Lutech DATALYS V Series User manual

Operator’s Manual
DATALYS V SERIES VETERINARY MONITORS
LUTECH VETERINARY INDUSTRIES, INC.
Queensland Office
Unit 6/1 Lear-Jet Drive,
Caboolture, Qld, 4510
Ph: 07 5428 3666
Fax: [phone]
Toll Free: 1300 785 401
E: [email protected]
Melbourne Office
17-19 Horne Street,
Hoppers Crossing, VIC, 3029
Ph: 03 9360 9700
Fax: [phone]
Toll Free: 1300 785 405
E: [email protected]
www.dlc.com.au

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Notice
Thank you for purchasing a Lutech Datalys multiparameter veterinary monitor. Before operating, please
read this manual carefully to ensure proper use. Please keep this Manual close by in a safe location for
future reference.
Product: Multiparameter Veterinary monitor.
Model: Datalys V Series: Datalys V5, Datalys V7
Structure and Components: The Datalys V series veterinary monitors consist of a master unit, display,
ECG cable and electrodes, SpO2 extension cord and probe, blood pressure tube and cuffs, and
temperature probes. Optionally, the monitor may include a printer, CO2 module and anesthesia gas
module.
Scope of Application: Monitors patient ECG, respiration rate (RESP), blood oxygen saturation (SpO2),
pulse rate (PR), noninvasive blood pressure (NIBP) and temperature (TEMP) as well as displays, reviews
and stores the monitoring information. If optional parameters are installed, the monitor also monitors
CO2 and anesthesia gas data and is able to print out specific data and waveforms upon request.
Manual Date of Issue: August 16, 2017
Manual Version: 2.0
NOTE: Throughout this operator’s manual, Lutech Veterinary Industries, Inc., Lutech, and
Company are used to mean the same thing.
Intellectual Property Rights
The intellectual property rights of this Operator’s Manual and the corresponding product belong to
Lutech.
This manual contains proprietary information protected by copyright law. Without written permission of
Lutech, no organization or individual is permitted to photograph, copy, modify or print any part of this
manual. Furthermore, without written permission of Lutech, no organization or individual is permitted to
translate this manual into any other language.
Lutech is not liable for any incidental or consequential damages due to errors in this Manual. Lutech does
not provide license conferred by patent law to any other parties. Lutech does not assume legal
responsibility for the legal consequences resulting from violating the patent law and the rights of any third
party.
Statement
Lutech reserves the right of final interpretation to this Manual. The content of this Manual is subject to
change without prior notice. Lutech will be responsible for the safety, reliability and performance of the
product only if the following requirements are met:

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•Assembly, expansion, re-adjustment, improvement and repair should only be performed by
qualified personnel approved by Lutech.
•All the replaced parts and supported accessories and consumables relate to the maintenance shall
be originally from Lutech or others approved by Lutech.
•The electrical equipment complies with relevant standards and the requirements of this Manual.
•The product is operated in accordance with this Manual.
•Lutech will make available upon request circuit diagrams, component part lists, descriptions,
calibration instructions, or other information that will assist service personnel to repair those parts
of equipment that are designated by Lutech as repairable by service personnel.
Service and Repair
Built to last and trained to serve, Lutech takes post sale services very seriously. Please contact Lutech via
the methods below to start your service request.
Phone: [phone]
Email: [e-mail]
Alternate email: [e-mail]
Website: www.lutechvet.com
Hours of operation: 9:00AM –5:00PM (EST)
Warranty Policy
The standard warranty period is 2 years for the main unit and 1 year for the main accessories. The main
accessories include: SpO2 extension cord and probe, ECG cable and leadwires, blood pressure tube,
temperature probe, power cord, and ground wire. Different distributors and packages may offer extended
warranty. Please ask your distributor or Lutech representative for more details.
Consumables are disposable materials that should be replaced after each use or wearing parts that should
be replaced periodically. The consumables are not covered by warranty except for open box failures.
The warranty period starts 30 days from the invoice date for the unit.
Lutech will be responsible for the safety, reliability and performance of the product if the following
requirements are met:
•The product is used in accordance with the Operator’s Manual.
•Product installation, repair and upgrade are carried out by personnel approved or authorized by
Lutech.
•The storage, operating and electrical environment meets product specifications.
•The S/N label or manufacturer logo of the product is clearly visible and not tampered with.
•The product is not physically damaged. (ex: the unit is dropped or something hit the unit causing
damage.)
Covered Under Warranty
For customers located within the United States who contact Lutech directly for service or repair, the
following are covered free of charge by the warranty:

