Mindray BeneFusion eSP Vet User manual

BeneFusion eSP Vet
Veterinary Syringe Pump
Operator’s Manual

I
© Copyright 2021 Shenzhen Mindray Animal Medical Technology Co., LTD. All rights
reserved.
Release date: 2021-04
Revision: 1.0

II
Intellectual Property Statement
Shenzhen Mindray Animal Medical Technology Co., LTD. (hereinafter called Mindray
Animal Medical) owns the intellectual property rights to this product and this manual.
This manual may refer to information protected by copyright or patents and does not
convey any license under the patent rights or copyright of Mindray Animal Medical, or of
others.
Mindray Animal Medical intends to maintain the contents of this manual as confidential
information. Disclosure of the information in this manual in any manner whatsoever
without the written permission of Mindray Animal Medical is strictly forbidden.
Release, amendment, reproduction, distribution, rental, adaptation, translation or any
other derivative work of this manual in any manner whatsoever without the written
permission of Mindray Animal Medical is strictly forbidden.
is the trademark of SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO.,
LTD. in China and other countries. All other trademarks that appear in this manual are
used only for informational or editorial purposes. They are the property of their
respective owners.
Responsibility on the Manufacturer Party
Contents of this manual are subject to changes without prior notice.
All information contained in this manual is believed to be correct. Mindray Animal
Medical shall not be liable for errors contained herein nor for incidental or consequential
damages in connection with the furnishing, performance, or use of this manual.
Mindray Animal Medical is responsible for the effects on safety, reliability and
performance of this product, only if:
■all installation operations, expansions, changes, modifications and repairs of this
product are conducted by Mindray Animal Medical authorized personnel;
■the electrical installation of the relevant room complies with the applicable
national and local requirements;
■the product is used in accordance with the instructions for use.

III
Warranty
THIS WARRANTY IS EXCLUSIVE AND IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESSED
OR IMPLIED, INCLUDING WARRANTIES OF MERCHANTABILITY OR FITNESS FOR ANY
PARTICULAR PURPOSE.
Exemptions
Mindray Animal Medical's obligation or liability under this warranty does not include any
transportation or other charges or liability for direct, indirect or consequential damages
or delay resulting from the improper use or application of the product or the use of parts
or accessories not approved by Mindray Animal Medical or repairs by people other than
Mindray Animal Medical authorized personnel.
This warranty shall not extend to
■Malfunction or damage caused by improper use or man-made failure.
■Malfunction or damage caused by unstable or out-of-range power input.
■Malfunction or damage caused by force majeure such as fire and earthquake.
■Malfunction or damage caused by improper operation or repair by unqualified or
unauthorized service people.
■Malfunction of the instrument or part whose serial number is not legible enough.
■Others not caused by instrument or part itself.
Company Contact
Manufacturer: Shenzhen Mindray Animal Medical Technology Co., LTD.
Address: Room 702, Tower 4, YESUN Intelligent Community III, No.1301-88
Guanguang Road, Xinlan Community, Guanlan Street, Longhua
District, Shenzhen 518110, P. R. China
Website: www.mindrayanimal.com
E-mail Address: [e-mail]
Tel: [phone]
Fax: [phone]

IV
Preface
Manual Purpose
This manual contains the instructions necessary to operate the product safely and in
accordance with its function and intended use. Observance of this manual is a
prerequisite for proper product performance and correct operation and ensures patient
and operator safety.
This manual is based on the maximum configuration and therefore some contents may
not apply to your product. If you have any question, please contact us.
This manual is an integral part of the product. It should always be kept close to the
equipment so that it can be obtained conveniently when needed.
Intended Audience
This manual is geared for clinical professionals who are expected to have a working
knowledge of medical procedures, practices and terminology as required for monitoring
of critically ill patients.
Illustrations
All illustrations in this manual serve as examples only. They may not necessarily reflect
the setup or data displayed on your equipment.
Conventions
■Italic text is used in this manual to quote the referenced chapters or sections.
■Bold text is used to indicate the screen texts.
■→is used to indicate operational procedures.

