Bomba de Infusion Medifuion d1-2000

MEDIFUSION
DI-2000
User Manual
Imported by:
DEAM S.R.L, 30 64222464 - 2
Av. Maip 380 Local 1, Crdoba,
X5000IBH - Argentina.
Technical Director: Bioengineer Juan Pablo Giulioni, Mat: 5348 28676206

Authorized by A.N.M.A.T
PM- 1317 -30
Condition of sale: exclusive professional and Health Institutions
DAIWHA
Copyright 2010, DAIWHA Corporation. All rights reserved.
Manual No: DW-DI2000-OP-EN(Rev 1.10)
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Table of Contents
1. Precautions
1.1 Overview .............................................................................................. 4
1.2 Warnings .............................................................................................. 4
1.3 Cautions ............................................................................................... 5
1.4 Symbols ............................................................................................... 8
2. Specifications
2.1 Specifications ....................................................................................... 9
2.2 Occlusion Detection Characteristics .................................................... 11
2.3 Usable IV Sets ..................................................................................... 12
2.4 Characteristics Curves ......................................................................... 13
2.5 Memory Function ................................................................................. 15
2.6 Drop Sensor Functions (Optional) ....................................................... 15
3. Names and Functions

3.1 Keys ..................................................................................................... 16
3.2 Display Section .................................................................................... 18
3.3 Rear Mounting Section ........................................................................ 19
3.4 Inside of Door....................................................................................... 20
3.5 Accessories.......................................................................................... 20
4. Installation
4.1 Installing DI-2000 and Connecting Power ........................................... 21
4.2 Installing the IV Set .............................................................................. 23
4.3 Installing the Drop Sensor (Optional)................................................... 24
5. Menu
5.1 Infusion Mode 1, 2 ............................................................................... 25
5.2 Setting Mode 1, 2 ................................................................................. 26
6. Settings
6.1 Infusion Mode 1 (Normal) .................................................................... 30
6.1.1 Setting Flow Rate (ml/h) ...................................................................... 30
6.1.2 Setting Total Volume (ml) .................................................................... 30
6.1.3 Resetting Accumulated Volume (ml) ................................................... 31
6.1.4 Titration Function ................................................................................. 31
6.2 Infusion Mode 2 (Time) ........................................................................ 32
6.2.1 Setting Infusion Time ........................................................................... 32
6.2.2 Setting Total Volume............................................................................ 32
6.3 Infusion Mode 2 (Gtt) ........................................................................... 33
6.3.1 Setting Gtt ............................................................................................ 33
6.3.2 Setting IV Set Drop .............................................................................. 33
6.4 Infusion Mode 2 (Dosage).................................................................... 34
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6.4.1 Setting Dosage mcg............................................................................. 34
6.4.2 Setting Weight...................................................................................... 35
6.4.3 Setting Dosage (mg) ............................................................................ 35
7. Operation
7.1 Standby (Before Operation) ................................................................. 37
7.2 Start Infusion (Start Operation) ............................................................ 38
7.3 Stop and Pause Operation................................................................... 39
7.4 Viewing Infused Volume and Time Remaining .................................... 39
7.5 Key Lock Function ............................................................................... 40
7.6 History Log Function ............................................................................ 40
8. Alarms
8.1 Air Bubble Alarm .................................................................................. 41
8.2 Occlusion Alarm ................................................................................... 41
8.3 Door Open Alarm ................................................................................. 42
8.4 Battery Low Alarm................................................................................ 42
8.5 Battery Empty Alarm ............................................................................ 43
8.6 Abnormal Drop Alarm .......................................................................... 43
8.7 Completion of Infusion Alarm............................................................... 43
8.8 AC Power Alarm................................................................................... 44
8.9 DC Power Alarm .................................................................................. 44
8.10 Standby Alarm...................................................................................... 44
8.11 Start Reminder Alarm .......................................................................... 44
8.12 Tubing Misloading Alarm ..................................................................... 45
8.13 Near Complete Alarm .......................................................................... 45
8.14 Error Code............................................................................................ 45
8.15 Troubleshooting Alarms ....................................................................... 45
9. User Settings
9.1 Setting Mode 1 ..................................................................................... 49
9.2 Setting Mode 2 ..................................................................................... 50
9.3 Setting Range ...................................................................................... 56
9.4 Set Initialization .................................................................................... 57
10. Precautions During Use

10.1 Maintenance ....................................................................................... 58
10.2 Cleaning and Disinfecting .................................................................... 59
10.3 Disposal ............................................................................................... 59
10.4 Storage................................................................................................. 59
10.5 Technical description ........................................................................... 59
10.6 Warranty and Service Information ....................................................... 60
11. GUIDANCE AND MANUFACTURERS DECLARATION ON

ELECTROMAGNETIC EMISSIONS 61
Document History ............................................................................................ 64
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1. Precautions
1.1 Overview
This manual describes how to use the infusion pump (Model: DI-2000), manufactured by
DAIWHA Corporation, and its technical specifications.
The pump is designed to meet the fluid and drug delivery requirements of todays changing
clinical environment including general wards, critical and intensive care, neonatal, operating
rooms and emergency rooms.
The pump is suitable for use only by appropriately trained clinicians and nurses.
Infusion rates are programmable from 0.1 to 1200 ml/h.
The pump is available enteral feeding purpose.
In case the pump is used for feeding, use only feeding solutions prescribed by the responsible
physician, registered dietitian, registered nurse, or other licensed practitioner.
The pump can operate in Infusion Mode 1 (Normal) and Infusion Mode 2 (Time, Gtt, Dosage)
with variety of dosing units.
Repair or circuit alteration of this equipment can only be carried out by personnel authorized by
manufacturer or its authorized service representative. The warranty shall not apply to defects or
damage caused by repairs or disassembly by anyone other than personnel authorized by the
manufacturer or its authorized service representative, and safety shall not be assured.
Parts or circuits which are used for this equipment can be replaced to improve the safety and
performance of this equipment.
Read this manual carefully before using the pump, and understand its functions and how to use
it for safe use.
Contact manufacturer or its authorized service representative if you have any questions
regarding the User Manual.
This manual is applicable only to pumps with Program Version v0.xxxx or above.
Safety precautions are classified as below in accordance with expected danger,

seriousness of damage and urgency of danger occurrence.
A precaution which can result in critical personnel injury or immediate loss of
Danger life if instructions are not followed.
A precaution which could result in critical personnel injury or loss of life if

Warning instructions are not followed.
A precaution which could result in minor personnel injury or damage to the

Caution product if instructions are not followed.
1.2 Warnings
1. Do not operate the DI-2000 infusion pump in the presence of flammable anesthetics, flammable
liquids, or explosive gases (danger of fire or explosion).
2. Do not touch the inlet section with a wet hand or get it wet (danger of electric shock or short-circuit).
3. Do not operate the pump in an area where strong sources of high frequency waves and
electromagnetic fields are present or where high pressure oxidation ignites (cause of failure or
low performance).
4. Ensure that the top and the bottom of the IV set are installed correctly.
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If it is installed upside down, the patients blood can stream back into the pump.
5. Check the infusion volume, flow rate, time, Micro and settings carefully prior to infusion.
Infusion differences or critical errors may occur, since this pump does not have means to
determine actual infusion rate.
6. Check the functions and infusion differences of the pump if the pump has been severely
impacted, since this pump does not have a device to detect force of impact automatically.
7. Do not use the pump where radiation and MRI equipment are used or where high pressure
oxidation could ignite. Do not use and leave an IV line in a high pressure oxidation therapy
room. (It can cause product failure, degradation or explosion.)
8. Do not leave the infusion pump in a damp environment or where there is active gas
(comprehensive disinfecting gas). (These environments may affect internal electrical parts and
cause degradation of or damage to the equipment.)
9. Do not keep or use the infusion pump in the presence of flammable liquid or gas. Doing so may
cause ignition or explosion.
10. Do not use the infusion pump with gravity infusion. (1. The pump may not detect occlusion
below the connector. 2. If the gravity IV line is empty at the beginning, incorrect infusion may
occur and the alarm may not go off due to infiltration of the air below the connector.)
11. Do not use the infusion pump in an environment, e.g., an extracorporeal circuit, where positive
pressure and negative pressure occur. (Infusion may not be accurate and the occlusion alarm
function may not work properly.)
12. Do not use the infusion pump for infusing blood.
(1. The accuracy of infusion is not guaranteed. 2. It may hemolyze the blood.)
13. To use Enteral Feeding Pump, please make sure to check following advice.
1) Make sure to check using correct Feeding IV set for Nutrition.
2) Make sure to check maximum Flow Rate for each Nutrition.
3) Make sure to check Nutrition Viscosity is suitable to use.
1.3 Cautions
1. Only designated personnel (trained, experienced) are permitted to operate the pump for safe
use.
2. Operate the pump using the correct procedure.
3. The following must be ensured when installing the pump.
1) Be careful of safety, e.g. vibration, impact (including transport).
2) The location for installation shall not be affected by temperature, humidity and pressure.
3) Ensure that the pump is always clean.
4) The correct electric power has to be provided.
5) The location must be securely grounded.
6) Avoid strong direct sunlight.
4. The following must be ensured when operating the pump with an external power source.
1) The power plug has to be plugged into a grounded outlet for the hospital, and check the
rated voltage and the frequency beforehand.
2) Do not use an extension cord containing two wires without it being grounded.
3) Check the power plug prior to use.
4) Do not connect the DC power and AC power to the pump simultaneously.
5) Be careful of the polarity and voltage when using electric power.
5. The following must be ensured when operating the pump with a battery.
1) Be careful of the usage time when operating the pump with a battery.
(The battery can support a running rate of 25 ml/h for up to 6 hours when fully charged.)
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2) Charge the battery if the BATT lamp on the front blinks or if the alarm goes off.
3) Charge the battery at least once a month to prevent its life-span from being reduced if the
battery is not being used for an extended period of time.
4) Fully recharge the battery if possible, since the battery charging lasts for approx. 10 hours
after being completely discharged.
5) The battery capacity is indicated on the battery capacity display bar.
6) Turn the switch on the back of the pump off after use. The battery discharges faster if the
switch remains on without being connected to an external power source.
6. The following must be ensured during infusion.
1) Check the operating conditions of the pump and the patients condition regularly.
2) Check if there is any damage to the IV set, e.g. leakage, broken filter.
3) Use the Key Lock on the back of the pump to prevent the settings from being altered even
if some keys are pressed while the pump is in use.
7. The following must be ensured when using the IV set.
1) Use the IV set designated for medicinal infusion only, otherwise the flow rate may differ
from the desired rate and cause malfunction of the air and occlusion alarms. Contact a
manufacturer or its authorized service representative or the head office if you can't use the
IV set designated in this user manual.
2) Do not reuse the IV set. If you reuse the IV set, it may result in the malfunctioning of
infusion volume or sensors.
3) Change the position of the IV set tube at least 15 cm if it is used for more than 24 hours.
You must follow the instructions in order to use the IV set within the range of tolerance.
4) Do not extend the IV set during installation, as it may result in an incorrect flow rate and
infusion volume.
5) Free flow or leakage may occur if the IV set is not installed correctly.
6) Do not link and use other devices or products to infuse a drug into a patient who is
connected to the IV set section (Patient Line). It may result in an incorrect flow rate and
infusion volume, and may affect the alarm functions.
7) Only use IV sets specified in the operator's manual. Use of unauthorized sets may lead to
PATIENT RISK.
8 Beware that infusion volume may differ in the following conditions when;
1) a solution with high viscosity, e.g., Dextrose 50% is used,
2) activation time of the occlusion alarm is long and infusion does not happen,
3) the pump is operated in an environment other than ambient temperature (10C ~ 40C),
relative humidity (20% ~ 90%) and atmospheric pressure (70 kPa ~ 106 kPa).
9. The following must be ensured when cleaning the pump.
1) Do not disinfect the pump with Ethylene Oxide gas or by autoclaving.
2) Do not wipe the pump with thinner, solvents, benzene, ammonia or acetone. Wipe down
the pump with damp gauze and then dry with a smooth, dry cloth.
3) Do not operate the pump in wet conditions.
4) Do not submerge the pump in water or dry the pump forcibly.
10. Do not open or disassemble the pump.
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Sales & Address: Daiwha B/D, 733-18 Yeoksam-dong, Gangnam-gu, Seoul, Korea
Service Tel: +82 - 2 - 558 - 1711 6
Center Fax: + 82 - 2 - 554 - 0317
Website: http://www.daiwha.com
Address: mdi Europa Gmbh Langenhagener Str. 71 30855 Hannover-

