag
6
Display
7
SET button
8
User 2 touch button
9
ON/OFF switch for
User 1 and User 2
touch button
10
User 1 touch button
11
Connector jack for
the cuff hose
12
Date indicator
13
Time indicator
14
Indicator for
systolic pressure
15
Indicator for diastolic
pressure
16
Air release indicator
17
Memory slot indicator
18
Pulse indicator
19
Indicator for mea-
surement classifica-
tion according to the
WHO
20
Bluetooth® indicator
21
Battery indicator
22
Arrhythmia indica-
tor/pulse indicator
23
User indicator
7General information
IREGB
General information
General information
Reading and storing the instruction
manual
This instruction manual accompanies this
Bluetooth® blood pressure monitor. It con-
tains important information on how to set
up and handle the device.
For improved readability, the Bluetooth®
blood pressure monitor will be referred
to merely as the “blood pressure monitor”
below.
Before using the blood pressure monitor,
read the instruction manual carefully. This
particularly applies for the safety notes.
Non-observance of this instruction manual
may cause damage to the blood pressure
monitor.
The instruction manual is based on the
standards and rules in force in the European
Union. When abroad, you must also observe
country-specific guidelines and laws.
Store the instruction manual for future use.
Make sure to include this instruction manual
when passing the blood pressure monitor
on to third parties.
8 General information
GB IRE
Explanation of symbols
The following symbols and signal words are used in
this instruction manual, on the packaging or on the
blood pressure monitor.
WARNING! This signal word designates
a hazard with a moderate degree of risk
which may lead to death or severe injury if
not avoided.
CAUTION! This signal word designates a
hazard with low risk that, if not avoided,
may result in minor or moderate injury.
NOTICE! This signal word warns against pos-
sible damage to property or provides you
with useful additional information on use.
Declaration of conformity (see chapter “Dec-
laration of conformity”): Products marked
with this symbol fulfil the requirements of
the CE directive for medical products.
This symbol indicates that the warranty for
the blood pressure monitor amounts to 36
months (3 years).
9General information
IREGB
This symbol identifies devices classified as
type BF.
This symbol indicates that the device must
be protected against wetness.
This symbol indicates that you should read
the instruction manual and hold onto it.
This symbol identifies information from the
manufacturer (see chapter “Manufacturer
information”).
This symbol identifies information from the
manufacturer's representative in the Eu-
ropean Union (see chapter “Manufacturer
information”).
This symbol identifies devices that emit
non-ionising electromagnetic radiation (see
chapter “Electromagnetic compatibility”).
This symbol signalises disposal instructions
for packaging material (see chapter “Dis-
posal instructions”).
This symbol identifies devices that are oper-
ated with direct current (see chapter “Tech-
nical data”).
10 Safety
GB IRE
This symbol signalises legal regulations for
the disposal of electrical devices (see chap-
ter “Disposal instructions”).
This symbol signalises legal regulations
for the disposal of rechargeable batter-
ies and batteries (see chapter “Disposal
instructions”).
This symbol identifies the serial number of
the device.
Operation
RH 15% - 93%
+40°C
+5°C
This graphic identifies permissible oper-
ating conditions (see chapter “Technical
data”).
Storage
RH
<
93%
+70°C
-25°C
This graphic identifies the permissible
storage conditions (see chapter “Technical
data”).
Safety
Proper use
The blood pressure monitor is designed for non-invasive
measuring and monitoring of arterial blood pressure
levels of adults (patients). Your pulse rate is also shown
on the display of the blood pressure monitor.
The blood pressure monitor issues a warning in the
11Safety
IREGB
event of cardiac arrhythmia. The levels measured are
classified and rendered in accordance with the guide-
lines of the WHO (World Health Organisation).
The patient is also intended to be the user. The blood
pressure monitor is exclusively intended for private use
and is not suitable for commercial or clinical use. The
blood pressure monitor is not a children's toy.
Only use the blood pressure monitor as described in this
instruction manual. Any other use is deemed improper
and may result in injury to persons or damage to the
blood pressure monitor.
The manufacturer or vendor accepts no liability for dam-
age caused by improper or incorrect use.
12 Safety
GB IRE
Safety notes
WARNING!
Danger for children and per-
sons with impaired physical,
sensory or mental capacities
(e.g. partially disabled per-
sons, older persons with re-
duced physical and mental
capacities) or lack of expe-
rience and knowledge (e.g.
children).
The blood pressure monitor may not
be used by children under the age of 8.
Keep the blood pressure monitor and its
accessories away from children under
the age of 8.
The blood pressure monitor may be
used by children ages eight and over as
well as persons with impaired physical,
sensory or mental capacities or those
lacking experience and/or knowledge if
they are supervised or have been in-
structed in how to safely use the blood
pressure monitor and have understood
13Safety
IREGB
the risks associated with operating it.
Do not allow children to play with the
packaging wrapper. They may get
caught in it and suffocate.
WARNING!
Risks associated with improper
handling of the batteries!
The blood pressure monitor is bat-
tery-operated. Improper handling
of the batteries may result in injury
and damage to property.
Store the batteries in an area that is not
accessible for children. If you suspect
that a child has swallowed a battery,
immediately contact a physician.
Never expose the batteries to exces-
sive heat such as direct sunlight, open
flames or similar.
Do not charge the batteries and do not
reactivate them with other means.
Do not short circuit the batteries.
Do not open the batteries.
14 Safety
GB IRE
To prevent the batteries from leaking,
only insert batteries of the same type in
the blood pressure monitor.
If necessary, clean the battery and de-
vice contacts before inserting the bat-
teries.
Make sure that the polarity is correct
when inserting the batteries.
Promptly remove empty batteries from
the blood pressure monitor.
If a battery in the blood pressure moni-
tor has leaked, put on protective gloves
and use a dry cloth to clean the battery
compartment.
Do not allow battery acid to come into
contact with skin, eyes or mucus mem-
branes. In the event of contact with bat-
tery acid, immediately flush the applica-
ble areas with plenty of clean water and
consult a physician immediately.
