Amsco 3085 SP User manual

OPERATOR MANUAL
Amsco®3085 SP

Surgical Table
(10/01/04) P150830-026

i
Table of Contents Operator Manual 150830-026
A WORD FROM STERIS CORPORATION
This manual contains important information on proper use and maintenance of
the Amsco®3085 SP™ Surgical Table. Allpersonnelinvolvedintheuseand
maintenanceofthisequipmentmustcarefullyreviewandcomplywiththe
warnings, cautions, and instructions contained in this manual. These
instructions are important to protect the health and safety of personnel
operating a 3085 SP table and should be retained in a conveniently accessible
area for quick reference.
Complete instructions for uncrating have been furnished. If missing, contact
STERIS for a replacement copy, giving the serial and model numbers of the
unit.
STERIS carries a complete line of accessories for use with this table. A STERIS
representative will gladly review these with you.
A listing of the
Safety Precautions to be observed when operating and
servicing this equipment can be found in SECTION 1 of this manual. Do not
operate or service the equipment until you have become familiar with this
information.
Any alteration of this equipment not authorized or performed by STERIS
Engineering Service will void the warranty, could violate federal, state, and
local regulations, and jeopardize your insurance coverage.
The Amsco 3085 SP Surgical Table is a mobile, electrohydraulically operated
general surgical table providing flexible articulation of the surgical patient.
A thorough preventive maintenance program is essential to safe and proper
unit operation. This manual contains maintenance schedules and procedures
which should be followed for satisfactory equipment performance.
Customers are encouraged to contact STERIS concerning our comprehensive
preventive maintenance agreement. Under the terms of this agreement,
preventive maintenance, adjustments, and replacement of worn parts are done
on a scheduled basis to help assure equipment performance at peak capability
and to help avoid untimely or costly interruptions. STERIS maintains a global
staff of well equipped, factory-trained technicians to provide this service, as
well as expert repair services. Please contact STERIS for details.
NOTE:Apatientgroundingpost/potentialequalizationterminal(maleconnec-
tor, DIN 42801) is provided. The mating female connector is not furnished by
STERIS.
©2004, STERIS Corporation. All rights reserved. Printed in U.S.A.
Indications for Use
Advisory
Service Information

ii
150830-026 Operator Manual Table of Contents
ECAuthorizedRepresentative
STERIS Limited
STERISHouse
Jays Close
Viables
Basingstoke
Hampshire
RG224AX
UNITEDKINGDOM
Manufacturedby:
STERISCorporation
2720GunterParkEast
Montgomery, AL 36109 • USA
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 use.

The base language of this document is
ENGLISH. Any translations must be
made from the base language document.
STERIS Corporation,
Montgomery, Alabama is an
ISO 13485 certified facility.

