Alcon Infiniti Vision System Operator's Manual

Manufacturer: Alcon 6201
U.S.A.
Produced
Alcon
15800
Irvine,
USA.
Laboratories,
South
Worth,
Freeway
Texas
By:
Laboratories,
Alton
Parkway
California
DNFI
Operator's
Inc.
76134-2099
92618-3818
MI
VISION
Manual
EU
Authorized
Alcon
Boundary
Hertfordshire,
United
CE
TI
SYSTEM
Representative:
Laboratories
Way,
Hemel
HP2
Kingdom
(U.K.)
Hempstead
7UD
Telephone:
FAX:
8065751606 905-2100-006
R,
B,
949/753-1393
800/832-7827 949/753-6614
CATALOG
TEXT
ONLY
NUMBER
Directive
93/42/EEC
©
Alcon,
Inc.
DATE
July
2009
September
REVISION
N
2009
R
Infiniti?
:-
ECN
20091225 - Initial
8065751606,
consoles
IP
20091528 - Add
Vision
MANUAL
NUMBER
feature,
and
and
System
8065751606
REVISION
software
the
note
Operator's
AND
DESCRIPTION
release
905-2100-006
version
23
gauge
on
text
RECORD
of
operator's
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Infiniti?
cover
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Manual
manual
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manual
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inspect
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catalog
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includes
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Vision
the
QIP
System
Ozil®
manual.
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and
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product
in
the
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Patent & Trademark
is a trademark
is a registered
is
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are
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END
USER
contains
of
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trademark
Micro
Medical
trademarks
LICENSE
software
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of
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Devices,
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licensed
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IP
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8065751606
vii
PREFACE
This
operator's
available
apply
to
your
to
the
specific
manual
customer;
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unit.
your
written
therefore,
guide
to
the
reading
Infiniti?
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manual,
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ignore
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NOTE:
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If
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attention
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attention protect
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this
manual
to
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individuals
the
text,
to
highlighted
or
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carefully
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support
exists
supplied
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on-going
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Cautions,
from
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written
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want
additional
Services
Department
before
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meant
personnel
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with a consumable
bodily
to
protect
operating
to
restrict
should
the
process
and
Notes
harm. A Caution
the
information,
at:
Alcon
Irvine,
Laboratories,
15800
FAX
Alton
California
(949)
(949)
the
instrument.
the
surgeon;
be
experienced
instructions
pak
and,
as
such,
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this
manual. A WARNING!
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instrument
Parkway
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753-6614
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CAUTION:
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USS.
Federal
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LAST
this
PAGE
device
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to
sale
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or
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order
of a physician.
8065751606
ONE
INTRODUCTION
INTL
Alcon’s safe,
lens
handpieces. that along the
The
intended
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process
eye controls
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to
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salt
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and
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include a footswitch
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Vision
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and
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instrument
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8065751606
Figure
1-1
The
Infiniti?
Vision
System
11
GENERAL
INFORMATION
The
Infiniti?
require
simultaneous associated purpose: and every
to
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Infiniti?
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options:
ultrasonic
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control
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fluidic
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achieved
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and
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surgeon
the
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technology,
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of
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with
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power
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flow
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and
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and
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8065751606
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status
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Table
1-1
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maximum
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watts
and d is
meters
from
by an
less
than
range”.
may
marked
distance:
80
MHz
to
800
(W)
the
(m).
electromagnetic
the
occur
with
800
MHz
to
output
according
recommended
fixed
RF
compliance
in
the
vicinity
following
propagation
accuracy.
If
the
above,
than 3 V/m.
and
To
measured
the
(equipment
may
be
is
affected
land
mobile
access
field
necessary,
by
absorption
radios,
the
electromagnetic
strength
or
system)
such
in
as
re-orienting
MHz
2.5
GHz
power
rating
to
the
transmitter
separation
transmitters,
site level
of
symbol.
and
reflection
amateur
the
should
radio,
environment
location
be
or
to
the
as
survey’,
in
each
(0)
from
AM
in
which
observed
relocating
and due
the
to
15
Table
1-3
Rated
power
For
transmitters
be
estimated
transmitter
Note
1-
Note
At
2-
These structures,
Recommended
Equipment
electromagnetic
or
the
maintaining a minimum
(transmitters) output
maximum
of
transmitter:
AM
0.01
0.1
1
10
100
rates
using
the
in
watts
(W)
80
MHz
and
guidelines
objects,
and
user
of
and
power
china
outpui
at a maximum
equation
according
800
may
applicable
MHz,
not
and
the
of
to
people.
Separation
the
Infiniti?
environmentin
Infiniti?
distance
the
Infinit?
the
communications
0.12
0.38
output
power
to
the
the
apply
the
transmitter
separation
in
all
situations.
Distances
Vision
which
Vision
between
Vision
1.2
3.8
12 12
not
listed
frequency
manufacturer.
distance
Electromagnetic
Between
System - The
radiated
System
System
can
portable
as
equipment.
above,
the
of
for
the
the
recommended
transmitter,
higher
Portable
Infiniti?
