idi Aspect100-4 User manual

Aspect100-4
Mobile Imaging Table
Operator Manual

Operator Manual Aspect 100-4
L100-3058 REV A www.imagediagnostics.com ii
Table of Contents
PRODUCT DATA ............................................................................................................................................ 1
INTRODUCTION ............................................................................................................................................ 2
CUSTOMER SUPPORT ................................................................................................................................... 3
SYMBOLS AND DATA PLATE......................................................................................................................... 4
SPECIFICATIONS............................................................................................................................................ 6
ELECTROMAGNETIC COMPATIBILITY STATEMENT...................................................................................... 7
SETUP ............................................................................................................................................................ 8
SAFETY HAZARDS.......................................................................................................................................... 9
SAFETY HAZARD ALERTS ............................................................................................................................ 10
SAFETY INSTRUCTIONS............................................................................................................................... 10
ACCESSORIES ..............................................................................................................................................13
OPERATOR CONTROLS ............................................................................................................................... 21
ELECTRIC SYSTEM .......................................................................................................................................23
BATTERY FUNCTION ...................................................................................................................................24
POWER SUPPLY AND RELAY FUNCTION .................................................................................................... 24
GENERAL CLEANING ................................................................................................................................... 25
MAINTENANCE ........................................................................................................................................... 27
DISPOSAL OF COMPONENTS...................................................................................................................... 28
WARRANTY................................................................................................................................................. 29
Linak documentation can be found at their web site: www.linak-us.com
Select “Products | User manuals” and click on “Actuators & Electronics”.
The text of this manual was originally written, approved
and published by the manufacturer in English.

Operator Manual Aspect 100-4
L100-3058 REV A www.imagediagnostics.com 1
PRODUCT DATA
•Low attenuation carbon fiber tabletop
•Tabletop: 76 cm x 203 cm (30 in x 80 in)
53 cm (21 in) upper abdominal area
•Longitudinal travel: 102 cm (40 in)
•Transverse tabletop travel: 25 cm (10 in)
•Height range: 71 cm to 97 cm (28 in to 38 in)
•Patient capacity: 204 kg (450 lbs)
•Table weight: ~175 kg (~385 lbs)
•Locking swivel casters
•Hand operator control standard
•Foot operator control optional

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INTRODUCTION
Overview
This manual pertains to the specified product only. It is intended for qualified medical
personnel who have been trained in the use of medical equipment. It is not designed to
replace or substitute for certified training in the application of this equipment.
Functional capabilities and operation of the equipment described herein which can be
employed in a variety of diagnostic, therapeutic, and surgical applications. It is designed
for use as either a fluoroscopic or radiographic table.
Owner Responsibilities
The owner is responsible to ensure system compatibility, the qualifications of the
operator and maintenance personnel. The operator must be properly trained and have
obtained credentials from the appropriate authorities.
This equipment should only be installed in an area provided with the proper electrical
power.
The owner is responsible for verifying continued compliance with all applicable
regulations and standards. Consult local, state, federal and/or international agencies
regarding specific requirements and regulations applicable to the use of this equipment.
Image Diagnostics, Inc. certifies this equipment. After-sale operating practices and safety
are the responsibility of the owner and operator. Image Diagnostics, Inc. assumes no
liability or responsibility for after-sale operating or safety practices; nor can it be
responsible for personal injury or damage resulting from misuse.
Never make modifications or adjustments to the equipment unless directed by a qualified
Image Diagnostics representative. This equipment, when properly assembled, meets US
federal regulations and international standards. Unauthorized modifications to the
equipment may impact adherence to these standards and make the equipment unsafe to
operate.

