INFUSOVET IP

INFUSION PUMP
USER MANUAL

Item no. 402085

TELEPHONE +49 7461 96 580 0

www.eickemeyer.com
Release date: 2022-05

Revision: 2.0

I
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 animal
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 veterinarians who are expected to have a working
knowledge of medical procedures, practices and terminology as required for
monitoring of critically ill animals.

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.
 [ ] is used to enclose screen texts.
 <> is used to enclose the keys.
 → is used to indicate operational procedures.

II
Contents
Preface ............................................................................................................................. II

1 Safety ......................................................................................................................... 1-1

1.1 Safety Information ................................................................................................ 1-1
1.1.1 Dangers ...................................................................................................... 1-1
1.1.2 WARNING .................................................................................................. 1-2
1.1.3 CAUTION ................................................................................................... 1-3
1.1.4 NOTE ......................................................................................................... 1-4
1.2 Equipment Symbols.............................................................................................. 1-5

2 Overview .................................................................................................................... 2-1

2.1 Description ........................................................................................................... 2-1
2.1.1 Indications for Use ...................................................................................... 2-1
2.1.2 Contraindications ........................................................................................ 2-1
2.1.3 Appearance, Parts and Features ................................................................ 2-1
2.2 Host ...................................................................................................................... 2-2
2.2.1 Front View .................................................................................................. 2-2
2.2.2 Front View with the Door Opened............................................................... 2-4
2.2.3 Rear View ................................................................................................... 2-5
2.3 Screen Display ..................................................................................................... 2-6
2.4 Cursor ................................................................................................................... 2-6

3 Installation and Setting ............................................................................................. 3-1

3.1 Installation ............................................................................................................ 3-1
3.1.1 Out of Box Audit (OOBA) ............................................................................ 3-2
3.1.2 Operating Conditions .................................................................................. 3-2
3.1.3 Mount the Clamp ........................................................................................ 3-3
3.1.3.1 Standard Pole Clamp3-3
3.1.3.2 Advanced Pole Clamp (Optional)3-4
3.1.4 Connect the AC Power Source ................................................................... 3-5
3.1.5 Install and Operate the Drop Sensor (Optional) ......................................... 3-5
3.2 Conventional Settings ........................................................................................... 3-7
3.2.1 Set Language ............................................................................................. 3-7
3.2.2 Adjust Screen Contrast ............................................................................... 3-7
3.2.3 Set Date and Time ...................................................................................... 3-8
3.2.4 Adjust Volume ............................................................................................. 3-8
3.3 Restore Factory Default ........................................................................................ 3-8

4 Basic Operation......................................................................................................... 4-1

4.1 Infusion Flow Chart ............................................................................................... 4-1

1
 4.2 Operational Procedures ........................................................................................ 4-2
4.2.1 Turn on the Pump ....................................................................................... 4-2
4.2.2 Load the Infusion Set ................................................................................. 4-2
4.2.3 Change the Infusion Set ............................................................................. 4-4
4.2.4 Change the Infusion Bottle (Bag) ............................................................... 4-4
4.2.5 Select Infusion Set Brand ........................................................................... 4-4
4.2.6 Infusion Mode ............................................................................................. 4-5
4.2.7 Purge .......................................................................................................... 4-6
4.2.8 Set Infusion Parameters ............................................................................. 4-6
4.2.9 Infusion ....................................................................................................... 4-6
4.2.10 BOLUS ..................................................................................................... 4-7
4.2.11 Change the Rate during Operation ........................................................... 4-7
4.2.12 Complete .................................................................................................. 4-8
4.2.13 Standby .................................................................................................... 4-8
4.2.14 Turn off the Pump ..................................................................................... 4-8

5 Setting Parameters ................................................................................................... 5-1

5.1 KVO ...................................................................................................................... 5-1
5.2 Occlusion Pressure .............................................................................................. 5-1
5.2.1 Set Occlusion Pressure .............................................................................. 5-1
5.2.2 Set Pressure Unit ....................................................................................... 5-2
5.2.3 Dynamic Pressure Scanning (DPS) ........................................................... 5-2
5.2.4 Automatic Pressure Release Function (Anti-Bolus) .................................... 5-2
5.3 Set the Air Bubble Size ......................................................................................... 5-2
5.4 Acumulated Bubble............................................................................................... 5-3
5.5 Key Lock Function ................................................................................................ 5-3
5.6 Reminder Function ............................................................................................... 5-3
5.7 Time Near End...................................................................................................... 5-4
5.8 Common Infusion Set Brands ............................................................................... 5-4
5.9 Bed No. Settings................................................................................................... 5-4
5.10 View Department ................................................................................................ 5-5
5.11 Set the Sensitivity of Empty Bottle Alarm ............................................................ 5-5

6 Other Functions ........................................................................................................ 6-1

6.1 Nurse Call ............................................................................................................. 6-1
6.2 Wireless Networking (Optional) ............................................................................ 6-2
6.3 Data Export........................................................................................................... 6-3
6.4 WLAN Setting ....................................................................................................... 6-3

7 Alarms ........................................................................................................................ 7-1

7.1 Alarm Level ........................................................................................................... 7-1
7.2 Alarm Types .......................................................................................................... 7-1
7.2.1 Multi-level Alarm Rules ............................................................................... 7-2
7.3 Alarm Handling Rules ........................................................................................... 7-2

2
 7.4 Alarm Countermeasures ....................................................................................... 7-3

8 Battery........................................................................................................................ 8-1
8.1 Battery Performance Optimization ........................................................................ 8-2
8.2 Check the Battery ................................................................................................. 8-2
8.3 Battery Recycling.................................................................................................. 8-3

9 Preservation and Sanitation ..................................................................................... 9-1

9.1 Description ........................................................................................................... 9-1
9.2 Cleaning ............................................................................................................... 9-1
9.3 Disinfection ........................................................................................................... 9-2

10 Maintenance .......................................................................................................... 10-1

10.1 Inspection ......................................................................................................... 10-1
10.2 Maintenance Plan ............................................................................................. 10-2
10.3 View Information ............................................................................................... 10-2
10.4 Safe Disposal and Recycling ............................................................................ 10-2

11 Accessories ........................................................................................................... 11-1

A Product Specifications ............................................................................................ A-1

A.1 Safety Specifications ............................................................................................ A-1
A.1.1 Product Classification................................................................................. A-1
A.1.2 Operating Environment .............................................................................. A-2
A.2 Physical Specifications ......................................................................................... A-2
A.3 Hardware Specifications ...................................................................................... A-3
A.3.1 Display ....................................................................................................... A-3
A.3.2 Battery........................................................................................................ A-3
A.3.3 Host LED.................................................................................................... A-3
A.3.4 Auditory Indicator ....................................................................................... A-4
A.3.5 External Ports ............................................................................................ A-4
A.3.6 Signal Output Interface .............................................................................. A-4
A.4 Wi-Fi Specifications.............................................................................................. A-5
A.5 Specifications ....................................................................................................... A-5
A.6 A Reference Table Showing Occlusion Alarm Delay and Possible Dose .............. A-7
A.7 Infusion Accuracy Curve and Trumpet Curve ....................................................... A-8

B EMC and Radio Regulatory Compliance ............................................................... B-1

B.1 EMC ..................................................................................................................... B-1
B.2 Radio Regulatory Compliance.............................................................................. B-6

C Default Factory Settings ......................................................................................... C-1

C.1 Alarms ................................................................................................................. C-1
C.2 Interface .............................................................................................................. C-1

3
 C.3 Parameters ......................................................................................................... C-1
C.4 System Time ....................................................................................................... C-2

D Alarm Information .................................................................................................... D-1

E Symbols and Terms .................................................................................................. E-1

E.1 List of Units .......................................................................................................... E-1
E.2 List of Symbols ..................................................................................................... E-2
E.3 List of Terms ......................................................................................................... E-2
E.4 List of Unit Conversion ......................................................................................... E-4

F Toxic and Hazardous Substances or Elements ...................................................... F-1

4
1 Safety
1.1 Safety Information
The safety statements presented in this chapter refer to basic safety information that
the operator must pay attention to and abide by when using the veterinary infusion
pump. There are additional safety statements in other chapters or sections, which may
be the same as or similar to the following, or specific to particular operations.

Dangers
 Indicates an imminent hazard that, if not avoided, could result in death,
serious injury or damage to product/property.

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 Dangers
This Manual does not contain any information at the "Danger" level.

1-1
1.1.2 WARNING

WARNING

 Device, cables and accessories must be inspected before use to

guarantee their normal and safe operation.
 This equipment can only be connected to the socket with ground
protection. Please adopt a rechargeable battery instead of the socket as
the power supply if the socket is not provided with a ground lead.
 To prevent fire or explosion, do not operate the equipment in the
presence of anesthetic, flammable or explosive materials.
 Do not open the equipment casing as there is the impending danger of
electric shock. Equipment maintenance and upgrades must be carried
out by maintenance technicians whom are trained and licensed by the
manufacturer. Moreover, the process must be done only after the AC
power supply is disconnected. Maintenance carried out by individuals
non-affiliated to the manufacturer or by non-licensed personnel may
affect the safety, performance and function of the product.
 When used with electrosurgery equipment, the safety of animals should
be ensured.
 The animal's condition and the working condition of the veterinary
infusion pump must be monitored carefully, the alarm volume and alarm
levels need to be set according to the actual needs. Operation and
performance relying solely on the auditory alarm system alone is not
sufficient, and setting the alarm at a low volume may endanger the
animal. If the alarm volume is less than the surroundings volume, which
can further lead to operators identify alarm mistakenly.
 Please carefully install the power line and cables with various
accessories to prevent the animal from choking or suffocation caused
by entanglement of the cables or by electrical disturbance.
 The packaging materials must be disposed of in compliance with local
laws and regulations or the pet hospital policy on waste
management.They must be kept out of the reach of children.
 Infusion set knots, filter coagulation and occlusions arising from needle
insertion can cause the pressure inside the infusion set to rise during
infusion. When this occurs, removing the occlusion can cause
excessive liquid drug to be infused into the animal, so appropriate
measures should be taken.
 It is recommended that veterinary infusion pump is used with infusion
sets recommended by manufacturers (please refer to 5.8 Recommended
Infusion Sets List for specific brands). When use of non-recommended

1-2
 infusion sets, please make sure to confirm relevant infusion
performance (such as accuracy, bubble and pressure) on veterinary
infusion pump, and contact the company for calibration service, the
infusion sets can only be used after confirmation, otherwise we is not
responsible for infusion performance (such as accuracy, bubble and
pressure) and relevant alarm function of the veterinary infusion pump.
 Its accuracy cannot be guaranteed when the pump is used with an
infusion set without calibration.
 Do not touch the animal when connecting the peripheral equipment via
the input/output signal ports to prevent animal leakage current from
exceeding the requirements specified by the standard.
 In the process of defibrillation, do not touch animal and other non-
defibrillation equipments to prevent electric shock damage, and
defibrillation will not affect the basic performance (such as infusion
accuracy, alarm and signal transmission) of the pump.

