Eickemeyer INFUSOVET CONNECT User manual

USER MANUAL
INFUSOVET CONNECT
INFUSION PUMP
Item no. 402090
Version 3.0, 7/2020
TELEPHONE [phone]
www.eickemeyer.com

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USER MANUAL INFUSOVET CONNECT INFUSION PUMP
T [phone] | F [phone] | [e-mail] | www.eickemeyer.com

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USER MANUAL INFUSOVET CONNECT INFUSION PUMP
T [phone] | F [phone] | [e-mail] | www.eickemeyer.com
CONTENT
Preface............................................................................................................................................... 6
1. Application Scope of the User Manual.......................................................................................6
2. Applicable Object of the User Manual........................................................................................6
3. Use Instructions..................................................................................................................................6
4. Paraphrase............................................................................................................................................6
1. Safety Instructions ................................................................................................................... 7
1.1 Warnings.............................................................................................................................................7
1.2 Cautions..............................................................................................................................................8
1.3 Dialogue Window............................................................................................................................9
1.4 Symbols ........................................................................................................................................... 10
2. Overview .................................................................................................................................11
2.1 Application Scope ........................................................................................................................ 11
2.1.1 Expected Purpose............................................................................................................ 11
2.1.2 Expected Working Environment................................................................................. 11
2.1.3 Suitable Objects............................................................................................................... 11
2.2 Contraindications ......................................................................................................................... 11
2.3 Working Principle......................................................................................................................... 11
2.4 Structure and Performance....................................................................................................... 11
2.4.1 Structure and Performance.......................................................................................... 11
2.4.2 Functional Specifi cations ............................................................................................. 12
2.5 Product Specifi cation.................................................................................................................. 12
3. Appearance .............................................................................................................................15
3.1 Front View....................................................................................................................................... 15
3.2 Operation Panel............................................................................................................................ 16
3.3 Display Screen................................................................................................................................17
3.3.1 Title Bar ...............................................................................................................................17
3.3.2 Interface Icons Description.......................................................................................... 18
3.4 Rear View ........................................................................................................................................ 19
3.5 Drop Sensor (Optional, Item No. 40209001) ...................................................................... 19
4. Installation.............................................................................................................................. 20
4.1 Unpacking and Checking........................................................................................................... 20
4.2 Installation ..................................................................................................................................... 20
4.2.1 Install the Infusion Pump............................................................................................. 20
4.2.2 Install the Drop Sensor ................................................................................................. 21
5. Preparation and Precautions Before Use.............................................................................22
5.1 Use Preparation ............................................................................................................................ 22
5.2 Operation Cautions...................................................................................................................... 22
6. Basic Operation ......................................................................................................................23
6.1 Operation Flow............................................................................................................................. 23
6.2 Infusion Operation....................................................................................................................... 23
6.2.1 Starting and Self Test..................................................................................................... 23
6.2.2 Infusion Apparatus Installation.................................................................................. 24
6.2.3 Replace Infusion Line/ Infusion Container............................................................. 25
6.2.4 Selecting the Infusion Set Brand............................................................................... 25
6.2.5 Set Infusion Mode........................................................................................................... 25
6.2.5.1 ml/h Mode............................................................................................................. 25
6.2.5.2 Body-weight Mode............................................................................................. 25
6.2.5.3 Drip Mode.............................................................................................................. 26
6.2.5.4 Drug Library Mode ............................................................................................. 26
6.2.5.5 Sequence Mode................................................................................................... 26
6.2.6 Purge Air............................................................................................................................. 26
6.2.7 Set the Infusion Parameters ........................................................................................ 26
6.2.8 Start Infusion.................................................................................................................... 26
6.2.9 Changing Infusing Parameters during Infusion.................................................... 26