RF
disturbances
help
prevent
and
recommended
according
A)
80-MHz
frequency
to
dep:
0.12
0.38
1.2
38
where P is
propagation
and
Mobile
Vision
mobile
800-MHZ
System
are
electromagnetic
RF
communications
below,
to:frequency-of.transmitter
di
RF
is
intended
controlled.
according
800
|
separation
range
is
the
maximum
applies.
affected
distance
output
by
absorption
d in
meters
power
NE
Communications
to
MHZ
d
and
for
use
in
The
customer
interference
eguipment
the
maximum
to
2.5
2.3YP
GHz
0.23
0.73"
23-
73
23
(m)
can
rating
of
the
reflection
from
an
by
1.6
8065751606
ON
FINE
WARNINGS
AND
CAUTIONS
Most
of
these
they
are
repeated
contact
There footswitch.
your
are
no
The
Infinit?
service
Good and
Ensure
Do result ardous
Inadvertent hazardous
engineer.
clinical
operation
that
not
exceed
condition
warnings
in
local
Alcon
user
serviceable
Refer
all
Vision
practice
as
the
tubings
maximum
exceeding
actuation
condition
are
stated
greater
service
System
Access
applicable
for
detail
service
by
dictates
are
capacity
drain
the
patient.
of
Prime
that
may
elsewhere
here.
If
representative,
components
issues
battery
untrained
testing
for
each
not
occluded
bag
maximum
or
result
to
your
WARNINGS!
can
only
for
handpiece
of
drain
Tune
in
in
this
manual;
additional
inside
factory-trained
be
personnel
adequate
during
bag
capacity
while a handpiece
patient
information
or
the
Technical
the
/nfiniti®
serviced
can
irrigation,
prior
any
and
injury.
lead
to
phase
however,
Vision
Alcon
by a factory-trained
to
entering
Excessive
potentially
is in
for
is
required,
Services
System
service
injury.
aspiration
eye.
of
operation.
result
the
eye
easy
Department.
console
engineer.
flow,
pressure
in a haz-
can
reference
please
or
Alcon
reflux,
can
create
a
Inadvertent shut
down.
If
the
handpiece
irrigation
turn,
Avoid
in a lower
If
the
Canada,
Keep from off,
Keep hair,
Aqualified
every
*
* *
In
case
flow
may
cause a shallowing
setting
irrigation
Infiniti?
it
should
clear
being
priming,
clear
of
and
/or
technician
twelve
Warning
Power Fuses
of a deficiency,
pressing
test
through
the
patientabove
Vision
be
of
the
IV
trapped
and
bottle
display
clothing
months:
Labels
of
Standby
chamber
the
handpiece
pressure
System
used
on a center-tapped,
pole
when
in
the
IV
height
base
when
from
being
must
(see
section
do
not
switch
is
collapsed
or
collapsing
the
FMS.
indicated
is
it
is
pole
mechanism.
adjustment.
raising
trapped
perform a visual
one
use
the
and
Operating
at
the
in
motion
display
at
of
this
system;
system
after
tuning,
may
result
of
the
anterior
with
the
on
the
display,
220V - 240V
240V
to
prevent
The
IV
from
the
base.
inspection
manual)
call
Alcon
is
active
there
in a fluidic
chamber.
patient
single
pole
stored
of
and
range
skin,
moves
the
Technical
above
in
phase
position
following
is a
potential
imbalance.
the
possible
the
United
circuit.
hair,
and/or
during
to
Services.
cause
FMS
underventing.
components
This,
will
States
clothing
power
prevent
of
low
result
on/
skin,
to
in
or
8065751606
A
qualified
twelve
EN60601-1/IEC601-1).
standards,
Technicai
technician
months
or
Services.
to
50%
ensure
Values
above
check
they
are
initial
ground
within
be
measurement,
the
recorded,
continuity
applicable
and
if
do
not
for
leakage
standards
are
use
the
above
system;
current
(for
example:
the
applicable
call
every
Alcon
17
WARNINGS!
Use
of
accessories
emissions communications
or
and
decreased
equipment
cables
immunity
can
other
affect
than
of
those
the
medical
provided
system.
electrical
may
result
Portable
equipment.
and
in
increased
mobile
RF
Handpiece
The
Infiniti?
handpieces
should
the
handpiece
dry
before
Directions
If
in undergoes processed
The
Infiniti?
temperature
after
autoclaving;
Never
U/S
handpieces;
Care
AquaLase®,
are
surgical
not
touch
connecting for
the
ultrasonically
any
solid
must
be
thoroughly
it
Use
(DFU)
medical
according
NeoSonix® , OZil®
just
a
high
before
never
opinion
risk
clean
irreparable
OZil®
instruments
to
to
use.
immerse
torsional,
object
console.
supplied
procedure,
local
while
cleaned. Be
of
the
requirements.
torsional,
Allow
the
and
For
with
physician a patient
the
CAUTIONS
the
Infiniti®
damage
NeoSoniX®,
must
be
in
operation.
cleaning
the
handpiece.
WARNING!
the
instrument
and
U/S
handpiece
handpiece
AquaLase®,
may
result.
handled
Immediately
sure
handpiece
and
sterilization
handpieces
to
air
in
liquid
and
high
with
care.
connector
with a prion
should
must
cool
for
when
OZiP
torsional,
performance
The
following
procedures,
related
destroyed
be
at
least
hot.
U/S
handpiece
surgery
is
completely
disease
at
room
15
minutes
NeoSoniX®,
tip
see the
or
be
or
Prior
U/S the
during
Do immersed use.
