Aitecs SP-12S Pro, SEP-12S Plus, SEP-10S Plus User manual

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SP-12S Pro, SEP-12S Plus,
SEP-10S Plus
SYRINGE INFUSION PUMPS
SERVICE MANUAL
BS037016EN-P02
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CONTENTS
2. TECHNICAL DATA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
3. EXTERNAL VIEW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
5. TECHNICAL DESCRIPTION
5.1. PRINCIPLE OF OPERATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
5.2. ELECTRICAL SCHEMATIC DIAGRAM OF THE PUMP . . . . . . . . . . . . . . 9
5.3. ELECTRICAL SCHEMATIC DIAGRAM
OF ELECTRONIC BOARD B7043 . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
6. SETUP MENU . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
7. CHECKING PARAMETERS
7.1. MEANS REQUIRED FOR PARAMETERS CHECKING . . . . . . . . . . . . . 19
7.2. CHECKING INFUSION VOLUME . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
7.3. CHECKING INFUSION RATE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
7.4. CHECKING BOLUS VOLUME . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
7.5. CHECKING OCCLUSION PRESSURE . . . . . . . . . . . . . . . . . . . . . . . . . 21
8. CHECKING ALARM SIGNALS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
10. PUMP REPAIR
10.1. DISASSEMBLING THE PUMP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
10.2. REPLACING INTERNAL BATTERY . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
10.3. REPLACING RUBBER BELLOWS . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
10.4. REPLACING OPTICAL SENSOR TAX1 . . . . . . . . . . . . . . . . . . . . . . . . 33
10.5. REPLACING END SWITCH S1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
10.6. REPLACING PRE-ALARM SWITCH S2 . . . . . . . . . . . . . . . . . . . . . . . . 33
10.7. REPLACING SYRINGE SENSOR S3 . . . . . . . . . . . . . . . . . . . . . . . . . . 34
10.8. REPLACING ELECTRONIC BOARD . . . . . . . . . . . . . . . . . . . . . . . . . . 34
10.9. REPLACING KEYBOARD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
10.10. REPLACING MICROCONTROLLER . . . . . . . . . . . . . . . . . . . . . . . . . 35
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10.11. REPLACING SYRINGE SIZE SENSOR . . . . . . . . . . . . . . . . . . . . . . . 35
10.12. REPLACING BUZZER UNIT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
10.13. REPLACING POWER SUPPLY INLET . . . . . . . . . . . . . . . . . . . . . . . . 36
10.14. REPLACING SUPPLY UNIT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
ANNEX A
ELECTRICAL SCHEMATIC DIAGRAM
OF THE PUMPS SP-12S Pro and SEP-12S Plus . . . . . . . . . . . . . . . . . . . . . . . . . . 40
ANNEX B
ELECTRICAL SCHEMATIC DIAGRAM OF THE PUMP SEP-10S Plus . . . . . . . . . 42
ANNEX C
ANNEX D ELECTRICAL SCHEMATIC DIAGRAM OF ELECTRONIC BOARD B7043 . . . 46
ANNEX E
ASSEMBLY DRAWING OF ELECTRONIC BOARD B7043 . . . . . . . . . . . . . . . . . . 52
ANNEX F
DRAWING OF CABLES FOR MULTIFUNCTIONAL CONNECTOR (MFC) . . . . . . 54
ANNEX G
ANNEX H
PREVENTIVE MAINTENANCE CHECKLIST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
ANNEX I
ANNEX J
ANNEX K
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1. INTRODUCTION
u This SERVICE MANUAL describes how to check,
troubleshoot and repair SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps. The purpose and maintenance of the pumps are described in the appropri­ate OPERATING INSTRUCTIONS.
If when repairing your pump you have encountered prob­lems, which you cannot solve, or the pump parameters are changed after the repair, please, in all these cases contact the manufacturer.
NOTE:
The manufacturer’s authorized personnel may carry out the technical servicing of the pump only!
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2. TECHNICAL DATA
Power supply:
220–230 VAC ±10%, 50/60 Hz, or 115 VAC ±10%, 50/60 Hz, or internal rechargeable battery
Fuses:
T80 mA/L250 V – for 220–230 VAC T160 mA/L250 V – for 115 VAC
Power consumption:
10 VA (max)
Internal battery:
9.6 V 1300 mAh NiMH battery
Cordless work time:
8 h (minimum) at 5 ml/h infusion rate; 2 h (minimum) at 100 ml/h infusion rate.
Battery recharging time: 24 hours. Classification: Class II, CF, splash proof. RS232 (optional) 12 VDC supply connection (optional) Nurse Call connection (optional) Operating temperature range:
+5 to +40 °C.
Storage temperature range:
-20 to +40 °C.
Air pressure:
60 to 106 kPa.
Relative humidity:
90% max., no condensation (operation and storage).
Dimensions:
135 x 305 x 195 mm
Weight:
2.6 kg.
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3. EXTERNAL VIEW
Fig. 1.
Front view of the pump SEP-10S Plus
Front view of the pumps SP-12S Pro, SEP-12S Plus
1 – display 2 – indicators 3 – keypad
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Fig. 2.
Rear view of the pumps SP-12S Pro, SEP-12S Plus and SEP-10S Plus
1 – syringe driver arm 2 – slot for inserting the push-
button of the syringe
plunger 3 – rubber bellows 4 – slot for inserting the finger
grips of the syringe barrel 5 – syringe clamp
6 – handle 7 – cap 8 – mounting pole clamp
9 – fuse holder 10 – mains inlet 11 – MFC* 12 – Audio volume control*
* – optional
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4. KEYBOARD DESCRIPTION
– green indicator, indicating pump connected to the AC line 220–
230V and battery charging.
– green LED is on when pump runs on internal battery; flashing
if LOW BATTERY alarm condition occurs.
– during infusion, three yellow LEDs are sequentially flashing. If
the rightmost LED is on permanently – the infusion is stopped.
– key to switch the pump on/off; keep it pressed for several sec-
onds in order to switch off. – key to start/stop the infusion. – key to move the syringe driver arm rapidly to the left-hand side
during syringe insertion or to initiate the Bolus mode; it is also
intended for air removal from the extension set after syringe in-
sertion. – key to move the syringe driver arm to the right-hand side. – keys to scroll up/down the list of parameters and syringe brands
or answer positively or negatively the dialog questions. – key to select dimensions of parameters when programming (only
in SP-12S Pro and SEP-12S Plus). – key to program (modify) parameters. Pressing it once more re-
stores previous values. – key to confirm the selected parameter.
...
– numerical keys to enter digits of the parameter being pro-
grammed. – key to select additional functions or to review programmed pa-
rameters. – key to cancel the numerical value or the meaning of the param-
eter or silence the alarm signal. It deletes TOTAL INFUSED
and INFUSED DOSE values and clears the numerical value on
display when programming.