If you do not use the blood pressure
monitor for a prolonged period, remove
the batteries from the battery compart-
ment.
15Safety
IREGB
NOTICE!
Risk of damage!
Improper use of the blood pres-
sure monitor may result in inaccu-
rate measurements and damage
to the blood pressure monitor.
Do not expose the blood pressure moni-
tor to strong magnetic fields (e.g. trans-
formers). Otherwise this could cause
err
ors in data transmission or damage to
the blood pressure monitor.
Only use the blood pressure monitor
at an ambient temperature of + 5°C to
+40°C and a humidity of 15% to 93%.
Do not open the blood pressure monitor.
Protect the device against dirt, direct sun
-
light, severe temperature fluctuations,
chemicals and mechanical shocks.
Do not let the device fall down.
Only use enclosed or original replace-
ment cuffs to ensure that
the measure-
ments are correct.
Do not start the measurement process
until the cuff has been fitted.
Do not immerse the blood pressure
16 Checking the product contents
GB IRE
monitor in water and do not rinse it off
under running water.
Protect the cuff and cuff hose from sharp
and pointy objects.
Do not kink the cuff hose.
Do not place any heavy objects on the
blood pressure monitor, the cuff or cuff
hose.
Checking the product contents
NOTICE!
Risk of damage!
If you are not cautious when open-
ing the packaging with a sharp
knife
or other pointy object, you
could damage the blood pressure
monitor.
You should therefore be very
careful when opening it.
1. Take the blood pressure monitor out of the packaging
and remove the packaging material.
2. Take the protective plastic foil off of the display of the
measurement computer.
17Crane Connect app
IREGB
3. Check to make sure that the delivery is complete (see
fig. A).
4. Check whether the blood pressure monitor or the
individual parts exhibit damages. If this is the case,
do not use the blood pressure monitor. Contact the
manufacturer at the service address specified on the
warranty card.
Crane Connect app
The blood pressure monitor is designed to measure
blood pressure and pulse. The data measured are
transmitted to a smartphone or tablet via Bluetooth®.
With the free Crane Connect app (hereinafter referred
to as “app”) you can save and analyse this data on your
smartphone or tablet.
If the Internet connection on your smartphone or tablet
is active, the Crane Connect app will automatically up-
load the measurements to the website
www.cranesportsconnect.com and permanently save
them in your user account.
The blood pressure monitor can record, save and trans-
fer data from two different users.
You can also use the blood pressure monitor without
being connected to the app. The blood pressure monitor
has 60 memory slots for each user. Once all 60 memory
slots are occupied, the next measurement will overwrite
the oldest entry.
18 Description of the device
GB IRE
The data saved is transferred to the app the next time
you connect the blood pressure monitor with the app.
Compatibility
The following smartphones and tablets with
Bluetooth® Smart Ready (Bluetooth®4.0) are compati-
ble with the blood pressure monitor and app:
Apple® iPhone® 4s and more recent versions
Apple® iPad® 3rd generation and more recent ver-
sions
Apple® iPad mini™ 1st generation and more recent
versions
Apple® iPad Air™ and more recent versions
Smartphones and tablets with Android™ 4.3 and
more recent versions
You can find a detailed list of compatible devices on the
following website:
www.cranesportsconnect.com/compatibility.
Description of the device
The blood pressure monitor consists of a measurement
computer, a cuff that inflates automatically and a cuff
hose that connects the cuff with the measurement
computer.
A display, multiple LEDs and function buttons are locat-
ed on the measurement computer. They are described
below.
19Description of the device
IREGB
Control elements
The control elements can be used to make various set-
tings on the measurement computer (see Fig. A).
Control element Functions
User 1 touch button
10
and user2 touch
button
8
Start/stop the measure-
ments
Access the measurements
In Setting mode: Decrease
and/or increase the value
Changing the mode
SET button
7
Save the data and time
settings
Stop the measurements
Manually connect to the
app
Change of mode when an
error is displayed
ON/OFF switch
9
Activate and/or deactivate
the user 1 and user 2 touch
buttons
20 Description of the device
GB IRE
Display
Different data will be shown on the display (see fig. B).
Display Description
Date indicator
12
The date is shown here. It
will be saved with the meas-
urements. It therefore makes
sense to set the right data on
the measurement computer.
Time indicator
13
The time is shown here. It is
saved with the measurements.
It therefore makes sense to set
the correct time on the meas-
urement computer.
Indicator for systolic
pressure
14
The systolic pressure is shown
in mmHg here (millimetres of
mercury).
Indicator for diastolic
pressure
15
The diastolic pressure is shown
in mmHg here (millimetres of
mercury).
Air release indicator
16
This symbol is shown when the
blood pressure monitor releas-
es air from the cuff.
Memory slot
indicator
17
Here, the memory slot being
used for the current measure-
ment is shown. 60 memory
slots are available per user.
21Description of the device
IREGB
Display Description
Pulse
indicator
18
Here, the pulse recorded
during blood pressure meas-
urement is shown in beats per
minute (bpm).
Display of the meas-
urement classifica-
tion according to the
WHO
19
The LEDs indicate the classifi-
cation of the blood pressure
levels measured according to
the WHO scale. You can find
details in the chapter “Evaluat-
ing measurements”.
Bluetooth®
indicator
20
This symbol indicates whether
data transmission via Blue-
tooth® is active.
Battery indicator
21
The battery indicator lights up
when the batteries are empty
and have to be replaced.
Arrhythmia indica-
tor/pulse indicator
22
This symbol blinks during the
measurement to show that a
pulse is being measured.
Once the measurement is
complete, the indicator will
report any potential cardiac ar-
rhythmia detected during the
measurement. You can find
details in the chapter “Evaluat-
ing measurements”.
22 Description of the device
GB IRE
Display Description
User indicator
23
The user currently performing
a measurement or retrieving
measurements is shown here.