Ensure tuning
may
Quenching a hot
Be handpiece
to
sterilization,
handpieces
sterilization
handling,
not
operate
in
BSS®
Irreparable
that
test
OZil®
result
sure
torsional,
in
premature
handpiece
and
console
the
should
tray.
This
and
especially
OZil®
torsional,
sterile
damage
chamber
handpiece
is
completely
Infiniti?
always
will
AguaLase?,
have
prevent
during
NeoSoniX®,
irrigating
to
the
handpiece
is
filled
with
NeoSoniX®,
tip
failure
in
water
dry
may
result
the
connector
damage
autoclaving.
solution
and
BSS®
or
U/S
handpieces.
and
breakage.
can
cause
before
if
plugged
OZiF
torsional,
end
to
the
connectors
or
0/5
handpieces
or
distilled
tip
can
sterile
connecting
in
irrigating
damage
when
wet.
NeoSoniXº,
cap
secured
water
result
if
and
and
handpieces
unless
or
run
solution
is
in
dry.
the
surgical
before
placed
tip
Tuning a handpiece
and
will
void
warranty.
it
to
console.
Damage
and
in
is
dry
to
18
8065751606
DN
FINIT
L
Use
absence
can
of
the
cause
OZIiF
of
irrigation
excessive
torsional,
flow
heating
Infiniti?
and/or
in
and
WARNINGS!
NeoSoniX®,
the
presence
potential
thermal
U/S,
of
or
AquaLase®
reduced
injury
or
to
adjacent
handpiece
lost
aspiration
eye
in
the
flow
tissues.
Appropriate
for
successful
heights, conditions power, result lead
to
Use
of
or
U/S
not
permitted,
patient
The
U/S
ОР
torsional,
be
ordinances.
Use
0.9
1.1
mm
tips
and
Directing
use
high
power
(beeping
excessively
in
significant
severe
an
ultrasonic
handpiece,
and/or
tips
supplied
mm
U/S
liquefaction
infusion
energy
of
Infiniti?
procedures.
settings,
tones), tight
temperature
thermal
and
operator.
Infinit®
eye
handpiece
or
use
may
result
in
the
NeoSonixX®,
per
case,
exclusively
tips
exclusively
sleeves
toward
Vision
incisions,
of a handpiece
may
non-lens
Use
of
extended
failure
increases
tissue
other
in
patient
/nfinitP”
and
create
System
low
to
sufficiently
and
damage.
Vision
or
with
material
parameters
vacuum
power
usage,
combinations
at
incision
than
the
OZiF
repaired
injury,
U/S
disposed
0.9
potentially
including
System
handpieces.
mm
infusion
1.1
mm
may
and
limits,
power
aspirate
site
torsional,
without
pak
of
according
sleeves.
infusion
hazardous
cause
tissue
accessories
low
rates,
usage
during
viscoelastic
of
the
above
and
inside
Infinit®
Alcon
potential
are
Each
sleeves.
authorization,
only
to
U/S
tip
to
Use
Mismatching
fluidic
damage.
is
important
low
occlusion
prior
to
actions
the
eye,
NeoSonix®,
shock
hazard
be
used
is
intended
local
governing
1.1
mm
U/S
imbalances.
bottle
using
may
and
is
to
on
the
to
and
U/S
IV
Pole
Once bottle
IV
negatively causing
Empirical technique.
and
Extender
the
height
bottle
IV
pole
tothe
impact
false
numbers
The
extender
by
manually
lower
the
indications
for
surgeon
is
installed,
hanging
introduce
performance
at
low
bottle
should
heights
visually
WARNINGS!
the
upper
the bottle on
an
error
of
the
Infusion
bottle
levels.
are not a replacement
and
physically
hook
the
in
lower
the
displayed
Pressure
monitor
is
to
hook.
be
used.
Manually
height
Drop
detection
for
competent
intraocular
Do
not
change
lowering
indication
feature,
surgical
pressure.
the
and
8065751606
1.9
Феи
Ultraflow™*
Prior
Ultraflow™ * handpiece.
contact Alcon's
Use Alcon with
cause a shallowing
Exceeding
cause
capsule.
VA
Recommended
to
each
of
surgical
the
anterior
tips
(I/A)
Handpiece
procedure
Technical
non-Alcon
Infinit®
the
are
not
Vacuum
inspect
If
damaged
Services
surgical
specifications,
Vision
or
recommended
chamber
to
be
Range
reusable
System,
collapsing
shallowing
used
with
for
the
two
O-rings
or
missing,
Department.
WARNINGS!
or
or
use
of
may
result
of
the
level
of
100
and/or
NeoSoniX®,
I/A
Tips
where
replace
disposable
an
Alcon
in a fluidic
anterior
mmHg
incarceration
OZiP
the
tip
the
I/A
handpieces
handpiece
imbalance.
chamber.
with a 0.5
or
torsional,
screws
o-rings.
that
not
specified
This,
mm
or
larger
tearing
or
of
U/S
handpieces.
onto
If
in
do
in
the
the
doubt,
not
meet
for
turn,
I/A
tip
posterior
use
may
may
It
is
important
vacuum.
100
mmHg.