1
Contents
1 Safety ..........................................................................................................................................1 - 1
1.1 Safety Information .......................................................................................................................................1 - 1
1.1.1 Warnings ..........................................................................................................................................1 - 1
1.1.2 Cautions ............................................................................................................................................1 - 2
1.1.3 Notes ..................................................................................................................................................1 - 3
1.2 Equipment Symbols ....................................................................................................................................1 - 3
2 Equipment Introduction ............................................................................................................2 - 1
2.1 Intended Use ..................................................................................................................................................2 - 1
2.2 Applied Part ....................................................................................................................................................2 - 1
2.3 Main Unit .........................................................................................................................................................2 - 1
2.3.1 Front View ........................................................................................................................................2 - 1
2.3.2 Rear View ..........................................................................................................................................2 - 4
2.3.3 Bottom View ...................................................................................................................................2 - 5
2.4 Screen Display ...............................................................................................................................................2 - 5
2.4.1 On-screen Symbols .......................................................................................................................2 - 6
2.4.2 Menus ................................................................................................................................................2 - 7
2.4.3 Operation Keys ...............................................................................................................................2 - 7
2.4.4 Using the Touchscreen ...............................................................................................................2 - 8
2.4.5 Using the On-Screen Keyboard ................................................................................................2 - 9
3 Equipment Preparation .............................................................................................................3 - 1
3.1 Equipment Preparation Safety Information .......................................................................................3 - 1
3.2 Environmental Requirements ..................................................................................................................3 - 2
3.3 Installation ......................................................................................................................................................3 - 2
3.3.1 Pole Clamp Installation ...............................................................................................................3 - 2
3.3.2 Stack Rack Installation .................................................................................................................3 - 2
3.4 Setting Up the Equipment ........................................................................................................................3 - 3
3.4.1 Connecting the AC Mains ..........................................................................................................3 - 3
3.4.2 Charging the Battery ....................................................................................................................3 - 3
3.4.3 Adjusting the Screen Brightness .............................................................................................3 - 4
3.4.4 Setting the Date and Time .........................................................................................................3 - 4
4 Getting Started ...........................................................................................................................4 - 1
4.1 Quick Start Guide ..........................................................................................................................................4 - 1
4.2 Setting Up the Pump ...................................................................................................................................4 - 1
4.3 Loading the Syringe ....................................................................................................................................4 - 2
4.4 Starting Infusion ............................................................................................................................................4 - 4
4.5 Purge .................................................................................................................................................................4 - 5
4.6 Bolus Infusions ...............................................................................................................................................4 - 5
4.6.1 Setting the Bolus Rate .................................................................................................................4 - 6

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4.6.2 Automatic Bolus Infusion ...........................................................................................................4 - 6
4.6.3 Manual Bolus Infusion .................................................................................................................4 - 6
4.6.4 Setting the Bolus Volume Unit .................................................................................................4 - 7
4.7 Changing the Infusion Parameters ........................................................................................................4 - 7
4.8 Pausing the Infusion ....................................................................................................................................4 - 7
4.9 Setting Keep Vein Open (KVO) Rate .......................................................................................................4 - 7
4.10 Unloading a Syringe ..................................................................................................................................4 - 8
4.11 Viewing the Infused Volume ..................................................................................................................4 - 9
4.12 Entering the Standby Mode ................................................................................................................ 4 - 10
4.13 Turning Off the Pump ............................................................................................................................ 4 - 10
5 Using the Dock ............................................................................................................................5 - 1
5.1 Securing the Pump in the Dock ..............................................................................................................5 - 1
5.2 Relay Infusion .................................................................................................................................................5 - 2
5.2.1 Setting up a Relay Infusion ........................................................................................................5 - 2
5.2.2 Canceling the Relay ......................................................................................................................5 - 2
5.3 Performing Day’s Prescription .................................................................................................................5 - 3
5.4 Configuring Pumps in Batches through the Dock ............................................................................5 - 3
6 Alarms .........................................................................................................................................6 - 1
6.1 Alarm Safety Information ..........................................................................................................................6 - 1
6.2 Understanding the Alarms ........................................................................................................................6 - 1
6.2.1 Alarm Priorities ...............................................................................................................................6 - 1
6.2.2 Alarm Indicators ............................................................................................................................6 - 1
6.2.3 Alarm Screen ...................................................................................................................................6 - 2
6.3 Resetting Alarms ...........................................................................................................................................6 - 3
6.4 Pausing Alarm Sound ..................................................................................................................................6 - 3
6.5 Setting the Alarm Sound ...........................................................................................................................6 - 4
6.5.1 Setting the Alarm Volume .........................................................................................................6 - 4
6.5.2 Setting the Alarm Sound Mode ...............................................................................................6 - 4
6.6 Nurse Call .........................................................................................................................................................6 - 4
6.7 Alarm Solutions .............................................................................................................................................6 - 5
6.8 Occlusion Alarm ............................................................................................................................................6 - 8
7 Menu Options .............................................................................................................................7 - 1
7.1 Main Menu Options .....................................................................................................................................7 - 1
7.2 General Option ..............................................................................................................................................7 - 1
7.3 System Options .............................................................................................................................................7 - 3
8 Infusion Modes ...........................................................................................................................8 - 1
8.1 Rate Mode/Time Mode ...............................................................................................................................8 - 1
8.2 Dose Mode ......................................................................................................................................................8 - 2
8.3 Loading Dose Mode ....................................................................................................................................8 - 2

