User Manual
User Manual
Blood Pressure Monitor
TMB-1018-BT
Mistakes and changes are reserved.
BodyGauge is a registered trademark.
Arm Type
BodyGauge, Postbus 654, 3720 AR Bilthoven, The Netherlands
Tel. +31 858769819, email: [email protected]
GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO.,LTD
Zone A, 5/F., Investment Building, No. 12, Huizhan East Rd., Torch
Development District, Zhongshan, Guangdong, 528437, China
EC
REP
Version:1.0
Please do read the user manual carefully and thoroughtly so as to
ensure the safe usage of this product, and keep the manual well for further
reference in case you have problems.
This blood pressure monitor could also easily be used seperately. All
functions will be available, without the usage of a Bluetooth® Smart device
with BodyGauge app isn’t necessary.
TABLE OF CONTENTS
Table of Contents
INTRODUCTION ............................................................... 2
General Description
Indications For Use
Measurement Principle
Safety Information
LCD Display Signal
Monitor Components
BEFORE YOU START ...........................................................6
The Choise of Power Supply
Installing and Replacing the Batteries
Data Transmission via Bluetooth® Smart
Apply the Cuff
Settings
Select User ID
Pair-up the Blood Pressure Monitor with Your Device
START MEASUREMENT
...........................................................11
Start Measurement
DATA MANAGEMENT ...........................................................12
Recall the Records
Delete the Records
Data Transmission
INFORMATION FOR USER.......................................................14
Tips for Measurement
Maintenance
ABOUT BLOOD PRESSURE
.......................................................16
What are systolic pressure and diastolic pressure?
What is the standard blood pressure classification?
Why does my blood pressure fluctuate throughout the day?
Why the blood pressure I get from the hospital is different from home?
The result is different that you measuring on the different arm.
TROUBLESHOOTING ............................................................18
SPECIFICATIONS ...............................................................19
AUTHORIZED COPMONENT
.......................................................20
COMPLIED EUROPEAN STANDARDS LIST........................................20
EMC GUDIANCE ................................................................21
1
INTRODUCTION
General Description
Thank you for selecting BodyGauge arm type Blood Pressure Monitor (TMB-1018-BT).
The monitor features blood pressure measurement, pulse rate measurement and
auto-save the result. The design provides you with two years of reliable service.
Reading taken by the TMB-1018-BT are equivalent to those obtained by a trained
observer using the cuff and stethoscope auscultation method.
This manual contains important safety and care information, and provides step by step
instruction for using the product.
Read the manual thoroughly before using the product.
Features:
141mm x 36mm Blue LCD display with white backlight
Up to 60 pieces of record stored for each user
Measure-during-inflating Technology
Bluetooth® Smart data transmitting function
Indications For Use
The BodyGauge Blood Pressure Monitor is digital monitors intended for use in
measuring blood pressure and heartbeat rate with arm circumference ranging
from 22 cm to 32 cm (8.7-12.6 inches).
It is intended for adult indoor use only.
Measurement Principle
This product uses the Oscillometric Measuring method to detect blood pressure.
Before every measurement, the unit establishes a “zero pressure” equivalent to
the air pressure.Then it starts inflating the arm cuff, meanwhile, the unit detects
pressure oscillations generated by beat-to-beat pulsatile, which is used to determine
the systolic and diastolic pressure, and also pulse rate.The device also compares
the longest and the shortest time intervals of detected pulse waves to mean time
interval then calculates standard deviation.The device will display a warning signal
with the reading to indicate the detection of irregular heartbeat when the difference
of the time intervals over.
INTRODUCTION
Safety Information
The below signs might be in the user manual, labeling or other component.
they are the requirement of standard and using.
Symbol for “THE OPERATION
GUIDE MUST BE READ”
Symbol for “TYPE BF APPLIED
PARTS”
Symbol for “ENVIRONMENT
PROTECTION – Waste electrical
products should not be disposed of
with household waste. Please follow
local guidelines.”
