Surdial Service Manual PDF
Surdial Service Manual PDF
Surdial Service Manual PDF
Procedures for operation and cautions for safety contained in the manual are
only applicable to the case when the machine is used for specified purpose.
It shall be noted that any danger caused by use of the machine based on any
procedures not specified in the manual shall be responsible for user.
(1) Messages for safety are classified into the following three categories:
DANGER
Cases critically causing death or severe injury of user by misuse of the
machine
WARNING
Cases potentially causing death or severe injury of user by misuse of the
machine
CAUTION
Cases potentially causing injury of user and/or loss of property by
misuse of the machine
DANGER
Before use of the machine, read and understand this Operation Manual.
• The machine can be used safely and reliably when operated and maintained as
specified in the manual.
• The machine shall be operated by well trained and qualified person only to
avoid danger and/or the machine damage due to incorrect use.
DO NOT touch board, wiring and terminal with hand in the case other than
maintenance.
• DO NOT touch wiring and terminal not insulated.
• DO NOT touch board with wet hand.
• Turn OFF the power breaker and remove plug when touch terminal.
Take the following care to avoid potential danger to patient when blood line
connection and disconnection:
• DO NOT enter air bubbles into patient body.
• DO NOT connect blood line to the patient before completion of priming
operation.
• DO NOT connect blood line to the patient during rinsing operation.
• DO NOT enter harmful virus or chemical into patient body.
WARNING
DO NOT touch power cable on the floor to prevent electric shock due to fluid
beak caused by the machine trouble.
DO NOT touch switch unnecessary for the machine operation during dialysis.
CONTENTS
PREFACE ..................................................................................................................... PREFACE-1
CAUTIONS FOR SAFETY............................................................................................ CAUTION-1
DANGER........................................................................................................... CAUTION-2
WARNING......................................................................................................... CAUTION-3
CAUTION .......................................................................................................... CAUTION-4
1. APPLICATION .............................................................................................................. 1-1
2. CONTRAINDICATION ................................................................................................. 2-1
3. CAUTIONS.................................................................................................................... 3-1
4. SYMBOL FOR SAFETY................................................................................................ 4-1
5. FLOW CHART
5.1. Fluid and blood line ............................................................................................ 5-1
5.1.1. Flow chart ................................................................................................. 5-1
5.1.2. List of input components .......................................................................... 5-2
5.1.3. List of output components ........................................................................ 5-3
5.1.4. List of other components ......................................................................... 5-4
6. DISASSEMBLING AND REPLACEMENT
6.1. Input components................................................................................................ 6.1.1-1
6.1.1. Conductivity cell Assy (CD) ...................................................................... 6.1.1-1
6.1.2. Dialysate pressure sensor Assy (PD) ...................................................... 6.1.2-1
6.1.3. Blood leak sensor Assy (BLD) ................................................................. 6.1.3-1
6.1.4. Pressure SW: AW-3200-63-A (PS) .......................................................... 6.1.4.1
6.2. Output components............................................................................................. 6.2.1-1
6.2.1. Two way electromagnetic valve : AV-3200-318-SC
(V2/V3/V12/V13/V14(V15/V17)) .......................................................................... 6.2.1-1
6.2.2. Two way electromagnetic valve: AV-3202-63-S (V4 / V11) ....................... 6.2.2-1
6.2.3. High vacuum electromagnetic valve: AV-3202-63-SH (V10) ..................... 6.2.3-1
6.2.4. Three way electromagnetic valve:
AV-3302-63-S (V5 / V6 / V7 / V8)......................................................................... 6.2.4-1
6.2.5. Bellowphragm pump: VCP-60 (Vpa / VPb) ............................................... .6.2.5-1
6.2.6. Blood pump Assy (BP / BPC) .................................................................... .6.2.6-1
6.2.7. Micro gear pump Assy (P1/P2) .................................................................. .6.2.7-1
6.2.8. Venous clamp Assy (CLV) ........................................................................ .6.2.8-1
1. APPLICATION
(a) Single patient dialysis machine, SURDIAL is applied to treatment of patients with
acute or chronic renal failure by dialysis when the application is instructed by
doctor.
(b) SURDIAL can be used at both hospital and home.
2. CONTRAINDICATION
Any application other than dialysis using SURDIAL is contraindicated.
3. CAUTIONS
Take care of the followings in use of the machine:
(2) Install the machine at place without fear of adverse effects caused by abnormal
(5) Frequency, voltage and amperage (power consumption) of power supply should be
as specified.
(6) Connect the machine with earth correctly.
(4) Take care that operation of the machine combined with other device may cause
adverse effects.
(5) Recheck integrity of lines connected to patient directly.
(2) If trouble of the machine or patient is detected, take appropriate actions such as
2) Store the machine at place without fear of adverse effects caused by abnormal
(4) Clean accessories, cords, 7 and the like in order and clean them to store.
(5) Store the machine after cleaning it for the next use without any trouble.