Langenhagener
Tel: +49 - 511 - 39 08 95 30
This is medical equipment.
DAIWHA Corporation
1656-2 Dongwha-ri, Munmak-eup, Wonju city, Kangwon, Korea
Product Name Infusion Pump
Model DI-2000
Approval No. 03-123
Packaging Unit 1 Set
Purpose Consistent infusion of medicine
Storage Preserve at room temperature.
Usages and Precautions See the User Manual.
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1.4 Symbols
Power Off Power On
AC DC
Down Key Up Key
BOLUS (Fast Infusion) Serial Number
STOP/CLEAR
Start Key (Start Infusion)
(Stop motor and delete infusion volume)
Date of Manufacture Manufacturer
Device Complies With The Attention

Requirements of MDD (Read the User Manual carefully prior to
93/42/EEC directive use)
Type CF Feeding Formula
Protected against dripping

IPX1 Reference Number
water
European Authorized Recycle electrical and electronic

Representative equipment
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2. Specifications
2.1 Specifications
Product Name Volumetric Infusion Pump

Model DI-2000
Pumping Mechanism Peristaltic Transit Finger
Micro (On): 0.1 ~ 99.9 ml/h (in 0.1 ml/h increments)

Flow Rate 0.1 ~ 1200 ml/h 100 ~ 1200 ml/h (in 1 ml/h increments)
Micro (Off): 1 ~ 1200 ml/h (in 1 ml/h increments)
5% ( Korea Vaccine CODE S203 Type)

Accuracy Measured every hour at room temperature (25) using water or saline
solution (above 1.0 ml/h of flow rate).
* Accuracy may differ depending on the type of medical fluid and IV set.
Micro (On): 0.1 ~ 99.9 ml (in 0.1 ml increments)
0.1 ~ 9999 ml
Total Vol. 100 ~ 9999 ml (in 1 ml increments)
or infinity Micro (Off): 1 ~ 9999 ml (in 1 ml increments)
Infusion
Range
0.1 ~ 99.9 ml (in 0.1 ml increments)
Infused Vol. 0.0 ~ 9999 ml 100 ~ 9999 ml (in 1 ml increments)
Bolus Rate (Purge) 700 ml/h (default) - 1 ~ 1200 ml/h

Bolus Volume (Purge) 5 ml (default) - 1 ~ 9999 ml
1 ml/h (default)
At flow rate 1.0 ~ 1 2 0 0 m l / h
1 ~ 9 ml/h
KVO Rate
0.1 ml/h (default) At flow rate 0.1 ~ 0.9 ml/h
Occlusion pressure 100mmHg ~ 950mmHg(13~126kPa)
Display 7 segments (4 digits * 3 lines)
* Air Bubble alarm

* Occlusion alarm (detection capacity: 100 ~ 950 mmHg)
- seven adjustable steps for downstream occlusion
* Door Open alarm
* Battery Low, Battery Empty alarm
* Abnormal Drop alarm
* Infusion Complete alarm (automatic switch-over to KVO feature)
Alarms * AC/DC Power Shut-off alarm
* Start Reminder alarm (pause set time elapsed)
* Standby alarm (at an interval of 2 minutes when not infusing)
* Near complete alarm
* The pump stops operating when alarms go off except for battery low,
start reminder and infusion completion signals.
* Malfunction
- The status of the pump is displayed and an alarm goes off.
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* Door Open: Infusion is unavailable when the door is open.
* Key Lock: Only the START, STOP and ON/OFF keys work.
* Air Sensor: Detects air bubbles.
Safety Features
* Occlusion Sensor: Detects clogging of the tube.
* Drop Sensor: Detects medical fluid drops.
* Nurse Call: Monitoring is possible if an alarm goes off.
* Time Mode: Calculates the flow rate by setting the infusion time.
* Gtt Mode: Calculates the flow rate by setting the number of infusion
drops.
* Dosage Mode: Calculates the flow rate by setting the dosage.
* Titration: Flow rate can be altered during infusion (available only
when the remaining time for infusion is more than 5 minutes).
* Battery Low, Empty: Alarms go off 30 minutes and 3 minutes before
the battery goes flat.
* Date and Time: The date and time can be checked without a power
supply, since a clock is installed.
Other Functions * Pause: Infusion resumes automatically after preset time elapses
when the pause key is pressed and infusion is stopped (default 24
hours, setting range from 1 minute to 24 hours in 1 minute units).
* Event History: Saves up to 2000 and it can view by separate PC
utility. Please refer service manual for detailed usage of event
history.
* Alarm log event: Saves up to 50 in the pump and it can view in the
pump at setting mode1. Please refer service manual for detailed
usage of alarm log event.
* The electronic data of the infusion pump are stored for over 2 years
even if it has been turned off.
* AC 100~240 VAC, 50~60 Hz (Fuse: 250 V, T3.15 A)

* DC 12V (500 mA)
* Ni-MH Rechargeable Battery
Power
- 2,100 mA/h, AA, 1.2V x 10cell
- operating time approx. 4 hours at a flow rate of 25 ml/h
- recharging time approx. 10 hours
Power Requirements 35VA
* Protection from electric shock: Class

Protection Type * Protection capacity for electric shock: Type CF
Protection from liquid infiltration: IPX 1 (drip-proof)
Size (DWH) 120130206 mm

Weight approx. 1.7 kg
Temperature: 10~ 40, Humidity: 20 ~ 90%

Operating Environment
Atmospheric Pressure: 70 ~ 106 kPa (525.04 ~ 795.06 mmHg)
Temperature: -10 ~ 60, Humidity: 10 ~ 95%

Storage Environment
Atmospheric Pressure: 65 ~ 120 kPa (487.54 ~ 900.07 mmHg)
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User Manual 1 ea (Manual No.: Refer to the front cover of the manual.)
Infusion Pole Clamp 1 ea (Model: PoleClamp-A)
Accessories Drop Sensor (Model: DropSensor-A) (Optional)
AC Power Cable 1 ea (4 meters, 0.75 x 3C, KS C IEC 60227-5
300/500V 60227 KSIEC 53)
Communication USB
2.2 Occlusion Detection Characteristics
1. Occlusion Pressure, Time to Alarm and Bolus Volume are measured at a 1 ml/h and 25 ml/h of
flow rate.
2. IV set for measurement: Korea Vaccine CODE S203 Type (at ambient temperature 25)
3. Measurement position: The occlusion clamp is placed 1 m below the pump.
NOTE: The following figures are only for reference.

(Measurement Instrument: FLUKE IDA4PLUS)
Occlusion Occlusion Time to BOLUS
Flow Rate Level Pressure Alarm Volume
(Setting) (mmHg) (min : sec) (ml)
1 275.5 36 : 02 0.55
1 ml/h 4 524.5 54 : 03 0.9
7 775.0 90 : 06 1.5
1 278.0 01 : 30 0.58
25 ml/h 4 532.0 02 : 10 0.95
7 771.5 03 : 50 1.45
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2.3 Usable IV Sets
1. KoreaVaccine (Type S203T), Baxter,Sendal, Bbraun, Ferraril etc
2. Various kinds of IV sets will be available through continuous product updates.
Please refer service manual for setting user IV sets.
Caution
The infusion amount may differ depending on the types of IV sets.
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2.4 Characteristics Curves
* The following characteristics curves were achieved in the same conditions as those of IEC
60601-2-24.
1. Start-up Curve: This curve shows an infusion every 30 seconds within 2 hours of measuring
time, and the characteristics of the infusion when the ratio becomes stable after onset of the
infusion.
2. Trumpet Curve: This curve shows the fluctuation ratio through the maximum and the minimum
differences in the flow rate on the horizontal and the vertical axes. (The smaller the gaps get,
the less fluctuations occur.)
NOTE: The following figures are only for reference.
(Measurement Instrument: FLUKE IDA4PLUS)
Flow Rate: 1 ml/h
Flow Rate: 25 ml/h
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Influences of Back Pressure at 25ml/h(Pressure 100mmHg)
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2.5 Memory Function
1. Recent flow rates and intended infusion volume are stored in the internal memory after the
power is turned off, and the data saved in the memory are semi-permanently stored.
2. The date, time, infusion volume and status are stored, and these data can be checked on the 7
segment character display, or the history log can be downloaded via USB.
2.6 Drop Sensor Function (Optional)
1. Detects free flow caused by abrupt device malfunctioning
2. Detects No Drop caused by an empty bottle or clogging of the tube.
3. It is advisable to reinforce the safety of the drop sensor.
4. See Drop S ensor Installation for other installation.
Caution
Do not connect or disconnect the Drop sensor during infusion.
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3. Names and Functions
3.1 Keys
SEL Key ( ) - This key is used when selecting the total volume, flow rate and infusing time in
Infusion Mode 1. When pressing the SEL Key, STOP/CLEAR Key and holding it down, you
access Setting Mode 1. When pressing the SEL Key and holding it down in Setting Mode 1, you
access Setting Mode 2. The desired display for setting will blink.
MODE Key ( ) - Pressing this key and holding it down in Infusion Mode 2 will allow you to
switch between TIME - GTT - DOSAGE
UP Key ( ) in units of 100 - This key is used for setting the total volume, flow rate and Setting
Mode, and increases by 100 whenever pressed.
DOWN Key ( ) in units of 100 - This key is used for setting the total volume, flow rate and
Setting Mode, and decreases by 100 whenever pressed.
BOLUS Key ( ) - The flow rate and volume set in the Setting Mode (BOLUS volume and rate)
are infused during pause or infusion when pressing the BOLUS key. If this key is pressed
continuously, the infusion continues at the rate set in the Setting Mode (BOLUS rate). When
pressing this key quickly in Infusion Mode 2, Setting Mode 1 or Setting Mode 2, the pump will
change to the standby mode.
(Only the occlusion sensor is detected while the BOLUS is operating during infusion.)
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PAUSE Key ( ) - The infusion is paused for a time set in the Setting Mode if this key is
pressed. The infusion resumes when the set time elapses.
(Press the STOP/CLEAR key when resuming the infusion before the set time has elapsed.
Pressing the STOP/CLEAR key completes the set time and continues on to a normal state.)
STOP/CLEAR Key ( ) - This key is used when pausing medical fluid infusion, Bolus and KVO.
Pressing this key and holding it down in standby for an infusion will initialize the blinking display
information (total volume, flow rate and accumulated infusion volume).
START Key ( ) This key is used when starting an infusion and after completing the infusion
settings. However, only when the total volume is larger than the volume to be infused, can
infusion start.
ON/OFF Key ( ) The pump is turned on when pressing this key, but when pressing and
holding this key, it turns off.
(This key does not work during infusion, but works in the infusion standby mode.)
R.TIME Key ( ) - Infusion volume is displayed when starting infusion. Pressing this key will
display the remaining time to complete the infusion.
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3.2 Display Section
OCCL LED- This LED is turned on if the IV set is clogged.