LED indicator
The 6 LEDs on the left side of the display indicate the
classification of the measurements according to the
WHO scale. The indicator is colour-coded. For details
on the WHO classification, see the chapter “Evaluating
measurements”.
Colour Meaning
Green Optimal
Green Normal
Green Elevated normal
Yellow Slight hypertension
Orange Moderate hypertension
Red Severe hypertension
Device modes
The blood pressure monitor has five different modes,
which are explained below.
In all modes, the display light turns off after 30 seconds
of user inactivity.
23Description of the device
IREGB
After 1 minute of user inactivity, the measurement com-
puter will switch to sleep mode.
Sleep mode
After all settings have been made and the device is acti-
vated, the blood pressure monitor automatically switch-
es to sleep mode. The display light and WHO-LEDs are
deactivated in this mode.
You can also manually transfer data to the app on your
smartphone or tablet from sleep mode (see chapter
“Manual data transfer”).
From sleep mode, you can switch to the other modes as
follows:
Mode Switching modes
Setting mode for
date and time
Push the “SET” button to access
the setting mode for date and
time and to activate or deacti-
vate Bluetooth®.
Measurement
mode
Tap the user1 touch button once
to access the measurement
mode for user 1.
Tap the user2 touch button to
access the measurement mode
for user 2.
24 Description of the device
GB IRE
Mode Switching modes
Transmission
mode
Hold the SET button for approx.
three seconds to access the
transmission mode for manual
data transmission.
Memory mode Press and hold the user 1 touch
button for approx. three seconds
to access the save mode for
user1.
Press and hold the user 2 touch
button for approx. three seconds
to access the memory mode for
user 2.
Setting mode
In setting mode, you can set the time format, date, time
and automatic data transmission after a measurement
(see chapter “Setting the measurement computer”).
Measurement mode
In measurement mode, you can measure blood pres-
sure and automatically transfer the data to the app on
your smartphone or tablet (see chapter “Performing a
measurement”).
Transmission mode
In transmission mode, data from the blood pressure
monitor is transferred to the app on your smartphone
25Start-up
IREGB
or tablet. With automatic data transmission, the blood
pressure monitor will directly switch to transmission
mode once the measurement has been performed (see
chapter “Performing a measurement”).
For manual data transmission, you must switch the
blood pressure monitor to transmission mode yourself
(see chapter “Manual data transfer”).
Memory mode
In memory mode, you can have the measurements
shown on the display of the measurement computer
(see chapter “Viewing the measurements on the meas-
urement computer”) and erase the measurements for a
user (see chapter “Erasing measurements”).
Start-up
Inserting batteries
NOTICE!
Do not use your blood pressure monitor
with rechargeable batteries.
1. Open the battery compartment on the bottom of the
device.
2. Insert the four batteries contained in the product
contents in the battery compartment. In the process,
observe the marking for the correct polarity.
26 Start-up
GB IRE
3. Close the battery compartment. All indicator segments
will briefly appear on the display
6
(see fig. A and
B). Then the display will switch on and the “24 h” time
format will blink on the display.
The measurement computer is now ready for the basic
settings.
Setting the measurement computer
The results from each successful measurement are
saved together with the time and date. For this, first
the time format, date and time must be entered on the
measurement computer properly. Proceed as follows:
1. If “24 h” blinks on the display, tap the touch buttons
for user 1
10
or user 2
8
to switch between the “12
h” and “24 h” time formats (see fig.A).
2. Push the SET button
7
to save the time format set-
ting. The year indicator will now blink.
3. Tap the touch buttons for user 1 or user2 to set the
current year.
4. Confirm your setting with the “SET” button.
5. You can set the month, day, hours and minutes in
the same manner. Then “On” or “OF” will blink on the
display.
6. Tap the touch buttons for user1 or user 2 to activate
or deactivate Bluetooth® on the measurement com-
puter. Bluetooth® is activated by factory default.
In general, you should only switch Bluetooth® off
27Start-up
IREGB
if you don't want to transfer measurements to your
smartphone or tablet.
7. Confirm the Bluetooth® setting with the “SET” but-
ton. The display will switch off.
The measurement computer is now ready for use.
Installing the app
1. Download the free Crane Connect app from the App
Store or from the Google Play Store. You can also
download the app by scanning one of the following
QR codes:
For iOS: For Android™:
You can also download the app under the following
URL:
www.cranesportsconnect.com/downloads.
2. Install the app on your smartphone or tablet. For this,
follow the on-screen instructions.
Creating a user account
The blood pressure monitor has 2 user memory slots
for storing your individual measurements and those of
family members for example. For this purpose, an own
user account must be set up in the app for each of these
users.
28 Start-up
GB IRE
To create a user account with the app, follow the steps
below:
1. Start the app.
You will be directed to the “Home” menu.
2. Select the app icon “All Settings”.
3. To create a new user or log on with an existing user,
select the app icon “User Settings”.
4. Follow the step-by-step instructions provided in the
app.
5. Once the user settings are complete, return to the “All
Settings” menu.
You can also create your user data on the following
website: www.cranesportsconnect.com.
Configuring users
In order for the blood pressure monitor to send the cor-
rect data to your smartphone or tablet, you must now
assign user 1 or 2 from the blood pressure monitor to
your user account.
1. Start the app on your smartphone or tablet if you
have not already done so.
2. Select the app icon “All Settings”.
3. Select the icon “Blood Pressure Monitor”. You will
access the other settings for the blood pressure
monitor.
4. Set user 1 or user 2 in the “Settings” menu. With the
user set here, you must perform the measurements
29Start-up
IREGB
on the blood pressure monitor later on so that the
app properly recognises your data.
5. After you have selected the user, return to the
“Home” menu. From there, you can access all anal-
yses of the measurements via the app icon “Blood
Pressure Monitor”.
The app is now ready to receive measurements from the
blood pressure monitor.
30 Handling
GB IRE
Handling
Performing a measurement
Caution!
Risk of injury!
Using the blood pressure monitor
improperly poses a risk of injury,
among other things by impaired
circulation of blood.