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6.2.10 Bolus...................................................................................................................................27
6.2.11 Infusion Completion .....................................................................................................27
6.2.12 Stop Infusion...................................................................................................................27
6.2.13 Remove IV Set.................................................................................................................27
6.2.14 Power off or Standby....................................................................................................27
7. System Setting ....................................................................................................................... 28
7.1 Settings ............................................................................................................................................ 28
7.1.1 Drug Library....................................................................................................................... 28
7.1.1.1 Introduction to Drug Library........................................................................... 28
7.1.1.2 Setting Drug Library........................................................................................... 28
7.1.2 KVO Rate............................................................................................................................. 28
7.1.3 Bolus Rate .......................................................................................................................... 28
7.1.4 Occlusion Pressure .......................................................................................................... 28
7.1.5 Bubble Detecting Level ................................................................................................. 29
7.1.6 Cumulative Bubble.......................................................................................................... 30
7.1.7 Finish Pre-Alarm............................................................................................................... 30
7.1.8 Reminder Alarm................................................................................................................ 30
7.1.9 Weight Unit ........................................................................................................................ 30
7.1.10 Pressure Unit................................................................................................................... 31
7.1.11 Micro Mode...................................................................................................................... 31
7.1.12 Drop Sensor..................................................................................................................... 31
7.1.13 Tube Brand....................................................................................................................... 31
7.2 General............................................................................................................................................. 32
7.2.1 Network............................................................................................................................... 32
7.2.1.1 Connection Mode................................................................................................ 32
7.2.1.2 WLAN....................................................................................................................... 32
7.2.2 Sound................................................................................................................................... 32
7.2.3 Date & Time ...................................................................................................................... 32
7.2.4 Screen Lock........................................................................................................................ 32
7.2.5 Brightness........................................................................................................................... 33
7.2.6 Night Mode ........................................................................................................................ 33
7.2.7 Nurse Call ........................................................................................................................... 33
7.2.8 Nurse Call Alarm Level................................................................................................... 33
7.2.9 Battery Capacity Display................................................................................................ 33
7.3 Patient .............................................................................................................................................. 33
7.3.1 Patient Information......................................................................................................... 33
7.4 Records............................................................................................................................................. 33
7.4.1 History Entries................................................................................................................... 33
7.4.2 Last Therapies................................................................................................................... 33
7.4.3 Export History Records .................................................................................................. 34
7.5 System .............................................................................................................................................. 34
7.5.1 Language ............................................................................................................................ 34
7.5.2 SN (Serial Number).......................................................................................................... 34
7.5.3 Version ................................................................................................................................. 34
7.6 Reset Total Volume....................................................................................................................... 34
7.7 Electronic Memory Function..................................................................................................... 34
8. Alarm Prompt and Troubleshooting.....................................................................................35
8.1 Introduction to Alarm Level...................................................................................................... 35
8.2 Multi-level Alarm Rules............................................................................................................. 35
8.3 Alarm Handle................................................................................................................................. 35
8.4 Fault Analysis and Solution...................................................................................................... 36
9. Maintenance ........................................................................................................................... 37
9.1 Cleaning, Disinfecting and Sterilizing....................................................................................37
9.1.1 Cleaning...............................................................................................................................37
9.1.2 Disinfecting ........................................................................................................................37
9.2 Periodical Maintenance ..............................................................................................................37

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9.2.1 Check the Appearance ................................................................................................... 38
9.2.2 Performance Check......................................................................................................... 38
9.2.3 Maintenance Plan............................................................................................................ 38
9.3 Add new Brand and Calibration .............................................................................................. 38
9.4 Repair ............................................................................................................................................... 40
9.4.1 Normal Repair Process .................................................................................................. 40
9.4.2 Maintenance for Long Term Store ............................................................................. 40
9.5 Equipment Components /Accessories................................................................................... 40
9.6 Production Date............................................................................................................................ 40
9.7 Recycling ......................................................................................................................................... 41
10. Battery.................................................................................................................................... 41
10.1 Check the Battery Performance ............................................................................................ 41
10.2 Replaced the Battery................................................................................................................ 41
11. After Sale Service...................................................................................................................42
12. Appendix.................................................................................................................................43
Appendix A: Occlusion Response Property................................................................................. 43
Appendix B: Alarm and Solution.................................................................................................... 44
Appendix C: EMC Electro Magnetic Compatibility Declaration........................................... 46
Appendix D: Wireless Module Information ................................................................................ 50
Appendix E: Factory Default Data Set.......................................................................................... 50