LOCK LED - This LED is turned on if the the keys are locked.
AIR LED - This LED is turned on if air gets into the pump body.
DOOR LED - This LED is turned on if the door is kept open.
COMP LED - This LED is turned on when completing infusion.
BATT LED - This LED blinks when the battery capacity that is left is 30 minutes long when using
battery power. This LED is turned off when the battery capacity that is left is 3 minutes long.
Micro LED - This LED is turned on when operated in the Micro Mode
T.Vol (ml) Display Desired total infusion volume is displayed.
I.Vol (ml) Display, R.TIME Display - The infused volume to a patient and the remaining time are
displayed.
F.Rate (ml/h) Display - The flow rate, alarm messages and error codes are displayed.
AC/DC LED - This LED is turned on when electric power (AC/DC) is supplied.
Battery Capacity Display Bar LED The battery status is displayed in three levels (high,
middle, low).
<Battery level display based on the battery capacity>
No. Battery Status Battery Capacity Display Bar BATT Alarm Led
1 70 % ~ 100% Full Off
2 15 % ~ 70% Middle Off
3 Battery Low Low Blink
4 Battery Empty Empty Blink
5 Battery Removed Empty On
The current charge level is The corresponding
6 Charging
displaying. status is indicated.
7 Charging Complete Full Off
Caution
The battery is not charged when DC power is supplied.
Status Indication LED:

- Green and red LEDs Off: standby for infusion
- Green LED blinking: infusing or communicating
- Green LED On: infusing KVO
- Red LED blinking: alarm occurred
- Red LED On: error occurred
- Green and Red LEDs blinking alternatively: during pause
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3.3 Rear Mounting Section
RS485 Port Used when downloading History

Log and communicating via RS485.
Drop Sensor Port The Drop Sensor is

connected to this port.
Nurse Call Port Connected to the Nurse Call

equipment with a Nurse Call cable and warning
signals are sent to the Nurse Call equipment
during the infusion.
USB Port Used when downloading History

Log and communicating via USB.
DC Power Port - 12 ~ 15 VDC can be supplied.
Key Lock - Only the START( ) and
STOP/CLEAR Key ( ) and ON/OFF ( )

keys work.
Power Switch Turns power on or off.
Battery Built-in battery
Power Inlet The power cord is plugged into

this inlet.
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3.4 Inside of Door
Air Detector Prevents the patient from getting

injected with air by detecting the air in the IV set.
Auxiliary Door Lock Used when opening this

door.
Pumping Unit Infuses medical fluid by pressing

the tube of the IV set.
Door Lock Lever Used when opening or closing

the door.
Occlusion Detector Detects whether the tube at

the bottom of the equipment is clogged.
Auxiliary Door Holds the IV set in position for

safe infusion of medical fluid.
Door Lock Prevents the door from opening.
3.5 Items supplied with pump
AC Power Cable
Infusion Pole Clamp
Drop Sensor (Optional)
User Manual
5 IV sets (Optional)
AC Power Cable Infusion Pole Clamp Drop Sensor
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4. Installation
4.1 Installing DI-2000 and Connecting Power
Installing DI-2000 on the infusion stand
1. Mount the pole clamp onto the infusion stand by fastening

the knob of the pole clamp.
2. Align the pump to the pole clamp hole and gently press it
down. Press the pole clamp lever down to detach the pump.
Before Assembling After Assembling
Caution
DI-2000 can not work in horizontal or other position.
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Connecting external power
1. Plug the power cord into the AC power cord inlet on the back of
the pump.
2. Turn on the power switch at the back of the pump, and the
AC/DC orange LED will turn on.
3. Press the ON/OFF key on the front.
4. The display on the front turns on and the functions of the pump
will be checked automatically.
Using the battery power
AC Power
1. Turn on the power switch at the back of the pump, and the Green
Battery Capacity Bar LED will turn off.
2. Press the ON/OFF key on the front.
3. The display on the front turns on and the functions of the pump
will be checked automatically.
4. The F.Rate window blinks after completing the self-test, and the
settings for the flow rate are displayed.
ON/OFF
Key
AC/DC LED
BAT. LED
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4.2 Installing the IV Set
1. Place the roller clamp of the IV set at the bottom of the

pump and close the roller clamp.
2. Put the injecting needle into the IV solution container and

fill the solution in the chamber to between 1/3 and 1/2.
3. Open the roller clamp to remove the air from the tube and
then close the roller clamp.
4. Mount the IV solution container on the pole. The solution

container must not be placed more than 1 m above the
patients heart.
5. Push the door knob upwards to open the door.
6. Press the auxiliary door lock to open the pumping unit.
7. Hold with a hand and gently stretch in the direction of .
8. Press the IV set tightly onto the air detector to keep the
tube in position.
9. Hold with a hand so as not to stretch and press the

Occlusion Detector to hold the tube in position.
10. The Air Alarm or the Occlusion Alarm may be triggered if

the IV set is not properly installed.
11. Press the door knob downwards to close the door. The
auxiliary door will automatically close with door.
12. Open the roller clamp in the IV set.
13. Remove the air in the tube and check if there is leakage
prior to putting the needle into the patients vein.
Caution
1. Verify if the IV set is approved. Using an inappropriate IV set may result in triggering the
occlusion or air alarm, or not achieving a desired flow rate.
2. Make sure that the IV set is installed straight without being bent or twisted, otherwise it may
result in not achieving a desired flow rate.
3. Close the roller clamp prior to opening the door or removing the IV set, otherwise leakage may
occur.
4. Follow the above instruction when replacing the liquid container or IV set.
5. It is recommended to place the IV solution container more than 50 cm above the patients heart.
6. Do not use the IV set in the same position over 24 hours, The tubing may deform and cause a
flow error when used continuously over a long period. It is recommended either to side the tubing
by at least 15cm once in every 24 hours or to replace with a new IV set.
- 24 -
4.3 Installing the Drop Sensor (Optional)
1. Connect the drop sensor to the drop sensor port on the back of
the pump.
Caution: Do not connect the drop sensor to the Nurse Call port
or the RS485 port.
Do not connect or disconnect the drop sensor during infusion.
2. Set the drop sensor according to the IV set drops/ml.
3. Place the drop sensor between the drip chamber nozzle and the
surface of the liquid.
Do not install the drop sensor too close to the nozzle, do not tilt
the chamber, do not install the drop sensor below the surface of
the solution, otherwise drops cannot be counted.
4. Install the drop sensor vertically to the drip chamber, otherwise it

may not operate properly.
5. Always ensure the surface of the IV set chamber is kept clean

when using the drop sensor.
Ensure that there is no dirt or in the chamber, otherwise drops
cannot be counted.
.
Caution
1. Do not expose the drop sensor to direct sunlight.
- 25 -
5. Menu
* Letter Display
5.1 Infusion Mode1, 2: Use the UP and DOWN ( , ) keys to change the values.
Infusion Mode1
Press and
hold down
Press quickly
Press quickly
Pressing the SEL ( ) key quickly will switch the mode to Infusion Mode 1.
Infusion Mode2
Press and
hold down
Press quickly
Press quickly
Press quickly
- 26 -
Pressing the MODE ( ) key and holding it down will switch the mode to Infusion Mode 2.
- 27 -
5.2 Setting Mode1, 2: Use the UP and DOWN ( , ) keys to change the values.
* When pressing the SEL ( ) key and STOP ( ) key simultaneously and holding it down,
Setting Mode 1 appears. When pressing the SEL( ) key again in Setting Mode 1 and holding
it down, the mode switches to Setting Mode 2.
* HLOG (History Log) and CLAC(Calibration) menu is accessible by service personnel only.
- 28 -
6. Settings
1. Infusion Mode 1 (Normal) and Infusion Mode 2 (Time, Gtt, Dosage) can be set by pressing the
SEL ( ) key or the MODE ( ) key. (See Changing infusion mode.)
2. Enter set values according to each infusion mode. (See Infusion Mode.)
3. Infusion set values can be changed in Micro Mode. (See Micro Mode.)
4. To set values, use the UP and DOWN ( , ) keys. (See Changing Infusion
Mode values.)
Changing infusion mode

Mode
Button Operation Description
Category
Accesses and
Infusion Mode 1 Press the SEL ( ) key quickly to access and
changes Infusion
(Normal) change. Mode 1.
Press the MODE ( ) key and hold it down to

Accesses Infusion
access. Press this key quickly to switch Mode 2.
Infusion Mode 2
between Time, Gtt, and Dosage.
(Time, Gtt,
Dosage) In Infusion Mode 2, press the SEL ( ) key Changes Infusion
quickly to switch to a submenu. Mode 2.
Micro Mode
Mode
Display Setting Range Remarks
Category
Total desired infusion volume
100 ~ 9999 ml (in 1 ml increments)
Flow rate
0.1 ~ 99.9 ml/h (in 0.1 ml/h increments)
Micro On 100 ~ 1200 ml/h (in 1 ml/h increments)
Accumulated infusion volume
0.1 ~ 99.9 ml (in 0.1 ml increments) See 9.1.3 Setting
100 ~ 9999 ml (in 1 ml increments) Micro Mode On
or Off
Total desired infusion volume
Flow rate
1 ~ 1200 ml/h (in 1 ml/h increments)
Micro Off Accumulated infusion volume
- 29 -
Infusion setting mode
Mode
Display Description Remarks
Category
The normal infusion mode can

Infusion Mode 1 be set by using the flow rate
(ml/h) and total volume (ml). See 6.1
(Normal)
The time infusion mode can be

set by using the infusion time
Time (ml/min) and total volume (ml). See 6.2
The Gtt infusion mode can be

set by using the Gtt (Gtt/min),
Infusion
Gtt no. of IV set drops (drop/ml) See 6.3
Mode 2
and total volume (ml).
The dosage infusion mode can

be set by using the dosage
Dosage (mcg/kg/min), weight (kg), See 6.4
dosage volume (mg) and the
total volume
Changing infusion mode values

