FP-960
OPERATION MANUAL
NIPRO CORPORATION
INTRODUCTION
CONTENT
1. Precausions in use of pump ·1
9. Ni-cd battery 20
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2.COMPONENTS OF PUMP ANO FUNCTIONS
I FRONT VIEW I
Handle I REAR VIEW I Name plate
Power switch
Name plate
I.V. pole clamp Fuse (O.8A)
Bubble sensor
I
I Battery cover (Emitter)
1
I
Door clamp I~; __ --'IIt~-WARNING for
tube setting
Pressure sensor
Bubble sensor Harness Infusion
(Receiver) tube outlet
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3.COMPONENTS ON OPERATION PANEL ANO (J)AC POWER
FUNCTIONS The LEO is turned on during connection of the pump with external
power supply.
(?lCHARGE
The LEO is turned on during charge of encased Ni-Cd battery.
About 6 hours are required to full charge the battery When full
charged, the LEO is turned off. The battery is charged as far as the
® ~ OCCLUSION alarm
1 h LEO is turned on when occlusion in infusion tube is detected.
Alnrrn range is between 68.65 and 1l768kPa (0.7 and 1.2kgUcm') and the
.uarrn limit is directly proportional to infusion rateo
1, I OW BATTERY alarm
111 \ LEO is turned on when voltage of the battery is reduced to preset
1I v 1 and further operation
is disabled under normal condition.
"AIR-IN-LlNE alarm
111 ' LEO is turned on when a bubble of a size to be alerted is detected
()f infusion tube is not set to the pump. Flashing of the LEO indicates
dI l ction of a dangerous bubble a little smaller than the above siz e.
IllOOR OPEN alarm
111 \ LEO is turned on when door is fully or partially opened.
Il KVO (Keep-Vein-Open)
111 LEO is turned on when the pump is in KVO condition after the
lnluslon is complete.
11 HATE
1110 LEO is turned on when infusion rate is displayed on data screen.
IDI) LlMIT
20 lile LEO is turned on when delivery limit is displayed on data screen.
11'1 l, TOTAL
111 LEO is turned on when delivery total is displayed on data screen.
I? 1111
111 LEO is turned on when data displayed on screen is mL unit.
13 II1I/h
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@OATA SCREEN 4.SPECIFICATIONS ANO PACKAGE
RATE, OELlVERY LlMIT, OELlVERY TOTAL or fast infusion rate during
its setting or the pump operation ; or error message is displayed on +SPECIFICATIONS
data screen by 7 segment LEO. e Product name infusion pump
@SELECT SW e Model FP-960
By each pressing of the SW, cycle of "RATE •• O.LlMIT •• O.TOTAL" i e Power supply AC220V±20V, 50/60Hz
repeated. If O.LlMIT or O.TOTAL is left to be displayed for 10 seconds Ni-Cd battery 9.6V, 700mA/h
after the pressing, it is changed to RATE automatically. (usable for 2-3 hours after charge for about
@RESET SW 6 hours)
The SW is used to clear O.TOTAL. To reset the volume, press the S *AC110V± 1OV, 50/60Hz type FP-960 is also
for 2 seconds or more after displaying O.TOTAL. available upon request.
e Maximum power consumption 25VA
@UPSW
eRATE setting range 1-1000mL/h(1mLlh steps)
The SW is used to increase RATE or O.LlMIT displayed on data scree
el .LlMIT setting range 1-9999m Uh(1 mLlh steps)
by pressing. When the SW is pressed one second or more, th
en,TOTAL display range 1-9999mL/h(1 mUh steps)
displayed rate or volume is increased continuously.
e, ast infusion rate About 1000mLlh
@OOWN SW elllfusion pressure 68.65 - 11768kPa (0.7 -1.2kgf /cm )
The SW is used to decrease RATE or O.LlMIT displayed on dat elllfusion accuracy + 10% with Nipro FPC-96 infusion set.
screen by pressing. When the SW is pressed one second or more, th el\pplicable infusion set FPC-96 series
displayed rate or volume is decreased continuously.
@STOP/MUTE SW el\lnrms and notice Occlusion, low battery, Air-In-Line, door open,
The SW is used to stop the pump operation or to mute buzzing. KVO and drive error
e Monitors
@)STOP LEO
The LEO is turned on when the pump operation is stopped.
e, IJ es
External power connection, charge and ready
0.8A/250VX2
*1.5A/125V X2 for AC110V type FP-960.
@START/FAST SW e 01' ration environment Ambient temperature 10~35'C
The SW is used to start infusion or fast infusion. To start infusion, pres
atmospheric pressure 700~ 1060hPa
the SW momentarily. To start fast infusion, press the SW for 1-
Relative humidity 30~85%(No dew condensation)
seconds or more. By the pressing, fast infusion rate is displayed o ')Ior ge environment Ambient temperature -1O~40'C
data screen.