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USER MANUAL INFUSOVET CONNECT INFUSION PUMP
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PREFACE
1. Application Scope of the User Manual
Applicable to InfusoVet Connect infusion pumps of EICKEMEYER®.
This User Manual describes the product’s most complete confi guration, accessories and functions which may not exist in the
product of the user, for more detailed information, please contact EICKEMEYER®.
2. Applicable Object of the User Manual
Applicable to professionally trained veterinary nurses, veterinary equipment repairers, etc.
3. Use Instructions
This User Manual covers the basic information on the safety and effectiveness of the product for guiding the operator to
correctly install, test, operate, use and maintain the product. Please read this manual thoroughly before use and use the
product in a correct way. Please carefully keep the User Manual for future use.
EICKEMEYER® is responsible for the reliability and performance of the equipment only all following conditions are met:
• Use the equipment according to this User Manual.
• The equipment can only be disassembled, assembled, replaced, tested, improved and repaired by the professional
technicians of EICKEMEYER®.
• All components and accessories as well as consumables for repairing are provided by EICKEMEYER®.
• Relevant electric devices meet the international standard IEC/ EN 60601-1 and this User Manual.
4. Paraphrase
【】 means mechanical button
『』 means touch button
( ) further Information
- means inapplicable
√ means accordant
→ means operation steps
Bolus: Infuse large volume of liquid in a short time.
KVO: Keep vein open, prevent blood back to the IV tube and needle blocked.
Anti-bolus: Motor automatically reverse while the IV tube with high pressure.
DPS: Used to indicate real-time detection and dynamic display of blocking pressure.
Warning /Attention: It may possibly cause physical injury or death if the cautions covered in the Warning are not obeyed.
Caution: It may possibly cause physical injury or property loss if the cautions are not obeyed.
Note: In case fails to follow the supplementary or prompt information on the operation instructions may
possibly cause physical injury the equipment fault or property loss if it is not obeyed.
Accessories: The optional components which are necessary and (or) suitable for using with the equipment in order
to achieve the expected purpose, or provide convenience for achieving the expected purpose,or improve
the expected purpose, or increase the additional functions of the equipment.

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1. SAFETY INSTRUCTIONS
1.1 Warnings
Warning!
• Before using, please check the equipment, connecting wire and accessories to ensure that it can work normally
and safely. If there’s anything abnormal, immediately stop working and contact our after sale service department.
Additionally, the adhesion or intrusion of fl uid / drug may possibly cause the equipment fault and malfunction.
Therefore, please clean the equipment after use, and store it correctly.
• This equipment must be operated by trained professional medical care personnel.
• It is not allowed to put and use the equipment in the environment with anesthetic and other infl ammable or
explosive articles to avoid fi re or explosion.
• It is not allowed to store or use the equipment in the environment with active chemical gas (including gas for
disinfecting) and moist environment since it may infl uence the inside components of the infusion pump and
may possibly cause performance drop or damage of the inside components.
• The operator shall guarantee that the set infusion parameters of this equipment are the same as the medical
advice before starting infusion.
• Please correctly install the infusion apparatus according to the infusion indication direction of this equipment,
ensure that infusion tube smoothly and straightly cross the creep device. Otherwise, it may possibly suck blood
from the animal or fails to reach the expected performance.
• Please do not only depend on information prompt during use, please periodically check it to avoid accident.
• Tightly fi x this equipment on the infusion stand and ensure the stability of the infusion stand. Be careful when
moving the infusion stand and this equipment to avoid the equipment dropping and infusion stand falling or
knocking the surrounding objects.
• If the infusion tube is twisted, or the fi lter or needle is obstructed, or blood in the needle which may obstruct
the infusion, the pressure in the infusion tube will rise. When removing such occlusion, it may possibly cause
“bolus injection” (temporary excess infusion) to the animal. The correct method is to tightly hold or clamp the
infusion tube near the puncturing position, then open the door to drop the pressure in the infusion tube. Then
loosen the infusion tube, solve the reason of occlusion, and restart infusion. If infusion is restarted when the
occlusion reason exists, then it may cause occlusion alarm persistently, and the pressure in the infusion tube
may keep rising, and may break or cut off the infusion tube, or hurt the animal.
• This equipment injects fl uid / drug through extruding the infusion tube, but it can’t detect the leakage if the
infusion line is cut off or broken.Therefore, please periodically check it to avoid above fault during the working
period.
• During infusion, please periodically check the dripping state of the fl uid and the fl uid / drug in the intravenous
infusion bag / container, so as to ensure the correct working during infusion. This equipment doesn’t directly
measure the quantity of infusion fl uid, therefore, it is possible that this equipment can’t detect the free infusion
fl ow under the extremely special condition.
• This equipment has the occlusion detection function for detecting and alarming when the infusion needle
deviates the position in the vein or the needle is not correctly punctured in the vein. However, it only alarms
when the occlusion pressure has reached certain numerical value, and the puncturing part may possibly have
become reddish, swelling or bleeding, additionally, it is possible that the device doesn’t alarm for a long period
if the actual occlusion pressure is lower than the alarm threshold value, therefore, please periodically check the
puncturing part. If there’s any abnormal phenomenon for the puncturing part, please timely take suitable
measures, such as puncturing again.

