OPERATOR MANUAL

Amsco® SQ240TM Surgical Lighting Systems

Centra Mount/Track Mount

Amsco® SQ240 SurgiVisionTM Surgical Lighting and

Video System
Centra Mount
(05/29/01) P-150824-909
Rev. 10
 A WORD FROM STERIS CORPORATION

This manual contains important information on proper use and care of this
surgical lighting fixture. All operators and department heads are urged to
carefully review and become familiar with the warnings, cautions, and instruc-
tions contained herein. Your new surgical lighting fixture features an advanced,
state-of-the-art design, with cool, shadow-reduced light, and ease of maneu-
verability. It produces light of a quality necessary for the most demanding and
complex of surgical procedures.
A thorough preventive maintenance program is essential to safe and proper
operation of your surgical light. You are encouraged to contact STERIS concern-
ing our Annual Maintenance Agreement. Under terms of this agreement,
preventive maintenance, adjustments, and replacement of worn parts are done
on a scheduled basis to assure lighting fixture performance at peak capability
and to help avoid untimely or costly downtime. STERIS maintains a nationwide
staff of well-equipped, factory-trained technicians to provide this service, as well
as expert repair services. Contact your STERIS representative for details.
12345678901234567890123456789012
12345678901234567890123456789012 The Amsco® SQ240 SurgiVisionTM Surgical Lighting and Video System from
Indications for Use STERIS is a high-resolution video system integrated into the lighthead of an
12345678901234567890123456789012
12345678901234567890123456789012 SQ240 light. This video system, designed into the camera housing that
accepts the sterilizable handle, enables the Customer to document surgical
procedures for a variety of reasons, including teaching and archival purposes.
A remote hand-held wireless control allows the Customer to control the key
video functions of the system; zoom, image-field rotation, and focus of the
camera. An optional foot control accessory (not available on Hermes-ready
systems) is available to activate the video system zoom and rotation functions.
The Hermes-ready system requires the use of a Hermes control center (not
supplied by STERIS) that allows the customer to control key video functions
(zoom, image-field rotation and focus) using verbal commands or a hand-held
touch screen pendant.
The Amsco® SQ240TM Surgical Lighting System provides cool, color-cor-
rected, shadow-controlled illumination of the surgical field during surgical
procedures in the operating theatre.

12345678901234567890123456789012 The following is an important message from STERIS about the

12345678901234567890123456789012 advantages and limitations associated with the use of high
Advisory
12345678901234567890123456789012
intensity surgical lighting systems.
12345678901234567890123456789012 Because of the variety of surgical procedures performed and the wide range
of individual preferences of surgical staffs, it is desirable that the surgical
lighting system be capable of selective control across a wide range of
illumination intensities. The Illuminating Engineering Society (IES) stresses
that in addition to providing control of intensity, surgical lighting systems
should provide shadow control, correct color rendition, and a suitable depth
of field to provide sharp, consistent lighting into deep body cavities.
The IES states that the surgical lighting system should be capable of providing
a minimum of 2,500 footcandles of light directed to the center of the pattern.
Although the IES does not recommend a maximum illumination intensity, it
cautions that as illumination intensities increase to maximum settings, radiant
heat will also increase. The IES further cautions that for most operations, infrared
radiant energy in the spectral region of 800 to 1000 nm should be kept to a
© 2000, STERIS Corporation. All rights reserved. Printed in U.S.A.

i
150824-909
 minimum. In certain neurosurgical or intestinal procedures on delicate, thin, dry
or abnormal tissue, the user of surgical lights should take care to utilize the
lowest possible illumination intensity suitable for the procedure.
The Amsco SQ240 Surgical Lighting System has been designed to provide
maximum illumination flexibility and at the same time minimize potentially
damaging infrared heat in the surgical field. Illumination intensity of the SQ240
Surgical Light can be adjusted through five intensity settings on the Variable
Intensity Controller (VIC). Typical illumination performance can be expected to
range between approximately 6,000 footcandles at position number 1 on the
VIC and 12,000 footcandles at position number 5. For the protection of
surgically exposed tissues and for the comfort and efficiency of the surgeon
and assistants, radiant energy can be effectively controlled by limiting the time
of exposure at the higher intensity settings on the VIC.
NOTE: This device is in compliance with IEC 60601-1-2 (1st Edition, 1993-04),
Medical Electrical Equipment – Part 1: Gneral Requirements for Safety;
Electromagnetic Compatibility (EMC). There is, however, apotential for electro-
magnetic or other interference between this equipment and other devices.
Should you experience interference, relocate the device or minimize the use
of the affected equipment while this device is operating.

EC Authorized Representative Manufactured by:

STERIS Ltd. STERIS Corporation

The Stable Block, Cornbury Park 2720 Gunter Park East
Charlbury Montgomery, AL 36109 • USA
Oxfordshire OX7 3EH TEL: 334 277 6660
ENGLAND FAX: 334 271 5450

Class 1 Equipment
Type B Equipment
Ordinary Equipment (enclosed equipment without protection of ingress of water)
Equipment not suitable for use in the presence of a flammable anesthetic mixture with
air or oxygen or nitrous oxide.
Suitable for continuous operation.
Power Rating: 110-130 VAC, 50/60 Hz, 3.5 A (Single) / 7 A (Dual)
220-250 VAC, 50/60 Hz, 2 A (Single) / 4 A (Dual)
NOTE: Optional equipment may have other power requirements.

STERIS offices worldwide:

Canada 800 661 3937
Germany 49 2233 6999 400
Hong Kong 852 2 563 3623
Italy 39 0141 590429
Japan 81 78 252 1901
Korea 82 2 554 1661
Latin America 305 442 8202
Singapore 65 841 7677
Spain 34 91 658 5920
United Kingdom 44 1 608 811 822

Manufactured ISO 9001

Exclusively by EN 46001
STERIS Corporation ISO 13485
Montgomery, AL Certified

The base language of this document is

ENGLISH. Any translations must be
made from the base language document.

ii
150824-909
 TABLE OF CONTENTS

Section Title Page

1 Listing Of Warnings And Cautions .................................................. 1-1

Definition of Symbols ......................................................................................................... 1-3

2 Installation Verification .................................................................. 2-1

Pre-operation Checklist ..................................................................................................... 2-1

3 Operating Instructions .................................................................... 3-1

Advisory ............................................................................................................................. 3-1
Lighthead Positioning ........................................................................................................ 3-2
Check Lamp Failure LEDs ................................................................................................. 3-2
Variable Intensity Controller ............................................................................................... 3-2
Light Pattern Adjustment ................................................................................................... 3-4
Sterilizable Handle ............................................................................................................. 3-5
Camera Installation or Removal ......................................................................................... 3-7
Surgivision Camera Operation........................................................................................... 3-8
Install Video Monitor .......................................................................................................... 3-9
Install Video Cassette Recorder ........................................................................................ 3-9

4 Cleaning the Equipment .................................................................. 4-1

Cleaning Equipment .......................................................................................................... 4-1
General Cleaning/Disinfecting Procedure ......................................................................... 4-3
Areas To Be Cleaned Before Each Use ............................................................................. 4-3
Areas To Be Cleaned/Disinfected Once A Month .............................................................. 4-3

5 Operator Troubleshooting ............................................................... 5-1

6 Maintenance .................................................................................... 6-1

Preventive Maintenance Record ........................................................................................ 6-1
Inspect Lamp Change Mechanism ................................................................................... 6-3
Check Vertical Suspension Tube ....................................................................................... 6-3
Check Battery Backup (As Applicable) ............................................................................. 6-3
Check Hub Cap (Centra Mount) ........................................................................................ 6-5
Check Variable Intensity Controller .................................................................................... 6-5
Check Yoke Plug Button .................................................................................................... 6-5
Lamp Replacement ........................................................................................................... 6-6

7 Replacement Parts .......................................................................... 7-1

iii
150824-909
 Track Mounting
Alternative
Suspension

Ceiling
Mounted
Track

Carriage
Assembly

Vertical
Suspension
Tube
Lamp
Failure
LED
Track Mounted Systems Only Upper
(track mounting not available Horizontal
for SurgiVision systems). Arm(s) Centra Mount

Vertical
Suspension
Tube Top Cover Lighthead
Yoke
Suspension
Arm

2
Knuckle Sterilizable Non-sterile
Assembly Handle Handle (4)
Serial
Number
Tag

SQ240
SurgiVision
Lighthead with
Integral
SurgiVision
Video System

Amsco SQ240 Lighting System and SQ240 SurgiVision Lighting and Video System

iv
150824-909
LISTING OF WARNINGS AND CAUTIONS 1
The following is a summary of safety precautions which must be observed when operating or servicing this lighting
fixture. WARNINGS indicate the potential for danger to personnel, and CAUTIONS indicate the potential for
damage to equipment. The precautions are repeated (in whole or in part), where applicable, throughout the
manual. Carefully read all precautions before proceeding to use or service this equipment.