iii
Table of Contents Operator Manual 150830-026
TABLE OF CONTENTS
A WORD FROM STERIS CORPORATION ............................................ i
1 SAFETY PRECAUTIONS ................................................................. 1-1
2 IMPORTANT USER INFORMATION ................................................. 2-1
2.1 Pinch Point Warnings ................................................................................................... 2-1
2.2 Patient Positioning and Weight Limitation ................................................................... 2-1
2.2.1 Prevent Possible Tipping ...................................................................................... 2-3
2.2.2 For Reverse Patient Orientation ............................................................................ 2-3
2.2.3 Other Considerations ............................................................................................ 2-4
2.3 General Description ..................................................................................................... 2-4
2.4 Technical Specifications ............................................................................................... 2-5
2.4.1 Overall Size (W x L x H) ....................................................................................... 2-5
2.4.2 Weight .................................................................................................................. 2-5
2.4.3 Utility Requirements ............................................................................................. 2-5
3 INSTALLATION INSTRUCTIONS .................................................... 3-1
3.1 Install and Route Power Cord ...................................................................................... 3-2
3.2 Install Hand Control and Lock Table in Place .............................................................. 3-3
3.2.1 Standard 3085 SP Tables Hand Control ................................................................ 3-3
3.2.2 Operating Room Control System (ORCS) Hand Control ........................................ 3-3
3.2.3 Lock Table in PLace ............................................................................................. 3-4
3.3 Hand Control Interchangeability .................................................................................. 3-5
4 OPERATING INSTRUCTIONS .......................................................... 4-1
4.1 Attach Headrest and Orient Patient ............................................................................. 4-1
4.2 Tabletop Positioning .................................................................................................... 4-3
4.2.1 Hand Control Operation ........................................................................................ 4-3
4.2.2 Optional Foot Control Operation ........................................................................... 4-5
4.2.3 Care of Controls When Not In Use ........................................................................ 4-7
4.3 Optional Operating Room Control System (ORCS) Operation ..................................... 4-8
4.3.1 HERMES-Ready System Operation ...................................................................... 4-8
4.3.2 ACT Enabled System Operation ........................................................................... 4-9
4.4 Headrest Positioning ................................................................................................... 4-10
4.5 Kidney Bridge Elevation ............................................................................................. 4-10
4.6 Pads and Accessories ................................................................................................ 4-11
4.6.1 Tabletop Pads ..................................................................................................... 4-11
4.6.2 X-Ray Top Accessories ....................................................................................... 4-11
4.6.3 General Accessories Applied to Side Rails ......................................................... 4-12
4.6.4 Accessories Specific to Amsco 3085 SP Tables.................................................. 4-13
Section Title Page

iv
150830-026 Operator Manual Table of Contents
TABLE OF CONTENTS (Cont'd)
5 AUXILIARY OVERRIDE SYSTEMS ................................................. 5-1
5.1 Articulation With Electric Pump Power Available ......................................................... 5-2
5.2 Articulation With No Electric Pump Power Available .................................................... 5-3
5.3 Floor Lock Override Systems ...................................................................................... 5-3
6 ROUTINE MAINTENANCE ............................................................... 6-1
6.1 Preventive Maintenance Schedule ............................................................................... 6-1
6.2 Cleaning/Disinfecting Procedures ................................................................................ 6-3
6.2.1 Post-Usage ........................................................................................................... 6-3
6.2.2 End-of-Day ........................................................................................................... 6-4
6.2.3 Weekly ................................................................................................................. 6-4
6.3 Biweekly Maintenance ................................................................................................. 6-5
6.4 Monthly Maintenance ................................................................................................... 6-5
6.5 Battery Charging Procedure ........................................................................................ 6-6
6.5.1 Electric-Powered Tables........................................................................................ 6-6
6.5.2 Battery-Powered Tables ........................................................................................ 6-6
7 TROUBLESHOOTING....................................................................... 7-1
8 SERVICE PROCEDURES ................................................................. 8-1
8.1 Reset Circuit Breakers ................................................................................................. 8-1
8.2 Change Fuses.............................................................................................................. 8-2
8.3 Disconnect the Motor Battery ...................................................................................... 8-2
8.4 Replacement Parts ...................................................................................................... 8-3
9 DISPOSAL HAZARDS ...................................................................... 9-1
Section Title Page

