SKYTRON, a Division of the KMW Group, Inc. (SKYTRON) warrants all new products sold by it directly or through a dealer or other
authorized representative, with exception to replacement parts, spares, bulbs (surgical lights), pads, and accessory items (surgical tables)
to be free from defects in material or workmanship, under normal use and service, for a period of two (2) years. This warranty shall include
the cost of repair or replacement of defective parts including the cost of service labor and travel time to the site of equipment use. Delays
caused by the user in accessing the equipment for repair will be chargeable at the normal hourly rate for service by SKYTRON’s authorized
service representative. The warranty period shall begin with the initial operation or one (1) year after receipt of the product, whichever shall
occur first.
Replacement parts, spares, bulbs (surgical lights), pads and accessory items (surgical tables) are warranted to be free from defects in material
or workmanship, under normal use and service, for a period of ninety (90) days from receipt by the ultimate user, with exception to replacement
parts supplied by SKYTRON, for products under warranty, which shall be covered for any remaining period of the original product warranty,
or for 90 days, whichever is of greater benefit to the ultimate user.
SKYTRON’s responsibility and liability shall be limited to the repair or replacement of any part which we, SKYTRON, determine to be defective
within the applicable warranty period. Minor adjustments required as a result of normal wear during the use of the product within the warranty
period are not covered under warranty. The labor portion of this warranty is covered by SKYTRON’s Authorized Service Agent. Repairs
made by others are not authorized nor covered by SKYTRON with respect to labor costs.
SKYTRON shall not be liable for any other expense, loss or damage, whether direct, incidental, consequential or exemplary arising in connection
with the sale or use of or the inability to use SKYTRON products.
NO EXPRESS WARRANTY IS GIVEN BY SKYTRON WITH RESPECT TO ITS PRODUCTS EXCEPT AS SPECIFICALLY SET FORTH
HEREIN. ANY WARRANTY IMPLIED BY LAW, INCLUDING ANY WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR
PURPOSE, IS EXPRESSLY LIMITED TO THE TWO-YEAR AND 90-DAY TERMS SET FORTH ABOVE. THE FOREGOING STATEMENTS
OF WARRANTY ARE EXCLUSIVE AND IN LIEU OF ALL OTHER REMEDIES.
No dealer, agent, employee or other representative of SKYTRON is authorized to extend or enlarge this warranty.
REV. 1/05
Although current at the time of publication, SKYTRON’s policy of continuous development makes this
manual subject to change without notice.
TABLE OF CONTENTS
TitlePage
EQUIPMENT LABELS AND SPECIFICATIONS.................................................................................... 2
6600 Series General Purpose Surgical Table Specifications .................................................................. 3
SPECIAL USER ATTENTION ................................................................................................................ 4
SECTION I INTRODUCTION ................................................................................................................. 7
4-3. Service ....................................................................................................................................... 21
1
TYPE B
EQUIPMENT
EQUIPMENT LABELS AND SPECIFICATIONS
INDICATES DANGEROUS VOLTAGE, 120 V, 60 Hz
CLASS I DEFIBRILLATION PROOF, TYPE B EQUIPMENT- IPX4 RATED.
INTERNALLY POWERED EQUIPMENT
PROTECTIVE GROUNDING.
IN ORDER TO ENSURE PROPER GROUNDING RELIABILITY,
THIS TABLE MUST BE CONNECTED TO A PROPERLY GROUNDED
HOSPITAL GRADE OUTLET.
NN
IPX4
V
A
HZ
CONNECTION FOR NEUTRAL CONDUCTOR SUPPLIED
UNIT TO BE USED ONLY IN SPECIFIED ENVIRONMENTAL CONDITIONS
TEMPERATURE: 15˚ - 30˚ C (60˚ - 85˚ F)
HUMIDITY: 30% - 60% RELATIVE HUMIDITY, NON CONDENSING
AC VOLTAGE
ENCLOSURE CLASS
VOLTAGE RATING OF THE UNIT
AMPERAGE RATING OF THE UNIT
FREQUENCY OF THE UNIT
ATTENTION, CONSULT MANUAL FOR FURTHER INSTRUCTIONS.
