Sun-Tech Vet30E User manual

Continuous Vital Signs Monitor
for Animals
User Manual

Changes
This manual is identified as part number: 80-0084-00-RevB. This manual is for use with Vet30E models M30AE and
M30BE. An updated version may be available for download from the SunTech Medical website. Should you notice
errors or omissions in this manual, please notify us at:
SunTech Medical, Inc.
507 Airport Boulevard, Suite 117
Morrisville, NC 27560 USA
Tel: [phone]
919.654.2300
Fax: [phone]
Email: [email protected]
Web: www.SunTechMed.com
Copyright Information
All content in this manual is the proprietary information of SunTech Medical and is provided solely for purposes of
operation of the SunTech Vet30E. This manual and the Vet30E described in it are protected under copyright law under
which they may not be copied, in whole or in part, without written consent of SunTech Medical.
The information in this manual is furnished for guidance only, is subject to change without notice, and should not be
construed as a commitment by SunTech Medical. SunTech Medical assumes no liability for errors or inaccuracies
that may appear in this manual.
© 2019 SunTech Medical. All rights reserved.
Other office location:
SunTech Medical, Inc.
507 Airport Blvd, #117
Morrisville, NC 27560-8200
Phone: [phone]
1-800-421-8626
Fax: [phone]
SunTech Medical, Ltd.
Oakfield Industrial Estate
Stanton Harcourt Road
Eynsham, Oxfordshire OX29 4TS
England
Phone: + 44 (0) 1865-884-234
Fax: + 44 (0) 1865-884-235
SunTech Medical (Shenzhen) Co., Ltd.
105 HuanGuan South Road, Suite 15 2~3/F
DaHe Community Guanlan,
LongHua District, Shenzhen
GuangDong PRC 518110
Tel: + 86-755-29588810
+ 86-755-29588986 (Sales)
+ 86-755-29588665 (Service)
Fax: + 86-755-29588829

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Welcome to the SunTech Vet30E
Thank you for choosing the Vet30E vital signs monitor! For over 30 years, SunTech Medical has been the preeminent
supplier of leading edge technology and innovative products to obtain blood pressure (BP) measurements.
Developed specifically for the veterinary care environment, the Vet30E can perform automatic BP, pulse oximetry
(SpO2), and body temperature measurements for veterinary professionals.
For measuring BP, a BP cuff is placed around the patient’s forelimb or tail. The cuff is inflated automatically and
blood pressure is determined by the oscillometric method, which senses pressure waves in the artery when occluded
by pressure in the cuff. Measurement of the frequency of the pressure waves enables heart rate to also be measured.
The pulse oximetry function measures the patient’s percent functional oxygen saturation of arterial hemoglobin using
principles of plethysmography via a SpO2sensor placed on the patient. Arterial oxyhemoglobin saturation is
determined by measuring the absorption of red and infrared light passing through the tissue. Changes in absorption
caused by pulsations of blood in the vascular bed are used to determine arterial saturation and pulse rate. The
Vet30E provides two options for SpO2: AccuVetTM or MasimoTM SET®. The oximeters require no routine calibration or
maintenance. The display features a pulse oximetry focus screen, which displays the SpO2plethysmograph. The
waveform is not normalized.
Temperature can be measured using a rectal temperature probe. The temperature probe contains a thermistor that
generates a voltage based on changes in temperature, and these voltages are recorded by the temperature circuitry.
The Vet30E is a portable device, weighing approximately 2.65 lb (1202 g). Control buttons allow the user to turn on or
off the device and stop/start a BP measurement. The touchscreen display shows the device status and measurement
information and allows for selection of settings. The device uses a microprocessor with software, which is not
accessible to the user. The unit is powered by a single rechargeable lithium-ion battery at the bottom of the device.
Bluetooth can be used to wirelessly connect and send data to a PC application, which may be downloaded from the
SunTech website at: https://www.suntechmed.com/Vet30E-data-capture.Upper and lower alarm limits can be set for
all parameters.
Intended Use
The SunTech Vet30E and Vet25E monitors are clinical grade automated blood pressure measurement devices that
provide oscillometric non-invasive blood pressure. The Vet30E provides additional pulse oximetry and temperature
measurement capabilities. These portable devices are for use in the veterinary clinic on companion animals (cats
and dogs) and horses. The devices can be used for spot-check or continuous monitoring activities. The devices are
not intended for human use.
The devices are contraindicated for use on humans or any species other than those described above.
Vet30E Essential Performance:
The Essential Performance of the Vet30E models are designed to measure, record, and display a patient’s blood
pressure within a blood pressure accuracy range of +/- 5 mmHg mean error & 8mm Hg standard deviation (max
inflate 280 mmHg).
Additionally, these models are designed to measure, record, and display a patient’s functional oxygen saturation over the
range of 70% to 100% with an increment of 1% within an accuracy of +/- 3%. These models shall also measure, record,
and display a patient’s continuous temperature within an accuracy of no greater than 0.3⁰C (+/- 3 digits) when
used with a minimum temperature range of 26⁰C to 46⁰C.
User Responsibility
The Vet30E is designed to perform in conformity with the description thereof contained in this operation manual
when operated. This operation manual is for use with Vet30E models M30AE and M30BE. The user of this monitor
shall have the sole responsibility for any malfunction which results from improper use, faulty maintenance, improper
repair, damage or alteration by anyone other than SunTech Medical or their authorized service personnel. The Vet30E
is for use only by or on the direction of a licensed veterinarian.

