Manual Bomba Daiwha mp1000
Manual Bomba Daiwha mp1000
MP-1000
OPERATING MANUAL
This Manual describes the use of infusion pump (model: MP-1000) manufactured by
DAIWHA Corp., Ltd.
Only the person who is authorized by the company can repair this equipment and
change a circuit. The equipment that is dismantled or repaired without prior
permission cannot get any post-management service.
Parts and circuits used in this equipment can be changed for better performance
and safety reasons.
After reading this manual, put it in a place with easy access so that everybody can
use it.
If you have any questions or concerns regarding this equipment and user manual,
feel free to contact at the below company.
Safety precautions are divided into the following categories depending on the level
of the expected hazard and damage caused by inappropriate use of the product and
the level of urgency that requires actions.
TABLE OF CONTENTS
1. PRECAUTIONS……………………………………………………… 1
2. TECHNICAL SPECIFICATIONS………………………………. 4
3. CHARACTERISTICS………………………………………………. 5
3.1 PRODUCT OVERVIEW……………………………………………………. 5
3.2 MEMORY FUNCTION………………………………………………………. 5
3.3 CHARACTERISTICS OF THE OCCLUSION DETECTION…….. 5
3.4 FUNCTION OF THE DROP SENSOR (OPTION)…………………. 5
3.5 FLOW RATE ACCURACY…………………………………………………. 7
5. OPERATION…………………………………………………………… 17
5.1 ATTACH THE PUMP TO AN INFUSION STAND…………………. 17
5.2 HOW TO CONNECT THE POWER………………………………………. 17
5.3 HOW TO INSTALL AND SET UP AN INFUSION SET………….. 17
5.4 HOW TO INSTALL THE DROP SENSOR (OPTION)…………….. 19
5.5 HOW TO SET UP A FLOW RATE………………………………………. 19
5.6 HOW TO SET UP TOTAL VOLUME (VOLUME TO BE INFUSED) 19
5.7 HOW TO START THE OPERATION…………………………………….. 20
5.8 HOW TO STOP & RESTART THE OPERATION……………………. 20
5.9 HOW TO VIEW INFUSED VOLUME…………………………………….. 21
5.10 INFUSION COMPLETION………………………………………………….. 21
5.11 PURGE FUNCTION …………………………………………………………. 21
TABLE OF CONTENTS
6. ALARM……………………………………………………………………. 22
6.1 AIR (BUBBLE) ALARM………………………………………………………. 22
6.2 OCCLUSION ALARM…………………………………………………………. 22
6.3 DOOR OPEN ALARM…………………………………………………………. 23
6.4 LOW BATTERY ALARM…………………………………………………….. 23
6.5 FREE FLOW & NO DROP ALARM………………………………………. 23
6.6 TUBING MISLOADING ALARM………………………………………….. 23
6.7 OTHERS………………………………………………………………………….. 24
7. USER SETTING………………………………………………………. 25
7.1 HOW TO SET UP CALIBRATION (ACCURACY)…………………. 26
7.2 HOW TO SET UP DOWN STREAM OCCLUSION SENSITIVITY 27
7.3 HOW TO SET UP ALARM VOLUME……………………………………. 27
7.4 HOW TO SET UP PURGE RATE…………………………………………. 28
7.5 HOW TO SET UP PURGE VOLUME……………………………………. 28
7.6 HOW TO SET UP SAVE FUNCTION……………………………………. 29
7.7 HOW TO SET UP K.V.O. RATE…………………………………………. 29
7.8 HOW TO SET UP INFUSION SET Drops/ml (OPTION)……….. 30
7.9 HOW TO SET UP NURSE CALL (OPTION)………………………….. 30
7.10 HOW TO SET UP STANDBY ALARM………………………………… 31
7.11 HOW TO SET UP TUBING MISLOADING ALARM……………… 31
7.12 HOW TO SET UP AIR SENSITIVITY………………………………… 32
7.13 OTHERS (TEST MODE)…………………………………………………… 32
8. MAINTENANCE………………………………………………………. 33
8.1 CHECKOUT THE PUMP …………………………………. 33
8.2 CLEANING AND STERILIZATION………………………………………. 34
8.3 STORAGE OF THE INFUSION PUMP…………………………………. 34
8.4 LIFE SPAN………………………………………………………………….…. 34
9. WARRANTY………………………………………………………………………… 35
Danger Warning Caution
Definition of Terms
Please use the infusion Pump with extreme care & correctness after reading this
- Danger : Possible hazards that could cause serious injury or even INSTANT DEATH.