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5. TECHNICAL DESCRIPTION
5.1. PRINCIPLE OF OPERATION
u The pump is intended for precise dosing of medicine at the
rate programmed by the operator. The speed of syringe driver arm is set by the microcontroller, which evaluates the syringe volume and features of the syringe model. The microcontroller controls the step motor, which transfers movement to the syringe driver arm via the helical gear. The microcontroller monitors also voltage of the internal battery, mains voltage, occlusion pressure, Bolus volume and rate. Data on pump status and programming data are outputted to the alphanumeric 2x16 symbol display. Op­eration of the microcontroller is monitored by the special circuit (watch-dog), which unconditionally switches off the motor in case of failure of the microcontroller. In case of mains voltage failure, the pump automatically continues its operation being powered from the internal rechargeable battery and warns the operator on this by means of audible and visual signals.
5.2. ELECTRICAL SCHEMATIC DIAGRAM OF THE PUMP
5.2.1. Principle of operation
u The electrical schematic diagram of the pumps are pre-
sented in theAnnex A, B. The interconnection diagram of the pump is presented in Annex C. Diagrams of the pump are composed of the following main parts:
w power supply; w keyboard; w drive; w syringe size sensor; w electronic board B7043.
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5.2.2. Power supply
u 220-230 VAC (or 115 VAC) voltages via the mains filter
MF1 and fuse F1 is fed to the primary winding of the step-down transformer TR1. Voltage from the secondary winding of the transformer TR1 reduced to 10-11 VAC is rectified by the diode bridge D1 and capacitor C1 (11­13,5 VDC) and via the fuse F1(A2) is fed to the remain­ing part of the circuit. The resistor R1 sets the charging current for the rechargeable batteries GB1, GB2 which shall be in range of (70-130) mA. When the pump is powered from the internal battery, power supply current goes via the diode D2. The fuse F2(A2) protects batteries by limiting charging and load currents. There is fed a sig­nal to the electronic board B7043 via the diode D3 and the resistor R2 informing the pump is powered from the external mains of 50/60 Hz, 220-230 VAC (or 115 VAC). The electronic board B7043 controls the buzzer Z1.
5.2.3. Keyboard
u The keyboard is composed of 21 keys (SEP-10S Plus
20 keys) in form of a matrix having 7 inputs and 3 out­puts. Electronic board B7043 performs scanning of the keyboard and reading of information from it. The key ON/OFF controls the circuit of electronic power supply switch located on the electronic board B7043.
5.2.4. Drive
u The stepper motor SM1 rotates the lead screw with a nut
on it converting rotating movement of the motor to lin­ear movement of the tube. The tube supported by four guiding bearings is connected to the syringe driver arm. Marginal positions of the tube with syringe driver arm are limited by: w limit switch S1 at the right extreme position which is actuated by the end of the tube;
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w rotational optical sensor TAX1 at the left extreme po­sition when the tube covers the raster of rotating cou­pling of the optical sensor TAX1. In case of occlusion when pressure in the syringe in­creases to the prohibited level, it stops movement of the syringe driver arm and at the same rotation of the step­per motor SM1. Rotation of the stepper motor is controlled by the optical sensor TAX1 which reads a signal, reflected from the raster of rotational coupling. This signal is fed to the micro­controller U18 located on the electronic board B7043, and this signal switches on the emergency signal. There is some delay between beginning of occlusion on one hand and stepper motor SM1 stopping and emergency signal actua­tion on the other hand depending on infusion rate, length, thickness and elasticity of extension tube.
u The pre-alarm switch S2 is activated when the distance
between syringe finger flange and syringe thumb rest is equal to 45 mm. When this distance is equal to 27 mm, the end switch S1 is activated, which in this case acts as the second pre-alarm switch. When the pre-alarm switch has been activated, the pump calculates distance to the end of appropriate syringe. Based on this there are calcu­lated and activated the following warning messages:
Xmin. PREALARM!Xmin. PREALARM!
Xmin. PREALARM!
Xmin. PREALARM!Xmin. PREALARM!
where X ≤ 5 min., and
SYRINGE EMPTY!SYRINGE EMPTY!
SYRINGE EMPTY!
SYRINGE EMPTY!SYRINGE EMPTY!
u In case of occlusion the stepper motor SM1 executes
some number of steps back depending on syringe type. This reduced pressure in the syringe and extension tube and at the same time reduces unwanted Bolus volume injected to the patient when the cause of occlusion is re­moved.
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5.2.5. Syringe size sensor
u Syringe size sensor is implemented as a sliding poten-
tiometer R1. Depending on syringe diameter, potentio­meter slider position is changed and its output voltage at the same time, which is linearly proportional to the out­put resistance of the potentiometer R1. This output volt­age is fed to the electronic board B7043.
5.3. ELECTRICAL SCHEMATIC DIAGRAM OF ELECTRONIC BOARD B7043
u The electrical schematic diagram of electronic board
B7043 is shown in the annex C. It is composed of the following main parts:
w microcontroller circuit; w display circuit; w „watch-dog” circuit; w stabilized power supply; w electronic power-supply switch circuit; w syringe size sensor signal processing circuit; w DAC; w pulse current stabilizers; w switches.
5.3.1. Microcontroller circuit
u There is used the T89C51RD2 microcontroller U18 having
internal RAM of 256 bytes for data, internal flash memory of 64 kB and external EEPROM of 32 kB for software and external time keeper SRAM U14 with clock for log. The quartz resonator Q2 of 12,288 MHz sets clock fre­quency for microcontroller. The microcontroller U18 se­lects addresses of the SRAM U14 (lower addresses from port P0 via register U13, higher addresses from port P2 directly). The microcontroller U18 via port P0 and regis­ter U11 generates instructions for step motor control,
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writes information to display MD1, writes and reads in­formation to/from SRAM U14, controls the buzzer, LEDs D26, D27, D28 „RUN”. Also via port P0 and register U13, it scans the keyboard. Information from the key­board is read via register U12 to port P0.
u The microcontroller U8 AT89C2051 receives informa-
tion from the microcontroller U18 T89C51RD2 to its inputs P3.0 and P3.2 on step motor rotation direction, period between steps and power. The restart signal for the microcontroller U8 (pin 1) is generated by means of ele­ments C46 and R51 in time of power switching on. When master „watch-dog” circuit is activated, a high-level signal is applied to the restart input of the micro­controller U8 interrupting its operation.
5.3.2. Display circuit
u Information to display MD1 (addresses and data) is writ-
ten from the port P0 of microcontroller U18. The resis­tors R88—R91 sets current via transistor T15 and at that same time current for backlighting LED of display MD1. This current shall be equal to 70 ± 10 mA when backli­ghting is switched on and 10 ± 5 mA when backlighting is switched off. The backlighting current is controlled by the signal from microcontroller U18 via register U10. Re­sistor R93 defines brightness of the display MD1.
5.3.3. “Watch-dog” circuit
u The special „Watch-dog” circuit monitors operation of
the microcontroller U18. In case of disturbances in microcontroller U18 operation, this circuit prevents func­tioning of the pump, stops the motor and activates audi­ble alarm. The basis of master „Watch-dog” circuit is monostable multivibrator U5A, U5B and the trigger U3A. They compose the frequency discriminator with pass-band of 500 Hz to 2 kHz.
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u The slave watch-dog circuit is composed of elements
U17A, D25, C61, C74. When for some reason the pulses cease to arrive to capacitor C61, 0.5 sec later a low-level signal is generated at the output 6 of the Schmitt trigger U17A initiating actuation of the master watch-dog circuit.
