Bionet BM3VET Touch User manual

BM3VET Touch User’s Manual
Veterinary Patient Monitor
Rev. 1.1(20160401)

Rev. 1.1 2
BM3VET Touch User’s Manual
Table of Contents
Table of Contents.............................................................................................................................2
1. BASIC................................................................................................................................. 7
1.1 CE Standard Information.........................................................................................................8
1.2 Read before Use.......................................................................................................................10
How to Contact Us .....................................................................................................................................10
Warranty Period..........................................................................................................................................11
Warning, Caution, Note..............................................................................................................................11
General Precaution on Environment...........................................................................................................12
General Precaution on Electric Safety........................................................................................................17
Equipment Connection ...............................................................................................................................18
Maintenance and Washing Equipment Connections ..................................................................................25
1.3 Product Components...............................................................................................................27
Product Outline...........................................................................................................................................27
Principal features of Product ......................................................................................................................27
Product Configuration ................................................................................................................................28
Option Product ...........................................................................................................................................28
Features of Main Body...............................................................................................................................29
1.4 Function and Key ....................................................................................................................35
External Function .......................................................................................................................................35
Operation Key ............................................................................................................................................35
1.5 Standard Power Supply Application.....................................................................................37
1.6 Battery Power Supply Application ........................................................................................38
1.7 General Menu Operation........................................................................................................42
Screen Composition....................................................................................................................................42
Menu Selection...........................................................................................................................................44
Menu Composition.....................................................................................................................................45
2. ANIMAL/DATA MANAGEMENT.................................................................................. 49
2.1 ADMIT.....................................................................................................................................50
ANIMAL TYPE.........................................................................................................................................51
CHANGE ANIMAL INFO ........................................................................................................................51

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DEFAULT SETTING................................................................................................................................52
HEIGHT.....................................................................................................................................................52
WEIGHT ....................................................................................................................................................53
2.2 ALARM....................................................................................................................................54
Alarm for the Product.................................................................................................................................55
PARAMETER1 LEVEL ............................................................................................................................56
PARAMETER2 LEVEL ............................................................................................................................56
ARRHYTHMIA LEVEL ...........................................................................................................................57
ALARM REVIEW.....................................................................................................................................57
ALARM VOLUME....................................................................................................................................59
ALARM PRINT.........................................................................................................................................60
NURSE CALL ...........................................................................................................................................60
3. SETUP.............................................................................................................................. 63
3.1 SETUP......................................................................................................................................64
SET PARA .................................................................................................................................................65
UNIT SELECT...........................................................................................................................................65
USER SERVICE ........................................................................................................................................66
SYSTEM ....................................................................................................................................................73
NETWORK................................................................................................................................................74
MAKER SERVICE....................................................................................................................................77
FREEZE MENU.........................................................................................................................................77
4. TREND ............................................................................................................................. 78
4.1 TREND.....................................................................................................................................79
GRAPHIC TREND ....................................................................................................................................80
TABULAR TREND...................................................................................................................................81
TREND WINDOW SETUP.......................................................................................................................82
5. ECG................................................................................................................................... 85
5.1 Introduction.............................................................................................................................86
Colors and Standards of Cables..................................................................................................................86
Position of ECG Connector and Measuring Cable .....................................................................................86
Attaching Electrodes to the Animal............................................................................................................89
Choosing an ECG lead for Arrhythmia Monitoring ...................................................................................90
Information on the ECG waveform............................................................................................................90