1.1.3 CAUTION

CAUTION
 Use the accessories specified in this Operator’s Manual to guarantee
the animal’s safety.
 When this veterinary infusion pump and its accessories exceed their
service life, they must be disposed of in accordance with local statutes
or pet hospital regulations. If you have any queries, please contact your
distributor or the manufacturer.
 After loading the infusion set and before infusion, check for leakages. If
any are found, they should be rectified as soon as possible.
 For SK series infusion sets, it is recommended to replace the infusion
set or adjust the fixing site of the infusion set after the infusion has
been running for 36 hours to guarantee accuracy. For infusion sets of
other brand, it is recommended to test the service life of the infusion set
to determine the time interval of changing the fixing site of the infusion
set; if the service life of the infusion set is not tested, it is recommended
to adjust the fixing site of the infusion set every 4-8 hours after infusion
begins to guarantee accuracy.
 Electromagnetic fields may affect equipment performance. This makes
it necessary for other equipment used in the vicinity of the pump to
meet EMC standards. Mobile phones, X ray and MRI equipment are all

1-3
 potential interference sources because of their high-intensity
electromagnetic radiation.
 Before the equipment is connected to the power supply, check that the
voltage and frequency of the power supply match the specifications on
the label or in this Operator’s Manual.
 Please install and carry the equipment correctly to protect the
equipment from damage from drops, impacts, violent shaking or other
external mechanical forces.
 Disposable accessories must be disposed of after use in accordance
with the relevant pet hospital regulations.
 Avoid direct sunshine, high temperatures and dampness.
 Check the built-in battery before use to make sure it has sufficient
power. Recharge the battery if necessary.
 The infusion set with the luer taper is recommended for use, which can
effectively prevent animals from under current caused by the
occurrence of the cannula to slip out when under tension.

1.1.4 NOTE

NOTE
 Install the equipment in a position where it can be easily accessed for
inspection, operation and maintenance.
 Keep this Operator’s Manual near to the equipment for future ease of
reference.
 The software of the equipment is developed according to the software
development demands of IEC60601-1 standard, which can minimize the
possibility of the risk caused by program error.
 This Operator’s Manual describes the most complete functional
configuration of the equipment. The product you are using may not
have some of the settings or functions described herein.
 Do not insert devices that are not specified by the manufacturer into the
DB9 interfaces.
 During infusion, the veterinary infusion pump can accurately control the
rate, infusion volume and infusion time, and monitor the operation in
real-time, to effectively prevent over currents, under currents and
instances of backflow.
 The device is not in touch with the drugs or animals directly. Thus,
there is no need to process Biocompatibility test on it.

1-4
1.2 Equipment Symbols
The equipment you purchased may not provide you with all the following symbols.

Consult instructions for ON/OFF

use

Alternating current power

Battery
supply (AC)

Alarms AUDIO PAUSED

Clear/Back Start

Bolus Confirm

Stop Menu

Move up/Increase Move down/Decrease

Move left Move right

Infusion set Caution

Wireless modules work in

Wireless transceiver
order

DB9 interface Drop sensor interface

Protected against
Lock defibrillation CF
applied parts

Date of manufacture Manufacturer

This way up Keep dryy

Stacking limit by
Fragile, handle with care
number

1-5
 Protected against solid
foreign objects with a Environmentally-
diameter no less than friendly use periods of
IP34 2.5mm and protected electronic products (20
against spraying liquid years)
water

Temperature limit CE mark

NRTL certification
Recycle
mark

Atmospheric pressure
Humidity limitation
limitation

Serial number / /

The following definition of the WEEE label applies to EU member

states only: the use of this symbol indicates that waste electrical
and electronic equipment must not be disposed of as unsorted
municipal waste and must be collected separately. By ensuring that
this product is disposed of correctly, you will help prevent bringing
potential negative consequences to the environment and human
health. For more detailed information with regard to returning and
recycling this product, please consult the distributor from whom you
purchased the product

1-6
2 Overview
2.1 Description
2.1.1 Indications for Use
The veterinary infusion pump is used in conjunction with the infusion set to control the
dose of liquid infused into the animal’s body.

This veterinary infusion pump is expected to be used in institutes or units with

healthcare capabilities.

WARNING
 The veterinary infusion pump is for accurate and continuous infusion to
animals. It must only be used under appropriate conditions by
professional veterinarians or by suitably trained veterinarians.
Personnel using this product must receive sufficient training. This
product must not be operated by anyone who has not been authorized
to do so or has not received suitable training.

2.1.2 Contraindications
None

2.1.3 Appearance, Parts and Features

The veterinary infusion pump primarily consists of a housing and built-in battery.
Eccentric camshaft is driven by stepper motor during operation, making the fixed
upper slider moves up and down sequentially and regularly, infusion set is extruded
regularly, and liquids in infusion set can flow directionally at a certain rate, and all
components are suitable for use in animal environment. The drop sensor and wireless
module are optional. Optional functions of the software comprise Rate Mode and Anti-
bolus function.

Since some parts and functions are optional, the veterinary infusion pump you
purchased may not contain these additional parts and their relevant functions.

2-1
2.2 Host
2.2.1 Front View

1. Alarm light
The alarm light indicates different alarm levels in different colors and flash
frequencies, please refer to Chapter 7 Alarms for details.
2. Display
Used for displaying infusion parameters and relevant content.
3. <CLEAR/BACK>
 Under non-setting status, indicate to return to the previous menu or
operation.
 Under the setting status, indicate to clear the current set or cancel
the edit.

4. <DIRECTION>
Used for adjusting value, change lines and pages.
5. <OK>
Used for confirming input operation and saving values.
6. <MENU>
 Under non-operation status, used for switching [Main Menu]
interface and other interfaces.
 Under operation status, press and hold this key to lock; in locked
state, press and hold to unlock.

2-2
7. AC/DC indicator light
 On: The pump is connected to an AC/DC power supply (including
shutdown).
 Off: The pump is not connected to an AC/DC power supply.

8. Battery indicator
 Steady green indicates that the battery is charging.
 Flashing indicates that the battery is providing power.
 Light off indicates that there is no battery or the equipment is turned
off and not connected to an AC power supply.

9. <POWER>
 Used for turning power on, entering in standby state and turning off
operations.
 When power off, press and hold (>3 s) the key.

10. <BOLUS>
 During infusion, press this key to enter the Bolus settings screen.
 When the pump is stopped, press this key to enter the Purge prompt
screen.

11. <AUDIO PAUSED>

Pauses alarm sound.
12. <START>
After loading the infusion set correctly and completing setting infusion
parameters, press this key to start the infusion.
13. <STOP>
During infusion, press this key to stop infusion. Infusion stops caused by
alarms, such as occlusion and so on, press this key to cancel the alarm.
14. Handle
15. Door
16. Door holder
Pull it to open the door.

2-3
2.2.2 Front View with the Door Opened

1. Liquid check clip button

2. Liquid check clip
3. Infusion set slot

2-4
2.2.3 Rear View

1. DB9 interface, which combines the following interface functions:

 DC power input interface
 RS232 interface
 Nurse call interface

2. Alternating current power supply (AC) port

Connected by three-core-type power cord and AC power source.
3. Drop sensor interface
4. Pole clamp
5. Product label

2-5
2.3 Screen Display
This veterinary infusion pump has a monochrome LCD screen. The display
information comprises two main parts:

1. Parameter area
Display battery icon, every parameter and the parameter value of the current
screen, etc.
2. Prompt bar
Display run icon. The run icon on the screen displays the running operation:
The icon indicates normal running.
Arrows move from right to left, and the
■
running speed increases as the rate is
increased.
Motor stops caused by alarms during
■
infusion, no icon.

2.4 Cursor
In the main screen and parameter settings screen, when the cursor is located at an
option or at a data value, the grounding of the option or the data value will turn to white

and the font will become blue. Press or to move cursor up or down and

confirm the location. Press to select the option or data value for further operation.

Note: Press or to "locate" cursor; press to "Select".

2-6
3 Installation and Setting
3.1 Installation

WARNING
 Equipment assembly and refit (including correct protective grounding
connection) during life period must be carried out by maintenance
technicians whom are trained and licensed by the manufacturer, and
evaluated according to the specified IEC60601-1. Please contact the
company if you have any queries.
 The software copyright for this equipment belongs to the manufacturer.
Unless explicitly authorized, any alteration, reproduction or sale by any
means or in any form by any organization or individual is prohibited.
 All the analog equipment and digital facilities should be certified
according to the specified IEC standard (such as: IEC60950 Information
Technology Equipment Safety and IEC60601-1 Medical Electrical
Equipment Safety). Moreover, all equipment should be connected based
on the requirements of the valid version of the IEC60601-1 system. The
qualified individual responsible for connecting auxiliary equipment to
the input and output signal ports is also accountable for making the
system in accordance with the IEC60601-1 standard. Please contact the
company if you have any queries.
 When this equipment combining with other electrical equipments forms
a combination with a special function, and the user cannot determine
whether there is an impending danger from each equipment
specification (such as a danger of electric shock due to aggregation of
current leakage), please contact the company or a specialist in the field
at the pet hospital, to guarantee that all equipment in the combination
are safe enough and will not be damaged.
 Please make sure this equipment is securely fixed and positioned.
Positioning changes and severe shock can lead to minor changes in the
delivery accuracy.

3-1
 NOTE
 This equipment is in accordance with the EN 1789:2007+A1:2010
standard. It can be fixed on cross bar (square cross bar: 10 x 25 mm) or
vertical bar (round vertical bar with diameter size of 15-38mm) of
ambulance with advanced pole clamp. Please refer to 3.1.3.2 Advanced
Pole Clamp (Optional) for detailed operation of advanced pole clamp.

3.1.1 Out of Box Audit (OOBA)

Please check the packing case carefully before opening the box. If there is any
damage, please contact the distributor or manufacturer immediately.

Please carefully remove the equipment and its accessories from the packaging in a
correct manner, and inspect them against the packing list. Examine the equipment for
any mechanical damage and ensure that the box includes all items on the packing list.
Please contact the company if you have any queries.

NOTE
 Keep the packing case and packaging materials for future
transportation or storage.

WARNING
 They must be kept out of the reach of children.The packaging materials
must be disposed of in compliance with local laws and regulations or
the pet hospital policy on waste management.
 The equipment may be contaminated by microbes during storage,
transport and use. Please ensure that the package is undamaged before
using, do not use if there is any damage.

3.1.2 Operating Conditions

The operating environment of this veterinary infusion pump must meet the
requirements in A.1.2 Operating Environment, and in accordance with the
emergency medical care requirements of medical equipment short-time operation of
the valid version of the IEC60601-1-12 system.

