Bionet BM3 User manual

BM3
Operation Manual
Patient Monitor
Ver. 2.62
2016.12.23
www.ebionet.com

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BM3 Operation Manual
Table of Contents
Table of Contents...................................................................................................................2
1. BASIC.......................................................................................................9
1.1 CE Standard Information............................................................................................. 10
1.2 Read before Use.............................................................................................................. 11
How to Contact Us.................................................................................................. 11
Warranty Period...................................................................................................... 12
Warning, Caution, Note........................................................................................... 13
General Precaution on Environment....................................................................... 14
General Precaution on Electric Safety .................................................................... 17
Cleaning Applied Parts ........................................................................................... 23
1.3 Product Components .....................................................................................................25
Product Outline....................................................................................................... 25
Principal Characters of Product .............................................................................. 25
Product Configuration............................................................................................. 26
Option Product........................................................................................................ 26
Product Body Configuration.................................................................................... 27
Accessories............................................................................................................ 29
Equipment Sign ...................................................................................................... 30
1.4 Function and Key........................................................................................................... 33
External Function.................................................................................................... 33
Operation Key......................................................................................................... 33
1.5 Standard Power Supply Application............................................................................35
DC Power............................................................................................................... 35
1.6 Battery Power SupplyApplication ...............................................................................36
Operation................................................................................................................ 36
The Impact of Lithium-Ion Battery Technology on the Battery................................. 38
Conditioning Guideline............................................................................................ 38
Storage Guideline................................................................................................... 38
How to Recycle the Battery..................................................................................... 38
To insert and remove the battery pack.................................................................... 39
1.7 DISPLAY MODE ( MONITOR OR SPOT )............................................................... 40
MONITORING MODE..............................................................................41
1. General Operation..................................................................................42
1.1 General Manu Operation.............................................................................................. 42
Screen Composition................................................................................................ 42
Menu Selection....................................................................................................... 43
Menu Composition.................................................................................................. 43
2. PATIENT/DATAMANAGEMENT.......................................................47
2.1 ADMIT............................................................................................................................ 48
ADMIT TYPE.......................................................................................................... 48
CHANGE ADMIT INFO........................................................................................... 49
DISCHARGE ( Discharge Patient )......................................................................... 49
ADMIT( Admit patient ) ........................................................................................... 50
HEIGHT.................................................................................................................. 50

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WEIGHT................................................................................................................. 51
DEFAULT SETTING............................................................................................... 51
2.2 ALARM........................................................................................................................... 52
ALL LIMITS............................................................................................................. 54
ALARM PRINT........................................................................................................ 54
ALARM VOLUME................................................................................................... 55
ALARM LEVEL....................................................................................................... 55
PARAMETER LEVEL ............................................................................................. 56
ALARM REVIEW.................................................................................................... 57
ALARM LIST........................................................................................................... 58
SAVE CONDITION................................................................................................. 59
NURSE CALL......................................................................................................... 60
3. SETUP ....................................................................................................61
3.1 SETUP.............................................................................................................................62
DISPLAY ................................................................................................................ 62
SET PARA.............................................................................................................. 63
WAVE SELECT...................................................................................................... 64
SET DATE & TIME ................................................................................................. 64
SET TIME............................................................................................................... 65
SET DATE.............................................................................................................. 65
HR SOURCE.......................................................................................................... 66
SWEEP SPEED...................................................................................................... 66
KEY SOUND .......................................................................................................... 67
DEMO..................................................................................................................... 67
USER SERVICE..................................................................................................... 67
SET UNIT NAME.................................................................................................... 68
SET BED NUMBER................................................................................................ 68
AC FILTER............................................................................................................. 69
SYSTEM................................................................................................................. 70
W-LAN.................................................................................................................... 71
DISPLAY MODE ( MONITOR or SPOT )................................................................ 71
MAKER SERVICE.................................................................................................. 71
Freezing and Unfreezing......................................................................................... 71
4. TREND ...................................................................................................72
4.1 TREND............................................................................................................................73
GRAPHIC TREND.................................................................................................. 74
TIME PERIOD ........................................................................................................ 75
TABULAR TREND.................................................................................................. 76
TIME INTERVAL..................................................................................................... 77
TREND WINDOW SETUP...................................................................................... 78
TIME PERIOD ........................................................................................................ 79
SET TREND ........................................................................................................... 80
TREND PRINT........................................................................................................ 80
5. ECG.........................................................................................................81
5.1 Outline.............................................................................................................................82
Colors and Standards of Cables ............................................................................. 82
Position of ECG Connector and Measuring Cable .................................................. 82
Attaching Electrodes to the Patient......................................................................... 83
Information on the ECG waveform.......................................................................... 83

