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Potential electrom agnetic or o ther interference between medical equipments and other
devices being operated together in the same environmental may expert an ad verse
unctioning of the medic al equipment.
Non-medical equipm ents not in
co mpliance with the requirements of EN 60601
used to gether in the same environmental as the medical equipm ents
This equipment has been tested and found t
o comply with the limits for medical devices in
These limits are designed to provide reasonable protection against
harmful interference in a typical medical installation
For use of equipment in rated voltage less than 125V
One end with Hospital Grade Type, NEMA 5
end with appliance coupler. For use of equipment in rated voltage less than 2 50Vac
This product may malfunction due to electromagnetic waves caused by portable personal
telephones, transceivers, radio
controlled toys, etc. Be sure to avoid having objects such as,
affect this product, brought near the product.
The information in this publication has been carefully checked and is believed to be entirely
accurate at the time of publication. HUVITZ assumes no responsibility, ho we ver, for possible
or for any consequences resulting from the use of the ormation

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HUVITZ reserves the right to make changes in its products or product specifications at any
time and without prior notice, and is not required to update this docume ntation
435-862, Republic of Korea
Under copyright laws, this manual may not be copied, in whole o r in part, without the prior
ritten conse nt of HUVITZ Co., Ltd.

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63.Features & Operating Condition
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Assembling the Instrument
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Protection fuses replacement
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Guidance and manufacturer’s declaration
Guidance and manufacturer’s declaration
Guidance and manufacturer’s de
Recommended separation distances between portable and mobile RF
communications equipment and the EUT
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Immunity and Compliance Level
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Guidance and manufacturer’s declaration
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7000 is intended for use in eye examination of the ant eye
segments, from the cornea epithelium to the posterior capsule. It is u
diagnosis of diseases or trauma which
the structural properties of the anterior
Protection against electric shock: Class I
Applied Parts: Type B applied parts.
Protection against harmful ingress of wa
Degree of safety in the presence of a flammable anesthetics mixture with air
or with oxygen or with nitrous oxide: Not suitable for use in the presence of a
flammable anesthetics mixture with air or with oxygen or with nitrous oxide.
-Mode of operation: Continuous
Light Hazard protection Classification: Group 2 by ISO15004
Do not try to move this equipment without help.
heavy and should maintain stationary. Always get two persons to help lift this
Federal law restricts this device to sale by or on the of a physician

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s responsibility. The safe use of this equipment is largely dependent
upon the installer, user, operator, and maintaine
r. It is imperative that personnel study
and become familiar with this entire manual before attempting to
service or adjust this equipment and any associated accessories. It is paramount that
the instructions contained in this manual ar
e fully understood and followed to enhance
safety to the patient and the user/operator. It is for this reason that the following safety
notices have been placed appropriately within the text of this manual to highlight safety
related information or informa
tion requiring special emphasis. All users, operators, and
maintainers must be familiar with and pay particular attention to all Warnings and
Cautions incorporated herein.
indicates the presence of a hazard that could result in severe persona
death or substantial property damage if ignored
Note”describes information for the installation, operatio n, or maintenance of which is
important but hazard related if ignored.
indicates the presence of a hazard th at coul
d result in minor injury, or
property damaged if ignored.

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(IEC) has established a set of symbols
for medical electronic equipment which classify a connection or warn of any potential
The classifications and symbols are shown below.
This applies only to the instrument that has the certification symbol printed explicitly on
the product label or sticker.
I and O on po wer switch represent ON and OFF respectively.
Type B Isolated patient connection.
This symbol identifies a safety note. Ensure you understand
the function of this control before using it. Control on
described in the appropriate User ’s or Service M anual.
Identifies the point where the
fastened to the chassis. Protective earth connected to
Class I equipment for safety purposes.