Symbol for “COMPLIES WITH
MDD93/42/EEC
REQUIREMENTS”
Symbol for “MANUFACTURER”
Symbol for “SERIAL NUMBER”
Symbol for “DIRECT CURRENT”
EC
REP
For indoor use only
The Bluetooth Smart Mark
®
Symbol for “Authorised Representative in the European Community”
Symbol for “Class II Equipment”
F1
T1A/250V Φ3.6*10CCC
Symbol for “MANUFACTURE
DATE”
CAUTION
Please do read this user manual carefully and thoroughly before use.
This device is intended for adult use in the home/domestic only.
This device is intended for non-invasive measuring and monitoring of arterial blood pressure. It is not
intended for use on extremities other than the upper arm or for functions other than obtaining a blood
pressure measurement.
Do not confuse self-monitoring with self-diagnosis. This unit allows you to monitor your blood
pressure. Please start or end medical treatment basing solely on physician’s treatment advice.
If you are taking medication, consult your physician to determine the most appropriate time for your
measurement. Never change a prescribed medication without your physician’s consent.
This unit is not suitable for continuous monitoring during medical emergencies or operations.
If the pressure of the cuff exceeds 40 kPa (300 mmHg), the unit will automatically deflate. Should the
cuff not deflate when its pressure exceeds 40 kPa (300 mmHg), detach the cuff from the upper arm
and press the homologous button to stop inflation.
Do not use the monitor under the conditions of strong electromagnetic field (e.g. mobile) that radiates
interference signal or electrical fast transient / burst signal, especially when the AC adaptor is applied.
Do not touch the output of AC adapter and the patient simultaneously.
The device is not AP/APG equipment. It is not suitable for use in the presence of a flammable
anesthetic mixture with air (or oxygen, nitrous oxide).
Please keep the unit out of reach of infants or children, since inhalation or swallowing of small parts
is dangerous or even fatal.
Please use ACCESSORIES and detachable parts specified / authorised by MANUFACTURER.
Otherwise, it may cause damage to the unit or danger to the user / patient.
The materials of the cuff have been tested and found to comply with requirements of ISO 10993-5:
2009 and ISO 10993-10:2010. It will not cause any potential alergic reaction or contact injury.
Please make sure the unit functions safely and it is in proper working conditions before use.
2
3
INTRODUCTION
INTRODUCTION
LCD Display Signal
Monitor Components
CUFF
AIR HOSE
SYMBOL
4
DESCRIPTION
EXPLANATION
Systolic Blood Pressure
High blood pressure
Diastolic Blood Pressure
Low blood pressure
Puls
Beat/minute
User 1
Start measurement for user 1 and transmit the
measuring result automatically.
User 2
Start measurement for user 2 and transmit the
measuring result automatically.
Memory Review Mode
The query log, and a few memories
Successful Bluetooth®
Smart Connection
Bluetooth® Smart is turned on
Average Value
Average value of last three measurements.
Error
The monitor detects error.
Low Battery
Low battery and please replace the batteries.
Unit
Measurement unit of blood pressure
Current Time
Month:Day (Hour:Minute)
Irregular Heartbeat
Detector
Detects irregular heart beats.
DC POWER SOCKET
SET/UP BUTTON
START/STOP BUTTON
MEM/DOWN BUTTON
LCD DISPLAY
BATTERY COMPARTMENT
AIR CONNECTOR PLUG
List
1.Blood Pressure Monitor
(TMB-1018-BT)
2.Cuff
4.User manual
3. 4*AAA alkaline batteries
5.AC Adaptor
(UE08WCP-060100SPA)
5
BEFORE YOU START
BEFORE YOU START
The Choice of Power Supply
Apply the Cuff
1.Battery powered mode:
1.Insert the plug of cuff’s air pipe into
the interface located on the right side
of the monitor.
6VDC 4*AAA alkaline batteries
2.AC adaptor powered mode:
100-240V~, 50-60HZ,400mA
(Can be supplied by AC adaptor model
UE08WCP-060100SPA only!)
Please unplug the adaptor to depart from the
using utility power.
AC adaptor
2.As pictured on the right, wear the
cuff on your upper arm.
CAUTION
In order to achieve the best performance and protect you monitor,
please use the authorized / specified battery and power adaptor.
