Medinox Econocare ECO-BP01 User manual

FUNCTION OF MEMORY
TIPS ON TAKING BLOOD PRESSURE MEASUREMENT
Model: ECO-BP01
INSTRUCTION MANUAL
1.It is necessary to know that arterial blood pressure is subjected to sharp
fluctuations. The level of the arterial blood pressure depends on many factors.
Generally arterial blood pressure is lower in summer and higher in winter. Arterial
blood pressure changes with atmosphere pressure and is affected considerably by
many factors, e.g. physical loads, emotional excitability, stress, meals, etc.
Medicines, drinking, smoking affects greatly the level of individual blood pressure.
When blood pressure is measured in hospital, the value is always higher than that
at home. The reason is the tensity and such case is especially serious in given
group patients, which is known as ‘White coat effect’ medically. Blood pressure will
raise in low temperature, so it is better to take blood pressure measurement in
room temperature (approximately 20℃). If this device was stored in low tempera-
ture, it is necessary to leave it in room temperature for at least 1 hour, otherwise
the measurement can be inaccurate. Blood pressure does vary with age and
individual, and it is recommended to write down the readings in blood pressure
record daily, then you can check with your doctor to find out what is “normal blood
pressure” for you.
2.Take measurement under doctor’s instruction for patients with
cardio-vascular diseases.
Under no circumstances should you alter the dosages of any drugs prescribed
by your doctor!
3.Accurate measurement of blood pressure may be difficult in arrhythmia,
premature beat, atrial fibrillation atreriosclerosis hypoperfusion diabetes pregnan-
cy nephropathy , weak pulse, or in patients with obvious fluctuation of heart
contraction rhythm. Please consult a qualified physician to interpret your blood
pressure readings.
4.It is necessary to keep quiet during measurement to get accurate
readings. Measurement should be conducted in quiet environment at
room temperature. Don’t eat or smoke before a measurement.
This device is supplied with the standard cuff and adult large cuff which
are fit for the arm size 22-32 cm and 32-42cm. Care should be taken to
ensure that the cuff size is appropriate for the person whose blood
pressure is being taken. Children and adults with cuff size fall outside the
range of the standard cuff size and large adult cuff size should select special
size cuffs. Please contact the dealer to get these special size cuffs.
ATTENTION: Do not use cuffs other than the original cuff contained in
this kit!
5.Repeated measurements with interval at 3 minutes are recommend-
ed, so you can calculate the average to get more accurate measure-
ment. Atherosclerosis patients are required longer interval (10-15
minutes) as elasticity of patients’ vessels decreased significantly in
these diseases. 10-15 minutes interval is also applicable for patients
suffering from diabetes for a long time.
The illustration is from British Hypertension Society.
AUTOMATIC INFLATION
There are 4 given levels of given inflation pressure for
this device: 190mmHg, 230mmHg, 270mmHg and
300mmHg. When 190mmHg is not enough or movement
of arm occurs, the device will automatically inflate to
reasonable pressure level to ensure a successful
measurement. It is not a fault.
RAPID DEFLATION DURING MEASUREMENT
If you do not feel well during measurement or want to stop the measure-
ment for some reason, you can press the “ ” button. The device will
quickly release the air in cuff and the device will be switched off.
MEMORY RECALL
1.ECO-BP01 can store 90 sets of readings and automatically calculate the
average value of the latest 3 readings. When the memory is full (90 sets of
readings are stored), the oldest reading will be replaced by new one automati-
cally. Memory will not clear away even if power supply is removed;
2.After a measurement or when the device stands by,
the user can press button Memory to recall memory.
Press button Memory, the display will show the
average value of the latest 3 readings as Fig. 5;
3.Press again, the display will show ‘01’, which
means the latest reading, then turns to another
screen to show readings as Fig. 6;
4.Press again, the display will show ‘02’, which
means the second to the latest reading…
MEMORY CLEARANCE
After a measurement is finished or when the device
stands by, hold down button Memory for at least 5
seconds, the display will show ‘CLR’ which means all
the stored reading are removed as Fig.7.