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5-Leadwire Electrode Placement............................................................................ 84
3-Leadwire Electrode Placement............................................................................ 84
Electrode Placement for Neonates.......................................................................... 85
5.2 ECG Data Window.........................................................................................................86
5.3 ECG Setup......................................................................................................................88
LEAD SELECT ....................................................................................................... 88
ALARM LIMIT......................................................................................................... 89
ALARM LEVEL....................................................................................................... 90
ALARM SOUND ..................................................................................................... 91
QRS VOLUME........................................................................................................ 92
DISPLAY ................................................................................................................ 92
ECG SWEEP SPEED............................................................................................. 93
ECG SIZE............................................................................................................... 93
HR SOURCE.......................................................................................................... 94
ANALYSIS SETTING.............................................................................................. 94
6. SpO2.........................................................................................................98
6.1 Outline.............................................................................................................................99
SpO2 Connector Location and Measuring Cable.................................................... 99
6.2 SpO2 Data Window .....................................................................................................100
Signal and Data Validity........................................................................................ 101
6.3 SpO2Setup....................................................................................................................102
RATE VOLUME.................................................................................................... 102
ALARM................................................................................................................. 102
ALARM LIMIT....................................................................................................... 103
ALARM LEVEL..................................................................................................... 104
ALARM SOUND ................................................................................................... 104
Probe Off Condition.............................................................................................. 105
SPO2 Messages................................................................................................... 105
7. RESPIRATION ....................................................................................107
7.1 Outline...........................................................................................................................108
7.2 Respiration Data Window...........................................................................................109
7.3 Respiration Setup......................................................................................................... 109
RESPIRATION SPEED ........................................................................................ 110
RESPIRATION SIZE............................................................................................. 110
ALARM................................................................................................................. 111
ALARM LIMIT....................................................................................................... 111
ALARM LEVEL..................................................................................................... 112
ALARM SOUND ................................................................................................... 112
8. NIBP .....................................................................................................113
8.1 Outline........................................................................................................................... 114
8.2 NIBP Data Window ..................................................................................................... 116
8.3 NIBP Setup ................................................................................................................... 117
ALARM................................................................................................................. 117
ALARM LIMIT....................................................................................................... 118
ALARM LEVEL..................................................................................................... 119
ALARM SOUND ................................................................................................... 119
NIBP STAT........................................................................................................... 120
CUFF SIZE........................................................................................................... 120
UNIT SELECT ...................................................................................................... 120

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INTERVAL............................................................................................................ 121
INFLATION SET................................................................................................... 121
NIBP Status Messages......................................................................................... 122
Erroneous NIBP measurement............................................................................. 122
9. EtCO2....................................................................................................123
9.1 Introduction..................................................................................................................124
9.2 EtCO2 Parameter Window ......................................................................................... 129
9.3 EtCO2 Parameter Setting Menu.................................................................................130
EtCO2 SWEEP SPEED........................................................................................ 132
10. TEMPERATURE ...............................................................................137
10.1 Outline.........................................................................................................................138
10.2 Temperature Data Window ......................................................................................139
10.3 Temperature Setup....................................................................................................140
ALARM................................................................................................................. 140
ALARM LIMIT....................................................................................................... 141
ALARM LEVEL..................................................................................................... 142
ALARM SOUND ................................................................................................... 142
UNIT SELECT ...................................................................................................... 143
Check list.............................................................................................................. 143
TEMP Message.................................................................................................... 143
11. PRINT.................................................................................................144
11.1 Print.............................................................................................................................145
Printer and Heat Sensitivity Paper ........................................................................ 145
Function and Setup Menu..................................................................................... 146
11.2 Paper Change..............................................................................................................148
12. MESSAGE LIST ................................................................................149
13. DEFAULT SETTING VALUE ..........................................................150
1. Adult-ICU Mode ............................................................................................................150
2. Neonate-ICU Mode........................................................................................................ 152
3. Pediatric-ICU Mode.......................................................................................................154
SPOT MODE............................................................................................156
1. General Operation................................................................................157
1.1 Function and key.......................................................................................................... 157
Operation Keys..................................................................................................... 157
1.2 Screen Generating Power Mode................................................................................. 158
1.3 Standard Menu Operation..........................................................................................161
Menu Select.......................................................................................................... 163
Menu Icon Composition........................................................................................ 163
Numeric Value Window......................................................................................... 164
Select Menu Using by Trim Knob Key................................................................... 164
Select Arrow Item Menu........................................................................................ 164
Letter Arrangement Menu..................................................................................... 164
List selective menu............................................................................................... 165
Operation Menu.................................................................................................... 165