WARNING — EXPLOSION HAZARD:

Do not use lighting fixture in the presence of flammable anesthetics.

WARNING — ELECTRIC SHOCK HAZARD:

Do not remove covers or perform service other than as described in this operator manual. Refer
servicing to qualified service personnel. (Maintenance Manual P-764326-998.)

Do not remove variable intensity controller covers. Refer servicing to qualified service personnel.

WARNING — RISK OF FIRE:

Replace fuses (F-1) and (F-2) as noted: 24V- FLM 20 250 V. Contact STERIS Corporation for
replacement fuses.

WARNING — PERSONAL INJURY HAZARD:

Do not use lighting fixture if red band is visible below rubber cap at top of vertical suspension
tube.

Do not attempt to replace the lamp unless power is turned off at variable intensity controller by
disengaging the circuit breaker(s) and the lighthead has cooled sufficiently.

Do not attempt to clean lighthead unless power is turned off at variable intensity controller by
disengaging the circuit breaker(s) and the lighthead has cooled sufficiently.

Do not attempt to adjust suspension system. Refer servicing to qualified service personnel.

CAUTION: POSSIBLE EQUIPMENT DAMAGE

Do not bump lightheads into walls or other equipment.

Use only recommended cleaning/disinfecting and/or anti-static agents on this light. Some degree
of staining, pitting, and/or discoloration could occur if a phenolic-, iodophor-, or glutaraldehyde-
based disinfectant is used on the surfaces of this light. Also, use of alcohol or aerosol spray
cleaner/disinfectants (e.g., Lysol®) containing a substantial amount of alcohol in the formula can
damage the acrylic plastic lens.

Use of any disinfectant solution other than those listed below may cause discoloration or
deformation on the acrylic lens surface: Coverage Spray TB, Germicidal Cloth, Coverage Spray
HBV, Coverage HBV Concentrate, T.B.Q., or Coverage Plus. Cleaning solutions other than those
listed have NOT been tested for compatibility or effectiveness. Always follow manufacturer
instructions for concentrations and use of cleaning products.

1-1
Operator Manual Preventive Maintenance 150824-909
 Prevent leakage of fluids into interior of lighthead.

Do not scratch optical coating on accessible portions of optical core when cleaning; always wear
rubber gloves and use only a clean, white, lint-free cloth when wiping internal surfaces.

Do not touch glass portion of lamp during re-lamping or cleaning.

Manual actuation of the lamp change mechanism may result in permanent damage to the gear
motor.

To prevent camera or camera replacement unit from falling, tighten thumb screws securely.

Do not operate circuit breaker with the intensity controller knob in any of the “ON” positions.

Do not use circuit breaker as routine operation ON/OFF switch.

Do not immerse the hand-held control in fluid.

1-2
150824-909 Listing of Warnings and Cautions Operator Manual
12345678901234567890123456789
12345678901234567890123456789
Definition of Symbol Definition
Symbols
12345678901234567890123456789
12345678901234567890123456789 ON

OFF (Standby)

ON

STANDBY

Lamp Out

Protective Earth (Ground)

Attention, consult manual for further instructions

Hot

SER. NO. Serial Number of Unit

V~ Voltage Rating of Unit, Alternating Current

A Amperage Rating of Unit

Hz Frequency of Unit

Zoom

Rotate

Manual Focus

Auto Focus

1-3
Operator Manual Preventive Maintenance 150824-909
INSTALLATION VERIFICATION 2
WARNING - ELECTRIC An Equipment Drawing showing all of the space and utility requirements was
sent to the purchaser after the order for this surgical light was received. The
SHOCK HAZARD: Do not
clearance space shown on the drawing is necessary for proper installation,
remove covers or perform
operation, and maintenance of this fixture.
service other than as de-
scribed in this operator Installation and Uncrating Instructions were furnished with the Lighting
manual. Refer servicing Fixture.
to qualified service per-
sonnel (Maintenance If any of these documents are missing or misplaced, contact STERIS, giving
Manual P-764326-998) the serial, unit and model numbers of the equipment. Replacement copies will
be sent to you promptly.
12345678901234567890123456789
12345678901234567890123456789
Before operating the equipment, complete the pre-operation checklist. It is
Pre-operation essential to the safe operation and continuing maintenance of this equipment
to ensure the installation is complete and correct. (Refer to Figures 1 through
Checklist
12345678901234567890123456789 5 to locate parts.)
12345678901234567890123456789

2-1
Operator Manual Installation Verification 150824-909
 Check Track Mounting For Seismic If Required (see
Figure 2-1)
NOTE: 4'6" track uses eight outer holes for seismic and four central holes for
non-seismic installations.
NOTE: Seismic installations require track to be mounted using the eight hole
mounting pattern only (see Figure 2-1). Contact STERIS if there are any
questions regarding seismic building code regulations.

These holes required for These holes required for

Top View
all seismic installations all seismic installations

Holes used for non-seismic installations

Figure 2-1. Track Mounting Hole Patterns for 9' Track

2-2
150824-909 Installation Verification Operator Manual
 Check Vertical Suspension Tube (see Figure 2-2)
WARNING - PERSONAL
INJURY HAZARD: Do not Inspect vertical suspension tube. A red colored band has been applied to the
use lighting fixture if red surface of the tube normally hidden under the rubber boot at the top. If the
band is visible below rub- mounting configuration has been properly assembled, the red band will not
ber cap at top of vertical be visible. If the red band is visible, do not attempt to use the light fixture.
suspension tube. Additionally, when properly assembled the vertical suspension tube should
not move back and forth or side to side (i.e., “wobble”). If the vertical
suspension tube does move back and forth or side to side, do not use the light
fixture because the installation is not correct. In either case, call your STERIS
service representative immediately.
Check Suspension Movement
The lighthead assembly should move smoothly and easily. When positioned,
the lighthead should not drift. If any binding or drifting is present in the
movement of the lighthead, call your STERIS service representative to make
adjustments. Ensure that suspension system (e.g. counterbalance, vertical
suspension tube pivot) moves through all articulations smoothly without
binding.

Red Band
Showing
(INCORRECT)

Red Band Red Band NOT Showing

Showing (CORRECT)
(INCORRECT)
Red Band NOT Showing
(CORRECT)

Centra Mount Track Mount

Figure 2-2 Check Vertical Suspension Tube

2-3
Operator Manual Installation Verification 150824-909
 Check Operation of Fixture
Ensure that electrical power to the Variable Intensity Controller (VIC) is on.
Variable Intensity Controller: Turn the controller on by pressing the circuit
breaker(s) to the “ON” position. This control has five discrete intensity
settings. Turn the rotary knob clockwise until it points to #1 (lowest intensity
setting). The “ON” LED should illuminate to indicate power to the lighthead.
Turning the knob clockwise to the #2, #3, #4, and #5 positions will increase
Lamp Failure LED the light intensity. Check all five positions for operation and change in
(One on each side of the lighthead) intensity. (See Figure 2-3.)
NOTE: Turn power OFF using intensity control knob when testing is
complete. (See Figure 2-3.)
Check Lamp Failure LEDs: If the LEDs on the lighthead cover are
blinking, one or both of the fixture's lamps may have to be replaced. (Refer
to Lamp Replacement, Section 6.)
Check Operation of SurgiVision Video Camera
Turn the video controller on by pressing the circuit breaker to the “ON”
position. Press the power “ON” touch button on the touch pad to turn on
camera. (See Figure 2-4.) Verify that power LED illuminates.
Video: Ensure a clear signal is reaching the video display device
(monitor) from the camera. (Check cable connection between wall control
and monitor, if necessary.)
Wall Control: Verify zoom, rotation and focus functions with the wall
control membrane switches.
Hermes-ready Wall Control: Refer to Hermes Control Center operating
manual to verify verbal command operation (check Hermes interface cable
connections between wall control and Hermes control center if necessary).
Wireless Hand-held Control: Verify zoom, rotation and focus functions
with the wireless control. (Check batteries in control if necessary.)
NOTE: Transmitter on wireless control must be within 15 feet (maximum)
and directed within 50° of receiver on wall control.