Atmospheric pressure 700~1 060hPa
@START LEO Relative humidity 30~85%(No dew condensation)
The LEO is turned on when the pump operation is started. I It ctric shock protective class and type Class 1, type CF
Flashing of the LEO indicates that the pump is being operated. Highe e p ration mode • Continuous operation
(Iower) infusion rate is reflected by higher (Iower) flashing frequency. Ollt r dimension (W)86mmX(L)130mmX(H)155mm
(excluding protruded part)
Wüight about 1.5kg
+ ACKAGE
l 'ump · · 1
f'owor cord ····· ·· ·1
Op ration manual ·1
''1)1cifications and design may be changed without giving prior notice.
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To unlock tube clamp, press tube clamp lever marked with ~shown in
5.DIRECTIONS FOR USE Ihe lower right Fig, of P.9.
1.0peration
( Y closing door, the tube clamp is released.
G)Set the pump to I.V. pole or on table.
~Connect the pump to external power supply .
• Connect power cord to power (11) ot infusion rate (1 mUh steps).
inlet ~ placed at rear side of -:. Ouring infusion, infusion rate
the pump and connect plug change is disabled.
placed at opposite side of the After stopping the pump operation,
cord to AC220V * receptacle provid change the rate by pressing
-ed with ground connection. "UP" SW and/or "OOWN" SW
*For AC110Vtype FP-960, connect m rked with ••.
plug to AC110V receptacle .
• After the connection completion,
LEO's of" . r "and"CHARGE"
on operation panel are turned on
if battery is not full charged. '1o ot O.LlMIT (mL), display the volume on data screen by pressing
"',1 LECT" SW followed by pressing "UP" SW and/or "OOWN" SW
Q)Turn on power SW Q) placed at
111ukod with ••.
rear side of the pump.
• f)uring infusion, the volume change is disabled.
At the moment of the turning on,
LEO's on operation panel are turned on from upper left end laterally on "11 et to OmL, KVO mode can not be executed.
by one toward lower end. Check the stepwise turning on. .·LJ ually infusion rate (mLlh) is displayed on data screen. By each
pt ssing of "SELECT" SW, cycle of "RATE" •• "O.LlMIT" ••
®Fill infusion set (FPC-96 series) with solution. it i "D.TOTAL" is repeated. If "O.LlMIT" or "O.TOTAL" is left to be
Remove bubbles from infusion tube completely. If n~t removed, di played for 10 seconds, the display is changed to "RATE"
detected by BUBBLE sensor, disabling the pump function. .uuornatically,
@Set infusion tube firmly as : "tube clamp" •• "tube guide" ••. "ea 1 1111
opon roller clamp of infusion set.
blades" •• "BUBBLE sensor (emitter)". Close door and check turrunq o
'1I'fl s "START/FAST" SW for 1-2 seconds or more to start fast infusion.
of "OOOR OPEN" alarm LEO.
1'11H "STOP 1M UTE" SW to stop the infusion after checking few drops
,,1 ',olution discharge from needle tip and no bubbles in infusion tube.
Ilocause the fast infusion volume is integrated, reset by pressing
"HESET" SW for 2 seconds or more after displaying "O.TOTAL" by
prossing "SELECT" SW.
1il',Ioltllnfusion by pressing "START" SW after venipuncture.
11111ch ck O.LlMIT or O.TOTAL during infusion, press "SELECT" SW to
di play it.
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* During infusion, change of RATE or D.LlMIT is disabled.
.Fast infused volume is added to D.TOTAL.
.To check D.TOTAL during fast infusion, press "SELECT" SW.Relevant
RATE change O.LlMIT change LED is turned on and D.TOTAL is displayed. O.TOTAL
Fast infusion rate display display during fast infusion
.ln1uslon completion.
• Press "STOP/MUTE" SW.
4.Fast infusion • Remove infusion set from the pump.
• During fast infusion, fast infusion rate is displayed on data screen. • Turn off "POWER" SW.
• About 2 seconds after releasing press of "START/FAST" SW, t
display is changed to infusion rate and infusion is continued.
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6.ALARMS ANO NOTICE
1.Alarms
e No solutio 1,,1' lnluslon or start after refilling e Flashing of AIR-IN-L1NE LEO shows
Pi,Pi,Pi ...
AIR-IN-L1NE (intermittent) e Bubble in •11111 ItII!. small bubble inclusion in infusion tube.
tube. 110''''IVI bubble or replace infusion When bubble of alarm limit size is
e Unloaded ,1 detected, pump operation is stopped
tube or tub 1" 111111 tube or set it to sensor with the LEO ON and buzzing.
-ed from 1111'I Ily. eOuring DOOR OPEN, the LEO is ON
e oa.maged 11,11111 ' t supplier to check/repair. irrespective of presence/absence of infusion
tube because sensor (receiver) is placed
at door inside.
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BUZZING NOTE
ALARM DISPLAY PATTERN CAU ACTION
E--1
• Affected by
frequency nois
E--3
. 4 I ms is not displaved .
• Durinq infuslon. E-- a ar
E--4 • Damaged mot uppuer to check/repair. The alarm is displayed only w~en .POW.ER
• Damaged SW is turned on. If alerted dunng mfusl.on
rotation sens without error display, stop pump operatlon
• Internal elect and press the SW to see error codeo
circuit error.