(2) When the machine is used after storage for some time, check and maintain so that
a) The symbol shown below means that user of SURDIAL must read and understand
this Service Manual before starting operation of the machine for safe and effective
use of it.
b) The symbol shown below means that electric shock is caused by contact with high
voltage applied live part.
5. FLOW CHART
Sensor
1 Valve body 1
2 Seat 1
3 Packing 1
4 Seat holder 1
5 Spring 1
6 Lock nut 1
7 Casing 1
8 Name plate 1
Sampling port
1 Body ACB060 1
Seat holder ACH090 1
2 Check valve seat Assy
Seat ACL010 1
3 Spring 1
4 Lock nut ACH080 1
5 O-ring P9DC 1
6 Sub-body ACB070 1
1 Socket QJ-2P,NPT1/8 1
2 Silicone tube φ 5 x φ 11 x 50L 1
3 ………..FEP tube TF185 1 φ 6 x φ 8 x 330L
#9193 59 32 010 2 1 Pink for A concentrate
4 Color seal
#9193 59 33 010 2 1 Orange for B concentrate
[Connection]
[Adjustment]
Not required
[Replacement]
(1) Turn off power SW of machine.
(2) Remove left side cover from upper part of machine
(3) Disconnect flexible cable from connector by unlocking it.
CAUTION
• Replace operation panel sheet after turning off power SW under care not to be charged with
static electricity.
• Handle flexible cable carefully so that it is not folded and/or damaged. Otherwise malfunction
may be caused.
• DO NOT apply excess external force to operation panel because key SW's and patterns
encased in the panel may be folded and/or damaged, resulting in malfunctioning of them, in
particular when the panel itself is stored or handled.
• DO NOT reused removed panel sheet.
• Disconnect flexible cable from connector after unlocking it. If the cable is pulled out under
unlocking the connector, electrodes placed at the connector surface may be separated,
causing machine failure.
[Connection]
• CN1: Connect to CN22 of [main board] through harness.
• CN2: Connect to CN10 of [main board] through harness.
• CN3: Connect to flexible cable of [operation panel).
• CN4: Connect to CN2 of [LCD module] through harness.
• CN5: Connect to CN1 of [LCD module].
[Adjustment]
See “10.17. Adjustment of contrast”.
[Replacement]
(1) Turn off power SW of machine.
(2) Remove left cover from upper part of machine.
(3) Disconnect all connectors.
(4) Remove green cap from upper part of knob of blood pump flow rate setting volume placed
at front side of machine and loosen exposed screw by screwdriver under pressing the knob
by hand to remove it.
(5) Remove board fixing nuts from machine inside to remove the board.
(6) Prepare new board.
(7) Remove seal, if provided, from buzzer (BZ1).
(8) Attach the new board.
(9) Attach knob of blood pump flow rate setting volume under care of correct 0 point
positioning.
(10) Connect the all disconnected connectors.
(11) Turn on power SW of machine.
(12) Try to adjust contrast as per the procedure specified in “10.17. Adjustment of contrast”.
(13) Check correct functioning of each LED.
(14) Check correct functioning of each SW of operation panel.
(15) Return the removed cover to the original position.
CAUTION
• Replace operation panel board after turning off power SW under care not to be charged with
static electricity.
• It is recommended to replace the board after cooling to room temperature because temperature
of resistors placed on the board immediately tuning off power is high, potentially causing burn.
• Handle flexible cable carefully so that it is not folded and/or damaged. Otherwise malfunction
may be caused.
• Disconnect flexible cable from connector after unlocking it. If the cable is pulled out under
unlocking the connector, electrodes placed at the connector surface may be separated, causing
machine failure. Unlock as per the procedure specified in “8.1 Operation panel”.
• LCD may not function normally after the board replacement. If so, adjust contrast.
[Connection]
• CN1: Connect to CN5 of [operation panel board].
• CN2: Connect to CN4 of [operation panel board] through harness.
[Adjustment]
See “10.17 Adjustment of contrast”.
[Replacement]
(1) Turn off power SW of machine.
(2) Remove left cover from upper part of machine.
(3) Disconnect CN1 and CN2 from LCD module.
(4) Remove 4 fixing screws or nuts to take out the module.
(5) Prepare new LCD module.
(6) Remove protective sheet from the new module surface.
(7) Attach the module under care of correct positioning of “UP” mark on the board.
(8) Connect CN1 and CN2 to LCD module.
(9) Turn on power SW of machine.
( 1 0 ) Try to adjust contrast as per the procedure specified in “10.17 Adjustment of contrast”.
CAUTION
[Connection]
• CN601: Connect to connector of [bubble sensor].
• CN602: Connect to CN3 of [main board] through harness.
[Adjustment]
See “10.15 Adjustment of bubble sensor”.
[Replacement]
(1) Turn off power SW of machine.
(2) Remove left cover from upper part of machine.
(3) Disconnect all connectors.
(4) Remove bubble sensor board under pressing spacer lock used to fix it.
(5) Prepare new bubble sensor board.
(6) Attach the new board and check correct locking.
(7) Connect all the disconnected connectors.
(8) Turn on power SW of machine.