1-1
Safety Precautions Operator Manual 150830-026
The following SafetyPrecautions mustbe observed when operating and servicing this equipment. WARNING indicates
the potential for personal injury, and CAUTION indicates the potential for damage to equipment. These Safety
Precautions are repeated, where applicable, throughout the manual.
WARNING – PINCHING HAZARD:
Pinch points are created during extreme tabletop articulation. Carefully review illustrations in Figure 2-1 before
operating the table.
WARNING – TIPPING HAZARD:
Do not place patient on the table unless floor locks are engaged.
Do not release floor locks while patient is on table.
Do not use this table for patients exceeding the 1,000-lb (452-kg) limit when patient is positioned in normal
orientation. The maximum safe patient weight on this table for standard surgical positions in normal orientation is
1,000 lb (452 kg) with floor locks locked.
Do not use this table for patients exceeding the 500-lb (226-kg) limit when patient is positioned in reversed
orientation. The maximum safe patient weight on this table for standard surgical positions in reversed orientation
is 500 lb (226 kg) with floor locks locked.
When performing surgery requiring a headrest accessory in reversed patient orientation, or when using a Fem/Pop
board or the 3080/3085 Ortho Extension accessory, do not exceed the 400 lb (181 kg) patient weight.
Do not use the Fem/Pop Board with X-ray Tops for bariatric patients.
Foot Extension Accessory or combination of Foot Extension and Headrest Accessories from previous design
STERIS tables must not be used for reverse orientation on the 3085 SP Table.
Do not use two or more Uro-Endo/Image Amplification Extension accessories together on the 3085 SP Table.
Do not articulate table with auxiliary override systems unless floor locks are engaged.
During an articulation if the tabletop sections contact an obstruction, the table may tip. Before lowering either the
table top or individual sections, remove possible obstructions. Do not allow leg section, when lowered, to contact
the floor.
Fem/Pop Board must be installed into leg section only. Board must be used to support the legs only. It is not
intended to support upper body weight.
Do not use the Fem/Pop Board with patients exceeding 400 lbs (181 kg).
WARNING – EXPLOSION HAZARD:
Table must not be used in the presence of flammable anesthetics.
WARNING – TRIPPING HAZARD:
Route the power cord to the receptacle in a position so it will not be tripped over by personnel in the area.
SAFETY PRECAUTIONS 1

1-2
150830-026 Operator Manual Safety Precautions
WARNING – PERSONAL INJURY HAZARD:
Healthcare professionals must ensure patients are positioned and monitored to prevent compromising respiration,
nerve pathways, or circulation.
When installing any table accessory, check for correct attachment and tighten securely (if appropriate). Do not
use worn or damaged accessory. Check installation before using any accessory.
There is a 1,000-lb (452-kg) patient weight limit if patient is in normal orientation and a 500-lb (226-kg) patient weight
limit if patient is in reversed orientation; however, the accessory load rating may be lower. Do not exceed the
accessory load rating if it is lower than the table rating.
Unanticipated table movement could cause patient injury. Patient must be secured to the table in accordance with
recommended positioning practices.
Do not immerse any part of foot control in liquids; this could cause unanticipated table movement, leading to patient
injury. Always cover control with a plastic bag before using.
If the integrity of the external protective earth conductor installation or arrangement is in doubt, operate the table
from its internal power source.
WARNING – INSTABILITY HAZARD:
Stabilize table when transferring patient.
Possible patient or user injury, as well as table or accessory failure, may result from using STERIS table accessories
for other than their stated purpose - or from using, on STERIS tables, accessories manufactured and sold by other
companies.
Patient Transfer Board must be used as a leg support only. It is not intended to support upper body weight of a
patient.
WARNING – PINCHING AND TIPPING HAZARD:
Patient injury may result if the operator of this table is not completely familiar with the controls for patient positioning
and table operation.
WARNING – PERSONAL INJURY AND/OR EQUIPMENT DAMAGE HAZARD:
Safe and reliable operation of this equipment requires regularly scheduled preventive maintenance, in addition to
the faithful performance of routine maintenance. Contact STERIS to schedule preventive maintenance.
Repairs and adjustments to this equipment must be made only by fully qualified service personnel. Nonroutine
maintenance performed by inexperienced, unqualified personnel or installation of unauthorized parts could cause
personal injury, invalidate the warranty, or result in costly damage. Contact STERIS regarding service options.
WARNING – INFECTION HAZARD:
To protect against aerosols being reflected from contaminated surfaces, wear rubber or plastic gloves, masks and
eye protection and follow OSHA blood-borne pathogens standards when cleaning.
WARNING – DISPOSAL HAZARD:
This product contains materials which may require disposal through appropriately licensed and permitted
hazardous waste management firms.