Mode
Button Operation Remarks
Category
A value can be set and changed in

, units of 100.
Infusion Volume A value can be set and changed in See Setting Each
Setting Mode , units of 10. Menu.
A value can be set and changed in
, units of 1.
- 30 -
DPS(Dynamic Pressure System) Monitoring and setting
DPS function is to monitor the pressure in IV tube in real time, and it shows both of pressure setting
value and real-time pressure value together.
1. Infused Vol., DPS, Remaining Time are displayed by pressing R.TIME ( ) key.
DPS Function Active
You can check the pressure setting level.
You can check the real-time pressure during operation.
You can check the pressure down.
- 31 -
6.1 Infusion Mode 1 (Normal)
1. Infusion Mode 1 (Normal) can be set in the order of flow rate, total volume and accumulated
infused volume.
2. When pressing the SEL ( ) key, the display blinks in the following order: F.Rate (ml/h) T.Vol
(ml) I.Vol (ml).
3. A value can be set within the set value range.
6.1.1 Setting Flow Rate (ml/h) Infusion Mode 1 (Normal)
1. In Infusion Mode 1 (Normal), press the SEL ( ) key until the F.Rate(ml/h)
display starts to blink.
2. Set the desired flow rate (ml/h) using the UP and DOWN ( ,
) keys.
3. The flow rate is displayed down to the decimal point when the Micro LED is
turned on. If the Micro LED is turned off, then the decimal point is not
displayed. (See 9.1.3 Setting Micro Mode On or Off)
1) Micro Mode
- Micro LED On: 0.1 ~ 99.9 ml/h (in 0.1 ml/h increments)
100 ~1200 ml/h (in 1 ml/h increments)
- Micro LED Off: 1 ~ 1200 ml/h (in 1 ml/h increments)
4. Press the STOP/CLEAR ( ) key and hold it down to reset the set value on
the F.Rate(ml/h) display.
5. Set a flow rate (ml/h) and press the R.TIME ( ) key to view the time
remaining.
6. Press the BOLUS ( ) key quickly to switch to the standby mode.
7. Press the START ( ) key to access the infusion state.
Only the flow rate can be changed for titration.
6.1.2 Setting Total Desired Volume (ml) Infusion Mode 1 (Normal)
1. In Infusion Mode 1 (Normal), press the SEL ( ) key until the T.Vol (ml) starts blinking.
2. Set the desired total volume (ml) using the UP and DOWN ( , ) keys.
3. The total volume is displayed down to the decimal point when the Micro LED is turned on. If the
Micro LED is turned off, then the decimal point is not displayed. (See 9.1.3 Setting Micro Mode On
or Off)
1) Micro Mode
- Micro LED On: 0.1 ~ 99.9 ml (in 0.1 ml increments)
- 32 -
100 ~1200 ml (in 1 ml increments)
- Micro LED Off: 1 ~ 1200 ml (in 1 ml increments)
the T Vol (ml) display.
5. After setting the total desired volume, press the R.TIME ( ) key to view the
time remaining.
* Setting infinite infusion mode: Press the STOP/CLEAR ( ) key and hold it
down to reset the set value on the T.Vol (ml) display, and set the desired
volume using the UP and DOWN ( , ) keys.
- - - - is displayed on the display.
6.1.3 Resetting Accumulated Volume (ml) Infusion Mode 1 (Normal)
1. In Infusion Mode 1 (Normal), press the SEL ( ) key until the I.Vol (ml)
display starts to blink.
2. Accumulated infusion volume is displayed as follows regardless of the Micro

Mode.
the I.Vol (ml) display.
4. Set a flow rate (ml/h) and press the R.TIME ( ) key to view the time
remaining.
6.1.4 Titration Function Infusion Mode 1 (Normal)
1. To set a flow rate, press the SEL ( ) key during infusion until the F.Rate (ml/h) display starts to blink.
2. Press the START ( ) key to infuse using the changed flow rate.
3. Press the STOP/CLEAR ( ) key to switch back to the previous set value.
- 33 -
6.2 Infusion Mode 2 (Time)
1. Press the MODE ( ) key to set Infusion Mode 2 (Time) when the time is displayed on the T.Vol
(ml) display.
2. Pressing the SEL ( ) key will change Time (ml/min) TVOL (ml) on the I.Vol (ml) display and
the corresponding F.Rate (ml/h) display will blink.
6.2.1 Setting Infusion Time Infusion Mode 2 (Time)
1. Press the MODE ( ) key and hold it down until the time appears on the
T.Vol (ml) display.
2. When pressing the SEL ( ) key in Time Mode, the time is displayed on
the I.Vol (ml) display. When the F.Rate (ml/h) display starts to blink, you
can set the infusion time.
3. Set the desired infusion time using the UP and DOWN ( ,

) keys.
Set time 00.00 ~ 24.00 (00.01 (in 1 min increments))
6.2.2 Setting Total Volume Infusion Mode 2 (Time)
1. Press the MODE ( ) key and hold it down until the time appears on the
T.Vol (ml) display.
2. When pressing the SEL ( ) key in Time Mode, TVOL is displayed on the
I.Vol (ml) display. When the F.Rate (ml/h) display starts to blink, you can set
the total volume (ml).
3. Set the desired infusion volume using the UP and ( ,

) keys.
4. The total volume is displayed down to the first decimal point when the Micro
LED is turned on. If the Micro LED is turned off, then the decimal point is not displayed. (See 9.1.3
Setting Micro Mode On or Off)
1) Micro Mode
- 34 -
6.3 Infusion Mode 2 (Gtt)
1. Press the MODE ( ) key and hold it down to set Gtt Mode until Gtt appears on the T.Vol (ml)
display.
2. Pressing the SEL ( ) key will change Gtt (gtt/min) Drop(Drops/ml) T.VOL (ml) on the I.Vol
(ml) display and the corresponding F.Rate (ml/h) display will blink.
6.3.1 Setting Gtt Infusion Mode 2 (Gtt)
1. Press the MODE ( ) key and hold it down until Gtt appears on the T.Vol
(ml) display.
2. When pressing the SEL ( ) key in Gtt Mode, Gtt is displayed on the I.Vol
(ml) display. When the F.Rate (ml/h) display starts to blink, you can set the
Gtt rate (gtt/min).
3. Set the desired infusion time using the UP and DOWN ( ,

) keys. Gtt can be set 0.1 ~ 500 (1 gtt/min).
6.3.2 Setting IV Set Drop Infusion Mode 2 (Gtt)
(ml) display.
2. When pressing the SEL ( ) key in Gtt Mode, the no. of drops is displayed
on the I.Vol (ml) display. When the F.Rate(ml/h) display starts to blink, you
can set the no. of IV Set drops (drops/min).
3. Set the desired infusion no. of drop using the UP and ( ,

) keys. The drops can be set only to 15, 20 or 60. There are three
types of IV Set drops: 15 (drops/ml), 20 (drops/ml), 60 (drops/ml).
6.3.3 Setting Total Volume Infusion Mode 2 (Gtt)

(ml) display.
2. When pressing the SEL ( ) key in Gtt Mode, TVOL is displayed on the
I.Vol (ml) display. When the F.Rate (ml/h) display starts to blink, you can set
the total volume (ml).
3. Set the desired infusion volume using the UP and ( ,

) keys.
4. The total volume is displayed down to first decimal point when the Micro
- 35 -
1) Micro Mode
6.4 Infusion Mode 2 (Dosage)
1. Press the MODE ( ) key and hold it down to set Dosage Mode until DOSG appears on the T.Vol
(ml) display.
2. Pressing the SEL ( ) key will change MCG (mcg/kg/min) KG (kg) -> MG (mg) -> T.VOL (ml)
on the I.Vol (ml) display and the corresponding F.Rate (ml/h) display will blink.
6.4.1 Setting Dosage Order mcg Infusion Mode 2 (Dosage)

1. Press the MODE ( ) key and hold it down until DOSG appears on the
T.Vol (ml) display.
2. When pressing the SEL ( ) key in Dosage Mode, MCG is displayed on
can set the mcg amount (mcg/kg/min).
3. Set the desired infusion dosage using the UP and DOWN ( ,

) keys.
4. The mcg volume is displayed down to the first decimal point when the
Micro LED is turned on. If the Micro LED is turned off, then the decimal point is not displayed.
(See 9.1.3 Setting Micro Mode On or Off)
1) Micro Mode
- Micro LED On: 0.1 ~ 99.9 ml (in 0.1 mcg/kg/min increments)
100 ~200 ml (in 1 mcg/kg/min increments)
-Micro LED Off: 1 ~ 200 ml (in 1 mcg/kg/min increments)
- 36 -
6.4.2 Setting Weight Infusion Mode 2 (Dosage)
T.Vol (ml) display.
2. When pressing the SEL ( ) key in Dosage Mode, KG is displayed on the
I.Vol (ml) display. When the F.Rate (ml/h) display starts to blink, you can
set the weight (kg).
3. Set the desired infusion weight using the UP and DOWN ( ,

)keys.
4. The weight (KG) is displayed down to the first decimal point when the Micro
1) Micro Mode
- Micro LED On: 0.1 ~ 99.9 kg (in 0.1 kg increments)
100 ~ 150 kg (in 1 kg increments)
- Micro LED Off: 1 ~ 150 kg (in 1 kg increments)
5. Press the BOLUS ( ) key to switch to the standby mode.
6.4.3 Setting Dosage (mg) Infusion Mode 2 (Dosage)

T.Vol (ml) display.
2. When pressing the SEL ( ) key in Dosage Mode, mg is displayed on the
I.Vol (ml) display. When the F.Rate (ml/h) display starts to blink, you can
set the dosage (mg).

)keys.
Dosage setting range: 1 ~ 800 mg (in 1 mg increments and 0.1 mg increments with
micro on)
6.4.4 Setting Total Volume Infusion Mode 2 (Dosage)

T.Vol (ml) display.
2. When pressing the SEL ( ) key in Dosage Mode, TVOL is displayed on
can set the total volume (ml).
)keys.
4. The total volume is displayed down to the first decimal point when the Micro
LED is turned on. If the Micro LED is turned off, then the decimal point is
not displayed. (See 9.1.3 Setting Micro Mode On or Off)
1) Micro Mode
- 37 -
7. Operation
* Please ensure that you operate the infusion pump in a safe indoor area.
1. Operation states can be categorized as follows.

Types of Operation States
Mode
Display Description
Category
The infusion pump can be operated immediately when

Standby
pressing the START ( ) key.
Infusion The START ( ) key was pressed, and infusion has started.
Purge Infusion Press the BOLUS ( ) key in the standby mode.
Bolus Infusion Press the BOLUS ( ) key in the normal infusion state.
When infusion reaches the volume limit, it switches to the KVO

KVO Infusion
Mode automatically.
Pause When the PAUSE ( ) key is pressed in the normal infusion

state, the infusion pauses.
Infusion Mode 1 At least one display out of T.Vol (ml), I.Vol (ml) and F.Rate
(Normal) (ml/h) blinks in this mode.
Infusion Mode 2
Press the MODE ( ) key to enter Infusion Mode 2 (Time, Gtt,
(Time, Gtt,
Dosage) Dosage).
- 38 -
Press the SEL ( ) key and STOP ( ) key simultaneously
and holding it down to enter Setting Mode 1.
Setting Mode 1,2
Press the SEL( ) key and holding it down to enter Setting
Mode 2 from Setting Mode 1.
(In detail, please refer Chapter 9. user setting)
7.1 Standby (Before Operation)
1. The infusion pump can be operated immediately when pressing the START ( ) key in the
standby mode.
2. You can access any mode in the standby mode. However ensure that the Key Lock switch is
turned off. (See 7.5 Key Lock Function.)
3. The Standby alarm goes off if no keys are pressed for 2 minutes in the standby mode.
The red status LED and 'STBR' on the F.Rate (ml/h) display blink.
See Chapter 9 Setting Standby Alarm in Setting Mode 2.
4. When pressing the BOLUS ( ) key quickly, infusion starts at the set BOLUS F.Rate with the set
bolus infusion volume in Setting Mode 2.
5. When pressing the BOLUS key ( ) and holding it down, infusion continues at the BOLUS F.Rate
set in Setting Mode 2.
Standby Alarm Purge State
Caution
When pressing the BOLUS key ( ) in standby mode, the occlusion sensor is detected in Purge
Mode, but the air sensor is not detected. Note that excessive liquid may be infused abruptly.
- 39 -
7.2 Start Infusion (Start Operation)
1. Press the START ( ) key to start the pump.