Power ON
Symbol

Power OFF
Symbol
Variable
Intensity
Positions

Circuit Fuse(s)
Breaker

Figure 2-3. SQ240 and SurgiVision

Variable Intensity Controller

2-4
150824-909 Installation Verification Operator Manual
 Optional Foot Control: Verify zoom and rotation functions with the optional
foot control. (Check cable connection between foot control and wall control,
if necessary.)
NOTE: When testing is complete, press the power “STANDBY” touch
button on the touch pad, then turn circuit breaker “OFF”. (See Figure 2-4.)

Infrared Transmitter
Amsco® SQ240 SurgiVisionTM
Surgical Lighting and Video System

Infrared
Function Controls for Receiver
SurgiVision Camera

ZOOM
ON/OFF
Switch
ROTATE

MANUAL
FOCUS

AUTO
FOCUS POWER
ON STANDBY

VIDEO OUT
FOOT CONTROL SVHS COMPOSITE

Connector Jack for

Foot Control Cable
Hand-held Circuit Breaker Connector Jacks for
Wireless Control Video Monitor

Standard Wall Control

Amsco® SQ240 SurgiVisionTM

Surgical Lighting and Video System HERMES-Ready

Infrared
Receiver

Amsco® SQ240 SurgiVisionTM

ZOOM
Surgical Lighting and Video System
ON/OFF
Switch
ZOOM ROTATE
ROTATE

Function Controls for

SurgiVision Camera MANUAL
FOCUS

AUTO
FOCUS POWER
ON STANDBY

VIDEO OUT

Optional Foot Control SVHS COMPOSITE HERMES

Circuit Breaker Connector Jacks for Hermes Interface

Video Monitor Connector

Hermes-ready Wall Control

Figure 2-4. Standard SurgiVision Wall Control, Hermes-ready Wall Control,

Hand-held Wireless Control, and Optional Foot Control

2-5
Operator Manual Installation Verification 150824-909
OPERATING INSTRUCTIONS 3
12345678901234567890123456789
12345678901234567890123456789 The following is an important message from STERIS about the
Advisory advantages and limitations associated with the use of high
12345678901234567890123456789
12345678901234567890123456789 intensity surgical lighting systems.
Because of the variety of surgical procedures performed and the wide range of
individual preferences of surgical staffs, it is desirable that the surgical lighting
system be capable of selective control across a wide range of illumination
intensities. The Illuminating Engineering Society (IES) stresses that in addition
to providing control of intensity, surgical lighting systems should provide
shadow control, correct color rendition, and a suitable depth of field to provide
sharp, consistent lighting into deep body cavities.
The IES states that the surgical lighting system should be capable of providing
a minimum of 2,500 footcandles of light directed to the center of the pattern.
Although the IES does not recommend a maximum illumination intensity, it
cautions that as illumination intensities increase to maximum settings, radiant
heat will also increase. The IES further cautions that for most operations,
infrared radiant energy in the spectral region of 800 to 1000 nm should be kept
to a minimum. In certain neurosurgical or intestinal procedures on delicate,
thin, dry or abnormal tissue, the user of surgical lights should take care to utilize
the lowest possible illumination intensity suitable for the procedure.
The Amsco SQ240 Surgical Lighting System has been designed to provide
maximum illumination flexibility and at the same time minimize potentially
damaging infrared heat in the surgical field. Illumination intensity of the SQ240
Surgical Light can be adjusted through five intensity settings on the Variable
Intensity Controller (VIC). Typical illumination performance can be expected to
range between approximately 6,000 footcandles at position number 1 on the
VIC and 12,000 footcandles at position number 5. For the protection of
surgically exposed tissues and for the comfort and efficiency of the surgeon
and assistants, radiant energy can be effectively controlled by limiting the time
of exposure at the higher intensity settings on the VIC.
NOTE: This device is in compliance with IEC 60601-1-2 (1st Edition, 1993-04),
Medical Electrical Equipment – Part 1: Gneral Requirements for Safety;
Electromagnetic Compatibility (EMC). There is, however, apotential for electro-
magnetic or other interference between this equipment and other devices.
Should you experience interference, relocate the device or minimize the use of
the affected equipment while this device is operating.

3-1
Operator Manual Operating Instructions 150824-909
12345678901234567890123456789
12345678901234567890123456789 A wall-mounted Variable Intensity Controller (see Section 2, Figure 2-3) allows
Variable Intensity the user to adjust the fixture's light intensity (brightness) by rotating a control
knob. An identifying number on the rotary knob corresponds to the same
Controller
12345678901234567890123456789
12345678901234567890123456789 number on the lighthead suspension knuckle.
To operate the controller:
WARNING - EXPLOSION 1. Push circuit breaker(s) to the ON position.
HAZARD: Do not use in
the presence of flammable 2. One or two rotary knobs on the face of the controller are used to adjust the
anesthetics. intensity level of lightheads. Generally, rotating a knob clockwise increases
intensity, rotating a knob counterclockwise decreases intensity. Each
CAUTION: Do not operate knob can be positioned to five discrete intensity levels.
circuit breaker with the Positions:
intensity controller knob
in any of the “ON” posi- NOTE: Trying to leave knob indicator at a point between discrete positions can
tions. damage the controller.
– OFF
CAUTION: Do not use cir-
cuit breaker as routine – Power ON, indicator LED
operation ON/OFF switch.
1, 2, 3, 4, 5 – (also note increasingly larger circle beside each number).
The higher the number (or the larger the circle), the greater level of
illumination from the lighthead.
NOTE: For longer lamp life, use lowest intensity level suitable for surgical
procedure.
3. To turn lighthead OFF, rotate knob until indicator points to the OFF symbol
on the controller panel.

12345678901234567890123456789
12345678901234567890123456789
Lamp Failure LEDs, with accompanying symbols, are located on the front and
Check Lamp back of lighthead cover (see illustration at left for location). These indicators
are used to determine if the lighthead is operating on the secondary lamp.
Failure LEDs
12345678901234567890123456789
12345678901234567890123456789 • Check the Lamp Failure LEDs each time the surgical light is used.
• A secondary lamp inside the lighthead turns on when the primary lamp
fails and automatically moves into the primary position. This function takes
approximately one second.
• If the lamp failure LEDs are blinking, replace the failed lamp(s). (See Lamp
Replacement, Section 6.) After the lamp is replaced and power is restored
to the lighthead, the LEDs stop blinking, the primary lamp lights and
returns to the primary position.
Lamp Failure LED
(One on each side of the lighthead)

12345678901234567890123456789
12345678901234567890123456789 The lighthead movements shown in Figure 3-1 can be made by using either
Lighthead the sterile handle or the four non-sterile handles positioned around the edge
of the lens retainer (see Figure 1 for position of handles). The following two
Positioning
12345678901234567890123456789 paragraphs describe the positioning characteristics of the SQ240 SurgiVision
12345678901234567890123456789
lighthead from outside or within the sterile field. To optimize shadow control,
CAUTION: Do not bump position the lighthead as appropriate before starting the intended surgical
lightheads into walls or procedure.
other equipment.

3-2
150824-909 Operating Instructions Operator Manual
 • Centra-Mounted
Lighthead may (1) rotate continuously around vertical suspension tube; (2)
rotate continuously around central hub; (3) rotate continuously about suspen-
sion arm; (4) tilt forward or backward in yoke approximately 310 degrees; and
(5) move up or down by pivoting at suspension fork 15 degrees up, and 90
degrees down until vertical tube and suspension arm describe a straight line
(i.e., full movement up and down through 105 degrees, see Figure 3-1).