1-3
Safety Precautions Operator Manual 150830-026
CAUTION – POSSIBLE EQUIPMENT DAMAGE:
When moving the table to point of use, roll it carefully at moderate speed and only over smooth floors. Maximum
floor clearance is 1/4" (6 mm). Avoid door jambs, elevator jambs, and obstructions greater than 1/4" (6 mm). If
necessary, lift uncrated table over obstructions, onto trucks, etc. Lift table evenly and only by the table base. DO
NOT transport articles (including accessories) on top of the table and DO NOT use a forklift to move the uncrated
table.
Route the hand control cord (and optional HERMES®-Ready1or ACT Enabled™ interface cord and/or optional foot
control cord, if applicable) clear of any pinch points where the cord(s) could be damaged.
The use of incorrect hydraulic oil may severely damage the table and/or cause malfunction. Contact STERIS for
the proper oil to use.
For ORCS equipped tables, use the HERMES®-Ready1or ACT Enabled™ 3085 SP hand control with the blue strain
relief on the plug. The standard 3085 SP hand control has a red strain relief on the plug. Thesetwohandcontrols
arenotinterchangeable.
Hang the hand control from side rail (or end rail) of the table when not in use, to avoid possible damage to the control.
During some extreme articulations, the tabletop may contact the base and/or column shrouds. Take care to avoid
positioning the table in such a way as to cause damage to the shrouds.
Use caution when raising the seat section or back section while the kidney bridge is elevated. The section may
contact the elevated kidney bridge and damage the bridge and/or section.
When cleaning/disinfecting table, do not use phenolics, which may cause patient skin burns if inadequately rinsed
off, or alcohol, which does not have sufficient cleaning/disinfection properties.
When cleaning/disinfecting table, thoroughly read the cleaning fluid directions for use and follow all directions and
cautions as shown.
Do not spray cleaning fluid into electric receptacles and avoid spraying directly on override switches or into
clearance space above column. Spray or drippage may settle onto electric circuits inside table causing corrosion
and loss of function.
Cleaning procedures requiring articulation of the table should be performed only by persons familiar with table
operation.
After performing cleaning procedures, ensure pads and X-ray tops are completely dry before reinstalling. Moisture
trapped between pads and X-ray tops may contribute to equipment damage, such as X-ray top warpage.
Table may cause dimpling of cushioned vinyl flooring or other soft flooring. When fully loaded to 500 lb (226 kg)
patient load, the floor lock feet exert up to 380 psi (2,619 KPa) pressure on the floor. The pressure may reach
440 psi (3,033 KPa) with a 1,000-lb (452-kg) patient load.
The table has internal switches for setting to various AC-input voltages. Improper setting of switches may damage
table electrical system and/or cause improper operation of the table.
The HERMES®-Ready1and ACT Enabled hand controls are interchangeable for control of table functions;
however, ORCS voice-activation control will NOT operate properly with improper hand control.
1HERMES-Ready is a registered trademark of Computer Motion.

1-4
150830-026 Operator Manual Safety Precautions
Definition of
Symbols Symbol Definition
Protective Earth (Ground)
Attention, Consult Manual for Further Instructions
AAmperage Rating of the Unit
VVoltage Rating of the Unit
~Alternating Current
kW Power Rating of the Unit
Hz Frequency of the Unit
Equipotentiality
Type B Equipment
Powered by AC
Powered by Battery
Battery Charged
Battery Down
Optional HERMES-Ready System Installed
ON
OFF
Following is a key to symbols which may be on your table or controls.
Continued ...

1-5
Safety Precautions Operator Manual 150830-026
Symbol Definition
Floor Lock (Function Touch Pad)
Floor Lock: Lock
Floor Lock: Unlock
Patient Orientation (Function Touch Pad)
Normal Orientation
Reverse Orientation
Trendelenburg
Reverse Trendelenburg
Height Up (Raise)
Height Down (Lower)
Tilt Left
Tilt Right
Back Up
Back Down
Leg Up
Leg Down
Continued ...