TA
adjustable
Handpiece
Ensure an
error
not
too
Use
of a tool
and/or
During
touching
of
metal
ultrasonic
that
Only
0.2
vacuum
Tips
that
handpiece
may
be
generated
tight
so
that
other
handpiece.
clinical
performance
any
ultrasonic
of
the
particles
energy
only
the
mm
or
0.3
range
tip
is
and/or
it
can
be
than
tip
procedure,
ultrasonic
resulting
causing
proper
fully
wrenches
size
mm
I/A
is
0-650+.
tightened
inadequate
removed
result
tip
with a second
from
micro
abrasion
I/A
tip
tips
should
to
the
tuning
after
use.
supplied
WARNING!
if
tip
is
metal
any
particles
ultrasonic
of
be
used
when
be
used with
handpiece.
will
by
Alcon
not
secured
may
instrument.
handpiece
the
ultrasonic
operating
If
occur.
may
cause
tightly
result
Another
vacuum
not
securely
Ensure
damage
to
the
from
potential
may
be
with
maximum
limits
that
above
attached,
the
tip
to
the
handpiece.
inadvertent
source
the
result
is
tip
of
1.10
Check
tips. tubing
for
Never
may
the
presence
attempt
result
and
correct
to
remove
in a hazardous
the
position
tubing. condition
Use
of
of
for
the
the
the
polymer
Mackoo/"
patient.
tubing
tips
on
the
without
Mackoof*
polymer
8065751606
ONFINITÙÀ
Infiniti®
Aspiration/Vacuum
Vitrectomy
The
Infiniti?
Do
not
test
BSS®
sterile
damage
After
erly
good position Prior
the
is
the
actuated,
*
If
»
If priming,
+ H a
procedure,
to
filling
actuating
visualization.
1.
to
entry
surgeon
cutting;
cutter
cutting
air
bubbles
reduction
vitrectomy
or
irrigating
the
and
If
cutting
alternatively,
is
replace
replace
Probe
probe, a guillotine
operate
solution
handpiece
testing,
and
aspirating.
The
port
into
the
should
observed
stop
the
probe.
is
partially
are
observed
the
of
cutting
immediately
Adjustments
vitrectomy
and
tip
and
before
port
should
is
partially
eye,
and
on
the
press
the
to
not
fully
closed
in
probe.
capability
WARNINGS!
probes
or
distilled
can
surgical
This
always
closed
with
footpedal
Test
close,
while
the
aspiration
or
and
replace
vitreous
unless
water
result
may
tip
button
require
remain
while
of
probe
for
or
idle,
vacuum
the
if
does
cutter,
tip
oris
run
dry.
verify
lowering in
in
position
in
visual
on
the
not
replace
line
or
is
observed
probe.
is
intended
of
probe
in
surgical
the
cut
open
position
1,
replace
sterile
verification
Vitrectomy
the
exiting
move
irrigating
when
probe.
the
during
for
single
is
immersed
use.
İrreparable
probe
rate
in
that the
Setup
the
probe
the
use
is
prop-
to
achieve
footpedal
the
probe.
solution,
probe
Screen:
probe
tip
during
surgical
only.
in
if
is
Adjusting
aspiration
Dynamic
Care
must
Adjusting the
IV
which
Presurgical
Presurgical section. the
If
Troubleshooting
When
fluidics adequate
aspiration levels
pole
may
Check-out
an
filling
(volumes)
values
be
taken
aspiration
below
result
check-out
error
message
handpiece
response
irrigation
rates
or
of
1,2,3,
not
to
engage
rates
the
preset
in
patient
Tests
tests
must
or
section
will
of
test
be
jeopardized.
and
aspiration
vacuum
exceeding
or 4 will
non-lens
WARNING!
or
vacuum
values,
injury.
be
performed
advisory
this
manual.
WARNINGS!
chamber,
flow
limits
above
irrigation
achieve
material.
limits
may
message
Good
If
the
if
stream
prior
above
cause
as
clinical
the
preset
inflow.
vacuum
the
chamber
outlined
is
displayed
problem
of
fluid
practice
to
entering
values
in
shorter
preset
in
persists,
values,
shallowing
the
Operating
on
the
DO
is
weak
dictates
the
eye.
may
periods
front
NOT
or
absent,
the
result
or
or
panel,
in
of
time.
lowering
collapse
Instructions
refer
PROCEED.
good
testing
for
to
8065751606
Ensure
that
tubings
are
not
occluded
or
pinched
during
any
phase
of
operation.
1.11
Footswitch
ONE
INET
|
Never
footswitch
If
required,
germicidal
Do
not
compatible Damage
High
Altitudes
Vitrectomy
Service
Occlusion
Two
different
that
the stopped when
or
AquaLase®
single
intermittent ultrasonic
pick
up
or
can
cause
the
footswitch
solution
clean
may
the
with
result.
cutting
for
additional
Tones
occlusion
vacuum
to
avoid
occlusion
system
beep.
The
double
power
move
the
irreparable
that
is
footswitch
plastic
parts
performance
information.
tones
is
near
or
exceeding
occurs
during
magnitude),
second
or
type
beep,
AquaLase®
footswitch
damage.
may
be
wiped
compatible
using
solvents,
made
may
(intermittent
at
its
preset
the
limit.
aspiration
The
of
occlusion
and
sounds
system
by
the
cable.
with
with
the
CAUTION
abrasives,
of
GE
Cycoloy
vary
at
high
beeping
limit,
and
The
first
only
I/A
occlusion
tone,
when
occlusion
magnitude.