• Track-Mounted
Lighthead may (1) provide motion along the length of the track system; (2)
rotate continuously around the carriage; (3) rotate continuously about suspen-
sion arm; (4) tilt forward or backward in yoke approximately 310 degrees; and
(5) move up or down by pivoting at suspension fork 15 degrees up, and 90
degrees down until vertical tube and suspension arm describe a straight line
(i.e., full movement up and down through 105 degrees, see Figure 3-1).

310°

35°

Typical Centra-Mounted Lighting System

105°

Typical Track-Mounted Lighting System

(Not available for SQ240 SurgiVision)

Figure 3-1. Lighthead Positioning

3-3
Operator Manual Operating Instructions 150824-909
12345678901234567890123456789
12345678901234567890123456789 • See Figure 3-2
Light Pattern
IMPORTANT: SQ240 lightheads equipped with the SurgiVision video sys-
Adjustment
12345678901234567890123456789 tem (or “SurgiVision-ready” lightheads capable of being equipped with the
12345678901234567890123456789
video system) do not possess the pattern change feature.
• Adjust the light pattern by rotating the sterilizable handle counterclockwise
to decrease pattern size. Rotate the handle clockwise to increase pattern
Pattern Adjustment Symbol size.
• A pattern adjustment symbol on the sterile handle support indicates
direction of rotation to increase or decrease the size of the light pattern.

Smaller Pattern
Larger Pattern

Prefocused Lens

Non-sterile Handles

Non-sterile Handles

Small Pattern Large Pattern

Sterilizable Handle for

Positioning Light and Pattern
Size Adjustment

Figure 3-2. Light Pattern Adjustment

3-4
150824-909 Operating Instructions Operator Manual
12345678901234567890123456789
12345678901234567890123456789 • Refer to Figure 3-3
Sterilizable Handle
12345678901234567890123456789
12345678901234567890123456789
The sterile handle is used to position the SQ240 lighthead and to adjust the
light pattern size.
The SurgiVision light fixture can be used without the video camera. When used
without the camera, an optional sterile handle fixture is attached to the camera
mounting plate.
• The sterilizable handle can be removed for sterilization by unscrewing it
from the threaded, white nylon extension.
• An optional disposable cover can be used over the sterilizable handle.
(Disposable cover not supplied by STERIS.)
• The handle can be sterilized using standard hospital cycles. Always
sterilize handle between surgical procedures.
• When reinstalling the sterilizable handle on the white, nylon extension,
ensure that the handle is firmly tightened before usage.

Sterilizable Handle
Mounting Plate
(Removable)

Knurled-Head
Mounting Screw

White Nylon White Nylon

Extension Extension
Fastening
Hardware
(Captive)

Sterilizable Handle
Sterilizable Handle
Handle used Replacement Handle used
with SQ240 Lightheads with SurgiVision Lightheads

Figure 3-3. Sterilizable Handles

3-5
Operator Manual Operating Instructions 150824-909
 Sterilizable Handle (SQ240 SurgiVision with camera attached)
Refer to Figure 3-4
When the lighthead is used with the camera, a sterile handle is attached to the
camera housing. The sterile handle is used to position the lighthead, and
direct illumination from the lighthead.
• The sterilizable handle can be removed for sterilization by unscrewing
it from the threaded nylon extension.
• An optional disposable cover can be used over the sterilizable handle.
(Disposable cover not supplied by STERIS.)
• Handle can be re-sterilized using standard hospital cycles. Always
sterilize handle between surgical procedures.
» Following sterilization allow the handle to air cool for three to five
minutes before installing on camera housing.
» Do Not immerse the handle in a sterile solution to aid cooling.
• When reinstalling the sterilizable handle on the nylon extension, ensure
that the handle is firmly tightened before usage.

Figure 3-4. Metal Sterilizable Handle

3-6
150824-909 Operating Instructions Operator Manual
12345678901234567890123456789
12345678901234567890123456789 • Installation
Camera
1. Rotate lighthead until lens faces the room ceiling.
Installation or
Removal
12345678901234567890123456789
2. Loosen two knurled-head thumb screws to either side of sterile hand
12345678901234567890123456789 support, and remove sterile handle support.
3. Refer to Figures 3-5 and 3-6.
The camera is secured to the lighthead by two knurled-head thumb screws.
a. Align the camera drive gear and connector properly, and install camera
assembly to lighthead.
b. Tighten thumb screws until screw heads are snug against camera
CAUTION: To prevent housing. Rotate lighthead until lens and camera face room floor.
camera or replacement 4. Position wall control circuit breaker to ON (switch should be illuminated).
unit from falling, tighten
thumb screws securely. 5. Press the ON touch pad on the face of the wall control. (Power LED should
be lit.)
6. Verify that all functions of the camera operate correctly using the positioning
controls on the wall control. Then verify functions using the wireless hand-
held control (and the optional foot control, if applicable).
7. Once camera functions are verified, press the STANDBY touch pad on the
face of the wall control.
8. Turn off circuit breaker when the camera is not in use.

• Removal
1. Rotate lighthead until lens faces the room ceiling.
2. Loosen two knurled-head thumb screws to either side of camera body
and remove camera.
3. If necessary, install sterile handle support.

Camera/Lighthead
Mating Surface

Drive Gear Thumb Screw

Thumb Screw
Video
Connector

Figure 3-5. Align Camera Drive Gear and Figure 3-6. Tighten Thumb Screws
Video Connector Until Secure

3-7
Operator Manual Operating Instructions 150824-909
12345678901234567890123456789
12345678901234567890123456789 General: STERIS recommends connecting a monitor approved for medical
Install Video applications to the SQ240 SurgiVision system. The wall control provides two
Monitor different output signals: Composite and SVHS.
12345678901234567890123456789
12345678901234567890123456789 Recommended monitor for use with SQ240 SurgiVision: SONY® PVM-20M2MDU
Amsco® SQ240 SurgiVisionTM
Surgical Lighting and Video System
NOTE: This SONY monitor is recommended due to its conformance with
medical safety standards, including UL 2601-1, CSA 601.1 and EN 60601-1, and
is available directly from STERIS Corporation.
ZOOM
1. Determine the required type of output signal:
ROTATE

• For Composite signals, use cable P-134470-549

MANUAL
FOCUS

AUTO
FOCUS POWER
ON STANDBY
• For SVHS signals, use cable P-134470-550

FOOT CONTROL SVHS

VIDEO OUT
COMPOSITE
2. Refer to the monitor's instruction manual for specific details, and connect
the appropriate cable between the wall control and the monitor.
For Hermes-ready systems, refer to the Hermes control center operating
manual for additional monitor connections.
Connect Output to
SVHS Device Here
Connect Output to
Composite Device Here

12345678901234567890123456789
12345678901234567890123456789 General: STERIS recommends connecting a Video Cassette Recorder (VCR)
Install Video approved for medical applications to the SQ240 SurgiVision system. The wall
control provides both Composite and SVHS output signals.
Cassette Recorder
12345678901234567890123456789
12345678901234567890123456789 Recommended VCR for use with SQ240 SurgiVision: SONY® SVO-9500MD S-
VHS Videocassette Recorder.
NOTE: This SONY VCR is recommended due to its conformance with safety
standards, including UL 544, and is available directly from STERIS Corporation.
1. Determine the required type of output signal and select the appropriate
cable from those provided with the VCR.
2. Refer to the VCR instruction manual for specific details, and connect the
appropriate cable between the wall control and the VCR.
3. Connect monitor to VCR following instruction provided with the VCR and
monitor.

SONY® is a registered trademark of Sony Corporation of America.

3-8
150824-909 Operating Instructions Operator Manual
12345678901234567890123456789
12345678901234567890123456789 The SurgiVision camera is integrated into the sterile handle of the lighthead. The
SurgiVision camera itself is provided with a metal sterilizable handle. This handle allows the
Camera Operation camera to be grasped and used in the same way as a standard sterile handle,
12345678901234567890123456789
12345678901234567890123456789 both to direct light from the fixture for optimal illumination, and to position the
video image field for the best view of the procedure.
The metal sterilizable handle must be removed from the camera and sterilized
between procedures. Use a general purpose hospital steam cycle to sterilize
the camera cover. Following sterilization allow the handle to air cool for three
to five minutes before installing on the camera housing. Do Not immerse the
handle in a sterile solution to aid cooling.
The SurgiVision video and control signals are turned on or off at the wall control,
the wall control and the hand-held wireless control provide the same control
functions.
Metal Sterilizable Handle Camera functions may be controlled by three remote devices: a hand-held
wireless control, Hermes control center (verbal commands and hand-held
pendant) or an optional foot control (not available on Hermes-ready systems).