3-2
 The operating environment should also be appropriately protected from noise,
vibration, dust, and corrosive, inflammable or explosive substances. If installed inside
the equipment case, a sufficient space before and after the equipment case should be
ensured to facilitate operation, maintenance and repairing work.There should be a 2"
(5 cm) gap around the veterinary infusion pump to ensure that air can circulate freely
for a better cooling effect.

When the pump is transferred from one place to another, differences in temperature
and humidity can cause condensation to form inside the pump. If this occurs, do not
switch the pump to the "ON" state until the condensation has gone.

WARNING
 Please use only when the operating environment meets the
requirements specified above. Otherwise, the pump's performance will
not match the technical specifications in A Product Specifications.
Device failure and other unexpected consequences may also result.

3.1.3 Mount the Clamp

3.1.3.1 Standard Pole Clamp
1. Turn counterclockwise to
loosen the pole clamp until an
IV stand can be inserted in.

3-3
 2. Tighten the pole clamp
clockwise to firmly fix the
device on the IV stand (round
vertical bar with diameter size
of 15-32mm).

3.1.3.2 Advanced Pole Clamp (Optional)

Press the button of pole clamp, horizontally or vertically adjust pole clamp, the button
will pop-up after loosening the pole clamp. Turn the handle, pump can be fixed to cross
bar (square cross bar: 10 x 25 mm) or vertical bar (round vertical bar with diameter
size of 15-38mm).

3-4
3.1.4 Connect the AC Power Source
1. Please confirm to use the original three-core-type power cord.
2. Insert one end of the power line into the AC socket on the back panel of the
veterinary infusion pump.
3. Insert the other end of the power line into the matched three-plug connector
connecting to the AC power.

WARNING
 The earthing wire in the three-plug connector should be grounded. The
connection of the protective earthing terminal of all fixed or
permanently installed medical devices and external protective earthing
system should be connected and verified based on the requirements of
the valid version of the IEC60601-1-12 system. If there is a doubt
whether the AC power system is grounded or not, please adopt the
built-in battery and contact an electrical technician at the pet hospital or
the company.
 Do not touch the power plug with wet or moist hands! If there is a liquid
drug or residue on or around the power socket or plug, the user should
completely clean and dry the area before plugging into the power
supply, or accidents or injuries may result!

NOTE

 Compatible power supply: 100–240 V～, 50/60 Hz.

 The AC power cable should be correctly inserted and secured into the
socket.
 Removing power cord is to disconnect equipment from power supply.
Please ensure suitable clearance around the device to facilitate connect
and remove power cord.

3.1.5 Install and Operate the Drop Sensor (Optional)

NOTE
 This section should be used with the optional drop sensor. The user
may skip the instructions in this section if a drop sensor is not included
with the veterinary infusion pump.

3-5
1. Firmly insert the signal line of drop sensor into the connecting port on the right
side panel of the pump.
2. Clip the drop sensor to the drip chamber, making sure that the drop sensor is
above the surface of the liquid.

3. Press to start the infusion. The light of drop sensor flashes green when
liquid is detected in normal infusion status.

WARNING
 For 60drop/ml infusion sets, it is recommended to set the rate
<1000ml/h. Otherwise, the [Empty bottle] alarm will be triggered
mistakenly.
 Small liquid drops in drip chamber might be left on its wall after long
time infusion, the medical staffs need to confirm and eliminate the
drops. Otherwise, the accuracy of drop rate check will be affected, and
the [Empty bottle] alarm will be triggered.

3-6
 NOTE
 The surface of the liquid in the drip chamber must be lower than the
drop sensor, which should be between 1/3 and 1/2 of the drip chamber.
 The positioning block of the drip chamber must be inserted vertically
through the positioning groove on the drop sensor.
 Do not excessively tilt the drop sensor, or expose it to direct sunlight
during infusion. Otherwise, accuracy of the drop sensor may be
influenced.
 Make sure that the drip chamber is not clamped too tightly by the drop
sensor.
 It is suggested that the singal line of drop sensor should be changed
every six months.

3.2 Conventional Settings

This chapter only introduces the general settings for the veterinary infusion pump,
please refer to other relative chapters for parameters and other feature settings.

3.2.1 Set Language

1. Select [Main Menu]→[Language].
2. Select [Language] from the [Language] according to actual needs.

3.2.2 Adjust Screen Contrast

1. Select [Main Menu]→[Brightness].
2. Select [Brightness]: 1-8. 8 for the brightest setting, and 1 for the darkest setting.
When operating on battery power, you can set a low Contrast to save the power
of the battery.

3-7
3.2.3 Set Date and Time
1. Select [Main Menu]→[System Date and Time].
2. Set [Time] and [Date].

CAUTION
 Please check the system date and time to keep accurate records in the
History function.

3.2.4 Adjust Volume

1. Select [Main Menu]→[Volume].
2. Select [Volume]:1-8.1 for the lowest volume;8 for the highest volume.

3.3 Restore Factory Default

During operation, you may change some settings in some situations. However, the
changes may not be appropriate or correct, especially when animal or infusion set
brands are changed. Therefore, you should restore the system to the default factory
settings during operation according to actual needs, to guarantee that each
configuration of the veterinary infusion pump is applicable for animal use. For some
default factory settings of this equipment, please refer to C Default Factory Settings.

Select [Main Menu]→[System Maintenance]→Input User Maintenance

Password→[Restore factory default], and restore the factory default settings as
prompted on screen, some parameters will be restored to default values.

3-8
4 Basic Operation
4.1 Infusion Flow Chart

Turn pump on Press to activate and turn on the pump, the

pump will run start-up checks and display the start-
up screen;
Load infusion set
Please refer to 4.2.2 Load the Infusion Set;

Select according to the infusion set brand currently

Select brand
being used;

Purge Refer to 4.2.7 Purge;

Set infusion parameters Refer to 4.2.8 Set Infusion Parameters;

Connect animal Connect to the animal;

Start infusion
Press ;

Finish Press ;

Shut down the Robert clip (or flow rate regulator),

Remove infusion set disconnect from the animal, and remove the
infusion set in a correct manner;

Turn pump off Hold down (>3 s) , until the Power Off progress
bar complete.

4-1
4.2 Operational Procedures
4.2.1 Turn on the Pump
Please turn on the device as the following steps:
1. Perform a safety inspection referring to 10.1 Inspection before turning on the
pump.

2. Press , the system will initiate the self-test and the screen will display the
[System Self-test] interface:
3. The system will give out a sound "di" —— indicating the self-testing of the
loudspeaker to be successful.
4. The color of the alarm indicator lamp will change from red to yellow, turn on and
off orderly —— indicating the self-testing of the alarm lamp to be successful.
5. The system will give out a sound of "di" —— indicating the self-testing of the
buzzer to be successful.
6. Enter the operation interface after successfully completing the system self-test,
and now you can operate the system through the key board.

WARNING
 Please monitor the self-test process to make sure that the speaker, the
alarm light, and the buzzer are all self-tested successfully. Otherwise,
please contact the company and do not operate the pump until
maintenance is performed.
 Please contact the company if the veterinary infusion pump is damaged
or cannot operate properly, and it cannot be used for animal infusion.

4.2.2 Load the Infusion Set

System will inspect whether infusion set is loadesd after completing the self-test: If
infusion set is loaded, enter the [Infusion set selection] interface; If infusion set is not
loaded, enter the infusion set [Installation Guide] interface. If the infusion set is not

required to load, please press to skip the step.

Load infusion set according to the following method:

4-2
 2. Pull the free flow clamp button upward
1. Pull the door holder and open the door. left, and open the free flow clamp.

3. Load the set, confirm it is firmly loaded into 4. Close the door, the interface will enter
the tube slot. [Infusion set selection] interface,
indicating that the infusion set is loaded
correctly; otherwise, it needs to be

4-3
 reloaded.

WARNING
 The infusion set should be firmly loaded into the slot, and not jutting on
the outside of the slot.
 Before using this veterinary infusion pump, the veterinary infusion
pump, infusion set, and other accessories should be loaded correctly.

4.2.3 Change the Infusion Set

Follow the steps below to change the infusion set:
1. To prevent animal injury due to free flow, before changing the infusion set or
extruded tube, please shut down the Robert clip (or flow rate regulator). During

infusion, press to stop the pump.

2. Pull the door holder, open the door, pull the free flow clamp button upward left,
and take out the loaded infusion set.
3. Please refer to 4.2.2 Load the Infusion Set to reload the infusion set.

4.2.4 Change the Infusion Bottle (Bag)

Follow the steps below to change the infusion bottle (bag):
1. To prevent animal injury due to free flow, before changing the infusion bottle (bag),
please shut down the Robert clip (or flow rate regulator). During infusion, press

to stop the pump.

2. Take out the loaded infusion bottle (bag), and reload it.

4.2.5 Select Infusion Set Brand

On the [Infusion set selection] screen, press to select the infusion set

brand, and press for confirmation. Specific brand, please refer to 5.8 Common
Infusion Set Brands.

CAUTION

4-4
  Please confirm that the current selected brand is the same as the brand
actually used.

4.2.6 Infusion Mode

 Unit of Rate (ml/h)

Press to exit [Main Menu], and enter the [Rate Mode Setting/Running]
interface.

Mode Parameters Parameter Range

Rate 0.1 - 1500ml/h

Rate
Mode
VTBI 0.1 - 9999ml

 Unit of Rate (drip/min)

1. Select [Main Menu]→[Drip setting].
2. Select [drip/min]→[On], and set the “drip”. If [Off] is selected, the following steps
cannot be conducted.

3. Press to exit [Drip setting] interface, and enter the [Rate Mode Setting]
interface.

4. Change the unit of Rate to “drip/min”, set the parameters, and then press to
start the infusion.

Mode Parameters Parameter Range

Rate 1 - (400*drip/60) drip/ min

Rate
Mode
VTBI 0.1 - 9999ml

4-5
4.2.7 Purge
During infusion, the user should prevent air bubbles from entering the blood with the
liquid drug, which may form an aeroembolism and put animals in serious danger.
Therefore, air bubbles in the infusion set should be eliminated before the infusion.

On infusion parameters setting interface, press to enter [Purge] prompt

screen. Hold down to enter [Purge] running screen, release after the air
bubbles are purged.

WARNING
 During the purge, please disconnect the pump from the animal.

Otherwise, the animal will be in serious danger！

NOTE
 Purge rate can not be changed.
 [Air in line] alarm will not be triggered during purge.

4.2.8 Set Infusion Parameters

Under rate mode, users can set infusion parameters by pressing , , ,

, and .

4.2.9 Infusion

When ready, connect the infusion set to the animal. Press to start the infusion,
and the screen will display the running icon, the arrows will move from right to left, and
the running speed will increase, which will indicate that the rate will also increase.

