ee
The
Introduction
The
AK-10
two
basic
Fluid
modified
variety
This
in
the
monitor
monitors
tem.
standard
amount
of
infusion
ment.
system
building
Monitor.
by
adding
of
needs
manual
The
describes
AK-10
system.
for
extracorporeal
the
blood
HFM
hemofiltration.
of
filtrate
solution
blocks,
The
and
circulation
10-1
drawn
AK-10
for
hemofiltration
the
Blood
system
or
treatment
is
given
can
interchanging
the
operation
The
BMM
circulation.
the
hemofiltration
It
controls
from
the
to
the
is
designed
Monitor
easily
be
expanded
monitors
techniques.
of
two
10-1
is
the
It
controls
in
the
extracorporeal
fluid
and
monitors
patient
patient
and
during
system
around
and
the
or
to
meet
a
of
the
monitors
standard
and
monitor
the
the
amount
the
treat-
blood
sys-
for
for
hemofiltration.
Contents
Introduction
Description
The
Blood
Monitor
The
Hemofiltration
Hemofiltration
Attaching
Starting
Priming
Initiating
Changing
Discontinuing
the
the
machine
and
hemofiltration
parameters
hemofiltration
Fluid
preparations
blood
and
fluid
rinsing
procedure
during
Monitor
lines
treatment
11
12
14
15
16
spetto;
Note:
operated
are
manual.
When
equipment
sured.
The
AK-10
by
familiar
unpacking,
is
hemofiltration
persons
with
the
check
damaged
trained
operation
in
equipment
proper
machine
hemotiltration
procedure
operation
for
damage.
may
given
cannot
only
and
in
be
who
this
If
be
as-
Alarms
Blood
Monitor
Hemofiltration
Error
alarms
Operator
Technical
Cleaning
Technical
Technical
data
data
alarms
action
error
BMM
HFM
Monitor
table
codes
10-1
10-1
alarms
17
18
19
20
21
24
25
26
27
The
The
BMM
10-1
number
trol
other
so
operational
alarm
certain
and
“depress”
pushing
1.
2
of
functional
and
monitor
monitors
that
mode
handling
selector
“out”
(light
and
in
The
MAIN
and
the
button
silence
the
buzzer
the
MUTE
to
sound.
The
heparin-protamine
control
ments.
monitor
the
in
selection
settings
buttons
buttons
off).
“release”
and
letting
SWITCH
hemofiltration
lights
the
audible
for
button
knob.
can
be
groups
extracorporeal
the
AK-10
For
are
up
on
30
seconds. A power
The
is
made
with
are
have
these
used
out
the
alarm
alarm.
to
blink
knob
which
system,
knobs.
two
powers
fluid
conveniently
work
blood
the
with
white
Alarm
always
buttons.
is
red.
positions,
buttons
and
Pressing
pump
to
designate
both
monitor.
is
used
and
an
and
the
graduated
the
failure
intermittent
together
BMM
instructions
the
its
Blood
divided
to
circuit.
indication
On
The
to
in
As
isdesigned
buttons
“in”
the
blood
button
and
this
monitor,
(lighton)
action
monitor
MUTE
temporarily
silences
will
cause
alarm
flow
rate
ml/h
incre-
intoa
con-
the
and
of
Monitor
The
arterial
pressure
arterial
out
the
rotating
The
arterial
clamps
alarm
The
single
and
the
Owing
filtration,
such
as
single
The
air
(AIRDET.BYPASS)
ton
(AIRDET.RESET).
justable
18—30
detect
ml/min
pressure
alarm
pressure
sensor
the
pressure
and
clamp
situations.
needle
arterial
to
the
high
the
the
AK-10
needle
mode.
detector,
to
accommodate
mm
diameter.
at
least
and
give
indicator
sensor
plate.
The
venous
the
arterial
mode
and
blood
use
ofa
BMM
the air
0.2
ml
air/min
an
alarm.
sensor
and
(ARTER.PRESS.).
can
be
bypassed
sensitivity
plate.
line
clamps.
and
venous
selector
venous
double-pump
time-setting
flow
rate
10-4,
is
detector
and
the
air
The
air
most
drip
The
ultrasonic
at
blood
the
arterial
by
pulling
can
be
adjusted
The
lines
in
button
(SN
knobs.
needed
recommended
detector
detector
in
blood
monitor,
bypass
chambers
air
detector
flows
hemo-
button
reset
head
below
The
by
solenoid
certain
ON)
for
but-
is
ad-
of
will
300
AiRDEY
BYPASS
AIROET
RESET
ARTER
PRESS
VENOUS
PRESS
3
Theblood
control
rate
blood
white
pump
4a
The
limits
(VENOUS
4b
The
knob.
in
ml/min.
can
be
handle
in
the
venous
and
venous
pump,
flow
The
blood
In
the
returned
on
the
blood
direction
pressure
the
venous
PRESS.).
pressure
meter
flow
meter
event
ofa
to
the
patient
pump
indicated
meter
with
pressure
connector
and
its
flow
indicates
power
failure,
by
pulling
and
turning
by
the
arrows.
adjustable
alarm
(male).
rate
the
button
the
flow
the
out
the
alarm
The
a)
The
b)
The
c)
The
Note
blood
back
interface
mains
monitor
that
the
monitor
of
the
cable.
fuse(s).
type
serial
may
machine
label
with
number
be
for
different.
serial
number.
the
hemofiltration
and
The
The
HFM
10-1
groups
circuits.
Mode
alarms
and
2
3
4
which
control
selection
are
indicated
buttons.
The
filtrate
Thefiltrate
Thetransmembrane
alarm
limits,
control
The
venous
selected
TMP
The
ton
knob.
The
The
The
and
ALARM).
34°C
The
knob
monitor
indicates
pressure
TMP
is
shown
blood
(BLOOD
infusion
infusion
infusion
temperature
and
42°C.
heater
is
monitor
scale
pump
alarm
and
is
on
leak
Internal
not
consists
and
is
made
with
and
dealt
(maximum
and
indicator
and
filtrate
the
TMP
the
pressure
automatically
the
transmembrane
detector,
LEAK)
scale
(maximum
pump
and
heater
with
alarm
alarm
activated
Hemofiltration
ofa
monitor
pressure
and
until
the
white
with
load:
its
flow
(TMP
pressure
as
the
caused
held
constant
the
blood
its
sensitivity
its
flow
temperature
indicator
limits
the
AUTO
number
control
using
rate
meter
difference
by
pressure
load:
rate
are
of
filtrate
and
buttons,
red
35
kg).
control
with
ALARM),
connector.
between
the
filtrate
by
the
meter.
leak
alarm
control
35kg).
control
control
(TEMP.
normally
mode
ts
functional
infusion
while
indicators
knob.
adjustable
TMP
the
pump.
The
monitor.
entered.
but-
knob.
knob
set
at
The
Fluid
8
The
with:
a)
b)
C)
d)
©)
f)
When
sed
mulated
During
treatment
type
Q)
The
operating
buttons
will
page
Monitor
automatic
The
(AUTO).
The
The
wheel
Theinfusion
The
thumb
The
(max
(Blinking
gaining
The
the
button
filtrate
The
pressed
remaining
minutes
last
hour
in
minutes.
simultaneously
of
(blinking
indicate
treatment
automatic
weight
desired
desired
display.
filtrate
time
error
20.
loss
weight
selectors.
infusion
wheel
9.9
kg)
display
weight).
flow
is
flow
rate
button
the
display
treatment
(3.5
of
treatment
the
UF
infusion
the
first 10
parameters
hemofilter
indicator
fault
red
light).
are
pressed
is
monitored
treatment
selector
loss
is
quantity
selectors.
The
is
continuously
pressed
in
means 3 hours
RATE
minutes
used,
selector
quantity
accumulated
indicates
rate
button
the
display
l/min
(TIME).
will
indicate
time
the
and
the
display
volume
of
have
been
the
indicator
(ERROR)
(steady
red
When
the
simultaneously
an
error
code.
selector
(kg
DIFF).
selected
(kg
is
selected
weight
shown.
that
the
(UF
will
(UF
rate).