2. The infusion volume on the I.Vol display increases as the pump keeps running.
3. When pressing the R.TIME ( ) key, the time remaining before the infusion is complete displays
on the I.Vol display. (Infusion volume remaining infusion time)
4. When pressing the BOLUS ( ) key quickly, infusion starts at the set BOLUS F.Rate with the set
bolus infusion volume in Setting Mode 2.
5. When pressing the BOLUS key ( ) and holding it down, infusion continues at the BOLUS F.Rate
set in Setting Mode 2.
Caution
When pressing the BOLUS ( ) key during operation, the occlusion sensor is detected, but the air
sensor is not detected. Note that excessive liquid may be infused abruptly.
6. Press the SEL ( ) key to change the flow rate during infusion. See 6.1.4 Titration function
7. When pressing the PAUSE ( ) key during infusion, the pump is paused for the time set in Setting
Mode 2, as described in Chapter 9 Setting Pause Time. The green and red status LEDs start to
blink. After the set time elapses, the Start Reminder Alarm goes off, and operation starts again.
8. When the infused volume reaches 5 minutes before total volume, the Near Complete alarm
displays on the F.Rate (ml/h) display at intervals. See Chapter 9 Setting Near Complete Alarm.
9. When the total volume is infused, the infusion mode switches to the KVO infusion mode. The
Infusion Complete alarm goes off and the green status LED turns on. (See Chapter 9 Setting
KVO.)
10. The KVO infusion mode stays on until the STOP/CLEAR ( ) key is pressed.
11. If the Save function is on, the infusion volume and flow rate are saved. When the power is turned
off and turned on again, the previous data are displayed.
If the Save function is not set, the infusion volume and flow rate are not saved. Therefore when the
power is turned off and turned on again, the infusion volume and flow rate are displayed as "0".
(See Chapter 9 Setting Save Function in Setting Mode 2.)
Infusion Infusion remaining time Bolus infusion
- 40 -
KVO infusion Near Complete alarm Infusion Mode 1 (Normal) - Titration function,
Infusion Complete alarm Air detection alarm
Caution
1. Prior to infusion, verify that the IV Set is installed properly, and that the flow rate and the total
volume are set properly.
2. Press the START ( ) key and monitor the infusion to ensure that it is working properly.
7.3 Stop and Pause Operation
1. If the STOP/CLEAR ( ) key is pressed while the pump is operating normally,

infusion stops and the green status LED turns off.
2. When pressing the PAUSE ( ) key, infusion is paused for the preset time.
(Factory default pause time set to 24 hours and it may change as preset) The
Flow rate display shows alternatively the Remaining time to resume and
PAUS to show current status. The status indicator LED shows green and red
blink alternately.
7.4 Viewing lnfused Volume and Time Remaining
1. When pressing the R.TIME ( ) key during infusion, the following are displayed: Infusion volume
Remaining infusion time.
[Infusion Volume, Remaining Infusion Time]
- 41 -
7.5 Key Lock Function
1. This function is used to disable the keys during infusion.
2. The Lock LED turns on when pressing the Key Lock on the back of the pump, and only the START
( ), STOP/CLEAR ( ) and ON/OFF ( ) keys work.
(3.3 See No.7 in Rear Mounting Section.)
7.6 History Log Function

1. The History Log function saves the events of the equipment in the memory.
2. Up to 2,000 events can be saved, and when there are more than 2,000 events, the oldest ones
are overwritten (actually, only 50 events can be displayed in the pump).
3. Events are saved when starting, completing and pausing infusion, and when alarms occur.
4. Events contain the Date & Time (the date and time when an event occurs), Operation Mode, Total
Volume, Flow Rate, Infused Volume and Types of Alarms.
1) Date & Time: Year, Month, Day, Hour, Minute, Second
2) Operation Mode: Ready, Normal, Bolus, Purge, KVO, Pause
3) Total Vol.: 0 ~ 9999.9
4) Flow Rate: 0 ~ 1200.0
5) Infused Vol.: 0 ~ 9999.9
6) Types of Alarms
5. Optional History Log software is used to download history log data to PC.
6. In addition to history log event, latest 50 alarm log events stored at different memory location with
history log event. The alarm log event can view on display of pump in setting mode1. Please refer
service manual for detailed usage of alarm log event.
- 42 -
8. Alarms
Alarm
The following describes alarms and corrective actions when the pump is not working properly.
For the patients safety, there are many safety alarms. Alarms go off and each state is notified to the
user by triggering alarms and displaying the status LEDs, the front indicators and the FND(Flexible
Numeric Display) window.
If the pump operates abnormally, infusion will stop

The Alarm functions include the Status Indicator Lamp, Alarm LED and Alarm Sound. The visibility
of each of them is:
Status Indicator, Alarm Sound : 3 meters
Alarm LED : 1 meter
It is recommended to position the operating pump with a front side always visible for the operator.
1. LED display
- Green and Red LEDs Off: standby for infusion
- Green LED Blinking: infusing or communicating
- Green LED On: during KVO infusion mode
- Red LED Blinking: when an alarm goes off and an error
occurs
- Green and Red LEDs blinking alternately: during pause
mode
8.1 Air Bubble Alarm

1. The pump stops if the Air sensor detects air in the tube during infusion, and
the Air Bubble alarm is triggered.
2. The following alarm and LED are displayed when the Air Bubble alarm is
triggered.
- An alarm goes off.
- Status LED: red LED blinking
- F.Rate Display: "Air"
- "Air" LED Indicator: On
3. Press STOP/CLEAR ( ) key to clear the Air Bubble alarm.
(However, the Air LED indicator stays On until the air is removed.)
4. To adjust the air sensor sensitivity, see 9.2.6.
When the Air Bubble alarm occurs, remove the air from the IV Set prior to use.
8.2 Occlusion Alarm

1. The Occlusion alarm is triggered and infusion stops when the IV set is twisted during infusion or
installed incorrectly, or when the needle of the IV Set is clogged and thus the liquid is not being
injected into the patient.
- 43 -
2. The following alarm and LED are displayed when the Occlusion alarm is
triggered.
- F.Rate Display: "Occl"
- "OCCL" LED Indicator: On
3. Press STOP/CLEAR ( ) key to clear the Occlusion alarm sound off.
(However, the OCCL LED indicator stays On until the occlusion state is
cleared.)
4. To clear the OCCL LED and occlusion state, do close the roller clamp to eject the IV set from
machine. Then Remove the pressure and mount correctly the IV Set again, and open the roller
clamp to start infusion.
Caution
In case the Occlusion alarm occurs due to the locking of the roller clamp, do not open the roller
clamp immediately. It can cause a globule of bolus to the patient.
Corrective action for influx of bolus in a globule
1. Check that the manual roller clamp is closed.
2. To solve this problem, remove the tubing from the pump and clear the pressure.
3. Check that the pressure is being cleared from the tubing.
8.3 Door Open Alarm

1. The pump stops if the Door LED is triggered when the door is opened during
infusion.
2. The following alarm and LED are displayed when the Door Open alarm is
triggered.
- F.Rate Display: "Door"
- "DOOR" LED Indicator: On
3. Press STOP/CLEAR ( ) key to clear the Door Open alarm.
(However, the Door LED indicator stays On until the door is closed.)
8.4 Battery Low Alarm

1. The Battery Low alarm is triggered 30 minutes before the pump stops working if the pump is
operating on battery power without an external power source.
2. The following alarm and LED are displayed when the Battery Low alarm is triggered.
- "BATT" LED Indicator: On/Off blinking
3. When external power is supplied to the pump, the Battery Low alarm is cleared.
(However, the BATT indicator stays On until the battery is charged by an external power source.)
- 44 -
8.5 Battery Empty Alarm
1. If the pump is operating on battery power without an external AC mains power supply, the Battery
Empty alarm is triggered and stops the infusion, 3 minutes before the remaining battery shuts
down the pump.
2. The following alarm and LED are displayed when the Battery Empty alarm is triggered.
- An alarm goes off. (The Battery Empty Alarm is not stop by press STOP/CLEAR ( )key. Only
the Battery Empty Alarm can stop by connect AC mains supply or turn off the pump.)
- Status indicator LED: red LED blinking
- "BATT" LED Indicator: On/Off blinking
3. Supply external power to clear the Battery Empty alarm.
4. After the Battery Empty alarm occurs, the pump stays on for 3 minutes, and then shuts down.
8.6 Abnormal Drop Alarm

1. The Drop Sensor alarm is triggered;
- when an abrupt free flow, leakage or an empty liquid bottle occurs during infusion.
- when the number of drops detected is much larger or smaller than the one set on the drop sensor
during infusion.
2. The following alarm and LED are displayed when the Abnormal Drop alarm is triggered.
- F.Rate Display: "Drop"
3. Press STOP/CLEAR ( ) key to clear the Abnormal Drop alarm.
When connecting or disconnecting the Drop sensor during infusion, an alarm goes off and "Drop" is
displayed on the F.Rate display for one second before it disappears.
8.7 Completion of Infusion Alarm

1. When the set infusion volume is completed, infusion doesn't stop and the KVO (Keep Vein Open)
function is activated. Infusion continues at the KVO rate set in Setting Mode 2 (see 9.2.2 Setting
KVO(Keep Vein Open)) and the Infusion Complete alarm is triggered.
The infused volume increases as well at this time.
2. The following alarm and LED are displayed when the Infusion Complete alarm is triggered.
- Status LED: green LED On
3. Press STOP/CLEAR ( ) key to stop infusion and to clear the Infusion Complete alarm.
- 45 -
8.8 AC Power Removal Alarm
1. The AC Power Removal alarm is triggered if AC power stops being supplied.
2. The alarm sounds out for 3 minutes at 5 seconds interval when the AC Power Removal alarm is
triggered.
3. If AC power is supplied again, the AC Power Removal alarm is cleared and it goes off for two
seconds.
8.9 DC Power Removal Alarm

1. The DC Power Removal alarm is triggered if DC power stops being supplied.
2. The alarm goes off for 3 minutes at 5 seconds interval when the DC Power Removal alarm is
triggered.
3. If DC power is supplied again, the DC Power Removal alarm is cleared and goes off for two
seconds.
8.10 Standby Alarm