Fig.5
PARTS AND COMPONENTS
1.Main Body
2.LCD Display
3.Air Connector
4.Tube Plug
5.Air Hose
6.Cuff
7.D-ring
8.Button ‘M’
9.Button ‘ ’
10.Batteries (Optional)
7
8
9
10
2
3
4
5
6
1
Symbols Meaning
Manufacturer
Authorized Representative in the
European community
CE marking in conformity with EC
directive 93/42/EEC
Keep dry
Attention, consult accompanying
documents
Type BF Applied Part
Stand by
Symbol for the marking of electrical and
electronics devices according to
Directive 2002/96/EC.
The device, accessories and the
packaging have to be disposed of waste
correctly at the end of the usage. Please
follow Local Ordinances or Regulations
for disposal.
SYMBOLS
TABLE OF CONTENT
1. GENERAL
- PRINCIPLE OF OPERATION
- NEW TECHNOLOGIES USED
2. TIPS ON TAKING BLOOD PRESSURE MEASUREMENT
3. BATTERY INSTALLATION
4. USE THE DEVICE WITH AC POWER ADAPTER
5. CORRECT POSTURE FOR MEASUREMENT
6. ASSEMBLY THE CUFF
7. CARRY OUT A MEASUREMENT
- AUTOMATIC INFLATION
- RAPID DEFLATION DURING MEASUREMENT
8. FUNCTION OF MEMORY
- MEMORY RECALL
- MEMORY CLEARANCE
9. WHO BLOOD PRESSURE CLASSIFICATION INDICATION
10. ERROR AND LOW BATTERY INFORMATION
11. CARE, STORING, REPAIR AND RECYCLING
12. TROUBLESHOOTING
13. WARRANTY OBLIGATIONS
14. SPECIFICATIONS
15. BLOOD PRESSURE RECORD
16. MANUFACTURER’S DECLARATION
17. QUALITY GUARANTEE
18. REQUIRING RECORD
19. PERIODIC SAFETRY CHECKS
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2
2
3
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3
3
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4
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5
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6
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6
GENERAL
This instruction manual is intended to assist the user for safe and efficient
operation of the automatic digital blood pressure monitor (hereinafter: device)
model ECO-BP01. The device must be used in accordance with the procedures
described in the manual. It is important to read and understand the entire manual,
especially the section <Tips on taking blood pressure measurement>.
This device is intended for the non-invasive measurement of systolic and diastolic
arterial blood pressure and pulse rate in adults(age 15 and above). Consult the
physician if measurement is taken in children or persons with arrhythmia as errors
may occur.
PRINCIPLE OF OPERATION
This device adopts the oscillometric technology with Fuzzy Algorithm measuring
the arterial blood pressure and pulse rate. The cuff is wrapped around the arm and
automatically inflated by the air pump. The sensor of the device catches weak
fluctuation of the pressure in the cuff produced by extension and contraction of the
artery of the arm in response to each heartbeat. The amplitude of the pressure
waves is measured, converted in millimeters of the mercury column, and is
displayed by digital value.
Annotation: This device can not provide reasonable accuracy if used or stored in
the temperature or humidity beyond the range stated in the section
<SPECIFICATIONS> of this manual.
CAUTION: DO NOT USE THE DEVICE OUTDOORS
NEW TECHNOLOGIES USED
Fuzzy Algorithm is the processing algorithm taking into account of the speciality of
individual heartbeats, which provides higher accuracy of measurement.
Software version: V1.1
ME EQUIPMENT not intended for use in an oxygen rich environment
or in the presence of flammable mixers.
Internally powered equipment (without adapter), Class II equipment
(with adapter).
Type BF applied part, recognize the cuff as applied part.
CLASSIFICATION
BATTERY INSTALLATION
USE THE DEVICE WITH AC POWER ADAPTER
1.Open the battery cover and install four ‘AA’ type batteries into the battery
compartment as indicated. Make sure that the polarity is correct;
2.Close the battery compartment cover.
Besides batteries you can use AC power adapter as the power supply. AC
power adapter is optional for the device for sale.
Insert the AC adapter cord into the jack on the right side of the monitor .
Insert the AC adapter plug into the outlet.
To remove the AC adapter, disconnect the adapter plug from the AC outlet first
and then disconnect the cord from the monitor’s jack.
CAUTION
When using optional AC adapter, the AC adapter must comply with the
requirements of standard IEC60601-1.