When
the
in
hours
and
50
minutes).
remaining
TIME
button
will
infused
light)
into
the
treatment,
adjusted
is
indicates
or
UF
RATE
For
error
not
technical
and
controlled
button
with
the
INF).
with
loss
patient
RATE).
indicate
the
button
calculated
and
tens
During
time
is
are
show
the
the
patient.
before
to
the
patient
very
accurate.
either
and
the
display
codes
thumb
the
inkg
is
When
the
is
of
the
shown
pres-
accu-
the
and
fault
TIME
see
8a-g
—
;
ERROR
|
AUTO
|
(,
=
40
-100.200
309
400
500
The
AUTO
the
manual
ERROR
mode
indicator
is
activated.
mode.
will
This
be
steadily
is
to
notify
lit
the
until
the
operator
of
The
back
a)
Theinterface
b)
The
mains
monitor
The
c)
that
Note
blood
of
fuse(s).
the
monitor
the
cable.
label
type
serial
may
machine
with
for
numer
be
different.
numer.
serial
hemofiltration
the
and
Hemofiltration
First
check
that
the
mains
cables
are
failure
alarm
connected.
that
the
(BMM)
correctly
connected.
not
operate.
Setting
1
Hang
up
tion
for
2
Hang
up
Make
sure
to
contain
of
the
infusion
will
result
interface
and
placed.
cable
the
hemofiltration
An
alarm
Ifimproperly
up
container/bags
the
treatment
empty
that
the
selected
solution
on
container/bags
the
container/bags
quantity
connected
ifthe
between
will
connected
with
the
infusion
plus
the
to
power. A power
mains
cables
the
blood
fluid
monitor
result
if
the
sufficient
scale.
on
the
have
of
filtrate
patient’s
are
not
monitor
(HFM)
the
cable
monitors
infusion
filtrate
scale.
the
capacity
i.e.
the
weight
is
is
not
will
solu-
volume
loss.
preparations
Arterial
1
Arterial
arterial
sides
2
Blood
blood
the
3
Hemofilter
nector
4
Heparin-protamine
pulling
one
line
5
Arterial
into
blood
pressure
of
the
pump-
pump.
blood
to
down
of
the
into
place.
the
line
line
pressure
sensor.
pillow
by
Thread
When
pump
door.
blood
the
blood
the
housing.
two
grooves.
line
clamp
clamp
sensor — Place
Secure
adjusting
the
the
pump
port-
port
at
pump — Open
Push
-—
Place
colour-coded
Attaching
the
it
into
pump
segment
segmentis
Attach
the
Place
bottom
the
the
housing
the
pre-pump
with
the
the
pillow
blood
the
hemofilter
of
the
heparin
the
in
line
on
line
holders.
into
in
place,
the
hemofilter.
pump
line
up
tolock
arterial
red
dot.
the
the
both
the
close
con-
by
into
the
blood
line
and
fluid
lines
Note:
The
accuracy
removed
Place
with
Note: / is
throughout
treatment.
Place
and
matic
sterility
of
or
touched
the
hemofilter
the
arterial
the
the
blood
connect
diagram
ofall
container/bags
the
scale
important
priming
lines
to
the
on
connectors.
must
during
the
during
treatment.
in
the
end
at
the
that
the
and
rinsing
and
hemofilter
page
9.
hang
free
treatment.
holder
bottom.
hemofilter
procedure
the
fluid
lines
according
Take
care
so
as
to
guarantee
They must
in a vertical
remains
to
not
in
this
as
well
as
on
the
machine
to
the
sche-
maintain
position
during
the
the
be
position
Venous
1
Air
detector - Place
way
2
Venousline
venous
blue
3
Venous
pressure
connector.
4
Hemofilter
nector
blood
down
line
dot.
pressure
to
line
into
the
air
clamp — Place
into
the
transducer
blood
the
blood
the
venous
detector.
line
clamp
drip
the
post-drip
colour-coded
chamber
connector — Attach
protector
port—
port
Attach
on
the
to
the
top
the
of
venous
hemofilter
the
half-
chamber
with
the
the
venous
pressure
con-
hemofilter.
Starting
Infusion
1
Theheater - Pull
heating
part
out
the
Note:
heater,
heater
2
The
(coming
non-return
ber.
3
Theinfusion
the
line
bag
of
the
lines
of
the
heater
heater.
infusion
Close
The
lines
infusion
is
not
properly
venous
out
valve
out
and
to
the
vertical
into
the
line
so
that
the
and
push
must
not
be
kinked
pump
and
filtrate
inserted.
drip
chamber — Connect
from
the
upper
connector
pump-
Thread
pump.
open
the
bar
at
holders
bag
is
in
the
or
pump
part
of
at
the
the
heater.
the
back.
and
pull
correctly
heater.
twisted
in
will
not
the
the
heater)
venous
pump
Fasten
Press
the
the
lines
placed
the
heater.
function
infusion
to
the
drip
cham-
segment
the
soft
in
The
if
the
line
into
Before
starting
Place
clamps
followed
ped
Connect a physiological
terial
hemofilter.
empty
Ifthe
heparin
in
close
to
blood
bottle.
heparin
solution
the
Place
the
on
the
lines
unit.
(The
the
hemofilter).
line
for
priming
the
line
is
to
(bag
machine
according
solution
free
end
be
used,
or
syringe).
filtrate
line
(2000
and
rinsing
of
the
connect
to
the
procedure
should
ml)
the
venous
it
to
be
to
the
lines
line
the
clam-
ar-
and
into
an
the
machine
Starting
4
Depress
Wait
(0—9 + error
should
hemofiltration.
Ifthe
—
pull
—
depress
—
move
pressure
—
release
—
depress
sitivity
—
move
brane
the
MAIN
until
the
now
buzzer
out
the
AIRDET.
the
adjustable
AUTO
BLOOD
control
the
adjustable
pressure
machine
SWITCH
count-down
code
symbols).
be
lit,
since
sounds
arterial
meter
apart.
(light
LEAK
knob
meter
(light
on).
on
the
display
Several
the
machine
continuously:
pressure
BYPASS
alarm
sensor
(light
limits
off).
(light
off)
to
10.
alarm
limits
apart.
alarm
is
not
on).
on
the
and
on
the
has
ended
lights
yet
ready
plate.
venous
turn
the
transmem-
for
sen-
4
Container/bags — Clamp
fore
attaching
Lf a pyrogen
Separate
Filtrate
1
The
blood
half-way
turbulence
2
Thefiltrate
pressure
to
filter
instructions
line
leak
down
into
might
pressure
transducer
connector.
3
Thefiltrate
the
filtrate
4
Thehemofilter
line
to
5
The
drain
of
the
container.
pump - Thread
pump.
the
filtrate
line-
drain
line
all
multiconnector
the
is
used
for
infusion
this
container/bags.
in
the
infusion
device.
detector — Place
the
blood
leak
cause
false
alarms).
connector — Attach
protector
to
the
filtrate
port
Remove
and
port-
of
the
place
Connect
hemofilter.
the
protection
the
line
line
please
the
filtrate
detector.
the
filtrate
pump
segment
into
the
lines
follow
chamber
(Otherwise
the
filtrate
pressure
into
the
filtrate
cap
at
the
filtrate
be-
end
If
the
AUTO
having
The
buzzer
not
yet
SWITCH
10
minutes.
The
TEMP.
until
AUTO
mode
started
will
ready
for
twice
ALARM
is
not
activated
the
machine
sound
and
the
hemofiltration
to
reset
the
and
is
pressed.
within
there
will
be
an
MUTE
is
lit.
treatment
alarm function
ERROR
10
minutes
AUTO
If
the
machine
press
for
another
buttons
will
after
alarm.
MAIN
be
is
lit
10
11
Priming
General
For
priming
continue
rinsing
by
the
in
steps
cedure.
Check
1
Arterial
the
alarm
Blood,
the
clamp
2
Airdetector-—
AIRDET.
will
The
reactivate
off).
the
3
Venous
to
pressure.