1. The Standby alarm is triggered if no keys are pressed for 2 minutes during
standby for infusion.
2. The following alarm and LED are displayed when the Standby alarm is
triggered.
3. Press STOP/CLEAR ( ) key to clear the Standby alarm temporarily.
4. The Standby alarm is triggered again if no keys are pressed for 2 minutes.
8.11 Start Reminder Alarm (Pause Mode)

1. While infusion is being paused using the Pause key, if no keys are pressed until the preset pause
time elapses, infusion restarts. The Start Reminder alarm is triggered and then the pump operates
normally.
2. The following alarm and LED are displayed when the Start Reminder alarm is triggered.
- An alarm goes off twice.
- Status LED: The red LED blinks twice.
- 46 -
8.12 Tubing Misloading Alarm
1. When the IV Set tube is installed incorrectly or the tube is dislocated from its original position due
to being used for an extended period of time, the Air alarm or the Occl. alarm occurs.
8.13 Near Complete Alarm

1. The following alarm and LED are displayed 5 minutes before the infusion completes, in accordance
with the set total volume and the infused volume.
- Status LED: green LED blinking
- F.Rate Display: "N.C.A"
2. Press STOP/CLEAR ( ) key to clear the Near Complete alarm, and for
infusion to continue.
8.14 Error Code

1. When the error occurs during operation, the Error Code is displayed in F.Rate(ml/h) window.
2. When the error occurs, turn the Power Switch off and turn on again. If the the Error Code continues
to occur, please contact our after service team.
Err Code Display(F.Rate(ml/h) Cause
E001 Motor Check Error
E002 System Error
The maximum volume that may be infused under SINGLE FAULT CONDITION is 0.1 ml.
8.15 Troubleshooting and checking Alarms

Alarms (HIGH priority) automatically stop the infusion and require immediate attention before the
infusion can be restarted. During an alarm condition, the pump indicates a message on the display. In
addition, the red indicator flashes and the alarm tone sounds.
It is recommended to position the operating pump with a front side always visible for the operator.
It is possible to regenerate already cancelled alarm by pressing the STOP/CLEAR ( ) key and the
START Key ( ) afterwards (available if alarm conditions remain active).
Table 1 Troubleshooting Pump Alarm Messages

MESSAGE CAUSE CORRECTION CHECKING
Alarm LED An air inflow is Remove air from the Install the IVSET in
detected: IVSET in use. which air has flowed in
F.Rate(ml/h) This alarm occurs if air the air detection part.
flows in during infusion.
- 47 -
Alarm LED The inside of the Check whether the Lock the IVSET infusion
IVSET is clogged or a IVSET is clogged and regulator.
pressure more than the remove the pressure.
F.Rate(ml/h) set sensitivity applied.
Alarm LED The door is opened Press the Open the door during
forcibly during infusion. STOP/CLEAR key to infusion.
F.Rate(ml/h) clear this alarm.
Check that the door
is properly closed.
Alarm LED Battery charge low with Connect the pump to Run the pump on
30 minutes operation AC power supply and battery until alarm is
remaining. charge the internal generated.
No Message battery.
(LOW BATTERY)
Alarm LED Battery charge low with Connect the pump to Run the pump on
3 minutes operation AC power supply and battery until alarm is
F.Rate(ml/h) remaining. charge the internal generated.
battery.
The drop sensor is Press the Install or uninstall drop

installed or uninstalled STOP/CLEAR key to sensor during infusion.
F.Rate(ml/h) during infusion. clear this alarm.
A drop error has Install the drop Imitate no drop or free
occurred. sensor correctly or flow drop situation
remove water drops during infusion when
from the IVSET drop sensor is installed.
chamber.
Alarm LED The total infusion Press the After the total volume
estimation amount is STOP/CLEAR key to amount has been
infused. clear this alarm. infused, infusion starts
F.Rate(ml/h)
with the K.V.O set rate.
No Message The AC/DC LED is Press the Connect the mains

(AC/DC Power turned off when AC STOP/CLEAR key to cable to the pump.
Removal Alarm) mains power supply or clear this alarm Ensure that AC Mains
DC power supply temporarily. Power Supply Removal
AC/DC LED adapter is removed. The alarm sounds out Alarm Setting is turned
for 3 minutes at 5 on. Switch on the pump
seconds interval. and launch infusion.
After few seconds
disconnect the mains
cable.
F.Rate(ml/h) There is no key Press the Having enabled standby
operation during the STOP/CLEAR key to function, turn on the
Standby Alarm setting clear this alarm pump and leave it for 2
time. temporarily. minutes.
F.Rate(ml/h) The pump stops Resume infusion Pause key is pressed
temporarily when the after the pause during infusion.
Pause key is pressed. setting time has
passed.
- 48 -
The remaining infusion Cleared automatically The remaining infusion
F.Rate(ml/h) time is within the Near when the total time is within the Near
Complete setting time infusion estimation Complete setting time.
when infusion is amount is infused.
performed up to the
total infusion
estimation amount.
Alarm LED The IVSET is not Install the IVSET The IVSET is
installed: When correctly in the air disconnected or
infusion is started by detection part. installed wrongly in the
F.Rate(ml/h) pressing the START air detection part.
key, this alarm occurs if
the IVSET is not
installed in the air
detection part.
Alarm LED The IVSET is not Install the IVSET The IVSET is
installed: When correctly in the disconnected or
infusion is started by occlusion detection installed wrongly in the
F.Rate(ml/h) pressing the START part. occlusion detection part.
key, this alarm occurs if
the IVSET is not
installed in the
(Tubing occlusion detection
Misloading Alarm) part.
T.Vol(ml) Motor Check error It will be removed If the motor check error
occurs when the motor temporarily by turn continues to occur
rotation is in abnormal. the Power Switch off remove the pump from
I.Vol(ml) and on again. service.
F.Rate(ml/h)
T.Vol(ml) System error occurs Turn the Power If the system error
when the system Switch off and on continues to occur
encounters abnormal again. remove the pump from
I.Vol(ml) operation. service.
F.Rate(ml/h)
Caution
Install the IV Set on the product properly prior to use.
Contact the vendor you purchased the product from or the

customer service center for other error statuses or problems with
the product.
- 49 -
9. User Settings
User Setting
This function helps the user use the pump more easily and safely, since the user can set values
according to the operating environment. This function can be selected only when infusion is stopped.
1.In standby mode, press the SEL ( ) key and STOP ( ) key simultaneously and holding it down
to enter Setting Mode 1.
2. Press the SEL ( ) key and hold it down to switch between Setting Mode 1 and Setting Mode 2.
3. Press the SEL key quickly in the corresponding setting mode to change the set menu.
4. In Setting Mode 1 or 2, press the UP and DOWN ( , , , , , ) keys to change the
values to the desired set values.
5. Press the BOLUS ( ) key to switch to the standby mode when entering set values in each mode.
Changing setting mode

Category
Button Operation Description
Mode
Press the SEL ( ) key and STOP ( ) key

simultaneously and holding it down to enter Changes each set
Setting Mode 1, 2 Setting Mode 1. menu.
Press the SEL( ) key and holding it down to
enter Setting Mode 2 from Setting Mode 1.
Changing set values

Category
Button Operation Remarks
Mode
,
Setting Mode , Changes set values.
- 50 -
9.1 Setting Mode 1
In Standby Mode, press the SEL ( ) key and STOP ( ) key simultaneously and holding it down to
enter Setting Mode 1.
9.1.1 Setting IV Set Maker

1. When pressing the SEL ( ) key quickly in Setting Mode 1, IVST is displayed on the T.Vol (ml)
display. When the F.Rate (ml/h) display starts to blink, you can set an IV Set maker.
2. Press the MODE ( ) key quickly to change SET 1 or SET 2, and select the type of IV set on the
F.Rate (ml/h) display.
No IV Set Maker and Model
K001 Korea Vaccine / S203T
AItE Viltechmeda, UAB Aitecs IVset
Table 9.1.1 IV set listed
- 51 -
9.1.2 Setting Drop
1. When pressing the SEL ( ) key quickly in Setting Mode 1, DROP is displayed on the T.Vol (ml)
display. When the F.Rate (ml/h) display starts to blink, you can choose one of 15, 20 and 60 as
the number of drops for the IV Set.
9.1.3 Setting Micro Mode On or Off

1. When pressing the SEL ( ) key quickly in Setting Mode 1, MICR is displayed on the T.Vol (ml)
display. When the F.Rate (ml/h) display starts to blink, you can set Micro Mode.
9.2 Setting Mode 2
In Setting Mode 1, press the SEL ( ) key and hold it down to switch to Setting Mode 2.
9.2.1 Setting Bolus

1. When pressing the SEL ( ) key quickly in Setting Mode 2, BOLU is displayed on the T.Vol (ml)
display.
Use the MODE ( ) key to switch the Bolus flow rate and Bolus volume.
2. When FRAT is displayed on the I.VOL (ml) display and the F.Rate (ml/h) display starts to blink,
you can set Bolus flow rate.
3. When TVOL is displayed on the I.VOL (ml) display and the F.Rate (ml/h) display starts to blink,
you can set the Bolus volume.
- 52 -
9.2.2 Setting KVO(Keep Vein Open)
1. When pressing the SEL ( ) key quickly in Setting Mode 2, KVO is displayed on the T.Vol (ml)
display. When the F.Rate (ml/h) display starts to blink, you can set the KVO flow rate.
9.2.3 Setting Pause Time

1. When pressing the SEL ( ) key quickly in Setting Mode 2, PAUS is displayed on the T.Vol (ml)
display. When the F.Rate (ml/h) display starts to blink, you can set the pause time.
9.2.4 Setting Standby Alarm

1. When pressing the SEL ( ) key quickly in Setting Mode 2, STBA is displayed on the T.Vol (ml)
display. When the F.Rate (ml/h) display starts to blink, you can set the standby alarm.
- 53 -
9.2.5 Setting Infusion Time Near Complete Alarm
1. When pressing the SEL ( ) key quickly in Setting Mode 2, NCR is displayed on the T.Vol (ml)
display. When the F.Rate (ml/h) display starts to blink, you can set the Infusion Time Near
Complete Alarm.
9.2.6 Setting Air Sensor Bubble Size

1. When pressing the SEL ( ) key quickly in Setting Mode 2, AIR is displayed on the T.Vol (ml)
display. When the F.Rate (ml/h) display starts to blink, you can set the bubble size of the air
sensor.
Insensitive -> Sensitive

Presentation LARG(Large) MEdi (Medium) SMAL (Small)
Measured Bubble above 15mm above 10mm above 5mm
9.2.7 Setting Occlusion Sensor

1. When pressing the SEL ( ) key quickly in Setting Mode 2, OCCL is displayed on the T.Vol (ml)
display. When the F.Rate (ml/h) display starts to blink, you can set the sensitivity of the Occlusion
sensor.
Pressure level 1 2~8 9

Measured pressure 100mmHg 200~800mmHg 900mmHg
* The infusion pressure level may differ depending on the types of IV sets.
- 54 -
9.2.8 Setting Nurse Call
1. When pressing the SEL ( ) key quickly in Setting Mode 2, NRSC is displayed on the T.Vol (ml)
display. When the F.Rate (ml/h) display starts to blink, you can set the Nurse Call function.
9.2.9 Setting Sound Volume