1-6
150830-026 Operator Manual Safety Precautions
Symbol Definition
Flex
Reflex
Level

2-1
Important User Information Operator Manual 150830-026
2IMPORTANT USER INFORMATION
During extreme tabletop articulation, various possible pinch points exist. These
points are identified in Figure 2-1. All personnel involved in tabletop positioning
should examine and be aware of these points before operating the table.
The Amsco®3085 SP™ Surgical Table is designed to safely support a 1,000-lb
(452-kg) patient in the normal orientation only with limited posturing, or a
500-lb (226-kg) patient in the reversed orientation.
• RefertothefollowingSectionsandFigures2-2and2-3forPrecau-
tionaryTippingrecommendations,typicalPatientPositioning,and
MaximumWeight Limitations.
• Accessoriesmayhaveaspecifiedlesserweightlimitationthanthe
table. Do not exceed the lowest weight limit, table or accessory.
• For patient weights exceeding 500 lb (226 kg), do not use an
accessorythathas nolabeled weightlimit. Accessories available
forpatientweightsexceeding500lb(226kg)willbelabeledassuch
with the allowable limit.
• Alwayscheckpatientstability whenpatientispositioned.
IMPORTANT: When normal patient loads exceed 700 lb (318 kg), note the
following:
• Reflex and Return-to-Level articulations may be slow or not operate. Use
other articulations to move the table tops to the desired position.
• Moving the table from an extreme Right Tilt may require the table tops be
level. When normal patient loads exceed 900 lb (408 kg), moving the table
from an extreme Right Tilt may be slow or not operate.
2.1 Pinch Point
Warnings
WARNING–TIPPING
HAZARD:
• Do not place patient on the
table unless floor locks are
engaged.
• Do not release floor locks
while patient is on table.
• Do not use this table for pa-
tients exceeding the 1,000-lb
(452-kg) limit when patient is
positioned in normal orienta-
tion. The maximum safe pa-
tient weight on this table for
standardsurgicalpositionsin
normal orientation is 1,000 lb
(452kg)withfloorlockslocked.
• Do not use this table for pa-
tientsexceedingthe500-lb(226-
kg) limit when patient is posi-
tionedinreversedorientation.
The maximum safe patient
weight on this table for the
standardsurgicalpositionsin
reversed orientation is 500 lb
(226 kg)withfloorlockslocked.
• When performing surgery re-
quiring a headrest accessory
inreversedpatientorientation,
or when using a Fem/Pop
board or the 3080/3085 Ortho
Extension accessory, do not
exceed400lbs(181kg) patient
weight.
2.2 Patient
Positioning and
Weight Limitation
WARNING - PINCHING HAZ-
ARD: Pinch points are cre-
atedduringextremetabletop
articulation.Carefullyreview
theillustrationsinFigure2-1
beforeoperatingthetable.

2-2
150830-026 Operator Manual Important User Information
Typical Pinch Point and
Tipping Hazard When
Lowering
Between Column
Skirt and Column Cap
Between Ratchet Handle
and Table Frame
Between Table Frame
and Column Skirt
Column
Cap
Column Skirt
Figure 2-1. Pinch Points
Between Headrest (if
Present) and Back
Section
Between Headrest (if Present)
and Base Cover
Between Leg Section or Headrest
(if Present) and Column Cover
Between Leg Section or
Headrest (if Present) and Base
Between Leg Section or
Headrest (if Present) and Base
Cover
Cover
Between Leg Section or
Headrest (if Present) and
Floor
Between Kidney Bridge and
Tabletop or Between Kidney
Bridge and X-ray Set
Between Saddle and
Table Frame

