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-------------------------------------------------------------------------------------SLIT LAMP HS-5000 5X 1
Operator’s Manual
SLIT LAMP MICROSCOPE HS-5000 5X
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IMPORTANT NOTICE
!
WARNING
Potential electromagnetic or other interference between medical equipments and other
devices being operated together in the same environmental may expert an adverse
influence on functioning of the medical equipment. Non-medical equipments not in
compliance with the requirements of EN 60601-1 and EN 60601-1-2 should not be
used together in the same environmental as the medical equipments
This equipment has been tested and found to comply with the limits for medical devices in
IEC 60601-1-2:2001. These limits are designed to provide reasonable protection against
harmful interference in a typical medical installation
Power Cord
use of equipment in rated voltage less than 125Vac,minimum 6A,Type SJT or SVT ,
For
18/3AWG,10A, max 3.0m long : One end with Hospital Grade Type, NEMA 5-15P Other
end with appliance coupler. For use of equipment in rated voltage less than
250Vac,minimum 6A,Type SJT or SVT , 18/3AWG,10A, max 3.0m long : One end
terminatesd with blade attachment plug(HAR) Type, NEMA 6-15P.
This product may malfunction due to electrom
telephones, transceivers, radio-controlled toys, etc. Be sure to avoid having objects such as,
which 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, however, for possible
errors or omissions, or for any consequences resulting from the use of the information
contained herein.
agnetic waves caused by portable personal
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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 documentation to reflect such
changes.
©2006 HUVITZ Co., Ltd.
689-3, Geumjeong-dong, Gunpo-si, Gyeonggi-do,
435-862, Republic of Korea
All rights are reserved.
Under copyright laws, this manual may not be copied, in whole or in part, without the prior
written consent of HUVITZ Co., Ltd.
Document Number: 9000OMSL001-A, published in 2006/07/20
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Contents
1. Introduction ................................................................................................................6
1.1.
Outline of the instrument..................................................................................6
1.2. Classification....................................................................................................6
2. Safety Information......................................................................................................7
2.1.
Introduction ......................................................................................................7
2.2. Safety Symbols ................................................................................................8
2.3. Environment factors .......................................................................................10
2.4. Safety Precautions.........................................................................................12
3. Features & Operating Condition.............................................................................14
3.1.
Brief Description.............................................................................................14
3.2. Operating Condition .......................................................................................14
4. Standard Components.............................................................................................16
5. Accessories..............................................................................................................17
6. Composition .............................................................................................................18
7. Installation ................................................................................................................23
Assembling the Instrument ............................................................................23
7.1.
8. Trial Operations........................................................................................................27
9. Main Features...........................................................................................................28
10. Ordinary Maintenance .............................................................................................29
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10.1.
Halogen Projection bulb ................................................................................ 29
10.2. Protection fuses replacement ........................................................................ 31
10.3. Cleaning & Disinfection ................................................................................. 32
11. EMC Information...................................................................................................... 33
11. 1.
Guidance and manufacturer’s declaration – electromagnetic emissions ......33
11. 2. Guidance and manufacturer’s declaration – electromagnetic immunity........ 34
11. 3. Guidance and manufacturer’s declaration – electromagnetic immunity........ 36
11. 4. Recommended separation distances between portable and mobile RF
communications equipment and the EUT................................................................... 38
11. 5. Immunity and Compliance Level ................................................................... 39
11. 6. Guidance and manufacturer’s declaration – electromagnetic immunity........ 40
12. Electric Diagram ...................................................................................................... 42
13. Technical Specifications .........................................................................................43
14. Service Information .................................................................................................45
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1. Introduction
1.1. Outline of the instrument
The device works like all slit lamps:
- stereomicroscopic examination of the eye under the slit light.
- microscopic examination of the ocular fundus and posterior vitreous body (using
hubry’s lens).
These devices are designed for use by ophthalmologists and optometrists(within the
realms of their respective professions) for specific diagnostic procedures(bio-
microscopic examination of the eye)
1.2. Classification
Protection against electric shock: Class I
Applied Parts: Type B applied parts.