WARNING
 Users should regularly monitor the connection between the infusion
set, pump and animal, and infuse according to the method mentioned in
the manual.

4-6
 NOTE
 When in running status, if there is no operation in other interface over 2
minutes, it will return to the running screen automatically.

4.2.10 BOLUS

In run screen of rate mode, press to enter [Bolus] settings screen. Follow the
ways to start the bolus:

 Manual Bolus: Set [Bolus] rate, and then press and hold to start a

manual bolus. The system returns to the original rate when is

released, or is hold for 10 seconds.

NOTE
 If the previous bolus rate ≤current rate, the default bolus rate is 600ml/h.
 If no operation is performed within 2 minutes, the veterinary infusion pump
will automatically exit the Bolus Settings screen and the procedure must be
repeated.
 [VTBI Near Done] alarm will not be triggered during bolus.
 Occlusion pressure will automatically switch to "High" level when bolus,
animal's clinical condition and working condition of the veterinary infusion
pump must be monitored carefully.

4.2.11 Change the Rate during Operation

In run screen of rate mode, press , or to change the value of the [Rate]

into the adjustable state, thus to set the expected rate, press or again for
confirmation, then start to infuse under the new set rate.

4-7
4.2.12 Complete
When [VTBI] is not set during the infusion and infusion is completed, if drop sensor is
installed and the switch of [Drip rate check] is on, the [Empty bottle] alarm will be
triggered; if drop sensor is not installed, the [Air in line] alarm will be triggered.
When [VTBI] is set during the infusion and the remaining infusion time is close to the
[Near end] time set by the users, the [VTBI Near Done] alarm will be triggered. If no
action has been taken, the alarm will not be canceled automatically until the infusion
is completed, and then switch to [VTBI Done] alarm. Set [Near end] time, please refer
to 5.7 Time Near End. When infusion is completed, enter to [KVO] mode, and KVO
mode will run for 30 mins at most. Infusion will stop automatically after the KVO is
finished, and the [KVO Finish] alarm will be triggered. Set KVO rate, please refer to
5.1 KVO.

4.2.13 Standby

Under non-operation status, tap (<3 s) to enter [Standby] interface, default

display the previous standby time, press to modify standby time (range is 00:01-

99:59 hh:mm), press for confirmation after modifying. The pump cannot be put
in standby mode if there is a high-level alarm.

When the standby state is ended, the title bar will display [Standby Time Expired],

press to confirm quit, and the screen will enter to the interface before standby

appears. Press to remain in standby status.

4.2.14 Turn off the Pump

Follow the steps below to turn off the veterinary infusion pump:
1. Disconnect from the animal;

2. Hold down (>3 s) , until the Power Off progress bar complete, and the power
will turn off.

4-8
NOTE
 The current operating data and saved data will always be autosaved
when the device is powered off properly. The effective storage duration
of the data is equal to the service life of the device.

4-9
FOR YOUR NOTES

4-10
5 Setting Parameters
5.1 KVO
KVO (Keep Vein Open) means to keep the vein open, during which the veterinary
infusion pump continues infusion at a very low rate after finishing the infusion in order
to prevent blood backflow or vascular occlusion.

Select [Main Menu]→[KVO rate]: 0.5ml/h is unadjustable.

5.2 Occlusion Pressure

Occlusion pressure is adjustable, which can meet the requirements for occlusion
pressure of different animals during infusion. Pressure in the infusion tube can be
measured by the built-in pressure sensor, pressure can be calculated by the internal
CPU, which is compared with the preset occlusion alarm threshold. [Occlusion] alarm
will be triggered if pressure exceeds the threshold.

5.2.1 Set Occlusion Pressure

1. Select [Main Menu]→[Occl. pressure].
2. Occlusion pressure Degree 3, lowest at 150mmHg, and highest at 900mmHg.
Occlusion pressure should be selected according to actual needs.

CAUTION
 If the animal experiences discomfort at a higher occlusion pressure,
monitor the animal's physical conditions under the higher occlusion
pressure closely, and take measures instantly if any abnormal condition
occurs.
 When the infusion set with ultrafilter at a lower occlusion pressure, the
[Occlusion] alarm might be triggered at high rate due to resistence
generated from liquid flow of ultrafilter. Select a higher occlusion
pressure or lower rate to cancel alarm.

5-1
5.2.2 Set Pressure Unit
1. Select [Main Menu]→[Pressure unit].
2. Select [Pressure unit]: The 4 various forms of pressure units, mmHg, kPa, bar
and psi are converted automatically, and can be selected according to actual
needs.

CAUTION
 Carefully confirm the edit when changing the current pressure unit.

5.2.3 Dynamic Pressure Scanning (DPS)

During the infusion, the bottom-right corner of the Run screen demonstrates real-time
pressure changes of the animal, in order to find the cannula occlusion at an earlier
time and to prevent the occurrence of further complications.

The pressure icon on the screen indicates the condition of the current
pressure:
1 solid area indicates low occlusion pressure
2 solid areas indicate medium occlusion pressure
3 solid areas indicate high occlusion pressure

5.2.4 Automatic Pressure Release Function (Anti-Bolus)

When occlusion occurs, infusion will stop and the [Occlusion] alarm will be triggered.
After the alarm is triggered, the motor is reversed, and the cannula pressure is then
released. This prevents an additional aggressive dose to the animal after the occlusion
is eliminated.

5.3 Set the Air Bubble Size

Air bubble size indicates the size of air bubble that can be monitored in the tube. The
lower of the bubble size, the smaller air bubble can be identified. Bubble in the infusion
tube can be measured by the built-in ultrasonic sensor, bubble size can be calculated
by the internal CPU, which is compared with the preset threshold. [Air in line] alarm
will be triggered if bubble size exceeds the threshold.
1. Select [Main Menu]→ [Bubble size].

5-2
 2. Select [Bubble size], five levels of air bubble can be selected, lowest at 50μl, and
highest at 800μl. Air bubble level should be selected according to actual needs.

CAUTION
 If the animal experiences discomfort or danger at a higher air bubble
filter level, monitor the animal's physical conditions and select the
actual needed level. Measures should be taken instantly if any abnormal
condition occurs.

5.4 Acumulated Bubble

1. Select [Main Menu]→[Accum. bubble].
2. Select [Accum. bubble]: 0.1-4.0ml/h is adjustable.

5.5 Key Lock Function

When locked, an icon in the upper-right corner of the screen merges.The

following are two ways for automatic locking and manual locking:

 Automatic Locking:
1. Select [Main Menu]→[Auto-lock].
2. Select [Auto-lock]: Off, 1-5min. After a specific time is set during the running state,
and if there is no operation or high-level alarm within the set auto-lock time, the
key board will be auto-locked. [Off] indicates closing automatic locking function.
 Manual Locking: In the running interface, under the unlocking condition, press

and hold (>3 seconds) to lock the key board.

If unlocking is needed, press and hold (>3 seconds) to unlock, it is automatically

locked during the high-level alarm.

5.6 Reminder Function

1. Select [Main Menu]→[Reminder].
2. Select [Reminder]: Off, 1-5min. After a specific time is set, the infusion set is
loaded. If no operations are performed to the pump within the set time (including
operations on the keyboard, the slider and the pull handle), and the [Reminder]

5-3
 alarm will then alert the user to proceed to the next step. [Off] indicates closing
the function.

5.7 Time Near End

1. Select [Main Menu]→[Near end].
2. Select [Near end]: Off, 1-30min (when <10min, the stair-step is 1min, and when
≥10min, the stair-step is 5min). After a specific time set, when the remaining
infusion time is close to the [Near end] set by the users, [VTBI Near Done] alarm
will be triggered. [Off] indicates closing the function.

5.8 Common Infusion Set Brands

There are multiple commonly used infusion set brands installed inside the veterinary
infusion pump, making it convenient for the user to select from. For specific infusion
set brands, please refer to actual infusion device.

1. Select [Main Menu]→[Commonly used tube].

2. Select in [Commonly used tube] according to actual needs.
Note: Please ensure that at least one “Commonly used tube” to be selected.

Recommended Infusion Sets List

No. Infusion Set Brand Specifications and Model
1 B. Braun Intrafix SafeSet
2 SK ZPQ, JMB,150ml, SK-B

WARNING
 This equipment has to be used with high elastic tube. If you are not sure
whether the tube is high elastic tube, please contact us for tube test.

5.9 Bed No. Settings

1. Select [Main Menu]→[System Maintenance]→Input User Maintenance
Password “4321” →[Bed No.].
2. Select [Bed No.]: 1-999. [---] indicates invalid values. Beds can be differentiated
through setting Bed No.

5-4
5.10 View Department
The veterinary infusion pump are net-connected with BeneFusion CS5 Infusion
Supervision System through the approach of wireless networking, and the system
contains department information, the system will automatically distribute department
information to all veterinary infusion pumps when pumps are on.

Select [Main Menu]→[System Maintenance]→Input User Maintenance Password

“4321”→[Department] to view the department information.

5.11 Set the Sensitivity of Empty Bottle Alarm

1. Select [Main Menu]→[Empty Alarm].
2. Select [Empty Alarm]: High and Low. [High] indicates high sensitivity of [Empty
bottle] alarm detection, [Empty bottle] alarm will be triggered in shorter time;
[Low] indicates low sensitivity of [Empty bottle] alarm detection, [Empty bottle]
alarm will be triggered in longer time. It can be selected according to actual needs.
Note: [Empty Alarm] option is not visible when the switch of [Drop sensor] is off.

5-5
FOR YOUR NOTES

5-6
6 Other Functions
6.1 Nurse Call
Select [Main Menu]→[System Maintenance]→Input User Maintenance Password
→[Nurse call], and set in the open menu:

 Switch
On: indicates the opening of the nurse call function.
Off: indicates the closing of the nurse call function.

 Signal type
1. Cont.
Indicates that the output nurse call signal type is the same as that of the alarm
existence time, i.e., from the occurrence of the alarm to the end of it.
2. Pulse
Indicates the output nurse call signal is a pulse signal with the type of 1 second. When
several alarms exist at the same time, only one pulse signal can be outputted. If the
current alarm is not removed and another alarm occurs, then one additional pulse
signal is outputted.

 Trigger type
1. Normally Closed: Select when the pet hospital call system is set as [NC].
2. Normally Open: Select when the pet hospital call system is set as [NO].

 Alarm level: Three options: [High], [Medium] and [Low].The system sends
nurse call signals according to the alarm at the selected alarm level or
above.

WARNING
 Non-veterinarians are forbidden to modify the nurse call setting.
 The nurse call function must be used in conjunction with a special
cable.

6-1
 NOTE
 Veterinarians should not consider the nurse call function as the main
alarm notice approach, and rather combine the sound and visual alarms
of the veterinary infusion pump and the performances and symptoms of
the animal in order to judge the animal's conditions and take further
attention as needed.