INDICATES SPECIAL USER ATTENTION.
BATTERY TYPE:
FUSE:
2
POWERED BY AC VOLTAGE
BATTERY MODELS
POWERED BY BATTERY
SEALED
LEAD ACID 12V, VALVE REGULATED
16AH, 10HR (530W/10MIN)
15 AMP FAST ACTING INTERNAL FUSE
15A
6600 Series General Purpose Surgical Table Specifications
15"
10"19-1/2"21-1/2"24"
60˚
90˚
9"
6"
14-1/2"
TOP VIEW
76"
36-1/2"
SIDE VIEW
3"
19-3/4"
21-3/4"
45" MAX
26" MIN
5-3/4"
19"
END VIEW
Electrical Specifications
Power requirements
Current Leakage
Power Cord
15 feet w/hospital grade connector(removeable)
ENTELA CERTIFIED
TO UL2601-1
CAN/CSA601.1, IEC 60601-2-46
120 VAC, 60Hz, 450 Watts
Less than 100 micro amps
3
SPECIAL USER ATTENTION
The extreme positioning capabilities of the 6600
Series Table requires special attention for possible
interference points when using multiple function
positioning. As with the operation of any surgical
table, a certain amount of care should be exercised
to position the patient safely. Although the thick
pads and sheets substantially protect the patient,
pinch points, located at the joints of the top section
should always be considered. BE SURE THAT
THE ARMS, HANDS AND FINGERS OF THE
PATIENT AND THOSE OF THE OPERATING
ROOM PERSONNEL ARE CLEAR OF ALL MOVING PARTS BEFORE MOVING THE TABLE.
Proper restraints should always be used for patient
safety.
Certain accessories such as the Uro-Drain Tray,
Armboards and X-Ray top can be damaged when
changing the position of the table top sections.
Always look first to see if a desired movement is
going to interfere with any accessories in use.
The operator has the ultimate responsibility of
preventing damage to the table and surrounding
equipment or possible injury to the patient or staff.
NOTE
Activating any function button will activate the brake system. Using the TABLE
UP function to set the brakes provides
a visual assurance that the brakes are
locked without altering the table position, except when emergency brake is
released.
WARNING
Prior to operating the table, observe
all table caution labels and review the
SPECIAL USER ATTENTION section in the front of this manual.
WARNING
Possible explosion hazard exists if table
is used in the presence of FLAMMABLE
ANESTHETICS.
NOTE
The table will operate correctly on battery power with the power cord connected to a wall outlet or disconnected.
The operator must ensure proper positioning is
maintained to prevent compromizing respiration,
nerve pathways or circulation.
In general, common sense will dictate when there
is a potential hazard.
The following precautions should be reviewed
by all personnel prior to operating the table.
A routine Instructional Program should be
implemented by the facility for proper usage
instructions for all personnel that may operate
this table
.
WARNING
Indicates a possibility of personal injury.
CAUTION
Indicates a possibility of damage to
equipment.
NOTE
Battery Operation must be turned OFF
at the pendant control. It can not be
turned Off using the main power switch.
NOTE
Turning the Main Power Switch ON will
change the table operation to 120 VAC
power.
NOTE
If the table is stored for a period greater
than 6 months, the batteries should be
removed and stored in a dry, clean condition at a storage temperature of 68° F
(20° C). Batteries should be recharged
every 6 months of product storage.
NOTE
When the red light starts to blink (indicating low power in battery) the table
will operate for approximately 5 continuous minutes, typically long enough
to use the table for the rest of the day.
NOTE
Indicates important facts or helpful hints.
4
NOTE
The charging system operates ONLY
when the table is in AC120V operation
mode.
SPECIAL USER ATTENTION
NOTE
In battery mode, only the red indicator
light will be on. In AC 120V mode, both
the green indicator light and red indicator light will be on.
NOTE
The table can be operated on 120VAC
power while the battery is being recharged.