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5 Position of 5-Lead ...................................................................................................................................91
Position of 3-Lead Wire Electrodes............................................................................................................92
5.2 ECG Data Window..................................................................................................................93
5.3 ECG Data Setup ......................................................................................................................96
ALARM LIMIT..........................................................................................................................................96
LEAD SELECT..........................................................................................................................................97
QRS VOLUME ..........................................................................................................................................97
DISPLAY...................................................................................................................................................98
ARRHYTHMIA SETTING .....................................................................................................................101
ST/PVC ....................................................................................................................................................102
6. SpO2................................................................................................................................ 108
6.1 Outline....................................................................................................................................109
SpO2 Connector Location and Measuring Cable .....................................................................................109
6.2 SpO2 Data Window...............................................................................................................110
Signal and Data Validity...........................................................................................................................111
6.3 SpO2 Data Setup....................................................................................................................113
ALARM....................................................................................................................................................114
RATE VOLUME......................................................................................................................................114
LEAD FAULT Condition.........................................................................................................................115
SPO2 Messages ........................................................................................................................................115
7. RESPIRATION ...............................................................................................................116
7.1 Outline....................................................................................................................................117
7.2 Respiration Data Window ....................................................................................................119
7.3 Respiration Data Setup.........................................................................................................120
ALARM....................................................................................................................................................121
APNEA DETECT ....................................................................................................................................121
RESPIRATION SPEED...........................................................................................................................122
RESPIRATION SIZE...............................................................................................................................122
8. NIBP ............................................................................................................................... 123
8.1 Outline....................................................................................................................................124
8.2 NIBP Data Window...............................................................................................................126

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8.3 NIBP Data Setup....................................................................................................................128
ALARM....................................................................................................................................................129
CUFF SIZE...............................................................................................................................................130
INFLATION.............................................................................................................................................130
INTERVAL..............................................................................................................................................131
NIBP STAT..............................................................................................................................................132
NIBP VITAL SIGN..................................................................................................................................133
UNIT SELECT.........................................................................................................................................134
9. EtCO2.............................................................................................................................. 135
9.1 Introduction...........................................................................................................................136
9.2 EtCO2 Parameter Window ..................................................................................................142
9.3 EtCO2 Parameter Setting Menu..........................................................................................143
ALARM LIMIT........................................................................................................................................144
WAVEFORM SCALE .............................................................................................................................145
EtCO2 SWEEP SPEED............................................................................................................................145
APNEA DETECT ....................................................................................................................................146
MODULE INFO.......................................................................................................................................147
MODULE SETUP....................................................................................................................................148
ZERO .......................................................................................................................................................150
MODULE RESET....................................................................................................................................151
9.4 TROUBLESHOOTING........................................................................................................152
10. TEMPERATURE ......................................................................................................... 154
10.1 Outline..................................................................................................................................155
10.2 Temperature Data Window................................................................................................156
10.3 Temperature Data Setup ....................................................................................................157
ALARM....................................................................................................................................................158
UNIT SELECT.........................................................................................................................................158
11. PRINT........................................................................................................................... 159
11.1 Print......................................................................................................................................160
Printer and Heat Sensitivity Paper............................................................................................................160
Function and Setup Menu.........................................................................................................................161

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11.2 Paper Change.......................................................................................................................167
12. MESSAGE LIST .......................................................................................................... 168
13. DEFAULT SETTING VALUE..................................................................................... 169
13.1 HORSE-ICU Mode..............................................................................................................169
13.2 DOG-ICU Mode...................................................................................................................172
13.3 PUPPY-ICU Mode...............................................................................................................174
13.4 CAT-ICU Mode...................................................................................................................176
14. TROUBLE SHOOTING .............................................................................................. 178
14.1 Noise in ECG........................................................................................................................178
14.2 SpO2 malfunction................................................................................................................179
14.3 Temp malfunction ...............................................................................................................179
14.4 NIBP malfunction................................................................................................................180
14.5 Abnormality in NIBP measurements.................................................................................180
14.6 Failure in battery recharge.................................................................................................181
14.7 Power failure........................................................................................................................182
14.8 Periodic noises......................................................................................................................183
14.9 Print failure..........................................................................................................................184
15. SPECIFICATION........................................................................................................ 185
Ease of use................................................................................................................................................186
Additional Function..................................................................................................................................186
Monitor Environmental Specifications.....................................................................................................186
Power........................................................................................................................................................186
Specification.............................................................................................................................................187
Accessories Included................................................................................................................................189
Option.......................................................................................................................................................189
Abbreviations and Symbols................................................................................................ 190
PRODUCT WARRANTY ................................................................................................... 193