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• Only those infusion apparatus, line, infusion needle and other medical components that meet the local laws
and regulations and the requirements covered in and this User Manual can be adopted, it is suggested to adopt
the infusion apparatus with same brand as this equipment.It can’t ensure the infusion accuracy if the unsuitable
infusion line is adopted.
• It is not allowed to disassemble or refi t this equipment or use it for other purposes except normal infusion.
• No one is allowed to repair this equipment except EICKEMEYER® or the authorized repair technician of
EICKEMEYER®.
• Maintenance or replacement of spare parts is prohibited during the clinical use of the equipment.
• To avoid risk of electric shock, this equipment must only be connected to AC with Ground Protection.
1.2 Cautions
Caution!
• Before its fi rst use after purchase, or this equipment is not used for a long period, please charge the equipment
with AC power supply. If it is not fully charged, under power failure, the equipment can’t continue working with
built-in battery power supply.
• This equipment can not be used in the places with radiological installation or magnetic resonance equipment
as well as the places with high pressure oxygen therapy.
• Not to position ME Equipment to make it diffi cult to operate the disconnection device.
• The DC power supply is only suitable for applications where a backup power supply is required. Only use the
DC power supply line provided by EICKEMEYER®.
• Other devices near this equipment must meet corresponding EMC requirements, otherwise, it may infl uence the
performance of this equipment.
• Under general conditions, please use AC power supply as much as possible since it can prolong the service life
of the battery at a certain degree. When using AC power supply, ensure that the grounding wire is reliably
connected with the ground, and only the AC power wire attached with this equipment shall be adopted. The
built-in battery can only be used as the assistant power supply when the AC power supply can’t reliably
connected with the ground and is not under normal conditions (power failure or moving infusion).
• Before connecting this equipment with power supply, please keep the power socket and plug dry, and the
power voltage and frequency meet the requirements listed in the equipment label or this User Manual.
• The equipment is equipped with the audible and visual alarm system, and the red and yellow alarm indicators
will light on by turn to check if the alarm system can work normally, and the speaker makes the “beep” sound.
• Please keep the equipment away from the AC power socket for a certain distance to avoid fl uid / drug splashing
or dropping in the socket, otherwise, it may possibly cause short circuit.
• Please use the fl uid / drug after it has reached or nearly reached room temperature. When the fl uid / drug is
used at low temperature, the air which is dissolved in the fl uid / drug may cause more air bubbles and result in
frequent air bubble alarm.
• It is not allowed to press and operate the button with sharp object (such as pencil tip and nail), otherwise, it
may possibly cause early damage to button or surface fi lm.
• Please do not use the infusion tube for 8h at the same pumping position. Infusion tube may distort after using
for a long time and cause fl ow rate error. It is suggested to replace the pumping position or directly replace the
infusion tube every 8h.
• Please tightly close the fl ow rate adjuster of the infusion apparatus before taking out the infusion apparatus
to avoid liquid leakage.
• Under the condition of low fl ow rate infusion, please pay special attention on occlusion. The lower the infusion
fl ow rate, the longer the time of detecting occlusion, and it in turn may possibly cause a long time infusion stop
during this period.