2-3
Important User Information Operator Manual 150830-026
Do not exceed the maximum patient weight indicated in Figures 2-2 and 2-3.
Do not place patient on the table unless floor locks are engaged.
Do not release floor locks while patient is on table.
Do not attempt to move table while patient is on it.
Do not extend (lengthen) the patient support surface beyond that shown, unless
using a STERIS table accessory intended for this purpose and the accessory
weight limitation is not exceeded.
When using Fem/Pop Board or the 3080/3085 Ortho Extension accessory, do
not exceed 400 lbs (181 kg) maximum patient weight.
Head Section
(For Patient Head
or Feet Only)
Back Section
Leg Section
Seat Section
2.2.1 Prevent Possible
Tipping
Figure 2-2. Normal Patient Orientation
(For up to 1,000-lb [452-kg] Patient Weight)
2.2.2 For Reverse Patient
Orientation
Seat Section
Section
Head Section
(For Patient
Head or Feet
Only)
Leg Section Back
Figure 2-3. Reverse Patient Orientation
(For up to 500-lb [226-kg] Patient Weight)
When performing surgery requiring a headrest accessory in a reversed patient
orientation, do not exceed 400-lb (181 kg) patient weight limit.
For Patients Over
500 lb (226 kg),
Always Position
With Patient Head
on Table Head
Section.
WARNING–TIPPING
HAZARD:
• Do not use this table for pa-
tientsexceedingthe1,000-lb
(452-kg)limitwhenpatientis
positionedinnormalorienta-
tion. The maximum safe pa-
tient weight on this table for
standard surgical positions
innormalorientationis1,000
lb (452 kg) with floor locks
locked.
• Fem/Pop Board must be in-
stalled into leg section only.
Board must be used to sup-
port the legs only. It is not
intended to support upper
bodyweight.
• Do not use the Fem/Pop
Board with patients exceed-
ing 400 lbs (181 kg).
WARNING–TIPPING
HAZARD:
• Do not use this table for pa-
tients exceeding the 500-lb
(226-kg) limit when patient is
positionedinreversedorien-
tation.Themaximumsafepa-
tient weight on this table for
standardsurgicalpositionsin
reversedorientationis500lb
(226kg)withfloorlockslocked.
• When performing surgery re-
quiring a headrest accessory
inreversedpatientorientation,
orwhenusingaFem/Popboard
or the 3080/3085 Ortho Exten-
sionaccessory,donotexceed
400lbs(181kg)patientweight.
• Foot Extension Accessory or
combinationofFootExtension
andHeadrestAccessoriesfrom
previousdesignSTERIStables
must not be used for reverse
orientation on the 3085 SP
Table.

2-4
150830-026 Operator Manual Important User Information
Use extreme care when transferring patients to or from table.
Ensure all accessories are properly installed and secured.
Check for and eliminate harmful patient pressure points once patient is
positioned.
Have a qualified medical professional monitor patient during surgery for all
possible patient positioning hazards.
Amsco 3085 SP Surgical Tables are remote control, Image Amplification
compatible units with auxiliary override (backup) systems for the control and
hydraulic systems. Tables are furnished with 2" (51 mm) thick pads and are
available in the following two configurations:
• Electric Powered
• Battery Powered
Both tables are operated in the same manner.
NOTE:Twohandcontrolsareavailable:Thestandardhandcontrolunit(witha
redstrainreliefontheplug)isforstandardtables;theOperatingRoomControl
System(ORCS)hand control(withablue strainreliefonthe plug)isfortables
equippedwitheithertheHERMES
®
-Ready
1
orACTEnabled™interfacecontrol
options.Thehand controlsarenot interchangeable.
Image Amplification Coverage
Head End −28" (711 mm) with headrest attached (plus 3" [76 mm] maximum
extension of headrest).
Foot End −33" (838 mm) without headrest attached.
−45" (1,143 mm) with headrest attached (no extension of headrest
allowed when at this end).
Width −14.5" (368 mm) average on both ends.
2.2.3 Other
Considerations
2.3 General
Description
WARNING – PERSONAL
INJURYHAZARD:
• Health care professionals
must ensure patients are po-
sitionedandmonitoredsoas
topreventcompromisingres-
piration, nerve pathways, or
circulation.
• There is a 1,000-lb (452-kg)
patient weight limit if patient
isinnormalorientationanda
500-lb(226-kg)patientweight
limit if patient is in reversed
orientation;however,the ac-
cessory load rating may be
lower. Do not exceed the ac-
cessory load rating if it is
lower than the table rating.
1HERMES-Ready is a registered trademark of Computer Motion.
CAUTION – POSSIBLE
EQUIPMENTDAMAGE:
• For ORCS equipped tables,
use the HERMES®-Ready1or
ACT Enabled 3085 SP hand
control with the blue strain
relief on the plug. The stan-
dard 3085 SP hand control
has a red strain relief on the
plug. These two hand con-
trolsarenotinterchangeable.
• TheHERMES®-Ready1andACT
Enabled hand controls are in-
terchangeable for control of
table functions; however,
ORCSvoice-activationcontrol
willNOToperateproperlywith
improperhandcontrol.