Dropping
alcohol,
plastic
parts.
CU
altitudes.
tones
aspiration
type,
the
(in
the
absence
tone
the
phaco
occurs
or
mild
soap
or
any
6800
Consult
during
flow
I/A
occlusion
of
is a lower,
occlusion
during
kicking
and water,
cleaner
and
the
LEXAN
Alcon
occlusion)
is
reduced
tone,
ultrasonic
intermittent
tone,
is a higher,
application
or
any
is
not
920A.
Technical
indicate
or
sounds
power
of
The
I/A
occlusion maximum phaco
The and/or
Use of
excessive
Vacuum
A
vacuum
high
in
volume,
allowed
occlusion
phaco
prolonged
of
the
irrigation
Tone
tone
vacuum
but
and
preset
tone
occlusion
use
NeoSoniX®,
flow
and/or
heating
can
not
and
is
provided.
indicate
turned
phaco
value.
cannot
bell
may
OZiF
in
potential
that
occlusion
The
be
turned
WARNINGS!
indicates
lead
to
torsional,
the
presence
thermal
The
pitch
little
to
tones
I/A
occlusion
off.
no
thermal
U/S,
of
will
no
flow
indicate
aspiration
injury.
or
AquaLase®
reduced
injury
vary
to
relative
is
occuring.
that
tone
can
flow.
or
lost
adjacent
to
the
vacuum
be
turned
Use
of
high
handpiece
aspiration
eye
tissues.
the
amount
This
tone
has
off,
U/S
in
the
flow
of
can
reached
while
the
settings
absence
can
cause
vacuum.
be
reduced
8065751606
its
A
WARNINGS!
A
moderate
the
NeoSonix®,
irrigation
excessive
Do
not
result
hazardous
Coagulation
to
flow
heating
exceed
exceeding
condition
Function
OZiF
and/or
and
maximum
vacuum
torsional,
in
the
potential
capacity
drain
for
the
may
U/S,
presence
thermal
bag
maximum
patient.
indicate
or
of
of
drain
little
AquaLase®
reduced
injury
to
bag
capacity
to
handpiece
or
lost
adjacent
(500
mi).
no
aspiration
eye
Excessive
and
potentially
is
occuring.
in
the
absence
flow
tissues.
pressure
Use
can
cause
result
of
of
can
in
a
8065751606
Listed
+
below
To
ensure
and
accessories
performance
endorsed
*
To
reduce
operating
¢
Interference adversely
«
Accessories checked
+
Operation
*
The
lowest
intended
*
Skin-to-skin
should
«
When equipment
should
electrodes
+
In devices
«
The contact
*
Temporarily from
*
The
and the
*
Non-flammable
¢
Flammable
should
materials,
be
*
Accessories coagulation
be
HF
be
all
cases,
cables
with
the
use
oxygen
thorax
be
ignited
are
general
safe
operation
can
precautions
must
be
guaranteed
components.
the
of
accidental
high-frequency
produced
influence
should
for
possible
of
the
power
purpose.
contact
avoided,
(high
are
placed
are
monitoring
are
recommended.
to
the the unused
patient.
of
flammable
should
or
the
agents
allowed
for
by
sparks
should
output
the
be
damage
coagulation
level
(for
for
frequency)
used
simultaneously
as
far
not
recommended.
surgical
patient
active
be
head,
agents
used to
example
produced
have a rated
voltage.
to
of
the
coagulation
be
used
(See
only
burns,
surgical
by
the
operation
operation
checked
in
example
example
as
systems
or
anaesthetics
avoided
unless
should
for
evaporate
cotton,
regularly;
to
the
step
coagulation
by
surgical
possible
incorporating
electrodes
other
leads
electrodes
if a
these
be
used
cleaning
before
wool
in
normal
voltage
be
followed
function,
your
Alcon
when
using
caution
equipment.
of
high-frequency
of
other
electronic
electrode
insulation.
is
limited
step
should
between
the
insertion
equipment
on
the
same
from
the
should
is
avoided.
should
or
oxidizing
surgical
agents
for
or
and
procedure
are
cleaning
disinfecting,
the
application
gauze,
use
equal
when
using
the
only
approved
representative).
Alcon
components
г
should
to
extraocular
arms
of
dry
surgical
high
be
positioned
be
sucked
of
to
always
surgical
equipment.
cables
uses
always
and
be
body
gauze.
and
physiological
patient,
stored
gases
and
when
the
or
any
electrodes.
frequency
in
so
that
such
is
carried
away.
disinfection
or
as
solvents
of
HF
saturated
HF
surgical
greater
should
as
Coagulation
Coagulation
be
taken
equipment
particularly
only.
selected
of
the
monitoring
monitoring
Needle
current-limiting
such a way
they
are
nitrous
out
wherever
of
surgery.
with
equipment.
than
the
function:
cables
or
Alcon-
for
the
patient)
electrodes
monitoring
that
isolated
oxide
in
the
region
possible.
adhesives,
Some
oxygen
maximum
may
be
(N,O)
of
may
1.13
Coagulation
Do
not
defibrillatory pacemakers irreparable
may
occur
or
defibrillatory
Failure unintended
The
Infiniti?
discharge.