To avoid possible damage to the monitor, use only the exclusive AC adapter
that can be purchased from authorized dealers. Other adapter may damage the
blood pressure monitor.
Replace the batteries when the replacement indication “ ”appears in the
display or nothing after “ ” button is pressed;
Batteries in this kit are intended to check work capacity of the device and the
life-span of the batteries can be shorter than the recommended;
Use R6,LR6 or AA alkaline batteries, do not use rechargeable batteries;
Only same type batteries are allowed to use together. Replace all batteries
simultaneously;
If the device is to be unused for long time, please take out the batteries;
Don’t leave the worn batteries in the device.
CORRECT POSTURE FOR MEASUREMENT
ASSEMBLY THE CUFF
The AC adapter is used as an isolating means, the AC adapter plug shall
insert into the outlet nearby the operator, make it easy to disconnection the
device from the outlet.
If long time work, remove the plug after the adapter cools, and prevent bums.
Note: The monitor is designed not to draw power from the batteries when
the AC adapter in use.
Optional AC adapter technical feature:
Output voltage: 6V±5%
Max. output current: At least 600 mA
Output plug polarity: <-> inner
1.Sit beside the table and let the table support your
arm as you take the measurement. Make sure that
the cuff on the upper arm no cross, and is at
approximately the same level as the heart,make
sure that your feet lie on the ground and no cross.
2.You may lie on your back and take measurement.
Look at the ceiling, keep calm, and don’t move your
neck or body during the measurement. Make sure
that the cuff on the upper arm is at approximately
the same level as the heart.
1.Insert the edge of the cuff approximately 5
centimeters into the D-ring as shown in figure.
2.Put the cuff on the left upper arm with the tube
pointing to the direction of palm. If measurement on
your left arm is difficult, you can use right arm for
measurement. In this case, it is necessary to know
that the readings may differ about 5-10 mmHg
between left arm and right arm.
3.Wrap cuff around your upper arm with the lower
edge of the cuff approximately 2-3 centimeters above
the elbow. The mark <ARTERY> must be over the
artery of the arm.
4.Press the cuff to make sure that it is attached secure-
ly. The cuff should not be too tight or too loose. Two
fingers should be easily put in between cuff and upper
arm.
5.The mark <INDEX> on the cuff must point to area
<NORMAL> or <LARGE CUFF>. This means the cuff size
is correct. If mark <INDEX> points to the area beyond area
<NORMAL> or <LARGE CUFF>, please consult your
dealer whether you need another size cuff.
6.Sometimes it is difficult to make the cuff regular
owning to the shape of the user’s upper arm, the
cone-shape assembly of cuff is also acceptable.
7.If your clothes restrict blood circulation of your
upper arm, or you roll your sleeve up so as to result in
such restriction. Please take off your clothes to get
accurate measurement if necessary.
CARRY OUT A MEASUREMENT
1.Insert the tube plug into the air connector. Before the measurement, take
3~5 times deep breath and relax yourself. Don’t talk or move your arm;
2.Press button ‘ ’, and all symbols will appear on display
in 2 seconds as Fig.1.
Then two short beep will sound and ‘0’ will appear on the
screen. Pump begins to inflate with display showing the
reading of pressure. Generally the pressure will reach
190mmHg as Fig.2;
3.The pump stop inflating and pressure begins to decrease
gradually, during which the user’s blood pressure and pulse
will be calculated as Fig.3;
4.There will be a long beep following the accomplishment of
measurement. The air in the cuff will deflate quickly and the
blood pressure reading, pulse reading will show in the
display as Fig.4;
5.Press the button ‘ ’ to turn off the device. Please rest
for at least 3 minutes for another measurement. If the power
supply is not switched off and the device keeps unused for
3 minutes, the device will be switched off automatically.
Fig.1
Fig.2
Fig.3
Fig.4
Fig. 6
Fig. 7
123

CARE, STORING, REPAIR AND RECYCLING
TROUBLESHOOTING
WARRANTY OBLIGATIONS
1. It’s necessary to protect this device against high moisture, direct
sunlight, shock, solvent, alcohol and gasoline.
2. Remove the batteries if the device is to be stored for a long time and
keep the batteries far from the children.