2-5
Important User Information Operator Manual 150830-026
24-13/32 x 75-15/16 x 27 to 44"
(620 x 1,928 x 686 to 1,118 mm)
737 lbs (334 kg); maximum anticipated floor lock pressure exerted on floor:
380 psi (2,619 KPa) with a 500-lb (226-kg) patient load, 440 psi (3,033 KPa) with
a 1,000-lb (452-kg) patient load.
Electric:*
•100 V, 5 A, 1-Phase •220 V, 3 A, 1-Phase
•120 V, 4.5 A, 1-Phase •230/240 V, 2.5 A, 1-Phase
2.4.1 Overall Size
(WxLxH)
2.4.2 Weight
2.4.3 Utility Requirements
2.4 Technical
Specifications
* Each table is shipped from the factory configured to the electrical requirement
specified on the factory order. If required to be changed in the field, consult STERIS
for the procedure/materials required. Tables intended to be shipped to other than
USA or Canada will have procedure/materials included in shipping container.

3-1
Installation Instructions Operator Manual 150830-026
3INSTALLATION INSTRUCTIONS
NOTE: Patientgroundingpost/potentialequalizationterminal (maleconnector,
DIN 42801) is provided. Mating female connector is not furnished by STERIS.
IMPORTANT: Before connecting the table to your AC power system, check
that table internal voltage switches are set for your power system (100, 120, 220,
or 230/240).
IMPORTANT: Battery powered tables should be completely charged prior to
initial operation. Charge batteries as indicated in SECTION6,ROUTINEMAINTENANCE ,
before proceeding.
If table is to be placed in extended storage, have table prepared for storage by
a qualified service technician. Ensure batteries are disconnected and check
batteries before reconnecting. Every six months the table must be operated
through all articulations and the batteries charged.
WARNING – PERSONAL
INJURYHAZARD:Iftheinteg-
rityoftheexternalprotective
earth conductor installation
or arrangement is in doubt,
operate the table from its in-
ternalpowersource.
WARNING – EXPLOSION
HAZARD: Table must not be
usedinthepresenceofflam-
mableanesthetics.
WARNING–TRIPPING
HAZARD: Route power cord
toreceptacleinapositionso
it will not be tripped over by
personnel in the area.
CAUTION – POSSIBLE
EQUIPMENTDAMAGE:
• When moving the table to
pointofuse,rollitcarefullyat
moderatespeedandonlyover
smooth floors. Maximum
floorclearanceis1/4"(6mm).
Avoid door jambs, elevator
jambs, and obstructions
greater than 1/4" (6 mm). If
necessary,liftuncratedtable
overobstructions,ontotrucks,
etc.Lifttableevenlyandonly
by the table base. DO NOT
transport articles (including
accessories) on top of the
tableandDONOT useafork-
lifttomovetheuncratedtable.
• Thetablehas internalswitches
forsettingtovariousACinput
voltages.Impropersettingof
switches may damage table
electricalsystemand/orcause
improper operation of the
table.