(9) Adjust the sensor as per the procedure specified in “10.15 Adjustment of bubble sensor”.
(10) Check correct function of bubble sensor.
( 1 1 ) Return the removed cover to the original position.
[Connection]
• CN701: Connect to connector of [dialysate pressure sensor].
• CN702: Connect to CN14 of [main board] through harness.
[Adjustment]
See “10.3. Adjustment of dialysate pressure sensor”.
[Replacement]
(1) Turn off power SW of machine.
(2) Remove left cover from upper part of machine and left cover from lower part of it.
(3) Remove dialysate pressure sensor ASSY as per the procedure specified in “6.1.2 Dialysate
pressure sensor ASSY”.
(4) Disconnect all connectors.
(5) Loosen screws used to fix dialysate pressure sensor board to remove it.
(6) Prepare new dialysate pressure sensor board.
(7) Attach the new board.
(8) Connect all the disconnected connectors.
(9) Attach dialysate pressure sensor ASSY.
(10) Turn on power SW of machine.
(11) Adjust dialysate pressure sensor as per the procedure specified in “10.3.
Adjustment of dialysate pressure sensor”.
(12) Check correct function of dialysate pressure sensor.
(13) Return the removed covers to the original positions.
CAUTION
• Replace dialysate pressure sensor board after turning off power SW of machine
under care not to be charged with static electricity.
[Connection]
• CN1: Connect to CN413 of (sub-board] through harness.
• CN2: Connect to [blood leak sensor] through harness.
• CN3: Connect to CN602 of [bubble sensor board] through harness.
• CN4: Not connected.
• CN5: Connect to CN408 of [sub-board] through harness.
• CN6: Not connected.
• CN7: Connect to [photo-sensor board of Bellowphragm pump A] through harness.
• CN8: Connect to [photo-sensor board of Bellowphragm pump B] through harness.
• CN9: Connect to CN502 of [DSUB board] through harness.
• CN10: Connect to CN2 of [operation panel board] through harness.
• CN11: Connect to CN701 of [arterial pressure sensor board] through harness.
• CN12: Connect to V3,V4,V9,V10,V12 and V17 through harnesses.
• CN13: Connect to CN701 of [venous pressure sensor board] through harness.
• CN14: Connect to CN701 of [dialysate pressure sensor board] through harness.
• CN15: Connect to LS2 and FS through harnesses.
• CN16: Connect to harness of LS3.
• CN17: Connect to LAMP through harness.
• CN18: Connect to harness of CLV.
• CN19: Connect to PS, FSW and LS1 through harnesses.
• CN20: Connect to V5,V6,V7 and V8 through harnesses.
• CN21: Connect to V2,V11,V13,V14 and V15 through harnesses.
• CN22: Connect to CN1 of [operation panel board] through harness.
• TM1: Connect to temperature sensors (T1,T2 and T3) and concentration sensor.
[Adjustment]
See “10.16. Adjustment of concentration”.
«ROM»
(1) Turn on power SW of machine and record all set values.
(2) Turn off power SW of machine.
(3) Remove right cover from upper part of machine and right cover from DENSO box.
(4) Remove ROM using tool specially designed for the removal.
(5) Prepare new ROM.
(6) Attach the new ROM under care that it is positioned correctly and pins of it are
not damaged.
(7) Turn on power SW of machine.
(8) If ROM of different version is attached, initialization alarm is actuated.
(9) Input all the set values recorded at step (1).
(10) If EEPROM initialization alarm is actuated, adjust concentration as per the
procedure specified in "10.16. Adjustment of concentration".
(11) Check correct function of machine.
(12) Return the removed covers to the original positions.
Fig. 8.6-2 Attachment of ROM
CAUTION
• Replace main board or ROM after turning off power SW of machine under care not to be charged
with static electricity.
• After the board replacement, re-input set values. It should be noted that the values found in
maintenance modes 5 and 6 are specific to machine.
NIPRO SURDIAL (SEM) ver. OR2102-9902
8.7.1
[Connection]
When used as venous pressure sensor:
• CN701: Connect to CN13 of [main board] through harness.
[Adjustment]
See “10.2. Adjustment of venous and arterial pressure sensors”.
[Replacement]
(1) Turn off power SW of machine.
(2) Remove right cover from upper part of machine and right cover from DENSO box.
(3) Disconnect all connectors.
(4) Remove snapper to take out tube.
(5) Remove venous or arterial pressure sensor board under pressing spacer lock used to fix it.
(6) Prepare new venous or arterial pressure sensor board.
(7) Attach the new board and check correct locking.
(8) Attach tube and snapper.
(9) Connect all the disconnected connectors.
(10) Turn on power SW of machine.
(11) Adjust venous or arterial pressure sensor as per the procedure specified in 10.2.
“Adjustment of venous and arterial pressure sensors”.
(12) Check correct indication of venous or arterial pressure.
(13) Return the removed covers to the original positions.
CAUTION
• Replace venous or arterial pressure sensor board after turning off power SW of machine under
care not to be charged with static electricity.