Protection against harmful ingress of water: Ordinary, IPX0
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
Stationary: Do not try to move this equipment without help. This microscope is
heavy and should maintain stationary. Always get two persons to help lift this unit
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2. Safety Information
2.1. Introduction
Safety is everyone’s responsibility. The safe use of this equipment is largely dependent
upon the installer, user, operator, and maintainer. It is imperative that personnel study
and become familiar with this entire manual before attempting to install, use, clean,
service or adjust this equipment and any associated accessories. It is paramount that
the instructions contained in this manual are 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 information requiring special emphasis. All users, operators, and
maintainers must be familiar with and pay particular attention to all Warnings and
Cautions incorporated herein.
!
WARNING
“Warning” indicates the presence of a hazard that could result in severe personal injury,
death or substantial property damage if ignored.
NOTE
“Note” describes information for the installation, operation, or maintenance of which is
important but hazard related if ignored.
!
“Caution” indicates the presence of a hazard that could result in minor injury, or
property damaged if ignored.
CAUTION
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2.2. Safety Symbols
The International Electrotechnical Commission (IEC) has established a set of symbols
for medical electronic equipment which classify a connection or warn of any potential
hazards. 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.
Save this instruction
I and O on power 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 function
is described in the appropriate User’s or Service Manual.
Identifies the point where the system safety ground is
fastened to the chassis. Protective earth connected to
conductive parts of Class I equipment for safety purposes.
Hot surface.
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MEDICAL EUIPMENT
UL60601-1
CAN/CSA C22.2
NO.601.1
Disposal of your old appliance
When this crossed-out wheeled bin symbol is attached to a
product it means the product is covered by the European
Directive 2002/96/EC.
All electrical and electronic products should be disposed of
separately from the municipal waste stream via designated
collection facilities appointed by the government or the local
authorities.
The correct disposal of your old appliance will help prevent
potential negative consequences for the environment and
human health.
4. For more detailed information about disposal of your
appliance, please c
service or the shop where you purchased the product.
Alternating Current
WITH RESPECT TO ELECTRIC SHOCK
FIRE AND MECHANICAL HAZARDS
ONLY IN ACCORDANCE WITH UL 606011, AND CAN/CSA C22.2 NO.601.1
old
ontact your city office, waste disposal
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2.3. Environment factors
Avoid the following environments for operation or storage:
Where the equipment is exposed to water vapor.
Don’t operate an equipment with a wet hand.
Where the equipment is exposed to direct sunlight.
Where the temperature changes extremely.
Normal operating temperature range is from 10° C to 40°C,
Humidity is from 30% to 75%.
Altitude is from 700 to 1060hpa
Where it is near the heat equipment.
Where the humidity is extremely high or there is a ventilation
problem.
Where the equipment is subject to excessive shocks or
vibrations.
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Where equipment is exposed to chemical material or
explosive gas.
Be careful not to be inserted dust, especially, metal.
Don’t disassemble the product or open. We aren’t
responsible for it for nothing.
Be careful not to close the fan located on the lateral or back
side of the equipment.
Don’t plug the AC power cord into the outlet before the
connection between devices of the equipment is completed.
This can generate the defect.
Pull out the power cord with holding the plug, not the cord.
Avoid places w
normal operation, or below -10℃ or exceeds 40℃ (14℉-104℉) for transportation and
storage. Humidity should be maintained between 30 and 75% for normal operation,
transportation and storage. The atmospheric pressure in operation, transportation and
storage is from 700 to 1060hpa.
here the ambient temperature falls below 10℃ or exceeds 40℃ for
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2.4. Safety Precautions
This equipment has been developed and 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 device. The correct handling of this equipment is
imperative for its safe operation. Therefore, please read carefully all instructions before
switching on this device. For more detailed information, please contact our Customer
Service Department or one of our authorized representatives.
1. This equipment must not be used (a) in an area that is in danger of explosions
and (b) in the presence of flammable, explosive, or volatile solvent such as
alcohol, benzene or similar chemicals.