Operator Manual Aspect 100-4
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CUSTOMER SUPPORT
Image Diagnostics will make available, on request, circuit diagrams,
component part lists, calibration instructions, or other information which
will assist the user’s appropriately qualified technical personnel to repair
those parts of equipment which are designated by the manufacturer as
repairable.
For technical assistance, call IDI at [phone] or send fax to (978)
829-0027. Be prepared to give the complete model and serial number
found on the dataplate on the table base at the time of contact.
This X-ray component manufactured by Image Diagnostics, Inc. complies
with applicable FDA performance standards contained in 21CFR at date of
manufacture.

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SYMBOLS AND DATA PLATE
Intertek Testing Service
The system was tested and found to be in compliance with the
requirements of all relevant directives and standards in effect within
the European Union at the time of manufacture.
Attention! Consult accompanying documents.
Failure to follow these instructions can cause accidents resulting in
serious personal injury or damage to equipment. CD ROMs
containing file copies of all relevant drawings, BOMs, and
documentation are included with this manual, one for general
operators and one for the BIOMED department.
Type B equipment
Alternating current
Data Plate
Maximum Patient Weight
204 kg
450 LBS

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LATEX
Recycle
Some of the material can be recycled rather than discarded.
Not for Patient Transport
The table should not be relocated with a patient on it nor should it
be used to move a patient.
Do Not Sit
This label is found on parts that are not designed to support the
sitting weight of a patient.
Not made with natural rubber latex
Single Use Item.
This symbol, when used in this manual, indicates the potential of
exposure to harmful x-rays. Be sure to read and comply with all
warnings.
European Authorized
Representative
Warning! Information or instructions shown near this symbol must
be adhered to in order to prevent a potentially hazardous situation
which if not avoided, could result in death, personal injury or
damage to the equipment.
2
EC
REP
Advena Ltd. Pure Offices, Plato Close,
WARWICK CV34 6WE UK

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SPECIFICATIONS
Mode of Operation:
For continuous operation with short time loading
Duty Cycle: 10% (6 min/hr)
Type of Equipment:
Class I Type B (as defined by IEC 60601-1, UL 60601-1,
EN 60601-1, CSA 601.1, IEC 60601-2-32:1994)
Type B protection against electrical shock
Electrical:
Supply Voltage: 120±5% Vac 60Hz or 23010% Vac 50Hz
Duty Cycle: 10% (6 min/hr)
Current Rating: Less than 10 Amps
Internally Battery Powered
Environmental:
Operating Temperature Range: -10C to +40C
Operating Humidity Range: 30% to 75% relative humidity, noncondensing
Operating Pressure Range: 700hPa to 1060 hPa
Transport & Storage Temperature Range: -40C to +60C
Transport & Storage Humidity Range: 30% to 75% relative humidity, noncondensing
Transport & Storage Pressure Range: 500hPa to 1060 hPa
Rated IPX4 (Protected against splashing water)
Meets EMC requirements of EN 60601-2 (1993)
Tabletop:
The tabletop is made of carbon fiber and is certified to meet all the requirements of 21
CFR Subchapter J

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ELECTROMAGNETIC COMPATIBILITY STATEMENT
This equipment may generate and use radio frequency energy. The equipment must be
installed and used according to the manufacturer’s instructions in order to avoid radio
frequency interference.
If this equipment generates or receives interference:
•Verify that the equipment is the cause by turning the system off and on.
•In the event of unintended motor actuation, immediately remove power to the
equipment.
•Use only cables supplied by Image Diagnostics, Inc.

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SETUP
Unpack
No special handling is required for unpacking this equipment at the site. Conventional
shipping materials are used.
When using a forklift, pad the forks to protect the paint. Lift from under the metal base.
Install
Hand controls are standard with this table with foot controls as optional. The operator should
become familiar with the controls before using.
The table operates on 110Vac (or 230Vac) or on internal battery backup. Swing the hinged cover
open to find the power input terminal block. When power is applied, the green indicator on the
control box will illuminate.
Activate tabletop UP or DOWN using the operator control to initiate battery charging after
connecting to mains. During an AC failure, the table will automatically run on battery backup
without any manual switching required. It is recommended that power be applied at all times,
even when not in use, to keep a proper charge on the batteries and achieve maximum battery life
and table function. (Batteries are being charged during normal use).
Where the integrity of the external protective earth conductor is in doubt, this equipment shall be
operated from its internal electrical power source by unplugging the power cord from the mains.
Note: The electromagnetic brakes that release when the mushroom panhandle (if hand
control equipped) is depressed or the brake release pedal (if foot control equipped) is
depressed (allowing the top to “float”) will not operate when the table is disconnected from
the ac power and the table is operating in battery backup mode.
Recycle or dispose of shipping
material per local regulations.