• Connect tube to left side of sensor and expose right side of it to atmosphere. If connected to the
right side, measured pressure is incorrect.
• After connecting tube to sensor, attach snapper. If not attached, tube may be disconnected by
pressure application, resulting in blood inflow.
• Connect tubes for venous and arterial pressure monitoring to respective boards correctly.
[Connection]
• CN501: Connect to external monitor (option).
• CN502: Connect to CN9 of [main board] through harness.
• CN503: Connect to CN402 of [sub-board] through harness.
• CN504: Connect to CN810 of [buzzer board] through harness.
[Adjustment]
Not required
[Replacement]
(1) Turn off power SW of machine.
(2) Remove right cover from upper part of machine and right cover from DENSO box.
(3) If battery (option) is provided, disconnect its connector.
(4) Disconnect all connectors.
(5) Remove knob from BP BACKUP volume.
(6) Remove spacer used to fix DSUB board and nuts used to fix the volume to take out the
board.
(7) Prepare new DSUB board.
(8) Attach the new board.
(9) Return the removed knob to BP BACKUP volume.
(10) Connect all the disconnected connectors.
(11) If battery (option) is used, connect its connector. Turn BP BACKUP volume to check correct
blood pump operation under no power supply.
(12) Turn on power SW of machine.
(13) Check correct function.
(14) Return the removed covers to the original positions.
CAUTION
• Replace DSUB board after turning off power SW of machine under care not to be charged
with static electricity.
• After the replacement, set BP BACKUP volume to OFF position.
• DO NOT miss parts used to fix. Spacer is fixed by nuts at its rear side.
[Connection]
• CN801: Connect to CN504 of [DSUB board] through harness.
[Adjustment]
Not required
[Replacement]
(1) Turn off power SW of machine.
(2) Remove right cover from upper part of machine and right cover from DENSO box.
(3) Disconnect all connectors.
(4) Remove buzzer board under pressing spacer lock used to fix it.
(5) Prepare new buzzer board.
(6) Attach the new board and check correct locking.
(7) Connect all the disconnected connectors.
(8) Turn on power SW of machine.
(9) Make error to check buzzing.
(10) Return the removed covers to the original positions.
CAUTION
• Replace buzzer board after turning off power SW of machine under care not to be charged
with static electricity.
8.10. Sub-board
Board No. is silk screen printed at upper right side of sub-board. SBY0157 is for AC230V and
SBY0163 is for AC110V. Unnecessary Nos. are soldered. And also, concerning SBY0163 for
AC110V, components are attached to CN416.
«Fuse»
(1) Turn off power SW of machine.
(2) Disconnect power plug from receptacle.
(3) Remove left cover from upper part of machine and left cover from DENSO box.
(4) Remove fuse.
(5) Prepare new fuse. Select fuse to be replaced by referring to the following purposes and
ratings of fuses:
FUSE402: AC250V 3A P1 pump protection
FUSE403: AC250V 3A RY402 detect power failure relay protection
FUSE404: AC250V 3A P2 pump protection
FUSE405: AC250V 5A BP driver protection
CAUTION
• Replace sub-board or fuse after disconnecting power plug from receptacle. Only power
SW OFF is insufficient to avoid danger because AC supply placed at left side in DENSO
box is not disconnected, potentially causing electric shock.
• Handle sub-board under care not to be charged with static electricity.
• Power rating of sub-board should conform to that of power source of machine.
Otherwise, fire and/or machine failure may be caused.
• Use fuse of correct rating. Otherwise, fire and/or machine failure may be caused.
9. MAINTENANCE MODES
9.1 Display
LCD is used to display various dialysis related information and setting screens by 40
letters in each of 4 lines.
Many information and setting screens are available and desired screen can be displayed
by SW operation on operation panel.
CAUTION
• LCD is easily scratched. DO NOT press or scratch its surface by pencil point or hard
tool.
• Glass is mainly used in LCD. DO NOT apply mechanical impact.
• DO NOT press operation panel SW by pencil point or hard tool.
Dialysis related data indication, alarm setting, alarm release, machine function monitoring
or concentration calibration can be executed in selected maintenance mode.
10 maintenance modes are available. There are mode to indicate information only,
mode enabling setting at any time required and mode enabling setting under specified
condition only.
• Indication only
Mode to indicate information only. Setting is disabled.
(4) Operation SW's [+]/[-] are displayed above [F-1][F-2] and items enabled to
be set blink.
DANGER
• Setting or setting change of item to be maintained during dialysis is danger. DO NOT set or
change item to be maintained under the condition that patient is connected to machine.
• DO NOT change set value without direction of doctor or technician.
• Protect modes 2, 4, 5, 6 and 7 to prevent malfunction of machine always by setting
“20.MAINTENANCE MODE FREE” to OFF. Release the protection only when setting change
is required.
CAUTION
• If ROM of different version is loaded, some maintenance values may be initialized. In such
case, reset the values.
• When ROM or main board is replaced, or CPU is reset, set maintenance mode values
followed by checking them.
• It is recommended to record maintenance mode values. Use supplement of this service
manual to record them.