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Use of Vet30E
Use only veterinary BP cuffs supplied by SunTech Medical. Observe the patient carefully during the measurement.
Accuracy of any BP reading or oxygen saturation measurement may be affected by the position of the patient, their
physical condition and use outside of the operating instructions detailed in this guide. The interpretation of BP and
oxygen saturation measurements should only be made by a veterinarian.
AccuVet SpO2Module: Use only AccuVet SpO2 sensors supplied by SunTech Medical.
Masimo SET SpO2Module: Use only original Masimo SpO2sensors and cables.
Check the application site of the SpO2sensor frequently to confirm proper positioning of the sensor and to check the
circulation and skin sensitivity of the patient.

Table of Contents
Changes.................................................................... 2
Copyright Information.............................................. 2
Welcome to the SunTech Vet30E............................ 3
Intended Use ............................................................ 3
1. Warnings and Precautions................................. 6
2. Icons and Symbols ............................................ 8
3. Getting to Know SunTech Vet30E .....................10
3.1 Applied Parts and Patient Environment .......... 10
3.2 Device Placement ............................................ 10
3.3 Front Panel ....................................................... 11
3.4 Connect Power, Hose, and Sensors ................ 11
3.5 Display .............................................................. 14
3.6 Start/Stop Button ............................................. 16
4. Selecting Your Settings .....................................16
4.1 Animal Mode .................................................... 16
4.2 Volume ............................................................. 16
4.3 Settings............................................................. 16
5. Blood Pressure Measurement ...........................21
5.1 Cuff Sizing ........................................................ 21
5.2 Applying the Cuff and Taking a BP
Measurement on Small Animals ........................... 21
5.3 Applying the Cuff and Taking a BP
Measurement on Horses ....................................... 22
5.4 Interval BP Mode.............................................. 22
5.5 STAT Mode....................................................... 23
5.6 Interrupting/Stopping a Measurement ........... 23
5.7 Heart Rate Measurement ................................ 23
6. Temperature Measurement ...............................24
6.1 Where to Apply the Temperature Probe.......... 24
6.2 Taking a Temperature Measurement ............. 24
7. SpO2Measurement............................................24
7.1 Masimo Pulse Oximetry................................... 25
7.2 AccuVet Pulse Oximetry .................................. 28
7.3 Heart Rate Measurement ................................ 29
8. Reviewing and Transferring Data .......................29
8.1 Viewing Stored Measurements ....................... 29
8.2 Averaging Measurements ............................... 30
8.3 Bluetooth Connection ...................................... 30
8.4 Data Transfer ................................................... 31
8.5 Reviewing Data and Creating Reports............. 31
9. Alarms ..............................................................33
9.1 Technical Alarms ............................................. 33
9.2 Clinical Alarms ................................................. 34
10. Taking Care of the SunTech Vet30E .................34
10.1 Battery ............................................................ 34
10.2 Cleaning.......................................................... 34
10.3 Preventative Maintenance............................. 35
10.4 System Components ..................................... 36
10.5 Accessories & Replacement Parts................ 37
10.6 Status Messages ........................................... 38
10.7 SpO2Status Messages .................................. 39
11. Frequently Asked Questions ............................40
12. Limited Warranty............................................. 41
13. Technical Information ..................................... 42
13.1 Monitor Model Numbers ............................... 42
13.2 Factory Default Settings ................................ 42
13.3 Performance Specifications.......................... 43
13.4 Radio Frequency Compliance Requirements 45
13.5 Electromagnetic Compatibility (EMC)........... 45
Appendix A: Service Screens................................. 50
Service Information................................................ 50
Calibration Check................................................... 50
Air Leak Check........................................................ 51
Restore Factory Defaults ....................................... 52
Software Update .................................................... 53