6.2 Wireless Networking (Optional)

The veterinary infusion pump can be configured with the wireless modules, and be
net-connected with BeneFusion CS5 Infusion Supervision System through the
approach of wireless networking. Through the network:
 The veterinary infusion pump sends real-time infusion parameters, alarm
information, prompt information, Bed No. and other information to BeneFusion
CS5 Infusion Supervision System.
 BeneFusion CS5 Infusion Supervision System and veterinary infusion pump can
display synchronously. For detailed descriptions, please refer to the instructions
of BeneFusion CS5 Infusion Supervision System (hereinafter called CIMS).

Normal communication of the pump and CIMS depends on whether the network
connection is successful, operators are unable to observe the operation status of the
pump in real time when the communication is interrupted. After the network connection
settings of the pump and CIMS are modified, operators shall reset the network
connection as required in the manual to ensure the communication of the pump and
CIMS are restored.

When using wireless modules to connect to the Internet while using the veterinary
infusion pump, the wireless icon on the upper-right corner indicates the working
condition of the wireless modules:

Wireless modules work in order

No No wireless modules configured or connect BeneFusion

icons CS5 Infusion Supervision System

6-2
 NOTE
 Wireless security transmission distance is no more than 50 meters.
 2.4 GHz Wi-Fi frequency range, WEP and WPA/WPA2 security modes
and 802.11b/g/n wireless standard are supported.
 The settings of the wireless network must be conducted by technicians
approved by the company or maintenance staff designated by the
company.

6.3 Data Export

To export the data in the veterinary infusion pump, please refer to the following steps:
1. Log on PC tools, and connect the PC to the veterinary infusion pump;
2. When the veterinary infusion pump is in working communication with the PC, the
PC automatically reads all the data in the pump;
3. Select [History Record] in PC tools;
4. Export data.

6.4 WLAN Setting

The pump can be net-connected through built-in Wi-Fi module.

1. Select [Main Menu]→[WLAN Setting], then select [On] to enable Wi-Fi function.
2. Select [Advanced Settings], there are two ways to distribute IP address:
 DHCP: Check the checkbox to activate DHCP, IP address, subnet mask and
gateway can not be modified, automatically obtain an IP address.
 Manually: Uncheck the DHCP checkbox, enter IP address, subnet mask and
gateway.
3. Available networks shall be displayed:
 If password is required for to-be-connected network, please enter the password.
 If password is not required for to-be-connected network, you can connect the
network directly.

6-3
FOR YOUR NOTES

6-4
7 Alarms
The alarm is used in order to alert the veterinarian by means of sound and light when
abnormal situations occur during the infusion procedure which can lead to infusion
changes or when the infusion of the animal cannot continue due to the unexpected
breakdown or pause/delay of the veterinary infusion pump.

WARNING
 It is potentially hazardous to use the same or similar equipment with
different alarm presets within the same area.

7.1 Alarm Level

According to the severity scale of the alarm, the alarms of the veterinary infusion pump
can be classified to high-level alarms, mid-level alarms and low-level alarms.

7.2 Alarm Types

When an alarm is triggered, the veterinary infusion pump will use the following visual
and audible methods to alert the user:
 Visible alarms
 Audible alarm
 Alarm Information
Among the visible alarms and audible alarms, the alarm information will distinguish
alarm levels in different ways.

Audible
Color of Flashing light Light/no-light
Alarm level alarm
alarm light frequency ratio
frequency

High-level
Red 10 seconds 2.0±0.6Hz 20%-60%
alarms

Mid-level
Yellow 15 seconds 0.6±0.2Hz 20%-60%
alarms

7-1
 Low-level
Yellow 20 seconds Steady 100%
alarms

7.2.1 Multi-level Alarm Rules

When several alarms occur simultaneously, the alarms proceed according to the
following rules:
 When several alarms at different levels occur, the visible alarms and audible
alarms are consistent with the highest-level alarms.
 When several alarms at different levels occur, only the highest-level alarm is
displayed, and after it is cancelled, the lower-level alarm will then be displayed.
 When several alarms at the same level occur, the alarm information will be
demonstrated in an alternate manner.

The title bar of the veterinary infusion pump screen will display the corresponding
alarm information during the alarm blast, to see more details in D Alarm Information.

NOTE
 The [No Communication] alarm of the pump and BeneFusion CS5
Infusion Supervision System are delayed for 3 minutes, while other
alarms are delayed for less than 5 seconds.

7.3 Alarm Handling Rules

Under normal working conditions, when an alarm occurs, all the alarm types of the
veterinary infusion pump will alert according to their respective alarm levels. In addition,
the user can pause the alarm sound according to demands.

 For high level (except battery empty) and medium level alarms, press to
pause alarm sound for 2 minutes, no alarm sound is made in any case. When

the alarm pause time expires, the alarm tone will sound. Press to cancel
high level alarms (except battery empty and system error).

 For low level alarms, press , no alarm sound, alarm information and alarm
light, until it is triggered next time.

NOTE
 [Battery Empty] alarm sound is unable to be paused.

7-2
7.4 Alarm Countermeasures

WARNING
 When an alarm is triggered, the animal's condition should be checked
firstly and operation should only be allowed to proceed after the reason
for the triggering of the alarm is ruled out.

When an alarm is triggered, please follow these steps and take appropriate action:
1. Check the animal;
2. Check the alarm type and the parameter which triggered the alarm;
3. Determine the reason for the alarm;
4. Eliminate the reason for the alarm;
5. Check whether the alarm has cleared.

NOTE
 Please refer to D Alarm Information for specific handling procedures for
each alarm.
 The operator position shall be the normal operating position of the
veterinary infusion pump (0.5m). Otherwise, operators might identify
alarm mistakenly.

7-3
FOR YOUR NOTES

7-4
8 Battery
WARNING
 The battery can not be disassembled. The battery should be changed by
maintenance staff designated by the company only. Inserting fuel cell or
changing battery by personnel who has not received suitable training
may cause such danger as overtemperature, fire or explode.

The veterinary infusion pump is configured with rechargeable Lithium batteries to

ensure that the veterinary infusion pump can be used normally under the condition of
the animal's migration within the pet hospital or during the circumstance of a power
failure. When the veterinary infusion pump switches to the AC power, the battery can
be charged regardless of whether the veterinary infusion pump is on or off. The battery
is chargeable only within the veterinary infusion pump. During charge, the battery icon
in the upper-right corner of the screen floats left and right. If the battery icon stops
floating and is completely filled, it indicates that the battery is fully charged. Under the
condition of a sudden power failure, the pump will automatically use the battery to
provide power as a backup.

The battery icon on the screen indicates the condition of the battery:
The battery jar of the veterinary infusion pump is installed
with batteries, and the white fill area indicates the quantity
of electricity.
Low battery electric quantity indicates that charging is
needed.

When the battery is empty, charging is needed immediately.

The power supply by the battery can only be sustained for a limited period of time. The
[Battery Empty] alarm will be triggered when the battery voltage is too low, and red
alarm light will flash. The alarm will continue within the remaining time of the battery’s
electric quantity and cannot be paused. Now, the veterinary infusion pump should be
switched on to AC power for charging.

8-1
8.1 Battery Performance Optimization
When the battery is used for the first time, at least two complete optimizing cycles
should be ensured. A complete optimizing cycle contains the following: Charging
incessantly, and then discharging until the power of the veterinary infusion pump runs
out. During usage, regularly optimizing the battery performance will extend its lifespan.
It is suggested that the battery should be optimized when in use or in storage for three
months, or when the running time of the battery is significantly shortened.
Please follow the steps below during optimization:
1. Disconnect the pump from the animal and stop the infusion.
2. Switch the veterinary infusion pump on the AC power and charge the battery
incessantly for over 10 hours.
3. Disconnect the AC power and use the battery to charge the veterinary infusion
pump until the veterinary infusion pump is closed.
4. Switch the veterinary infusion pump over to AC power again and charge the
battery incessantly for over 10 hours.
5. The battery optimization is now complete.

8.2 Check the Battery

The performance of the battery may decrease over time. Please follow the steps below
when checking the battery:
1. Disconnect the pump from the animal and stop the infusion.
2. Switch the veterinary infusion pump on the AC power and charge the battery
incessantly for over 10 hours.
3. Disconnect the AC power and use the battery to charge the veterinary infusion
pump until the veterinary infusion pump is closed.
4. The length of the battery’s lifetime reflects the performance of the battery.
Note: If the length of the battery’s lifetime is obviously shorter than that claimed in the
specifications, please consider changing the battery or contact us.

8-2
 NOTE
 The lifespan of the battery depends on how frequently it is used and on
how long it has been used, battery capactiy decreases with increase in
charging and discharging times. If the maintenance and storage of the
battery is appropriate, the lifespan of the Lithium battery is no less than
300 times of full charging and discharging. If the use of battery is
improper, its lifespan shall be shortened or in failure status. We
recommend replacing the lithium battery every 3 years.
 Please connect to the AC power source if [Battery Empty] alarm is
triggered. To prevent battery not used for a long time or in battery
empty status, if battery is not charging more than two months after
battery is empty, battery will be in failure status. Do not charge the
failure battery, and replace the failure battery.
 If battery will not be used for a long time, we recommend keeping the
battery in a fully charged state and charging the battery every two
months for lifespan guarantee. Please replace the battery if the length of
its lifetime is obviously shortened during optimization.
 The length of the battery’s lifetime depends on the device configuration
and operation, for example: Under the condition of the power supply by
the battery, frequent infusion at a high rate will also shorten the length
of the battery’s lifetime.

8.3 Battery Recycling

If there is any obvious damage to the battery or to the battery capacity exhausts, it
should be replaced and recycled appropriately. Please follow the applicable laws on
recycling.

WARNING
 The battery must not be disassembled, burned or short-circuited.
Burning, exploding or leaking batteries can cause animal injury.

8-3
FOR YOUR NOTES

8-4
9 Preservation and Sanitation
The pump must be cleaned or disinfected using the materials and methods listed in
this section. The manufacturer will not be responsible for any damage or accident
caused by cleaning and disinfection using other materials and methods.

The manufacturer shall not be held responsible for the efficacy of the following
chemicals or methods for infection control. Please contact your pet hospital's infection
prevention department or epidemiology specialists for advice on infection control
practices.

9.1 Description
Please make sure that your device and other fittings are clean without dust. In order
to prevent any damage to the device, please abide by the following rules:
 Dilute all cleaning agents and disinfectants in accordance with the
manufacturer’s instructions, or use as low a concentration as possible.
 Do not immerse or submerge the device in liquid.
 Do not pour liquid on the device or accessories.
 Avoid liquid from entering the pump body.
 Do not use abrasive materials (such as steel wool or silver polishes), or any
strong solvent (such as acetone or any detergent containing acetone).

WARNING
 Turn off the pump and disconnect the AC power source line from the
socket before cleaning. Do not clean and disinfect the device, export
history record and perform other operations when animals are using the
pump.