INDICATION DESCRIPTION
MODE1: DATA Dialysis related data indication mode
MODE2: ALARM SETTING Alarm setting mode
MODE3: ALARM FORCED OFF Alarm release mode
MODE4: FUNCTION MONITOR Function monitor and manual operation mode
MODE5: CONCENTRATE DATA Concentration calibration mode
MODE6: CHARACTERISITICS Instrument adjustment mode
MODE7: SYSTEM System setting mode
MODE8: SERVICE FREQUENCY Operation frequency indicating mode
MODE9: MACHINE FILLING
Air purge mode
PROCEDURE
MODE10: ALARM HISTORY Alarm history indicating mode
In maintenance mode 1 screen, real time indication of various data during dialysis
operation is executed. In the mode, only data indication is enabled and setting is disabled.
Press [F-3] or [F-4] SW to check data.
Press [F-5] SW to display maintenance mode menu screen.
INDICATION DESCRIPTION
1. TREATED BLOOD VOLUME Treated blood volume indication
2. TREATMENT TIME Executed dialysis time indication
3. SN AVG.BLOOD FLOW Mean SN blood flow rate indication
4. SN STROKE VOLUME One stroke SN1 blood volume indication
5. BLD REAL VALUE Leaked blood level indication
6. BLD AUTO ZERO Bood leak auto zero value indication
7. BLD SENS VALUE Blood leak SENS value indication
8. BLD RED RIGHT Blood leak red value indication
9. BLD GREEN RIGHT Blood leak green value indication
INDICATION DESCRIPTION
1.V.PRESS MAX RANGE Auto-setting of upper venous pressure alarm limit
2.V.PRESS MIN RANGE Auto-setting of lower venous pressure alarm limit
3.A.PRESS MAX RANGE Auto-setting of upper arterial pressure alarm limit
4.A.PRESS MIN RANGE Auto-setting of lower arterial pressure alarm limit
5.D.PRESS MAX RANGE Auto-setting of upper dialysate pressure alarm limit
6.D.PRESS MIN RANGE Auto-setting of lower dialysate pressure alarm limit
7.TMP(I) Setting of TMP alarm limit
8.CONDUCTIVITY MAX Setting of upper conductivity alarm limit
9.CONDUCTIVITY MIN Setting of lower conductivity alarm limit
10.TEMPERATURE MAX Setting of upper dialysate temperature alarm limit
11.TEMPERATURE MIN Setting of lower dialysate temperature alarm limit
12.BLOOD LEAK Setting of blood leak alarm limit
13.UF MAX AGAINST BLF Setting of upper UF alarm limit
14.SN HIGH/LOW RANGE Setting of upper and lower SN alarm limits
15.SN STROKE TIME Setting of SN stroke time alarm limit
16.VCS UF LEAK TEST Setting of leak detection level from closed circuit
17.UF LEAK VALUE a Setting of leak detection level a from closed circuit
18.UF LEAK VALUE b Setting of leak detection level b from closed circuit
19.UF LEAK TIME c Setting of leak detection time c from closed circuit
20.UF LEAK TIME d Setting of leak detection time d from closed circuit
21. RESET SW TIME Setting of no reset SW press alarm time
22.DIALYSIS SW TIME Setting of no dialysis SW press alarm time
23 BYPASS SW TIME Setting of no bypass SW press alarm time
WARNING
• DO NOT release any alarm during dialysis. Otherwise, machine failure may be caused.
CAUTION
Press [F-3] or [F-4] SW to check data. If not protected, press [F-3] or [F-4] SW to
shift blink and press [F-1] or [F-2] SW to operate component.
FUNCTION WHEN
SYMBOL COMPONENT SYMBOL IS MARKED WITH NOTE
O IN DRAWING
V2~V4
Two way electromagnetic valve During power supply
V10~V17
V5~V9 Three way electromagnetic valve During power supply
P1 Deaeration pump During power supply
P2 Dialysate pump During power supply
CLV Clamp During power supply
FAN Fan During power supply
VPA A chamber viscous pump During power supply CW rotation
VPa A chamber viscous pump During power supply CCW rotation
VPB B chamber viscous pump During power supply CW rotation
VPb B chamber viscous pump During power supply CCW rotation
H Heater During power supply
BP Blood pump During power supply
SP Syringe pump During power supply
PH1 Viscous pump position sensor Shaded photo-sensor Original point detection.
PH2 Viscous pump position sensor Shaded photo-sensor Rotation signal
PH3 Viscous pump position sensor Shaded photo-sensor Original point detection
PH4 Viscous pump position sensor Shaded photo-sensor Rotation signal
LS2 Coupler SW Coupler being set
LS3 Syringe overload SW Overload detection
LS5 Clamp position sensor Being clamped
PS Pressure SW Pressurized water
FS Flow sensor Float drop
FSW Float SW Air detection
P1F P1 pump fuse Burnt out
P2F P2 pump fuse Burnt out
DANGER
• DO NOT operate any component manually under the condition that patient is connected to
machine to avoid his/her injury.