2. 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 equipment or devices.
3. The equipment must be operated only by, or under direct supervision of a
properly trained and qualified person.
4. Modifications of this equipment may only be carried out by Huvitz’s service
technicians or other authorized persons.
5. Customer maintenance of this equipment may only be performed as stated in
the User’s Manual and Service Manual. Any additional maintenance may only
be performed by Huvitz’s service technicians or other authorized persons.
6. The manufacturer is only responsible for 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, operated,
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and maintained according to this manual and Service Manual.
7. The manufacturer is not liable for damage caused by unauthorized tampering
with the device(s). Such tampering will forfeit any rights to claim under
warranty.
8. This equipment may only be used together with accessories supplied by
Huvitz’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.
10. Keep the User’s Manual and Service Manual in a place easily accessible at all
times for persons operating and maintaining the equipment.
11. Do not force cable connections. If a cable does not connect easily, be sure that
the connector (plug) is appropriate for the receptacle (socket). If you cause any
damage to a cable connector(s) or receptacle(s), let the damage(s) be repaired
by an authorized service technician.
12. Please do not pull on any cable. Always hold on to the plug when
disconnecting cables.
13. Before every operation, visually check the equipment for exterior mechanical
damage(s) and for proper function.
14. Do not cover any ventilation grids or slits.
15. Immediately turn off and unplug any equipment that gives off smoke, sparks,
strange noises, or odors.
16. Power Supply Cord set (international) - (Detachable) Rated 10 A, 250 V. Plug
type CEE 7/VII, Connector type IEC 60320/C13, and Cord type H05VV-F3G,
min. 0.75 mm2, 3-conductor terminating in molded-on grounding type
attachment plug. <HAR> marked on the cord. Maximum 4.0 m long.
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3. Features & Operating Condition
3.1. Brief Description
The device works like all slit lamps:
- stereomicroscopic examination of the eye under the slit light.
- microscopic examination of the ocular fundus and posterior vitreous body (using
hubry’s lens).
These devices are designed for use by ophthalmologists and optometrists(within the
realms of their respective professions) for specific diagnostic procedures(bio-
microscopic examination of the eye)
3.2. Operating Condition
z 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 for shipping and storage
without risk of damage:
- Temperature range : from –10˚ C to +40˚C;
- Relative humidity range: from 30% to75%;
z The device is made to operate under the following environmental conditions:
- Temperature range : from +10˚ C to +40˚C;
- Relative humidity range: from 30% to 75%;
The device neither generates nor receives electromagnetic interference when used
near other equipment. Therefore, no preventive or corrective measures are required
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!
Because prolonged intense light exposure can damage the retina, the use of the device
for ocular examination should not be unnecessarily prolonged, and the brightness
setting should not exceed what is needed to provide clear visualization of the target
structures. This device should be used with filters that eliminate UV
radiation(<400nm)and, whenever possible, filters that eliminate short-wavelength blue
light(<420nm).
The retinal exposure dose for a photochemical hazard is a product of the radiance and
the exposure time. If the value of radiance were reduced in half, twice the time would
be needed to reach the maximum exposure limit.
While no acute optical radiation hazards have been identified for slit lamps, it is
recommended that the intensity of light directed into the patient’s eye be limited to the
minimum level which is necessary for diagnosis. Infants, aphakes and persons with
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 apply
particularly if the eye has been exposed to retinal photography
CAUTION
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4. Standard Components
The instrument is delivered in package. Taking it out of the package, make sure that
none of the following parts is missing.
z 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);
z A base with orthogonal movements.
z A microscope with either dual magnification or a system(31) including
eyepieces.
z An optical group of the slit projector.
z A head rest module(59).
z A microscope arm(45).
z This manual.