» Wall Control and The wall control functions by transmitting signals along the main control cable
Wireless Hand-held to the camera located in the lighthead. The wireless control functions by
Control Functions transmitting infra-red signals to the wall control. To initiate camera functions
with either control press the appropriate touch pad on the control face panel.
The hand-held control's IR (infra-red) transmitter must be within approximately
15 feet maximum and 50° of the wall control receiver. The control touch pads
are used to control the following camera functions:
Zoom – for determining the level of detail visible in the image field. The Zoom
function adjusts the image field continuously between two extremes:
+ (Telephoto). At extreme telephoto, the camera captures an image
showing great detail in a small area.
NOTE: At extreme telephoto, any motion of the lighthead/camera will be
exaggerated (jerky). The field of focus has little depth at this extreme,
forcing the Auto Focus function (if enabled) to refocus the camera when any
object (such as a hand) enters the image field, or if camera position is
adjusted. The camera is also sensitive to light level changes at extreme
telephoto.
– (Wide Angle). At extreme wide angle, the camera captures a large,
image with less detail than telephoto.
NOTE: At extreme wide angle, the image field possesses a greater depth
of focus and less sensitivity to light level changes.
Rotate – Use this function to change orientation of the video field. Image field
can be rotated in either clockwise or counter-clockwise directions.
Manual Focu s–
Focus–
s–Use this function to manually set the focus for close-up shots
or other special applications. The Auto Focus function must be toggled off to
enable manual focusing. Adjust the clarity of focus by pressing the + or –
touchpads.
NOTE: + touch pad moves the lens slightly CLOSER to subject; – touch pad
moves the lens slightly AWAY from subject.

3-9
Operator Manual Operating Instructions 150824-909
 Control Touch Pad

Infrared Transmitter

Zoom:
"+" close (tight)
Rotate: "-" far (wide)
" " counterclockwise
" " clockwise Manual Focus:
"+" moves lens closer to subject
Auto Focus: "-" moves lens further from subject
Automatic lens
movement controlled
by camera.

Hand-Held Wireless Control

Amsco® SQ240 SurgiVisionTM

Surgical Lighting and Video System

Control Touch Pad

ZOOM

ROTATE

MANUAL
FOCUS Infrared Receiver
AUTO
FOCUS POWER
ON STANDBY

VIDEO OUT
FOOT CONTROL SVHS COMPOSITE

Video System
ON/STANDBY
Switches
Circuit Breaker
Wall Control

Figure 3-7. SurgiVision Controls

Control Cable Connects to

Keyed Jack on Bottom of Wall Activate Foot Control
Control Functions by Pressing on
Appropriate Side of Foot
Pedals.
Figure 3-8. Optional Foot control

3-10
150824-909 Operating Instructions Operator Manual
 Auto Focus –Use this function to toggle Auto Focus on or off. When Auto Focus
is ON, the camera automatically focuses on the object in the image field closest
to the camera lens. When Auto Focus is turned OFF, the camera maintains
focus on the last object upon which it was focused, until Auto Focus is turned
back on.
NOTE: It may be necessary to toggle Auto Focus OFF when using the camera
at extreme telephoto (or close up), to prevent the camera from refocusing on
hands and other objects introduced into the image field during the shot.
HERMES-Ready Control Center– The Hermes Control Center functions by
transmitting signals through a interface cable connected to the wall control.
When used, the interface cable should be routed to avoid surgical personnel
foot traffic. The control center is intended to allow personnel within the sterile
field to operate all camera functions using verbal commands or a hand-held
pendant. Refer to the Hermes operating manual for more information.

» Optional Foot Control The foot control functions by transmitting signals through a cable connected
to the wall control. When the foot control is used, the cable should be routed
to avoid surgical personnel foot traffic. The foot control is intended to allow
personnel within the sterile field to operate the zoom and rotation functions of
the camera.
Foot control is used to control zoom and rotation functions. Press on
appropriate sides of foot pedals to activate foot control functions. Functions
controlled through the foot control unit are identical to those controlled through
the hand-held wireless control or wall control. See Figure 3-8.

» Guidelines for The following steps will aid in maximizing video imaging effectiveness.
Maximizing Video Image
• Energize the light at setting 3 on the variable intensity controller (VIC), and
position the lighthead approximately 42" (1067 mm) from the surgical site.
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789 • Using the hand-held remote, or the wall control, zoom in or out (+ or -) until
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789 the desired image fills the viewing screen of the monitor.
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789 NOTE: Zooming completely out causes image distortion within the illuminated
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789 area.
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
Light Pattern If the light pattern (white circle) does not fill the monitor’s screen (shaded
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
(Illuminated Area)
12345678901234567890123456789012123456789 square), the image inside the pattern will be distorted.
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789 Reposition the camera to orient the focal point (center of the desired image)
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789 at the center of the viewing screen.
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789 Adjust zoom and rotation as needed:
12345678901234567890123456789012123456789
12345678901234567890123456789012123456789
Monitor's Screen (Image Area) • The camera may be zoomed to the full 12x zoom and rotation orientation
adjusted as needed.
• Clockwise and/or counterclockwise orientation is adjusted by using the
curved arrow(s) on the hand-held control, the wall control or the optional foot
control.

3-11
Operator Manual Operating Instructions 150824-909
 » Engage Manual Focus As instruments are introduced and removed from the surgical field, the auto
(Optional) focus will attempt to focus on the nearest object, causing the image to blur
intermittently. To prevent his effect, once the camera has been positioned and
focused onto the surgical site, the manual focus mode may be engaged to
maintain image clarity during the procedure.
For deep cavity illumination, it may be necessary to engage the manual focus
to focus beyond the nearest object (i.e., the surface area surrounding the
incision) so that the desired image can be viewed clearly.

3-12
150824-909 Operating Instructions Operator Manual
CLEANING THE EQUIPMENT 4
12345678901234567890123456789
12345678901234567890123456789 • Pail
Cleaning • Sponge
Equipment
12345678901234567890123456789
12345678901234567890123456789 • Cloth Wipes
• Rubber Gloves
WARNING - PERSONAL
• Mild Household Detergent (e.g., Joy)
INJURY HAZARD: Do not
attempt to clean lighthead • Disinfectant cleaners such as:
unless power is turned off » Coverage® Spray TB (1424-63)
at variable intensity
» Germicidal Cloth (NK350, NK352)
controller by disengaging
the circuit breaker(s) and » Coverage® Spray HB (1424-63)
the lighthead has cooled » Coverage® HB Concentrate (1420-08)
sufficiently. » T.B.Q.® (6345-08)
Use of any disinfectant so- » Coverage Plus® (6367-08)
lution other than those All listed disinfectant cleaning products are available from STERIS for use
listed below may cause dis- on this equipment.
coloration or deformation
on the acrylic lens surface:
Coverage Spray TB, Ger-
micidal Cloth, Coverage
Spray HB, Coverage HB
Concentrate, T.B.Q., or
Coverage Plus. Cleaning
solutions other than those
listed have NOT been tested
for compatibility or effec-
tiveness. Always follow
manufacturer instructions
for concentrations and use
of cleaning products.