5.3.4. Stabilized power supply
u There are used two stabilized +5VDC voltages Vcc1 and
Vcc2. The voltage Vcc1 is supplied to the microcontroller U18, „Watch-dog” circuit and electronic power supply switch. When powering of the pump is switched off by means of the key ON/OFF, voltage Vcc1 goes down to 2V (voltage Vcc2 becomes equal to 0V). The IC U1 is the voltage stabilizer. The transistor T1 is a current amplifier and the transistor T2 is a power supply switch. Adjustable resistor R13 sets threshold for emergency sig­nal actuation on discharge of batteries GB1, GB2 (volt­age on pin 7 of the IC U1 shall go down from +5V to 0V when battery voltage drops to 9.2V).
u DC/DC converter U2 generates necessary negative volt-
age of —(4,7÷5,0)V at its output (pin 5).
5.3.5. Electronic power-supply switch
u When the pump is switched on by pressing the key
ON/OFF, there is set at the same time inhibition to switch it off, i.e. the low-level signal is applied to pin 13 of the trigger U3B. This inhibition may be removed either by the microcontroller U18 having received an ap­propriate request or by the „watch-dog” activated. The microcontroller U18 via the input T0 receives informa­tion on depressed key ON/OFF. Then when the key ON/OFF is kept depressed for 3 sec the microcontroller U18 switches off the pump by applying high-level pulse to the pin 10 of the trigger U3B.
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Electronic power-supply switch output signals control the power supply stabilizer and switch the microcontroller U18 to mode of low power consumption or to normal mode. These signals via capacitor C67 generate start (re­set) pulse for microcontroller U18.
5.3.6. Syringe size sensor signal processing circuit
u The voltage taken from the potentiometer for syringe di-
ameter and proportional to the syringe diameter is fed to ADC U7. Information on syringe diameter in digital form from U7 is transferred via the serial port to the in­put P1.0 of the microcontroller U18.
5.3.7. DAC (digital to analog converter)
u The DAC is composed of resistor network, amplifier U6A
and inverter U6B. Depending on the code at the port P1 of the microcontroller U8, voltage at the output 7 of the operational amplifier U6A is changing in the range 0 to -
0.4V. The inverter is based on the operational amplifier U6B and converts this voltage to positive one. The volt­age from the output 1 of U4B is fed to two (separate for each phase of the motor) sample-and-hold units for analogous signal, implemented on elements T6, C55 and T7, C57 accordingly. There are generated two independ­ent voltages on capacitors C11, C12 being proportional to currents flowing through motor phases.
5.3.8. Pulse current stabilizers
u The pulse current stabilizer for the 1st phase is composed
of elements U15A, T5, R56, D18, D19, L4, R61, R60, and that for the 2nd phase - of elements U15B, T4, R57, D15, D20, L5, R67, R69. Further is described operation of the pulse current stabilizer for the 1st phase only. The voltage from the capacitor C55 is fed to the inverting input 2 of
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the comparator U15A. The non-inverting input of the comparator receives the signal equal to voltage drop across the resistors R61, R60 and proportional to current flow­ing through them. When this voltage is lower than that on the capacitor C55, then transistor T5 becomes open. Then the power source VCC-NS is connected to the inductor L4 and the current through it starts to increase. When volt­age drop across resistors R61, R60 exceeds voltage from the capacitor C55, the transistor T5 becomes closed and cur­rent through the reactor L4 starts to decrease. The new cy­cle is started, and its frequency depends on inductance of the reactor L4, phase current value and comparator hyster­esis.
5.3.9. Switches
u Currents for both phases flow to the common conductors
of motor phase coils via accumulating reactors L4 and L5. Direction of motor rotation is defined by appropriate or­der of current switching in both phase coils. This switch­ing is implemented by current switches T8, T9 and T10, T13 for the 1st and the 2nd phases accordingly.
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6. SETUP MENU
u In order to access optional functions or certain param-
eters, keep the START/STOP key in pressed position and switch the pump on by pressing the ON/OFF key. When short beep is heard, release the START/STOP key, enter appropriate code with the numerical keys and confirm it by pressing the ENTER key. The total list of optional functions/parameters and their access codes are presented in the Table 1:
Table 1
CODE NAME DESCRIPTION NOTE
100 Pump modes 137 Syringe list 147 Drug list 157 DEFAULT GRUG SET restoring default
237 Functions Configurable
257 DEFAULT restoring default
PARAMETERS SET (manufacturer’s) parameters
337 LANGUAGE SET:
ENGLISH and other installation of dialog language
537 SYRINGE SIZE to calibrate syringe sensor for calibration needs spacers:
CALIBRATION B8640027, B8640027-01,
547 OCCLUSION calibration of occlusion level
CALIBRATION
637 DATE, TIME setting of date and time
(manufacturer’s) jist of drug
functions/parameters
B8640027-02, B8640027-03,
u List of optional functions may be reviewed using the
scroll keys. If displayed name is marked with the asterisk, it means that function is active. To activate an inactive function press the ENTER key, and the asterisk will ap­pear in front of the item name. To deactivate a function, press the C key. The asterisk shall disappear.
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u To change flow rate upper limit select appropriate item, press the
PROG key, enter the new value using the numeric keys and confirm it by pressing the ENTER key.
u To enter a new drug name open the drug list and select the drug name
to be replaced by the new one. Press the PROG key, and enter the new drug name using keys in accordance with the table below (e.g. to en­ter letter Z press the 9 key four times):
Key 1 2 3 4 5 6 7 8 9 0 . YES NO, C Cha-
1 A,B, D,E, G,H, J, K, M, N, P,Q, T, U, W, X, %, 0, . Space Backspace
rac­ter
C,2 F, 3 I, 4 L, 5 O, 6 R, S, 7 V, 8 Y, Z, 9 /, -
Confirm the new drug name by pressing the ENTER key.
NOTES:
1. Entered character can be reset by means of the C or NO keys.
2. Old drug name can be restored by means of the PROG key until new name is confirmed.
u To exit setup menu press the START/STOP key. u To change date and time settings enter new values when appropriate
demand is displayed and press the ENTER key to confirm them and exit setup menu.
ATTENTION !
It is recommended to minimize number of parameters, types of syringes, drug names and other functions leaving only that necessary for work. It will help to avoid errors in parameters programming and thereby decrease patient’s risk.
u If the high occlusion level value after actions specified in section 7.5 are
performed is beyond specified limits, occlusion level shall be calibrated. For this sake factual value of high occlusion level pressure obtained dur­ing testing is entered into pump. Typical value for CORRECT END is 60 kPa.
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7. CHECKING PARAMETERS
7.1. MEANS REQUIRED FOR PARAMETERS CHECKING
u Prepare the following means:
w 50 ml BD Plastipak syringe, w standard 90 cm long extension tube, w stop-watch, w glass test-tube with graduation (one point equal
to 0.1 ml), 60 ml or more volume,
w pressure gauge with graduation up to 160 kPa,
(accuracy 2.5%).