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•Labor fees associated with the repair or service.
•Main unit parts replacement associated with the repair or service.
•Main accessories replacement associated with the repair or service when falling within
accessories warranty period.
•Loaner unit for the duration of the repair.
•Shipping of loan unit via ground shipment to and from the customer.
•Shipping of repaired unit back to the customer.
For customers located outside of the United States, Lutech may repair or service the unit or direct them to
a local distributor or service center that may be able to assist them with their repair or service needs.
Each distributor or service center will have their own repair procedures. However, the following should
remain covered free of charge by the warranty:
•Labor fees associated with the repair or service.
•Main unit parts replacement associated with the repair or service.
•Main accessories replacement associated with the repair or service when falling within
accessories warranty period.
Not Covered Under Warranty
For customers located outside of the United States, the following is not covered under the warranty if the
unit were to be repaired in the USA repair center:
•Any freight (including customs fees, duties or any other import/export fee) associated with the
import or export of the unit for repair or service. This includes shipping to and from the repair
center.
•Any freight (including customs fees, duties or any other import/export fee) associated with the
import or export of the loaner unit if one is available in that territory. This includes shipping to
and from the repair center.
Out of Warranty Repair and Service
For units that are no longer in warranty, contact your Lutech representative or distributor for service
information. Service and repair requests may also be made through Lutech’s website by filling out a
repair request form.
Return Process
NOTE: Please do not send anything to Lutech without first obtaining a Return Material
Authorization (RMA) number.
To request repair service, please follow the steps below:
1. Collect the following information:
a. Product Model Number
b. Serial Number
c. Customer Name

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d. Distributor Name (if applicable)
2. Contact Lutech to obtain an RMA number via one of the methods below:
a. Phone: [phone] (between 9:00AM –5:00PM EST)
b. Email: [e-mail]
c. Alternate email: [e-mail]
d. Website Form: www.lutechvet.com
3. Our customers are our priority. A response to a service inquiry will be sent within 24 business
hours of receiving the request via one of the above methods.
4. An RMA number will be provided once it is determined that the problem cannot be resolved
without sending the unit in to be serviced.
5. If a loaner has been requested, the customer will need to complete and return the loaner
agreement. The loaner will not be shipped unless the loaner agreement is completed, submitted
and approved by Lutech. The customer may use the loaner box to ship back the repair unit
should the loaner come before the repair unit is shipped out.
6. If a loaner unit is not necessary, the customer should send the unit back in its original packaging
whenever possible. If that is no longer available, the customer must package the unit very
carefully. Any damage during shipping will be the responsibility of the customer.
7. The RMA number must be written on the outside of the package so that it can be received
properly and in a timely manner. Otherwise, the repair may be delayed.
8. Once the repair unit is received, the unit will be diagnosed. If the unit is under warranty, it will
be repaired immediately. If it is out of warranty, a quote for repair is sent to the customer. Upon
customer approval and payment, the repair is made.
9. Once the repair is complete, the unit will be shipped back to the customer. The repaired unit must
be shipped in a proper packaging material. The customer will be charged a packaging material
fee should Lutech need to provide packaging to safely ship the unit back.
10. The customer will be asked to ship back the loaner unit as soon as the repaired unit has been
delivered per carrier record.
11. The customer will be sent a survey on Lutech’s service performance so that we can continuously
improve.
The turnaround time for a typical RMA cycle is 5 days or less once the repair unit has been received by
Lutech. Should additional time be necessary, Lutech will proactively alert the customers and maintain an
open line of communication.