4-1
Operator Manual Cleaning the Equipment 150824-909
12345678901234567890123456789
12345678901234567890123456789 1. Wear rubber gloves
General Cleaning/ 2. Use sponge and a mild detergent and water solution. The following
Disinfecting cleaning/disinfecting agents are compatible with the outer surfaces of the
suspension arm, yoke, lighthead and acrylic lens when used in accordance
Procedure
12345678901234567890123456789 with label instructions: Coverage Spray TB, Germicidal Cloth, Coverage
12345678901234567890123456789
Spray HB, Coverage HB Concentrate, T.B.Q., or Coverage Plus.
3. Prepare cleaning or disinfecting solution in accordance with directions on
the container labels.
WARNING - PERSONAL
INJURY HAZARD: Do not 4. Using a soft cloth and the cleaning solution, thoroughly wipe the areas to
attempt to clean lighthead be cleaned (see Figure 4-1). Make sure to wring out excess solution
unless power is turned off before wiping.
at variable intensity con-
troller by disengaging the 5. Rinse all surfaces with a soft cloth wipe and clear water.
circuit breaker(s) and the 6. Wipe all surfaces dry with a clean, dry cloth.
lighthead has cooled
sufficiently. 7. Ensure sterile camera cover or sterile handle is sterilized between each
procedure using a standard hospital cycle.
CAUTION: Use of any dis-
infectant solution other Cleaning Hand-held Control
than those listed below
Clean the hand-held control once a day, or as needed between procedures.
may cause discoloration
or deformation on the 1. Soak a soft cloth in a solution of water and a recommended agent. Wring
acrylic lens surface: Cov- the cloth until excess moisture has been eliminated.
erage Spray TB, Germi-
cidal Cloth, Coverage 2. Wipe all surfaces of the hand-held control, removing any accumulated
Spray HB, Coverage HB debris or soil.
Concentrate, T.B.Q., or 3. Using a clean, dry cloth, wipe the surfaces of the control until
Coverage Plus. Cleaning completely dry.
solutions other than those
listed have NOT been
tested for compatibility or
effectiveness. Always
follow manufacturer
instructions for concen-
trations and use of
cleaning products.

CAUTION: Do not
immerse the hand-held
control in fluid.

4-2
150824-909 Cleaning the Equipment Operator Manual
12345678901234567890123456789
12345678901234567890123456789 • Refer to Figure 4-1
Areas To Be
The following areas of the lighthead must be cleaned and disinfected before
Cleaned Before each use of the lighthead (see "General Cleaning/Disinfecting Procedure" for
Each Use
12345678901234567890123456789
12345678901234567890123456789
instructions):
• Suspension Arm – Wipe the entire suspension arm, including the
CAUTION: Use only rec- suspension fork and yoke.
ommended cleaning/disin- • Lighthead – Wipe both top and side surfaces.
fecting and/or anti-static
agents on this light. Some • Sterile Handle Support – Wipe all areas of the support, including those
degree of staining, pitting, covered when the handle is installed.
and/or discoloration could
occur if a phenolic-, iodo-
phor-, or glutaraldehyde-
based disinfectant is used
on the surfaces of this
light. Also, use of alcohol
or aerosol spray cleaner/ Top Cover
disinfectants (e.g., Lysol®) Lighthead
Yoke
containing a substantial
amount of alcohol in the Suspension Arm
formula can damage the
acrylic plastic lens.

CAUTION: Do not scratch

optical coating on acces-
sible portions of optical
core when cleaning; al-
ways wear rubber gloves Non-Sterile
Counterbalance Camera
Handle (4)
and use only a clean, white, Knuckle Assembly Sterilizable Cover
lint-free cloth when wip-
ing internal surfaces. Figure 4-1. Areas To Be Cleaned
CAUTION: Prevent leak-
age of fluids into interior
of lighthead.
12345678901234567890123456789
12345678901234567890123456789
• Lens
Areas To Be
IMPORTANT: Clean only the exterior surface of the lens.
Cleaned/
Disinfected Once a 1. Remove the sterile handle.

Month
12345678901234567890123456789 2. Clean/disinfect the outer surface of the lens as outlined in General
12345678901234567890123456789 Cleaning/Disinfecting Procedure.
3. Wipe the outer surface of the lens with an antistatic acrylic cleaner and
WARNING - PERSONAL
soft cloth.
INJURY HAZARD: Do not
attempt to clean lighthead 4. Do not reinstall a sterile handle until immediately before the light is to
unless power is turned off be used in a surgical procedure. Always sterilize handle between
at variable intensity surgical procedures.
controller by disengaging
the circuit breaker(s) and NOTE: Always sterilize handle between each surgical procedures using
the lighthead has cooled conventional hospital sterilization procedures and a standard sterilization
sufficiently. prevacuum or gravity cycle.

4-3
Operator Manual Cleaning the Equipment 150824-909
OPERATOR TROUBLESHOOTING 5
WARNING - PERSONAL
Use the following Troubleshooting Chart to identify problems and probable
INJURY HAZARD: Do causes should they occur.
not attempt to replace
the lamp unless power If you are unable to correct the problem with this Troubleshooting Chart, or if
is turned off at variable a problem occurs not described on the chart, please call your STERIS
intensity controller by representative, who will arrange to have your equipment promptly put into
disengaging the circuit working order by a factory-trained representative. Never permit unquali-
breaker(s) and the light- fied persons to service the lightheads or suspension arms.
head has cooled suffi-
ciently.

WARNING - PERSONAL
INJURY HAZARD: Do
not attempt to clean
lighthead unless power
is turned off at variable
intensity controller by
disengaging the circuit
breaker(s) and the light-
head has cooled suffi-
ciently.

WARNING - PERSONAL
INJURY HAZARD:
Do not attempt to adjust
suspension system. Re-
fer servicing to qualified
service personnel.

PROBLEM POSSIBLE CAUSE AND/OR CORRECTION

1. Lighthead drifts 1. Brake adjustment incorrect — call your service representative, or — if

once set in qualified — consult section concerning suspension arm adjustments in
position and Maintenance Manual P-764326-998.
released.
2. Centra Mount not level — call your service representative, or — if
qualified — consult section concerning suspension arm adjustments in
Maintenance Manual P-764326-998.
3. Centra Mount Units — Track Mount not level — call your service
representative, or — if qualified — consult Section concerning
suspension arm adjustments in Maintenance Manual P-764326-998.

2. Light flickers 1. Possible contact problem at yoke commutator, horizontal/vertical arm

when moved. commutator, or centra hub commutator— contact STERIS Service.
2. Track Mount Units — Possible contact problem with electrical brushes
(at carriage; internal and external brushes; and at the yoke/horizontal
arm assembly; commutator assembly)—contact STERIS Service.

5-1
Operator Manual Operator Troubleshooting P-150824-909
 PROBLEM POSSIBLE CAUSE AND/OR CORRECTION

3. Light will not turn on. 1. Possible malfunctions at variable intensity controller — check circuit
breakers and turn ON if tripped to OFF.
2. Check fuses — replace if failed.
IMPORTANT: If fuses fail again immediately, call your service
representative. Do not attempt to use the light.
3. Both lamps in lamp change mechanism may have failed — replace if
failed. Lamp failure LEDs on lighthead will be blinking if both lamps have
failed.

4. Lamp change 1. Inspect lamp change mechanism to ensure secondary lamp has intact
mechanism will filament, or is fully seated in socket.
not work.
2. If lamps appear operable, refer problem to qualified STERIS or STERIS-
trained service technician.

5. Poor light pattern. 1. Bent lamp filament; lightheads knocked together while lit — check lamp
filament position. Replace lamp if bent.

6. Light pattern will 1. Refer problem to qualified STERIS or STERIS-trained service technician.
not change.

7. Video system 1. Hand-held Wireless control:

does not respond • Check batteries in hand-held wireless control.
to commands
from hand-held • Ensure wall control receiver is not covered.
wireless control or 2. Foot Control:
optional foot
• Check connection of foot control cable to wall control.
controls.

8. Video system 1. Check Hermes interface cable connection from Hermes control center to
does not respond wall control (refer to Hermes control center operating manual).
to verbal
commands or
hand-held
pendant.

5-2
P-150824-909 Operator Troubleshooting Operator Manual
MAINTENANCE 6
12345678901234567890123456789
12345678901234567890123456789
NOTE: This schedule is supplied for the customer’s reference only, any actual
Preventive service should be done by a qualified service technician.
Maintenance These procedures should be performed at regular intervals as indicated. This
Record frequency is minimum and should be increased with increased light usage.
12345678901234567890123456789
12345678901234567890123456789

SCHEDULE
Procedure Frequency Paragraph (if applicable**)

Inspect lamp change mechanism and lamp each inspection Inspect Lamp Change Mechanism
Change secondary lamp every year Lamp Replacement

Check for movement in vertical suspension each inspection Check Vertical Suspension Tube
tube and for red band at top of vertical
suspension tube.