Avoid prolonged exposure to
the pressure exerted by the
cuff, e.g. by kinking the cuff
hose and by performing pro
-
longed or frequent measure-
ments.
Do not place the cuff over
wounds to prevent further
injury.
Remove the cuff from your arm
in the event of a malfunction.
31Handling
IREGB
NOTICE!
For ideal measurement results,
follow the basic rules below when
measuring your blood pressure.
If possible, always measure your blood pressure at
the same time of day for comparable results.
At least 30 minutes before you perform a measure-
ment, do not smoke, eat or drink and avoid physical
exertion.
Give your circulatory system about five minutes to
calm down each time before you perform a meas-
urement.
If the measurements are not plausible, repeat the
measurement.
Wait at least five minutes before taking another
measurement for the same person.
The results of your blood pressure measurements
are for your information and are no substitute for
a medical examination. Do not make any medical
decisions based on your own measurements (e.g.
with respect to taking medication or their dosage).
Consult your physician if you have questions about
the measurements.
Do not use this blood pressure monitor to perform
any measurements on preeclampsia patients or
newborn babies.
32 Handling
GB IRE
Consult your physician before you use
the blood pressure monitor on pregnant persons.
Do not use the blood pressure monitor together with
high-frequency surgical devices.
Only use the device for persons with an upper arm
circumference between 22 and 35cm.
The function of the affected body part may be im-
paired when inflating the cuff.
The cuff hose may not be kinked, compressed or
otherwise restricted.
Always measure your blood pressure on the same
arm – ideally, the left arm.
Do not use the cuff on limbs whose arteries or veins
are undergoing medical treatment e.g. in the form of
intravascular access, intravascular therapy or arterio-
venous (A-V) shunt.
Do not fit the cuff on persons, who have undergone a
mastectomy.
Please keep in mind that the restriction of circulation
through the inflation of the cuff may temporarily
cause other measurement devices connected to the
same body part to temporarily malfunction.
Avoid performing frequent measurements and pro-
longed pressure in the cuff to prevent injury.
The blood pressure monitor is battery-operated.
Data transmission and data storage are only possi-
ble if the power supply is intact. The blood pressure
monitor will lose the date and time if the batteries
33Handling
IREGB
are empty or have been changed. However, meas-
urements that have been saved will remain intact.
To save battery power, automatic switch-off will
automatically switch the blood pressure monitor to
sleep mode after more than 1 minute of key inactivity
on the measurement computer.
The following illnesses or symptoms may result in incor-
rect measurements or affect the measurement accuracy
of the blood pressure monitor:
Diseases of the cardiovascular system,
very low blood pressure,
diabetes,
circulatory disorder and cardiac arrhythmia,
shivering,
shaking.
Preparing a measurement
Establishing a Bluetooth® connection
If you would like to perform the measurement without
direct data transmission, the data will be saved on the
measurement computer. You can transfer them to the
app later (see chapter “Manual data transfer”).
If you would like to automatically transfer the measure-
ments to the app once measurement is complete, pro-
ceed as follows:
1. Make sure that the Bluetooth® function of your
smartphone or tablet is switched on.
34 Handling
GB IRE
2. Start the app if you have not already done so.
3. Activate the user touch buttons with the
ON/OFF switch
9
(see fig.A).
4. Make sure that Bluetooth® on your measurement
computer is also on (see chapter “Setting the meas-
urement computer”).
Fitting the cuff
1. Expose the arm where you would like to measure the
blood pressure. Use your left arm if possible.
2. Wrap the cuff
2
around the exposed upper arm
(see fig. C).
The bottom edge of the cuff must be 2–3 cm above
the elbow and over the artery. The cuff hose
3
must point towards the middle of your palm.
3. Now place the free end of the cuff around your arm.
The cuff must be fitted tightly enough so that two
fingers fit under the cuff.
4. Once the cuff has been properly fitted, close the Vel-
cro strap.
5. Now connect the cuff hose with the connector
jack
11
on the measurement computer
1
(see fig. A and D).
Assuming the correct posture
You can perform the measurement while sitting or lying
down (see fig. E and F). Be absolutely sure to observe
the following instructions:
35Handling
IREGB
1. The cuff must be roughly at the height of your heart,
but no higher.
2. Rest your arms in a relaxed position.
A chair with armrests or a table are required for
measurements performed while sitting.
3. Do not move and do not speak while performing a
measurement.
If you would like to measure your blood pressure while
sitting, you must also observe these instructions:
4. Sit in a relaxed position when measuring your blood
pressure and lean back.
5. Place your feet flat on the ground.
6. Do not cross your legs.
Starting a blood pressure measurement
NOTICE!
You can cancel blood pressure measure-
ments that are in progress by pushing the
SET button or the user 1 or user 2 touch
button.
Proceed as follows to start the blood pressure monitor:
1. On the measurement computer
1
, tap the user
1 touch button
10
or the user 2 touch button
8
depending on which user you have configured for
yourself in the app (see fig. A and B).
All display elements will be shown briefly. The last
36 Handling
GB IRE
measurement will then appear on the display
6
for one second. If no measurement has been per-
formed yet, the device will not show any values.
2. The cuff will now inflate
2
and you will feel it tight-
en (see fig. A).
If no measurements have been saved, the blood
pressure monitor will inflate the cuff up to a pressure
of 190mmHg. Otherwise, the device will calculate
the average systolic pressure of all previous meas-
urements, add 40mmHg and inflate the cuff to that
value.
3. As soon as the blood pressure monitor detects your
pulse, the pulse indicator will blink on the display
22
. If this is not the case, the device will inflate
again (see fig. B).
4. Once the measurement is complete, the entire air
will be released from the cuff. The measurements
for systolic pressure
14
, diastolic pressure
15
and
pulse
18
will appear on the display and be saved.
The WHO-LED corresponding to the measured values
will light up (see fig.B).
5. If you do not want to perform automatic data trans-
mission, use the user 1 touch button
10
or the user 2
touch button
8
to switch the blood pressure moni-
tor to sleep mode (see fig.B).