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• If the equipment suffered from dropping or impacting, please immediately stop using it, and contact our after
sale service department, because the inside components of the equipment may be possibly damaged even the
appearance is not damaged and abnormality is not occurred when working.
• It is recommended to use the accessories specifi ed in this manual to ensure animal safety.
1.3 Dialogue Window
Dialogue window mainly content include operation select, operation confi rm etc. tips information. For instance:
Figure 1.3-1 Operation select information Figure 1.3-2 Parameter error reminder

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1.4 Symbols
Not all of the below symbols are existed in the equipment you have purchased.
Marks Description Marks Description
LOT
Batch code IP44
Dustproof and waterproof prevent the pouring of
solid objects larger than 1.0 mm in diameter and
the intrusion of splashing water in all directions
Serial number Both direct and alternating current
Caution Battery
Date of Manufacture Handle with harmless method
Input / output Manufacturer
Unlock Non-ionizing electromagnetic
Lock Direct current
Keep dry This side up
Please refer to the instruction manual/ manual Fragile items
Transportation package temperature limit range is
-20 ~ 60°C Stacking level limit
Protective earth (ground) The limited humidity range of transportation
package is 10 ~ 95%
The environmental pressure of transportation package is limited to 50 ~ 106kPa
Table 1.4-1

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2. OVERVIEW
2.1 Application Scope
2.1.1 Expected Purpose
The infusion pump is used together with infusion set to control the dose of liquid infused into animal’s body, for example
intravenous infusion.
2.1.2 Expected Working Environment
Animal Hospital, Pet clinic.
2.1.3 Suitable Objects
Animals.
2.2 Contraindications
No.
2.3 Working Principle
This equipment is a kind of instrument which can drive the pump to extrude the infusion tube for accurately control of the
infusion drops or infusion fl ow rate with the motor, and is capable of guaranteeing to convey drug fl uid safely in the vein of
animal with even rate and accurate dosage.
2.4 Structure and Performance
2.4.1 Structure and Performance
The infusion pump is mainly composed of a control system, a motor driving unit, a peristaltic pressing mechanism, a detecting
device, an alarm device, an input and display device, a housing, a supporting structure thereof and a software component.
Optional drop number sensor, DC power cable, DB15 serial communication cable. Double CPU has been adopted to our pump
to ensure infusion safety. This equipment provides several infusion modes, such as ml/h mode, body weight mode, drip mode,
sequence mode. Additionally, it also has functions such as history records, drug library, Anti-bolus, and alarm and so on.

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2.4.2 Functional Specifi cations
Function / Model InfusoVet Connect
Infusion Mode
ml/h Mode ●
Body-weight mode ●
Drip mode ●
Drug library mode ○
Micro Mode ●
Sequence Mode ●
Occlusion alarm level
5 Levels adjustable:
Level 1: 50mmHg
Level 2: 150mmHg
Level 3: 300mmHg
Level 4: 600mmHg
Level 5: 900mmHg
Drug library ≥2,000
History entries ≥5,000
Brand Library ≥200
WiFi ○
Remarks: ●means standard; ○means optional.
Attention!
This User Manual describes the most confi guration and most complete functions, due to model difference or
optional components, not all functions are equipped in the product you purchased.
2.5 Product Specifi cation
Safety Classifi cation
Electric protection Type Class I
Electric protection Level Defi brillation proof type CF applied Part
Protection against fl uid
ingress IP44
Working mode Continuous operation
Classifi cation Portable equipment, non-portable infusion pump
Specifi cation Parameters
Infusion apparatus
specifi cation 10–60 drops/ml
Infusion Rate
10 – 20 drops/ml specifi cation infusion apparatus: 0.1 – 2,000ml/h
21 – 40 drops/ml specifi cation infusion apparatus: 0.1 – 800 ml/h
41 – 60 drops/ml specifi cation infusion apparatus: 0.1 – 400 ml/h
Minimum step is 0.01 ml/h
< 100 ml/h step is 0.01ml/h
< 1,000 ml/h step is 0.1ml/h
≥ 1,000 ml/h step is 1ml/h