Cautery,
The Diathermy,
Diathermy,
Infiniti®
Function
use
the
devices.
or
damage
and
of
the
HF
increase
Vision
Vision
based
(from
coagulation
defibrillatory
device
Coagulation
System
on
prior
If
electrosurgery
to
the
to
ventricular manufacturers
surgical
of
output power.
System
the
is
uses
following
pacemaker
equipment
page)
WARNINGS!
function
devices
on
fibrillation.
CAUTION
not
protected
Definition
the
word
definition:
patients
is
used
or
pacemaker
or
defibrillatory
for
their
(coagulation
against
“Coagulation”
on
patients
Please
recommendations.
the
pacemakers
with
electrodes,
device
check
circuitry)
effects
in
place
or
implanted
be
and
its
the
pacemaker
could
of
of
result
defibrillator
Cautery
implanted
cardiac
aware
that
function
in
or
an
Coagulation - Isolated, forceps). “Coag”
Infiniti?
Do Refer
Do
*
Do
*
Use to
Current
in
some
VideOverlay
not
remove
servicing
not
simultaneously
not
use
multiple
only
the
Alcon-supplied
the
IVO.
bipolar,
passes
of
between
the
text
System
VideOverlay
to
gualified
portable
of
this
(IVO)
touch
high
frequency
these
electrodes,
operator’s
WARNINGSI
cover;
service
serial
there
the
VideOverlay
CAUTIONS
socket
cable
personnel.
current
manual.)
are
outlets
to
connect
supplied
halting
no
user-serviceable
enclosure
with
this
the
to
conductors
bleeding.
and
system.
Infiniti®
(Abbreviated
the
Vision
parts
patient.
inside.
System
(e.g.
8065751606
Consumable
Consumable
to
be
All
Infiniti®
stand
the
NOTE: manual accessory,
Mismatch a
particular
Do
Sterile
been
paks
DFU’s
If
an
and
follow
of
not
use
disposable
designed
items
used
with
and
discarded,
contain
prior
inconsistency
the
Directions
the
consumable
combination
paks
for
to
DFU
that
have
medical
one
use.
Directions
time
the
Infiniti?
unless
exists
For
between
Use
‘WARNINGS!
components
of
consumable
exceeded
devices
use
only;
for
Use
(DFU)
and use
the
should
do not
Vision
labeled
(DFU).
the
supplied
of
components
expiration
not
be
reuse.
System
instructions
during
otherwise.
It
is
important
with a consumable
settings
reused!
may
date.
not
create a patient
These
surgery
to
in
the
specially
components
are
designed
read
and
under-
operator’s
pak
adjusted
hazard.
or
for
The
equipment
plete
surgical
system contributed voidance
In
all
cases,
thoroughly
Read
Miscellaneous
all
Do
not Avoid handpiece Do at should Do
The
for
spilling
not
the
rear
be
not
USB
use
Tray
in
conjunction
system.
performance
to
the
of
the
the
understood
package
use
the
/nfiniti®
BSS®
connectors.
push
or
pull
and
sides
pulled
place
more
connector ( *&* ) and
by
Alcon
support
Use
and
malfunction
contract
instrument
prior
label
material
Vision
solution,
the
unit
of
the
and
not
pushed,
than a 20
trained
must
personnel
be
create
and/or
of
disposables
potential
of
the
invoicing
setup
instructions
to
using
printed
CAUTIONS
System
or
moisture
by
the
unit
are
provided
especially
lb.
load
Infiniti?
set
in
its
the
Alcon
other than
hazards,
equipment
at
any
of
on
the
near
flammable
of
display,
on
only.
the
for
over
tray
Failure
WARNING!
stored
position
disposables
Alcon
and
under
prevailing
contained
the
pak
configurations.
consumable
any kind,
tray,
or
moving
elevator
support.
to
comply
when
constitutes a com-
disposables
if
it
is
determined
contract,
hourly
in
anesthetics. around
the
the
and
located
moving
could
rates.
the
manual
paks
prior
the
electrical
IV
pole.
instrument.
door
thresholds.
on
the
will
void
instrument.
may
to
result
should
to
their
Handles
The
unit
panel
warranty.
affect
have
in
the
be
use.
located
are
8065751606
PRODUCT
SERVICE
For
product
number
service,
provided
please
below.
contact
Alcon’s
Technical
Services
Department
at
the
Operators Instructions should authorized
For
optimum maintenance year. Alcon’s quality
Safety least must
To
avoid
Department deemed
shipping
experiencing
and
be
referred
service
Additional
Field
of
workmanship.
performance
twice a year.
be
checked
unnecessary
prior
necessary, a Return
instructions.
problems
Troubleshooting
to
the
Alcon
representative.
performance,
service
Service
on
the
preventive
Engineers
should
Ground
to
appropriate
shipping,
to
return
Alcon
Irvine,
(800)
Technical
15800
832-7827,
with
sections
Technical
it
is
the
user’s system maintenance
be
resistance,
of
Material
California
and
are
trained
verified
national
please
any
system
Authorization
Services
Alton
or
leakage
Parkway
(949)
the
system
of
Services
responsibility
its
accessories a minimum
may
and
by
the
standard.
contact
or
should
this
manual. A problem
Department
be
required
equipped
user
(e.g.,
current,
your
and
Alcon
accessories.
will
Department
92618-3818
753-1393
refer
to
the
or
to
schedule
based
qualified
If
be
upon
to
provide
service
dielectric
Technical
return
of
issued
Operating
which
your
local
preventive
of
one
time
system
the
highest
personnel)
withstand
Services
the
equipment
with
appropriate
persists
per
use.
at
voltage
is
1.16
8065751606
LIMITED
WARRANTY
Alcon found from of
the
accordance
Alcon or
destruction
or
caused
any
Act
earthquake.