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2. PATIENT/DATAMANAGEMENT.....................................................166
2.1 Outline...........................................................................................................................167
2.2 Admit Type....................................................................................................................167
2.3 Select Patient in Admit Information...........................................................................169
2.4 Alarm Outline...............................................................................................................170
2.5 Alarm Setup.................................................................................................................. 171
2.6 Alarm Limit.................................................................................................................. 171
2.7 Alarm Print................................................................................................................... 172
2.8 Alarm Volume...............................................................................................................172
2.9 Alarm Level .................................................................................................................. 172
2.10 Nurse Call ...................................................................................................................173
2.11 Alarm Sound...............................................................................................................173
3. SAVE RECORD....................................................................................174
3.1 Outline...........................................................................................................................175
3.2 Adjust to Record SAVE Mode..................................................................................... 175
3.3 Measure with Monitor Mode ......................................................................................175
3.4 Measure with MANUAL Mode................................................................................... 176
3.5 Save................................................................................................................................176
3.6 Exit from Saving Mode................................................................................................177
4. SAVED DATA MANAGEMENT.........................................................178
4.1 Record List View..........................................................................................................179
4.2 Exit from Record List.................................................................................................. 180
4.3 View Specified Patients Record List...........................................................................181
4.4 View All Patients Record List......................................................................................182
4.5 Adjust Record............................................................................................................... 182
4.6 Delete a Record.............................................................................................................184
4.7 Delete a Patients Record..............................................................................................184
4.8 DeleteAll Patients Record........................................................................................... 185
5. SETUP ..................................................................................................186
5.1 SETUP...........................................................................................................................187
5.2. DISPLAY..................................................................................................................... 187
5.3 SAVE MODE................................................................................................................188
5.4 USER SERVICE..........................................................................................................188
5.5 SYSTEM.......................................................................................................................189
5.6 KEY SOUND................................................................................................................189
5.7 MAKER SERVICE......................................................................................................189
6. NIBP .....................................................................................................190
6.1 Outline...........................................................................................................................191
6.2 NIBP Data Window......................................................................................................192
6.3 NIBP Setup................................................................................................................... 192
ALARM LIMIT....................................................................................................... 193
CUFF SIZE........................................................................................................... 193
NIBP STAT........................................................................................................... 193
INFLATION SET................................................................................................... 194
UNIT SELECT ...................................................................................................... 194
INTERVAL............................................................................................................ 194
NIBP Status Messages......................................................................................... 195
Erroneous NIBP measurement............................................................................. 195