9.2 Cleaning
The pump should be cleaned regularly. If operating in dirty or sandy areas, cleaning
should be more frequent. Before cleaning, please consult or refer to the pet hospital's
specific regulations concerning medical device cleaning.

The recommended detergents include: Hydrogen peroxide (3%).

9-1
 To clean your equipment, follow these rules:
1. Turn off the pump and disconnect the AC power source line.
2. Wipe the display screen after soft cotton balls absorb an appropriate amount of
detergent.
3. Use a piece of soft cloth which absorbs a modest amount of cleaning agent to
wipe the surface of the device.
4. When necessary, use a piece of cloth to wipe off any excess cleaning agents.
5. Place the pump in a cool and ventilated environment to dry.

9.3 Disinfection
The operation of disinfection may cause certain damage to the veterinary infusion
pump. You are recommended to disinfect only when it is necessary in your desired
maintenance plan. Clean the equipment before disinfection.

The recommended disinfectants include: glutaraldehyde-type 2% liquid disinfectant.

CAUTION
 Never use EtO or formaldehyde for disinfection.
 Do not conduct high pressure or high temperature disinfection for the
veterinary infusion pump and its accessories.

9-2
10 Maintenance
WARNING

 The pet hospital or medical facility using this veterinary infusion pump
must set up a comprehensive maintenance plan. Failure to do so may
result in equipment failure or other unexpected consequences, and may
even jeopardize animal safety.
 All safety inspections or maintenance work involving the disassembly
of the device must be conducted by professional maintenance
personnel. Actions by unqualified persons may result in device failure
and may even jeopardize animal safety.
 Please contact the company immediately if you encounter problems
with the device.

10.1 Inspection
The veterinary infusion pump must be given a thorough inspection before use, after
6-12 months of continuous use, and after maintenance or upgrades, to ensure that it
is operating and functioning normally.

The inspection criteria are:

 The environment and power supply meet requirements.
 The equipment and accessories have no mechanical damage.
 The power cord is not damaged and has sufficient electrical insulation.
 Accessories used with the pump are correct.
 The alarm system functions correctly.
 Battery performance.
 Self-checking and pump functions are normal.
If there are any forms of damage or abnormal circumstances, do not use the veterinary
infusion pump and contact the company immediately.

10-1
10.2 Maintenance Plan
The following tasks must be conducted by professional maintenance personnel
approved by the company. Please contact the company if the following maintenances
are needed. Must clean and disinfect the device before the test or maintenance.

Inspection/Maintenance Items Frequency

Once every two years.Perform after the

Perform a safety inspection according
board is changed or the veterinary infusion
to the IEC60601-1 standard.
pump is accidentally dropped.

Preventive maintenance (refers to the Once every two years, or when you
Maintenance Manual for pressure suspect the occlusion alarm is abnormal,
calibration, sensor calibration, and the flow volume is inaccurate, or the
pump inspection). infusion set is incorrectly identified.

10.3 View Information

Select [Main Menu]→ [Version Information]. In the [Version Information] interface,
you can view the information of the version of the veterinary infusion pump system
software and other versions.

10.4 Safe Disposal and Recycling

Please contact the company for related information about safe disposal and recycling.

10-2
11 Accessories
WARNING
 Use the accessories specified in this chapter only. Other accessories
may cause damage to this veterinary infusion pump, or cannot reach the
specification in this manual.
 Please do not replace an accessory if its package or itself is damaged.

Materials PN

0020-20-12522
009-002755-00
009-002756-00
Power cord 009-002757-00
(Select PN according to sales area) 009-002758-00
009-003358-00
009-003651-00
009-002758-00

Standard pole clamp 115-031551-00

Advanced pole clamp 115-031552-00

Nurse call cable 115-034140-00

RS-232 communication cable 115-034142-00

DC input cable 115-034144-00

Drop Sensor 115-013821-01

Floor model infusion stand 034-000321-00

Multi-channel pump stand 045-001434-00

Pet bracket 115-033273-00

11-1
NOTE
 This Operator’s Manual describes the most complete functional
configuration of the system. The device you are using may not have
some of the settings or functions described herein.

11-2
A Product Specifications
A.1 Safety Specifications
A.1.1 Product Classification
Classifications of this veterinary infusion pump according to the IEC60601-1 standard
are as follows:

Safety

Components Host

Type of protection
I
against electrical shock
Degree of protection
CF Protected against defibrillation
against electrical shock

Ingress Protection IP34

Explosion protection
Unsuitable
level

Mode of operation Continuous

Mobile level Portable

NOTE:
 I: Type I devices
 CF: Class CF applied parts, can be directly used in the heart.
 IP34: Protected against solid foreign objects with a diameter no less than
2.5mm and protected against spraying water.
 Unsuitable: The equipment is not suitable for use in the presence of a
flammable anesthetic mixture with air or with oxygen or nitrous oxide.
 Portable devices: Can be moved from one place to another by one or more
persons or by other means when the devices are in use or being used.
 Portable veterinary infusion pump: Used to control the infusion of animals and
are devices which can be carried by the animals continuously.

A-1
A.1.2 Operating Environment
Work environment

Temperature 5 - 40ºC

Relative Humidity 15 - 95%, non-condensing

Atmospheric pressure 57 - 106 kPa

Storage environment

Temperature -20 - 60 ºC

Relative Humidity 10 – 95%, non-condensing

Atmospheric pressure 50 –106 kPa

Storage conditions Corrosive-free and ventilated indoors

AC Power Supply

Voltage 100 - 240 V～

Frequency 50/60 Hz

Current 0.40-0.14A

Fuse Low interrupting rating, T5AL/250V

External DC power supply

Voltage DC 10V-16V

Current 2.25-1.5A

A.2 Physical Specifications

Components Weight Size Remark

Less than 150 x 90 x 200 (mm)

Less than 1.8 kg Battery
Host (length × width × height)
(Without pole clamp) included
(Without pole clamp)

A-2
A.3 Hardware Specifications
A.3.1 Display
Display

Type Monochrome LCD

Size (diagonal) 2.5 inches

Differentiation 132 x 32 pixels

A.3.2 Battery
Internal battery

No. of batteries 1 (standard) or 2 (optional)

Battery type Lithium battery

Shutdown delay At least 30 mins (new battery, after the first low battery alarm)

Rated battery voltage 7.4 VDC

Battery capacity 2600 mAh (1 battery) or 5200 mAh (2 batteries)

Continuously operate at a rate of 25 ml/h, disable Wi-Fi

function, discharge for at least 4h (1 battery) or 8h (2 batteries)
using a fully charged new battery.
Power supply time
Continuously operate at the maximum selectable rate, disable
Wi-Fi function, discharge for at least 2h (1 battery) or4h (2
batteries) using a fully charged new battery.
When the pump is off, the charging time is not longer than 6h
Charging time
(1 battery) or 12h (2 batteries).

A.3.3 Host LED

Host LED

Alarm light 1 (two colors: red and yellow)

AC/DC indicator light 1 (green)

Batterys indicator light 1 (green)

A-3
A.3.4 Auditory Indicator
Produce an alarm, the sound pressure is 55 - 80 dB(A) and key
Speaker beep; Support multi-level volume functions; The alarm sound
meets the requirements of the IEC60601-1-8 standard.

A.3.5 External Ports

Ports

AC power supply
1 AC power supply port
port
DB9 interface 1 DB9 interface, which combines the following interface
functions:
 DC power input interface
 RS232 interface
 Nurse call interface

Drop sensor
1 Drop sensor interface
interface

A.3.6 Signal Output Interface

Nurse call signal output

Driving mode Relay drive

Electric
≤60W, ≤2A, ≤36VDC, ≤25VAC
specification
Isolation voltage >1500 VAC

Action mode Normally open or normally closed (optional)

A-4
A.4 Wi-Fi Specifications
Protocol IEEE 802.11b/g/n

Modulation mode CCK and OFDM

Operating
2412~2484MHz
frequency
Channel spacing 5MHz
IEEE 802.11b: 1–11 Mbps
Data rate IEEE 802.11g: 6–54 Mbps
IEEE 802.11n: 6.5–150 Mbps
802.11b: +18dBm(Max)
Transfer power 802.11g: +16dBm(Max)
802.11n: +15dBm(Max)
Operating mode STA/AP/STA+AP

Data security WEP/WPA-PSK/WPA2-PSK

A.5 Specifications
Parameters Specifications

Infusion set used in conjunction with veterinary infusion pump

Infusion set should meet the requirements of ISO 8536-4:2004 Infusion
standard equipment for medical use— Part 4: Infusion sets for single use,
gravity feed, MOD

Compatible infusion Infusion set diameter: 3.5-4.5mm

set sizes (ml) Infusion set thickness: 0.8-1.2mm
 Unit of Rate (ml/h): 0.1-1500, the increment is 0.1 ml/h
Rate range  Unit of Rate (drop/min): 1-(400 ml/h *drip/60), the
increment is 1 drop/min

Drip range 10-60 drop/ml, the increment is 1 drop/ml

0.1-1500ml/h
Bolus rate range
Note: Bolus accuracy is not declared.

Purge rate range 600ml/h, nonadjustable

VTBI range 0.1-9999 ml, the increment is 0.1 ml

Volume range 0.1-9999 ml, the increment is 0.1 ml

Time display range 00:00:01-99:59:59 h:m:s

A-5
Standby time range 00:01-99:59 hh:mm

Infusion mode Rate Mode

KVO rate 0.5ml/h, nonadjustable

Anti-bolus On, Off

Low, Medium and High, respectively are

150±125 mmHg(20.0±16.7 kPa),
Occl. pressure 525±125 mmHg(70.0±16.7 kPa),
900±180 mmHg(120.0±24.0 kPa).
Maximum occlusion pressure is about 1300mmHg.

Pressure unit mmHg, kPa, bar and psi

1 - 5, respectively are (50, 100, 250, 500, 800) μl

Bubble size
Sensitivity of single bubble is 50μl.

Accum. bubble 0.1-4.0ml/h

Auto-lock Off, 1 - 5 min, step for 1min

Reminder Off, 1 - 5 min, step for 1min

Off, 1- 30 min
Near end when the time is <10min, step for 1min,
and step for 5 min when the time is ≥10 min

Bed No. 1-999

Volume 1-8

Brightness 1-8

System Date and Time:_ _:_ _

Time Date:_ _ _ _-_ _-_ _

System language You can select language according to actual needs.