VENOUS
buzzer
To
+200
4
Blood
until
will
and
the
turn
and
rinsing
with
the
of
other
hemofilters,
manufacturer
1--5
below
safety
pressure
arterial
buzzer
pressure
will
be
heparin,
sounds.
and
adjust
of
procedure
should
should
functions
sensor - Clamp
pillow.
activated:
infusion
To
the
Release
RESET
be
activated:
arterial
If
venous
simulate a decrease
reactivate
BLOOD
be
the
alarm,
the
and
the
necessary,
drip
pressure — Move
The
PRESS
sounds.
mmHg.
leak — Turn
activated:
arterial
depress
sensitivity
All
venous
alarm,
adjust
chamber
venous
(light
The
the
alarm,
the
LEAK
All
and
the
control
(light
pumps
arterial
pumps
venous
the
Gambro
on
this
page.
the
procedure
be
followed.
be
incorporated
The
arterial
ARTER.
and
filtrate
reactivate
sensor
plate
AARDET.
on).
The
stop,
solenoid
press
AIRDET.
the
fluid
using a syringe.
the
adjustable
and
an
increase
pressure
sensitivity
lights
BLOOD
on).
set
the
clamps
knob
alarm
All
and
alarm
up.
The
stop,
LEAK
pumps
venous
up
Fiber
For
recommended
The
into
the
line
PRESS.
pumps
the
alarm,
ifnecessary.
BYPASS
air
detector
the
buzzer
clamps
RESET
to
the
correct
of
will
limits
control
blood
the
buzzer
close.
button
two
degrees
and
Hemofilters
priming
instructions
this
pro-
just
before
pressure
(light
on).
stop
and
remove
(light
off);
alarm
sounds.
close*.
To
(light
levelin
alarm
limits
the
venous
be
activated:
stop,
the
clamps
close*.
at + 10
knob
down
leak
alarm
sounds
Jo
reactivate
and
(light
rinsing
and
the
and
procedure
Gambro®
Approximately
infusion
procedure
should
An
and
pass
circuit.
recommended
be
followed.
additional
prime
the
through
1
Remove
fusion
2
When
the
infusion
venous
3
Remove
pump
circuit.
4
Prime
air
from
gently
5
Unclamp
should
venous
6
Rinse
ml
of
7
Unclamp
again.
priming
8
Just
before
used
remove
cuit.
Adjust
chamber
(10
mm)
2000
rest
the
pump
500
at
with
tapping
not
and
priming
Rinse
Fiber
500
Ifa
of
membrane
any
drip
any
150
the
be
line
solution.
with a syringe
below
Hemofilters
ml
of
infusion
pyrogen
filter
by
the
ml
of
priming
the
system.
to
obstructing
to
rinse
ml
of
infusion
pump
and
chamber.
obstructing
ml/min
500
ml
of
blood
compartment
the
upper
the
filtrate
in
position
at
the
top
prime
the
solution.
the
venous
and
prime
the
2000
any
remaining
the
amount
the
solution
is
included
manufacturer
solution
At
least
half
the
filtrate
compartment.
clamps
and
prime
solution
clamp
the
clamps
to
rinse
and
priming
line
in
the
of
filtrate
line
ml
top
header
(the
filtrate
filtrate
the
hemofilter.
compartment
and
with
of
priming
air
of
fluid
until
of
the
solution
clamp
the
the
drip
is
used
to
in
the
for
priming
will
be
required
of
this
volume
and
start
the
infusion
has
been
infusion
and
start
prime
and
in
the
with
the
pump
pump)
the
remaining
solution
from
the
in
the
venous
level
is
chamber.
prime
the
infusion
hemofilter
and
line
and
rinsing
to
rinse
should
the
in-
circuit.
used,
stop
line
at
the
blood
the
blood
remove
hand.
segment
clamp
with
1000
filtrate
line
500
ml
has
been
blood
cir-
drip
at
least 1 cm
the
the
by
the
of
a
/A\
off).
9
5
Transmembrane
a)
b)
12
Move
the
decrease
sound.
Move
the
an
increase
sounds
and
To
reactivate
limits
at 0 and
knob
at
lower
in
TMP:
upper
100
pressure:
adjustable
TMP
adjustable
in
TMP:
the
filtrate
the
alarm,
200
mmHg.
mmHg.
TMP
TMP
(light
pump
set
alarm
on),
alarm
(lighi
stops.
the
adjustable
Set
the
(light
off).
*)
limit
the
limit
on),
the
TMP
Not
to
simulate
buzzer
to
simulate
buzzer
alarm
control
on
all
models
will
a
10
Turnoffthe
venous
Insert
pump
The
hemofilter
lines.
the
filtrate
and
unclamp
blood
is
now
pump
pump
the
ready
and
clamp
segment
infusion
for
use.
the
into
and
arterial
the
filtrate
filtrate
and
lines.
13
Initiating
Select
Start
initial
Set
the
dreds
of
Set
the
always
To
prevent
always
be 1 litre
amount
Ex:
If
the
desired
amount
the
Connect
Remove
cannula.
Start
(100
ml/min).
Start
correct
Remove
venous
solution
Stop
the
venous
Make
venous
Connect
Remove
cannula.
desired
grams
desired
in
whole
air
from
of
infused:
total
volume
of
blood
the
arterial
the
clamps
the
blood
the
heparin
flow
rate.
the
clamp
pressure
flush
blood
drip
chamber.
sure
that
line,
and
the
venous
the
clamps
settings
weight
quantity
loss
(1.5 = 1
kg
(litres).
coming
infusion
of
the
infusion
solution
(kg
kg
500g)
of
infusion
into
solution
container/bags
circulation
blood
from
the
pump
at a low
pump,
ifreguired,
from
the
is + 100
out.
pump
all
then
air
line
from
mmHg
when
has
clamp
to
the
DIFF)
the
infusion
in
should
line
arterial
initial
venous
the
been
it.
the
patient.
venous
in
solution
circuit,
excess
is
never
to
the
flow
and
line
and
let
blood
removed
line
kg
and
(kg
there
of
the
desired
20
litres,
exceed
patient.
line
and
rate
set
the
when
the
priming
reaches
from
and
hemofiltration
hun-
INF)
must
the
19
litres.
the
the
the
the
the
Start
11
12
Warning:
flow
to
to
weight
13
Select
14
15
Warning:
OmmHg.
16
hemofiltration
Start
the
infusion
rate
(otherwise
be
activated
automatically
Start
rate.
led
rates
start the
avoid
deviation
gain
Depress
ring
selected
solution.
Note:
settings
tioning.
on
page
Check
value.
Set
below
Set the
accordingly.
flow
order
when
the
filtrate
The
pump
by
the
selected
There
in
the
manual
infusion
or
loss
AUTO
the
first
weight
Check
correspond.
Discontinue
16
and
the
operating
that
the
venous
the
patient’s
The
lower
required
rate
before
to
prevent
pump.
Turn
the
buzzer
will
entering
be
controlled
is
no
and
of
the
before
(light
15
that
call
pump.
speed
will
TMP
control
mode.
filtrate
two
entering
on)
seconds
loss
and
the
data
If
not,
the
treatment
for
technical
AUTO).
when
Turn
when
of
flow
the
selected
on
the
values
the
blood
flow
pressure
alarm
TMP
It
is
the
alarm
stabilized
limit
and
important
TMP
hemoconcentration.
the
knob
sound
and
the
The
pump
AUTO
the
automatically
the
It
is
pumps
rates
the
-ERROR
display
is
knob
AUTO
infusion
therefore
at
max
and
consequent
AUTO
(light
will
quantity
the
display
and
patient
data
selector
according
service.
rate
is
at
the
limits
just
venous
should
set
to
is
set
the
have
to
alarm
the
pressure.
never
sufficient
desired
to
max
flow
heater
will
not
speed
will
depressed.
to
max
flow
be
control-
is
depressed.
and
filtrate
recommended
flowrate
mode.
off).
Du-
indicate
the
to
the
required
above
the
of
infusion
selected
is
malfunc-
procedure
and
be
set
below
limits
blood
valuein
|
Note:
It
is
of
touched
during
and
the
machine
weight
loss
already
procedure.
Ifa
mains
power
data
are
stored
reprogram
the
Changing
During
weight
1
2
3
the
treatment
loss.
Release
Setthenew
not
otherwise
Depress
During
new
solution.