- Warning : Possible hazards that may cause serious injury or even death.
- Caution : Possible hazards that may cause mild injury to user or patient or damage to product.
1. PRECAUTIONS
The following information is provided to help user operate the pump safely and
accurately and further prevent hazard, physical injuries or damages.
Danger
1. Keep the pump away from inflammable anesthetic.
Warning
1. Make sure that an inlet that is connected to the external power stays dry all the
time.
2. Do not use a mobile phone, radio set or defibrillator generating high frequency
near the pump.
3. Do not use this pump in MRI rooms, high-pressure rooms or places while high
electromagnetic radiation is generated.
4. Be sure to set the infusion set rightly. If it is set by reversed manner to a normal
pump operation, the patient’s blood will be drawn up into the tubing.
Caution
1. Operate the pump by the designated steps.
2. When the external power sources are used, keep in mind the following matters:
1) Use the power cord for the hospital and plug it into the grounded outlet.
2) Prior to use, check the rated voltage and frequency.
3) Be sure to check whether an extension cord is normal or not.
3. Use only the person educated about the pump or a skilled hand.
1
1. PRECAUTIONS
4. Attach the pump securely to an infusion stand and ensure its stability. If the pump
is dropped or given any hard shocks, do not use it. Please call the local agencies or
the company.
5. During infusion, frequently check the infusion line such as a rupture in the filter or
a leak in the line. Check both pump and patient’s conditions on a regular basis
while drugs are infused. To ensure a good connection between the patients with the
infusion line, a male-to-female luer-lock type connection is recommended.
6. Pay close attention to the following matters when the infusion set is used.
1) Use a designated infusion set for infusion pump. If any infusion set other than
specified is used, proper flow rate accuracy and alarm function (air and
occlusion) are not guaranteed. If the designated set is not available, contact to
the agent or company.
2) Do not pull on the tubing with excessive force. Then the intended flow rate may
not be achieved.
3) Fit the tubing inside of the door from the bottom to the top. Securely set the
tubing along the groove of the PUMPING UNIT 3○1. If not, free flow or leak can be
occurred.
4) Do not connect an infusion set administrated from an infusion pump to another
infusion line administrated only by the manual roller clamp (gravity infusion)
because this may influence the accuracy of infusion and alarm functions.
5) When drugs are infused for extended time, change the tubing location every 12
hours to use the tubing within the margin of errors.
6) Do not reuse the infusion set.
7. When the pump is operated under the shown described conditions, the flow rate
accuracy may be incorrect.
1) Using drugs of the higher viscosity such as Dextrose 50%.
2) Operating under the ambient temperature between +5 ℃ and 40 ℃, a relative
LOW BATTERY ALARM INDICATOR 2○1 on the front is turned on or the alarm
sounds.
3) Charge the internal battery to full capacity by connecting the pump to an AC
power supply for 15 hours at least.
4) When the external (AC/DC) power is supplied, 3 lamps of the Battery capacity
9. Never connect both AC and DC power sources to the infusion pump at the same
time. To use the DC power, be sure to check the polarity of the DC jack.
10. Do not sterilize the pump with autoclave or E.O. gas. Do not wipe the pump with
thinner, solvent, benzene, ammonia, acetone, etc. Use a wet cloth to clean.