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8.4 Micro-infusion Mode ...................................................................................................................................8 - 3
8.5 Sequential Mode ...........................................................................................................................................8 - 3
8.5.1 Adding/Deleting Sequences .....................................................................................................8 - 3
8.5.2 Changing the Infusion Parameters .........................................................................................8 - 4
8.6 Intermittent Mode ........................................................................................................................................8 - 4
8.7 Ramp Mode ....................................................................................................................................................8 - 5
8.8 Dose Time Mode ...........................................................................................................................................8 - 5
9 Drug Library/Drug Info Library .................................................................................................9 - 1
9.1 Importing the Drug Library/Drug Info Library ...................................................................................9 - 1
9.2 Dose Error Reduction Systems (DERS) ..................................................................................................9 - 2
9.2.1 Hard Limits ......................................................................................................................................9 - 2
9.2.2 Soft Limits ........................................................................................................................................9 - 2
9.3 Predefining the Infusion Mode ................................................................................................................9 - 2
10 Managing Patient ...................................................................................................................10 - 1
10.1 Discharging/Admitting a Patient ...................................................................................................... 10 - 1
10.2 Editing Patient Information ................................................................................................................. 10 - 1
10.3 Exporting Patient Information ........................................................................................................... 10 - 1
10.4 Importing Patient Information ........................................................................................................... 10 - 2
11 Password Protected Settings ................................................................................................11 - 1
11.1 Accessing the User Maintenance Menu ......................................................................................... 11 - 1
11.2 The Device Management Settings .................................................................................................... 11 - 1
11.3 The Patient Information Settings ...................................................................................................... 11 - 1
11.4 System Calibration .................................................................................................................................. 11 - 2
11.5 Network Setup ......................................................................................................................................... 11 - 2
11.5.1 The WLAN Settings ................................................................................................................. 11 - 2
11.5.2 The WLAN IP Settings ............................................................................................................. 11 - 2
11.5.3 The Central Station Setup ..................................................................................................... 11 - 3
11.5.4 The Device Discover Settings .............................................................................................. 11 - 3
11.6 The Brand Management ....................................................................................................................... 11 - 3
11.7 The Time and Language Settings ..................................................................................................... 11 - 4
11.8 The Parameter Switch Settings .......................................................................................................... 11 - 4
11.9 The Unit Settings ..................................................................................................................................... 11 - 4
11.10 Viewing the Version Information .................................................................................................... 11 - 5
11.11 The Alarm Settings ............................................................................................................................... 11 - 5
11.12 The Bolus Volume Unit Settings ...................................................................................................... 11 - 5
11.13 The Bolus Limit Settings ..................................................................................................................... 11 - 5
11.14 The Purge Limit Settings .................................................................................................................... 11 - 6
11.15 The Parameter Memory Setting ...................................................................................................... 11 - 6
11.16 The Loading Guide Setting ............................................................................................................... 11 - 6
11.17 The Brand Selection Setting ............................................................................................................. 11 - 6