3. Keep the cuff from sharp subject and don’t extend or twist the cuff.
4. Use only soft and dry cloth to clean the device.
5. The wrist cuff are sensitive and must be handled with care. You can
clean the cuff cover with damp cloth as daily maintenance.
To avoid across infection when share the cuff, you can sanitary
treatment of inner side of fabrics cover of the cuff and contacting with
help of cotton wool tampons, moistened by 3% solution of hydrogen
dioxide. After long using, it is allowed partial discoloration of fabrics
covering of the cuff. It is not allowed the laundry of the cuff, as well as
ironing by hot flatiron.
WARNING: Under no circumstances may you wash the inner bladder!
6. Since neither the device nor batteries are household waste, follow your
local recycling rules and dispose them at appropriate collection sites.
7. Do not open the device. It is delicate electrical components and an
intricate air unit that could be damaged. If you can not fix the problem
using the troubleshooting instruction, request service from your dealer.
8. It is generally recommended to have the monitor inspected every 2
years, to ensure proper functioning and accuracy and safety. Please
contact your dealer for maintenance.
WARNING: Do not modify the equipment without authorization of
the manufacturer.
9. Do not serve or maintain the cuff when in use with patient.
Adapter
Memory
Upper arm circumference
Complete kit
Operation temperature and
humidity, air pressure
Transport and storage temperature
and humidity, air pressure
Optional component, 6V, 600mA
90 sets of memory
+10℃to + 40℃, 85% and below
700hPa to 1060hPa
-20℃to + 50℃, 85% and below
500hPa to 1060hPa
Applicable for arm circumference 22-32cm
(standard cuff); 32-42cm(large adult cuff)
Main body, storage bag(Optional),
standard cuff, large adult cuff (Optional),
4×AA batteries (Optional), instruction
manual, warranty card
Pollution Degrees
Overvoltage category
High Altitudes (m)
Fuse
Category II
Adapter: T3.15AH250V
Main Unit: T630mAl250V
Degrees 2
≤2000m
SPECIFICATIONS
Model
Size
Weight
Measuring method
Measuring range
Measuring accuracy
Inflation
Rapid deflation
Batteries
Extreme Pressure
ECO-BP01
134mm(L) ×98mm(W) ×57(H)mm
Oscillometry
40 to 260 mmHg (blood pressure)
40 to 160 beats/minute (pulse rate)
Automatic by the pump
Automatic electronic valve
4“AA”×1.5V
± 3 mmHg for static pressure
± 5% of the reading for the pulse rate
Approximately 236g without batteries
300mmHg
No display when
connect the power.
Inflation stops and
re-inflate later.
The reading is
extremely low or
high.
Pulse rate is too
low or too high.
The batteries are
run down soon.
Faulty batteries are used.
The batteries have run down.
The polarity of battery is wrong.
The contact of battery
compartment is polluted.
Replace all the batteries
with new ones.
Install the batteries correctly.
Clean the battery terminals
with dry cloth.
See<AUTOMATIC
INFLATION>
Keep quiet and silent during
the measurement.
Make sure that your posture
is right.
Wrap the cuff correctly.
Relax during measurement.
Keep quiet and silent during
the measurement.
Keep quiet and silent during
the measurement.
Take measurement again
after resting for more than 5
minutes.
Use alkaline batteries of
known manufacturers.
The automatic inflation for
ensuring correct measurement.
Did you talk or move your arm
(or hand) during measurement?
Is the cuff at the same level as
the heart?
Is the cuff wrapped right?
Did you strain your arm during
measurement?
Did you talk or move your arm
(or hand) during measurement?
Did you talk or move your
arm (or hand) during
measurement?
Did you make measurement
right after exercise?
SYMPTOM CHECK POINT REMEDY
MANUFACTURER’S DECLARATION
The model ECO-BP01 Digital Blood Pressure Monitor is intended for use
in the electromagnetic environment specified below. The customer or the
user of the model ECO-BP01 Digital Blood Pressure Monitor should
assure that is used in such an environment.
Guidance and manufacturer’s declaration – electromagnetic immunity
Emission test
Compliance
level
Electromagnetic
environment-guidance
RF emissions CISPR 11 Group 1
The model ECO-BP01 Digital Blood
Pressure Monitor uses RF energy only for
its internal function. Therefore, its RF
emissions are very low and aren’t likely to
cause any interference in nearby
electronic equipment.