11. Do not dismantle the pump.
3
4
2. TECHNICAL SPECIFICATIONS
+ Product Name Volumetric Infusion Pump
+ Model Name MP-1000
+ Infusion Principle Peristaltic Semi-Transit Finger
0.1~999 ml/h
+ Range of Flow Rate 0.1~99.9 ml/h: increase and decrease by 0.1 ml/h
100~999ml/h: increase and decrease by 1 ml/h
+ Accuracy ±5% (BD KOREA: model PUMP A122)
+ Range of Volume
- Total Volume 1~9999ml or no limit: 1~9999ml: increase by 1 ml
0.1~9999 ml: 0.0~99.9ml: increase by 0.1ml
- Infused Volume
100~9999ml: increase by 1ml
+ Purge Rate 700ml/h (subject to change)
+ Purge Volume 3ml (subject to change)
1ml/h: Flow rate 1.0~999 ml/h (subject to change)
+ K.V.O. Rate
0.1ml/h: Flow rate 0.1~0.9ml/h
+ Display 7 segment (4 digit * 2 line)
2 hours at flow rate 25ml/h
+ Battery
Charging time – approx. 15 hours
Visible and Audible Alarm
- Door open
- Occlusion (Detection range: 100~950mmHg)
: Down stream Occlusion 3 steps are adjustable
+ Alarm : Maximum infusion pressure: 950 mmHg
- Air Bubble detection
- Low battery
- Infusion complete
- Alarm for malfunction
100~240 VAC, 50/60Hz (Fuse: 250V, T3.15A)
+ Power supply
12VDC
+ Power consumption Less than 30VA
+ Classification Class I, Type BF, IPX 1 (Drip-proof)
+ Dimension (D x W x H) 125 x 166 x 258 mm
+ Weight Approx. 3.2 Kg
Flow rate Occlusion level Occlusion Pressure Time to alarm Bolus volume
Low 371 mmHg 18min 20sec 0.18 ml
1 ml/h Middle 570 mmHg 39min 15sec 0.38 ml
High 950 mmHg 1h 30min 0.51 ml
Low 285 mmHg 30sec 0.15 ml
25 ml/h Middle 535 mmHg 1min 0.28 ml
High 921 mmHg 2min 50sec 0.73 ml
※ See the 5.4. HOW TO INSTALL THE DROP SENSOR (Option) section
===============================================================
CAUTION
1. Only use the drop sensor for Medifusion MP-1000.
2. During infusing, do not connect or disconnect the drop sensor at the pump.
===============================================================
8
3. CHARACTERISTICS
3.5 FLOW RATE ACCURACY
The graph of time (horizontal axis) versus flow rate (vertical axis) give a clear
and simple picture of the general stability with time. This is generated during
the stabilization period and produces the so-called START-UP CURVE. The start-
up time to reach the desired flow rate decreases as the desired flow rate is
increased.
50 10
[%] 8
S T AR T - U P C U R V E
T RU M P E T CU R V E
Flow rate (ml/h)
40 6
30 2
20 - 2
- 4
10 - 6
- 8
0 - 10
2 5 11 19 31
15 30 45 60 75 90 105 120
Tim e [ m in ] O b s e r v a t i o n i n t e r v a l [ m in ]
This key is used for the PURGE. When you press the purge, the setting up purge
volume will be infused automatically. (Note: It does not sense the air and
occlusion.)
This key is used for setting up the total volume or the flow rate. When you press
this key, the digits will be shifted to the left.
This key is used for stopping infusion. If you press the button during 1 or 2 seconds,
the selected infused volume, flow rate and total volume will be cleared off.
9. UP KEY – 3○4
This key is used for setting up total volume or flow rate. The number will be
increased by one each time and will rapidly increase while the key is being held
down.
This key is used for setting up total volume or flow rate. The number will be
decreased by one each time and will rapidly decrease while the key is being held
down.