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1.Warnings and Precautions
General warnings and cautions are listed here and repeated where relevant throughout this guide.
A WARNING indicates a situation which, if not avoided, could result in serious injury or death.
WARNING: DO NOT connect patient hose or monitor to any other devices or connections, especially intravenous (IV)
tubes as there is potential for air to be pumped into a blood vessel which could cause serious injury.
WARNING: DO NOT use in the presence of flammable anesthetics; this could cause an explosion. This device is not
suitable for use in an oxygen enriched environment.
WARNING: This monitor may cause radio interference or may disrupt the operation of nearby equipment. It may be
necessary to take mitigation measures such as re-orienting, relocating or shielding the location.
WARNING: The cuff should not be applied over a wound as this can cause further injury.
WARNING: DO NOT use a defibrillator, full body irradiation, or ultrasonic device on the patient at the same time as it
may affect the operation and/or safety of the patient due to interactions.
WARNING: DO NOT immerse the monitor in any fluid or attempt to clean the unit with liquid detergents, cleaning
agents, or solvents. This may cause an electrical hazard. Do not use the monitor if accidental wetting occurs. Refer
to the cleaning section of this guide for instructions on cleaning.
WARNING: Check the limb frequently to ensure that operation of the monitor does not result in prolonged
impairment of the circulation of the patient.
WARNING: DO NOT apply the BP cuff to a limb being used for IV infusions or any other intravascular access, therapy,
or an arteriovenous (A-V) shunt. The cuff inflation can temporarily block blood flow, potentially causing harm to the
patient.
WARNING: Pressurization of the cuff can temporarily cause loss of functionality of SpO2if simultaneously using
device on the same limb.
WARNING: DO NOT use if device is dropped and/or is damaged. Have a qualified service representative check the
unit before using again. Repairs should only be conducted by an authorized SunTech Medical service representative.
WARNING: Before performing a procedure when device is not plugged into main power, ensure there is sufficient
battery charge. If battery loses charge, device must be plugged into power supply to function.
WARNING: The USB port is only a service port and cannot be used to download data or interface with the monitor.
When updating the software, the monitor cannot be in use and the accessories should not be contacting the patient.
WARNING: Do not open the memory screen while readings are in progress. If the memory screen is open while pulse
oximetry or temperature readings are being taken, any new readings will not be added to memory, or be recoverable
in any way.
WARNING: As with all medical equipment, carefully route patient cabling to reduce the possibility of patient
entanglement or strangulation.
WARNING: Do not place the monitor or accessories in any position that might cause it to fall on the patient.
WARNING: Do not start or operate the monitor unless the setup was verified to be correct.
WARNING: Do not use the monitor during magnetic resonance imaging (MRI) or in an MRI environment.
WARNING: Do not use the monitor if it appears or is suspected to be damaged.
WARNING: Explosion hazard: Do not use the monitor in the presence of flammable anesthetics or other flammable
substance in combination with air, oxygen-enriched environments, or nitrous oxide.
WARNING: To ensure safety, avoid stacking multiple devices or placing anything on the device during operation.
WARNING: To protect against injury, follow the directions below:
•Avoid placing the device on surfaces with visible liquid spills.
•Do not soak or immerse the device in liquids.
•Do not attempt to sterilize the device.