Installing and Replacing the Batteries
1. Open the battery door.
2. Insert the batteries according to the polarity
indications.
3. Close the battery door.
3.Tighten the cuff up. Make sure the
cuff is fixed 2 to 3 centimeters above
your elbow.
Appropriate to insert one finger
when the cuff is tightened around
your upper arm.
Battery Life: Approx. 44 days
(Battery capacity: 600 mAH. If measured three times per day, each measurement takes 35s,
measuring result display takes 20s and data transmission takes 10s. The current for measurement is
400 mA and that for records display and data transmission is 50 mA and 50 mA separately, while the
current when shutdown is 35 uA.
Replace the batteries under following circumstances:
displays on the LCD.
The LCD display dims.
When powering on the monitor, the LCD doesn’t light up.
CAUTION
Remove batteries if the device is not likely to be used for some time.
4.Correct Posture:
Bare your arm or wear tights only when
starting measurement.
Sit comfortably and relaxed on a
proper-size chair.
The central of the cuff should maintain at
the same level as your heart.
Legs relaxed with the feet falling outwards.
Palms up.
Worn batteries are harmful to the environment. Do not dispose with daily garbage.
Remove the old batteries from the device following your local recycling guidelines.
6
7
BEFORE YOU START
BEFORE YOU START
Settings
Please proceed to time setting before your initial use so as to ensure
each piece of record is labeled with a time stamp. (The range of the
year is 2000 to 2050. Time Format: 24 Hours)
NOTE: The monitor will shut off automatically in 60 seconds after last
operation when in Setting Interface.
1.When the monitor is OFF,
press and hold SET button to
enter [HOUR] and [MINUTE]
setting.
2.Press MEM button to
change the numeral. Each
press will increase the
numeral by one in a
cycling manner.
3.Press SET button to
confirm the [HOUR] and
[MINUTE]. Then the
monitor diverts to
[MONTH] and [DAY]
setting automatically.
Select User ID
NOTE: The monitor will shut off automatically in 60 seconds after last
operation when under User ID selection mode.
1.When the monitor is OFF,
press and hold MEM
button to enter User ID
selection mode.
HOUR
2.The current User ID
blinks.
MINUTE
4.Repeat step 2 and 3 to confirm [MONTH] and [DAY]. Then the monitor
diverts to [YEAR] setting automatically.
MONTH
6.After confirming the [YEAR], the LCD will display “dOnE” and the
monitor will shut off automatically.
3.Press MEM button to switch
between User 1 and User 2.
DAY
5.Repeat step 2 and 3 to confirm [YEAR].
4.Press SET button to
confirm the selected User
ID.
8
YEAR
9
Start Mearsurement
BEFORE YOU START
Pair-up the Blood Pressure Monitor
with Your Device
1.Turn on Bluetooth® Smart
and the app. Make sure
both are ON when pair-up
is proceeding.
Start Mearsurement
After correctly positioning the cuff and selecting User ID, press START·STOP
button to turn on the monitor, and it will complete the measurement process
automatically.
1.LCD display
2.When the monitor is OFF,
press and hold the START
button to start pair-up. The
symbol
blinks,
indicating pair-up is
proceeding.
2.Adjust to zero automatically.
3.Inflating and measuring automatically.
If SUCCEED, symbols
will be shown on the LCD
just like the picture on the
right.
If FAIL, symbols will be shown on
the LCD just like the picture on the
right.
4.Display and save the results will
automatically transmitted to the app.
The icon
blinks.
5. Press START·STOP button to turn off the monitor. Otherwise, the monitor will
3.The monitor will shut off automatically after Pair-up
process is complete.
10
shut off within 1 minute after last operation.
Tips:
A.when finish the whole measurement, press another button. Then the blood monitor
will begin measuring again.
B.Maximum 60 records are both for user 1 and user 2.
11
Data Management
Data Management
Data Transmission
Recall the Records
Automatic Data Transmission
1.When the monitor is OFF, press MEM
button to retrieve the memory. The monitor
will display the average value of last three
measurements.