If you have prepared the blood pressure monitor and
your smartphone or tablet accordingly, automatic
data transfer to the app will begin following the
measurement:
37Handling
IREGB
6. The Bluetooth® symbol
20
will blink on the display
6
. The blood pressure monitor will now attempt to
connect to the app for approx. 30 seconds (see fig. A
and B).
7. As soon as a connection has been established,
the Bluetooth® symbol will stop blinking and all
measurements will be automatically transferred
to the app. Following successful transmission, the
Bluetooth® symbol on the display will go out and
the device will switch to sleep mode. If a trans-
mission fails, the display will show the Bluetooth®
symbol and the error code “E7” (see chapter
“Troubleshooting”).
Manual data transfer
NOTICE!
All function buttons on the blood pres-
sure monitor are inactive during the data
transfer.
If it is not possible to automatically transfer the measure-
ments to your smartphone or tablet after the measure-
ment, you can perform a manual transfer as follows:
1. Activate Bluetooth® on your smartphone or tablet.
2. Open the app.
3. Press and hold the SET button
7
for three seconds.
The Bluetooth® symbol
20
will blink on the display
38 Handling
GB IRE
of the blood pressure monitor and a connect to the
app will be established (see fig.Aand B).
4. As soon as a connection has been established, the
Bluetooth® symbol will stop blinking and all meas-
urements will automatically be transferred to the
app.
5.
Once the transfer is successful, the Bluetooth® sym-
bol on the display will go out. The device will switch
t
o sleep mode. If it is not possible to perform a trans-
fer, the display will show the Bluetooth® symbol and
the error code “E7” (see chapter
Troubleshooting”).
Viewing the measurements on the
measurement computer
You can also view the measurements you saved directly
on the measurement computer without a smartphone
or tablet. Proceed as follows to do so:
1. Activate the user touch buttons on the
measurement computer with the ON/OFF switch
9
(see fig. A).
2. Switch to memory mode by touching user 1 touch
button
10
or user 2 touch button
8
for approx.
three seconds until the WHO-LED lights up with the
average value for all measurements (see fig. A).
3. You can now browse through the measurements of
the respective user with the user 1 touch button
10
or user2 touch button
8
(see fig.A). Tap the re-
spective button once to browse further.
39Handling
IREGB
The data will be displayed in this order:
Average values for all measurements
Average values for the last seven measure-
ments from 05:00 a.m. to 09:00 a.m.
Average values for the last seven measure-
ments from 06:00 p.m. to 08:00 p.m.
60th measurement (last) up to the 1st meas-
urement (oldest)
4. To view the values of the other user, touch the re-
spective user button.
5. After viewing all measurements, the measurement
computer will automatically switch to sleep mode.
If you would like to leave memory mode before this
time, touch the user 1 or user 2 touch button for three
seconds.
Erasing measurements
You can completely erase the measurements of a user.
Proceed as follows to do so:
1. Activate the user buttons on the measurement com-
puter with the ON/OFF switch
9
(see Fig. A).
2. Switch to memory mode by touching the user 1
button
10
or user 2 button
8
for three seconds
until the WHO-LED lights up with the average for all
measurements.
3. Touch the user button of the user whose values you
would like to erase.
40 Evaluating the measurements
GB IRE
4. Touch both the user 1 button
10
and the
user2 button
8
at the same time for 3 seconds. “CL
--” and then “CL 00” will appear on the display
6
(see fig. A).
All measurements of the respective user are erased.
5. You can now switch the measurement computer to
sleep mode by touching the user 1 or user 2 touch
button for three seconds.
Evaluating the measurements
Cardiac arrhythmia
NOTICE!
If the arrhythmia indicator
22
appears fre-
quently after a measurement, you should
advise your physician and get an in-depth
examination. Follow your doctor's orders.
Do not endanger yourself through self-di-
agnosis or taking your own therapeutic
measures.
Arrhythmia detection of the blood pressure monitor may
be able to detect potential cardiac arrhythmia. If the de-
vice detects an irregular pulse, this will be indicated with
the arrhythmia indicator
22
after the measurement
(see fig. B). Arrhythmia detection may provide an indi-
cation of an illness, but does not offer a sure diagnosis.
Arrhythmia is an illness involving a malfunction of the
41Evaluating the measurements
IREGB
bioelectric control mechanism for the heart beat that
results in an abnormal cardiac rhythm. Compared to a
normal cardiac rhythm, symptoms include missed or
premature heart beats or an overall slower or acceler-
ated pulse. The possible causes include, among other
things:
physical disposition,
advanced age,
cardiac illness,
excessive consumption of alcohol or nicotine,
stress,
lack of sleep.
If the arrhythmia indicator
22
appears, repeat the
measurement.
At the same time, make sure you comply with the basic
rules for correct measurement of blood pressure (see
chapter “Performing a measurement”).
WHO classifications
The World Health Organisation (WHO) has defined six
categories for the classification of blood pressure levels.
This classification is provided in the following table.
42 Evaluating the measurements
GB IRE
Range of
blood pres-
sure levels
Systoles
(in
mmHG)
Diasto-
les
(in
mmHG)
Measure
Optimal < 120 < 80 Check your
blood pressure
on your own
regularly.
Normal 120
– 129
80 – 84 Check your
blood pressure
on your own
regularly.
Elevated
normal
130
– 139
85 – 89 Have your
blood pressure
checked regular-
ly by a physician.
Level 1: Slight
hypertension
140
– 159
90 – 99 Have your
blood pressure
checked regular-
ly by a physician.
Level 2:
Moderate
hypertension
160
– 179
100
– 109
Have your phy-
sician examine
you promptly.
Level 3: Severe
hypertension
≥ 180 ≥ 110 Have your phy-
sician examine
you promptly.
43Evaluating the measurements
IREGB
The LEDs on the blood pressure monitor and the arrow
icons on the display indicate the range for the measured
blood pressure.
If the values for systoles and diastoles are within two
different WHO ranges, the device will display the higher
of the two ranges.