z 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 Halogen bulb(53); two
protection fuses(48); a breath screen(19); a chin-rest paper(47);a hole
cover(45); a power cable; two patient’s handles(50)
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5. Accessories
The following standard accessories are
provided with the instrument;
z protection cover(46)
z a setting rod(43)
z spare bulbs
12V 30W Halogen bulb(53)
z chin-rest paper(47)
z spare fuses
250Vac T2.0AL
z a breath screen(5)
z power cable
[ Figure 1. Accessories ]
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6. Composition
1) Fixation point
2) Control lever for changing enlargement
3) Removable eye-pieces
4) Knob for clamping the breath screen
5) Breath screen
6) Control handle for the slit rotation 90-0-90
7) Connecting plug of the projector lamp
8) Knurled ring for filters insertion
9) Joystick for lateral, longitudinal and vertical movements(x y z)
10) Base with orthogonal movements
11) Shaped tabletop
12) Warning light indicating the ignition of the SMPS is on
13) Main switch & Warning light
14) Luminosity selector
15) SMPS box
16) Drawer
17) Toothed guides
18) Wheel protection crankcases
19) Sliding plate
20) Knob to lock the projector
21) Scale for the projector position
22) Knob to lock the arm of the microscope
23) Hole cover
24) Knurled knob to lift the bulb holder
25) Ring for the vertical setting of the chin-rest
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26) Locking pins for chin rest paper
27) Chin rest
28) Knobs to change the slit width
29) Pointer for the eye positioning
30) Head rest
31) Microscope
32) Bulb feeding contacts
33) Knob to lock the base of the instrument
34) Knob to lock the microscope
35) Control handle for horizontal tilting
36) Control lever for vertical tilting
37) Microscope position stop
38) Graduated ring 90-0-90 determining the inclination of the slit during rotation
39) Lamp cover
40) fuse slots
41) Connecting plug
42) Fixation point connector
43) Setting rod
44) Microscope separation knob
45) Microscope arm
46) Protection cover
47) Chin rest papers
48) Guide screw
49) An optical group of the slit projector
50) Patient’s handle
51) Chin rest fastening screw
52) Wheel
53) Halogen bulb 12V 30W
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54) Bulb fastening knob
55) Mirror
56) Capture connector ( For the image system)
57) Capture switch
58) Luminosity selector connector ( Connect the Luminosity selector to the
SMPS)
59) Head rest module
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[ F
igure 2. Composition I ]
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[ F
igure 3. Composition Ⅱ]
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7. Installation
NOTE
The appliances are always supplied with excellent packaging to be able to stand up to
all kinds of transport and standard storage conditions. Please contact the suppliers if
any irregularities are found in the appliance due to transport after unpacking
7.1. Assembling the Instrument
z Put the table top on a very stable support. Block the two parts together by
tightening the screws
[ F
igure 4. Table Assembling ]
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z Place the head rest module(59) and make sure that its holes fit together with
those of the table top. Tighten the screw with the screw driver
[ Figure 5. Assembling the instrument I]
z
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
crankcase(59) and make sure that its holes fit together with those of the
toothed guides(17). Tighten the screw with the screw driver(+)
z Assemble the microscope arm(45) on the Base with orthogonal move
ments(10).
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z Assemble An optical group of the slit projector(49) on the Base with orthogonal
movements(10). Then tighten the Guide screw with the screw driver(-)
z 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)situated the right side of the
microscope.
z Fasten the breath screen(5) with the knob(4)
z Insert the connecting cable into the socket.
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igure 6. Assembling the instrument Ⅱ]
[ F
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8. Trial Operations
z Assemble the chin-rest paper(47) on the chin-rest(27).
z Let the patient sit down comfortable with his chin on the chin-rest and his
forehead against the forehead-rest.
z Lift or lower the chin-rest by moving the handle (25) so that the patient’s eyes
are in line with the notches on the chin-rest(29)
z Switch the instruments on, press the switch(13). You will see the warning light
on (12).
z Adjust the luminous intensity by moving the selector(14)
z Frame and focus the eye to be examined by moving the lever(9)
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9. Main Features
Principal operative characteristics of the instrument:
z Observation without settling or tiring and rapid change of enlargements.