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ALARM DISPLAY BUZZING
e
o=]§D
eDamaged moter,Degradation
IQ§J
~
AlE /
= = vEJ
Qml stuck of drive mechanism
h
=~,
Encoder trouble. 11
E-8
Pii···
e More moter rotation than settín 1- pller to check I repai r.
~rnrJ~ (Coutinuous)
-
OCClU lOW "'IR.IN
,r= E
(Q@J
@Q@
=
e Electronic noise, Encoder troub
e Electronic circuit error.
ER SW to find the noise
lhe source removal, turn
I1
2. Notice
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7.MONITORS ANO SPECIAL FUNCTIONS
1.REAOY LEO M INTENANCE ANO STORAGE
-1:0:. READY) Flashing indicates : I~complete. infusion preparatio
11111 pump is contaminated with solution, remove it immediately
Wlpll1(J wllh gauze, cloth or the like.
by
disable d pump operation I I r nr not to wet the pump with any fluid because it is not water
@-READY] Lighting indicates : Successfully completed infusi
I f J "el, Ign, in particular power inlet, POWER SW and fuses.
11'1I1 ( organic solvents such as thinner to clean the pump casing
preparation, ready for infusio 111, 11Is attcked.
start.
1" 111,f ump at an ambient temperature range from -10 to 40'C and
lo READY J Extinguishment indicates : f II\lVI humidity range from 30 to 85% in a place without fear of dew.
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L I
CAUTIONS IN USE OF ELECTRIC MEOICAL
© VICE FOR SAFE ANO NON-OANGEROUS
ALARMOFF !',m ON
PERATION
1;fQ
! ARNING
I 1lile, medical device shall be operated
ffiCAUTION
by authorized expert only.
I 1111,.medical device shall be set to a place of:
(1 )I~II contact with water
)r 11 idverse effects caused by exposure to abnormal atmospheric
1'11 ure, temperature or humidity; direct sunlight; or air containing
"" 1, ! alt and/or sulfur
)NII 111 itlnation, vibration or impact (also during transport)
11.GUARANTEE ANO SERVICE )tlll ,11 micals or no harmful gas generation
)1'1 1 nce of power supply of correct frequency/voltage and
The pump is guaranteed by Nissho for a . 111 ptable current level (or power consumption)
date ot your purchase If the umo : .penod of one year after the
)1 11 IlIqh frequency generating device such as electric knife or
due to our faulty work~anshi ~ d P IS f~,led oro damaged by defects
n WII( It s portable telephone
be repaired by us free of ch:rge p~atenals dunng the period, it shall
If failure or damage is caused b :ase contact your nearest agency. 11" following actions prior to use:
guarantee for one year is invalid Yd ny ?f the following reasons the 111t.k SW contacts, data setting SW's data screen and the like to
1. Misuse or unreasonable alterati~~ rep.alr cost shall be paid by y~u: IlIt correct functions of electric medical device.
person n reparr carned out by unauthorized )1 111ck correct and safe connection of all cords.
2. Drop or roug h transfer /trans t )1 111ck correct combination with other device(s) to eliminate potential
3. Fire, expOsure to salt or P~~r~~~~ the date of your purchase ""'11110 Is miss or danger
gas
abnormal voltage application o t f G , earthquake, storm, flood, )1 III ok Infusion line to be connected to patient to assure its safety.
r ac o od of any nature )1111I k correct ratings of power supply.
)11111'111 frequency generating device such as electric knife or wireless
1'"11(1)1 telephone is present near infusion pump, turn off the device.
11 lIu following actions during use
~1)1111ck whether limit time or volume required to diagnose or treat
l' ,lit nt ls not exceeded.
~ ) 11111110r patient and electric medical device frequently to assure safe
lid normal operation of the device.
~ )11 uouble of patient or electric medical device is detected, take
111111' lo cope with the trouble; for example, stop the device operation
111r.uustderation of the patient safety.
~ \)1 111ck no placement of high frequency generating device such as
I 1It le, knife or wireless portable telephone near infusion pump.
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5.Take the following actions after use:
(1)Return operation SW and the like to original states followed
turning off POWER SW in accordance with prescribed procedure.
(2)Store electric medical device at a place of:
1 No contact with water
TI No adverse effects caused by exposure to abnormal atmospheri
pressure, temperature or humidity; direct sun-light; or air containin
dust, salt and/or sulfur
III No inclination, vibration or impact
NNo chemicals or no harmful gas generation
(3)Store electric medical device after cleaning for the next normal use.
(4)lf electric medical device is damaged, indicate the fault condition
by suitable means. The device shall be repaird by authorized exper
only.
7.Don't alter electric medical device.
8.Maintenance and check
(1)Check and maintain electric medical device and its components
regularly.
(2)lf electric medical device is used after some time of resting, check
correct and safe functions of it prior to use.
9.0ther
(1)Use infusion set exclusively specified for infusion pump.
(2)Take care not to wet infusion pump with solution or the like.
(3)During infusion, monitor reduction of solution level in vial and infusion
pump operation frequently for assuring safety.
(4)When safety guard is operated, take corrective actions immediately
after finding the error cause.
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