The model ECO-BP01 Digital Blood
Pressure Monitor is suitable for use in all
establishments, including domestic
establishments and those directly
connected to the public low-voltage power
supply network that supplies buildings used
for domestic purposes.
Class BRF emissions CISPR 11
Class A
Complies
Harmonic emission
IEC 61000-3-2
Voltage fluctuations/
flickeremissions IEC
61000-3-3
IEC 60601
test level
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 floors are covered with
synthetic material, the relative
humidity should be at least 30%
Electrical fast
transient/burst
IEC 61000-4-4
±2 kV for
power supply
lines
±2 kV for
power supply
lines
Mains power quality should be that of
a typical commercial or hospital
environment.
Surge
IEC 61000-4-5
Voltage dips,
short
interruptions
and voltage
variations on
power supply
input lines
IEC
61000-4-11
±1 kV
differential
mode
<5% UT
(>95% dip in UT)
for 0.5 cycle
40% UT
(60% dip in UT)
for 5 cycles
70% UT
(30% dip in UT)
for 25 cycles
<5% UT
(>95% dip in UT)
for 5 sec
<5% UT
(>95% dip in UT)
for 0.5 cycle
40% UT
(60% dip in UT)
for 5 cycles
70% UT
(30% dip in UT)
for 25 cycles
<5% UT
(>95% dip in UT)
for 5 sec
±1 kV
differential
mode
Mains power quality should be that of
a typical commercial or hospital
environment.
Mains power quality should be that of
a typical commercial or hospital
environment. If the user of the
ECO-BP01 Digital Blood Pressure
Monitor Equipment requires
continued operation during power
mains interruptions, it is recommend-
ed that the ECO-BP01 Digital Blood
Pressure Monitor Equipment be
powered from an uninterruptible
power supply or a battery.
Note 1 At 80MHz and 800MHz, 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.
Radiated RF
IEC 61000-4-3
10 V/m
80 MHz to
2.5 GHz
3 V/m Where P is the maximum output power
rating of the transmitter in watts (W)
according to the transmitter manufac-
turer and d is the recommended
separation distance in metres (m). b
Field strengths from fixed RF
transmitters, as determined by an
electromagnetic site survey,c
should be less than the compliance
level in each frequency range.d
Interference may occur in the vicinity
of equipment marked with the
following symbol:
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. Electromag-
netic propagation is affected by absorption and reflection from
structures, objects and people.
Rated maximum
output power of
transmitter
(W)
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
Separation distance according to frequency of transmitter (m)
ª Field strength from fixed transmitters, such as base stations for radio
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
measured field strength in the location in which the Model ECO-BP01
Digital Blood Pressure Monitor is used exceeds the applicable RF
compliance level above, the Model ECO-BP01 Digital Blood Pressure
Monitor should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such
as re-orienting or relocating the Model ECO-BP01 Digital Blood
Pressure Monitor.
bOver the frequency range 150KHz to 80MHz, field strength should be
less than 3 V/m.
Recommended separation distances between
portable and mobile RF communications equipment and the ECO-BP01
Digital Blood Pressure Monitor
The ECO-BP01 Digital Blood Pressure Monitor is intended for use in an
electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the ECO-BP01 Digital Blood
Pressure Monitor can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communi-
cations equipment (transmitters) and the ECO-BP01 Digital Blood Pressure
Monitor as recommended below, according to the maximum output power of
the communications equipment.
P
V
d
=
1
5.3
P
E
d
=
1
5.3
P
E
d
=
1
7
0.01 0.117 0.117 0.233
0.1 0.369 0.369 0.738
1 1.167 1.167 2.333
10 3.689 3.689 7.379
100 11.667 11.667 23.333
The model ECO-BP01 Digital Blood Pressure Monitor is intended for
use in the electromagnetic environment specified below. The customer
or the user of the model ECO-BP01 Digital Blood Pressure Monitor
should assure that is used in such an environment.
Guidance and manufacturer’s declaration – electromagnetic immunity
Emission
test
Compliance
level
Electromagnetic
environment-guidance
Conducted RF
IEC 61000-4-6
3Vrms
150 kHz to 80
MHz
3 Vrms
Portable and mobile RF communica-
tions equipment should be used no
closer to any part of the ECO-BP01
Digital Blood Pressure Monitor
Equipment, including cables, than the
recommended separation distance
calculated from the equation applicable
to the frequency of the transmitter.