NOTE:
Programming infusion parameters, filling the sy­ringe and extension tube with drug solution, insert­ing the syringe into the pump and starting infusion are described in the OPERATING INSTRUC­TIONS of the pump.
7.2. CHECKING INFUSION VOLUME
u Take the 50 ml BD Plastipak syringe with extension tube
connected to it and fill it with distilled water up to the point of 55 ml. Insert the syringe into the pump and con­firm the 50 ml BD Plastipak syringe. Program the following infusion parameters:
w infusion rate — 100 ml/h, w volume limit — 50 ml, w occlusion pressure level — HIGH.
Expel the air from the extension tube. Insert the free end of the extension tube into the graduated test-tube and start the infusion. When the infusion is finished, the measured volume in the test-tube shall differ from the programmed volume not more than by ± 1 ml (± 2%).
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7.3. CHECKING INFUSION RATE
u Take the 50 ml BD Plastipak syringe with extension tube
connected to it and fill it with distilled water up to the point of 55 ml. Insert the syringe into the pump and con­firm the 50 ml BD Plastipak syringe. Program the following infusion parameters:
w infusion time — 12 min, w volume limit — 10 ml, w occlusion pressure level — HIGH.
Expel the air from the extension tube. Insert the free end of the extension tube into the graduated test-tube and start the infusion. Measure infusion time by the stop­watch and record the volume in the test-tube at the end of infusion. Calculate the infusion rate. It shall be 50 ml/h ± 1 ml/h (± 2%).
7.4. CHECKING BOLUS VOLUME
u Take the 50 ml BD Plastipak syringe with an extension
tube connected to it and fill it with distilled water up to the point 50 ml. Insert the syringe into the pump and confirm the 50 ml BD Plastipak syringe. Program the following infusion parameters:
w infusion rate — 50 ml/h, w volume limit — 50 ml, w bolus rate — 100 ml/h, w bolus dose — 20 ml, w occlusion pressure level — HIGH.
Expel the air from the extension tube. Insert the free end of the extension tube into the graduated test-tube and start the infusion. Record the volume delivered into the test-tube and starts the Bolus mode. Record the volume in the test-tube at the end of the Bolus cycle. The difference of these two volumes shall be 20 ml ± 0.4 ml (± 2%).
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7.5. CHECKING OCCLUSION PRESSURE
u Take the 50 ml BD Plastipak syringe with an extension
tube connected to it and fill it with distilled water up to the point of 30 ml. Insert the syringe into the pump and confirm the 50 ml BD Plastipak syringe. Program the following infusion parameters:
w infusion rate — 50 ml/h, w volume limit — 30 ml, w occlusion pressure level — LOW.
Connect the pressure gauge to the free end of the exten­sion tube. Start the infusion. As soon as the audible alarm is activated and there is displayed the message
OCCLUSION!!!OCCLUSION!!!
OCCLUSION!!!
OCCLUSION!!!OCCLUSION!!!
the pressure gauge shall read the pressure of (30 or 40)* kPa ± 15 kPa.
Press the key C. Reprogram the occlusion pressure to MEDIUM. Start again the infusion. As soon as the audi­ble alarm is activated and there is displayed the message
OCCLUSION!!!OCCLUSION!!!
OCCLUSION!!!
OCCLUSION!!!OCCLUSION!!!
the pressure gauge shall read the pressure of 60 kPa* ±15 kPa or 80 kPa* ± 20 kPa.
Press the key C. Reprogram the occlusion pressure to HIGH. Start again the infusion. As soon as the audible alarm is activated and there is displayed the message
OCCLUSION!!!OCCLUSION!!!
OCCLUSION!!!
OCCLUSION!!!OCCLUSION!!!
the pressure gauge shall read the pressure of 90 kPa* ± 20 kPa or 120 kPa* ± 25 kPa.
NOTE:
If measured values of pump parameters are out of ranges permitted, contact the Manufacturer.
* depends on the installed occlusion presure set (for SP-12S Pro only).
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8. CHECKING ALARM SIGNALS
u Alarm signals and their causes are listed in the Table.
No. Message in display Cause
OCCLUSION!!!OCCLUSION!!!
1.
OCCLUSION!!! The movement of the syringe driver arm is
OCCLUSION!!!OCCLUSION!!!
OCCLUSION or ENDOCCLUSION or END
2.
OCCLUSION or END The syringe driver arm stopped because the
OCCLUSION or ENDOCCLUSION or END
NO MAINS!!!NO MAINS!!!
3.
NO MAINS!!! No mains voltage. The pump is powered
NO MAINS!!!NO MAINS!!! Check power cordCheck power cord
Check power cord from the internal battery.
Check power cordCheck power cord
LOW BATTERYLOW BATTERY
4.
LOW BATTERY Low voltage of internal battery. There are left
LOW BATTERYLOW BATTERY
VERY LOW BATTERYVERY LOW BATTERY
5.
VERY LOW BATTERY Internal battery is fully discharged.
VERY LOW BATTERYVERY LOW BATTERY
X min. PREALARM!X min. PREALARM!
6.
X min. PREALARM! Not more than 5 min. left to the end of infusion.
X min. PREALARM!X min. PREALARM!
END of INFUSION!END of INFUSION!
7.
END of INFUSION! Infusion of a programmed volume is completed
END of INFUSION!END of INFUSION!
KOR X.X ml/hKOR X.X ml/h
8.
KOR X.X ml/h 1. Infusion was stopped and not resumed in
KOR X.X ml/hKOR X.X ml/h
stopped by increased pressure in the syringe.
syringe plunger reached the end of the syringe barrel or an occlusion happened.
from several minutes (at high infusion rates) to several tens of minutes (at low infusion rates) to the full discharge.
2 minutes.
2. Infusion is finished, but new infusion isn’t programmed or a syringe isn’t changed or the pump isn’t switched off.
3. Syringe is empty and not replaced.
SYRINGE EMPTY!SYRINGE EMPTY!
9.
SYRINGE EMPTY! Syringe is empty.
SYRINGE EMPTY!SYRINGE EMPTY!
CLAMP OPENED!CLAMP OPENED!
10.
CLAMP OPENED! Clamp is lifted during infusion
CLAMP OPENED!CLAMP OPENED!
ILLEGAL SYRINGE!ILLEGAL SYRINGE!
11.
ILLEGAL SYRINGE! Syringe diameter does not comply
ILLEGAL SYRINGE!ILLEGAL SYRINGE! Change SYRINGEChange SYRINGE
Change SYRINGE with any syringe installed.
Change SYRINGEChange SYRINGE
ERROR XXX!ERROR XXX!
12.
ERROR XXX! Pump failure (seeANNEX G)
ERROR XXX!ERROR XXX!
ATTENTION!ATTENTION!
13.
ATTENTION! The pump was left for 2 min with no action.
ATTENTION!ATTENTION! 2 min INACTIVE2 min INACTIVE
2 min INACTIVE
2 min INACTIVE2 min INACTIVE
STANDBY TIMESTANDBY TIME
14.