Example:
The systolic pressure is within the “Normal” range.
The diastolic pressure is within the “Elevated normal”
range.
The measurement computer shows “Elevated normal”.
However, the WHO only offers a general guideline.
Variances in the individual blood pressure of different
persons are not unusual. Ask your physician for blood
pressure levels that are normal for you and for levels
that are considered dangerous.
44 Cleaning and maintenance
GB IRE
Cleaning and maintenance
NOTICE!
Risk of damage!
If you do not clean the blood pres-
sure monitor properly, you can
damage the blood pressure mon-
itor.
Do not use any cleaners or
solvents.
Do not use any brushes with
metal or nylon bristles, sharp
or metallic cleaning utensils
such as knives, hard scrapers
or similar.
Clean the measurement computer, the cuff hose and
the cuff carefully with a damp cloth.
After cleaning, use a soft cloth to clean the blood
pressure monitor.
45Cleaning and maintenance
IREGB
Changing the batteries
NOTICE!
After you have changed the batteries, you
must reconfigure the data format, date and
time. The saved measurements will, howev-
er, remain intact.
If the display is blank after you switch on the measure-
ment computer or the battery indicator or error code
“E6” appears, the batteries are no longer supplying
enough energy.
To change the batteries, follow the steps described in
the chapter “Inserting batteries”.
Storage
If you do not use the blood pressure monitor for a pro-
longed period of time, please observe the following
notes:
Take the batteries out of the battery compartment.
Store the blood pressure monitor in the enclosed
bag to protect it from dust.
Do not store the blood pressure monitor near heat
sources.
Observe the information concerning the storage
environment (see chapter “Technical data”).
Do not place any heavy objects on the measurement
computer, the cuff or the cuff hose.
46 Troubleshooting
GB IRE
Troubleshooting
If a malfunction occurs, first check the points below
before you send the blood pressure monitor in to be
repaired.
If error codes are shown on the display, proceed as
follows:
1. Switch the measurement computer to sleep mode by
pushing the SET button, the user1 button
10
or the
user 2 button
8
(see fig. A).
2. Observe the solutions provided in the following
table.
Problem Causes and solutions
The error code “E1”
and the pulse in-
dicator appear on
the display.
The pulse is not being measured
correctly.
Fit the cuff correctly on your
arm.
Repeat the measurement.
The error code “E2”
appears on the
display.
You spoke or moved during the
measurement.
Repeat the measurement
without speaking or moving.
47Troubleshooting
IREGB
Problem Causes and solutions
The error code “E3”
appears on the
display.
The cuff is not on your upper
arm.
Fit the cuff correctly on your
arm.
Repeat the measurement.
The error code “E4”
appears on the
display.
A measurement error has
occurred.
Repeat the measurement.
The error code “E5”
appears on the
display.
A problem has occurred when
inflating the cuff (inflation pres-
sure > 300 mmHg).
Make sure that the cuff hose is
not kinked or clamped.
Fit the cuff correctly on your
arm.
Repeat the measurement.
The display is
blank.
or
The battery in-
dicator and the
error code “E6”
appear on the
display.
The batteries were not inserted
correctly.
Remove the batteries and put
them back in with the correct
polarity.
Batteries are empty.
Replace the empty batteries
with new ones.
48 Troubleshooting
GB IRE
Problem Causes and solutions
The
error code “E7” and
the Bluetooth® in-
dicator appear on
the display.
Bluetooth® transfer is not
possible.
Once you have prepared
everything for automat-
ic transmission, repeat the
measurement or transfer the
measurements manually.
Bluetooth® transfer is not
possible.
The Bluetooth® function of your
smartphone or tablet is switched
off.
Switch the Bluetooth®
function of your smartphone
or tablet on.
The Bluetooth® transmitter of
the blood pressure monitor is not
working properly.
Take the batteries out of the
battery compartment.
Put the batteries back in.
Switch the Bluetooth® func-
tion of your smartphone or
tablet off and back on.
49Troubleshooting
IREGB
Problem Causes and solutions
The
error code “E7” and
the Bluetooth® in-
dicator appear on
the display.
Your smartphone or tablet is not
working properly.
Switch off your smartphone or
tablet off completely and then
back on.
The app was not successfully
installed on your smartphone or
tablet.
Reinstall the app and log in
with your user data.
Your smartphone or tablet does
not support Bluetooth® Smart.
Exchange your smartphone
or tablet with a model that
supports Bluetooth® Smart.
50 Troubleshooting
GB IRE
Problem Causes and solutions
Not all measure-
ments saved are
transmitted.
You performed more than 60
measurements without connect-
ing to the app.
The blood pressure monitor can
save a total of 60 measurements
per user. Afterwards, the first
measurement will be overwritten
by the last one.
Connect the blood pressure
monitor with the app on a
regular basis to prevent losing
measurements.
Use the FAQs (frequently asked questions) on the fol-
lowing website as an additional help for your blood
pressure monitor: www.cranesportsconnect.com/faq.
If the measures described above have not resolved the
problem, please contact our service team. Use the infor-
mation provided below and also consider the chapter
Warranty”.
51Technical data
IREGB
Technical data
Type: MD 4000
Model: AE5-CDBP-1
Article number: 92126
EAN: 20021023
Power supply: Batteries, 4 x 1.5 V DC,
type LR03/AAA
Classification Type BF application part
Type of operation Continuous operation
Protection class Internal power supply
52 Technical data
GB IRE
IP code IPX 0
Anaesthesia safety The device is not approved in
accordance with category AP
or APG.