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WITH RESPECT TO ELEC TRIC SHOCK
ONLY IN ACCORDANCE W ITH U L
Disposal of your old applianc e
product is covered by the European
lectrical and electronic products should be dispose d of
separately from the municipal waste stream via de signated
collection facilities appointed by the government or the local
The correct disposal of your old appliance will help prevent
tial negative consequences for the environment and
4. For more detailed information about disposal of your old
appliance, please co ntact your city office, waste disposal
service or the shop where you purchased the pro duct.

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Avoid the following environments for operation or storage:
Where the equipment is exposed to water vapor.
Where the equipment is exposed to direct sunlight.
Normal operating temperature range is from 10
Humidity is from 30% to 75%.
Altitude is from 700 to 1060hpa
Where it is near the heat equipment.
Where the humidity is extre me ly high or there i
Where the equipme nt is subject to e xcessive shocks or

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Where equipment is exposed to chemical material or
Be careful not to be inserted dust, e specially, metal.
Don’t disassemble the product
respo nsible for it for nothing.
Be careful no t to close the fan located on the lateral or back
Don’t plug the AC power c ord into the outlet before the
co nnection between devices of the equipment is co mpleted.
This can generate the defect.
Pull out the power cord with holding the plug, not the cord.
Avoid places where the ambient temperature falls below 10
normal operation, or below
storage. Humidity should be maintained between 30 and for normal operation,
transportation and storage. The
operation, transportation and

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nd tested according to safety standards as well
as national and international standards. This guarantees a very high degree of safety
for this device. The legislator expects us to inform the user expressively about the
safety aspects in dealing with the de
vice. The correct handling of this equipment
imperative for its safe operation. Therefore, please read carefully all instructions before
switching on this device. For more detailed informatio please contact our Customer
Service Department or one of ou
r authorized representatives.
must not be used (a) in an area that is in danger of explosions
and (b) in the presence of flammable, explosive, or vo tile solvent such as
alcohol, benzene or similar chemicals.
Do not put or use this device
in humid rooms. Humidity should be maintained
between 30 and 75% for normal operation. Do not expose the device to water
splashes, dripping water, or sprayed water. Do not place containers containing
fluids, liquids, or gases on top of any electrical equi
The equipment must be operated only by, or under direct supervision of a
properly trained and qualified person.
Modifications of this equipment
may only be carried out by Huvitz
technicians or other authorized persons.
er maintenance of this equipment
may only be performed as stated in
s Manual and Service Manual. Any additional maintenance may only
s service technicians or other authorized persons.
The manufacturer is only responsible fo
r effects on safety, reliability, and
performance of this equipment when the following requirements are fulfilled: (1)
The electrical installation in the respective room corresponds to the
specifications stated in this manual and (2) This equipment is used

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maintained according to this manual and Service Manual.
The manufacturer is not liable for damage caused by unauthorized tampering
with the device(s). Such tampering will forfeit any rights to claim under
ly be used together with accessories supplied by
s. If the customer makes use of other accessories, use them only if their
safe usability under technical safety aspects has been proved and confirmed
by Huvitz or the manufacturer of the accessory.
9.Only persons who have undergone proper training and instructions are
authorized to install, use, operate, and maintain this equipment.
s Manual and Service Manual in a place easily accessible at all
times for persons operating and maintaining
Do not force cable connections. If a cable does not connect easily, be sure that
the connector (plug) is appropriate for the
(socket). If you cause any
damage to a cable connector(s) or receptacle(s), let the damage(s) be repair
by an authorized service technician.
Please do not pull on any cable. Always hold on to the plug when
Before every operation, visually check the equipment for exterior mechanical
damage(s) and for proper function.
ny ventilation grids or slits.
Immediately turn off and unplug any equipment that gives off smoke, sparks,
strange noises, or odors.
Power Supply Cord set (international)
(Detachable) Rated 10 A, 250 V. Plug
type CEE 7/VII, Connector type IEC 60320/C13
conductor terminating in molded
attachment plug. <HAR> marked on the cord. Maximum 4.0 m long