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•Use cleaning solutions only as instructed in this operator's manual.
•Do not attempt to clean the device while monitoring a patient.
WARNING: To protect from electric shock, always remove the sensor and completely disconnect the monitor before
bathing the patient.
WARNING: If any measurement seems questionable, first check the patient’s vital signs by alternate means and then
check the monitor for proper functioning.
WARNING: The monitor should not be used as the sole basis for medical decisions. It must be used in conjunction
with clinical signs and symptoms.
WARNING: The monitor is not an apnea monitor.
WARNING: The monitor may not be used during electrocautery.
WARNING: The monitor should not be used for arrhythmia analysis.
WARNING: Do not adjust, repair, open, disassemble, or modify the monitor or accessories. Injury to personnel or
equipment damage could occur. Return the monitor for servicing if necessary.
A CAUTION indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate injury to
the user, patient or damage to the equipment or other property.
CAUTION: For use only by or on the direction of a licensed veterinarian. NOT for use on humans.
CAUTION: DO NOT use the monitor for any purpose other than specified in this manual without written consent and
approval from SunTech Medical.
CAUTION: DO NOT use this monitor when oscillometric pulses may be altered by other devices or techniques.
CAUTION: DO NOT disassemble device. Doing so may increase the risk of electrical shock. This monitor does not
contain any user serviceable parts except for the battery. Substitution of a component or accessory different from
that supplied may result in measurement error. Repairs should be undertaken only by personnel trained or authorized
by SunTech Medical.
CAUTION: DO NOT sterilize this device.
CAUTION: Too frequent measurements may cause injury to the patient due to blood flow interference.
CAUTION: At the end of product life, the monitor, accessories, components and other consumable goods may
become contaminated from normal use. Consult local codes and ordinances for proper disposal of equipment and
other consumable goods.
CAUTION: This device contains a lithium ion battery that contains materials which may be hazardous to human
health. DO NOT dispose of battery in domestic waste! Instead, please dispose of in an environmentally responsible
way, or return the battery to SunTech Medical. A prepaid return label can be obtained. Please see our website for
more information about our environmental policy at http://www.suntechmed.com/about-suntech/environmental-
policy.
CAUTION: Accuracy of any blood pressure measurement may be affected by the position of the subject, the patient’s
physical condition, and use outside of the operating instructions detailed in this manual. Interpretation of BP
measurement should be made only by a veterinarian or trained medical staff. Minimize limb movement during the
measurement.
CAUTION: A compressed or kinked connection hose may cause continuous cuff pressure resulting in blood flow
interference and potentially harmful injury to the patient. If the cuff fails to deflate, the operator should be instructed
on how to remove the cuff.
CAUTION: Performance can be affected if used or stored outside the specified temperature and humidity ranges.
CAUTION: Replace user replaceable parts that are broken, worn, missing, damaged, incomplete, or contaminated.
Contact SunTech Medical for service on parts that are not user replaceable and stop using device until repaired.
Failure to repair a damaged product may cause injury to the user and/or patient.
CAUTION: Do not place the monitor where the controls can be changed by the patient.