4.2 DISPLAY
1. FLOW RATE DISPLAY WINDOW - ○
1
This Window displays infusion flow rate to the patient. It will be blinked when flow
rate set up function is selected (by pressing the Flow rate key 1○1).
This Window displays total volume or infused volume to the patient. It will be
○
2 will be turned on when infused volume is displayed (by pressing Infused volume
key 1○0).
13
3. TOTAL VOLUME INDICATOR - ○
3
This indicator will be turned on when selecting Total volume selection (by pressing
This indicator will be turned on when infused volume is selected (by pressing the
Infused volume key 1○0). At this time, Infused volume data will be displayed on the
5. PURGE INDICATOR - ○
5
This indicator will be turned on when purge starts (by pressing the PURGE key ○
8 ). It
6. STOP INDICATOR - ○
6
This indicator will be turned on when infusion is stopped. It will be turned off when
infusion starts.
7. INFUSION INDICATOR - ○
7
This indicator displays the battery capacity status in three levels (full, medium,
low). When external (AC/DC) power is supplied, 3 lamps of this indicator is turned
on, no concern with battery capacity.
This indicator will be blinked with the alarm sounding when an air (bubble) sensor
detects bubbles during the infusion process.
This indicator will be blinked with the alarm sounding when up or down occlusion
sensor detects the blocking of the infusion set during infusion process.
This indicator will be blinked with the alarm sounding when the door is open or
somebody opens the door forcefully during the infusion process. However, the
indicator will be turned on without the alarm sounding when the door is open after
the infusion is stopped.
This indicator will be blinked with the alarm sounding when the battery is
exhausted.
This indicator will be turned on only in micro mode (Flow rate 0.1 ~ 99.9ml/h).
16
4. NAMES AND FUNCTIONS OF EXTERNAL PARTS
4.3 INSIDE OF THE DOOR
This part senses whether or not the tubing is blocked on the upper part of the
pump.
2. KNOB - 3○0
Pull down the knob to open the Pumping unit (31) and push it back to close it.
When the door is closed without pushing the knob back, the knob will be pushed
back automatically.
This part is used to infuse drugs by pressing the tubing on the infusion set.
This part senses whether or not the tubing is blocked on the lower part of the pump.
If you connect the nurse call cable to the pump, the port will transmit the warning
to the nurse call in case of problem.
SYMBOLS
Power off
Power on
(Power : Disconnection form the
(Power : Disconnection to the mains)
mains)
Purge
Shift key
(The I/V and F/R which are set
(One step a movement the lift)
automatic pouring)
Down key Up key
(Figure one Decrease) (Figure one addition )
Stop/Clear
Start key
(Medicine water pouring into the
(Motor & Alarm stop, I/V & F/R & T/V
start)
clear)
Type BF equipment according to
Manufacturer’s serial number.
IEC60601-1
Date of Manufacture
Address of manufacturer.
EU Representative
1. PROVIDED ACCESSORIES
= AC Power cord
= Operating Manual For User
= Infusion set : 5 ea
2. SPECIAL ACCESSORIES
= Drop Sensor
= Nurse Call
= DC Cable
21
22
5. OPERATION
5.1 ATTACH THE PUMP TO AN INFUSION STAND
Secure the pump properly to the infusion stand by turning the handle of the clamp
at the backside of the pump. Be sure to check the stability of the infusion stand.
NOTICE!
7. At this time, make sure to install the tubing on the infusion set in the given space
as figure 2 and figure 3.
8. In particular, install the Occlusion Sensor 2○9, 3○2 and the Air sensor 3○3 by pressing
them with fingers.
9. If the infusion set is not installed normally, air alarm or occlusion alarm will sound.
10. Hold up the knob 3○0 to close the pumping unit 3○1. At this time, make sure to
install the tubing on the infusion set.
11. Close the door by pulling down the handle.
12. When the roller clamp on the infusion set is opened, check if there is any leakage
and then insert the needle into the patient’s vein.