Nurse call On, Off

Infusion accuracy Infusion accuracy error ≤±5%

Occlusion, VTBI Done, Battery Empty, VTBI Near Done,

Reminder, Battery Low, AC Power Disconnection, System Error,
Alarm Information System abnormal, KVO Finish, Standby Time Expired,
Tube not inserted, Air in line, Door opened, Empty bottle,
Drop error and No communication

Status indicators Stop, infusion, bolus, KVO, pause, standby, alarm and purge

Dose of single fault About 0.8ml

A-6
A.6 A Reference Table Showing Occlusion Alarm
Delay and Possible Dose
Occlusion Time of occlusion
Rate Bolus
pressure alarm
(ml/h) (ml)
(Level) (hh:mm:ss)

0.1 01:16:46 0.040

Low 1 00:07:25 0.033

25 00:00:08 0.021

1 00:25:57 0.050
Medium
25 00:00:48 0.028

0.1 08:36:34 0.069

High 1 00:44:08 0.055

25 00:01:45 0.037

NOTE
 Test conditions:
FLUKE IDA4 PLUS tester
Infusion set brand: SK
Test temperature: 20±2℃
Extension tube length: 1 meter
 Occlusion alarm pressure, alarm delays and bolus volume may vary
depending on test conditions, temperature and tube length.
 The above data are only typical values under normal test conditions. The
actual data may vary as test conditions change. Please refer to the test
data for the product you have purchased. Under the same standard
occlusion value and rate, the higher the value of the tested pressure is,
the longer the alarm time will be delayed.

A-7
A.7 Infusion Accuracy Curve and Trumpet Curve
The following typical infusion accuracy table expresses performance after infusion has
started and infusion fluctuations occurring within a certain period of time after normal
infusion flow volumes have been reached. The infusion accuracy table is for reference
only, detailed infusion accuracy curve is in accordance with the final device.

Plotted on the basis of data collected over a two-hour measurement period.

Infusion set brand: SK
Sampling quantity of pump: 3
Sampling quantity of infusion set: 3
Sampling interval: △t =0.5 min
Test period: t =240 mins
Infusion rate: Q (m/h)

Flow rate deviation over time (p△t)

Sampling interval: △t =0.5 min
Observation windows: p△t = 1, 2, 5, 11, 19, 31 mins
Maximum deviation over the course of a full observation window: Ep(Max) (%)
Minimum deviation over the course of a full observation window: Ep(Min) (%)
Average deviation: A (%) and B (%)

NOTE
 Infusion accuracy may be influenced by the pump's environment (such as
pressure, temperature, humidity and any infusion consumables used).

 Unit of Rate (ml/h)

A-8
A-9
  Unit of Rate (Drop/min)

Sampling rate: 20 Drop/

min
Sampling interval: △ t =1
min
Test period: t =120 mins
Infusion rate: Q (Drop/ min)

Sampling rate: 20 Drop/

min
Sampling interval: △ t =1
min
Observation windows: p△t
= 1, 2, 5, 11, 19, 31 mins
Maximum deviation over
the course of a full
observation window:
Ep(Max) (%)
Minimum deviation over
the course of a full
observation window:
Ep(Min) (%)
Average deviation: A (%)
Sampling rate: 20 Drop/
min
Sampling interval: △ t =1
min
Observation windows: p△t
= 1, 2, 5, 11, 19, 31 mins
Maximum deviation over
the course of a full
observation window:
Ep(Max) (%)
Minimum deviation over
the course of a full
observation window:
Ep(Min) (%)
Average deviation: B(%)

A-10
B EMC and Radio Regulatory Compliance
B.1 EMC
The device meets the requirements of IEC 60601-1-2:2014.

NOTE
 Use of accessories, transducers and cables other than those specified
or provided by the manufacturer of this device could result in increased
electromagnetic emissions or decreased electromagnetic immunity of
this device and result in improper operation.
 Use of this device adjacent to or stacked with other device should be
avoided because it could result in improper operation. If such use is
necessary, this device and the other device should be observed to
verify that they are operating normally.
 Portable RF communications equipment (including peripherals such as
antenna cables and external antennas) should be used no closer than
30 cm (12 inches) to any part of the this device, including cables
specified by the manufacturer. Otherwise, degradation of the
performance of this device could result.
 The non-ME EQUIPMENT (e.g. ITE) that is a part of an ME SYSTEM may
be disrupted by the electromagnetic interference of nearby equipment.
It may be necessary to take mitigation measures, such as re-orienting
or relocating the non-ME EQUIPMENT or shielding the location.
 This device is intended for use in professional healthcare facility
environment only. If it is used in special environment, such as magnetic
resonance imaging environment, the equipment/system may be
disrupted by the operation of nearby equipment.

B-1
 Guidance and Declaration - Electromagnetic Emissions
The device is intended for use in the electromagnetic environment specified below. The
customer or the user of the device should assure that it is used in such an environment.
Emission test Compliance Electromagnetic environment -
guidance
Conducted and radiated Group 1 The device uses RF energy only for its
RF EMISSIONS CISPR 11 internal function. Therefore, its RF
emissions are very low and are not likely
to cause any interference in nearby
electronic device.
Conducted and radiated Class A The device is suitable for use in all
RF EMISSIONS CISPR 11 establishments other than domestic and
those directly connected to the public low-
voltage power supply network that
supplies buildings used for domestic
purposes.
Harmonic distortion Class A The device is suitable for use in all
IEC 61000-3-2 establishments, including domestic
Voltage fluctuations and Complies establishments and those directly
flicker IEC 61000-3-3 connected to the public low-voltage power
supply network that supplies buildings
used for domestic purposes.

NOTE
 The device needs special precautions regarding EMC and needs to be
installed and put into service according to the EMC information
provided below.
 Other devices may affect this device even though they meet the
requirements of CISPR.
 The EMISSIONS characteristics of this device make it suitable for use in
industrial areas and hospitals (CISPR 11 class A). If it is used in a
residential environment (for which CISPR 11 class B is normally
required) this device might not offer adequate protection to radio-
frequency communication services. The user might need to take
mitigation measures, such as relocating or re-orienting the device.
 If the essential performance is lost or degraded, it may be necessary to
take mitigation measures, such as re-orienting or relocating the ME
EQUIPMENT or ME SYSTEM or shielding the location or stopping using
the veterinary infusion pump system and contact the service personnel.

B-2
 If the device is operated within the electromagnetic environment listed in Table
Guidance and Declaration —Electromagnetic Immunity, the system will remain
safe and provide the following essential performance:
 Operating mode
 Accuracy
 Function
 Protection against UNINTENDED BOLUS volumes
 Occlusion
 ALARM CONDITIONS regarded
 Data stored

Guidance and Declaration - Electromagnetic Immunity

The device is intended for use in the electromagnetic environment specified below. The
customer or the user of the device should assure that it is used in such an environment.
Immunity test IEC 60601 test Compliance Electromagnetic
level level environment -
guidance
Electrostatic ±8 kV contact ±8 kV contact Floors should be wood,
discharge (ESD) ±15kV air ±15kV air concrete or ceramic tile.
IEC 61000-4-2 If floors are covered with
synthetic material, the
relative humidity should
be at least 30%.
Electrical fast ±2 kV for power ±2 kV for power Mains power quality
transient/burst supply lines supply lines should be that of a
IEC 61000-4-4 ±1 kV for ±1 kV for typical commercial or
input/output lines input/output lines hospital environment.
(length greater (length greater than
than 3 m) 3 m)
Surge IEC ±1 kV line(s) to ±1 kV line(s) to
61000-4-5 line(s) line(s)
±2 kV line(s) to ±2 kV line(s) to
earth earth
Voltage dips and 0 % UT for 0,5 cycle 0 % UT for 0,5 cycle Mains power quality
Voltage should be that of a
interruptions 0 % UT for 1 cycle 0 % UT for 1 cycle typical commercial or
IEC 61000-4-11 and 70 % UT for and 70 % UT for hospital environment. If
25/30 cycles 25/30 cycles the user of our product
requires continued

B-3
 operation during power
0 % UT for 250/300 0 % UT for 250/300 mains interruptions, it is
cycle cycle recommended that our
product be powered
from an uninterruptible
power supply or a
battery.
RATED power 30 A/m 30 A/m Power frequency
frequency 50 Hz / 60 Hz 50 Hz / 60 Hz magnetic fields should
magnetic fields be at levels
IEC 61000-4-8 characteristic of a typical
location in a typical
commercial or hospital
environment.
Note: UT is the A.C. mains voltage prior to application of the test level.

Guidance and Declaration - Electromagnetic Immunity

The device is intended for use in the specified electromagnetic environment. The
customer or the user of the device should assure that it is used in such an environment
as described below.
Immunity IEC 60601 Complian Electromagnetic environment -
test Test level ce level guidance
Conducted 3 Vrms 10 Vrms Portable and mobile RF
disturbances 150 kHz to 80 communications equipment should
induced by RF MHz be used no closer to any part of the
fields device, including cables, than the
6 Vrms 6 Vrms
IEC61000-4-6 recommended separation distance
in ISM bands calculated from the equation
and amateur applicable to the frequency of the
radio bandsa transmitter. Recommended
between 0,15 separation distance:
MHz and 80
 3.5 
MHz d = P 150k to 80 MHz
 V 
Radiated 10V/m 10V/m  3.5 
RF EM d = P 80 MHz to 800 MHz
80 MHz to 2.7  E 
fields GHz 7
IEC61000- d =   P 800 MHz to 2.7 GHz
E
4-3
where P is the maximum output
Proximity fields 27 V/m 27 V/m
power rating of the transmitter in
from RF 380–390 MHz watts (W) according to the

B-4
wireless 28 V/m 28 V/m transmitter manufacturer and d is the
communication 430–470 MHz, recommended separation distance
s equipment 800–960 MHz, in meters (m).
IEC61000- 1700–1990 Field strengths from fixed RF
4-3 MHz, 2400– transmitters, as determined by an
2570 MHz electromagnetic site surveyb, should
9 V/m 9 V/m be less than the compliance level in
each frequency rangec.
704–787 MHz,
5100–5800 Interference may occur in the vicinity
MHz of equipment marked with the

following symbol: .
Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.
aThe ISM (industrial, scientific, and medical) bands between 150 kHz and 80 MHz are
6.765 MHz to 6.795 MHz; 13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and
40.66 MHz to 40.70 MHz. The amateur radio bands between 0,15 MHz and 80 MHz are
1,8 MHz to 2,0 MHz, 3,5 MHz to 4,0 MHz, 5,3 MHz to 5,4 MHz, 7 MHz to 7,3 MHz, 10,1
MHz to 10,15 MHz, 14 MHz to 14,2 MHz, 18,07 MHz to 18,17 MHz, 21,0 MHz to 21,4
MHz, 24,89 MHz to 24,99 MHz, 28,0 MHz to 29,7 MHz and 50,0 MHz to 54,0 MHz.
b Field strengths from fixed transmitters, such as base stations for radio
(cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio
broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess
the electromagnetic environment due to fixed RF transmitters, an electromagnetic site
survey should be considered. If the measured field strength in the location in which the
device is used exceeds the applicable RF compliance level above, the device should be
observed to verify normal operation. If abnormal performance is observed, additional
measures may be necessary, such as re-orienting or relocating the device.
cOver the frequency ranges 150 kHz to 80 MHz, field strengths should be less than
3V/m.