With the advanced Bluetooth® Smart technology applied, the mobile or portable
equipments, which are equipped with Bluetooth® Smart function in line with BLE
Technical Specifications as well as BLP Protocol established by global
organization App and Bluetooth® SIG, are capable to receive your personal health data.
When both BodyGauge App and Bluetooth® Smart are ON, TMB-1018-BT
will automatically transmit measurement data to your mobile via Bluetooth® Smart.
2.Press MEM button again to rotate the
records. Up to 60 records will be stored
under each user ID.
The measurement date and time will be
displayed alternatively.
1.After measurement, the symbol
lights
up, indicating the measuring result is being
automatically transmitted to BodyGauge app.
2.If SUCCEED, the LCD will display
“dOnE”.
3.If you would like to check another user
ID’s history, please follow the
instructions in Select User ID to
change to another User ID first.
3.If FAIL, the LCD will display “ERROR”.
No Record found for User 2!
Delete the Records
1.When under data enquiry mode, press
and hold both MEM button and SET button
for 3 seconds to clear memory. The LCD
will display “dEL dOnE”, indicating that the
memory is cleared.
CAUTION
Interference may occur in the vicinity of equipment marked with the following symbol
. And TMB-1018-BT may interfering vicinity electrical equipment.
Sensitive people, including pregnant women and those who implanted medical electronic instruments, should avoid using the unit whenever possible.
Keep the monitor at least 20 centimeters away from the human body (especially the
head) when the data transmission is proceeding after measurement.
To enable the data transmission function, this product should be paired to Bluetooth®
Smart end at 2.4 GHz.
How to mitigate possible interference?
1. The range between the device and Bluetooth® Smart end should be reasonably
close (1 - 10 meter). Please ensure no obstacles between device and Bluetooth®
Smart end so as to obtain quality connection and to lower the RF output range.
2. To avoid interference, other electronic devices (particularly those with wireless
transmission / Transmitter) should be kept at least 1 meter away from the monitor.
12
13
INFORMATION FOR USER
INFORMATION FOR USER
Maintenance
Tips for Measurement
It can cause inaccuracy if the measurement is taken in the following
circumstances.
Within 1 hour
after dinner or drinking
Within 20 minutes
after taking a bath
To obtain the best performance, please follow below instructions.
Put in a dry place and
avoid the sunshine
Avoid immersing it in the water.
Clean it with a dry cloth in case.
Avoid shaking and collision.
Avoid dusty environment and
unstable temperature surrounding
Immediate measurement
after tea, coffe, smoking
When talking or moving your fingers
Use the slightly damp cloth
to remove the dirt.
Avoid washing the cuff
Cleaning: Before Use - Pick out the whole unit of the storage bag. Use the soft cloth to
remove the dirt on the monitor and apply some alcohol to
disinfect the cuff before tying the cuff.
After Use - Use the soft cloth to wipe the unit and apply some alcohol to
disinfect the cuff before putting the whole unit back in the bag.
Please always disinfect the cuff before applying to another patient.
In a very cold environemnt
14
When you want to discharge urine
Please follow the instructinos for correct replacement of interchangeable or detachable
parts specified by BodyGauge as “replaceable”.
Disposal: Degraded sensors may result in inaccurate measurement while loosened
electrodes may cause the monitor’s failure to power on. The expected life of the monitor
is two years. Please dispose of ACCESSORIES, detachable parts, and the ME EQUIPMENT according to the local guidelines.
15
ABOUT BLOOD PRESSURE
ABOUT BLOOD PRESSURE
What are systolic pressure and diastolic pressure?
When ventricles contract and pump blood out
of the heart, the blood pressure reaches its
maximum value in the cycle, which is called
systolic pressure. When the ventricles relax,
the blood pressure reaches its minimum
value in the cycle, which is called diastolic
pressure.
Systolic
Diastolic
press
relax
blood discharging
artery
blood entering
vein
What is the standard blood pressure classification?
The blood pressure classification published by
World Health Organization (WHO) and
International Society of Hypertension (ISH) in
1999 is as follows:
3. Waiting at least 4-5 minutes for
another measurement.