z Base with cross-wise movement (which can be stopped) commanded by a
single joystick for all adjustments(x y z)
z Stereomicroscopical observation of the eye with enlargements 6X-10X-16X-25X-
40X(5 enlargements model).
z Tilting 5˚-10 ˚-15 ˚-20 ˚
z Microscopy of the back part and of the posterior vitreous body by means of
the Hruby lens or a contact options.(Goldman lens).
z Observation of the eye and valuation of the position of contact lenses in a
fluorescent light.
z Tonometry with Goldman tonometer.
z Measurement of the cornea diameter and contact lenses.
z Shooting and video recording of the eye
z Survey which reveals the axis of the contact lens, thanks to the possible reading
of the rotation angle of the slit which includes all the meridians.
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10. Ordinary Maintenance
!
WARNING
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 described below.
!
CAUTION
Please turn off the power switch before replacing lamps. Please place lamps after
cooling down. The heated lamp may burn your fingers.
NOTE
Don’t touch any other parts of glass tube with the bare fingers. Fingerprints, if any,
must be wiped off from the glass tube with alcohol
10.1. Halogen Projection bulb
T
o replace the Halogen projection bulb proceed as follow.
z Before doing anything else, disconnect the plug from the main supply socket;
z Remove the screws with the driver(24), Remove the cover(39),
z Remove the connectors(32) from the bulb stems;
z Rotate the knob(54) to loosen the bulb stop
z Remove the burnt out bulb; be careful , it could be very hot;
z Replace it with a new one(12V30W Halogen) using the plastic envelope(never
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touch the bulb whit fingers)
z Fasten the bulb with the knob
z Make sure that the stems of the bulb are completely inserted; insert the plug in
the main supply socket
[ Figure 7. Replace Halogen bulb ]
Don’t Touch to the Lamp House, During the Operation.
It’s Heating up.
!
WARNING
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10.2. Protection fuses replacement
To replace the fuses proceed as follows:
z The protection fuses are placed on the back of the SMPS, and inserted power
socket. Before doing anything else, disconnect the plug from the main supply
socket
z Remove the burned-out fuses
z Substitute the fuses and check
z Replace the plug in the main supply socket.
[ Figure 8. Replace the fuse ]
!
CAUTION
Replace fuses with the same rating and type(250Vac, T2.0AL)
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10.3. Cleaning & Disinfection
z To keep the device clean, apply clinical alcohol and cidex or cidex plus on a soft
cloth and scrub the body and the probe once a month. Do not use lacquer,
thinner, ethylene, or the oxidizing substance.
z 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 must be periodically removed with a very soft cloth
or with a small pump.
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11. EMC Information
11.1. Guidance and manufacturer’s declaration – electromagnetic
emissions
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
environment.
Immunity test Compliance Electromagnetic environment -
guidance
RF Emissions
CISPR 11
RF Emissions
CISPR 11
Harmonic
emissions
IEC 61000-3-2
Voltage
fluctuations/
Flicker emissions
Group 1 The EUT uses RF energy only for its
internal function. Therefore, its RF
emissions are very low and are not likely
to cause any interference in nearby
electronic equipment
Class B The EUT is suitable for use in ail
establishments, including domestic
establishments and those directly
connected to the public low-voltage power
supply network that supplies buildings
used for domestic purposes
Class A
Complies
IEC 61000-3-3
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11.2. Guidance and manufacturer’s declaration – electromagnetic
immunity
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
environment.
Immunity test IEC 60601
Test level
Electrostatic
discharge (ESD)
IEC 61000-4-2
Electrical fast
transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips,
short
interruptions and
voltage
variations
on power supply
input lines
IEC 61000-4-11
±6kV Contact
±8kV air
±2kV for power
supply lines
± 1kV for
input/output
lines
±1kV
differential
mode
±2kV common
mode
<5% Uт
(>95% dip in
Uт )
for 0.5cycle
40% Uт
(60% dip in
Uт )
for 5 cycle
70% Uт
(30% dip in Uт )
for 25 cycle
Compliance
level
±6kV Contact
±8kV air
±2kV for power
supply lines
± 1kV for
input/output
lines
±1kV differential
mode
±2kV common
mode
<5% Uт
(>95% dip in Uт)
for 0.5cycle
40% Uт
(60% dip in Uт )
for 5 cycle
70% Uт
(30% dip in Uт )
for 25 cycle
<5% Uт
(<95% dip in
Electromagnetic
environment -guidance
Floors should be wood,
concrete or ceramic tile.