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Contents
Notice........................................................................................................................................................ 2
Intellectual Property Rights ......................................................................................................................2
Statement ................................................................................................................................................. 2
Service and Repair .................................................................................................................................... 3
Warranty Policy.........................................................................................................................................3
Covered Under Warranty.......................................................................................................................... 3
Not Covered Under Warranty................................................................................................................... 4
Out of Warranty Repair and Service ......................................................................................................... 4
Return Process ..........................................................................................................................................4
Chapter 1: Manual Overview .....................................................................................................................13
1.1 Equipment Symbols ..........................................................................................................................13
1.2 Packaging Symbols............................................................................................................................14
Chapter 2: Safety.........................................................................................................................................15
2.1 Safety Instructions ............................................................................................................................15
2.2 Definition of Safety Terms ................................................................................................................15
2.2.1 DANGER......................................................................................................................................16
2.2.2 WARNING...................................................................................................................................16
2.2.3 CAUTION ....................................................................................................................................17
2.2.4 NOTE .......................................................................................................................................... 17
2.2.5 WARNING: Li-ion Battery ...........................................................................................................18
2.2.6 WARNING: Cleaning and Maintenance......................................................................................18
Chapter 3: Monitor Overview..................................................................................................................... 19
3.1 Overview ...........................................................................................................................................19
3.2 Composition and Structure...............................................................................................................19
3.2.1 Front View..................................................................................................................................19
3.2.2 Quick Access Buttons .................................................................................................................20
3.2.3 Side View –Connector Panel .....................................................................................................21
3.2.4 Side View –Printer.....................................................................................................................22
3.2.5 Rear View ................................................................................................................................... 22
Chapter 4: Preparing for Operation............................................................................................................24
4.1 Installation ........................................................................................................................................24
4.1.1 Unpacking and Checking............................................................................................................24

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4.1.2 Placement Requirements........................................................................................................... 24
4.1.3 Power Requirements .................................................................................................................24
4.1.4 Environmental Requirements ....................................................................................................24
4.2 Connecting to Power.........................................................................................................................25
Chapter 5: Basic Operation......................................................................................................................... 27
5.1 Turing the Monitor On...................................................................................................................... 27
5.2 Turning the Monitor Off....................................................................................................................27
5.3 Cable and Accessory Connection ......................................................................................................28
5.4 Mounting Solutions........................................................................................................................... 28
5.5 Screen Navigation .............................................................................................................................29
5.5.1 Accessing Menus........................................................................................................................29
5.5.2 Quick Access Icons .....................................................................................................................30
5.5.3 On Screen Keyboard...................................................................................................................32
5.5.4 The Main Setting Menu..............................................................................................................32
5.6 Operating Modes ..............................................................................................................................33
5.7 Display Modes...................................................................................................................................33
5.8 Volume Settings ................................................................................................................................ 34
5.9 Brightness Setting .............................................................................................................................35
5.10 Battery Status..................................................................................................................................35
5.11 Defining the Monitor ......................................................................................................................35
Chapter 6: Patient Information Management ............................................................................................37
6.1 Patient Setup Menu ..........................................................................................................................37
6.2 Quick Admit.......................................................................................................................................38
6.3 Admit Patient ....................................................................................................................................38
6.4 Discharge Patient ..............................................................................................................................39
6.5 Clear Alarm and Trend Info...............................................................................................................39
Chapter 7: Alarm.........................................................................................................................................40
7.1 Alarm Type ........................................................................................................................................ 40
7.2 Alarm Level........................................................................................................................................40
7.3 Alarm Method...................................................................................................................................41
7.3.1 Visual Alarm ...............................................................................................................................41
7.3.2 Audible Alarm ............................................................................................................................ 41
7.3.3 Alarm Message........................................................................................................................... 42