Only a physician can tell your normal BP range. Please
contact a physician if your measuring result falls out of the
range. Kindly note that only a physician could tell whether
your blood pressure value has reached a dangerous point.
Level
Optimal
Normal
High-normal
SYS
<120
120-129
DIA
<80
80-84
Mild
Moderate
Severe
130-139
140-159
160-179
≥180
85-89
90-99
100-109
≥110
Irregular Heartbeat Detector
This Blood Pressure Monitor is equipped with an intelligent function of Irregular
Heartbeat (IHB) Detector. During each measurement, this equipment records the
heartbeat intervals and works out the standard deviation. If the calculated value is
larger than or equal to 15, this equipment will light up the IHB symbol on the screen
when displaying the measuring result.
CAUTION
The appearance of the IHB icon indicates that a pulse irregularity consistent with
an irregular heartbeat was detected during measurement. Usually this is NOT a
cause for concern. However, if the symbol appears often, we recommend you
seek medical advice. Please note that the device does not replace a cardiac
examination, but serves to detect pulse irregularities at an early stage.
16
1. Individual blood pressure varies every in
one day, it also affected by the way you tie your
cuff and the your measurement position, so
please take the measurement at the same
condition.
2.The varies of the pressure is greater
if the person take medicine.
CAUTION
Blood
Pressure (mm Hg)
Why my blood pressure
is varies even in one
day?
Why the blood pressure
I get from the hospital is
different from home?
The blood pressure is different even
during 24 hour because of the
weather,emotion, exercise etc, specially
the “white coat” in hospital which makes
the results are higher than the ones at
home.
The attention need to pay
when you measure you blood
pressure at home:
If the cuff is tied properly.
If the cuff is too tight or too loose.
If the cuff is tied on the upperarm.
If you feel anxious pressured.
You had better take deep breath 2-3
times before beginning.
Advice:adjust yourself for 4-5 minutes
until you calm down.
If the result is the same
if measuring on the
right arm?
It is ok for both arms, but there will be
some different results for different arm,
so suggest you measure the same arm
every time.
17
TROUBLESHOOTING
PROBLEM SYMPTOM
No power
Low
batteries
Error
massage
Display is dim or
will not light up.
SPECIFICATIONS
CHECK THIS
Batteries are exhausted. Replace with new batteries
Batteries are inserted
incorrectly.
Show on
Batteries are low.
the display
E 1 shows
Data Communication
Failure.
E 2 shows
The cuff is very tight
E 3 shows
The pressure of the
cuff is excess.
E 10 or
E 11 shows
E 20 or
E 21 shows
Eexx,shows on
the display.
REMEDY
Insert the batteries
correctly
A calibration error
occurred.
Data Transmission
Failure.
Display mode
Please check below items:
Measurement mode
Oscillographic testing mode
Measurement range
Pressure: 0-40kpa(0~300mmHg)
pulse value:(40-199)times/minute
1.Bluetooth® Smart is ON.
2.Both devices are within
the transmission distance of
Bluetooth® Smart
Refasten the cuff and then
measure again.
Relax for a moment and
then measure again.
Retake the measurement.
If the problem persists,
contact the retailer or our
customer service
department for further
assistance.Refer to the
warranty for contact
information and return
instructions.
Press and hold START·
STOP button to start
manual data transmission.
Turn ON Bluetooth® Smart
Bluetooth® Smart is OFF. and try again.
The device is too far
away from your mobile.
18
Blue LCD with White Backlight
V.A. = 141mm(L) x 36mm(W)
Replace with new batteries
Relax for a moment
and then measure again.
movement can affect the
The monitor detected
measurement.Relax for a
motion while measuring. moment and then
measure again.
Measure incorrectly.
Power supply
Battery Powered Mode:
6V (4 x AAA-size alkaline-battery)
AC Adaptor Powered Mode:
100-240 V~, 50-60 Hz, 400 Ma
(Can be supplied by AC adaptor model
UE08WCP-060100SPA only!)
Keep the distance of Blood
Pressure Monitor and the
mobile within 2 to 3 meters.