STANDBY TIME Preset standby time elapsed
STANDBY TIMESTANDBY TIME ELAPSEDELAPSED
ELAPSED
ELAPSEDELAPSED
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SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
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All alarm signals are accompanied by the audible alarm. Alarm signals listed in the Table are checked in the fol­lowing ways:
u 1. Take a 50 ml BD Plastipak syringe with extension tube
and fill it with distilled water up to point of 30 ml. In­sert the syringe into the pump and confirm the 50 ml BD Plastipak syringe. Program the following infusion parameters:
w infusion rate — 100 ml/h, w volume limit — 30 ml, w occlusion pressure level — HIGH.
Connect the pressure gauge to the free end of the exten­sion tube. Start the infusion. When the pressure gauge shows the pressure 90 kPa* ± 20 kPa or 120 kPa* ± 25 kPa, there shall be displayed the message
OCCLUSION!!!OCCLUSION!!!
OCCLUSION!!!
OCCLUSION!!!OCCLUSION!!!
accompanied by the audible alarm.
u 2. Take a 50 ml BD Plastipak syringe and pull its plunger
out to point of 5 ml (may be without water). Insert the syringe into the pump and confirm the 50 ml BD Plastipak syringe. Program that same infusion parameters as in clause 1. Start the infusion. When the syringe plunger reaches the end of the syringe, there shall be dis­played the message
OCCLUSION or ENDOCCLUSION or END
OCCLUSION or END
OCCLUSION or ENDOCCLUSION or END
accompanied by the audible alarm.
u 3. Insert a 50 ml BD Plastipak syringe into the pump and
confirm it. Program the same infusion parameters as in clause 1.
* depends on the installed occlusion presure set (for SP-12S Pro only).
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Start the infusion. Disconnect the mains cord. There shall be heard the audible alarm and there shall be displayed the message
NO MAINS!!!NO MAINS!!!
NO MAINS!!!
NO MAINS!!!NO MAINS!!!
check power cord!check power cord!
check power cord!
check power cord!check power cord!
In spite of this, the pump shall continue to work.
u 4. Take a 50 ml BD Plastipak syringe and pull its plunger
out to point of 60 ml (may be without water). Insert a 50ml BD Plastipak syringe into the pump and confirm it. Program the following infusion parameters:
w infusion rate — 100 ml/h, w volume limit — 0 (no limit), w occlusion pressure level — HIGH.
Disconnect the mains cord. Start the infusion and record the time. Each time the syringe is empty, replace it (pull its plunger to point of 60 ml) as described in the OPERATING INSTRUCTIONS of the pump and re­start the infusion. Not earlier than 1 hour later* (in case the internal bat­tery of the pump was charged for 24 hours or more and there isn’t defined any other time value in the OPERAT­ING INSTRUCTIONS) there shall be heard the audible alarm and there shall be displayed the message
LOW BATTERY!LOW BATTERY!
LOW BATTERY!
LOW BATTERY!LOW BATTERY!
u 5. Checking of this alarm signal shall be carried out im-
mediately after the „Low Battery” checks. Continue the procedure described in step 4 and measure the time in­terval between the displayed messages
LOW BATTERY!LOW BATTERY!
LOW BATTERY!
LOW BATTERY!LOW BATTERY!
* In case the pump was in use for more than 2 years, this time may be shorter.
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SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
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and
VERY LOW BATTERYVERY LOW BATTERY
VERY LOW BATTERY
VERY LOW BATTERYVERY LOW BATTERY
The latter one accompanied by the audible alarm shall appear approximately in 10 minutes. Reconnect the pump to the mains. The green indicator shall glow.
u 6. Take a 50 ml BD Plastipak syringe and pull its plunger
out to point of 50 ml (may be without water). Insert a 50ml BD Plastipak syringe into the pump and confirm it. Program the following infusion parameters:
w infusion time — 6 min., w volume limit — 10 ml, w occlusion pressure level — HIGH.
Start the infusion. Soon the audible alarm shall be heard and there shall be displayed the message
5 min. PREALARM!5 min. PREALARM!
5 min. PREALARM!
5 min. PREALARM!5 min. PREALARM!
u 7. Checking of this alarm signal shall be carried out im-
mediately after the „5min. PREALARM” checks. Con­tinue the procedure described in step 6. 5 min later there shall be displayed the message
END of INFUSION!END of INFUSION!
END of INFUSION!
END of INFUSION!END of INFUSION!
KOR X.X ml/hKOR X.X ml/h
KOR X.X ml/h
KOR X.X ml/hKOR X.X ml/h
u 8. Don’t switch off the pump after the check of step 7.
Press the C key. There shall be displayed the message
END of INFUSION!END of INFUSION!
END of INFUSION!
END of INFUSION!END of INFUSION!
KOR X.X ml/hKOR X.X ml/h
KOR X.X ml/h
KOR X.X ml/hKOR X.X ml/h
Press the PROG key and restart the infusion with the pa­rameters set in step 6. Press the START/STOP key. 2 minutes later there shall be heard the audible alarm and there shall be displayed the message
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STOP X.X mlSTOP X.X ml
STOP X.X ml
STOP X.X mlSTOP X.X ml
KOR X.X ml/hKOR X.X ml/h
KOR X.X ml/h
KOR X.X ml/hKOR X.X ml/h
u 9. Take a 50 ml BD Plastipak syringe and pull its plunger
out to point of 20 ml (may be without water). Insert a 50ml BD Plastipak syringe into the pump and confirm it. Program that same infusion parameters as in clause 1. Start the infusion. When there is left about 2 mm to the end of the syringe, there shall be displayed the mes­sage
SYRINGE EMPTY!SYRINGE EMPTY!
SYRINGE EMPTY!
SYRINGE EMPTY!SYRINGE EMPTY!
KOR X.X ml/hKOR X.X ml/h
KOR X.X ml/h
KOR X.X ml/hKOR X.X ml/h
u 10. Take a 50 ml BD Plastipak syringe and pull its plunger
out to point of 20 ml (may be without water). Insert a 50ml BD Plastipak syringe into the pump and confirm it. Program that same infusion parameters as in clause 1. Start the infusion. Lift the syringe clamp. Infusion stops, the audible alarm shall be heard and there shall be dis­played the message
CLAMP OPENED!CLAMP OPENED!
CLAMP OPENED!
CLAMP OPENED!CLAMP OPENED!
u 11. Insert 50 ml BD Plastipak syringe into the pump.
Lift slowly the syringe clamp until the following message is displayed
ILLEGAL SYRINGE!ILLEGAL SYRINGE!
ILLEGAL SYRINGE!
ILLEGAL SYRINGE!ILLEGAL SYRINGE!
Change SYRINGEChange SYRINGE
Change SYRINGE
Change SYRINGEChange SYRINGE
u 12 alarm signal shall be left not checked because it is dif-
ficult to simulate such a situation without damaging the pump.
u 13. Insert a 50 ml BD Plastipak syringe into the pump
and confirm it. Leave the pump for 2 min with no action
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SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
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(no pressing of any key), the audible signal is activated and the following message is displayed:
ATTENTION!ATTENTION!
ATTENTION!
ATTENTION!ATTENTION!