CAUTION
• Manual operation of any component should be performed by engineer familiar with its
construction and function.
• DO NOT operate P1 or P2 pump without priming with fluid. Empty run may caused the
pump failure.
INDICATION DESCRIPTION
CAUTION
• Both BC1 and BC2 are bicarbonate dialysis modes. If different dialysate preparation
information is registered, it is recommended to record that the information is registered in
which mode BC1 or BC2 after checking concentrate type to be used.
• See “Concentration Calibration Procedure”.
INDICATION DESCRIPTION
1.VCa W+AC RATIO Setting of [water : AC] ratio in A chamber
2.VCb W+AC RATIO Setting of [water : AC] ratio in B chamber
3.THEORETICAL W+AC Setting of theoretical [water + AC] concentration
4.CHAMBER Indication of functioning chamber. Disabled setting
5.MODE Setting of dialysate preparation function at calibration
6.COND. W+AC Calibration of [water + AC] conductivity
7.CONC. W+AC Calibration of [water + AC] concentration
CAUTION
INDICATION DESCRIPTION
Indication of offset value to calibrate blood pump flow rate
18.BPF(OFFSET)
(instrument specific value)
19.ROLLING TUBE TYPE Setting of blood pump intended to be used
20.HEATER CONT.COEFFICIENT Kt Indication of coefficient in heater control
21.HEATER CONT.COEFFICIENT Kp Indication of coefficient in heater control
22.HEATER CONT.COEFFICIENT Ki Indication of coefficient in heater control
23.HEATER CONT.COEFFICIENT Kd Indication of coefficient in heater control
24. HEATER CONT.COEFFICIENT Kl Indication of coefficient in heater control
25. HEATER CONT.COEFFICIENT Kb Indication of coefficient in heater control
26.HEATER CONT.COEFFICIENT Lt1 Indication of coefficient in heater control
27.HEATER CONT.COEFFICIENT Lt2 Indication of coefficient in heater control
28.HEATER CONT.COEFFICIENT Lt3 Indication of coefficient in heater control
Indication of coefficient in temperature calibration of
29.TEMP.CORR.COEFFICIENT
conductivity
Indication of T1 determined by input value added T1
30. T1 OFFSET
temperature sensor value
Indication of T2 determined by input value added T2
31.T2 OFFSET
temperature sensor value
Indication of T3 determined by input value added T3
32.13 OFFSET
temperature sensor value
DANGER
• Change of setting other than calendar year, month and day; and clock hour and minute in maintenance
mode 6 may cause significant changes of UF volume, conductivity (concentration) and dialysate
temperature resulting in giving serious injury to patient. DO NOT change setting by any person other than
engineer familiar with the setting.
• After setting change, perform trial test of instrument to check its normal function.
Perform UF test to check that UF error is within specified range.
Measure conductivity to check that difference between the measured one and set one is within specified
range.
Check that measured blood pump flow rate is within ±5% of set flow rate.
Check also that temperature control is normal and dialysate temperature is stabilized.
WARNING
CAUTION
• BP flow rate calibration (GAIN and OFFSET) values are those determined using standard NIPRO
blood line. When blood line of smaller sized or other manufacturer is used, adjustment is required.
Also when blood line of smaller sized is used, adjust gap between BP rotors and housing.
In maintenance mode 7 screen, system and option settings can be performed. If setting
is protected, indication only is enabled and setting is disabled.
Press [F-3] or [F- 4] SW to check data. If not protected, press [F-1] or [F-2) SW to
change setting.
Press [F-5] SW to display maintenance mode menu screen.
INDICATION DESCRIPTION
WARNING
• Connection of each option should conform to its setting. Otherwise, disabled function of the
option or malfunction of machine may be caused.
CAUTION
INDICATION DESCRIPTION
1. POWER Indication of power connection time of machine
2.FAN Indication of fan operation time
3.P1 Indication of deaeration pump P1 operation time
4.P2 Indication of dialysate pump P2 operation time
5.CLV Indication of clamp operation frequency
6.V2 Indication of two way electromagnetic valve (EMV) V2 operation frequency
7.V3 Indication of two way EMV V3 operation frequency
8.V4 Indication of two way EMV V4 operation frequency
9.V5 Indication of three way EMV V5 operation frequency
10.V6 Indication of three way EMV V6 operation frequency
11.V7 Indication of three way EMV V7 operation frequency
12.V8 Indication of three way EMV V8 operation frequency
13.V9 Indication of three way EMV V9 operation frequency
14.V10 Indication of two way EMV V10 operation frequency
15.V11 Indication of two way EMV V11 operation frequency
16.V12 Indication of two way EMV V12 operation frequency
17.V13 Indication of two way EMV V13 operation frequency
18.V14 Indication of two way EMV V14 operation frequency
19.V15 Indication of two way EMV V15 operation frequency
20.V17 Indication of two way EMV V17 operation frequency
CAUTION
• Once zero cleared, the cleared operation time or frequency can not be resumed.
Press [F-3] or [F-4] SW to check data. Press [F-1] SW to clear the history.