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Features & Operating Condition
device works like all slit lamps:
examination of the eye under the slit light.
examination of the ocular fundus and posterior vitreou body (using
These devices are designed for use by ophthalmologists and
ive professions) for specific diagnostic
bio-microscopic examination of the eye)
As long as the slit lamp is in its original package it can be exposed to the
following environmental conditions for up to 15 weeks ship
C;-Relative humidity range: from 30% to75%;
The device is made to operate under the following environmental conditions:
40C;-Relative humidity range: from 30%
es electromagnetic interference when used
near other equipment. Therefore, no preventive or corrective measures are required

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Because prolonged intense light exposure c an damage the retina, the use of the device
for ocular examination should not be unne
cessarily prolonged, and the brightness
setting should not exceed what is needed to provide cl visualization of the target
structures. This device should be used with filters that eliminate UV
, whene ver possible, filters that elim
The retinal exposure dose for a photochemical hazard is a product of the radiance and
the exposure time. If the value of radiance were reduc in half, twice the time wo uld
be needed to reach the maximum exposure
While no acute optical radiation hazards have been identified for slit lamps, it is
recommended that the intensity of light directed into patient
minimum level which is necessary for diagnosis. Infants, aphakes and perso
diseased eyes will be at greater risk. The risk may also increased of the person being
examined has had any exposure with the same instrument or any other ophthalmic
instrument using a visible light source during the previous 24 hours. This will ap
particularly if the eye has been exposed to retinal photography

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The instrument is delivered in package. Taking it out the package, make sure that
none of the following parts is missing.
A table top(N.B. the table top isn
’t supplied with the slit lamp for twin table) on
which are placed: A SMPS box(15) including the main switch & a warning
light (13), Two sliding guides for the base with orthogonal movements(17), A
sliding plate for the position device(19), A drawer(16);
base with orthogonal movements.
A microscope with either dual magnification or a
An optical group of the slit projector.
A set of accessories including; two
wheels for the sliding guides(18); a setting
rod(43); a protective cover(46); a spare bulb 12V 30W ogen bulb(53); two
protection fuses(48); a breath screen(19); a chin
cover(45); a power cable; two patient

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The following standard accessories are provided with the instrument;
[ Figure 1. Accessories ]

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Control lever for changing enlargement
Knob for clamping the breath screen
Control handle for the slit rotation 90
Connecting plug of the projector lamp
Knurled ring for filters insertion
r lateral, longitudinal and vertical movements(x y z)
Base with orthogonal movements
Warning light indicating the ignition of the SMPS is on
Knob to lock the projector
Scale for the projector position
Knob to lock the arm of the microscope
for the vertical setting of the chin

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Locking pins for chin rest pa
Knobs to change the slit width
Pointer for the eye positioning
Knob to lock the base of the instrument
Knob to lock the microscope
Control handle for horizontal tilting
Control lever for vertical tilting
90 determining the inclination of the slit during rotation
Microscope separation knob
An optical group of the slit projector

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Capture connector ( For the image system)
Luminosity selector connector ( Connect the Luminos

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[ Figure 2. Composition I ]

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Assembling the Instrument
The appliances are always supplied with exce llent packaging to be able to stand up to
all kinds of transport and standard storage conditio ns. Please co ntact the suppliers if
y irregularities are found in the appliance due to transport after unpacking
Put the table top on a very stable support. Block the wo parts together by

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that its holes fit together with
those of the table top. Tighten the screw with the
Place the base with orthogonal movements on the guides situated on the
upper part of the table top, checking that the wheels are in line. Then Place the
and make sure that its holes fit together with those of the
. Tighten the screw with the
Base with orthogonal move
optical group of the slit
sembling the instrument I]

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10). Then tighten the Guide screw with the screw driver(
-)Put the microscope(31) in the right position making sure that it is placed well in
the stop(37); then tighten it with the knob(34)situate th
Fasten the breath screen(5) with the knob(4)
Insert the connecting cable into the socket.