=========================================================================
CAUTION
1. Check if the infusion set is available.
2. Make sure that the infusion set is not bent or twisted. If it is not straight,
occlusion or air alarm will occur or the flow rate will not be fully reached.
3. Before opening the door or removing the infusion set, be sure to close the tubing
by using a clamp on the infusion set. If not, it will cause leakage.
4. When the solution container or infusion set is replaced or change, follow the
above statements.
5. When the same section of the tubing is used for a long time, deformation of the
tubing may occur, resulting in a flow rate deviation. Either move the tubing at
least 20 cm every 12 hours, or replace the infusion set with a new one.
=========================================================================
24
5. OPERATION
5.4 HOW TO INSTALL THE DROP SENSOR (OPTION)
1. Insert the plug of the drop sensor into the drop sensor connector at the back of
the pump.
2. Set options of mode by the statements described at the 7.8 HOW TO SET UP
INFUSION SET Drops/ml.
3. Attach the drop sensor to the chamber of the infusion set by squeezing the drop
sensor with your fingers. The drop sensor should be located between the drop
nozzle of the chamber and the surface of the solution. Ensure the drop sensor’s
location to avoid any incorrect detection.
=========================================================================
CAUTION
1. When the drop sensor is used, the drop sensor must be positioned vertically at
the drop chamber. In addition, drop sensor is not exposed to the direct sunlight.
If not, sensor may work incorrectly.
2. Please do not connect it to nurse call port.
=========================================================================
=========================================================================
CAUTION
In case of purge infusion, air or occlusion is not detected; therefore the user should
pay a close attention to the pump.
27
=========================================================================
28
6. ALARM
=========================================================================
ALARM
This section covers the alarm that occurs when the pump is not operated normally
and provides efficient ways to deal with it.
For the safety of the patients, several alarm devices are prepared. When they operate,
the alarm indicator will be blinked and the alarm will sound. Press the STOP Key ⑭
to stop the alarm. Since each alarm has different sound, the user can tell the kinds of
problems just by listening to the alarm.
=========================================================================
6.5. FREE FLOW & NO DROP ALARM (IN CASE THE DROP SENSOR IS USED)
1. When the drop sensor is used, the drop sensor senses accidental free flow, liquid
leakage, flow error or empty container. And then the pump will stop the infusion
with alarm.
2. When the alarm is activated, “F.Err” is displayed at the Flow rate display
Windows ① in addition to the alarm sounding.
3. Press the STOP key ⑭ to deactivate the alarm.
※ See the 5.4. How to install the drop sensor (Option) section
6. ALARM
6.7 OTHERS
1. When the pump operates abnormally, infusion will stop, the error will be displayed
in Flow rate display windows ①, and alarm will sound.
2. Check the alarm message
1. When the Infused volume key ⑩ is pressed for two seconds, the program version in
the pump will be displayed for one or two seconds and the pump will enter into the
user setting mode. The User setting can be done when infusion is stopped.
2. Select the option of each function by pressing Up and Down key.
3. Press the SHIFT key ⑫ to switch to other function setting modes.
4. Press the Infused volume key ⑩ to save the setting option or STOP key ⑭ to
cancel the setting, and then go back to the initial mode. (Total volume or flow rate
setting mode)
5. The functions that the user can set up are as follows:
Table: Setting options When Released from the Factory (Program Version 2.08)
33
7. USER SETTING
7.1 HOW TO SET UP THE CALIBRATION (ACCURACY)
1. Enter into the user setting mode by press the Infused
volume key ⑩ for two seconds when infusion is stopped.
2. Change the mode by pressing the SHIFT key ⑫ until the
calibration-setting state is displayed.
3. To cancel the setting and go back to the initial mode, press
the STOP key ⑭.
4. Change the option to a desirable one by pressing Up and Down key. Then, press the
Infused volume key ⑩ to save the changed option and go back to the initial mode.