Accuracy
Pressure:
15℃-25℃ within ±0.4 kPa (3 mm Hg)
10℃-40℃(out of 15℃ -25℃ ) within ±0.7 kPa
(5 mm Hg); Pulse Value: ±5%
Working condition
Temperature:10℃-40℃
Relative Humidity 15%-90%RH
Atmospheric Pressure: 80-105 kPa
Storage & transportation
condition
Temperature:-20℃-60℃
Relative Humidity 10%-93%RH
Atmospheric Pressure: 50-106 kPa
Measurement perimeter
of the upper arm
About 22cm-32cm
Net Weight
External dimensions
Attachment
Approx.340g(Excluding the dry cells)
Approx.180*100*40mm
4*AAA alkaline batteries,user manual
Mode of operation
Continuous operation
Degree of protection
Type BF applied part
Device Classification
Battery Powered Mode: Internally Powered ME Equipment
AC Adaptor Powered Mode: Class II ME Equipment
IP Classification
IP22
Software Version
V01
WARNING: No modification of this equipment is allowed.
19
AUTHORIZED COPMONENT
The Matched Components
Please use the BodyGauge
authorized adaptor
2.Storage bag.
EMC Guidance
Table 1 Guidance and manufacturer’s declaration – electromagnetic emissionsfor all EQUIPMENT and SYSTEMS
Guidance and manufacture’s declaration – electromagnetic emission
Adaptor
Type: UE08WCP-060100SPA
Input: 100-240V, 50-60Hz,400mA
1A
Output: 6V
(Expected Service Life: 50,000 Hours)
Contact Information
For more information about our products, please visit:
BodyGauge, Postbus 654, 3720 AR Bilthoven, The Netherlands
Tel. +31 858769819, email: [email protected]
Manufactured by: GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO., LTD
Company: GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO., LTD
Address: Zone A, 5/F., Investment Building , No. 12, Huizhan East Rd., Torch
Development District, Zhongshan, Guangdong, 528437, China
Authorized European Representative:
Company: MDSS - Medical Device Safety Service GmbH
Address: Schiffgraben 41, 30175 Hannover, Germany
Complied European Standards List
Risk Management
EN/ISO 14971:2007
Labeling
EN 980:2008
User Manual
EN 1041:2008
The TMB-1018-BT is intended for use in the electromagnetic environment specified
below.The customer of the user of the TMB-1018-BT should assure that it is used in
such anenvironment
Emission test
Compliance
RF emissions
CISPR 11
Group 1
RF emission
CISPR 11
Class B
Harmonic emissions
IEC 61000-3-2
Not applicable
Voltage fluctuations/
flicker emissions IEC
61000-3-3
Not applicable
Electromagnetic environment - guidance
The TMB-1018-BT 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.
The TMB-1018-BT is suitable for use in all
establishments other than domestic and
those directly connected to the public
low-voltage power supply network that
supplies buildings used for domestic
purposes.
Generl Requirements EN 60601-1:2006/A1:2012
EN 62304:2006/AC:2008
for Safety
EN 60601-1-6:2010
EN 60601-1-11:2010
Non-invasive
EN 1060-1:1995+A2:2009
Sphygmomanometers
EN 1060-3:1997+A2:2009
General
Requirements
EN 1060-4:2004
Electromagnetic
Compatibility
20
EN 60601-1-2:2007/AC:2010
21
Table 2 Guidance and manufacturer’s declaration – electromagnetic immunity –
for all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacture’s declaration – electromagnetic immunity
The TMB-1018-BT is intended for use in the electromagnetic environment specified below.
The customer of the user of the TMB-1018-BT should assure that it is used in such an
environment
Electromagnetic
environment - guidance
Immunity test
IEC 60601 test level Compliance level
Electrostatic
discharge (ESD)
IEC 61000-4-2
±6 kV contact
±8 kV air
Electrical fast
transient/burst
IEC 61000-4-4
±2 kV for
power supply lines
Surge IEC
61000-4-5
±1 kV line(s)
to line(s)
±1 kV
differential mode
Mains power quality should
be that of a typical
commercial or hospital
environment.