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. Assembling the instrument

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Let the patient sit down comfortable with hi
forehead against the forehead
rest by moving the handle (25) so that the patient
are in line with the notches on the chin
Switch the instruments on, press the
ill see the warning light
Adjust the luminous intensity by moving the selector(14)
Frame and focus the eye to be examined by moving the lever(9)

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Principal operative characteristics of the instrument:
Observation without settli
ng or tiring and rapid change of enlargements.
wise movement (which can be stopped) commanded by a
single joystick for all adjustments(x y z)
observation of the eye with enlargements 6X
the posterior vitreous body by means of the
Hruby lens or a contact options
Observation of the eye and valuation of the position of contact lenses in a
ry with Goldman tonometer.
Measurement of the cornea diameter and contact lenses.
Survey which reveals the axis of the contact lens, tha to the possible reading
of the rotation angle of the slit which includes all the meridians.

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The repairs illustrated below should all be carried out with the power cable
disconnected from the main supply plug. Please contact the suppliers for any other
problems that cannot be resolved by the operations des ibed below.
he power switch befo re replacing lamps. Please place lamps after
cooling down. The heated lamp may burn your fingers.
Don’t touch any other parts of glass tube with the bare fingers. Fingerprints, if any,
must be wiped o ff from the glass tube with
To replace the Halogen projection bulb proceed as follow.
Before doing anything else, disconnect the plug from the main supply socket;
Remove the screws with the driver(24), Remove the cover(39),
(32) from the bulb stems;
(54) to loosen the bulb stop
Remove the burnt out bulb; be careful , it could be very hot;

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Replace it with a new one(12V30W Halogen) using the pl tic envelope(never
touch the bulb whit fingers)
Make sure that the stems of the bulb are completely inserted; insert the plug in
Don’t Touch to the Lamp House, During the Operation.

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Protection fuses replacement
The protection fuses are placed on the back of the SMPS, and inserted power
socket. Before doing anything else, disconnect the plu from the main supply
Substitute the fuses and check
e plug in the main supply socket.
Replace fuses with the same rating and type(250Vac, T2.0AL)

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llTo keep the device clean, apply clinical alcohol and cidex or cidex plus on a soft
cloth and scrub the body and the probe onc
e a month. Do not use lacquer,
thinner, ethylene, or the oxidizing substance.
If the instrument is not in use, dust must be kept away by covering the
instrument with the supplied plastic cover. Dust accumulating during the
functioning of the instrument m
ust be periodically removed with a very soft cloth

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Guidance and manufacturer
Electromagnetic environment
The EUT is intended for use in the electromagnetic environment specified below.
the user of the EUT should assure that it is used in such an
The EUT uses RF energy only for its
internal function. Therefore, its RF
are very low and are not likely
to cause any interference in nearby
The EUT is suitable for use in ail
establishments, including domestic
establishments and those directly
connected to the public low
supply network that supplies buildings
used for domestic purposes

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Guidance and manufacturer
The EUT is intended for use in the electromagnetic environment specified below.
The customer or the user of the EUT should assure that it is used in such an
concrete or ceramic tile.
If floors are covered with

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NOTE U? is the a.c. mains voltage prior to application of the test level.

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Guidance and manufacturer
Electromagnetic environment
Recommended separation distance
The EUT is intended for use in the electromagnetic environment specified below.
The customer or the user of t
he EUT should assure that it is used in such an
Portable and mobile RF communications
equipment should be used no closer to any
part of the EUT, including cables, than the
recommended separation distance
calculated from the equation
the frequency of the transmitter.
where P is the maximum output power
rating of the transmitter in watts (W)
according to the transmitter manufacturer