5. If this function is used for calibration, contact local agencies or the company.
6. The following table shows how the pump operates at specific options:
Displayed options 1 3 5 7 9 11 13 15 ……
Correction (%) -20 -10 0 10 20 30 40 50 ……
7. If errors occur while using the pump, correct options that were previously set up.
For example, if the option is set to '5' and its error is +8% (indicating that it is 8%
higher than the setting option), set the option to 3 or 4.
8. Please be informed that the maximum flow rate can be limited according to the
each ACC value. Please refer to the below table.
=========================================================================
CAUTION
1. Use a designated infusion set for infusion pump. If any infusion set other than
specified is used, proper flow rate accuracy and alarm function (air and occlusion)
is not guaranteed. If the designated set is not available, contact the local agency or
the company.
2. Pay close attention to the difference of the occlusion sensitivity, purge rate and
maximum flow rate by the Accuracy options.
3. If serious errors occur due to the extended use of the pump, contact the company.
It is recommended that the user make correction by testing once a year.
34
========================================================================
7. USER SETTING
7.2 HOW TO SET UP OCCLUSION PRESSURE
1. Enter into the setting mode by pressing the Infused volume
key ⑩ for two seconds when infusion is stopped.
2. Change the mode by using the SHIFT key ⑫ until occlusion
pressure setting state is displayed.
3. Press the STOP key ⑭ to cancel the setting and go back to
the initial mode.
4. Change the option to a desirable one by using Up and Down key. Then, press the
Infused volume key ⑩ to save the changed option and go back to the initial mode.
5. The following table shows how the pump operates at the specific options:
Displayed
Option
Pressure 100~450 mmHg 300~750 mmHg 600~950 mmHg
Displayed
Option
Volume Low Medium High
35
7. USER SETTING
7.4 HOW TO SET UP PURGE RATE
1. Enter into the user setting mode by pressing the Infused
volume key 1○0 for two seconds when infusion is stopped.
2. Change the mode by using the SHIFT key 1○2 until purge rate
setting state is displayed.
3. Press the STOP key 1○4 to cancel the setting and return to the
initial mode.
4. Change the option to a desirable one by pressing Up and 3○4 Down key3○5. Then,
press the Infused volume key 1○0 to save the changed option and go back to the
initial mode.
5. The following table shows how the pump operates at specific options:
6. The purge flow rate can be limited by the calibration data (ACC).
Acc. 1 ~ 13 14 ~ 15 16 ~ 21 22
Selectable purge rate 300, 500, 700, 300, 500, 300, 500, 300, 500
(ml/h) 900, 999 700, 900 700
7. USER SETTING
7.6 HOW TO SET UP SAVE FUNCTION
1. Enter into the user setting mode by pressing the Infused
volume key ⑩ for two seconds when infusion is stopped.
2. Change the mode by using the SHIFT key ⑫ until save
function setting state is displayed.
3. Press the STOP key ⑭ to cancel the setting and return to
the initial mode.
4. Change the option to a desirable one by pressing UP and Down key. Then, press the
Infused volume key ⑩ to save the changed option and go back to the initial mode.
5. The following table shows how the pump operates at specific options:
Displayed option
Total Volume,
Set up Not Set up
Flow Rate Save
Displayed option 1 2 3 4 5 6 7 8 9
K.V.O rate 1 ml/h 2 ml/h 3 ml/h 4 ml/h 5 ml/h 6 ml/h 7 ml/h 8 ml/h 9 ml/h
37
7. USER SETTING
7.8 HOW TO SET UP INFUSION SET Drops/ml (WHEN USING A
DROP SENSOR)
1. Enter into the user setting mode by pressing the Infused
volume key ⑩ for two seconds when infusion is stopped.
2. Change the mode by using the SHIFT key ⑫ until infusion set
drops/ml setting state is displayed.
3. Press the STOP key ⑭ to cancel the setting and return to
the initial mode.