If floors are covered with
synthetic material, the
relative humidity should
be at least 30%.
Mains power quality
should be that of a
typical commercial or
hospital environment.
Mains power quality
should be that of a
typical commercial or
hospital environment.
Mains power quality
should be that of a
typical commercial or
hospital environment. If
the user of the EUT
image intensifier require
continued operation
during power mains
interruptions,
it is recommended that
the
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<5% Uт
(<95% dip in
Uт )
for 5 s
Power frequency
(50/60Hz)
magnetic field
IEC 61000-4-8
NOTE Uт is the a.c. mains voltage prior to application of the test level.
3 A/m 3 A/m Power frequency
Uт )
for 5 s
EUT image intensifier be
powered from an
uninterruptible power
supply or a battery.
magnetic fields should
be at levels character
ristic of a typical location
in a typical commercial
or hospital environment.
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11.3. Guidance and manufacturer’s declaration – electromagnetic
immunity
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
environment.
Immunity
test
Conducted
RF
IEC
61000-4-6
Radiated
RF
IEC
61000-4-3
IEC
60601
test
level
3 Vrms
150
kHz to
80MHz
3 V/m
80
MHz to
2.5GHz
Complianc
e
level
3 Vrms
150 kHz to
80MHz
3 V/m
80MHz to
2.5GHz
Electromagnetic environment - guidance
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 applicable to
the frequency of the transmitter.
Recommended separation distance
w
here P is the maximum output power
rating of the transmitter in watts (W)
according to the transmitter manufacturer
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-------------------------------------------------------------------------------------SLIT LAMP HS-5000 5X 37
and d is the recommended separation
distance in meters (m).
Field strengths from fixed RF transmitters,
as deter-mined by an electromagnetic site
a
survey,
should be less than the compliance level in
each frequency range.
b
Interference may occur in the vicinity of
equipment marked with the following
symbol :
NOTE
1) At 80MHz and 800MHz, the higher frequency range applies.
NOTE 2) These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures, objects and
people.
a
Field strengths from 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 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
above, the EUT 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.
b
Over the frequency range 150kHz to 80MHz, field strengths should be less than
[V
] V/m.
1
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11.4. Recommended separation distances between portable and
mobile RF communications equipment and the EUT
The is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the EUT can help Prevent
electromagnetic interference by maintaining a minimum distance between portable
and mobile RF communications equipment (transmitters) and the EUT as
recommended below, according to the maximum output power of the communications
equipment.
Rated
maximum
output power
Separation distance according to frequency of transmitter [m]
150kHz to 80MHz 80MHz to
800MHz
800MHz to
2.5GHz
of transmitter
[W]
=3V/m E1=3V/m
=3Vrms
V
1
E
1
0.01 0.116 0.1166 0.2333
0.1 0.368 0.3687 0.7378
1 1.166 1.1660 2.3333
10 3.687 3.6872 7.3785
100 11.660 11.6600 23.333
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 the frequency of the transmitter, where p is the maximum
output power rating of the transmitter in watts (W) according to the transmitter
manufacturer.
NOTE 1) At 80MHz and 800MHz, the separation distance for the higher frequency
range applies.
NOTE 2) These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures, objects and
people.
Page 39
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11.5. Immunity and Compliance Level
Immunity test IEC 60601 Test
Level
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
3Vrms
150kHz to 80MHz
3Vrms
80MHz to 2.5GHz
Actual Immunity
Level
3Vrms 3Vrms
3V/m 3V/m
Compliance
Level
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40 SLIT LAMP HS-5000 5X ------------------- ----------------------------------------------------------------
11.6. Guidance and manufacturer’s declaration – electromagnetic
immunity
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.