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7. SpO2.......................................................................................................196
7.1 Outline...........................................................................................................................197
7.2 SpO2 Data Window .....................................................................................................198
7.3 SpO2Setup....................................................................................................................199
ALARM LIMIT....................................................................................................... 199
SWEEP SPEED.................................................................................................... 200
RATE VOLUME.................................................................................................... 200
ALARM LEVEL..................................................................................................... 200
PROBE OFF Condition......................................................................................... 201
SPO2 Messages................................................................................................... 201
8. TEMPERATURE .................................................................................202
8.1 Outline...........................................................................................................................203
8.2 Temperature Data Window ........................................................................................204
8.3 Temperature Setup......................................................................................................205
ALARM LIMIT....................................................................................................... 205
UNIT SELECT ...................................................................................................... 206
PROBE SITE (Measurement Position).................................................................. 206
Check list.............................................................................................................. 206
TEMP Message.................................................................................................... 206
9. PRINT...................................................................................................207
9.1 Print...............................................................................................................................208
Print and Heat Sensitivity Paper ........................................................................... 208
Function and Setup Menu..................................................................................... 208
9.2 Paper Change ............................................................................................................... 210
10. TROUBLE SHOOTING....................................................................211
1. Noise in ECG .................................................................................................................. 211
2. SpO2 malfunction ..........................................................................................................212
3. Temp malfunction..........................................................................................................212
4. NIBP malfunction ..........................................................................................................213
5. Abnormality in NIBP measurements...........................................................................213
6. Failure in battery recharge ...........................................................................................214
7. Power failure ..................................................................................................................215
8. Periodic noises................................................................................................................216
9. Print failure ....................................................................................................................217
SPECIFICATION....................................................................................218
Ease of use........................................................................................................... 219
Intended use......................................................................................................... 219
Indication for use .................................................................................................. 219
Additional Function ............................................................................................... 219
Monitor Environmental Specifications................................................................... 219
Power................................................................................................................... 219
Monitor Performance Specifications...................................................................... 220
Graphical and Tabular Trends .............................................................................. 220
ECG capacity........................................................................................................ 220
SpO2capacity....................................................................................................... 220
Respiration Performance Specifications................................................................ 221
NIBP capacity....................................................................................................... 221
Temperature Unit Performance Specifications...................................................... 221

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Accessories Included:........................................................................................... 221
Option................................................................................................................... 221
Abbreviations and Symbols......................................................................222
PRODUCT WARRANTY .........................................................................225

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1. BASIC
1.1 CE Standard Information
1.2 Read before Use
Warranty Period
Warning, Caution, Note
General Precaution on Environment
General Precaution on Electric Safety
Equipment Connection, Maintenance & Washing Equipment Connection
1.3 Product Components
Product Outline
Principal Characteristics of Product
Product Configuration and Option Product
Product Body Configuration
1.4 Function and Key
External Function
Operation Key
1.5 Standard Power Supply Application
1.6 Battery Power Supply Application
1.7 General Menu Operation
Screen Composition
Menu Selection
Menu Composition

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1.1 CE Standard Information
Electromechanical safety standards met:
- EN 60601-1: 1990 + A1:1993 + A2: 1995 Medical Electrical Equipment, Part 1, General
Requirements for Safety.
- IEC/EN 60601-1-2 :2001 Electromagnetic compatibility -Requirements and tests.
- EN 1060-1:1995 Non-invasive sphygmomanometers - Part 1: General requirements
- EN 1060-3:1997 Non-invasive sphygmomanometers - Part 3: Supplementary requirements for
electro-mechanical blood pressure measuring systems
- EN ISO 9919:2005 Medical electrical equipment - Particular requirements for the basic safety and
essential performance of pulse oximeter equipment for medical use (ISO 9919:2005)
- EN 60601-2-27:2006 Medical electrical equipment - Part 2-27: Particular requirements for the
safety, including essential performance, of electrocardiographic monitoring equipment
- EN 60601-2-30:2000 Medical electrical equipment - Part 2-30: Particular requirements for the
safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring
equipment
- EN 12470-4:2000 Clinical thermometers - Part 4: Performance of electrical thermometers for
continuous measurement
- EN 60601-2-49:2001 Medical electrical equipment - Part 2-49: Particular requirements for the
safety of multifunction patient monitoring equipment

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1.2 Read before Use
BIONET services are always available to you.
The followings are address and phone number for contacting information, services, and product
supplies.
How to Contact Us
Product Supply
Information
Bionet America Inc.
2691 Dow Ave Ste B
Tustin, CA 92780
Phone : [phone]
Fax : [phone]
E-mail : [e-mail],
Consumable Supplies
Request
Phone : [phone] - USA
Phone : [phone] - Intenational
A/S and Technical
Support
For any technical inquiries or repair on the equipment,
Phone : [phone]
E-mail : serv[email protected]
Home Page
URL : http://wwwbionetUS.com
※In the event of malfunction or failure, contact us along with the model name, serial number, and
product name of the equipment.
※If you need the supply circuit diagram, component list, description and calibration instruction
etc. you can contact us we will provide you with it.
The information in this manual only applies to BM3 patient monitor software version 1.10F .
Due to continuing product innovation, specifications in this manual are subject to change
without notice.