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Preparation for Patient Use
New Installation:
This equipment will need to be properly cleaned before patient use as it will inevitably come into
contact with contaminants during shipping, unpacking, storage, and installation.
After Installation:
This equipment will need to be properly cleaned between patient use as it will inevitably come
into contact with contaminants during procedures.
SAFETY HAZARDS
Operators using this equipment should understand the safety issues, emergency
procedures, and operating instructions provided.
Comments and questions regarding safety should be addressed to:
Customer Support
Image Diagnostics, Inc.
310 Authority Drive
Fitchburg, MA 01420
USA
Or call IDI at [phone] or send fax to [phone].
Or call toll-free at [phone].
Review the SAFETY INSTRUCTIONS before
operating table

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SAFETY HAZARD ALERTS
Alert
Circumstances for Use
DANGER
Indicates an imminently hazardous situation which, if
not avoided, will result in death or serious injury.
WARNING
Indicates a potentially hazardous situation which, if not
avoided, could result in death or serious injury.
CAUTION
Indicates a potentiallyhazardous situation which, if not
avoided, may result in minor or moderate injury or
equipment damage.
WARNING!
This equipment has not been tested for use with high
frequency surgical equipment, cardiac defibrillators, or
cardiac defibrillator monitors.
WARNING!
If an antistatic path is required, use the equipment on an
antistatic floor. Use only the tabletop pad (patient
mattress) supplied with the table.
WARNING!
This product may be used in conjunction with x-ray
equipment. This constitutes potential expose to harmful
x-rays for both the patient and operator. Be sure to use
proper radiation shielding.
CAUTION
Secure power cord when in use so that it does not get
entangled with other equipment and/or compromise
the safety of the operator and/or staff.
CAUTION
Do not modify this equipment without authorization of
the manufacturer.

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SAFETY INSTRUCTIONS
This manual should be accessible to all personnel installing, operating, or servicing this equipment.
Only a qualified technician may install or maintain this equipment.
Only qualified persons may operate this equipment.
Failure to follow safety precautions may result in serious injury to patient or user or damage to
equipment.
This symbol, when found marked on the equipment
means:
”Attention, consult accompanying documentation.”
WARNING!
Always safely position and secure patient on table
WARNING!
Do not exceed patient weight of 450 pounds (204kg)
CAUTION
Do not leave patient on table unattended
CAUTION
Patient must be restrained at all times. The restraining
straps are not intended to restrain an uncontrollable
patient.
CAUTION
The carbon fiber top is subject to damage or possible
damage from impact from other objects. Take caution
when using power driven diagnostic equipment around
table. Regular inspection of the tabletop is necessary for
the safety of patient and operator.

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Push down to lock
CAUTION
Ensure that the tabletop does not contact other
equipment as it moves.
CAUTION
During operation, listen for any unusual sounds and
watch for uneven operation.
CAUTION
Do not sit on the table top at the head of the table.
CAUTION
Secure wheel locks by depressing locks on all 4
wheels prior to patient usage and when table is not
in motion. Disengage to reposition.
CAUTION
Do not place or store any containers or large items
underneath the tabletop. As the tabletop is descending,
contact with an obstruction may cause permanent
damage to the table.
CAUTION
Do not use table for patient transport.
CAUTION
Retract tabletop to minimize overhang and lower
table position to a comfortable height before
performing CPR on a patient.