Check
data
As a safety
and
1
During
registered
continuously
If
minutes
AUTO
be
set
the
selected
that
on
the
filtrate
minute.
this
the
infusion
delay
the
utmost
treatment.
will
restart
obtained.
failure
occurs
for
10
minutes.
treatment
the
data.
weight
(light
weight
below
the
the
patient
AUTO
The
and
(light
first
15
weight
buzzer
the
display
thumb
precaution
pumps
stop
manual
mode
included
show
the
and
filtrate
before
the
importance
If
this
happens
the
treatment
To
reset
during
After
it
is
possible
off) - ERROR
loss
desired.
weight
will
on)
seconds
loss
and
will
corresponds
wheels.
the
buzzer
if
AUTO
the
in
the
accumulated
pumps
AUTO
Changing
that
MAIN
the
without
see
restart
treatment
10
minutes
loss
to
change
The
loss
already
get
reinfused.
-ERROR
the
display
the
quantity
sound
for 5 seconds.
will
sound
is
not
infusion
treatment
and
weight
are
turned
alarm
data.
SWITCH
programme
counting
and
the
it
is
(light
weight
achieved,
(light
will
with
and
reactivated
filtrate
The
loss.
off
will
be
parameters
will
be
the
weighing
actual
treatment
necessary
the
of
the
the
there
activated.
to
selected
on).
loss
should
off).
indicate
infusion
selected
infusion
within
flow
rates
display
will
is a 10
is
not
reset
the
are
during
Changing
Itis
also
possible
fusion
solution
cedure
above.
Restart
一
N
©
AB.
a
©
M
O
9
10
11
12
and
Read
and
Switch
off
SWITCH
Release
pumps.
Remove
fusion
scale,
Switch
SWITCH
occur.
Wait
until
error
code
Press
the
the
display.
Hang
up
scale.
The
display
solution.
Reprogram
the
patient’s
Turnon
Depress
treatment
the
quantity
to
change
during
the
treatment
weighing
record
the
weight
the
machine
(light
off).
AUTO
the
on
symbols)
the
AUTO
infusion
do
the
machine
(light
the
count-down
TIME
the
infusion
will
Kg
weight
infusion
and
turn
container/bags
not
touch
on)
and
has
ended.
button
now
INF
and
loss).
and
(light
of
infusion
the
selected
quantity
following
procedure
loss
on
the
by
releasing
off
the
infusion
the
filtrate
by
depressing
reset
any
alarm
on
the
display
(light
on):
0.015
container/bags
indicate
on).
the
Kg
DIFF
filtrate
pumps.
quantity
(with
solution
of
the
pro-
display.
MAIN
and
from
the
container.
MAIN
which
(0—9and
now
shown
on
the
infusion
of
respect
in-
filtrate
in-
may
on
infusion
to
14
10
Start
rate.
the
blood
pump
and
set
the
required
blood
flow
17
Recheck
cuits,
with
warm
Warning:
No
initiated.
as
all
the
red
connections
material
infusion
lights
solution
should
can
in
the
expand
and
be
lit
blood
due
blood.
when
and
fluid
to
the
the
treatment
cir-
contact
is
15
Discontinuing
1
If
the
Note:
volume
2
heparin-protamine
the
pump
at
the
treatment.
When
the
desired
obtained,
by
-
~
—
—
has
Turn
and
filter.
Turn
line
Release
Move
pressure
Adjust
0mmHg.
Turn
the
following:
AUTO
the
buzzer
the
infusion
the
filtrate
The
treatment
been
off
clamp
off
leading
the
the
off
the
treatment
blinks
sounds
pump
is
attained.
the
filtrate
the
the
infusion
to
AUTO
alarm
meter
lower
the
blood
prescribed
weight
pump
considered
filtrate
the
venous
(light
limits
apart.
venous
loss
should
stops
stops.
pump.
line
pump
blinks)
on
pump.
pump
has
time
before
and
infusion
be
terminated.
finished,
pressure
when
Set
TMP
coming
and
clamp
drip
chamber.
-ERROR
the
transmembrane
been
volume
the
at
out
of
alarm
used,
stop
finishing
have
been
This
is
indicated
preset
infusion
100mmHg
the
hemo-
the
infusion
(light
on).
limit
to
the
hemofiltration
Return
7
8
10
11
12
13
14
15
16
the
blood
Clamp
remove
Connect
physiologic
Invert
blood.
Start
flow
circuit.
Clamp
quate
When
turned
venous
patient.
When
Release
ary
fluid
the
it
the
the
rate
the
emptying
the
to
line
the
tient,
depress
to
reset
to
be
started
Remove
lines.
pulling
Remove
out
arterial
from
the
arterial
solution.
hemofilter
blood
to
remove
venous
required
the
and
blood
MAIN
the
and
Disarm
the
the
infusion
blood
line
the
patient.
blood
to
facilitate
pump
and
the
blood
line
repeatedly
of
the
hemofilter.
amount
patient,
AIRDET.
immediately.
discard
stop
cannula
lines
SWITCH
programme
sensor
and
are
disconnected
BYPASS
the
hemofilter,
the
arterial
plate.
and
and
line
to
set
the
from
of
blood
the
blood
disconnect
(light
even
pressure
the
filtrate
the
cannula
at
least
100
ml
the
rinse-back
desired
off).
ifa
rinse-back
the
extracorporeal
to
facilitate
has
been
pump,
clamp
it
from
from
the
(light
on).
This
is
necess-
new
treatmentis
blood
lines
alarm
containers/bags.
and
of
of
ade-
re-
the
pa-
and
by
the
General
The
AK-10
three
operational
Clinical
detection,
button
lit.
Ifa
ERROR
will
be
assistance.
Clinical
monitors
conditions — clinical
faults.
alarms,
will
and
the
deviation
indicator
displayed
Alarms
are
designed
alarms,
caused
result
indicator
occurs
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indicator
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will
blink.
staff
should
indicator
operator
can
there
button
An
error
be
informed
on
the
should
indicate
take
technical
tests
its
own
will
be
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audible
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be
lit
and
code
will
be
of
this.
hemofiltration
some
action.
function.
alarm,
the
ER-
displayed
monitor
16
ALARM
AIRDET.
ARTER.
VENOUS
BLOOD
TEMP.
TEMP.
TMP
TMP
ERROR
FLASHING
*Not
(high)
(low)
on
all
LIGHT
RESET | x
PRESS.
PRESS.|
LEAK
(high)
(low)
AUTO]
models
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17
Blood
In
analarm
patient
MUTE
if
the
Take
lit.
1
AIRDET.
clamps
lines.
the
the
Press
2
ARTER.
clamps
lines*.
between
by a fall
of
between
before
to
silence
fault
is
the
following
The
venous
air
from
AIRDET.
the
the
arterial
situation,
taking
the
not
rectified
steps
RESET
close
on
alarm
is
drip
chamber.
the
venous
RESET
PRESS
close
on
The
alarm
patient
and
in
the
patient’s
needle,
the
patient
first
check
any
other
buzzer.
the
activated
the
is
The
within
according
(red
light
arterial
if
After
drip
until
(red
light
arterial
activated
the
blood
blood
or a kink
and
the
the
connections
steps.
Then
buzzer
will
approximately
to
which
on).
AU
pumps
and
venous
there
is
too
much
rectifying
chamber
on).
by
an
pump.
pressure,
arterial
the
using a syringe.
the light
All
pumps
and
venous
increased
This
in
the
arterial
pressure
press
sound
alarm
blood
air
fault,
goes
stop.
blood
negative
may
altered
to
again
30
seconds.
lightis
stop.
or
foam
remove
off.
The
pressure
be
caused
position
line
pillow.
Monitor
the
The
in
[en
alarms
3
VENOUS
a)
b)
By
pressing
forced
occured.
*Not
BLOOD
LEAK
E
2
]
©)
K 2
PRESS
Too
high.
an
increase
ble
alarm
tion
of
the
change
Toolow.
the
arterial
is
activated
lower
adjustable
a
leaking
the
venous
blood
pressure
tion.
VENOUS
to
run
on
all
models
る
(red
All
pumps
of
the
venous
limit.
This
venous
in
the
patient’s
All
pumps
and
venous
by a decrease
alarm
or
separated
drip
chamber, a fall
or a change
so
as
to
determine
light
on).
stop.
pressure
may
be
line
after the
position.
stop.
in
the
limit.
line,
PRESS.