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7.3.4 Flashing Parameter ....................................................................................................................42
7.4 Alarm States......................................................................................................................................42
7.4.1 Alarm Reset................................................................................................................................42
7.4.2 Alarm Pause ...............................................................................................................................42
7.4.3 Alarm Audio Off .........................................................................................................................43
7.5 Alarm Setup.......................................................................................................................................43
7.6 Parameter Alarm Setup.....................................................................................................................44
7.6.1 ECG Alarm Setup ........................................................................................................................45
7.6.2 SpO2 Alarm Setup ......................................................................................................................45
7.6.3 NIBP Alarm Setup.......................................................................................................................46
7.6.4 Respiration Alarm Setup ............................................................................................................46
7.6.5 Temperature Alarm Setup .........................................................................................................47
7.6.6 IBP Alarm Setup .........................................................................................................................47
7.6.7 CO2 Alarm Setup........................................................................................................................ 48
7.6.8 Multigas/AG Alarm Setup ..........................................................................................................48
7.7 Manual Event .................................................................................................................................... 51
Chapter 8: ECG............................................................................................................................................ 52
8.1 Overview ...........................................................................................................................................52
8.2 Safety Information: ECG....................................................................................................................52
8.3 ECG Monitoring.................................................................................................................................53
8.3.1 Preparation for Electrodes.........................................................................................................53
8.3.2 Lead Name and Color.................................................................................................................53
8.3.3 Electrode Placement ..................................................................................................................53
8.3.4 Patient Position.......................................................................................................................... 55
8.4 ECG Display ....................................................................................................................................... 55
8.5 Monitoring Modes ............................................................................................................................56
8.6 ECG Setup..........................................................................................................................................56
8.7 Cleaning and Maintenance ...............................................................................................................57
8.8 Alarm Setup.......................................................................................................................................58
Chapter 9: Respiration ................................................................................................................................59
9.1 Overview ...........................................................................................................................................59
9.2 Safety Information ............................................................................................................................59
9.3 Skin Preparation and Electrode Placement ......................................................................................59

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9.4 Respiration Display ........................................................................................................................... 59
9.5 Respiration Setup..............................................................................................................................60
9.6 Alarm Setup.......................................................................................................................................61
Chapter 10: PR ............................................................................................................................................62
10.1 Overview ......................................................................................................................................... 62
10.2 PR Display........................................................................................................................................ 62
10.3 Setting PR Sound............................................................................................................................. 62
10.4 Alarm Setup.....................................................................................................................................62
Chapter 11: SpO2........................................................................................................................................63
11.1 Overview ......................................................................................................................................... 63
11.2 Safety Information ..........................................................................................................................63
11.3 Sensor Types ...................................................................................................................................63
11.4 Measuring SpO2..............................................................................................................................64
11.4.1 SpO2 Measurement Interference ............................................................................................64
11.5 SpO2 Display ...................................................................................................................................65
11.6 SpO2 Setup......................................................................................................................................66
11.6.1 Masimo SpO2 Setup.................................................................................................................66
11.6.2 Lutech SpO2 Setup................................................................................................................... 67
11.7 Cleaning and Disinfecting................................................................................................................67
11.8 Alarm Setup.....................................................................................................................................68
Chapter 12: NIBP.........................................................................................................................................69
12.1Overview..........................................................................................................................................69
12.2 Safety Information ..........................................................................................................................69
12.3 Patient Selection .............................................................................................................................70
12.4 Cuff Selection ..................................................................................................................................70
12.4 Cuff Placement................................................................................................................................71
12.5 Measuring NIBP...............................................................................................................................71
12.5.1 NIBP Measurement Interference.............................................................................................72
12.6 NIBP Display ....................................................................................................................................72
12.7 NIBP Setup ......................................................................................................................................73
12.8 Cleaning and Disinfecting................................................................................................................73
12.9 Alarm Setup.....................................................................................................................................74
Chapter 13: Temperature ...........................................................................................................................75