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CAUTION: Electrical shock and flammability hazard: Before cleaning, always turn off the device and disconnect from
any power source.
CAUTION: Do not place the monitor on electrical equipment that may affect the device, preventing it from working
properly.
CAUTION: To ensure that alarm limits are appropriate for the patient being monitored, check the limits each time the
monitor is used.
CAUTION: Electrical Shock Hazard: Carry out periodic tests to verify that leakage currents of patient-applied circuits
and the system are within acceptable limits as specified by the applicable safety standards. The summation of
leakage currents must be checked and in compliance with IEC 60601-1 and UL60601-1. The system leakage current
must be checked when connecting external equipment to the system. When an event such as a component drop of
approximately 1 meter or greater or a spillage of blood or other liquids occurs, retest before further use. Injury to
personnel could occur.
CAUTION: Disposal of product - Comply with local laws in the disposal of the device and/or its accessories.
CAUTION: To minimize radio interference, other electrical equipment that emits radio frequency transmissions
should not be in close proximity to the pulse oximeter.
2.Icons and Symbols
Some of the symbols, listed in the table below refer to the following FDA SDO Consensus standards:
•Recognition #5-103, ISO 7000: 2014: Graphical symbols for use on equipment - Registered symbols
•Recognition #5-116, ISO 7010: 2011: Graphical symbols - Safety colours and safety signs - Registered
safety signs
•Recognition #5-102, ISO 60417: 2002 DB: Graphical symbols for use on equipment
•Recognition #5-117, ISO 15223-1: 2016: Medical devices - Symbols to be used with medical device labels,
labelling, and information to be supplied - Part 1: General requirements
Symbol
Description
Standard/Source
General Warning Sign
ISO 7010-W001
Batch Code
ISO 7000-2492
Caution
ISO 7000-0434A
Classification –Class II
IEC 60417-5172
Refer to Instruction Manual
ISO 7010-M002
Authorized representative in the European Community
SunTech Design
USB-A or USB-B
Industry
Direct Current
IEC 60417-5031
Alternating Current
IEC 60417-5032
Polarity of DC power connector
IEC 60417-5926
Rechargeable battery
IEC 60417-5639
Consult Instructions for Use
ISO 7000-1641
This product meets the requirements of the applicable
Directives
EU Directive
Disposal in compliance with WEEE Directive
WEEE Directive

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Manufacturer
ISO 7000-3082
Date of Manufacture
ISO 7000-2497
Serial Number
ISO 7000-2498
Cuff index line must fall within range markings
SunTech Design
Arrow should be placed over artery
SunTech Design
Symbol indicating limb circumference
SunTech Design
Index line
SunTech Design
Not made with natural rubber latex
SunTech Design
Not made with PVC
SunTech Design
Reference Number
ISO 7000-2493
Type BF Applied Part
IEC 60417-5333
Fragile, handle with care
ISO 7000-0621
Humidity Limits
ISO 7000-2620
Temperature Limits
ISO 7000-0632
Keep Dry
ISO 7000-0626
Accesses Settings screen
SunTech Design
Small animal mode
SunTech Design
Large animal mode
SunTech Design
Equine mode
SunTech Design
Opens the Icon Menu
SunTech Design
Begins Interval BP Mode
SunTech Design
Adjusts volume
SunTech Design
View Memory
SunTech Design
Exits or closes a screen
SunTech Design
Goes back to previous screen
SunTech Design
Deletes all stored memory data
SunTech Design
Averages selected BP readings
SunTech Design
Begins STAT Mode
SunTech Design

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3.Getting to Know SunTech Vet30E
3.1 Applied Parts and Patient Environment
The applied parts are type BF. The following are the applied parts of the Vet30E:
•BP Cuffs
•SpO2 Sensors
•Temperature Probes
The Vet30E has been tested with specific parts of the system used within the patient environment. The parts of the
system that can be used in the patient environment are:
•Vet30E monitor
•All applied parts as defined above
•All accessories as defined in Section 10.5, excluding the AC Adapter
The patient environment is defined in the following diagram:
3.2 Device Placement
WARNING: As with all medical equipment, carefully route patient cabling to reduce the possibility of patient
entanglement or strangulation.
CAUTION: Do not position the monitor so that it is difficult to access and remove the AC adapter from the electrical
supply mains. The power supply is the means of disconnection to the supply mains.
Bluetooth
Bluetooth
Begins data transfer
SunTech Design
TIP:
Provides practical advice for using monitor
SunTech Design
Maximize or minimize a focus screen
SunTech Design
Standby (Powers device on/off)
IEC 60417-5009
Start/Stop a BP measurement
IEC 60417-5107B
IEC 60417-5110B
Battery Indicator
SunTech Design
IPX1
SpO2Sensors only: These items are protected against ingress
of vertically dripping water only
IEC 60529