The
above
caused
drip
The
blood
venous
This
may
an
obstruction
in
in
the
the
blood
why
the
alarm
is
activated
the
upper
by an
obstruc-
chamber
clamps
lines*.
pressure
The
below
be
caused
the
patient’s
patient’s
pump
alarm
by
adjusta-
ora
close on
alarm
the
by
before
posi-
can
be
has
4
TEMP.
a)
Too
high.
the
heater
tion,
both
temperature
activated
infusion
still
given
hemofiltration”
b)
Toolow
on.
~
The
heater
activated.
—
Low
temp
too
low
heater
de
whether
5
BLOODLEAK
clamps
lines.
presence
а)
Smallleaks:
10
and
the
transmembrane
leak
usually
Remember
original
transmembrane
b)
Major
risk of
At
this
her
or
Ifthe
with
"Discontinuing
structions
It
may
the
blood
the
light
the
sensitivity
ALARM
by a kinked
pump
after
(no
temperature
malfunction. A medical
close on
If
the
of
press
(red
light
The
infusion
is
turned
pumps
in
or a malfunction
buzzer).
is
The
alarm
the
leak
blood
Turn
BLOOD
off.
will
run
the
heater
infusion
15
minutes
and
call
No
turned
on
low
temp
when
of
treatment
(red
light
the
arterial
is
not
immediately
with a separate
up
the
LEAK
on).
and
(To
intermittently
is
line, a temporary
for
reaction
when
alarm
AUTO
incoming
should
on).
sensitivity
pressure
seals
itself
within
to
turn
the
sensitivity
position,
leaks:
contamination
point a medical
not
to
blood
be
necessary
leak
does
It
return
is
to
1—13.
detector
not
go
control
increase
pressure.
is
important
be
off
knob
the
from
decision
the
blood
returned
hemofiltration”
to
remove
in
order
when
BLOOD
is
set
Hemofiltration
filtrate
rectify
correct).
in
the
carry
technical
the
All
and
(light
and
approx. 5 minutes.
blood
to
the
filtrate
to
to
the
the
at
position
pumps
the
alarm
until
The
alarm
stop
heater.
If
the
out
""Discontinuing
service.
except
AUTO-mode
will
is
activated
infusion solution
decision
be
red
then
disappear.
must
continued
pumps
venous
visible,
test.
knob
off).
By
blood
flow
knob
back
flow
rate
consider
must
the
to
the
compartment.
be
made
patient.
patient
on
page
drip
chamber
start
the
LEAK
10).
stop,
condi-
the
might
of
the
alarm
is
light
is
indicates
or
be
ma-
or
not.
stop
and
blood
verify
the
to
position
decreasing
rate the
to
the
and
the
possible
whet-
proceed
16,
in-
from
pumps
is
(if
pressed and
monitor
be
alarms
Ifthe
blood
is
not
with ” Discontinuing
structions
Change
filtrate
Make
the
Carry
mofiltration”
instructions.
Note:
procedure
the
memory.
Ifthe
weighing
TMP
a)
Too
activated
above
caused
b)
Toolow.
and
filtrate
protector
pressure
MUTE
a)
position
turning
b)
having
Activate
twice
C)
The
stopped.
out
nical
1—6.
the
hemofilter
line.
The
sure
to
use
venous
drip
out’
Priming
The
machine
as
the
machine
procedure”
ALARM
high.
by
the
upper
by a blockage
chamber
on
patient’s
is
(red
The
an
No
MUTE
sounds.
transmembrane
limit.
This
buttons
The
may
pump,
not
connector.
(red
light
on,
The
infusion
The
AUTO
when
the
started
the
to
reset
rate
the
rate
mode
the
AUTO
the
microprocessor
Note
the
”Discontinuing
service.
to
be
returned
hemofiltration”
and
infusion
an
page
should
switched
circuit
aseptic
connection.
procedure”
14,
following
not
treatment
off
on
page
light
on).
filtrate
increase
in
the
adjustable
reaction
alarm
before
except
are
alarm
is
activated
pressure
being
below
be
caused
or
the
filtrate
properly
the
buzzer
control
knob
AUTO
machine.
alarm.
mode
control
is
not
activated
mode
in
the
hemofiltration
error
code
hemofiltration”.
to
the
patient
on
if
required,
technique
be
switched
parameters
follow ” Restart
15,
pump
transmembrane
the
lit
and
the
by
blood
is
not
to
when
and
’’
Initiating
the
appropriate
off
instructions 1 —
stops.
limit.
This
filtrate
the
TMP
the
by a decrease
lower
adjustable
an
air
leak
pressure
connected
sounds).
is
not
turned
is
activated.
knob
to
max
within
10
or
press
MAIN
monitor
if
possible
proceed
page
16,
in-
lines
and
be
removed.
handling
he-
during
this
are
banked
in
and
12.
The
alarm
is
pressure
may
be
pump.
ALARM
buzzer
in
the
alarm
before
the
transducer
to
the
on
or
is
in
min
Reset
by
position.
mintes
after
SWITCH
has
and
carry
Call
for
tech-
18
AUTO
filtrate
Carry
(blinking,
pumps
out
the
buzzer
stop.
The
treatment
”Discontinuing
hemofiltration”.
sounds).
The
has
infusion
finished.
and
19
Error
General
MUTE
is
а)
b)
is
lit,
blinking
or
Steadily
The
alarm
which
may
Note
the
TIME
layed
on
Blinking
The
alarm
Note
the
Carry
for
technical
the
buzzer
sounds
steadily
lit
error
buttons
the
lit.
ERROR
indicates a fault
be
caused
by a handling
code:
By
simultaneously
hemofiltration
ERROR
indicates a technical
error
code
as
out
’Discontinuing
service.
and
the
ERROR
in
the
gravimetric
mistake.
pressing
mentioned
the
UF
the
error
monitor.
fault.
in
pointa).
hemofiltration”
indicator
weighing
RATE
code
is
and
system
call
and
disp-
alarms
Error
Alarm
The
amount
sion
solution
into
the
been
within
30—300
during
code
condition
г
> >
/
tl
of
infused
patient
the
ml/min
the
last
infu-
has
not
limits
160
sec.
Reason
1
Runningin
1
The
infusion
2
Noinfusion
tainer/bags
Operation
manual
solution
line
mode
is
kinked.
in
the
con-
action
Action
Ifready
activate
Ifnot
alarm
Check
out
the
Discontinue
gard
on
the
table
to
initiate
the
ready
function
all
the
kink.
to
whether a new treatment
same
the
treatment
AUTO
press
lines
hemofiltration.
day.
MAIN
for
another
in
mode.
the
infusion
SWITCH
press
10
minutes.
circuit
Contact
should
AUTO
twice
to
reset
and
straighten
physician
be
performed
to
with
the
re-
Caution
After
having
the
alarm
approx. 5 minutes
the
alarm
supervised.
within
rectified
condition
is
maintained,
Ifthe
45
minutes,
the
will
automatically
(buzzer
alarm
(
carry
fault
caused
off,
lights
off).
the
patient
LI
orli
out
”Discontinuing
by
wrong
be
corrected
However,
must
be
я } does
handling
within
whilst
carefully
not
stop
hemofiltration”,
The
has
not
30—300
during
=
Lit
filtrate
flow
been
ml/min
the
last
rate
within
limits
160
the
sec.
3
Theinfusion
4
The
container/bags
hanging
1
The
filtrate
2
The
filtrate
in
the
filtrate
3
The
filtrate
4
The
container
hanging
free.
line
drain
pump
free.
pump
is
not
are
is
kinked.
line
container.
is
not
is
not
running.
not
is
not
placed
running.
Check
that
the
segment
Ifnecessary,
infusion
Make
Straighten
Place
much
patient’s
of
Check
less
on,
there
exchange
Make
sure
the
filtrate
the
patient’s
the
than
that
is
no
sure
is
correctly
pump.
that
out
drain
weight
preset
30
the
pump
kink.
the
pump
call
for
the
container/bags
the
kink.
line
was
lost
loss
weight
TMP
ml/min.
segmentis
Ifnecessary,
filtrate
that
the
is
switched
inserted
technical
in
(amount
Check
pump.
container
and
the
filtrate
and
ifnecessary
loss).
value.
that
correctly
call
on,
that
service
are
container.
of
lost
At
TMP=0
the
pump
for
is
hanging
that
the
pump
there
is
no
kink.
to
exchange
hanging
reprogram
filtrate = decrease
the
is
inserted
technical
free.
the
free.