1. When pressing the SEL ( ) key quickly in Setting Mode 2, SNDU is displayed on the T.Vol (ml)
display. When the F.Rate (ml/h) display starts to blink, you can set the sound volume.
2. Press the MODE ( ) key quickly to change SET1 or SET2. (SET1 : Alarm Sound, SET2 : Key
Sound)
Alarm Sound(left), Key Sound(right)

Low (1) <-----> Hi (11)
Alarm signal sound level Measured value

High: L11 66dB
Low: L1 52dB
9.2.10 Setting Date (Year, Month, Day)

1. When pressing the SEL ( ) key in Setting Mode 2, DATE is displayed on the T.Vol (ml) display.
Use the MODE ( ) key to change the year, month and day.
2. You can set the year when YEAR is displayed on the I.Vol (ml) display and the F.Rate (ml/h) starts
to blink.
3. You can set the month when MON is displayed on the I.Vol (ml) display and the F.Rate (ml/h)
starts to blink.
4. You can set the day when DAY is displayed on the I.Vol (ml) display and the F.Rate (ml/h) starts
to blink.
- 55 -
9.2.11 Setting Hour, Minute
1. When pressing the SEL ( ) key in Setting Mode 2, TIME is displayed on the T.Vol (ml) display.
Use the MODE ( ) key to switch the hours, minutes and seconds.
2. You can set the hours when HOUR is displayed on the I.Vol (ml) display and the F.Rate (ml/h)
starts to blink.
3. You can set the minutes when MIN is displayed on the I.Vol (ml) display and the F.Rate (ml/h)
starts to blink.
9.2.12 Setting Save for last Total Volume, Infused Volume, Flow rate.
1. When pressing the SEL ( ) key quickly in Setting Mode 2, SAVE is displayed on the T.Vol (ml)
display. When the F.Rate (ml/h) display starts to blink, you can set the Save Mode.
9.2.13 Drop Sensor Sensitivity Adjust
1. In setting mode2, press the SEL( ) key quickly then T.Vol(ml) displays DROP and
F.Rate(ml/h) display HI, Mid, LO in blinking.
2. Press the up and down key to change the drop sensor sensitivity.
3. Press the [BOLUS( )] key to save change and exit to stand by mode.
Sensitive Medium Insensitive

HI Middle Low
- 56 -
9.2.14 AC Mains Power Supply Removal Alarm Setting
1. In setting mode2, press the SEL( ) key quickly then T.Vol(ml) displays ACRE and
F.Rate(ml/h) display blinking.
2. Press the up and down key to choose the alarm on or off.
3. Press the [BOLUS( )] key to save change and exit to stand by mode.
9.2.15 Initializing Factory Settings

1. When pressing the SEL ( ) key quickly in Setting Mode 2, FCTS is displayed on the T.Vol (ml)
display. When the F.Rate (ml/h) display starts to blink, you can initialize to the Factory Settings by
input password. (Password is accessible only the designated personnel for safety.)
2. Press the BOLUS ( ) key to switch to the standby mode.
3. Please refer service manual for detailed usage of factory settings. (see 9.4 Set Initialization)
Caution
Factory Settings is Only designated personnel (trained, experienced) are permitted to operate the
pump for safe use and this function delete event log history and alarm log event.
- 57 -
9.3 Setting Range
1. The range of the set values for basic operation is as follows.
No. Setting Type Setting Value Range
1 IV Set Maker K001 (Korea Vaccine Type T), More IV Sets will be added.
2 DROP 15, 20, 60

3 Micro On, Off
4 Bolus Flow Rate (Purge) 1 ~ 1200 ml/h (Resolution 0.1 ml/h)
5 Bolus Volume (Purge) 0.1 ~ 9999 ml(with Micro On)
6 KVO Off, 1 ~ 9 ml/h (Resolution 1 ml/h)
7 Pause Timer 00:01 ~ 24:00 (1min)
8 Standby Alarm On, Off
9 Near Complete Alarm 00:01 ~ 24:00 (1min), Off
10 Air Sensor Bubble Size Off, Large (insensitive), Medium (normal), Small (sensitive)
11 Occl Pressure Level Sensor 1 ~ 9 (The higher the number, the more pressure it gets.)
12 Nurse Call On, Off
13 Sound Volume 1 ~ 11 (11: the highest sound, SET1: Alarm, SET2: Key)
14 Date Year: 2000 ~ 2099, Month: 01 ~ 12, Day: 01 ~ 31
15 Time Hour: 01 ~ 24, Minute: 00 ~ 59
16 Save On, Off
17 Drop Sensor Sensitivity Low (insensitive), Middle (normal), High (sensitive)
18 AC Mains Removal Alarm On, Off
19 Factory Initialization Enter the 4-digit password and then initialize.
20 Set Calibration Enter the 4-digit password and then initialize.
- 58 -
9.4 Set Initialization
1. This function changes the values back to the default factory values.
2. See 9.2.15 Initializing Factory Settings.
Enter the password. (The password is inaccessible to the user.)
No Setting Type Initial Setting Value
1 IV Set Maker K001
2 Drop 20
3 Micro Off
4 Bolus Flow Rate (Purge) 700 ml/h
5 Bolus Volume (Purge) 5 ml
6 KVO 1 ml/h
7 Pause Timer 24hours
8 Standby Alarm Off
9 Near Complete Alarm Off
10 Air Sensor Bubble Size LARG (Large, above 15mm)
Occl Pressure Level
11 7 (Pressure level=700mmHg, Relatively high pressure)
Sensor
12 Nurse Call Off
13 Sound Volume SET1 (Alarm sound): 11 (max.), SET2 (Key sound): 11(max)
14 Date Initialization doesnt change this parameters.
15 Time Initialization doesnt change this parameters.
16 Save On
17 Drop Sensor sensitivity Middle
18 AC Mains Removal Alarm On
19 Calibration Factory Calibration Value
* Note: All the existing set values are replaced with the initialized values if initialization is executed.
Caution
1. The actual infusion rate may differ from the desired rate, and malfunction of the air and the
occlusion alarms may occur if any IV sets other than the designated one are used. Contact the
manufacturer or its authorized service representative or the head office for assistance.
2. Note that occlusion pressure level (sensitivity), bolus flow rate and maximum flow rate change
depending on the IV set.
3. Contact the customer service center if drastic differences occur due to use for an extended
period of time. Test infusion volume regularly and carry out calibration at least once a year.
- 59 -
10. Precautions During Use
Perform regular inspection and maintenance of the pump to use it safely for a
long time.
Caution
Do not use the pump if the pump is found to be abnormal during inspection, and contact the
manufacturer or its authorized service representative for assistance.
Do not use the pump if it has any external signs of impact or is dropped, and contact the
manufacturer or authorized service representative for assistance.
The sensors inside the pump or its accuracy may deteriorate without the presence of external
issues.
The right to repair the pump or carry out periodical part replacements is reserved only to the
Manufacturer authorized service representative.
10.1 Maintenance
It is essential to inspect the pump regularly for safe and correct use. Contact the customer
service center if the pump is found to be abnormal.
Please refer the measurement method as the IEC60601-2-24 standards guides as figure10.1.
A. DI-2000 pump
B. IV set
C. Scale
B
A C
Figure 10.1 Measurement Method
1. Accuracy Inspection Monitor infusion volume regularly. Contact the customer service center if
there is a large difference in infusion volume.
2. Air (Bubble) Alarm Inspection Blow air bubbles (over 3 mm) into the pump and monitor if the air
alarm is triggered when the air bubbles pass the air sensor.
3. Occlusion Alarm Inspection Completely block the tube between the pump and the patient with a
roller clamp or by hand to prevent the influx of liquid, and monitor if the occlusion alarm is
triggered.
4. Door Open Alarm Inspection
- Check if the Door LED works if the door is opened.
- Open the door during infusion and check if the Door Open alarm and the Door LED work.
5. Battery Low Alarm Inspection
- Fully charge the batteries for 10 hours.
- Disconnect the external power source and use battery power. Set the flow rate to 25 ml/h and
press the START key to start infusion.
- Verify that infusion continues for 4 hours and that the remaining battery capacity LED turns off.
- Replace the batteries if they dont last for at least 2 hours.
- 60 -
10.2 Cleaning and Disinfecting
1. Clean and store the pump properly after use.
If the pump is not stored properly or is stored without cleaning, it may cause malfunctioning of the
pump.
2. If there is medical fluid or dirt on the occlusion sensor and/or the air bubble sensor, gently wipe it
with a cotton ball.
3. If the drop sensor is dirty, wipe it with gauze soaked in cold or warm water. If the stain is too heavy
to wipe off, or it is on the external casing, detach the drop sensor prior to cleaning.
The drop sensor can be washed with flowing water except for the connector. However, do not
submerge the sensor into water.)
Precautions
1. Disconnect the pump from any external power source when cleaning.
2. Do not disinfect the pump with Ethylene Oxide gas or by autoclaving.
3. Do not wipe down the pump with thinner, solvents, benzene, ammonia or acetone.
4. Dry the pump after cleaning.
10.3 Disposal
When the pump reaches the end of its life-span, dispose of or recycle the pump and the batteries in
accordance with local regulations, or contact the nearest vendor.
10.4 Storage
1. Avoid direct sunlight when storing the pump. Do not leave the pump in wet and humid conditions.
2. Avoid areas with a possibility of falling.
3. Storage conditions for the pump are as follows: Ambient temperature: -10 ~60 , relative
humidity: 10%~95%, atmospheric pressure: 65 kPa~120 kPa.
10.5 Technical description

General
The pump is intended for precise dosing of drug at the rate programmed by the operator.
The speed of flowrate is calculated by microprocessor based on the IV model and infusion
rate set.
Information on pump status and programming data are outputted to the FND( Flexible
Numeric Display) format display.
Operation of the microprocessor is monitored by the Guard Safe circuit which unconditionally
switches off the motor in case of failure.
Battery charging system

Pump comprises internal battery charging system based on the slow charge controller.
Once full charge is detected, the charging is stopped.
The device monitors three variables to determine when the battery reaches full charge:
voltage slope, battery temperature, and charge time.
Check the usage times of the batteries, since the batteries' life-span could be reduced if the
batteries are used for over a year. It is highly advisable to replace the batteries every year.
If it is not used for long time, it is recommended to switch off by rear switch to keep
battery energy longer.
Battery life-span may differ depending on the environment and the frequency of use.
Use the Ni-MH batteries designated by the manufacturer or its authorized service
representative when replacing.
- 61 -
Means to protect the patient
Alarm
Air Bubble alarm
Occlusion alarm (detection capacity: 100 ~ 950 mmHg)
seven adjustable steps for downstream occlusion
Door Open alarm
Battery Low, Battery Empty alarm
Abnormal Drop alarm
Infusion Complete alarm (automatic switch-over to KVO feature)
AC/DC Power Shut-off alarm
Start Reminder alarm (pause set time elapsed)
Standby alarm (at an interval of 2 minutes when not infusing)
Near complete alarm
Malfunction: The status of the pump is displayed and an alarm goes off.
Safety Features
Air Sensor: Detects air bubbles.
Occlusion Sensor: Detects clogging of the tube.
Drop Sensor: Detects medical fluid drops.
Nurse Call: Monitoring is possible if an alarm goes off.
10.6 Warranty and Service Information