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ACCESSORIES
•CRESCENT FACE CUSHION (supplied with some models)
Use this pad for patient comfort when the patient will be positioned face down. Place a
disposable cover over the pad.
LATEX
Crescent Face Cushion Head Pad
Part Number C000-0597
Disposable Covers
2
Part Number C000-0598 (box of 50)

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•Patient Restraint Straps
WITH THE SMALL RETAINING STRIP
SLIDE THE RESTRAINT STRAP OVER THE END OF THE TABLETOP
OVER THE TOP SURFACE OF THE TABLETOP.
PHOTO OF STRAP ARRANGEMENT:
•Patient Restraint Strap Set (Standard)
Part Number C000-0328
Two straps, one 3” wide and one 5” wide, with hook & loop fasteners
NOTE: Strap configuration shown above is recommended, however,
patient restraint is a case-by-case condition. Please refer to the
facility’s policy on restraining a patient.

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•CLAMP-ON ACCESSORY RAIL AND ARMBOARD (OPTION)
To install clamp to tabletop:
- Turn knob counterclockwise (as viewed from above) to open clamp enough
to slip onto tabletop
- Turn knob clockwise to tighten clamp to tabletop
A
B
C
D
A –Push to open latch to install to accessory rail or remove from accessory rail
B –Armboard pad
C –Pull trigger to rotate armboard to desired position
D –Hook & loop patient straps
Clamp-on Rail Accessory Part Number #A100-1007 (see note below)
Armboard with Pad & 2 Straps Part Number #A310-056 (see note below)
Replacement Armboard Pad Part Number #A100-1655 (see note below)
Replacement Armboard Straps Part Number #C000-0455 (pair)
Note: Part number is for quantity of 1 and fits either left or right side of table
WARNING!
25 LBS (11 kg) Maximum Load

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•Tabletop pads
•Tabletop Pad
Part Number X100-2650 Black
53.3/76.2cm X 203cm X 5.1cm thick (21/30in X 80in X 2in thick)
LATEX
Not made with natural rubber latex
Pads are held in place by hook and loop fasteners. Simply pull pad up gently to remove.
New replacement pads are supplied with new self-adhesive fasteners installed and new
mating pieces
for the tabletop or extension. Peel off old fasteners from tabletop or extension. Peel off
the
protective paper and carefully put new pad into position. Apply pressure to complete
installation.
Note: Pads comply to California Technical Bulletin 117 as well as
Underwriters Laboratories 94 (UL94).

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•Armboard
• Arm Board Option - Part Number A310-059 with hook & loop restraint straps and slip-
on pad.
• Replacement pad – Part Number C000-0689
• Replacement strap (single) – Part Number C000-0455
Carbon fiber construction
SLIP BASE UNDER TABLE PAD.
UNIT IS HELD IN PLACE
BY THE PATIENT'S WEIGHT.
ROTATES TO
ANY POSITION
USING TWO ARMBOARDS

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•VAB Armboard
VASCULAR ACCESS BOARD
Carbon fiber construction.
• Arm Board VAB Option for Tables with 2” thick Tabletop Pads
Part Number A100-2244 with pad and hook & loop restraint strap
• Arm Board VAB, 2” thick Tabletop Replacement Pad
Part Number X100-2243
• Arm Board VAB, Replacement Restraint Strap
Part Number C000-0709
•
LATEX
Not made with natural rubber latex
STRAP PASSES THROUGH
PAD
ARMBOARD
SELECTED LOOP ON BOTTOM OF PAD
HOOK SIDE UP
HOOK PIN
ON TABLETOP
TABLETOP
ARMBOARD SLIPS UNDER TABLETOP PATIENT PAD (IF EQUIPPED)
ROTATE ARMBOARD AS NEEDED, KEEPING PIN IN CONTACT WITH TABLETOP