Note
how
the
UF
rate
switched
and
that
service
is
to
21
Operator
Jf
loss
the
Reason
1
The
kinked.
2
The
infusion
not
running.
3
The
protector
filtrate
onthe
infusion
filtrate
is
pressure
HFM.
line
is
pump
pressure
not
connected
connector
is
transducer
Error
Alarm
code
condition
a
„LI
Linearity
a)
The
patient’s
weight
more
ted
value
of
selected
the
selected
is
less
alarm
calculated
200
g.
b)
The
patient’s
weight
than
500 g/15 min.
for
the
c)
The
patient’s
weight
than
selected
DIFF
alarm
loss
than
plus
weight
than
2.0
limit
value
loss
first
loss
plus
门
is
calcula-
10%
value.
kg,
is
set at
plus
is
more
hour.
is
more
kg
0.5
kg.
to
the
action
Action
Straighten
see
Connect
filtrate
When
alarm
having a higher
pump.
Supervise
reprogram.
patient.
table
out
the
kink.
/
İLİ | Actionon
the
pressure
the
fault
condition
ㆍ
filtrate
pressure
connector.
is
rectified
and
compensate
flow
rate
the
patient
Ifnecessary
the
in
during
page
21
transducer
HFM
for
the
infusion
the
IV
solution
will
automatically
the
patient’s
pump
alarm
can
protector
correct
excess
weight
than
in
the
filtrate
condition.
be
given
to
to
Do
the
loss
not
the
the
by
Error
Alarm
code
condition
—
L
Total
amount
a) A weight
of
more
on
the
scale
compared
the
tared
b)
Aweight
on
the
infusion
scale,
compared
the
tared
more
than
grammed
ofkg
INF + 200g.
|
I
alarm
increase
than
100
infusion
value.
decrease
value,
the
pro-
amount
to
to
of
g
Reason
1
Extra
added
AUTO
1
Theinfusion
have
was
activated.
infusion solution
to
the
was
been
removed
Operator
has
infusion
activated.
container/bags
scale
after
AUTO
been
after
action
Action
Reprogram
the
amountof
Hang
having
automatically
table
the
up
the
rectified
amount
kg
DIFF.
infusion
container/bags
the
fault
corrected.
of
the
kg
INF
alarm
and
if
necessary
again.
condition
After
will
be
Linearity
a)
The
weight
than
lue
selected
the
selected
is
less
alarm
calculated
200
g.
b)
The
gained
300 g within
first
c)
The
ight
0.5
ring
after a reprogram-
ming.
22
1.
ceo
LI
4
tto
alarm
patients
loss
calculated
minus
10%
value.
weight
than
2.0
limit
is
value
patient
more
hour.
patient’s
gain
exceeds
kg/15
min
the
first
is
less
kg,
set
has
than
the
we-
hour
va-
of
If
loss
the
at
minus
du-
1
The
2
the
filtrate
30
ml/min.
The
into
filtrate
filtrate
the
line
flow
drain
filtrate
is
kinked
rate
is
more
line
is
container
but
not
than
placed
Straighten
When
the
fault
alarm
condition
by
having a higher
pump.
Supervise
Do
not
reprogram.
Place
the
this
case
it
weight
loss.
out
the
is
rectified
and
flow
the
patient
filtrate
may
drain
be
kink.
the
HFM
compensate
necessary
rate
in
during
line
for
the
into
will
automatically
the
patient’s
filtrate
pump
the
alarm
the
filtrate
to
reprogramme
7
see
Li
D
3
The
filtrate
pump
is
not
running.
Actionon
page
2!
correct
excess
weight
than
in
the
condition.
container.
for
less
the
gain
infusion
In
全
Total
amount
a)
Aweight
of
more
on
compared
tared
b)
Aweight
of
more
programmed
amount
+
kg
on
compared
tared
.
1.
alarm
decrease
than
the
filtrate
to
value.
increase
than
of
kg
DIFF + 200g
the
filtrate
to
value.
100g
scale
the
the
INF
scale
the
1
The
filtrate
removed
vated.
1
Something
the
AUTO
after
filtrate
was
container
AUTO
has
container
activated.
been
has
been
was
placed
after
acti-
on
Hang
up
the
filtrate
Remove
to
treatment.
condition
place
the
anything
offending
After
will
be
container
article
on
the
having
automatically
again.
and
filtrate
container
rectified
the
corrected.
make
sure
never
during
fault the
alarm
23
Technical
dor
EU
Operating
Blood
Heparin
Pressures
Air
detector
Power
Dimensions
Weight
principle
pump
pump
supply
Double-needle
circulation
Self-threading
adjustable
Flow
regulation
50-500
Roller
pump
required
Flow
regulation
0-10
ml/h
Arterial
Venous
Mains
Power
Cable
Mains
Fuses
Leakage
pressure
Pressure
pressure
Measured
Instrument:
mmHg
Ultrasonic
voltage
240, 220,
(Mains
frequency
running-time
Max.
100
length
Approx.3m
socket
Standard
for
220
V;
220V:
2*x0.63
110V:
2*x
*Forsome
current
30
LA
Depth:
{with front
Width:
Height: 190
13kg
or
using
roller
occlusion
ml/min
for
protamine)
indicated
sensor
in
dripchamber
—200
detection
130,
110 V +10%;
meter)
W
earthed
ASA
for
ATT;
1.25
ATT;
countries 1 x0.63
400
mm
components
510mm
mm
data
single-needle
time
regulated
pump
indicated
two
plate
to + 400
must
socket; DIN
110
on
flow
lines
(heparin
on
regulating
with
microswitch
mmHg + 10%
at
dripchamber
50
be
specified
V
DINS5
x20
ASA6.3 x 22
450
ATT;
mm)
BMM
blood
clamps
instrument
and
when
knob
or
60
Hz
for
specifications
1.25
ATT
Alarm
Alarm
Sensitivity:
below
e
10-1
limits:
adjustable
limits:
adjustable
max.
300
The
electric
Classification
0.2 ml
ml/min
monitor
shock
is
protected
according
B.
—50
to
on
instrument
air/min
-500
mmHg
at
blood
」
against
to
IEC
601-1,
flow
Operating
Fluid
principle
balancing
Pressure/TMP
Temperature
Blood
leak
detector
Power
Dimensions
supply
Weight
Technical
Electronic
Pumps
Infusion:
Ultrafiltrate:
Infusion
Weighing
(including
Selectors
kg
Regulation
Oto
+
10%
Instrument
+
50
Alarm
limits
Adjustable;
Incoming
Transillumination
infrared
Mains
voltage
240, 220,
(Mains
running-time
Power
Approx.
Mains
socket
Standard
for
Fuses
220
DIN5x20
110V:
ASA6.3
*
Forsome
Cable
length
Approx.
Depth:
(with
Width:
Height:
23.5kg
feed-back
self-threading
self-threading
and
ultrafiltrate
range:
weighing
DIFF:
weight
500
mmHg
or + 10
to
-500
set
infusion
phototransistor
130,
frequency
400
earthed
220
V;
ASA
V:
2* x 0.63
2*«
1.25
x32
countries 1 x0.63
3m
400
mm
front
components
510mm
190
mm
meter)
W
data
control
scales
0—35
arms
loss
(0
to
66
mmHg
mmHg
(+7
with
two
solution:
of
the
110 V +
must
socket;
for
110
V
ATT
and
ATT
and3.0
roller
pump
roller
pump
kg
and
containers)
kPa)
(1.3
kPa)
to
~66
kPa)
indicators
min.
15°C
ultrafiltrate
10%;
50
or
be
DIN
1.6
450
60
specified
specifications
AF;
AF;
ATT;
1.25
mm)
HFM
towards
Hz
for
ATT
10-1
Flow
rate:
with
tube
Flow
rate:
with
tube 6 x
Overload
Weighing
suit
most
kg
INF:
Heated
Sensitivity:
sensitive
The
electric
R
Classification
0/approx.
6x
1.5
dia.
0/approx.
1.5
dia.
protection:
arms:
different
types
of
quantity
infusion
adjustable;
position
monitor
of
solution:
is
shock
20—200
20-200
mechanical
types
containers
infusion
solution
35—40°C+1°C
10
steps;
10
protected
according
B.
ml/min
ml/min
available
least
against
to
IEC
601-1
to
26
Contents
General
C
Field
Special
¡ÓN
Signal
Technical
description
Temperaturecontrolandalarm.............................................