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Warranty Period
This product is manufactured and passed through strict quality control and through
inspection.
We provide a 1-year warranty period for main body, with 6 months warranty for
accessories.
We will repair or replace any part of the BM3 found to be defective in usual operating
circumstance for free to you.
This warranty does not apply to any defect caused by improper use, misuse or abuse.

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Warning, Caution, Note
For special emphasis on agreement, terms are defined as listed below in user’s manual. Users
should operate the equipment according to all the warnings and cautions.
Warning
To inform that it may cause serious injury or death to the patient, property damage, material
losses against the “warning” sign
Caution
To inform that it may cause no harm in life but lead to injury against the “caution” sign
Note
To inform that it is not dangerous but important “note” sign for proper installation, operation, and
maintenance of the equipment.

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General Precaution on Environment
- Do not keep or operate the equipment in the environment listed below.
Avoid placing in an area
exposed to moist.
Do not touch the equipment
with wet hand.
Avoid exposure to direct
sunlight
Avoid placing in an area
where there is a high variation
of temperature.
Operating temperature
ranges from 10(C to
40(C. Operating humidity
ranges from 30% to 85%.
Avoid in the vicinity of
Electric heater
Avoid placing in an area where
there is an excessive
humidity rise or ventilation
problem.
Avoid placing in an area
where there is an
excessive shock or
vibration.
Avoid placing in an area where
chemicals are
stored or where there is danger
of gas leakage.
Avoid being inserted
dust and especially
metal
material into the
equipment
Do not disjoint or disassemble
the equipment.
We take no responsibility for it.
Power off when the
equipment is not fully
installed.
Otherwise, equipment
could be damaged.

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BM3 Operation Manual
CAUTIONS
Before Installation
Compatibility is critical to safe and effective use of this device. Please contact your local sales or
service representative prior to installation to verify equipment compatibility.
Defibrillator Precaution
Patient signal inputs labeled with the CF and BF symbols with paddles are protected against
damage resulting from defibrillation voltages. To ensure proper defibrillator protection, use only the
recommended cables and lead wires.
Proper placement of defibrillator paddles in relation to the electrodes is required to ensure
successful defibrillation.
Disposables
Disposable devices are intended for single use only. They should not be reused as performance
could degrade or contamination could occur.
Disposal of your old appliance
1. When this crossed out wheeled bin symbol is attached to a product it means
the product is covered by the European Directive 2002/96/EC.
2. All electrical and electronic products should be disposed of separately from
the municipal waste stream via designated collection facilities appointed by
the government or the local authorities.
3. The correct disposal of your old appliance will help prevent potential negative
consequences for the environment and human health.
4. For more detailed information about disposal of your old appliance, please
contact your city office, waste disposal service or the shop where you
purchased the product.
WARNING
This product contains a chemical known to the State of California to cause
cancer, birth defects, or other reproductive harm.
Electrocute Precautions
To prevent skin burns, apply electrocute electrodes as far as possible from all other electrodes, a
distance of at 15 cm/6 in. is recommended.
EMC
Magnetic and electrical fields are capable of interfering with the proper performance of the device.
For this reason make sure that all external devices operated in the vicinity of the monitor comply with
the relevant EMC requirements. X-ray equipment or MRI devices are possible source of interference
as they may emit higher levels of electromagnetic radiation.
Also, keep cellular phones to other telecommunication equipment away from the monitor.