This
warranty
by
any
provided
force
service credit service
will
repair
to
be
defective
the
date
of
system,
shall
of
person
and
personnel.
customer’s
or
when
with
not
of
by
God
does other
by
Alcon
effect
other
or
replace
in
material
initial
published
be
including,
if
alteration
installation.
said
obligated
systems
or
explosion
not
cover
than
with
respect
this
equipment
In
particular,
account
system
covered
an
at
its
option,
and/or
is
properly
instructions.
to
provide
where
of
any
but
not
limited
damage
Alcon-authorized
to
this
is
Alcon
for
the
cost
by
persons
any
workmanship
This
warranty
services
such
origin,
resulting
equipment
serviced
shall
of
the
other
system
installed,
damage
riot,
to
lightning,
service person,
by
have
equipment,
than
or
applies
under
civil
from
service
shall
anyone
no
obligation
Alcon-authorized
accompanying
for a period
to
the
original
maintained,
this
warranty
or
destruction
commotion,
windstorm,
become
other
which
and
repair
and
any
void
than
Alcon-authorized
to
has
service
accessories
of
one
(1)
year
purchaser
operated
for
damage
is a result
aircraft,
hail,
flood
|
or
other alteration
warranties
and
of
replace,
been
subject
in
to
of
or
or
an
no
further
repair
to
personnel.
or
The
express remedy agreements, including , without purpose. damages
The
constitute a complete handpieces
performance products malfunction
at
prevailing
warranty above
provided
guarantees,
Alcon
arising
consumable
shall
other
or
handpieces
of
above
out
and
hourly
is
is
in
or
watranties oral
limitation,
have
no
of
any
defect,
products
surgical
create
the
potential
equipment
rates.
the
sole
lieu
of
any
warranties
liability
used
those
not
whatsoever
improper
WARNING!
in
system.
manufactured
manufactured
during
warranty
and
all or
of
merchantability
use,
conjunction
Use
hazards.
warranty
obligation
other
remedies.
written,
or
If
by
expressed
for
any
unauthorized
with
Alcon
of
consumable
by
Alcon
it
is
determined
Alcon
period,
of
Alcon,
There
or
implied
or
fitness
incidental
have
service
or
service
instrument
may
affect
that
contributed
will
and
the
are
no
other
for a particular
consequential
or
repair.
products
products
consumable
be
and
system
to
the
provided
8065751606
1.17
CONSOLE
DIMENSIONS
WEIGHT
ENVIRONMENTAL. LIMITATIONS
Altitude:
Temperature:
Relative
Humidity:
ELECTRICAL
REMOTE
MAXIMUM PROTECTION CLASSIFICATION DATA
Table
REQUIREMENTS
CONTROL
INPUT
CURRENT:
AGAINST
CARD:
1-4 | SPECIFICATIONS
OF
MMC
(MultiMedia
system
Height:
Width:
Depth:
Unpacked:
Packed:
Operating
2438
meters
(8,000
feet)
10° G to
35°
(50° F to
95°
10%
to
95%
without
condensation
Method; Channels:
Batteries:
ELECTRIC
ALL
APPLIED
Card),
requirements,
160
cm
(63
58.5
cm
(23
76
cm
(30
107
kg
(235
150
kg
(330
Non-Operating
12,191
(40,000
C F)
220 - 240
SHOCK: Class
PARTS:
100 - 120
or
SD
-This
-40° C to
(-40° F to
10%
without
condensation
VAC, VAC,
Infrared 4 AAA
(3)
6A
Type
(Secure
table
and
inches)
inches)
inches)
pounds) pounds)
meters
feet)
60°
C
140°
F)
to
95%
50/60
Hz
50/60
Hz
1
BF
Digital)
32
Mb
is a quick
performance
PERFORMANCE
PHACOEMULSIFICATION
OZif?
AquaLase®
ANTERIOR
COAGULATION
VACUUM
mín.
POWER
reference
figures.
SPECIFICATIONS
Submodes:
Tip
Stroke @ 100%: Resonant Pulse
Burst
Longitudinal Torsional Pulse Burst
Pulse Burst
Submodes:
20
23 ga
10 76 200
Phacoemulsification:
Vitrectomy:
Irrigation/Aspiration: 0 to
Height With
Frequency:
Rate
Range:
Length:
TORSIONAL
Frequency:
Rate
Range:
Length:
LIQUEFACTION
Rate
Range:
Time
On:
VITRECTOMY
ga
Infiniti?
Infinit?
Watts
max.,
Vpp @ 1.5
Vpp
minimum,
SEA
IV
POLE
Range:
Alcon
IV
point
HANDPIECE
Frequency:
Vit
Probe:
UltraV#®
75
ohm
MHz
25%,
accessories
LEVEL
Pole
Extender
to
identify
DEVICE.