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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 and Washing Equipment Connection
1.3 Product Components
Product Outline
Principal features of Product
Product Configuration
Optional Products
Features of Main Body
1.4 Functions 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:
Information supplied by the manufacturer of medical devices
1. EN 60601-1(2006)
Medical electrical equipment Part1: General requirements for safety
2. EN 60601-1-2 (2007) (IEC 60601-1-2)
Electromagnetic Compatibility Requirement and tests
3. EN 55011:2007+A2:2007 Group 1 Class B(CISPR11) (EN 55011:2009/A1:2010)
Limits and methods of measurement of radio disturbance characteristics of industrial, scientific
and medical (ISM) radio-frequency equipment
4. IEC 60601-1-4:1996+A1:1999 (EN 60601-1:2006)
Part 1-4 General requirements for safety Collateral standard: Programmable electrical medical
system
5. IEC 60601-1-6:2010
Part 1-6 General requirements for safety Collateral standard: Usability
6. IEC 60601-1-8:2006 (EN 60601-1-8:2007)
Part 1-8 General requirements for safety Collateral standard: General requirements, tests and
guidance for alarm systems in medical electrical equipment and medical electrical systems
7. EN 60601-2-30:2000 (IEC 80601-2-30:2013)
Part 2: Particular requirements for the safety, including essential performance of automatic
cycling non-invasive blood pressure monitoring equipment
8. EN 60601-2-49:2001 (IEC 60601-2-49:2001)
Part 2: Particular requirements for the safety of multifunction patient monitoring equipment
9. EN 12470-4:2000+A1:2009
Performance test for Temperature Clinical thermometers - Part 4: Performance of electrical
thermometers for continuous measurement
10. EN 1060-1:1995+A2:2009, EN 1060-3:1995+A2:2009:(EN ISO 81060-1:2012)
Performance test for NIBP Non-invasive sphygmomanometers- Part 1: General requirements,
Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems
11. EN ISO 14971:2012
Medical devices - Application of risk management to medical devices
12. EN ISO 9919:2009 (ISO 80601-2-61:2011)
Particular requirements for the basic safety and essential performance of pulse oximeter
equipments for medical use.

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13. EN ISO 21647:2009 (ISO 80601-2-55:2011)
Medical electrical equipment -- Particular requirements for the basic safety and essential
performance of respiratory gas monitors
14. EN 980:2008 (EN ISO 15223-1:2012)
Symbols for use in the labeling of medical devices (Medical devices -- Symbols to be used with
medical device labels, labeling and information to be supplied -- Part 1: General requirements)
15. EN 1041:2008
Information supplied by the manufacturer of medical devices
16. IEC 60601-2-27:2006 : ECG Test
Medical electrical equipment - Part 2-27: Particular requirements for the safety including
essential performance, of electrocardiographic monitoring equipment
17. EN ISO 9919:2005
Medical electrical equipment -- Particular requirements for the basic safety and essential
performance of pulse oximeter equipment for medical use
18. EN 60601-2-34:2000 : IBP test
Medical electrical equipment –Part2: Particular requirements for the safety, including essential
performance, of invasive blood pressure monitoring equipment.

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1.2 Read before Use
BIONET services are always available to you.
The following are address and phone numbers for contacting information, services, and product
supplies.
How to Contact Us
Product Supply
Information
Bionet Ltd. –Sales Department
#1101 11F E&C Venture Dream Tower3 38-21, Digital-Ro, 31-Gil, Guro-
Gu, Seoul 08376, REPUBLIC OF KOREA
Overseas sales dept.
Tel:++82-2-6300-6410
Fax : ++82-2-6499-7789
E-mail : [e-mail]
URL : http:// www.ebionet.com
Refer to page.202 for more other country’s contact information
US Distributor
Bionet America, Inc.
2691 Dow Ave. Ste B
Tustin, CA 92780, USA
Toll Fee: 1-877-924-6638
Tel:[phone]
Fax: [phone]
www.bionetus.com
[email protected]
[email protected]
※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.