3-2
150830-026 Operator Manual Installation Instructions
1. Place table at desired location.
NOTE: Omit Steps 2 and 3 if table is battery-powered.
2. Connect female end of 20' (6 m) long power cord* to male connector located
on narrow end of table base (can only be connected one way). See Figure 3-1.
3. Route power cord to wall receptacle so it will not be tripped over, then plug
it into an appropriate receptacle.
4. For either electric-powered or battery-powered 3085 SP, power cord may
remain plugged into appropriate receptacle indefinitely. It will not harm table
or table batteries.
3.1 Install and Route
Power Cord
Figure 3-1. Power Cord Connection (Electric Table Only)
Connect AC Power Cord
WARNING–TRIPPINGHAZ-
ARD:Routethepowercordto
the receptacle in a position
so it will not be tripped over
by personnel in the area.
* The Australian medical power cord will be much shorter.

3-3
Installation Instructions Operator Manual 150830-026
Connect the hand control plug to the proper table receptacle.
NOTE:Aspring-loadedlockringlocksplugintoreceptacle.Whendisconnecting
the hand control, pull back on the lock ring before pulling the plug from the
receptacle.
Align the red dot on the hand control cord red plug with the red dot of the table
red receptacle and push into connected position (see Figure 3-2).
NOTE: The standard hand control and the ORCS hand control (for tables
equipped with either HERMES
®
-Ready
1
or ACT Enabled™ interface control
options)arenotinterchangeable.
Figure 3-3. Hand Control Connection for
ORCS Equipped 3085 SP Table
Blue Receptacle
(ORCS Hand
Control)
Gray Receptacle
(Foot Control)
Blue Strain
Relief
Black Receptacle
(ORCS Cable
Connection)
Align Red Dots
to Connect
Hand Control Plug
Figure 3-2. Hand Control Connection for
Standard 3085 SP Table
Red Receptacle
(Hand Control)
Gray Receptacle
(Foot Control)
Red Strain Relief
3.2 Install Hand
Control and Lock
Table in Place
Align the red dot on the hand control cord and the blue plug with the red dot of
the table blue receptacle, and push into connected position (see Figure 3-3).
NOTE: The standard hand control and the ORCS hand control (for tables
equipped with either HERMES
®
-Ready
1
or ACT Enabled™ interface control
options)arenotinterchangeable.
Align Red Dots
to Connect
Hand Control Plug
3.2.1 Standard 3085 SP
Tables Hand Control
CAUTION – POSSIBLE
EQUIPMENTDAMAGE:
• For ORCS equipped tables,
use the HERMES®-Ready1or
ACT Enabled 3085 SP hand
control with the blue strain
relief on the plug. The stan-
dard 3085 SP hand control
has a red strain relief on the
plug. These two hand con-
trols arenotinterchangeable.
• TheHERMES®-Ready1andACT
Enabled hand controls are in-
terchangeable for control of
table functions; however,
ORCSvoice-activationcontrol
willNOToperateproperlywith
improperhandcontrol.
3.2.2 Operating Room
Control System (ORCS)
Hand Control
1HERMES-Ready is a registered trademark of Computer Motion.
CAUTION – POSSIBLE
EQUIPMENTDAMAGE:
• For ORCS equipped tables,
use the HERMES®-Ready1or
ACT Enabled 3085 SP hand
control with the blue strain
relief on the plug. The stan-
dard 3085 SP hand control
has a red strain relief on the
plug. These two hand con-
trols arenotinterchangeable.
• TheHERMES®-Ready1andACT
Enabled hand controls are in-
terchangeable for control of
table functions; however,
ORCSvoice-activationcontrol
willNOToperateproperlywith
improperhandcontrol.

3-4
150830-026 Operator Manual Installation Instructions
UNLOCK
Actuate
Button
FLOOR LOCK
Function Button
LOCK
Actuate
Button
Figure 3-4. Standard Hand Control
1. Press ON button at top of hand control to turn table on. All LEDs on hand
control may light momentarily for control system self-test when power is
turned on.
Refer to Figure 3-4 for identification of hand control functions. See SECTION7,
TROUBLESHOOTING, to identify any problems with the hand control.
NOTE:Ifthewrongfunctionselectionbuttonisaccidentallypressed,pressthe
correct function button to override the incorrect selection.
ON
Button
3.2.3 Lock Table in Place