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BM3 Operation Manual
CAUTIONS
Instruction for Use
For continued safe use of this equipment, it is necessary that the instructions are followed. However,
instructions listed in this in no way supersede established medical practices concerning patient care.
Loss of Data
Should the monitor at any time temporarily lose patient data, the potential exists that active
monitoring is not being done. Close patient observation or alternate monitoring devices should be
used until monitor function is restored.
If the monitor does not automatically resume operation within 60 seconds, power cycle the monitor
using the power on/off switch. Once monitoring is restored, you should verify correct monitoring
state and alarm function.
Maintenance
Regular preventive maintenance should be carried out annually (Technical inspections). You are
responsible for any requirements specific to your country.
MPSO
The use of a multiple portable socket outlet (MPSO) for a system will result in an enclosure leakage
current equal to the sum of all individual earth leakage currents of the system if there is an
interruption of the MPSO protective earth conductor. Do not use an additional extension cable with
the MPSO as it will increase the chance of the single protective earth conductor interruption.
Negligence
BIONET does not assume responsibility for damage to the equipment caused by improperly vented
cabinets, improper or faulty power, or insufficient wall strength to support equipment mounted on
such walls.

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NOTES
Power Requirements
Before connecting the device to the power line, check that the voltage and frequency. Ratings of the
power line are the same as those indicated on the unit’s label. If this is not the case, do not connect
the system to the power line until you adjust the unit to match the power source.
In U.S.A, if the installation of this equipment will use 240V rather than 120V, the source must
be a center-tapped, 240V, single-phase circuit.
Restricted Sale
U.S.A federal law restricts this device to sale by or on the order of a physician.
Supervised Use
This equipment is intended for use under the direct supervision of a licensed health care practitioner.
Ventilation Requirements
Set up the device in a location which affords sufficient ventilation. The ventilation openings of the
device must not be obstructed. The ambient conditions specified in the technical specifications must
be ensured at all times.
·Put the monitor in a location where you can easily see the screen and access the operating controls.
·This product is protected against the effects of cardiac defibrillator discharges to ensure proper
recovery, as required by test standards. (the screen may blank during a defibrillator discharge but
recovers within second as required by test standards.)
Reference Literature
Medical Device Directive 93/42/EEC
EN 60601-1/1990 +A1: 1993 +A2 : 1995 : Medical electrical equipment.
General requirements for safety
EN 60601-1-1/9. 1994 +A1 12.95: General requirements for safety.
General Precaution on Electric Safety
Warning
BM3 OPERATION MANUAL
Check the item listed below before operating the equipment.
NOT
1. Be sure that AC power supply line is appropriate to use. (AC100 - 240V)
2. Be sure that the power source is the one supplied from Bionet. (DC18V, 2.8A , MW160KA1803)
3. Be sure that the entire connection cable of the system is properly and firmly fixed.
4. Be sure that the equipment is completely grounded. (If not, there might be the problem occur in
the product.)
5. The equipment should not be placed in the vicinity of electric generator, X-ray, broadcasting
apparatus to eliminate the electric noise during operation. Otherwise, it may cause incorrect result.

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Note
The Equipment should be placed far from generator, X-ray equipment, broadcasting equipment
or transmitting wires, so as to prevent the electrical noises from being generated during the
operation, When these devices are near the Equipment, it can produce inaccurate
measurements. For BM3, both independent circuit and stable grounding are essentially
required. In the event that the same power source is shared with other electronic equipment, it
can also produce inaccurate output.
Warning
Do not contacts with the patient while operate the machine It may cause serious danger to the
users. Use only the provided cable.
Warning
In case the Equipment does not operate as usual or damaged, do not use on patient, and
contact to the medical equipment technician of the hospital or the equipment supply division.
Note
BM3 is classified as follows:
- BM3 classifies as Class I, BF & CF concerning electric shock. It is not proper to operate this
Equipment around combustible anesthetic or dissolvent.
- Noise level is B class regarding IEC/EN 60601-1 and the subject of Nose is B level concerning
IEC/EN60601-1-2.
Equipment Connection
Caution
For measurements in or near the heart we recommend connecting the monitor to the potential
equalization system. Use the green and yellow potential equalization cable and connect it to the
pin labeled with the symbol .