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13.1 Overview ......................................................................................................................................... 75
13.2 Safety Information ..........................................................................................................................75
13.3 Measuring Temperature .................................................................................................................75
13.4 Temperature Display.......................................................................................................................75
13.5 Temperature Setup.........................................................................................................................76
13.6 Probe Resistance Type....................................................................................................................76
13.7 Cleaning and Disinfecting................................................................................................................76
13.8 Alarm Setup.....................................................................................................................................76
Chapter 14: IBP ........................................................................................................................................... 77
14.1 Overview ......................................................................................................................................... 77
14.2 Safety Information ..........................................................................................................................77
14.3 IBP Module Activation ....................................................................................................................77
14.4 IBP Display....................................................................................................................................... 78
14.5 Measuring IBP .................................................................................................................................79
14.6 Zeroing the IBP Sensor....................................................................................................................79
14.7 IBP Setup.........................................................................................................................................79
14.8 Cleaning and Disinfecting................................................................................................................80
14.9 Alarm Setup.....................................................................................................................................80
Chapter 15: CO2..........................................................................................................................................81
15.1 Overview ......................................................................................................................................... 81
15.2 Safety Information ..........................................................................................................................81
15.3 CO2 Module Activation................................................................................................................... 81
15.4 CO2 Display .....................................................................................................................................82
15.5 Zeroing the CO2 Probe....................................................................................................................82
15.5.1 Zeroing Masimo CO2 probes ...................................................................................................82
15.5.2 Masimo CO2 Probe Alarms ...................................................................................................... 83
15.5.3 Zeroing Respironics CO2 probes ..............................................................................................83
15.6 Preparing for CO2 Measurement....................................................................................................84
15.7 Measuring CO2: Masimo ................................................................................................................ 84
15.7.1 IRMA: Mainstream...................................................................................................................85
15.7.2 ISA: Sidestream ........................................................................................................................85
15.8 Measuring CO2: Respironics ...........................................................................................................86
15.8.1 Capnostat 5: Mainstream ........................................................................................................86

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15.8.2 LoFlo: Sidestream.....................................................................................................................87
15.9 CO2 Setup ....................................................................................................................................... 87
15.10 Cleaning and Disinfecting.............................................................................................................. 87
15.11 Alarm Setup...................................................................................................................................88
Chapter 16: Multigas (AG) .......................................................................................................................... 89
16.1 Overview ......................................................................................................................................... 89
16.2 Safety Information ..........................................................................................................................89
16.3 Nomoline Sampling Lines................................................................................................................90
16.4 Multigas/AG Module Activation ..................................................................................................... 90
16.5 Multigas Display.............................................................................................................................. 91
16.6 Zeroing Masimo Sweden Multigas/AG probes ...............................................................................92
16.6.1 Zeroing Masimo Sweden Multigas/AG Probes ........................................................................92
16.6.2 Masimo Sweden Multigas/AG Probe Alarms........................................................................... 92
16.7 Preparing for Multigas Measurement ............................................................................................93
16.8 Measuring Multigas ........................................................................................................................93
16.8.1 IRMA AX+: Mainstream............................................................................................................93
16.8.2 ISA AX+ and ISA OR+: Sidestream.............................................................................................94
16.9 Multigas/AG Setup..........................................................................................................................94
16.10 Cleaning and Disinfecting.............................................................................................................. 95
16.11 Alarm Setup...................................................................................................................................95
Chapter 17: Trend ....................................................................................................................................... 96
17.1 Reviewing Trend Chart....................................................................................................................96
Chapter 18: Battery.....................................................................................................................................99
18.1 Overview ......................................................................................................................................... 99
18.2 Battery Status..................................................................................................................................99
18.2 Replacing the Battery......................................................................................................................99
18.3 Battery Usage Guide .....................................................................................................................100
18.4 Battery Storage .............................................................................................................................100
18.5 Checking Battery Performance .....................................................................................................100
18.6 Battery Recycling...........................................................................................................................101
Chapter 19: Cleaning.................................................................................................................................102
19.1 Overview ....................................................................................................................................... 102
19.2 Cleaning.........................................................................................................................................102