Warranty
The Manufacturer warrants that pump is free from defects in material and workmanship
under normal use and service for a period of 12 months after the purchase date.
Repair or circuit alteration of this equipment can only be carried out by personnel
authorized by manufacturer or its authorized service representative. The warranty shall
not apply to defects or damage caused by repairs or disassembly by anyone other than
personnel authorized by manufacturer or its authorized service representative, and
safety shall not be assured.
This Warranty is not applicable to pumps with damaged seal or when failure was caused
by violations of requirements of this Operation Manual, by mains voltage non-conformity
to the requirements of IEC, by spills of liquids, by mechanical damages caused by
shocks or a pump being dropped, by pump damages caused during transportation, or
when packaging is damaged.
If the customer finds a defect in the pump during the Warranty period, he must report it
and inform the Manufacturer or its authorised representative within 30 days.
A pump sent for testing, repair or replacement shall be submitted to the Manufacturer or
its authorised representative in its original or equivalent packaging. The pump is sent for
repair and back at customer expense.
If no defect is found during testing, the Manufacturer or its authorised representative

reserves the right to submit the invoice to the customer for the work carried out.
Service Information
For service and repair contact manufacturer:
DAIWHA CO., LTD,
Daiwha B/D, 733-18 Yeoksam-dong, Gangnam-gu, Seoul, Korea.
Tel. : (+82) 2 - 558-1711~6
Fax : (+82) 2 - 554- 0317
E-mail : service@daiwha.com
Website: http://www.daiwha.com
- 62 -
11. GUIDANCE AND MANUFACTURERS DECLARATION ON ELECTROMAGNETIC EMISSIONS
Guidance and manufacturer's declaration - electromagnetic emission
The infusion pump DI-2000 is intended for use in the electromagnetic environment specified below. The customer or the user of
The infusion pump DI-2000 Series should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions Group 1 The infusion pump uses RF energy only for its internal
CISPR 11 function.
Therefore, its RF emissions are very low and are not likely
to cause any
interference in nearby electronic equipment.
RF emissions Class A The infusion pump is suitable for use in all establishments
CISPR 11 other
Harmonic emissions Class A than domestic and those directly connected to the public
IEC 61000-3-2 low-voltage power
supply network that supplies buildings used for domestic
Voltage fluctuations / Class A, purposes.
flicker emissions
IEC 61000-3-3
Guidance and manufacturer's declaration - electromagnetic immunity

Immunity test IEC 60601 Compliance level Electromagnetic environment -
test level guidance
Electrostatic 8 kV contact 8 kV contact Floors should be wood, concrete or
discharge (ESD) 15 kV air 15 kV air ceramic tile. If floors
IEC 61000-4-2 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 should be that of
transient/burst supply lines supply lines typical commercial
IEC 610004-4 1 kV for 1 kV for or hospital environment.
input/output lines input/output lines
Surge 1 kV differential 1 kV differential Mains power quality should be that of
IEC 61000-4-5 mode mode typical commercial
2 kV common 2 kV common or hospital environment.
mode mode
Voltage dips, short <5 % UT <5 % UT As the infusion pump DI-2000 is powered
interruptions and voltage (>95 % dip in UT) (>95 % dip in UT) by an internal battery, no special
variations on power for 0.5 cycle for 0.5 cycle precautions must be taken.
supply 40 % UT 40 % UT
input lines (60 % dip in UT) (60 % dip in UT)
IEC 61000-4-11 for 5 cycles for 5 cycles
70 % UT 70 % UT
(30 % dip in UT) (30 % dip in UT)
for 25 cycles for 25 cycles
<5 % UT <5 % UT
(>95 % dip in UT) (>95 % dip in UT)
for 5 sec for 5 sec
Power frequency 3 A/m 400 A/m
(50/60 Hz)
magnetic field
IEC 61000-4-8
NOTE UT is the a.c. mains voltage prior to application of the test level.
Guidance and manufacturer's declaration - electromagnetic immunity

Immunity test IEC 60601 test Compliance Electromagnetic environment -
level level guidance
Portable and mobile RF communications
- 63 -
equipment should not be used no
closer to any part of the infusion pump DI-
2000, including cables, than
the recommended separation distance
calculated from the equation
applicable to the frequency of the
3 Vrms transmitter.
Conducted RF 150 kHz to 80 MHz 10 Vrms
IEC 61000-4-6 outside ISM d = 1.2
10 Vrms 10 Vrms
150 kHz to 80 MHz d = 1.2
in ISM
10V/m
10 V/m d = 1.2 80 MHz to 800 MHz
Radiated RF 80 MHz to 2.5 GHz d = 2.3 800 MHz to 2.5 GHz
IEC 61000-4-3
where P is the maximum output power
rating of the transmitter in watts
(W) according to the transmitter
manufacturer and d is the recommended
separation distance in meters (m
Field strengths from fixed RF transmitters,
as determined by an electromagnetic site
survey should be less than the
compliance level in
each frequency range
Interference may occur in the vicinity 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.
a The 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 40.7 MHz.
b The compliance levels in the ISM frequency bands between 150 kHz and 80 MHz and in the frequency range 80 MHz to 2.5
GHz are intended to decrease the likelihood that mobile/portable communications equipment could cause interference if it is
inadvertently brought into patient areas. For this reason, an additional factor of 10/3 is used in calculating the recommended
separation distance for transmitters in these frequency ranges.
c 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 infusion pump DI-2000 is used exceeds the applicable RF compliance
level above, the infusion pump DI-2000 should be observed to verify normal operation. If abnormal performance is
observed, additional measures may be necessary, such as reorienting or relocating the infusion pump DI-2000.
d Over the frequency range 150 kHz to 80 MHz, field strength should be less than 10 V/m.
Recommended separation distances between portable and mobile RF

communications equipment and the Infusion pump DI-2000.
The infusion pump DI-2000 is intended for use in the electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the infusion pump DI-2000 can help prevent electromagnetic interference by
maintaining
a minimum distance between portable and mobile RF communications equipment (transmitters) and the infusion pump DI-2000
as recommended below, according to the maximum output power of the communication equipment.
Rated maximum output Separation distance according to frequency of transmitter
power of transmitter m
W 150 kHz to 80 MHz 150 kHz to 80 80 MHz to 800 MHz 800 MHz to 2.5 GHz
outside ISM bands MHz
- 64 -
d = 1.2 in ISM bands d = 1.2 d = 2.3
d =1.2
0.01 0.04 0.12 0.12 0.23
0.1 0.13 0.38 0.38 0.73
1 0.40 1.2 1.2 2.3
10 1.3 3.8 3.8 7.3
100 4.0 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (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 separation distance for the higher frequency range applies.
NOTE 2 The 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 40.7 MHz.
NOTE 3 An additional factor of 10/3 is used in calculating the recommended separation distance for transmitters in the ISM
frequency bands between 150 kHz and 80 MHz and in the frequency range 80 MHz to 2.5 GHz to decrease the likelihood that
mobile/portable communications equipment could cause interference if it is inadvertently brought into patient areas.
NOTE 4 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects and people.
- 65 -
-- DOCUMENT HISTORY
Original issue (DI-2000-OP-EN): Feb 2010

Revision 1.00 (DI-2000-OP-EN -P01): Jan 2010
Revision 1.01(DI-2000-OP-EN -P02): Jul 2010
Revision 1.02(DI-2000-OP-EN -P03): Aug 2010
Revision 1.03(DI-2000-OP-EN -P04): Oct 2010
Revision 1.04(DI-2000-OP-EN -P05): May 2011
st
Revision 1.05(DI-2000-OP-EN P06): 21 of May 2011
Revision 1.06(DI-2000-OP-EN P07): Jun 2011
Revision 1.07(DI-2000-OP-EN P08): Jun 2011
Revision 1.08(DI-2000-OP-EN P09): Aug 2011
Revision 1.09(DI-2000-OP-EN P10): Mar 2012
Revision 1.10(DI-2000-OP-EN P10): Apr 2012
- 66 -

Bomba de Infusion Medifuion d1-2000

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Bomba de Infusion Medifuion d1-2000

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MEDIFUSION

Technical Director: Bioengineer Juan Pablo Giulioni, Mat: 5348 28676206

Manual No: DW-DI2000-OP-EN(Rev 1.10)

3. Names and Functions

10. Precautions During Use

11. GUIDANCE AND MANUFACTURERS DECLARATION ON

Document History ............................................................................................ 64

Safety precautions are classified as below in accordance with expected danger,

A precaution which could result in critical personnel injury or loss of life if

A precaution which could result in minor personnel injury or damage to the

Address: mdi Europa Gmbh Langenhagener Str. 71 30855 Hannover-

This is medical equipment.

Power Off Power On

Down Key Up Key

BOLUS (Fast Infusion) Serial Number

Date of Manufacture Manufacturer

Device Complies With The Attention

Type CF Feeding Formula

Protected against dripping

European Authorized Recycle electrical and electronic

Product Name Volumetric Infusion Pump

Micro (On): 0.1 ~ 99.9 ml/h (in 0.1 ml/h increments)

5% ( Korea Vaccine CODE S203 Type)

Bolus Rate (Purge) 700 ml/h (default) - 1 ~ 1200 ml/h

Occlusion pressure 100mmHg ~ 950mmHg(13~126kPa)

Display 7 segments (4 digits * 3 lines)

* Air Bubble alarm

* AC 100~240 VAC, 50~60 Hz (Fuse: 250 V, T3.15 A)

Power Requirements 35VA

* Protection from electric shock: Class

Size (DWH) 120130206 mm

Temperature: 10~ 40, Humidity: 20 ~ 90%

Temperature: -10 ~ 60, Humidity: 10 ~ 95%

2.2 Occlusion Detection Characteristics

NOTE: The following figures are only for reference.

1. KoreaVaccine (Type S203T), Baxter,Sendal, Bbraun, Ferraril etc

2. Various kinds of IV sets will be available through continuous product updates.

Please refer service manual for setting user IV sets.

The infusion amount may differ depending on the types of IV sets.

NOTE: The following figures are only for reference.

(Measurement Instrument: FLUKE IDA4PLUS)

Flow Rate: 1 ml/h

Flow Rate: 25 ml/h

2.6 Drop Sensor Function (Optional)

1. Detects free flow caused by abrupt device malfunctioning

2. Detects No Drop caused by an empty bottle or clogging of the tube.

3. It is advisable to reinforce the safety of the drop sensor.

4. See Drop S ensor Installation for other installation.

Do not connect or disconnect the Drop sensor during infusion.

OCCL LED- This LED is turned on if the IV set is clogged.

<Battery level display based on the battery capacity>

The battery is not charged when DC power is supplied.

Status Indication LED:

RS485 Port Used when downloading History

Drop Sensor Port The Drop Sensor is

Nurse Call Port Connected to the Nurse Call

USB Port Used when downloading History

DC Power Port - 12 ~ 15 VDC can be supplied.

Key Lock - Only the START( ) and

STOP/CLEAR Key ( ) and ON/OFF ( )

Power Switch Turns power on or off.

Battery Built-in battery

Power Inlet The power cord is plugged into

Air Detector Prevents the patient from getting