Press [F-5] SW to display maintenance mode menu screen.
INDICATION DESCRIPTION
10. ADJUSTMENT
10.1. Measurement of chamber capacity and adjustment of silicone volume
10.1.1. Measurement of chamber capacity
In the cases such as replacement of viscous chamber or viscous pump, silicone oil
volume in the chamber may be changed. Measure the chamber capacity based on the
below procedures and input the measured result into machine.
(6) By pressing [PRIP.] SW to shift to preparation process, machine is started from console
mode.
(7) Check dialysate temperature stabilization.
(8) Isolate air discharge line of AS1 from drain line by clamping upper tube of AS1 by forceps
or the like.
(9) Measure RO water weight discharged from each of A and B chambers when each of [V5
and V6] and [V7 and V8] are ON using electronic balance under referring to data
displayed in maintenance mode 4 screen to derive each of the A and B chamber
capacities respectively. Calculate mean value of 3 measurements for each of the
chambers.
(10) Each of the capacities should satisfy the below requirement. If not so, adjust silicone oil
volume in each of the chambers followed by performing the measurement 3 times for
each of them.
snapper 6 from the plug by twisting latch along tooth line using radio pliers to remove the
plug.
(6) Turn on “V4” manually in maintenance mode 4 screen.
(7) Use silicone oil filled syringe 2 to add the oil to the
DANGER
• Take care for air not to be included in silicone oil to prevent conductivity (concentration) error or
UF error potentially causing patient injury.
WARNING
• Use silicone oil of acceptable quality, viscosity, purity and the like specified by manufacturer. DO
NOT use any other silicone oil.
• Add or aspirate silicone oil to or from chamber when the chamber capacity is larger or smaller
than specified volume.
(8) Connect syringe and manometer to venous pressure inlet port as shown in the below Fig.
(9) Expose manometer to atmosphere and try to indicate venous pressure of 0mmHg in the screen
by turning VR701.
(10) Pressurize manometer to 300mmHg by advancing syringe plunger and try to indicate venous
pressure of 300mmHg in the screen by turning VR702.
(11) Repeat the above steps (9) and (10) until each of 0mmHg and 300mmHg is indicated.
Manometer reading Adjusting means
0 mmHg PV_PCB VR701
300 mmHg PV_PCB VR702
(11) Input “6.V.PRESS OFFSET” value recorded at the above step (6) in maintenance mode 6
screen.
(12) Protect setting by selecting OFF of “20.MAINTENANCE MODE FREE” in maintenance mode 7
screen.
(13) Disconnect the syringe and manometer.
(14) Return the removed covers to the original positions.
Adjust arterial pressure sensor based on the same procedures as the case of the
venous pressure sensor. Offset value and adjusting means are as follows.
•Offset value
(8) Clamp tube connected to one side of dialysate pressure sensor using forceps and connect
syringe and manometer to tube connected to other side of the sensor as shown in the below
Fig.
(11) Input “8.D.PRESS OFFSET” value recorded at the above step (6) in maintenance mode
6 screen.
(12) Protect setting by selecting OFF of “20.MAINTENANCE MODE FREE” in maintenance mode
7 screen.
(13) Remove the syringe and manometer.
(14) Return the removed covers to the original positions.
(8) Adjust by checking indicated value when the resistor is connected. Check the
value in maintenance mode 6 screen and input offset value.
(11) Remove the syringe and manometer and return the pressure SW connection to the original.
(12) Return the removed cover to the original position.
NOTE
• Clean the Blood leak detector, before you calibrate it. Blood leak detector which is
not cleaned detect blood leak even it does not happen blood leak.
Adjusting value
Adjusting value
(11) Remove the manometer and the connection means to return to the original condition.
(12) Return the removed cover to the original position.
(7) By pressing [PRIP.] SW to shift to preparation process, machine is started from console
mode.
(8) Check dialysate temperature stabilization.
(9) Measure discharge flow time from start of discharge to end of discharge. Discharge flow is
intermittent.
Adjusting valve
10.12. Adjustment of gaps between housing and rotor rollers of blood pump
10.12.1. Adjustment by water head pressure
Adjust the gaps by application of water head pressure to blood line set to blood pump
based following procedures.
(1) Required devices
• Blood line
• Water receiver
• Water bottle
• Hexagon wrench (1.5mm)
(2) Turn off power SW of machine.
(3) Set rolling tube of blood line to blood pump and connect water bottle to inflow end of t??
(4) Prime blood line with water from the bottle by gravity flow of water.
(5) After the priming completion, turn rotor of blood pump manually to occlude rolling tube of 3
rollers of the rotor.
Fig. 10.12-1 Adjustment of gaps between housing and rotor rollers of blood pump
(6) Lift the bottle 1 so that height of water level in it from center of the rotor becomes above
Open outflow end of the rolling tube above water receiver.
(7) Loosen set screw 3 of the roller by hexagon wrench 2. Turn shaft 4 by screw repeat
narrowing and widening of gap between the roller and housing of blood pump set the gap to
allow water discharge from the outflow end.