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19.3 Disinfecting ...................................................................................................................................103
Chapter 20: Maintenance .........................................................................................................................104
20.1 Checking the Monitor ...................................................................................................................104
20.1.1 Basic Check Up .......................................................................................................................104
20.1.2 Comprehensive Check Up ......................................................................................................104
20.2 Software Version........................................................................................................................... 104
20.3 Maintenance Plan .........................................................................................................................105
Chapter 21: Accessories............................................................................................................................106
21.1 Accessory List................................................................................................................................ 106
21.1.1 Standard Accessories .............................................................................................................106
21.1.2 Optional Accessories..............................................................................................................106
AppendixA: Specifications......................................................................................................................... 107
A.1 Safety Specifications .......................................................................................................................107
A.2 Power Specifications.......................................................................................................................107
A.3 Dimension and Weight.................................................................................................................... 107
A.4 Parameter Specifications ................................................................................................................108
A.4.1 ECG...........................................................................................................................................108
A.4.2 SpO2......................................................................................................................................... 108
A.4.3 NIBP .........................................................................................................................................108
A.4.4 Temperature............................................................................................................................ 109
A.4.5 Respiration...............................................................................................................................109
A.4.6 IBP............................................................................................................................................109
A.4.7 CO2 ..........................................................................................................................................109
A.4.8 Multigas / AG ...........................................................................................................................110

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Chapter 1: Manual Overview
1.1 Equipment Symbols
These symbols are used on the Datalys V series monitors:
Symbol
Definition
DC power supply
Defibrillation-proof type CF applied part
Network interface
USB interface
Power adapter
Fuse
Equipotentiality
Power ON/OFF
Alternating
Current Earth Connector
Notified body code
Liquid protection class
Waste electrical and electronic equipment directive
Production date
Serial number
EU representative
Manufacturer info
Caution: U.S. federal law restricts this device for sale to or on the order
of a veterinarian.

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1.2 Packaging Symbols
These symbols are used on the packaging material for the Datalys V series monitors:
Symbol
Definition
Keep upright
Fragile, handle with care
Maximum stacking
Keep dry

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Chapter 2: Safety
2.1 Safety Instructions
The Datalys V series monitors meet the requirements of the IEC 60601-1: 2005 + A1: 2012 medical
electrical equipment general requirement for basic safety and essential performance standard, Class I, CF
type equipment, and complies with IEC 60601-1: 2005 + A1: 2012 part of electric shock protection
provisions. It also has anti-defibrillation capabilities.
Classifications:
Type of electric shock protection
Class I: internal and external power supply equipment. When the
integrity of the external protective earth or protective ground
conductor parameter of the equipment is in question, the device
must be powered by the internal power supply (battery).
Electric shock protection grade
ECG/NIBP /SpO2/PR/TEMP/RESP: CF (defibrillation
protection)
Explosion protection grade
Common equipment. No explosion protection.
Liquid inlet protection grade
IPX1 (prevents water from entering when the water drips
vertically)
Operating mode
Continuous
Movement
Portable
WARNING:
•Before using the monitor, the monitor and its attachments/accessories, etc. must be checked
for damage that may affect patient safety. If obvious damage or aging is found, the
attachment/accessory/part should be replaced before use. Only use parts and accessories
recommended by the manufacturer.
•The monitor must be maintained by authorized and qualified engineers. If not, Lutech will
not be responsible for monitor safety, reliability and performance.
2.2 Definition of Safety Terms
The following are symbols used in this operator’s manual:
Term
Definition
DANGER
Indicates an imminent hazard that, if not avoided, will result in death or
serious injury.
WARNING
Indicates a potential hazard or unsafe practice that, if not avoided, will
result in death or serious injury.
CAUTION
Indicates a potential hazard or unsafe practice that, if not avoided, could
result in minor personal injury or product/property damage.
NOTE
Emphasize important considerations or provides application tips or
other useful information to ensure that you get the most from your
product.