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Infusion accuracy ≤± 5%
Drop rate Infusion set drip pot setting range 10–60 drops/ml, drip rate 1–2,000 drops/min,
step is 1drops/min
Drop rate accuracy ≤± 5%
Bolus Rate (Bolus)
10 – 20 drops/ml specifi cation infusion apparatus: 1 – 2,000ml/h
21 – 40 drops/ml specifi cation infusion apparatus: 1 – 800 ml/h
41 – 60 drops/ml specifi cation infusion apparatus: 1 – 400 ml/h
Minimum step is 0.01 ml/h
< 100 ml/h step is 0.01ml/h
< 1,000 ml/h step is 0.1ml/h
≥ 1,000 ml/h step is 1ml/h
Bolus Rate accuracy ≤± 10%
Purge rate
10 – 20 drops/ml specifi cation infusion apparatus: 100 – 2,000ml/h
21 – 40 drops/ml specifi cation infusion apparatus: 100 – 800 ml/h
41 – 60 drops/ml specifi cation infusion apparatus: 100 – 400 ml/h
Minimum step is 0.1ml/h
< 1,000 ml/h step is 0.1ml/h
≥ 1,000 ml/h step is 1 ml/h
Purge rate accuracy ≤± 5%
VTBI 0 – 9,999.99ml
Minimum step is 0.01ml
Infusion accuracy ≤± 5%
Total Volume Infused 0 – 9,999.99ml
KVO rate 0 ~ 5ml/h
Minimum step is 0.01ml/h
KVO rate accuracy ≤± 10%
Micro mode setting range 0.1 ~ 200ml/h
Time Range 1s – 99hrs59min59s
Acti agentia 0.01–99,999
Volume 0.01 – 9,999ml
Conc. 0.01–99,999
Dose rate 0.01–9,999
Cumulative Bubble 50 ~ 1,000µl / 15 min
Single fault bolus Volume ≤2ml
Anti-bolus volume ≤0.2ml
Fuse Type T2AL 250V
Dimensions (in mm) 131.5 x 90 x 138 (No fastening clamp, no drop sensor hook)
Weight ≤1.55kg
Power Supply
AC power supply 100 – 240V AC, 50 / 60Hz, 0.25 – 0.1A
Input power 50VA
DC power supply DC 10 – 16V, 1.5 – 0.94A

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Battery
Battery quantity 2 pieces
Battery type Lithium battery
Rated battery voltage 7.4V
Battery capacity 5,200mAh
Charging time ≤8h
Running time
Use a new battery full of electricity to power:
Running at 25 ml/h, the running time from start-up to exhaustion of alarm batteries is not
less than 10 hours.
Running at 2,000 ml/h, the running time from start-up to exhaustion of alarm batteries is not
less than 5 hours.
Alarm
Alarm signal sound
pressure level
When the sound is set at lowest level, alarm signal sound pressure level ≥50dB(A)
When the sound is set at highest level, alarm signal sound pressure level ≤80dB(A)
Alarm information
VTBI near end, VTBI infused, Pressure high, Battery nearly empty, Battery empty, system error,
No power supply, Reminder alarm, Standby time expired, KVO fi nished, Drop sensor
connection, Drop error, Empty bottle, Single bubble, Cumulative Bubble, Door Open, Occlusion
pre-alarm, Drop in pressure, Drug dose limits exceeded, Backup battery power exhaustion
Environment
Non AP/APG type
equipment
Do not use it in the environment with infl ammable anesthetic gas mixed with air, and
infl ammable anesthetic gas mixed with oxygen or nitrous oxide
Operating
1. Temperature: 5 – 40°C
2. Humidity: 15 – 95%, non-condensable
3. Atmospheric pressure: 57 – 106kPa
Transport & Storage
1. Temperature: -20 – 60°C
2. Humidity: 10 – 95%, non-condensable
3. Atmospheric pressure: 50 – 106kPa

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3. APPEARANCE
3.1 Front View
① Tubing guide
② Air-in-line sensor (Detection of bubbles in infusion pipelines)
③ Pump door
④ Pressure plate
⑤ Waterproof fi lm
⑥ Door holder
⑦ Pressure sensor-DOWNSTREAM
⑧ Anti-free fl ow clamp
⑨ Display screen
⑩ Handle
Door switch
Note!
It is recommended that the waterproof fi lm be replaced once every two years.