Immunity
test
Conducted
RF
IEC
61000-4-6
Radiated
RF
IEC
61000-4-3
IEC 60601
test level
3 Vrms
150 kHz to
80MHz
3 V/m
80 MHz to
2.5GHz
Compliance
level
3 Vrms
150 kHz to
80MHz
3 V/m
80MHz to
2.5GHz
Electromagnetic environment -
guidance
The EUT must be used only in a
shielded location with a minimum RF
shielding effectiveness and, for each
cable 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,
as determined by an
electromagnetic site survey, should
be less than 3V/m.
Interfer
ence may occur in the vicinity
of equipment marked with the
following symbol:
a
Page 41
-------------------------------------------------------------------------------------SLIT LAMP HS-5000 5X 41
NOTE 1) These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures, objects and
people.
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
minimum specification.
a
Field strengths from 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 due to fixed RF
transmitters, an
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.
If abnormal performance 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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42 SLIT LAMP HS-5000 5X ------------------- ----------------------------------------------------------------
12. Electric Diagram
Page 43
-------------------------------------------------------------------------------------SLIT LAMP HS-5000 5X 43
13. Technical Specifications
MICROSCOPE - HS-5000 5X 5x
Type
Magnification 5 positions rotation drum
Eyepiece 12.5x
Total magnification 6x, 10x, 16x, 25x, 40x
Real field of view 38.5, 22.2, 15.2, 10.5, 6.7 mm
Interpupillary adjust 55-80 mm
SLIT ILLUMINATION
Slit length 0.3-12 mm(continuous)
Slit width 0-12 mm(continuous)
Slit projection 1x
Aperture diaphragms 0.3/1/3/5/9/12 mm
Filters
Slit rotation 0˚~180˚ continuous
Galileian converging binocular
cobalt blue, red-free, gray and heat-
absorption
Angle of incidence 0˚, 5˚, 10˚, 15˚, 20˚
Patient’s eye/mirror
surface working
distance
80 mm
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44 SLIT LAMP HS-5000 5X ------------------- ----------------------------------------------------------------
BASE
Vertical Movement Min. 28mm
Longitudinal Movement Min. 78mm.
Lateral Movement Min. 98mm
Fine base Movement Min. 10mm
Power supply 100~240 V AC 50/60HZ 2.0A
Power consumption 70VA
Instrument Voltage 12V DC
Halogem Projection
bulb
Fixation point bulb 6V 0.2A
12V 30W
Page 45
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14. Service Information
How to contact service: If there are any problems with the equipment, please follow the
steps below:
z First of all, refer to the 10. Maintenance and 11. Troubleshooting sections according
to the problem that you are encountered. And then follow the suggested sequences.
z If the problem persists, please contact the local distributor in your province or country
at first.
z Before calling to the local distributor, you’d better check these information such as
Model and Serial Numbers. To do so, fill up the following table as soon as you
purchase our product. You can look up these information at any time. The serial
number is found on the back of this unit. The serial number is unique to this unit.
You should retain this manual as a permanent record of your purchase. Please retain
your purchase receipt as your proof of purchase.
Date of Purchase:
Dealer’s Name:
Dealer Address:
Dealer Phone No. :
Model No.:
Serial No.:
z I
f you can’t contact with your local distributor, you can directly get in touch with the
service department of the HUVITZ using the phone number and the address written
in the below table.
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46 SLIT LAMP HS-5000 5X ------------------- ----------------------------------------------------------------
How to Contact HUVITZ Co., Ltd
Write us at:
HUVITZ Co., Ltd.
Huvitz B/D, 689-3 Geumjeong-dong
Gunpo-si Gyeonggi-do, South Korea
435-862
Tel: +82-31-442-8868
Fax: +82-31-442-8619
URL:http://www.huvitz.com