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2.2.1 DANGER
There are no known Dangers.
2.2.2 WARNING
•This monitor is intended for clinical veterinary monitoring and therefore, only trained and
qualified veterinary personnel may use this monitor.
•Before operating, the user must check the device to ensure its cables and accessories are
functioning properly and safely.
•The alarm volume, upper and lower alarm limit should be set according to the actual situation of
the patient.
•Never rely exclusively on the audio alarm system while monitoring the patient. Low alarm
volume or alarm failure may endanger patient safety. Please pay close attention to the actual
clinical situation of the patient.
•This device can only be connected to a grounded electrical outlet. Do not use any outlet that is
not properly connected to the ground wire. When in doubt, use the built-in rechargeable batteries.
•Do not position the device near the wall or other barriers as it makes it difficult to de-energize.
•Do not open the enclosure as it may cause an electric shock. Any repair, maintenance or upgrade
of the monitor must be performed by service personnel trained and/or authorized by Lutech.
•When handling packaging materials, abide by local laws and regulations or hospital waste
disposal regulations. Keep the packaging materials away from children.
•Do not use the monitor in a location where flammable gases such as anesthetics are not properly
contained and treated to prevent explosion or fire.
•Please connect and manage power and accessory cables carefully to avoid patient entanglement
or suffocation, cable entanglement or electrical interference.
•Any devices connected to the monitor should form an equipotential body (protective grounding
effectively connected).
•When the monitor is used together with electrosurgical devices, a properly trained veterinary
personnel should ensure the safety of the patient and instrument.
•The physiological data, waveform and alarm system displayed on the monitor is for reference
only and should not be directly used as the basis for clinical treatment.
•This is not a therapeutic unit.
•All analog and digital devices connected to the monitor must be certified by IEC standards (e.g.,
IEC 60950 Data Processing Equipment Standard and IEC 60601-1 Medical Equipment Standard).
Furthermore, all configurations shall comply with the valid version of IEC 60601-1 standard. The
personnel connecting additional devices to the input / output signal ports are responsible for the
compliance with IEC 60601-1 standard. If there are any questions, please contact Lutech.
•If the patient cable interface and network interface are connected with multiple devices, the total
electric leakage cannot exceed the allowable value.
•The copyright of the monitor software belongs to Lutech. Without permission, any organization
or individual shall not interpolate, copy or exchange by any means or form.
•When the monitor is combined with other devices, it must comply with IEC60601-
1:2005+A1:2012 and shouldn’t be connected with multi-socket wire board or extension cord.
•Do not connect the device on other equipment or NETWORK/DATA COUPLINGS, to which a
SIGNAL INPUT/OUTPUT PART may be connected.

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2.2.3 CAUTION
•To avoid damage to the monitor and to ensure patient safety, please only use the accessories
specified in this Manual.
•Make sure to install or transport the monitor properly to prevent damage due to falling, collision,
strong vibration or other mechanical forces.
•Avoid splashing the monitor with water.
•Avoid high temperatures. The monitor should be used within a temperature range of 41oF
~104oF (5oC ~40oC).
•Avoid using the monitor within an environment with high pressure, poor ventilation, high
concentrations of dust, salt, sulfur gas and/or other chemicals.
•Electromagnetic fields may affect the performance of the monitor. The use of devices within the
vicinity of the monitor must comply with relevant EMC requirements. For example: mobile
phone, X-ray or MRI equipment is likely to be a source of interference, since they will transmit
high intensity electromagnetic radiation.
•Before powering on the monitor, make sure that the power used by the monitor complies with the
supply voltage and frequency requirements.
•The monitor should be tested at least once a year by trained and qualified personnel. If there are
any problems detected by these maintenance tests, the monitor must be repaired or replaced
immediately.
•At the end of its life cycle, the monitor and/or accessories must be disposed of in accordance with
relevant local laws and regulations.
•Do not connect the monitor to unapproved network devices or equipment as it may cause
electrical damage to the monitor.
•SHOCK HAZARD –Do not connect non-medical electrical equipment, which has been supplied
as a part of the system, directly to the wall outlet when the non-medical equipment is intended to
be supplied by a multiple portable socket-outlet with an isolation transformer.
•SHOCK HAZARD –Do not connect electrical equipment, which has not been supplied as a part
of the system, to the multiple portable socket-outlets supplying the system.
•Do not connect any equipment or accessories that are not approved by the manufacturer or that
are not IEC/EN 60601-1-1 approved for the electrocardiograph. The operation or use of non-
approved equipment or accessories with the electrocardiograph is not tested or supported, and
electrocardiograph operation and safety are not guaranteed.
•Parts and accessories used must meet the requirements of the applicable IEC/EN 601 series safety
standards, and/or the system configuration must meet the requirements of the IEC/EN 60601-1-1
medical electrical systems standard.
•Ensure that the conductive parts of electrodes and associated connectors, including neutral
electrodes, do not come in contact with earth or any other conducting objects.
•The Monitor should only be used on one patient at a time.
2.2.4 NOTE
•Install the monitor in a location that is easy for observation, operation and maintenance.
•Keep the Operator’s Manual near the monitor for easy reference.