Voltage dips,
short interruptions
and voltage
variations on
power supply
input lines
IEC 61000-4-11
<5% UT
(>95% dip in UT )
for 0.5 cycle
<5% UT
(>95% dip in UT )
for 0.5 cycle
40% UT
(60% dip in UT )
for 5 cycles
40% UT
(60% dip in UT )
for 5 cycles
70% UT
(30% dip in UT )
for 25 cycles
70% UT
(30% dip in UT )
for 25 cycles
Mains power quality should
be that of a typical
commercial or hospital
environment. If the user of
TMB-1018-BT requires
continued operation during
power mains interruptions,
it is recommended that
TMB-1018-BT be powered
from an interruptible power
supply or a battery.
<5% UT
(>95% dip in UT )
for 5 sec
Power frequency 3A/m
(50Hz) magnetic
field
IEC 61000-4-8
NOTE
22
Floors should be wood,
concrete or ceramic tile. If
floors are covered with
synthetic material, the
relative humidity should be
at least 30%.
Mains power quality should
±2kV for
power supply lines be that of a typical
commercial or hospital
environment.
Table 4 Guidance and manufacturer’s declaration – electromagnetic immunity –
for ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING
Guidance and manufacture’s declaration – electromagnetic immunity
The TMB-1018-BT is intended for use in the electromagnetic environment specified below.The
customer of the user of the TMB-1018-BT should assure that it is used in such an environment.
Immunity test
IEC 60601
test level
Compliance
level
Portable and mobile RF communications
equipment should be used no closer to
any part of the TMB-1018-BT, including
cables,than the recommended separation
distance calculated from the equation
applicable to the frequency of the
transmitter.
±6 kV contact
±8 kV air
<5% UT
(>95% dip in UT )
for 5 sec
3A/m
Power frequency magnetic
fields should be at levels
characteristic of a typical
location in a typical
commercial or hospital
environment.
UT is the a.c. mains voltage prior to application of the test level.
Electromagnetic environment guidance
Recommended separation distance
Conducted RF 3 Vrms
IEC 61000-4-6 150 kHz to
80 MHz
3 Vrms
d = 1.167
Radiated RF
3 V/m
IEC 61000-4-3 80 MHz to
2.5 GHz
3 V/m
d = 1.167
80 MHz to 800 MHz
d = 2.333
800 MHz to 2.5 GHz
where P is the maximum output power
rating of the transmitter in watts (W)
according to the transmitter manufacture
and d is the recommended separation
distance 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 marked with the following
symbol:
23
Table 6 Recommended separation distances between portable and mobile
RF communications equipment and the EQUIPMENT or SYSTEM –
for ME EQUIPMENT or ME SYSTEM that are not LIFE-SUPPORTING
NOTE 1
NOTE 2
a
b
At 80 MHz and 800 MHz, the higher frequency range applies.
These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures, objects
and people.
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 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 TMB-1018-BT is
usedexceeds the applicable RF compliance level above, the TMB-1018-BT should be
observed to verify normal operation. If abnormal performance is observed, additional
measuresmay be necessary, such as re-orienting or relocating the TMB-1018-BT.
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than
3V/m.
Recommended separation distances
between portable and mobile RF communications equipment at the TMB-1018-BT.
The TMB-1018-BT is intended for use in an electromagnetic environment in which radiated
RF disturbances are controlled. The customer or the user of the TMB-1018-BT can help
prevent electromagnetic interference by maintaining a minimum distance between portable
and mobile RF communications equipment (transmittters) and the TMB-1018-BT as
recommended below, according to the maximum output power of the communications
equipment.
Rated maximum output
power of transmitter
(W)
Separation distance according to frequency of transmitter (m)
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
d = 1.167
d = 1.167
d = 2.333
0.01
0.167
0.167
0.233
0.1
0.369
0.369
0.738
1
1.167
1.167
2.333
10
3.690
3.690
7.338
100
11.67
11.67
23.33
For transmitters rated at a maximum output power not listed above, the recommended
separation distance d in metres (m) can be determined 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 80MHz and 800MHz, the separation distance for the higher frequency
range applies.
NOTE 4 These guidelines may not apply in all situations. Electromagnetic propagation
is affected by absorption and reflection from structures, objects and people.
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