Measurement method Oscillometric, non-invasive
measurement of blood pres-
sure on the upper arm
Measurement accuracy Maximum permissible standard
deviation according to clinical
examination: systolic 8 mmHg/
diastolic 8 mmHg
Measurement range
Cuff pressure: 30 – 250 mmHg
Systolic pressure: 50 – 250 mmHg
Diastolic pressure: 30 – 200 mmHg
Pulse: 40 – 180 bpm
Display accuracy: Pressure: +/- 3 mmHg
Pulse: +/- 5 % of the
measurement
Measurement
resolution:
Pressure: 1 mmHg
Pulse: 1 bpm
Cuff: Circumference of upper arm
22 – 35 cm
Bluetooth® version: 4.0 (Bluetooth® Smart),
~ 2.4 GHz
53Technical data
IREGB
Operating environment:
Temperature: + 5 °C to + 40 °C
Humidity: 15 % to 93 %
Storage environment:
Temperature: - 25 °C to + 70 °C
Humidity: up to 93 %
We reserve the right to make changes to technical data
without prior notice for updating reasons.
This device complies with the European standard EN
60601-1-2 and is subject to special precautionary meas-
ures with respect to electromagnetic compatibility. Port-
able or mobile high-frequency communication devices
could interfere with this device. You can request more
detailed information at the specified service address.
This blood pressure monitor corresponds to the following
guidelines, laws and standards:
EU Directive for Medical Products 93/42/EEC,
Medical Product Law (MPG) of the Federal Republic of
Germany,
Standard EN1060-1 (Non-Invasive Blood Pressure Mon
-
itoring Devices Part 1: General requirements),
Standard EN1060-3 (Non-invasive Blood Pressure
Monitoring Devices Part 3: Supplementary require-
ments for electromagnetic blood pressure monitoring
syst
ems),
Standard IEC80601-2-30 (Medical electrical devices
part 2-30: Special stipulations for safety including the
54 Technical data
GB IRE
essential features of automated non-invasive blood
pressure monitoring devices).
Full display reference
The following figure shows the display with all indicator
segments. You can use this figure to determine whether
the display is properly rendering the measurements.
AM
PM
55Manufacturer information
IREGB
Manufacturer information
Manufacturer:
Grandway Technology (Shenzhen) Limited
Block 7, Zhu Keng Industrial Zone,
Ping Shan District, 518118 Shenzhen,
PEOPLE'S REPUBLIC OF CHINA
Manufacturer's representative in the EU:
Shanghai International Trading
Corp. GmbH (Hamburg)
Eiffestrasse 80
20537 Hamburg
Germany
Declaration of conformity
R&TTE 1999/5/CE directive, RoHS 2011/65/
EU directive, 93/42/EEC medical products
directive:
Short text of the declaration of conformity: Krippl-Watch-
es hereby declares that the Bluetooth® blood pressure
monitor (model no. AE5-CDBP-1) complies with the fun-
damental requirements and other applicable provisions
56 Disposal
GB IRE
of the R&TTE 1999/5/EC, RoHS 2011/65/EU and 93/42/EEC
medical products directive.
You can access the complete text for the declaration of
conformity on our website:
http://www.produktservice.info
For this, enter the following EAN (European Article Num-
ber): 20021023.
Disposal
Disposing of the packaging
Dispose of the packaging separated into
single type materials. Dispose of card-
board and carton as waste paper and
foils via the recyclable material collection
service.
Disposing of old devices
(Applicable in the European Union and other European
states with systems for the separate collection of reusa-
ble waste materials)
57Disposal
IREGB
Old devices do not belong in the household
waste!
If the blood pressure monitor can no longer be
used, every user is required by law to dispose
of old devices separately from their house-
hold waste, e.g. at a collection point in his community/
borough. This ensures that old devices are recycled in a
professional manner and also rules out negative conse-
quences for the environment. For this reason, electrical
equipment is marked with the symbol shown here.
Batteries and rechargeable batteries may not be dis-
posed of with household waste!
As the end user you are required by law to
bring all batteries and storage batteries, re-
gardless whether they contain harmful sub-
stances* or not, to a collection point run by the
communal authority or borough or to a retailer,
so that they can be disposed of in an environmentally
friendly manner. Turn in the batteries and rechargeable
batteries at your collection point in a discharged state
only!
* labelled with: Cd = cadmium, Hg = mercury, Pb = lead
58 Electromagnetic compatibility
GB IRE
Electromagnetic compatibility
Electromagnetic emissions
Guidance and manufacturer’s declaration – electromagnetic emissions for
all EQUIPMENT and SYSTEMS
The Sphygmomanometer (MD4000) is intended for use in the electromagnetic environment specified below. The
customer of the user of the Sphygmomanometer (MD4000) should assure that it is used in such and environment.
Emission test Compliance Electromagnetic environment – guidance
RF emissions
CISPR 11
Group 1 The Sphygmomanometer (MD4000) uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to cause any interference
in nearby electronic equipment.
RF emission
CISPR 11
Class B The Sphygmomanometer (MD4000) is suitable for use in all establishments, inclu-
ding domestic establishments and those directly connected to the public low-volta-
ge power supply network that supplies buildings used for domestic purposes.
59Electromagnetic compatibility
IREGB
Electromagnetic immunity
Guidance and manufacturer’s declaration – electromagnetic immunity –
for all EQUIPMENT and SYSTEMS
The Sphygmomanometer (MD4000) is intended for use in the electromagnetic environment specified below. The
customer of the user of the Sphygmomanometer (MD4000) should assure that it is used in such and environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment
- guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
±6 kV contact
±8 kV air
±6 kV contact
±8 kV air
Floors should be wood, concrete or ceramic tile. If
floor are covered with synthetic material, the relative
humidity should be at least 30%.
Power frequency
(50Hz) magnetic field
IEC 61000-4-8
3A/m 3A/m Power frequency magnetic fields should be at levels
characteristic of a typical location in a typical com-
mercial or hospital environment.
60 Electromagnetic compatibility
GB IRE
Guidance and manufacturer’s declaration – electromagnetic immunity for
EQUIPMENT and SYSTEMS that are not LIFE-SUPPORTING
The Sphygmomanometer (MD4000) is intended for use in the electromagnetic environment specified below. The customer
or the user of Sphygmomanometer (MD4000) should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
Portable and mobile RF communications equipment
should be used no closer to any part of the Sphyg-
momanometer (MD4000), including cables, than the
recommended separation distance calculated from the
equation applicable to the frequency of the transmitter.