Ensure all three yoke plug buttons are each inspection

securely seated and tethered
Check light pattern and illumination levels every year

Inspect lighthead and arm wiring for every 6 months

deterioration

Inspect arm assembly for ease of each inspection

movement
Ensure force required to raise and lower each inspection
arm is similar

Check suspension system for drift each inspection

Ensure Centra hub rubber cap is secure each inspection Check Hub Cap (Centra Mount)
Check variable intensity control each inspection Check Light Intensity Control

Ensure lighthead moves through entire each inspection Lighthead Positioning

range of articulation

Check battery backup option (if applicable) each inspection Check Battery Backup
Check camera controls for smooth every 6 months
movement and full range of motion.
• Verify proper operation of zoom
controls
• Verify proper operation of rotation
controls
• Verify Manual Focus and Auto Focus
(ON/OFF and function)
• Check batteries in remote control
• Check operation of optional foot
control (if applicable)

6-1
Operator Manual Maintenance 150824-909
 SCHEDULE
Procedure Frequency Paragraph (if applicable**)

Verify secure mechanical attachment of each inspection

camera assembly to mounting plate.

Verify security of electrical connections each inspection

between the wall control and camera
Verify secure attachment of sterile handle each inspection
assemblies to lighthead, including
replacement handle of camera mount.

Inspect camera lens, clean if necessary. each inspection

Inspect plug buttons or other components each inspection

that may attach to the camera or arm

** When no paragraph is listed, operation should be performed by or referred to STERIS service representative (or other
qualified technician). Refer to Maintenance Manual P-764326-998.

NOTE: Any repairs or adjustments to lighthead and its suspension system should only be made by qualified STERIS
or STERIS trained service personnel while referring to Maintenance Manual P-764326-998.

6-2
150824-909 Maintenance Operator Manual
12345678901234567890123456789
12345678901234567890123456789 • Refer to Figure 6-1
Inspect Lamp 1. The lamp change mechanism assembly is accessed by removing the
Change Mechanism
12345678901234567890123456789 sterilizable handle, if present. Loosen the four quarter-turn, wing-head
12345678901234567890123456789
fasteners and carefully lower camera or handle mount until the lamp
change mechanism is visible. The assembly pivots to the side, allowing
WARNING - PERSONAL access to the lamps. The active lamp is positioned higher, and toward the
INJURY HAZARD: Do not center of the assembly.
attempt to replace the
lamp unless power is 2. Inspect the lamps for damage or discoloration. Be sure the element of the
turned off at variable in- lamp in the secondary position is intact. Replace if necessary.
tensity controller by dis-
3. Check that lamps are firmly seated in their sockets.
engaging the circuit
breaker(s) and the light- 4. Raise the lamp change mechanism into the lighthead and secure quarter-
head has cooled suffi- turn, wing-head mounting fasteners. Do not re-install the sterilizable
ciently. camera cover or sterilizable handle until the fixture is to be used. (Sterilize
handle, before returning to light.)
CAUTION: Do not touch
glass portion of lamp
during re-lamping or
cleaning.
CAUTION: Manual ac-
tuation of the lamp
change mechanism may
result in permanent dam-
age to the gear motor.
12345678901234567890123456789
12345678901234567890123456789 1. Turn on light.
Check Battery 2. Turn off AC power to Variable Intensity Controller.
Backup 3. Check that the battery backup indicator LED's and light are still on.
(as applicable)
12345678901234567890123456789
12345678901234567890123456789 4. Restore AC power and check that the indicator LED's have gone out.

WARNING - ELECTRIC
SHOCK HAZARD: Do not
remove variable intensity
controller covers refer
servicing to qualified ser-
vice personnel.
12345678901234567890123456789
12345678901234567890123456789 • Refer to Figure 6-2
Check Vertical 1. Inspect vertical suspension tube. A red colored band has been applied to
Suspension Tube
12345678901234567890123456789
the surface of the tube normally hidden under the rubber boot at the top of
12345678901234567890123456789 the tube. If the mounting configuration has been properly assembled, the
red band will not be visible. If the red band is visible, do not attempt to use
WARNING - PERSONAL the light fixture. Call your STERIS service representative immediately.
INJURY HAZARD: Do not 2. Attempt to push the vertical suspension tube back and forth or side to side.
use lighting fixture if red If the tube “wobbles,” mounting configuration has not been assembled
band is visible below rub- correctly. Call your STERIS service representative immediately.
ber cap at top of vertical
suspension tube. 3. Loosen screw and pull the lower plastic cap on the vertical tube away from
the top of the suspension fork. Inspect the four bolts at the bottom of the
tube. If any bolts have become loose, tighten them and replace the cap.

6-3
Operator Manual Maintenance 150824-909
 Primary
Lamp

Secondary
Lamp

Video Camera

Figure 6-1. Inspect Lamp Change Mechanism

CORRECT INCORRECT
(No Red Band) (Red Band Showing)

CORRECT
(No Red Band)

Ensure that the vertical suspension tube cannot move back-

and-forth or side-to-side.

Figure 6-2. Check Vertical Suspension Tube

Yoke Plug Button

Figure 6-3. Check Yoke Plug Button

6-4
150824-909 Maintenance Operator Manual
12345678901234567890123456789
12345678901234567890123456789 • Refer to Figure 6-3
Check Yoke
1. Remove the three plug buttons from the yoke assembly. Plug buttons are
Plug Button
12345678901234567890123456789 located on both sides of the lighthead and in the center of the yoke where
12345678901234567890123456789
the suspension arm is connected.
2. Check and make sure that the tether cable is not frayed or cut, if so,
replace with kit (P-764315-856).
NOTE: Make sure that the tab with the tether attached to it is bent inward toward
the plug's center.

12345678901234567890123456789
12345678901234567890123456789 • Refer to Figure 6-4
Check Hub Cap 1. Visually inspect fit of hub cap to central hub mount. There should be no
(Centra Mount)
12345678901234567890123456789 gaps between hub cap outer edge and surface of the mount at any point
12345678901234567890123456789 of 360 degree rotation. (See Figure 6-4.)
2. If any gaps are detected, contact qualified service technician to tighten
hub cap mounting screws.

Central Hub

Hub Cap

Figure 6-4. Check Hub Cap

12345678901234567890123456789
12345678901234567890123456789 1. Check operation of circuit breaker by cycling several times, insuring that
Check Variable breaker latches ON each time it is pressed.

Intensity 2. Rotate controller knob(s) from OFF to ON position, and then from lowest
intensity position ("1") through maximum intensity position ("5"). Make sure
Controller
12345678901234567890123456789 that the lighthead produces a higher intensity with each increase in the
12345678901234567890123456789
intensity position.

WARNING: ELECTRIC
SHOCK HAZARD: Do not
remove covers or per-
form service other than
those described in this
equipment manual.
Refer servicing to quali-
fied service personnel.
(Maintenance Manual
P-764326-998.)

6-5
Operator Manual Maintenance 150824-909
12345678901234567890123456789
12345678901234567890123456789 • Refer to Figure 6-5 and 6-6
Lamp Replacement
12345678901234567890123456789
12345678901234567890123456789
Each lighthead is equipped with two lamps. One of these lamps, called the
primary, is always positioned at a point in the optical core to provide best focus
and illumination. When the primary lamp fails, a secondary lamp lights
immediately and automatically moves to replace the primary lamp, yielding
WARNING: ELECTRIC equivalent optical performance. In this process, transmission of light to the
SHOCK HAZARD: Do operating table is interrupted for less than one second.
not remove covers or
perform service other If one lamp in the lighthead fails, the failure is indicated by a blinking LED on
than as described in this the side of the outer cover. Do not allow the lighthead to operate for any length
equipment manual. Re- of time with only one functional lamp. Always replace a failed lamp at the
fer servicing to qualified earliest opportunity. Primary lamp returns to position after it is replaced.
service personnel.
IMPORTANT: The procedure for accessing the lamps is slightly different,
(Maintenance Manual P-
depending on the type of lighthead. Types of lightheads can be separated into
764326-998.)
two categories:
WARNING - PERSONAL • SQ240 Lightheads (or SurgiVision lightheads without camera installed), or
INJURY HAZARD: Do • SurgiVision lightheads with camera installed.
not attempt to replace
the lamp unless power To replace a failed lamp, complete the appropriate procedure below:
is turned off at variable
intensity controller by
disengaging the circuit
breaker(s) and the light-
head has cooled suffi-
ciently.