Probe:
load
75
Continuous,
88.9
38.0 0-100
5
44.0
32.0 1-100 20
10-75 7-100
Cut
40
10
ohm
0 0
13
45
basic
127.0
+1.9
pps
to
500
2,0 KHz +2.0
pps
to
500
pps %
WA,
to
800
to
2500
loads
voltage
to
850
to
650 650
to
110
to
142
Pulse,
um
(.0035
KHz
mS
KHz
mS
VA
Cut
cpm
cpm
rating
mmHg mmHg mmHg
cm
cm
system
ONE
Burst
specifications,
+.0005
INIT)
in.)
Abbreviation
A AC Agi
Asp
Aspiration
BF
C
cc/min Coag CPM
Centigrade
DFU ESD F
FMS
Hz
VA IEC
Table
1-5
Description
Amperes Alternating
Current
AquaLase®
Floating
Cubic
centimeters Coagulation Cuts
Per
Minute
Directions Electro
Static
for
per
Use Discharge
Fahrenheit
Fluidic
Management
System
Footswitch High
Infusion
Sleeve
Handpiece
Hertz
Irrigation/Aspiration International
ABBREVIATIONS
Electrotechnical
minute
Commission
THE
/NFINITF
Abbreviation
International objects X (not (continuous
IRR
IT IVO
MMC mmHg PEL
PPS RCAT
SP
UL
U/S USB
V
Vac
Vit
Irrigation
Interchangeable Infinit®
MultiMedia Millimeters Patient
Pulses Remote Single-Piece
Underwriters
Ultrasonic Universal
Volts
Vacuum
Vitrectomy
VISION
Description
VideOverlay
Per
SYSTEM
protection
immersion)
Card
of
Mercury
Eye
Level
Second
Control
Laboratories
Serial
code - solid
specified),
water
Tip
Aseptic
Transfer
Bus
8
8065751606
Type
BF
equipment,
attributes
isolation.
Dangerous
CAUTION:
Equipotential
AC
Power for a part
of
Voltage
stand-by
of
basic
Voltage
Consult
equipment
insulation
accompanying
ground
state
providing
connection
both
and
the
“floated”
documents
REF
DEE
Catalog
Serial
Date
Manufacturer
Eject
U/S
Cable
AquaLase®
Cable
Vitrectomy
Tubing
Number
Number
of
Manufacture
FMS
Handpiece
Connector
Connector
Probe
Connector
Handpiece
Pb
Figure
1-2
ON
(POWER)
OFF
(POWER)
Footswitch
Fuse
Size
Use
appropriate
(see
Environmental
Pb
notation,
content
ICONS
that
are
and
greater
used
Rating
take-back
Considerations
if
present,
than
0.004%.
THE
with
the
system
indicates
Infinit
lead
/NFINITP
in
this
VISION
Vision
10101
manual)
c
SYSTEM - Icons
System
are
=) À
pi
©
>
É
7
US
identified
Bottle
Receptacle
AquaLase®/BSS®
Coagulation Cable
Connector
USB
Connector
Serial
Connector
Infinit®
ESD
NRTL electrical hazards
UL
IEC
identifying
in
this
Port
Sensitive
TUV
60601-1,
60601-1-2,
chart.
Connector
Mark - With
shock,
only
in
accordance
CSA
and IEC
modes,
for
Solution
respect
fire
and
mechanical
22.2
601-1,
60601-2-2
functions,
to
with
etc.,
8065751606
GNF
INIT
ENHANGED.
FOOTSWITCH
|
[Rer|
2065750405
M
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ko
DN E NT O TY
REMOTE
219-2384-001
(DG
4
SUNTROL
REV
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penál
그게
210-2437-003
REV
1
MEINI
Alcon
KA
6201
FORFWORTH,
MADE
USA
:
B.
|
|
LAHORATORIES,
SOUTH
FREEWAY
TX
7134-2099
MADE
210.2328-001
:
τ.
IN
ВЕУВ
le
INC,
USA
USA
FOR
APPLICABLE
SCREEN
ON
THE
Dr
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: +.
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DANCER:
DANGER: - SISQUE
GAUTION:
CAUTION:.
WARNING:
WARNING:
:
RISK
MALEANESTWENCS
"
PRESENCE
GROUNDING
고:
WHEN
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| . МРЕОАМСЕ
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=
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75
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Figure
1.20
1-3
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ON
here.
T6.3A/250.
INFINITF
The
labels
“WARNING:
PROTECTION
REPLACE
-AND:RATING
VISION
on
this
SYSTEM
page
FOR
CONTINUED...
AGAINST
ONLY
WITH
OF
FUSE.
-
Labels
are
intended
RISK'OF
SAME
TYPE
used
for
©
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on
the
reference
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only.
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System
8065751606
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40
9
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mx
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5
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8
7 в
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1
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25
VOLTAGE
20
PEAK
15
10
10
SETTING
20 30
(%)
POWER
40
50 60
ACROSS
75
OHM
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LOAD
80 90
100
Figure
8065751606
1-4
0
10
SETTING
COAGULATION
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in
the
20
(%)
POWER
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30
VOLTAGE
OUTPUTS - Set
operating
40
(PEAK)
mode
50
coagulation
in
60
ACROSS
reference
75
OHM
power
to
70 80
LOAD
at
the
figures
above.
90
intended
100
output
control
1.21
ÓN
E
TTF
THIS
PAGE
INTENTIONALLY
BLANK
1.22
LAST
PAGE
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8065751606
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