(8) Tighten the set screw 3 at a moment when the water discharge is stopped by turning 4
slowly.
(9) Repeat the above procedures until all the gaps are adjusted.
(1) Remove left cover form lower part of machine to expose PC1.
(2) Turn on power SW of machine.
(3) Turn on [DIALYSIS] SW to shift lo dialysis wait process.
(4) Press [PREP.] SW to shift to preparation process. Engage coupler with bypass connect
dialysate concentrate is not used, connect dumm? resistor to conductivity sensor.
(5) Check stabilization of dialysate temperature and concentration.
(6) Check that [BYPASS] SW is OFF (released bypassing and dialysate flow through coupler
(7) Adjust dialysate flow rate to 500ml/min by turning adjusting screw of NV2 under monitor
dialysate flow rate indication of flow meter.
(8) Turn on [BYPASS] SW to bypass dialysate line.
(9) Adjust bypass flow rate to 500ml/min by turning adjusting screw of PC1 under monitor
bypass flow rate indication of flow meter. Tube should be centered at PC1 and plates of
should be aligned correctly.
Fig. 10.12-2 Adjustment of gaps between housing and rotor rollers of blood pump
(6) Connect syringe 1 and manometer 5 to inflow end of the tube and open outflow end o??
above water receiver.
(7) Loosen set screw 3 of the roller by hexagon wrench 2. Turn shaft 4 by screwdriver repeat
narrowing and widening of gap between the rotor and housing of blood pump. Initially turn the
shaft to stop water discharge from the outflow end when a water pressure 0.2kgf/cm2 is applied
to the tube through the inflow end by operating the syringe.
(8) Tighten the set screw 3 at a moment when the water discharge is started under the pressure
application by turning the shaft 4 slowly.
(9) Repeat the above procedures until all the gaps are adjusted.
(10) Set blood pump flow rate to 400ml/min and operate the pump.
(11) Measure actually discharged water weight or volume/minute (ml/min).
(12) Input “17.BPF(GAIN)” value of blood pump flow rate in maintenance mode 6 screen value
t?? to adjust the actual flow rate to about 400ml/min. Decrease (increase) the value if the a??
flow rate is higher (lower) than the set flow rate.
(13) Repeat the above procedures (7) to (12) until each of the actual flow rates of 50 and
400ml/min is obtained.
(1) See chapter 10.12 and adjust gaps between housing and rotor rollers by using Small
Rolling Tube.
(2) Change “NORMAL” to “SMALL” at [19.ROLLING TUBE TYPE] in Maintenance mode 6
screen (Max blood flow change 500ml/min to 350mI/min)
(3) Set 2 pies of Tube holder (See Chapter 6.2 of Operation Manual) at inlet and outlet of
???? pump unit.
(4) See chapter 10.13.1 and adjust blood pump flow as same method. But adjust 50mL/min
to OFFSET and adjust 250mL/min to GAIN.
Fig. 10.14-1
(7) Under solenoid (5) fits to screw (3) correctly, tighten the 3 set bolts 2 to fix the solenoid to
upper pad of the clamp using spanner.
(8) Push rear side of the clamp by finger to check the adjusted gap.
Adjusting value
Clamp gap 1.3 to 1.5mm ( 1)
(9) After checking correct gap adjustment, tighten the set screw (nut) 3.
(10) Perform the leak test again to check whether the gap is correctly adjusted.
(11) Return the removed cover to the original position.
New dilution ratio = [Theoretical concentration of diluted A concentrate X Current dilution ratio] ÷ [Measured
concentration]
New dilution ratio: dilution ratio after adjustment
1
Input of into “1.VCa W+A RATIO” and “2.VCb W+A RATIO”
AA. AA
Current dilution ratio: dilution ratio before adjustment
1
Indication of in “1.VCa W+A RATIO” and “2.VCb W+A RATIO”
BB.BB
Measured concentration : Concentration measured using meter (mmol/L)
Theoretical concentration of diluted A concentrate A: (mmol/L)
Indicated in “3.THEORETICAL W+A”
(11) After the adjustment, wait until indicated conductivity is stabilized.
(12) Take dialysate specimen again from sampling port to measure its concentration using
concentration meter. Repeat the adjustment until the measured concentration (mmol/L)
becomes equal to theoretical concentration of “3 THEORETICAL W+A”.
(1) Remove right cover from upper part of machine and right cover from DENSO box to exp dip
SW’s placed on main board.
(2) Check Nos. of dip SW’s; SW1 to SW4 from the left in sequence.
(3) By shifting each dip SW to UP, it is turned on and by shifting it to DOWN, it is turned off.
CAUTION
• Usable functions are limited to those operated by SW1 and SW3. DO NOT operate SW2
because it is intended to be used by manufacturer only.
• Keep all dip SW's OFF during any process other than execution of maintenance.
1 Type name
CPU Main board µ PD784031 HN27C4096AG-10 2 Version No.
3 Registered date
2 The last letter of version No. indicates language (E: ENGLISH; S: SPANISH).