» Lamp Replacement 1. Turn OFF power to the lighthead at the circuit breaker on the variable
Procedure for SQ240 intensity controller.
lightheads or 2. Remove sterilizable handle, if present.
SurgiVision
3. Loosen four quarter-turn fasteners.
Lightheads without
Camera installed 4. Lower lamp change mechanism through circular aperture in the center of
the lens. The assembly pivots to the side, allowing access to the lamps.
Refer to Figure 6-5.
5. Normally, the failed lamp is in the lower of the two lamp sockets in the
lighthead. Remove failed lamps and replace with new lamps.
• If fixture provides no light at all, and LEDs on outer cover of lighthead
are blinking, both lamps may have failed.
CAUTION: Do not touch Remove each failed lamp by grasping the socket in one hand and the
glass portion of lamp lamp base in the other, then gently move the lamp base back-and-forth
during e-l-amping or while pulling it from the socket.
cleaning.
NOTE: Grasp the lamp base and lamp socket firmly when installing a new
CAUTION: Manual actua- lamp to prevent movement of the lamp change mechanism. Manual
tion of the lamp change actuation may cause permanent damage to the gear motor.
mechanism may result in 6. Grasp the new lamp by its ceramic base (do not remove protective wrapper
permanent damage to the do not touch glass) and press into the lower lamp holder. After replacing
gear motor. either lamp, remove wrapper(s) and inspect both lamps to ensure both
have intact filaments.

6-6
150824-909 Maintenance Operator Manual
 Loosen
Fasteners

Lower the Lamp

Change Mechanism

Primary Lamp

Secondary Lamp

Lamp Socket

Figure 6-5. Lamp Replacement Procedure for SQ240 Lightheads or SurgiVision

Lightheads without Camera installed

6-7
Operator Manual Maintenance 150824-909
 7. Raise the lamp change mechanism into the lighthead, and tighten quarter-
turn fasteners. Do not re-install the sterilizable handle until the fixture is to
be used. (Sterilize handle, if necessary, before returning to light.)
8. Return power to lighthead by pressing the circuit breaker at Variable
Intensity Controller to ON.
9. Verify that the Lamp Failure LEDs are not blinking. If the LEDs are still
blinking, access lamp change mechanism again and examine the filaments
of both lamps to ensure that one was not damaged during the lamp
replacement procedure.

» Lamp Replacement 1. Turn OFF power to the lighthead at the circuit breaker on the variable
Procedure for intensity controller.
SurgiVision 2. Turn off power to the camera by pressing the STANDBY button on the
Lightheads with SurgiVision wall control, if present.
Camera installed 3. Remove sterilizable camera handle, if present.
4. Rotate lighthead until lens faces ceiling.
5. Loosen four quarter-turn fasteners around the base of the camera.
6. Grasp camera body and raise assembly out of lighthead until hinges in
support cams are exposed.
7. Rotate lighthead approximately 90 and gently lower lamp change
mechanism and camera assembly until it rests against the face of the lens.
Refer to Figure 6-6.
NOTE: Next step may required the assistance of a second person to steady
the lighthead.
8. Normally, the failed lamp is in the lower of the two lamp sockets in the
lighthead. Remove failed lamps and replace with new lamps.
• If fixture provides no light at all, and LEDs on outer cover of lighthead
are blinking, both lamps may have failed.
Remove failed lamps by grasping the socket in one hand and the lamp
base in the other, then gently move the lamp base back-and-forth while
pulling it from the socket.
NOTE: Grasp the lamp base and lamp socket firmly when installing a new
lamp to prevent movement of the lamp change mechanism. Manual
CAUTION: Do not touch actuation may cause permanent damage to the gear motor.
glass portion of lamp
during re-lamping or 9. Grasp the new lamp by its ceramic base (do not remove protective wrapper
cleaning. do not touch glass) and press into the lower lamp holder. After replacing
either lamp, remove wrapper(s) and inspect both lamps to ensure both
CAUTION: Manual actua- have intact filaments.
tion of the lamp change
10. Return the lamp change mechanism into the lighthead, and tighten quarter-
mechanism may result in
turn fasteners. Do not re-install the sterilizable camera cover until the fixture
permanent damage to the
is to be used. (Sterilize camera cover, if necessary, before returning to
gear motor.
light.)

6-8
150824-909 Maintenance Operator Manual
 Remove
Sterilizable
Camera Cover, if
necessary

Rotate Lighthead Until Lens

Faces Ceiling, and Loosen
Quarter-turn Fasteners

Raise Camera Assembly and

Lamp Change Mechanism until
Hinges in Support Cams
are Exposed

Support Lighthead at Right Angle to

Floor,
Allow Lamp Change Mechanism and
Camera Assembly to Hang Toward Floor
Secondary
Lamp

Primary Lamp

Lamp Socket

Figure 6-6. Lamp Replacement Procedure for SurgiVision Lightheads

with Camera Installed.

6-9
Operator Manual Maintenance 150824-909
 11. Return power to lighthead by pressing the circuit breaker at Variable
Intensity Controller to ON.
12. Verify that the Lamp Failure LEDs are not blinking. If the LEDs are still
blinking, access lamp change mechanism again and examine the filaments
of both lamps to ensure that one was not damaged during the lamp
replacement procedure.

6-10
150824-909 Maintenance Operator Manual
REPLACEMENT PARTS 7
Parts listed in this section are those that would be necessary to do minor
maintenance on the lighting fixture. Quantities listed are the minimum number
of spares that we recommend you keep on hand.
When ordering, please include the part number, description, and quantity for
each replacement part requested.
Send your order directly to your nearest STERIS Regional Office.

Recommended
Description Part Number Spares
Fuse 20 Amp P-129362-213 5
Lamp P-129362-228 3
Sterilizable Handle P-93184-001 3
Sterilizable Camera Cover P-134470-429 2
• Quartz Lens Only P-134470-447 2
• Housing Only P-056938-816 1
Hermes Interface Cable P-134469-380 1

Associated Publications Part Number

Uncrating Instructions (Centra Mount) P-129362-443
Installation Instructions (Centra Mount) P-150824-819
Maintenance Manual P-764326-998
Uncrating Instructions (SQ-Track Mount) P-150824-929
Installation Instructions (SQ-Track Mount) P-150824-930

Equipment Drawings
SQ240 Centra Mounted, One 36" Arm, One Lighthead P-129378-078
SQ240 Centra Mounted, Two 36" Arms, Two Lightheads P-129378-079
SQ240 Centra Mounted, Three 36" Arms, Three Lightheads P-129378-080

Equipment Drawings (Wall Mounted Controls)

SQ240 Single, Surface Mounted VIC P-150824-833
SQ240 Single, Recess Mounted VIC P-150824-834
SQ240 Dual, Surface Mounted VIC P-150824-835
SQ240 Dual, Recess Mounted VIC P-150824-836
SQ240 SurgiVision Wall Control Mount P-129378-082
Continued on next page

7-1
Operator Manual Replacement Parts 150824-909
 Associated Publications Part Number

Equipment Drawings (Centra Mounted Fixture)

SQ240 Centra Mounted, One 36" Arm, One Lighthead P-150824-837
SQ240 Centra Mounted, Two 36" Arms, Two Lightheads P-150824-838
SQ240 Centra Mounted, One 24" Arm & One 36" Arm,
Two Lightheads P-150824-948
SQ240 Centra Mounted, Three 36" Arms, Three Lightheads P-150824-839
SQ240 Centra Mounted, One 36" Arm, One Lighthead
(with provision for future lighthead addition) P-150824-840
SQ240 Centra Mounted, Two 36" Arms, Two Lightheads
(with provision for future lighthead addition) P-150824-841

Equipment Drawings (Track Mounted Fixture)

SQ240 4'6" Surface Mounted Track, One Lighthead P-150824-922
SQ240 4'6" Recessed Mounted Track, One Lighthead P-150824-923
SQ240 9' Surface Mounted Track, One Lighthead P-150824-924
SQ240 9' Recessed Mounted Track, One Lighthead P-150824-925
SQ240 9' Surface Mounted Track, Two Lightheads P-150824-944
SQ240 9' Recessed Mounted Track, Two Lightheads P-150824-945

7-2
150824-909 Replacement Parts Operator Manual