2 min 2 min
2 min
2 min 2 min
INACTIVEINACTIVE
INACTIVE
INACTIVEINACTIVE
u 14. In the STOP mode press the ENTER key. Set
STANDBY time value of 1 min and wait. After 1 min delay an audible alarm shall be initiated together with the message
STANDBY TIMESTANDBY TIME
STANDBY TIME
STANDBY TIMESTANDBY TIME
ELAPSED!ELAPSED!
ELAPSED!
ELAPSED!ELAPSED!
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9. TROUBLESHOOTING
All failures are listed in the Table:
No SYMPTOM CAUSE CORRECTIVE ACTIONS
1 Message in the display
"NO MAINS!!! Check power cord" although the pump is connected to the mains (the green indicator glowing).
isn’t
1. External fuses are blown.
2. Faulty mains cord.
3. Faulty supply unit.
1. Check the external fuse and replace with identical one, if required. In case it blown again, consult the Manufacturer.
2. Check the mains cord and replace it, if necessary.
3. Check and replace if necessary the supply unit as described in section 10.14.
2 Short cordless work
time or no cordless work at all.
3 Rubber bellows
cracked.
4 Without syringe, the
syringe driver arm doesn’t move when pressing the <, >keys.
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SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
1. Fuse F2 is blown in the supply unit.
2. Decreased capacity of the battery.
Rubber ageing. Impermis­sible chemical substances were used for disinfecting and cleaning.
1. Faulty optical sensor ( Fig. 4 pos. 6) or dirty raster in the coupling (Fig. 4 pos. 4).
1. Open the pump as described in section 10.1. Check and replace the fuse with identical one. In case it is blown again, consult the Manufacturer.
2. Connect the pump to the mains for 24 hours in order to charge the internal battery. Disassemble the pump as pointed out in section 10.1. connect the
resistor of 20 Ω/10 W to the
battery and measure discharge time to the moment the battery voltage drops to 8V. In case this time is shorter than 2 hours (for 1300 mAh capacity battery), replace the battery as pointed out in section
10.2.
Replace the rubber bellows as described in sections 10.1 and 10.3.
1. Disassemble the pump as described in section 10.1 leaving the power connector P1 connected. Clean the
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No SYMPTOM CAUSE CORRECTIVE ACTIONS
coupling raster with a piece of soft cloth. Switch on the pump pressing the ON/OFF key. By means of an oscilloscope observe the signal at TP17 in the electronic board B7043 (rotate the coupling slowly by hand). The low level of the signal shall be not more than 1 V and the high level — not less than 3V during the full revolu­tion of the motor. Otherwise adjust R83 potentiometer or replace the optical sensor (section 10.4).
5 In the syringe insertion
mode, the syringe driver arm stops with noise when it reaches its right hand side position.
6 The pump doesn’t
display the messages "X min. PREALARM!" and "SYRINGE EMPTY!" although the syringe is filled with more than 50% of its nominal volume.
2. Broken connecting wires to the stepper motor.
Faulty end switch S1 (Fig. 4 pos. 11).
Faulty pre-alarm switch S2 (Fig. 4 pos. 8).
2. Disconnect the connector P1 of the step motor from the elec­tronic board B7043 and check the wires to the step motor for continuity according to the electrical schematic diagram by means of an ohmmeter. If the wires are broken, re­solder them. Re-connect the motor connector to the electronic board B7043.
Check the end switch and replace, if required, as described in the sections
10.1 and 10.5.
Check the pre-alarm switch and replace, if required, as described in the sections
10.1 and 10.6.
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No SYMPTOM CAUSE CORRECTIVE ACTIONS
7 Although the syringe is
inserted, there is displayed the message INCORRECT
Syringe sensor S3 is faulty
Disassemble the pump as described in the section 10.1. Replace the syringe sensor as described in the section 10.7.
INSERTION!
8 When a syringe is in-
serted, a wrong syringe size is displayed, or there is a message ILLEGAL SYRINGE! CHANGE SYRINGE
9 One or several keys
failto operate.
10 Audible alarm of the
pump fails to operate.
11 The keyboard
scratched, discolored or detached.
12 The pump fails to ope-
rate when switched on with ON/OFF key. No message or the message "ERROR XXX" is dis­played. Audible alarm is activated.
13 Indicator
glows, but the pump fails to operate.
Faulty syringe size sensor (Fig. 4 pos. 3).
Faulty keys.
Faulty buzzer Z1 in the power supply.
Impermissible chemical substances were used for disinfecting and cleaning.
Faulty electronic board B7043.
Fuse F1 blown in the supply unit (Fig.2. pos.8).
Calibrate syringe sensor (see section 6) or replace it (if calibration was not success­ful) as described in the sections 10.1 and 10.11.
Check and replace the keyboard, if required, as described in sections 10.1 and 10.9.
Check the buzzer and replace, if required, as described in the sections 10.1 and 10.12.
Replace the keyboard as described in the sections
10.1 and 10.9.
Replace the electronic board B7043 as described in the sections 10.1 and 10.8 (see also Annex F).
Open the pump as described in section 10.1. Check the fuse and replace it with identical one, if required. In case it is blown again, consult the Manufacturer.
14 When fixing the pump
to a stand, the stand surface is damaged
30
SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
The plastic cap (Fig. 2 pos. 4) of the cross knob is cracked.
Remove the cross knob of the mounting clamp rotating it counterclockwise until the cap falls down. Rotate the cross knob clockwise with the cylinder of 20mm x 20mm inserted and pressing the new cap between the cross knob
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No SYMPTOM CAUSE CORRECTIVE ACTIONS
screw and the cylinder until the cap seats on the screw.
Disassemble the pump as
15 Burned and cracked
power supply inlet
The power supply inlet was flushed with liquid and after connection to the mains 220-230 VAC
described in the section 10.1. Replace the power supply inlet as described in the
section 10.13. there has occurred short connection.
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31
Page 32
10. PUMP REPAIR
10.1. DISASSEMBLING THE PUMP (FIG. 1, ANNEX B)
u The syringe driver arm shall be moved to its end right
hand side extreme position. Remove six screws (6) located of the pump base. Carefully lift the pump housing and disconnect the supply unit connector P4 (Fig. 2 pos. 9), buzzer connector P5 (Fig. 2 pos. 16) from the electronic board B7043.
10.2. REPLACING INTERNAL BATTERY (FIG. 2, ANNEX B)
u Disassemble the pump according to section 10.1. Remove
screws (13) fastening the battery cover (14). Disconnect connectors P13, P14 (11) from the supply unit. Install new battery and reconnect connectors P13, P14 (11). Fix the battery cover with screws (13) and reassemble the pump in the reverse order to section 10.1.
10.3. REPLACING RUBBER BELLOWS (FIG. 3)
u Remove screw (4) and cover (1). Remove three screws (2)
fastening the plate (3) to the tube (10) and remove the plate. Remove screws (11). Remove the rubber bellows (6) and the support (5) from the tube (10). The new bellows (6) is inserted with its narrower end to­wards the notch on the tube (10). Spread the silicon sealer on the housing-side of the support (5) and install the support in such a way as to clamp the end of the rub­ber bellows (6) between the support and the housing (7). Replace the screws (11). Replace and fasten the plate (3) to the end of the tube (10) with screws (2) clamping the end of the rubber bel­lows (6). Fasten the cover (1) with the screw (4).