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Manufacturer’s declaration - electromagnetic emission
The BM3 system is intended for use in the electromagnetic environment specified below. The customer or
the user of BM3 system should assure that it is used in such an environment
Emission test
Compliance
Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1
The BM3 system 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 emissions
CISPR 11
Class B
The BM3 system is suitable for use in all establishm
ents other than domestic and those directly connect
ed to the public low-voltage power supplies building
s used for domestic purposes.
Harmonics emission
IEC 61000-3-2
A
Voltage fluctuation
IEC 61000-3-3
Complies
Manufacturer’s declaration - electromagnetic immunity
The BM3 system is intended for use in the electromagnetic environment specified below.
The customer or the user of the BM3system should assure that it is used in such an environment
Immunity test
IEC 60601
Test level
Compliance level
Electromagnetic
Environment -guidance
Electrostatic disc
harge (ESD)
IEC 61000-4-2
6 kV Contact
8 kV Air
6 kV Contact
8 kV Air
Floors should be wood, con
crete or ceramic tile. If floor
s are covered with synthetic
material, the relative humidit
y should be at least 30 %
Electrical fast
Transient / burst
IEC 61000-4-4
2kV for power supply lines
1kV for input/output lines
2kV for power supply line
s
1kV for input/output lines
Mains power quality should
be that of a typical commerc
ial or hospital environment.
Surge
IEC 61000-4-5
1 kV differential mode
2 kV common mode
1 kV differential mode
2 kV common mode
Mains power quality should
be that of a typical commer
cial or hospital environment.
Power frequency
(50/60Hz)
Magnetic field
IEC 61000-4-8
3.0 A/m
3.0 A/m
Power frequency magnetic fi
elds should be at levels cha
racteristic of a typical locatio
n in a typical commercial or
hospital environment.
Voltage dips, sh
ort
Interruptions and
Voltage variation
s
on power supply
input lines
IEC 61000-4-11
<5% Uт(>95% dip in Uт)
for 0.5cycle
40% Uт(60% dip in Uт )
for 5 cycle
70% Uт(30% dip in Uт)
for 25 cycle
<5% Uт(<95% dip in Uт )
for 5 s
<5% Uт(>95% dip in Uт)
for 0.5cycle
40% Uт(60% dip in Uт )
for 5 cycle
70% Uт(30% dip in Uт)
for 25 cycle
<5% Uт(<95% dip in Uт
)
for 5 s
Mains power quality should
be that of a typical commerc
ial or hospital environment. I
f th e u ser o f the BM3
system requires continued op
eration during power mains i
nterruptions, it is recommend
ed that the BM3 system be p
owered from an uninterruptib
le power supply or a battery
Note: Uт is the a.c. mains voltage prior to application of the test level.

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The BM3system is intended for use in the electromagnetic environment specified below.
The customer or the user of the BM3 system should assure that it is used in such an environment
Immunity test
IEC 60601
Test level
Compliance level
Electromagnetic environment -guidance
Conducted RF
IEC 61000-4-6
3 Vrms
150 kHz to 80 MH
z
3 Vrms
150 kHz to 80 MHz
Portable and mobile RF communications e
quipment should be used no closer to any
part of the BM3 system, including cables, t
han the recommended separation distance
calculated from the equation applicable to t
he frequency of the transmitter.
Recommended separation distance
Radiated RF
IEC 61000-4-3
3 V/m
80.0 MHz to 2.5 G
Hz
3 V/m
80.0 MHz to 2.5 G
Hz
Recommended separation distance
Where P is the maximum output power rat
ing of the transmitter in watts (W) accordin
g to the transmitter manufacturer and d is
the recommended separation distance in m
eters (m).
Field strengths from fixed RF transmitters,
as deter-mined by an electromagnetic site
survey,
(a) Should be less than the compliance lev
el in each frequency range (b).
Interference may occur in the vicinity of
equipment marked with the following symb
ol:
Note 1) Uт is the A.C. mains voltage prior to application of the test level.
Note 2) At 80 MHz and 800 MHz, the higher frequency range applies.
Note 3) These guidelines may not apply in all situations. Electromagnetic propagation is affected by a
bsorption and reflection from structures, objects and people.