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11.18 The Auto-Restart Setting ................................................................................................................... 11 - 6
11.19 The Concentration Setting ................................................................................................................ 11 - 7
11.20 Modify the Password ........................................................................................................................... 11 - 7
11.21 Import and Export ................................................................................................................................ 11 - 7
12 Maintenance ...........................................................................................................................12 - 1
12.1 Maintenance Safety Information ....................................................................................................... 12 - 1
12.2 Maintenance and Testing Schedule ................................................................................................. 12 - 2
12.3 Testing Methods and Procedures ..................................................................................................... 12 - 2
12.3.1 Performing Visual Inspection .............................................................................................. 12 - 3
12.3.2 Performing Power-on Test ................................................................................................... 12 - 3
12.3.3 Checking the Battery .............................................................................................................. 12 - 3
12.4 Maintaining the Battery ........................................................................................................................ 12 - 3
12.4.1 Battery Safety Information ................................................................................................... 12 - 3
12.4.2 Installing the Battery .............................................................................................................. 12 - 4
12.4.3 Charging the Battery .............................................................................................................. 12 - 5
12.4.4 Conditioning the Battery ...................................................................................................... 12 - 5
12.5 Checking Version Information ........................................................................................................... 12 - 6
12.6 Checking the History Record .............................................................................................................. 12 - 6
12.7 Exporting the History Record ............................................................................................................. 12 - 6
12.8 Disposing of the Equipment ............................................................................................................... 12 - 7
13 Care and Cleaning ..................................................................................................................13 - 1
13.1 Care and Cleaning Safety Information ............................................................................................ 13 - 1
13.2 Cleaning the Equipment ...................................................................................................................... 13 - 2
13.3 Disinfecting the Equipment ................................................................................................................ 13 - 2
13.4 Cleaning the Pole Clamp and Stack Rack ....................................................................................... 13 - 5
13.5 Disinfecting the Pole Clamp and Stack Rack ................................................................................. 13 - 5
13.6 Sterilization ............................................................................................................................................... 13 - 6
13.7 Impact of Improper Cleaning ............................................................................................................. 13 - 6
14 Accessories ..............................................................................................................................14 - 1
A Product Specifications .............................................................................................................. A - 1
A.1 Classifications ............................................................................................................................................... A - 1
A.2 Environmental Specifications ................................................................................................................. A - 1
A.3 Power Supply Specifications ................................................................................................................... A - 2
A.3.1 External Power Supply Specifications .................................................................................. A - 2
A.3.2 Battery............................................................................................................................................. A - 2
A.4 Physical Specifications .............................................................................................................................. A - 2
A.5 Hardware Specifications ........................................................................................................................... A - 3
A.5.1 Displays ........................................................................................................................................... A - 3
A.5.2 LEDs .................................................................................................................................................. A - 3
A.5.3 Audio Indicator ............................................................................................................................. A - 3

5
A.5.4 Interface Specifications ............................................................................................................. A - 3
A.5.5 Signal Output Specifications ................................................................................................... A - 3
A.6 Wireless Network ........................................................................................................................................ A - 4
A.7 Infusion Specifications .............................................................................................................................. A - 4
A.8 Recommended Syringes .......................................................................................................................... A - 6
A.9 Occlusion Alarm Delay and Bolus Volume ......................................................................................... A - 7
A.10 Infusion Accuracy Graphs ...................................................................................................................... A - 8
A.10.1 Infusion Accuracy at 1 ml/h ................................................................................................... A - 8
A.10.2 Infusion Accuracy at 5ml/h .................................................................................................... A - 9
B EMC and Radio Regulatory Compliance ...................................................................................B - 1
B.1 EMC ....................................................................................................................................................................B - 1
B.2 Radio Regulatory Compliance .................................................................................................................B - 7
C Abbreviations .............................................................................................................................C - 1
D Declaration of Conformity ....................................................................................................... D - 1

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1 - 1
1Safety
1.1 Safety Information
WARNING
•Indicates a potential hazard or unsafe practice that, if not avoided, could
result in death, serious injury or damage to product/property.
CAUTION
•Indicates a potential hazard or unsafe practice that, if not avoided, could
result in minor personal injury, product malfunction or damage to product/
property.
NOTE
•Provides application tips or other useful information to ensure that you get
the most out of the product.
1.1.1 Warnings
WARNING
•To avoid risk of electric shock, the equipment must only be connected to
mains power with protective earth. If a protective earth conductor is not
provided, operate it on battery power, if possible.
•To avoid explosion hazard, do not use the equipment in the presence of
oxygen-rich atmospheres, flammable anesthetics, or other flammable
agents.
•The equipment is not intended to be used within the Magnetic Resonance
(MR) environment.
•Do not use the multiple portable socket outlets (MPSO) or AC mains
extension cords. Ensure that the sum of the individual ground leakage
currents does not exceed the allowable limits.
•Do not open the equipment housings. All servicing and future upgrades must
be carried out by trained and authorized personnel.