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Warranty Period
This product is manufactured and passed through strict quality control and through
inspection.
Compensation standard concerning repair, replacement, refund of the product complies
with “Consumer’s protection law” noticed by Korea Fair Trade Commission.
Warranty period is 4 years.( Four years in USA).
We will repair or replace any part of the BM3VET Touch found to be defective in usual
operating circumstance for free to you.
This warranty does not apply to any defects caused by improper use, misuse or abuse
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.
Indicated in this manual In order to improve the product specifications and features are subject to
change without notice.
Warning
To inform that it may cause serious injury or death to the patient, property damage, or material
losses
Caution
To inform that it may cause no loss in life but lead to injury
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 moisture.
Do not touch the equipment
with wet hands.
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 placing 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 inserting dust or
especially metal
material into the
equipment
Do not disjoint or disassemble
the equipment.
This will void your warranty..
Power off when the
equipment is not fully
installed.
Otherwise, equipment
could be damaged.

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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.

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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 sources of
interference as they may emit higher levels of electromagnetic radiation.
Also, keep cellular phones and other telecommunication equipment away from the monitor.

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CAUTIONS
Intended Use
This device is designed to be used for monitoring the biological vital signs of Canine and Feline and
horses. Main functions of the product include displaying information such as ECG, respiration, SpO2,
NIBP, carbon dioxide (CO2) and temperature on its LCD screen and monitoring parameter, and
alarming. It also prints out waves and parameters via a printer.
Application Environment
This device is for use by trained veterinary personnel in veterinary centers. The device is restricted
to be used on one patient at a time.
Operator Requirement
Only veterinary personnel who have read the Operator’s Manual should use this monitor
Instruction for Use
For continued safe use of this equipment, it is necessary that the instructions are followed. However,
instructions listed in this manual 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 Animal 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 and locality.
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 licensed veterinarian..
Supervised Use
This equipment is intended for use under the direct supervision of trained veterinary personnel in
veterinary centers. The device is restricted to be used on one patient at a time.
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.

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General Precaution on Electric Safety
Warning
Check the items listed below before operating the equipment.
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, BPM050S18F02
Made in BridgePower Co., Ltd.)
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 problems in the
product.)
5. The equipment should not be placed in the vicinity of electric generators, X-ray, broadcasting
apparatus to eliminate electrical noise during operation. Otherwise, it may cause incorrect results.
Note
The Equipment should be placed far from generators, X-ray equipment, broadcasting
equipment or transmitting wires, so as to prevent electrical noise from being generated during
operation, When these devices are near the Equipment, it can produce inaccurate
measurements. For BM3VET TOUCH 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 make contact with the Animal while operating the machine It may cause serious danger
to the users. Use only the provided cables.
A warning that other cables and accessories may negatively affect EMC performance
Warning
In case the Equipment does not operate as usual or damaged, do not use on Animal, and
contact to the medical equipment technician of the hospital or the equipment supply division.

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Note
BM3VET TOUCH is classified as follows:
- BM3VET TOUCH 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
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 .
Manufacturer’s declaration - electromagnetic emission
The BM3VET TOUCH system is intended for use in the electromagnetic environment specified below. The
customer or the user of BM3VET TOUCH system should ensure that it is used in such an environment
Emission test
Compliance
Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1
The BM3VET TOUCH 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 BM3VET TOUCH system is suitable for use in al
l establishments other than domestic and those di
rectly connected to the public low-voltage power su
pplies buildings used for domestic purposes.
Harmonics emission
IEC 61000-3-2
A
Voltage fluctuation
IEC 61000-3-3
Complies

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Manufacturer’s declaration - electromagnetic immunity
The BM3VET TOUCH system is intended for use in the electromagnetic environment specified below.
The customer or the user of the BM3VET TOUCH system should ensure 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 the user of the BM3VET
TOUCH system requires cont
inued operation during powe
r mains interruptions, it is re
c o m m e n d e d t h a t the
BM3VET TOUCH system be
powered from an uninterrupti
ble power supply or a batter
y
Note: Uт is the a.c. mains voltage prior to application of the test level.

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The BM3VET TOUCH system is intended for use in the electromagnetic environment specified belo
w.
The customer or the user of the BM3VET TOUCH system should ensure 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 BM3VET TOUCH system, includ
ing cables, than the recommended separati
on distance calculated from the equation a
pplicable to the frequency of the transmitte
r.
Recommended separation distance