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3.2 Operation Panel
① ②③ ④ ⑤
⑥
⑦
⑧
①【Power】
Pump power switch, press and hold, pump power off. Stand-by selection button. Long press the power button until the
screen closes and the pump shuts down.
② Battery indicator (green)
Indicator fl ashing: device on, battery charging / power supply
Indicator lights on: the battery is full of electricity.
Indicator lights off: equipment shut down, no batteries
③【Menu】
Enter system home page.
④【Bolus / Purge】
⑤【Start / Stop】
⑥ AC/ DC indicator (green)
Turn on: connect AC/ DC power supply
Turn off: dis-connect AC/ DC power supply
⑦4.3 inches TFT(LCD) touch screen
⑧Alarm indicator (red/yellow)
While pump alarms, indicator light glitters, with different frequency and color, more information please refer to Chapter8.1.

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3.3 Display Screen
The display screen interface layout composes of title bar and typical interface.
Title bar
Interface
3.3.1 Title Bar
Title bar displays real-time state information and is not touchable, the left upper corner displays the name of current editing
parameter.
Icon Paraphrase Description
Infusion apparatus indication icon Infusion apparatus indication icon
Lock screen indication icon Unlock state icon is
Battery charging indication icon Display the current battery charging state
WiFi indication icon Indicate WiFi connection state.
Battery status indication icon
The percentage numerical or remaining time value at
the left side of the icon displays the remained battery.
Since the remained battery may change, it may possibly
show the following states:
Table 3.3.1-1

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USER MANUAL INFUSOVET CONNECT INFUSION PUMP
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3.3.2 Interface Icons Description
Icon Paraphrase Description
X / Y Page indication Arabic numerals mean, X is the current page, Y is the
total page
Up Click this icon, return to the back page
Down Click this icon to enter into the next page
Return / Cancel Click this icon, return to the back menu
Radio button-1 The current parameters is selected
Radio button-2 The current Level is selected
Confi rm Click to save the input parameters or the selected
parameters and exit
ON Mean this function is ON
OFF Mean this function is OFF
Clear button Click it to clear input
Backspace button Click it to backspace delete
/ Toggle key Click to switch into English or case input setting
Table 3.3.2-1

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USER MANUAL INFUSOVET CONNECT INFUSION PUMP
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3.4 Rear View
①Handle
②Drop sensor bracket
③DB15 Multi-functional interface, with following functions
• DC power input interface
• Software uploading interface
• Nurse call interface
• Drop sensor interface
Note!
The above functions cannot be used at the same time.
④Clamp
⑤Product label
⑥AC/ DC Adapter Port
⑦Loudspeaker
3.5 Drop Sensor (Optional, Item No. 40209001)
②
①
③
①Housing
②Slider
Push the slider to left direction to adjust the spacing, loosen the slider to automatically return.
③Cable

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USER MANUAL INFUSOVET CONNECT INFUSION PUMP
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4. INSTALLATION
4.1 Unpacking and Checking
1. Please check the appearance before unpacking, if broken, please contact the transportation company or our after-sale
service department quickly.
2. Please carefully open the package to avoid damaging the equipment and relevant accessories.
3. After unpacking, please check the objects according to the packing list, if there’re insuffi cient or damaged accessories,
please contact EICKEMEYER® as soon as possible.
4. Please keep the relevant accessories, User Manual.
5. Please keep the packing case and packing materials for future transportation or storage.
Warning!
Please put the packing materials out of reach of children. Please obey local laws and regulations or the hospital
waste treatment system to handle the packing materials.
4.2 Installation
Warning!
• This equipment shall be installed and used by trained medical personnel only.
• When connecting this equipment with other electric devices to form the combination with special function, if
the combination can’t be confi rmed dangerous or not, please contact the electric expert of hospital to ensure
that the necessary safety of all devices in the combination won’t be destroyed.
• This equipment must be used and stored in environment regulated by EICKEMEYER®.
4.2.1 Install the Infusion Pump
As shown in the fi gure, the infusion pump can be hung against the animal cage by the fastening clip.
Note!
Ensure the stability of the animal cage that is attached to the infusion pump. Be careful when moving the animal
cage and this equipment to prevent the equipment from slipping or colliding with nearby objects.