B-5
 Recommended Separation Distances between Portable and Mobile RF,
Communications Equipment and This Equipment
The equipment is intended for use in an electromagnetic environment in which radiated
RF disturbance are controlled. The customer or the user of the device can help prevent
electromagnetic interference by maintaining a minimum distance between portable and
mobile RF communications equipment (transmitters) and the device as recommended
below, according to the maximum output power of the communication equipment.
Rated Separation Distance According to Frequency of Transmitter (m)
Maximum
Output power 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.7 GHz
of Transmitter
 3.5   3.5  7
Watts d=  P d=  P d=  P
V   E  E
(W)
0.01 0.04 0.04 0.07
0.1 0.11 0.11 0.22
1 0.4 0.4 0.7
10 1.1 1.1 2.2
100 4 4 7
For transmitters at a maximum output power not listed above, the recommended
separation distanced in meters (m) can be determined using the equation applicable to
the frequency of the transmitter, where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.
Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.

B.2 Radio Regulatory Compliance

RF Parameter
Radio devices IEEE 802.11b/g/n (2.4GHz Wi-Fi)

Operating frequency 2412MHz to 2484MHz

Modulation mode CCK, OFDM
Output power ≤20dBm

The radio device used in this product is in compliance with the essential requirements
and other relevant provisions of Directive 2014/53/EU.

B-6
C Default Factory Settings
This chapter presents some default factory settings.User cannot change the factory
default, but may restore to the default factory settings when it is necessary.

C.1 Alarms
Alarm Setting Factory Default

Volume 4

Alarm sound Sound2

C.2 Interface
UI Factory Default

Brightness 4

C.3 Parameters
Setting Parameters Factory Default

KVO rate 0.5ml/h

Pressure unit mmHg

Occl. pressure 525mmHg

Bubble size 100μl

Accum. bubble 1.5ml/h

Auto-lock Off

Empty Alarm Low

Reminder 2min

Near end 3min

Commonly used tube B. Braun, SK

Bed No. ---

Standby time range 24:00

C-1
C.4 System Time
System Date and Time Factory Default

Time 00:00

Date 01/01/2015

C-2
D Alarm Information
This chapter presents the alarm information of the infusionpump.Prompt information
for operation guidance will not be presented in this chapter.

The table shows the appropriate countermeasures for each piece of information
related to alarm triggering.If the problem still exists after operating according to the
countermeasures, please contact the company.

Alarm Alarm
Reason Countermeasure
Information level

When occlusion occurs in Press to cancel alarm,

the infusion tube between eliminate the causes of the
[Occlusion] High the device and the animal, pressure of infusion tube,
and occlusion pressure
reaches the threshold value. and then press to
continue the infusion.

Size of single bubble or

bubbles accumulated in 1
[Air in line] High Press to cancel alarm.
hour reaches to the preset
value.
The veterinary infusion
[Door opened] High pump door is opened during Press to cancel alarm
infusion. and close the door correctly.

[VTBI Done] High VTBI volume is completed. Press to cancel alarm.

Alarm is triggered when

[KVO Finish] High Press to cancel alarm.
KVO model runs 30 minutes.
Only powered with built-in Connect to the power
[Battery Low] Low battery, battery charge is source to cancel alarm
insufficient. automatically.

Connect to the AC power

Only powered with built-in
[Battery Empty] High source, press or
battery, battery is empty.
to cancel alarm.

[AC Power Power cord disconnected Connect to the power

Low
Disconnection] when the network power source to cancel alarm

D-1
Alarm Alarm
Reason Countermeasure
Information level
source supply is powered. automatically.

The veterinary infusion

pump performs no operation
Operate the pump or open
[Reminder] Low during the set reminder time
the door to cancel alarm.
after the infusion set is
loaded to it.
Motor operation error, data Alarm cannot be cancelled.
[System Error] High communication error, sensor Please stop operation and
failure and etc. contact the company.
1. The alarm will not be
cancelled automatically until
Required time for the the infusion is completed,
[VTBI Near remaining VTBI volume and then switch to [VTBI
Low
Done] almost reaches the set [Near Done] alarm.
end].
2. Or press to cancel
alarm.

Press to cancel alarm,

[Standby Time and then exit standby or
Mid-level Standby is completed.
Expired] continue standby by

pressing .

Charging circuit error, Alarm cannot be cancelled.

[System
Mid-level supplying circuit error and Please stop operation and
abnomal]
etc. contact the company.

Door is opened during

[Tube not infusion, or infusion set is not Correctly load infusion set
Low
inserted] loaded, and start infusion and close the door.
when the door is closed.

D-2
Alarm Alarm
Reason Countermeasure
Information level

If drop sensor is installed

correctly and the switch of
[Drip rate check] is on,
[Drop error] High current rate is ≤400ml/h, Press to cancel alarm.
drop sensor detects that the
drop rate deviates the preset
value.

If drop sensor is installed

correctly and the switch of
[Drop sensor] is on, no liquid
drop.
Note: If drop sensor is not
[Empty bottle] High Press to cancel alarm.
correctly inserted or the
surface of the liquid in the
drip chamber is abnormal,
[Empty bottle] alarm might
be triggered.
Veterinary infusion pump
and BeneFusion CS5
Infusion Supervision System
are communicated Press or restore the
successfully over Wi-Fi, the
communication between
[No network communication is
Low veterinary infusion pump(s)
communication] abnormally interrupted for 3
and BeneFusion CS5
minutes. After the alarm is
Infusion Supervision
triggered, infusion of the
System.
pump will not be influenced,
and the pump continues
infusion.

NOTE

 All alarm sounds can be paused by pressing , except for the

circumstance of [Battery Empty].

D-3
FOR YOUR NOTES

D-4
E Symbols and Terms
E.1 List of Units
Abbreviation Meaning

A ampere

℃ centigrade

cm centimeter

dB decibel

g gram

hr hour

Hz hertz

inch inch

k kilo

kg kilogram

kPa kilopascal

l litre

lb pound

m meter

mg milligrams

min minute

ml milliliter

mm millimeters

mmHg millimeters of mercury

s second

μg Microgram

V volt

VA volt ampere

W watt

E-1
E.2 List of Symbols
Symbols Meaning

- minus

% percent

/ Per; divide; or

～ to

^ power

＋ plus

＝ equal to

< less than

> greater than

≤ less than or equal to

≥ greater than or equal to

± plus or minus

× multiply

© copyright

E.3 List of Terms

Abbreviation Meaning

AC Alternating current

Anti-Bolus Anti-Bolus

BOLUS Bolus

CCU(CICU) Cardiac Intensive Care Unit

CE Conformité Européenne

CISPR International Special Committee on Radio Interference

CPU central processing unit

DC Direct current

DPS Dynamic Pressure System

ECU(EICU) Emergency Intensive Care Unit

E-2
Abbreviation Meaning

EEC European Economic Community

EMC Electromagnetic compatibility

EMI Electromagnetic interference

EtO C2H4O

ICU Intensive Care Unit

ID Identification

IEC International Electrotechnical Commission

IEEE Institute of Electrical and Electronic Engineers

ISO International organization for Standardization

KVO Keep vein open

LED light emitting diode

Max Maximum

MDD Medical Device Directive

Min Minimum

MRI magnetic resonance imaging

N/A not applied

NICU Newborn Intensive Care Unit

OR operating room

SN Series Number

TIVA Total Intra Venous Anesthesia

VTBI Volume To Be Infused

E-3
E.4 List of Unit Conversion
Unit Symbols Unit Conversion

kPa 1kPa=7.5mmHg=0.145psi=0.01bar

psi 1psi=51.724mmHg=6.897kPa=0.069bar

bar 1bar=750mmHg=14.5psi=100kPa

lb 1 lb=0.454kg

drop/min drop/min = (ml/h×drip)/60

E-4
F Toxic and Hazardous Substances or
Elements

Pb Hg Cd Cr(VI) PBB PBDE

Name of the Parts
Pb Hg Cd Cr(VI) PBB PBDE

Front housing ○ ○ ○ ○ ○ ○

Back housing ○ ○ ○ ○ ○ ○
Device
Keys ○ ○ ○ ○ ○ ○
housing
Facing ○ ○ ○ ○ ○ ○

Labels ○ ○ ○ ○ ○ ○

Display Display ○ ○ ○ ○ ○ ○

Host hardware ○ ○ ○ ○ ○ ○

Host Internal cables ○ ○ ○ ○ ○ ○

PCBA ○ ○ ○ ○ ○ ○

Cartons (K=K ○ ○ ○ ○ ○ ○
crimp paper)
Packaging Foam packages ○ ○ ○ ○ ○ ○
(EPE)
Plastic bag (PE) ○ ○ ○ ○ ○ ○

Connecting pieces ○ ○ ○ ○ ○ ○
General
Power cord ○ ○ ○ ○ ○ ○

Battery Battery ○ ○ ○ ○ ○ ○

Accessories Accessories ○ ○ ○ ○ ○ ○

○: Indicates that this toxic or hazardous substance contained in all of

the homogeneous materials for this part is below the limit requirement
in Directive 2011/65/EU.
Remark
╳: Indicates that this toxic or hazardous substance contained in at
least one of the homogeneous materials used for this part is above the
limit requirement in Directive 2011/65/EU.

F-1
FOR YOUR NOTES

F-2
P/N: 046-00035A-00(2.0)
GERMANY SWITZERLAND POLAND

EICKEMEYER KG EICKEMEYER AG EICKEMEYER Sp. z o.o.

Eltastraße 8 Sandgrube 29 Al. Jana Pawła II 27
78532 Tuttlingen 9050 Appenzell 00-867 Warszawa
T +49 7461 96 580 0 T +41 71 788 23 13 T +48 22 185 55 76
F +49 7461 96 580 90 F +41 71 788 23 14 F +48 22 185 59 40
[email protected] [email protected] [email protected]
www.eickemeyer.de www.eickemeyer.ch www.eickemeyer.pl

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65015 Montesilvano (PE) 6500 Vojens 4104 BJ Culemborg
T +39 085 935 4078 T +45 7020 5019 T +31 345 58 9400
F +39 085 935 9471 [email protected] [email protected]
[email protected] www.eickemeyer.dk www.eickemeyer.nl
www.eickemeyer.it

UNITED KINGDOM CANADA

EICKEMEYER Ltd. EICKEMEYER Inc.

3 Windmill Business Village 617 Douro Street, Suite #205
Brooklands Close Stratford, Ont. Canada
Sunbury-on-Thames N5A 0B5
Surrey, TW16 7DY T +1 519 273 5558
T +44 20 8891 2007 F +1 519 271 7114
[email protected] [email protected]
www.eickemeyer.co.uk www.eickemeyercanada.ca