Pressure
Infusion
Ultrafiltrate
Bloodleakdetection.............................
Buzzeralarm..........................
Weighing
210
Power
Resetting
Alarm
Removing
Removing
Removing
Changingtheprintedcircuitboards.......................................
Removing
Changingthefan............................
Adjustinggthepumps............................
Changing
Changingtheloadcells..................................
Changingthevoltage............................................
Changing
Technical
Connections
Checking
Adjusting
Adjusting
Adjusting
Adjusting
Adjusting
Adjustingthebloodleakdetector......................
Zeroingtheweighingamplifier................................
Calibrating
Adjusting
Adjusting
monitoring
pump
pump
systemm
minutes”
supDy
сИсиИ$.. 이 니
1ist.
erene
service...............
thecover......................
the
the
the
thepump
the
adjustments
aids.
voltages,boardl.................................................
the
the
the
the
the
the
the
the
list.
data
and
control...
control...
Lube
control
i
eee
に に ユー
alarm
eee
이 이 이 아 아 아 아
還
instrument
front
panel..................
rear
section.
motors...................
signal
lamps............................................................
.Ne
Lie
e
cece
cece
temperature
temperaturcalarmcircuit.....................
pressure
pressure
TMP
weighing
load
pump
transducer........................................................
monitoring
alarm
system...........................
limits
eee
motor
トト
トー
トト
トト
トト
トス
0000000000000
아 아 아 아 이
panel...............
ϱϱϱϱϱᾖᾗὀὀϐβϱϱϱϱϱϐϱ-------Ἂ-
eee
eet
teen
control
delay.
circuit
circuits....................................,.........
e
circults.
이 아 어 아 리 리 어 며 러 이 어 이 이 아 어
eee
i
esere
eee
eee
enn
EEE
EERE EERE
トト
トト
トト
スト
er
DEERE
ez
eee
PKP P P K PKP P R K PKP P PK K R
ses
スト < トレ
eee
EERE
P
KP K K
トピ
ピー トト
トト
トート
리 여 아 아 아 이 이
EE
EG
ESE
EEE
EE
EE
een
ee
eee
P K 0 P R P en
et
nnenneee
onen
ーー
이이
ечинннь
0.0
OEE
EE
EES
ené
ーー
ee
nn
PK
né
Kn
ων
て
10
12
14
16
18
20
22
24
25
25
25
25
26
26
26
26
27
27
27
27
28
28
29
29
29
29
30
30
30
30
31
31
32
32
32
35
36
2
4
6
8
HC
E6911,
Rev.
02.1985
General
The
nitor
ent
at
drawn
The
function
the
infusion
of
the
infusion
hemofiltration
from
the
is
flow
patient
heated
hemofiltration
to
and
through
before
description
the
to
control
blood
the
it
is
monitor
stream
and
added
is
to
returning
monitor
hemofilter.
to
the
control and
to
the
the
ultrafiltrate
blood
stream.
mo-
pati-
The
transmembrane
nitored
and
alarm
limits
rature
and
hemofilter
errors.
pressure
maintained
can
undertemperature
and
certain
at a settable
be
set.
weighing
(TMP)
Alarm
in
across
level.
is
also
the
heater,
and
microprocessor
the
hemofilter
Both
given
blood
lower
at
leakage
is
mo-
and
upper
overtempe-
in
operating
the
Treatment
quantity
tinuosly
over
to
on
rate.
Infusion
is
values
shown
show
heater
automatic
and
selection
on a display.
calculated
To
air
detector
\
after
setting
of
The
remaining
of
weight
AUTO.
display
treatment
Infusion
The
can
weight
time
pump
loss
and
infusion
loss
also
be
switched
or
ultrafiltrati-
Blood
is
con-
Teak
The
detector
operating
Instrument
function
panel
is
made
clear
in
the
Ultrafiltrate
operator’s
pump
manual.
Instrument
panel
Ultrafiltrate
pump
motor
Infusion
Infusion
Infusion
pump
heater
load
mot«
cell
From
hemofilter
=
Infusion
scales
Ultrafiltrate
scales
Ultrafiltrate
load
cell
Board
“10
minutes
7
“alarm
Fan
Board
|
Power
supply
Board
2
Control
Board
Microprocessor
Board
Weigh
Board
Infusate
Board
Ultrafiltrate
logic
3
4
electronics
5
pump
6
pump
Mains
control
control
power
HC
E-6911,
Rev.
02.1985
HC
E-6911,
Rev.
02,1985
Temperature
ーー
|
|
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Rear
socket
・
| |
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Diagram
There
ducer
The
regulating
bridge
from
on
board 2 and
microprocessor.
potentiometer
to
the
(zero)
1
are
two
types
and a regulating
board
(TR
the
bridge
on
microprocessor.
and
addressed
of
temperature
transducer.
transducer
S!).
The
is
amplified
an
analog-digital
The
range
the
front
The
by
P1B5-7
in
the
heater-handle
bridge
and
is
set
panel,
analog
from
transducers.
is
zeroed
fed
through
converter
by
R24,
From
TMSV
is
selector
the
microprocessor.
An
is
by
R20.
an
on
board 3 to
the
fed
in
is
selected
alarm
connected
The
analog
selector
temperature
the
same
by
trans-
to
output
the
way
P1B4
|
Board
2
The
microprocessor
HENI
through
mains
a
power.
heater
in
pulsed
pending
also
controlled
sor
(speed
If
the
infusion
wise)
from a zero
switched
the
buzzer
series
to
turn
on
off
the
control
and
sounds.
compares
the
I/O
The
opto
with
the
heater
temperature
by
infusion
signal
potentiometer
position
in
AUTO
Mains
from
diagram
一
一
E
q
一
一
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normally
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then
L
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relay
1
7
一
|
|
|
|
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=
the
on
board 2 to
connects
for
longer
deviation.
flow
information
see
is
not
in
manaul
mode
the
TT
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|
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two
values
the
activated
or
shorter
The
Infusion
turned
mode
heater
Como
and
the
opto
mains
relay
pulsing
in
the
pump
far
enough
is
switched
Mains
issues
voltage
K3.
intervals
of
microproces-
the
PITA,
mí
|
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power
|
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7
signal
relay
in
the
to
HENI
de-
HENI
control).
(clock-
heater
is
off
and
Heater
the
is
is
TEMP
ALARM
Temperature
potentiometer
Infusion
heater
Safety
switch
m
There
are
two
1.
Software
The
microprocessor
blood
lead
(BLAO),
pressure
(DPAO),
exceeds
processor
lights
makes
low
tervals)
rotates,
2.
The
heater
second
potentiometer
the
lights
rature
above(
too
or a sensed
42°C.
turns
up
the
HENI
42°C
the
until
the
Hardware
alarm
and
input
comparator
the
TEMP
goes
1).
transducer
connected
below
types
of
alarms:
alarms.
turns
air
in
low
(APAO),
temperature
In
the
last
case
PC7
to
be
TEMP
ALARM
high,
stops
pump.
infusion
the
microprocessor
alarms.
to
pump
temperature
is
placed
to a comparator
the
comparator
R19.
If
the
issues a zero,
ALARM
42°C,
the
sensed
the
heater
blood
(temp
an
outport
lamp,
rotates
goes
turns
lamp,
infusion
Rear
off
circuit
venous
by
the
more
and
switches
After
the
at
least 5 x
below
PC7
to
adjacent
on
is
set
to
the
temperature
which
deactivates
stops
pumps.
pump
socket
at
five
different
(ADAO),
pressure
regulating
than
42°C)
deactivates
on
temperature
37°C.
be
an
to
the
board 2 (TS
equivalent
exceeds
After
works
arterial
out
transducer
the
the
buzzer,
1/2
rev.
When
outport.
handle
of
this
the
the
as
alarms:
of
limits
micro-
relay
K3,
goes
be-
(with
in-
the
pump
in
the
S1).