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SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
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10.4. REPLACING OPTICAL SENSOR TAX1 (FIG. 4)
u Disassemble the pump according to the section 10.1. Re-
move the screw (5) and then remove the optical sensor (6). Note the order of conductor connection and unsolder them. Re-solder the conductors to the new optical sensor (6) in the same order. Pull insulation tubes onto the sol­dering places. Spread an universal glue onto the optical sensor (6). Fasten the optical sensor (6) by means of the screw (5) so as to maintain the distance between the op-
tical sensor (6) and the coupling (4) equal to 4 ± 0.1 mm.
Reassemble the pump in reverse order to the section 10.1.
10.5. REPLACING END SWITCH S1 (FIG. 4)
u Disassemble the pump according to the section 10.1.
Unsolder two conductors from the end switch (11). Re­place the end switch (11) and re-solder the conductors to the same terminals. Pull insulation tubes onto the solder­ing places. Reassemble the pump in reverse order to the section 10.1.
10.6. REPLACING PRE-ALARM SWITCH S2 (FIG. 4)
u Disassemble the pump according to the section 10.1.
Unsolder two conductors from the pre-alarm switch (8). Replace the pre-alarm switch (8) and re-solder the con­ductors to the same terminals. Pull insulation tubes onto the soldering places. Fasten the pre-alarm switch (8) in such a position as to be activated when the distance be­tween the housing surface supporting finger flanges of the syringe and the syringe driver arm surface supporting thumb rest of the syringe is equal to 45 mm. Reassemble the pump in reverse order to the section 10.1.
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10.7. REPLACING SYRINGE SENSOR S3 (FIG. 1)
u Remove the screw (4) and the cover (1) (see Fig. 3). Dis-
connect the flexible cable (5) from the connector (4). Remove the syringe sensor (3) with its connector (4). Glue the new syringe sensor (3) with its connector (4) on the same place at the same depth. Connect the flexible cable (5) to the connector (4). Fasten the cover (1) with the screw (4) (see Fig.3).
10.8. REPLACING ELECTRONIC BOARD B7043 (FIG. 4, ANNEX C, E)
u Disassemble the pump according to the section 10.1. Re-
move four screws (10). Disconnect step motor connector P1 from electronic board B7043. Disconnect syringe sen­sor connector P2, sensors connector P3, MFC (multi­functional connector) connector P6, syringe size sensor connector P8 and keyboard connector J1 from the elec­tronic board B7043 and carefully take out the electronic board B7043. Install the new electronic board B7043, re­connect all connectors in reverse order. Reinstall four screws (10). Reassemble the pump in reverse order to the section 10.1.
10.9. REPLACING KEYBOARD (FIG. 1)
u Disassemble the pump according to the section 10.1. De-
tach the old keyboard (1). Disconnect keyboard (1) con­nector from the electronic board B7043 (2). Glue the new keyboard (1) taking openings for the dis­play and for LEDs as a reference. Glue from the left to the right pressing the keyboard (1) with a piece of soft clothes. Reconnect keyboard (1) connector to the elec­tronic board B7043 (2). Reassemble the pump in reverse order to the section 10.1.
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SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
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10.10. REPLACING MICROCONTROLLER (ANNEX D)
u Disassemble the pump according to the section 10.1.
Note the orientation of the key on the body of micro­controller U18 on the electronic board B7043. By means of the special tool lift carefully the microcontroller U18 out from its socket on the electronic board B7043. Insert the microcontroller into the socket on the elec­tronic board B7043 so as to have the same orientation of the key of its body as it was on the old micro­controller. Reassemble the pump in reverse order to the section 10.1.
10.11. REPLACING SYRINGE SIZE SENSOR (FIG. 4)
u Disassemble the pump according to the section 10.1.
Remove the screw (8) and remove the syringe clamp (9) (see Fig. 3). Disconnect the syringe size sensor (3) con­nector P8 from electronic board B7043 (9). Remove two screws (1) and lift the syringe size sensor (3) with other parts. Loosen two screws (2) and pull out the syringe size sensor (3). Install, fasten and reconnect the new sy­ringe size sensor (3) executing above-described actions in reverse order. Reassemble the pump in reverse order to the section 10.1. Perform syringe size calibration (see Chapter 6)
10.12. REPLACING BUZZER UNIT (FIG. 2)
u Disassemble the pump according to the section 10.1.
Detach buzer unit (17) (potentiometer and buzer) from the housing. Glue the new buzer unit to the housing in the same location. Glue potentiometer using ther­moglue. Reassemble the pump in reverse order to the section 10.1.
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35
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10.13. REPLACING POWER SUPPLY INLET (FIG. 2)
Disassemble the pump according to the section 10.1. Unsolder wires from power supply inlet (1). Remove two screws (2) and remove the power supply inlet (1). Install the new power supply inlet (1) and re-solder wires to it executing above-described actions in reverse order. Push insulating tubes onto soldering places. Re-assemble the pump in reverse order to section 10.1.
10.14. REPLACING SUPPLY UNIT (FIG. 2)
u Disassemble the pump according to the section 10.1.
Disconnect connectors P13, P14 (11) and P11, P12 (6) from supply unit (7). Remove four screws (10). Remove the supply unit (7). Install the new supply unit (7) and re-connect connectors executing above-described actions in reverse order. Re-assemble the pump in reverse order to section 10.1.
Fig.1
1. Keyboard
2. Electronic board B7043
3. Syringe sensor *
4. Connector *
5. Flexible cable *
6. Screws M4
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SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
* – optional
Page 37
Fig.2
1. Power supply inlet 10. Screws ∅ 3x6,5
2. Screw M3x10 with nuts M3 11. Battery connector
3. Fuse unit with fuse T80mA 12. Battery fuse
4. Plastic cap 13. Screw ∅ 3x10
5. Cross knob 14. Cover
6. Mains connector 15. Battery
7. Supply unit 16. Buzzer connector
8. Fuse T1A 17. Buzzer
9. Supply unit connector 18. Filter unit
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37
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Fig.3
1. Cover 7. Housing
2. Screw M3x8 8. Screw M2,5x12
3. Plate 172 9. Syringe clamp
4. Screw ∅ 3x10 10. Tube
5. Support 11. Screws M3x16
6. Rubber bellows 12. Plate 146
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SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
Page 39
Fig.4
1. Screw M4x8
2. Screw M3x10
3. Syringe size sensor
4. Coupling
5. Screw M3x8
6. Optical sensor
7. MFC
8. Prealarm switch S2
9. Electronic board B7043
10. Screws ∅ 3x6,5
11. End switch S1
39
Service manual
Page 40
ANNEX A
ELECTRICAL SCHEMATIC DIAGRAM OF THE PUMPS SP-12S Pro and SEP-12S Plus
40
SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
Page 41
*
*
Service manual
* – optional
41
Page 42
ANNEX B
ELECTRICAL SCHEMATIC DIAGRAM OF THE PUMP SEP-10S Plus
42
SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
Page 43
Service manual
* – optional
43
Page 44
ANNEX C
INTERCONNECTION DIAGRAM OF THE PUMPS
44
SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
Page 45
Service manual
* – optional
45
Page 46
ANNEX D
ELECTRICAL SCHEMATIC DIAGRAM OF ELECTRONIC BOARD B7043
46
SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
Page 47
Service manual
47
Page 48
ANNEX D
ELECTRICAL SCHEMATIC DIAGRAM OF ELECTRONIC BOARD B7043 (continue)
48
SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
Page 49
Service manual
49
Page 50
ANNEX D
ELECTRICAL SCHEMATIC DIAGRAM OF ELECTRONIC BOARD B7043 (continue)
50
SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
Page 51
Service manual
51
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ANNEX E
ASSEMBLY DRAWING OF ELECTRONIC BOARD B7043
52
SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
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Service manual
* – optional
53
Page 54
ANNEX F
DRAWING OF CABLES FOR MULTIFUNCTIONAL CONNECTOR (MFC)*
NOTE:
Use standard D Type — 9 pin connectors.