4. Change the option to a desirable one by pressing Up and Down key. Then, press the
Infused volume key ⑩ to save the changed option and go back to the initial mode.
5. The following table shows how the pump operates at specific options:
Displayed option 15 20 60
Infusion Set Type 15 Drops/ml 20 Drops/ml 60 Drops/ml
Displayed option
38
Nurse call Set up Not set up
7. USER SETTING
7.10 HOW TO SET UP STANDBY ALARM
1. Enter into the user setting mode by pressing the Infused
volume key 1○0 for two seconds when infusion is stopped.
2. Change the mode by using the SHIFT key 1○2 until standby
alarm setting state is displayed.
3. Press the STOP key 1○4 to cancel the setting and return to the
initial mode.
4. Change the option to a desirable one by pressing Up and Down key. Then, press the
Infused volume key 1○0 to save the changed option and go back to the initial mode.
5. The following table shows how the pump operates at specific options:
Displayed option
7. USER SETTING
7.12 HOW TO SET UP AIR SENSITIVITY
1. Enter into the setting mode by pressing the Infused volume
key ⑩ for two seconds when infusion is stopped.
2. Change the mode by using the SHIFT key ⑫ until air sensor
sensitivity setting state is displayed.
3. Press the STOP key ⑭ to cancel the setting and go back to
the initial mode.
4. Change the option to a desirable one by using Up and Down
key . Then, press the Infused volume key ⑩ to save the changed option and go
back to the initial mode.
5. The following table shows how the pump operates at specific options:
Displayed
Option
Bubble size below 3 mm below 7 mm below 10 mm
=========================================================================
CAUTION
This test function is designed to check the presence of problems in each sensor. For
the best results, the user needs to refer to the service manual or contact the
company directly.
=========================================================================
41
8. MAINTENANCE
8.1 CHECKOUT OF THE PUMP
* It is recommended that the user make correction by testing the pump once a year
for the more safe usage.
* If any problem occurs, contact the local agencies or company.
1. Accuracy
- Periodically check the infused volume. If the infused volume is not accurate, contact
the Local agencies or Company.
2. Checkout of the Air (Bubble) alarm
- Position the air(bubble) below the Pumping unit and above the air sensor. The
air(bubble) size should be bigger than 10mm. Start the infusion. When the air
reaches the air sensor, check the Air alarm is occurred.
3. Checkout of the Occlusion alarm
1) Upstream occlusion alarm
- Pinch off the tubing located between the drop chamber and above the pump with
roller clamp or fingers. And then check the Occlusion alarm is occurred.
2) Downstream occlusion alarm
- Pinch off the tubing located between below the pump and the patient line with
roller clamp or fingers. And then check the Occlusion alarm is occurred.
4. Checkout of the Door open alarm
1) Set the infusion set, and opens the door. Check the Door open alarm is occurred
when the START key ⑬ is pressed.
2) During infusion, open the door. And then check the Door open alarm is occurred.
5. Checkout of the Low battery alarm
1) Charge the internal battery to full capacity by connecting the pump to an AC
power supply for at least 15 hours.
2) Set the flow rate 25ml/h, and unplug the pump for operating the pump by the
internal battery. Start the infusion by pressing the START key ⑬
3) Check the pump is operated about approximately 2 hours and Low battery alarm
is occurred when 3 lamps of the Battery capacity indicator is turned off.
42
8. MAINTENANCE
8.2. CLEANING AND STERILIZATION
- Before cleaning the pump, be sure to turn off the pump by Power switch , and
disconnect the AC power port or DC power port from the pump.
- Do not sterilize the pump with autoclave or E.O gas.
- Do not use thinner, solvent, benzene, ammonia or acetone.
- Use a gauze moistened with cold or warm water.
- Before using it, be sure to dry the pump.
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.
If the Buyer 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.
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.
Serial No:
Delivery date:
Quality inspector:
DOCUMENT HISTORY