1 - 2
•Do not place the equipment or accessories in any position that might cause it
to fall on the patient.
•Do not start an infusion unless the setup was verified to be correct.
•To avoid inadvertent disconnection, route all cables in a way to prevent a
stumbling hazard. Wrap and secure excess cabling to reduce risk of
entanglement by patients or personnel.
•Clearing the occlusion result from line kinks, filter coagulation, etc. may
cause extra bolus to patients. Appropriate measures should be taken.
•Check that the syringe and the extension set are securely connected and
there is no leakage.
•Do not touch the patient and device connectors simultaneously. Otherwise
leakage current may result in patient injury.
•To avoid electric shock, do not touch patient and other non-defibrillation
proof equipments during defibrillation. Defibrillation will not affect the
performance of the equipment.
1.1.2 Cautions
CAUTION
•When several infusion lines are connected to the same vascular access, there
may be back flow or prolonged response time of occlusion alarm. Therefore,
use check valve at the line end or follow local hospitals’ instructions while in
connection with other infusion system.
•Ensure that the equipment is supplied with continuous electric power during
work. Sudden power failure may cause data loss.
•Electromagnetic fields may affect equipment performance. This makes it
necessary for other equipment used in the vicinity of this equipment to meet
EMC standards. Mobile phones, X ray and MRI equipment are all potential
interference sources because of their high-intensity electromagnetic
radiation.
•Always install or carry the equipment properly to avoid damage caused by
drop, impact, strong vibration or other mechanical force.
•Dry the equipment immediately in case of rain or water spray.
•Some settings are password protected and can only be changed by
authorized personnel. Contact your department manager or biomedical
engineering department for the passwords used at your facility.

1 - 3
1.1.3 Notes
NOTE
•The software was developed in compliance with IEC62304.
•The equipment provides power-down storage. Alarms limit setting and
history record are saved and will be maintained if the equipment is powered
down suddenly. The storage time is equals to the equipment’s service life.
The alarm limit settings before power-down are reloaded when the
equipment is restarted.
•This manual describes all features and options. Your equipment may not
have all of them.
1.2 Equipment Symbols
Some symbols may not appear on your equipment.
Refer to instruction manual/
booklet
Caution
Alternating current Input/output
Battery USB connector
Both direct and alternating
current
Direct current
Date of manufacture Manufacturer
IP33 Protected against solid
foreign objects with a
diameter no less than 2.5 mm
in diameter. Protected against
spraying liquid water.
DEFIBRILLATION-PROOF
TYPE CF APPLIED PART
Atmospheric pressure
limitations
Humidity limitations

1 - 4
THIS WAY UP Keep dry
Fragile, handle with care STACKING LIMIT BY NUMBER
CE mark Serial number
General warning sign Stop
Stand-by Non-ionizing
electromagnetic radiation
Temperature limitations Dispose of in accordance
to your country’s
requirements

2 - 1
2Equipment Introduction
2.1 Intended Use
The veterinary syringe pump is used in conjunction with the syringe to control the dose
of liquid infused into the patient’s body.
This veterinary syringe pump is expected to be used in institutes or units with healthcare
capabilities.
The veterinary syringe pump delivers infusion fluids through clinically accepted routes
of administration, including intravenous and intra-arterial routes.
WARNING
•This pump is intended for use only by clinical professionals or under their
guidance. It must only be used by persons who have received adequate
training in its use. Anyone unauthorized or untrained must not perform any
operation on it.
2.2 Applied Part
The applied part of the equipment is the syringe.
2.3 Main Unit
2.3.1 Front View
(1) (4)(3)(2) (5)
(7) (8)
(6)
(9)
(10)
(1) Extension set holder
Secures the extension set.

2 - 2
(2) Display
(3) Stop key
When an emergency happens during an infusion and unlocking the touchscreen
fails, press this key to stop infusion.
(4) Power switch
(5) Battery LED
• Green: the battery is being charged.
• Flashing green: the pump runs on battery power.
• Off: no battery is installed, or no external power is connected when the
equipment is off.
(6) External power LED
• On: when external power supply is connected.
• Off: when external power supply is not connected.
(7) Plunger grippers
Secures the plunger to the driver head.
(8) Driver head
Presses the plunger of the syringe.
(9) Alarm light
When a physiological alarm or technical alarm occurs, this lamp lights and flashes
corresponding with the alarm priority:
• High priority alarms: the lamp quickly flashes red.
• Low priority alarms: the lamp lights in yellow without flashing.
(10) Infusion status indicator
The indicator is on during infusion, purging, and bolus.

2 - 3
(1)
(3) (4)
(2)
(1) Extension set holder
Secures the extension set.
(2) Door
Open the door to load or unload the syringe.
(3) Barrel Clamp
Secures the barrel and the barrel flange to the pump and identifies the syringe
barrel size.
(4) Flange Retainer
Secures the barrel flange to the pump.

2 - 4
2.3.2 Rear View
(2) (3) (4)(1)
(1) Speaker
Provides sound for audible alarms and reminder.
(2) Multifunctional connector
• Connects the equipment to the hospital’s nurse call system through the nurse call
cable.
• Uses as a DC power input connector when the equipment is connected to the
dock.
• Uses as a RS232 connector for connecting the external devices.
(3) USB connector:
Connects the USB device.
(4) AC power input connector
Connects the AC power cord.