Recommended separation distance.
Conducted RF
IEC 61000-4-6
3 V
rms
150 kHz to 80 MHz
3 V
rms
Radiated RF
IEC 61000-4-3
3 V/m
80 MHz to 2.5 GHz
3 V/m
80 MHz to 800 MHz
800 MHz to 2.5 GHz
61Electromagnetic compatibility
IREGB
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
Where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation dis-
tance in metres (m).
Field strengths from fixed RF transmitters, as determined
by an electromagnetic site survey
a
should be less than
the compliance level in each frequency range
b
.
Interference may occur in the vicinity of equipment mar-
ked with the following symbol:
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures,
objects and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio,
AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy.
To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measu-
red field strength in the location in which the Sphygmomanometer (MD4000) is used exceeds the applicable RF compliance level above, the
Sphygmomanometer (MD4000) should be observed to verify normal operation. If abnormal performance is observed, additional measures
may be necessary, such as reorienting or relocating the Sphygmomanometer (MD4000).
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
62 Electromagnetic compatibility
GB IRE
Recommended separation distances
Recommended separation distances between portable and mobile RF communications
equipment and the EQUIPMENT or SYSTEM – for EQUIPMENT or SYSTEM that are not LIFE-
SUPPORTING
Recommended separation distances between portable and mobile RF communications equipment and the Sphygmomano-
meter (MD4000)
The Sphygmomanometer (MD4000) is intended for use in an electromagnetic environment in which radiated RF disturban-
ces are controlled. The customer or the user of the Sphygmomanometer (MD4000) can help prevent electromagnetic interfe-
rence by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and
the Sphygmomanometer (MD4000) as recommended below, according to the maximum output power of the communica-
tions equipment.
Rated maximum output
power of transmitter
(W)
Separation distance according to frequency of transmitter (m)
80 MHz to 800 MHz
800 MHz to 2.5 GHz
0,01 0.1167 0.2334
0,1 0.3689 0.7378
1 1.1667 2.3334
10 3.6893 7. 3 7 8 6
100 11.6667 23.3334
63Electromagnetic compatibility
IREGB
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m)
can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power
rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects and people.
64 Trademark protection notices
GB IRE
Trademark protection notices
Google Play™ and Android™ are trademarks of Google,
Inc.
Apple, the Apple logo, iPad, and iPhone are trademarks
of Apple Inc., registered in the U.S. and other countries.
App Store is a service mark of Apple, Inc.
The Bluetooth® word mark and logos are registered
trademarks of Bluetooth® SIG, Inc. and any use of such
marks by Krippl-Watches is under license. Other trade-
marks and trade names are those of their respective
owners.
65
IREGB
Warranty
Description of malfunction:
Return your comple-
ted warranty card to-
gether with the faulty
product to:
Krippl-Watches
Freepostcode:
RLTU-ZYZE-SKLG
Picadilly 180
W1J 9HF London
UNITED KINGDOM
Your details:
Name
Address
E-mail
Date of purchase *
* We recommend you keep the receipt with this warranty card.
Location of purchase
Please note: The helpline number
is a free phone number howe-
ver please allow time (up to 10
seconds) for the international
connection to take place.
YEARS
WARRANTY
WARRANTY CARD
BLUETOOTH® BLOOD PRESSURE
MONITOR
AFTER SALES SUPPORT
service@produktservice.info00800/52323000
Model: AE5-CDBP-1 Product Code: 92126
04/2015
66
GB IRE
Warranty
Warranty conditions
Dear Customer,
The ALDI warranty offers you extensive benefits compared
to the statutory obligation arising from a warranty:
Warranty period: 3 years from date of purchase.
6 months for wear parts and consu-
mables under normal and proper
conditions of use (e.g. rechargeable
batteries).
Costs: Free repair/exchange or refund.
No transport costs.
ADVICE: Please contact our service hotline by
phone, e-mail or fax before sending
in the device. This allows us to provide
support in the event of possible opera-
tor errors.
In order to make a claim under the warranty, please
send us:
together with the faulty item the original receipt
and the warranty card properly completed.
the faulty product with all components included
in the packaging.
67
IREGB
Warranty
The warranty does not cover damage caused by:
Accident or unanticipated events (e.g. light-
ning, water, fire).
Improper use or transport.
Disregard of the safety and maintenance inst-
ructions.
Other improper treatment or modification.
After the expiry of the warranty period, you still have the
possibility to have your product repaired at your own ex-
pense. If the repair or the estimate of costs is not free of
charge you will be informed accordingly in advance.
This warranty does not limit the statutory obligation of the
seller arising from a warranty. The period of warranty can
only be extended in accordance with a legal standard. In
countries where a (compulsory) warranty and/or spare
part storage and/or a system for compensation are/is re-
quired by law, the statutory minimum conditions apply. In
the event that a product is received for repair, neither the
service company nor the seller will assume any liability
for data or settings possibly stored on the product by the
customer.
Spend a little Live a lot.
Great care has gone into the manufacture of this product and it should there-
fore provide you with years of good service when used properly. In the event
of product failure within its intended use over the course of the first 3 years af-
ter date of purchase, we will remedy the problem as quickly as possible once it
has been brought to our attention. In the unlikely event of such an occurrence,
or if you require any information about the product, please contact us via our
helpline support services, details of which are to be found both in this manual
and on the product itself.
If you are not entirely satisfied with this
product please return it to the store
where it was purchased and we will be
pleased to replace or refund it. This does
not affect your statutory rights.
PRODUCED IN CHINA FOR:
ALDI STORES LTD. PO BOX 26, ATHERSTONE
WARWICKSHIRE, CV9 25H
ALDI STORES (IRELAND) LTD.
PO BOX 726, NAAS, CO. KILDARE.
visit us at www.aldi.co.uk
AFTER SALES SUPPORT
service@produktservice.info
Model: AE5-CDBP-1
Product code: 92126 04/2015
YEARS
WARRANTY
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