NOTE
The POWER SWITCH can be placed
in the OFF position to completely deactivate all table functions if required during certain procedures or in case of
emergency.
WARNING
DO NOT unlock brakes when a patient
is on the table. An uneven patient
weight load may cause instability.
NOTE
With an evenly distributed patient weight
load, all table positioning functions will
operate smoothly and quietly with a
patient weight of up to 600 pounds.
WARNING
To maximize patient safety, utilize
proper restraint methods during extreme
Trendelenburg positioning.
WARNING
To maximize patient safety, utilize
proper restraint methods during extreme
lateral tilt positioning.
NOTE
To prevent damage to the kidney lift, a
safety interlock prevents the back section from going above horizontal if the
kidney lift is not all the way down. If the
kidney lift is raised, an audible alarm will
sound when the BACK UP button is
pressed.
WARNING
The Leg section may hit the table base
or the floor if both the leg and elevation
systems are placed in their full down
position.
NOTE
When REFLEX button is activated, if
Kidney Bridge is up, the back section
will not go above horizontal.
NOTE
To prevent damage to the kidney lift, a
safety interlock prevents the kidney lift
from going up if the back section is
raised above horizontal. If the back
section is raised, an audible alarm will
sound when the KIDNEY UP button is
pressed.
NOTE
Elevation, kidney lift, and brake system
functions are not affected by the return
to level function.
CAUTION
The Back Section/Kidney Lift safety
interlock is not operational when the
emergency back-up control switches
are used.
CAUTION
The EMERGENCY BRAKE LOCK
switch does not activate the brake system timer. The switch must be held until
the brakes are completely locked, approximately 10 seconds.
NOTE
The emergency back-up control
switches on the battery powered models will function when the table is operating on 120VAC power, battery power,
or turned off.
NOTE
The Emergency Brake Release Valve
must be closed and tightened (clockwise) before activating any function.
•If the Emergency Brake Release Valve
has been operated, the UNLOCK button
on the pendant control will have to be
pressed before brakes will lock again.
5
SPECIAL USER ATTENTION
NOTE
To make the Back Section easier to
handle, remove the Head Section prior
to removing the Back Section.
WARNING
Ensure that the Leg and Back sections
are properly engaged and secured to
pins before use to prevent injury.
NOTE
The Leg and Back sections are labeled
for proper orientation. The Leg section
can not be installed on the Back section
pins.
NOTE
Normal table top position is with the
head (and back) section over the power
cord end of the base.
WARNING
When an antistatic pathway is required,
the table has to be used on an antistatic
floor.
WARNING
The antistatic properties of the table are
dependent on the use of the original pad
set which was furnished with the table
or an alternate approved replacement.
WARNING
Certain accessories may limit weight
capacities. Check with your SKYTRON
representative.
NOTE
Always follow current AORN Journal
Guidelines to ensure proper cleaning
and disinfection procedure.
WARNING
Always lock the table top in position
after rotation. DO NOT rotate the top
with an unevenly distributed patient
weight load as instability may result.
WARNING
•Make sure the TOP ROTATION LOCK
HANDLE is tightened and the brakes
are set before transferring the patient.
•Exercise caution with the table top
rotated 90° to the base since an improperly distributed patient load may cause
the table to be tipped over. A table
support rod is required for 90° positioning. See Specialty Positioning.
WARNING
Consult manufacturer's instructions
when using high frequency surgical
equipment, cardiac defibrillator and cardiac defibrillator monitors.
WARNING
Always follow OSHA blood-borne pathogens standards for protective clothing,
including gloves, masks and eye protection when cleaning the surgical table.
CAUTION
Thoroughly read and follow the
manufacturer's directions for all cleaning fluids. DO NOT use cleaners containing phenolics.
CAUTION
When using spray cleaners DO NOT
spray fluids directly into electrical receptacles or micro switches.
CAUTION
Before replacing pads on the table, make
sure the pads and all mating surfaces
are completely dry. Moisture trapped
between the pads and mating surfaces
may cause distortion of table tops.
6
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