54
SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
Connection data:
Ground (GND)
Normally Closed (NC)
Common (COM)
Normally Open (NO)
* – optional
Page 55
ANNEX G
DESCRIPTION OF ERRORS
All errors are listed in the Table:
Error
ERROR 001
ERROR 002
ERROR 004
ERROR 005
ERROR 006
ERROR 007
ERROR 008
ERROR 009
ERROR 011
ERROR 013
ERROR 016
ERROR 017
ERROR 018
ERROR 019
DESCRIPTION
Cannot read data from external EEPROM
Cannot write data to internal EEPROM
Occlusion koeff. settings failed
Language setting failed
Incorrect program CRC
Syringe size sensor calibration failed
Date and time setting failed
Drug set failed
Incorrect external EEPROM CRC
Watchdog activated
Data of current syringe failed
SRAM test failed
Incorrect program CRC (fast test)
Incorrect Bootloader CRC
CORRECTIVE
ACTIONS
Recycle power
Configure Setup menu
repeatedly (see Chapter 6)
Calibrate occlusion level
(see Chapter 6)
Select language
(see Chapter 6)
Consult the manufacturer
Calibrate syringe size
sensor (see Chapter 6)
Set date and time
(see Chapter 6)
Restore default drug set
(see Chapter 6)
Consult the manufacturer
Consult the manufacturer
Recycle power
Recycle power
Consult the manufacturer
Consult the manufacturer
NOTE:
When eliminated fault repeats consult the manufacturer.
Service manual
55
Page 56
ANNEX H
PREVENTIVE MAINTENANCE CHECKLIST
Serial number ...............
Service Manual Parameter Value section
7.2 Infusion volume accuracy %
7.3 Infusion rate accuracy %
7.4 Bolus volume accuracy %
7.5 Occlusion pressure accuracy: Low kPa
Service Manual Alarm signal Comment section
8(1) OCCLUSION!!!
8(2) OCCLUSION or END
8(3) NO MAINS!!! Check power cord
8(4) LOW BATTERY
8(5) VERY LOW BATTERY
8(6) X min. PREALARM!
8(7) END of INFUSION
8(8) KOR X.X ml/h
8(9) SYRINGE EMPTY!
8(10) CLAMP OPENED!
8(11) ILLEGAL SYRINGE! Change SYRINGE!
8(13) ATTENTION! 2 min INACTIVE
8(14) STANDBY TIME ELAPSED
Med kPa High kPa
Pump owner/ward ......................................................................................................
Tests performed by (name, surname, signature) ............................................................
Tests performed (date) ................................................................................................
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SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
Page 57
ANNEX I
COMPONENT LIST
No Description Code
1 2 3 4 5 6 7
8 9 10
11 12 13
14 15 16 17 18 19 20 21 22 23 24 25
Battery GB1, GB2 Rubber bellows Optical sensor TAX1 End S1 and prealarm S2 switch Syringe sensor S3 Electronic board B7043 Keyboard
Microcontroller U18 Syringe size sensor Buzzer unit Z1
Power supply inlet Supply unit Fuse T80 mA F1 Fuse T160 mA F1 Fuse T1A F1, F2(A2) Plastic cap Filter unit Cross knob Display MD1 LED yellow D26, D27, D28 LED green D29, D30 Mains cable Syringe clamp Plate 172 Plate 146 Support
Service manual
B6640004 B8703002 V5440101 V5500900 B6660016 B3087043 V6675033 (for SEP-10S Plus) V6675034 (for SP-12S Pro) V6675042 (for SEP-12S Plus) B6270010 B6666002 B6710005 (with volume control) B6710006 (without volume control) V5520180 B6340011 V5501002 (for 230 VAC mains) V5501000 (for 115 VAC mains) V5501020 B8123009 B6730006 B6370007 V5500442 V5430100 V5430200 V5570010 (European style) B8127002 B8600172 B8600146 B8126028 (without tooth) B8126046 (with tooth)
57
Page 58
ANNEX J
ACCESSORIES
Part number Description
B8640027 Spacer syringe sizing 1 B8640027-01 Spacer syringe sizing 2 B8640027-02 Spacer syringe sizing 3 B8640027-03 Spacer syringe sizing 4
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SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
Page 59
ANNEX K
COMMUNICATION PROTOCOL TECHNICAL DESCRIPTION
u Communication protocol is used for downloading „Event
Log” from the syringe pump in response to commands from a computer.
u The protocol uses a variation of the HDLC format for
data transfer. Following format is used to transfer com­mands from computer to the syringe pump:
BYTES CODE DESCRIPTION
1 0xC0 Flag 1 0x02 — 1 0x13 Control 1 0x00 Status (reserved) 1 — Command code (see below) 1 0x00 — 2 — CRC 1 0xC1 Flag
u Following commands are used for downloading „Event
Log” from syringe pump to computer:
CODE DESCRIPTION
0x01 Send Model and SN 0x30 Send Event Log Size 0x31 Send (repeat) frame 0x32 Send next frame 0x33 Quit
u Following format is used for transferring data from sy-
ringe pump to computer:
BYTES CODE DESCRIPTION
1 0xC0 Flag 1 0x03 — 1 0x13 Control 1 0x00 Status (reserved) 1 — Code of command from PC pump is responding to 1 0x00 —
45 — Data (5 events)
2 — CRC 1 0xC1 Flag
Service manual
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Page 60
u Technical specification of the RS232 Interface is shown
in the 1 table
1 table
RS 232 Specification
Connector 9-pin D-Socket
TX Pin 3
RX Pin 2
Baud rate 9600 baud
Bit format 1 start, 8 data, no parity, 1 stop
Character format Binary/ASCII (see below)
Ground Pin 5
Isolation socket/pump 4 kV, Air Gap ±15kV, Contact ±8kV
NOTE:
ASCII is used to transfer information regarding pump model in response to command „Send Model and SN”
u Cable connections scheme is shown in 2 table
2 table
PC Pump
Pin 3 (Tx) Pin 2 (Rx)
Pin 2 (Rx) Pin 3 (Tx)
Pin 5 (Ground) Pin 5 (GND)
Pin 4 Nc Pin 4, Pin 7 (Jumper)
Pin 7 Nc
60
SP-12S Pro, SEP-12S Plus and SEP-10S Plus syringe infusion pumps
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