Recommended separation distance
P
V
d
=
1
5.3
P
E
d
=
1
5.3
P
E
d
=
1
7
80 MHz to 800 MHz
800 MHz to 2.5 GHz
P575/1508/01
ERROR AND LOW BATTERY INFORMATION
INDICATION POSSIBLE REASON CORRECTION METHODS
The cuff is put on
wrongly or the tube plug
is inserted too loosely.
Movement of arm/hand
or talking during
measurement.
The cuff is not inflated to
necessary pressure.
Arrhythmia.
The batteries are weak Replace all 4 batteries with
new ones.
Make sure that cuff is put on
correctly and the tube plug is
inserted tightly and repeat the
measurement.
Repeat the measurement with
following completely recommenda-
tions of manual.
Repeat the measurement with
pumping cuff to higher pressure
Consult your personal physician.
WHO BLOOD PRESSURE CLASSIFICATION INDICATION
Standards for assessment of high or low blood pressure, regardless
of age, have been established by World Health Organization(WHO) as
show in the chart as right:
The indicator displays a segment, based on the current data,
corresponding to the WHO classification.
For example, if your blood pressure is 135mmHg (Systolic Pressure),
78mmHg (Diastolic Pressure),according to the world health organization
standard, your blood pressure level is High Normal.
Note:
1.If the systolic blood pressure and diastolic blood pressure fall into different
categories, the higher value should be taken for classification.
2. The WHO blood pressure classification indication in the device is only a
reminder, it can not be regarded as the final diagnosis.
1.Warranty for this automatic digital blood pressure monitor is 24 months
since the date of purchase. The 24 months warranty excludes the monitor
cuff. The cuff is warranted for 12 months.
2.The warranty obligations are prescribed by warranty certificate for buyer.
3.The addresses of organizations for guarantee maintenance are present
in the warranty certificate.
WARNING
Do not modify this equipment without authorization of the manufacturer.
All major maintains on the device must be performed by an authorized
service center or distributor. No use-serviceable parts inside, before
servicing to authorized representative or manufacturer!
DECLARATION:
When technical information for user requirements is not in the scope of
confidentiality of the Company, the Company committed to provide
information disclosure in accordance with procedure, including circuit
diagrams and parts lists, and other related type technology information that
do not involve commercial secrets may be disclosed. Access to information
channels and procedures, please contact your dealer or manufacturer.
BLOOD PRESSURE RECORD
DATE SYSTOLIC
(mmHg)
DIASTOLIC
(mmHg)
PULSE
(beats/minute)
Power
frequency
magnetic field
IEC 61000-4-8
3 A/m 3 A/m
Power frequency magnetic fields
should be at levels characteristic of a
typical location in a typical
commercial or hospital environment.
QUALITY GUARANTEE
MODEL
Date TROUBLE SERVICE MAN
Warranty period Two years from purchasing date
Purchasing date
Purchasing shop
Name: Telephone:
Telephone:
Address:
Name:
Address:
Guarantee
Regulation
REQUIRING RECORD
1.During warranty period the repair could be made at any BPM
repair department.
2. the following things not belong to warranty range:
(1) Operating BPM different from procedures or instructions of the
manual.
(2) The body is damaged artificially.
(3) Self-repairing or modifying the monitor construc tion in any way.
(4) Breakdown due to corrosion of battery leakage.
(5) Problem which occurs under natural calamity and other force
majeures.
The manufacturer reserves the right to make technical changes without notice
in the interest of progress.
Prior notices will not be given in case of any amendments within this manual.
The mentioned trademarks and names are owned by the corresponding
companies.
If you use the device with power adapter, preventive inspection and mainte-
nance to be performed including the frequency of sunch maintenance.
Every time before use, please check the adapter, once damaged, never to use.
Please clean the plug of adapter plug at least once a year. Too much
dust on plug may cause the fire.
PERIODIC SAFETRY CHECKS
Specially packaged for Medinox
P.O. Box 549, Glenvista, 2058
www.medinox.co.za
456
Customer