The
42°C
by
value,
relay
K3
tempe-
described
Board
3
The output
processor
The
regulating
alarm
is
amplified
ALARM
the
relay
safety
and
ultrafiltrate
The
heater
series
overheating
automatically
through
signal
lamp.
is
also
switch
for
220 V or
from
the
transducer
in
case
and
fed
deactivated
opens,
pumps
is
divided
guard
resets
Board
comparator
the
I/O
the
temperature
to
the
The
(see
up
in
in
paralell
which
breaks
when
2
circuit.
circuit
when
open
two
the
Mains
is
also
input
also
issues
goes
comparator
the
heater
safety
switch
diagram 3 and
elements,
for
110
V.
the
supply
element
has
power
to
the
low
below
34°C.
lighting
is
pulled
stops
4).
which
are
Each
circuit
cooled
the
micro-
temperature
the
up
the
out
the
infusicn
connected
element
at
75°C
down.
signal
TEMP
and
has
the
in
an
and
HC
E-6911,
Rev.
02.1985
HC
E4911,
Rev.
02.1985
Pressure
|
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Board
Board
2
3
Diagram
The
ultrafiltrate
amplifier
the
where
and a venous
Trimmer
Omm
venous
R25
pressure
serving
transducer,
it
is
added
R23
Hgultrafiltrate
pressure
is
used
2
pressure
asa + 10V/-5 V dcconverter.
NPTS
to a zero-setting
pressure
is
used
signal
to
adjust
transducer
is
amplified
signal
VEPA/VEPB.
to
set
the
pressure.
the
instrument
and
voltage
output
Trimmer
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fed
fed
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of the
R26is
at
the 0 mmHg
with
-5 V from
The
output
the
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NPTS
amplifier
used
to
from
point,
adjust
venous
an
at
the
The
summed
meter.
The
ultrafiltrate
microprocessor
digital
potentiometer
selector
microprocessor
the
ultrafiltrate
tive
of
voltages
converter.
is
selected
changes
and
through
In
on
the
by
will
pump
in
the
are
amplified
venous
the
the
same
front
P1B4
compare
to
keep
venous
pressure
in
analog
way
panel
to
and
addressed
set
and
the
TMP
pressure.
further
signals
selector
TPSV
is
the
microprocessor.
by
actual
at
the
and
are
and
fed
from
P1B5-7.
values
set
HC
E-6911,
fed
also
value
to
the
fed
the
analog-
the
The
and
control
irrespec-
Rev.
TMP
to
the
TMP
The
02.1985
in
HC
E-6911,
On
the
electronic
brane
pressure)
low.
The
through
gram
6).
The
upper
filtrate
Rev.
06.1984
meter
sensors,
signals
an
limit
pump
there
is
too
are
OR
gate
signal
(diagram
are
two
one
giving
high,
inverted
and
is
also
4).
alarm
the
and
to
fed
limit
PRAH
other
fedtothe
the
buzzer
to
the
indicators
when
PRAL
TMP
alarm
stop
circuit
TMP
when
with
(trans
TMP
ALARM
circuits
for the
opto-
mem-
is
too
lamp
(dia-
ultra-
Infusion
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|
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pump
control
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circuit
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Rear
socket
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motor
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sure
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leakage
pulled
the
of
BPMS
so
(BLAO)
out
drivers.
the
motor
ceases,
that
the
Board
3
Board
5
Board
7
Rear
socket
When
AUTO
is
can
be
stopped
either
from
or
at
air
venous
and
(TPMS).
For a quick
windings
the
stop
motor
does
at
the
detection
pressure
infusion
The
signal
stop
through
circuit
not
start
any
time
by
the
microprocessor
(ADAO),
temperature
enters a stop
this
are
out
of
limits
results
the
diodes
current
in a rush.
insufficient
in
limitation
BPMS
signal,
when
treatment
arterial
(DPAO),
above
circuit
short-circuiting
V1
42°C
which
and
in
blood
or
V2.
the
acts
drivers
which
is
pres-
heater
on
of
two
When
cuit
to
the
microprocessor
sion
potentiometer
zero
position
the
buzzer sounds. The
Signal
digital-analog
on
board
addressed
is
completed
MCV/T
2.
by
in
is
The
P1B5-7
the
selected,
AUTO
then
converter
out
signal
to
select
is
not
turned
mode
then
microprocessor
derived
analog
microprocessor
on
from
from
board 3 and
selector
the
AUSW
is
fed
through
automatic
far
enough
the
the
is
microprocessor.
will
(clockwise)
heater
is
lights
microprocessor
the
out
selected
cause
the
control
switched
the
AUTO
analog
by
P1B4
When
lamp
the
I/O
if
the
infu-
from
off
lamp.
through
selector
(one)
treatment
to
blink.
cir-
a
and
a
and
Diagram
3
When
the
infusion
zero
position, a switch
windings
windings
The
stead
Hall
R10.
of
are
motor
by
Hall
elements
PS01-04
the
infusion
each
has
no
elements
are
from
pump
speed
connects
pump
connected
mechanical
which
fed
with
the
Hall
potentiometer
+28 V to
motor.
The
to
their
own
commutator.
sense
the
position
+12 V (HESV)
elements
control
is
turned
one
end
other
driver.
It
is
of
and
the
HC
E-6911,
from
of
the
ends
of
the
controlled
the
rotor.
balanced
drivers.
Rev.
02.1985
the
four
in-
The
with
The
speed
of
signal
MCVI.
on
the
drivers.
ugh
the
drivers.
current.
automatically
HC
E6911,
In
Rev.
case
the
motor-
The
The
In
of
makes
02.1985
i.e
indirectly
signal
is
fed
regulating
case
of
momentary
prolonged
repeated
the
flow-
to a regulating
circuit
also
senses
overloading
overloading
attempts
it
at
is
regulated
circuit,
the
current
stops
the
starting.
which
it
limits
motor
by
the
acts
thro-
the
but
In
manual
converter-
POT],
and
the
heater
MCVI
from
turned
far
mode
then
Signal
AULA
gram
8).
mode
the
POTI
microprocessor.
transfering
is
on
quick
enough
the
heater
is
it
to
the
microprocessor
changes.
(clockwise)
is
switched
also
fed
to
signal
is
The
microprocessor
the
regulating
If
the
infusion
from a zero
off.
the
’’10
fed
to
analog
stage
filtrates
minutes’’
selector
is
only
copying
as
MCVI.
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to
potentiometer
position
alarm
in
board
in-A/D
When
prevent
is
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manual
(dia-
Blood
leak
detection
Blood
leak
detector
diz
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leak
detector
Sensitivity
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signal
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unit
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timer
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timer
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LEAK
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pump
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locked
gate
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reset
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fluid
causes a lower
on
board 2 and
signal
BLSV
occurs
the
comparator
lamp
is
lit.
the
timer
microprocessor
stop
circuits
stop
and
by
its
own
keeps
the
and
the
lamp
button.
signal
fed
to a comparator,
from
the
sensitivity
output
output
gets
for
heater
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arterial
and
output
acting
BLOOD
LEAK
extinguished
level
BLUD.
potentiometer.
gets
high
high,
i.e
the
switch-off
4)
and
to
venous
line
clamping.
through a NAND
lamp
lit.
by
depressing
HC
E-6911,
The
which
and
the
timer
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the
blood
ga-
the
Rev.
is-
06.1984
HC
E-6911,
Rev.
06.1984
Rear
socket
Y
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Board
2
13
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alarm
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At
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the
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At
TMP
out
of
can
be
set
by
From
the
microprocessor, a square
nostable
nous
square
be
tentionally
AUTOswitch
ting
The
microprocessor
system.
on
zero.
wave)
issued.
When
of a square
general
board
If
the
the
to
alarm
signal
i.e
at
limits,
R27.
2.
The
microcomputer
monostable
treatment
initiate
the
is
released
wave.
signal
for
later
BUZO
BLAO,
BUZO
monostable
output
is
finished,
alarm
the
microprocessor
BUZI
use
at
is
initiated
BUZO
will
be
wave
fails or
will
and
alert
from
the
connection
will
issued
P1B0is
will
then
issues
go
P4B1
the
blood
in
three
instances.
at
once
be
after a delay
fed
out
give
out a conti-
an
alarm(
high
and
BUZO
will
be
inhibited
operator.
continues
unit
is
input
of a central
E-6911,
HC
issued
which
toa
stops
After
genera-
to
alarm
Rev.
to
mo-
a
will
in-
the
the
02.1985
*
.
HC
E-6911,
Rear
socket
06.1984
Rev.
Board
2