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and d is the recommended separatio
Field strengths from fixed RF transmitters,
mined by an electromagnetic site
should be less than the compliance level in
Interference may occur in the vicinity of
NOTE 1) At 80MHz and 800MHz, the higher frequency range applies.
NOTE 2) These guidelines may not apply in all situatio Electromagnetic
propagation is affected by absorption and reflection from structures,
Field strengths from fixed transmitters, such as base tations for radio
(cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM
radio broadcast and TV broadcast cannot be predicted theoretically with accurac
To assess the electromagnetic environment due to fixed RF transmitters, an
electromagnetic site survey should be considered. If the measured field strength in
the location in which the EUT is used exceeds the applicable RF compliance level
UT should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as re
orienting or relocating the EUT.
Over the frequency range 150kHz to 80MHz, field strengths should be less than

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Recommended separation distances between portable and
mobile RF communications equipment and the EUT
Thisis intended for use in an electromagnetic environment which radiated RF
disturbances are controlled. The customer or the user the EUT ca
electromagnetic interference by maintaining a minimum nce between portable
and mobile RF communications equipment (transmitters) the EUT as
recommended below, according to the maximum output power of the communications
Separation distance according to frequency of transmitter
For transmitters rated at a maximum output power not listed above, the
recommended separation distance d in metres (m)
can be estimated using the
equation applicable to th
e frequency of the transmitter, where p is the maximum
output power rating of the transmitter in watts (W) according to the transmitter
NOTE 1) At 80MHz and 800MHz, the separation distance for the higher frequency
These guidelines may not apply in all situations. Electromagnetic
propagation is affected by
absorption and reflection from structures, objects and

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Immunity and Compliance Level

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Guidance and manufacturer
Electromagnetic environment
The EUT is intended for use in the electromagnetic
environment specified below.
The customer or the user of the EUT should assure that it is used in such an
electromagnetic environment.
The EUT must be used only in a
shielded location with a minimum RF
shielding effectiveness and, for each
able that enters the shielded
location with a minimum RF shielding
effectiveness and, for each cable that
enters the shielded location
Field strengths outside the shielded
location from fixed RF transmitters,
Interference may occur in the vicinity
of equipment marked with the

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NOTE 1) These guidelines may not apply in all situatio Electromagnetic
propagation is affected by absorpti
on and reflection from structures, objects and
NOTE 2) It is essential that the actual
shielding effectiveness and filter
attenuation of the shielded location be
verified to assure that they meet the
fixed transmitters, such as base stations for radio
(cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM
radio broadcast and TV broadcast cannot be predicted theoretically with
accuracy. To assess the electromagnetic environment
electromagnetic site survey should be considered. If the measured field strength
outside the shielded location in which the EUT is used exceeds 3V/m, the EUT
should be observed to verify normal operation.
formance is observed, additional measures may be necessary,
such as relocating the EUT or using a shielded location with a higher RF
shielding effectiveness and filter attenuation.

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Galilean converging binocular
5 positions rotation drum
6x, 10x, 16x, 25x, 40x(12.5x eyepiece )
or 5x, 8x, 12x, 20x, 32x( 10x eyepiece )
38.5, 24.0, 15.0, 9.0,6.0 mm
0˚, 5˚, 10˚, 15˚, 20˚Patient

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100~240 V AC 50/60HZ 2.0A

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If there are any problems with the equipment, please
First of all, refer to the 10. Maintenanc e and 11 . Troubleshooting sections according
to the problem that you are enco untered. And then fo llow the suggested
If the problem persists, please c
at first. Before calling to the local distributor, you
d better check the se information such as
Model and Serial Numbers. To do so, fill up the
purchase our produc t. You can loo k up these
number is found on the back of this unit. The serial number is unique to this unit.
Yo u should retain this manual as a permanent record of your purchase. Please retain
your purchase receipt as your proof of purchase.
t contact with your local distributor, you c an directly
of the HUVITZ using the phone number and the address written

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Relative spectral output graph

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ote: this graph be shown for the beam after it exist the instrument,
when the instrument is operating at
The light emitted from this instrument is potentially
hazardous. The longer the duration of exposure, the greater the risk of
ocular damage. Exposure to light from this instrument operated
tput will exceed the safety guideline after