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2.2.5 WARNING: Li-ion Battery
•Improper operation may cause the internal li-ion battery (hereinafter called battery) to become
heated or to ignite or explode. It may also lead a decrease in battery capacity. Please read the
Operator’s Manual carefully and thoroughly before operating the monitor.
•Do not reverse the anode and the cathode when installing the battery as it may cause an
explosion.
•Do not use the battery near a fire or in an environment where the temperature exceeds 140oF
(60℃).
•Do not heat the battery or throw it into fire.
•Do not splash the battery or throw it into water.
•Do not destroy the battery. Do not pierce, hit, step on, throw, drop, shock, or physically damage
the battery in any way.
•Do not disassemble or modify the battery as it could lead to overheating, smoking, deformation,
burning, or other dangerous results.
•If leakage or foul smell is found, stop using the battery immediately. If your skin or clothes come
into contact with the leakage liquid, cleanse it with clean water at once. If the leakage liquid
splashes into your eyes, do not wipe them. Irrigate them with clean water first and go see a doctor
immediately.
•Only qualified service engineers authorized by the manufacturer can open the battery
compartment and replace the battery.
•Only use batteries made specifically for this monitor.
•Properly dispose of or recycle the depleted battery according to local rules and regulations.
2.2.6 WARNING: Cleaning and Maintenance
•Turn off the power before cleaning and disinfecting. The mains supply must be switched off if it
is used, and the power cord and any patient cables must be removed.
•Do not allow any detergent to seep into the monitor.
•Never immerse the monitor and patient cables in liquid.
•Do not clean the monitor and accessories with abrasive fabric and avoid scratching the electrodes.
•Any remainder of detergent should be removed from the unit and the patient cable after cleaning.
•Do not use high-temperature, high-pressure vapor or ionizing radiation as disinfection methods.
Do not use chloric disinfectant such as chloride, sodium hypochlorite etc.

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Chapter 3: Monitor Overview
3.1 Overview
The Datalys V series veterinary monitors measures, records and displays the physiological data from a
patient such as ECG, NIBP, SpO2, respiration, temperature, CO2, IBP, and anesthesia gases. The data is
compared to preset values within each parameter and an alarm is given should any parameter value falls
over or under the preset values. The Datalys V series veterinary monitors are to be used by trained
veterinary personnel in veterinary hospitals or clinics. The monitor can only be used on one patient at a
time. There are no relevant contraindications.
3.2 Composition and Structure
The Datalys V series veterinary monitors consist of a master unit, display, ECG cable, SpO2 probe, blood
oxygen cuff, temperature probe, and a built-in lithium ion battery.
3.2.1 Front View
Figure 3.2.1-1 Datalys V series front view reference photo.
NOTE: The power button for the Datalys V series monitors is located on the side containing the
parameter connector panel. Please reference section 2.2.3 Side View –Connector Panel for more
details.