This product is provided with a CE marking in accordance with the
regulations stated in Appendix II of the Directive 93/42/EEC of June
14th, 1993 concerning medical devices.
In accordance with Appendix IX of the Directive 93/42/EEC, this
device is assigned to class II b.
The CE marking applies only to medical devices which have been
put on the market according to the above-mentioned EC Directive.
Unauthorized changes to this product invalidate this declaration.
Please observe the Safety Operator Manual.
Important information is given there.
The original version of this manual was written in English.
AXIOM Iconos R200
Overall Table of Contents
Lists
Operator Manual
Overall Table of Contents
Part: Lists
Chapter: Overall Table of Contents....................................................................................................... 1
Part: System Overview
Chapter: System Description.................................................................................................................. 5
System configuration ............................................................................................................................ 6
System overview .................................................................................................................................. 7
Unit overview ........................................................................................................................................ 8
Chapter: System Settings...................................................................................................................... 11
General notes ...................................................................................................................................... 11
Moving the X-ray system longitudinally .............................................................................................. 14
Additional Cu filter ............................................................................................................................... 30
Cup holder .......................................................................................................................................... 26
IV holder .............................................................................................................................................. 27
System .................................................................................................................................................. 5
Unit ....................................................................................................................................................... 6
Changing the bulb of the laser light localizer ....................................................................... 41
Testing the fit of the new bulb ................................................................................ 43
Accessories and auxiliary devices ..................................................................................... 43
AXIOM Iconos R200AXD3-340.620.13.01.023 / 44
System Overview
Table of Contents
4 / 44AXD3-340.620.13.01.02Operator Manual
System Overview
System Description
Application
The ICONOS R200 is an X-ray system for universal use and is suitable both as
intensively used universal workstation and as a highly loaded special workstation.
You can perform examinations with the following techniques:
❏ Fluoroscopy through image intensifier and television system
❏ Cassette exposures with spotfilm device (optional)
– Spotfilms
– Tomography (optional)
– Periscanning
– Peristepping (optional)
– DR scanning (optional)
– Digital subtraction angiography (optional)
❏ Tabletop cassette exposures
❏ Bed-side exposures
❏ Exposures onto the wall stand (optional)
Product description
ICONOS R200 universal X-ray diagnostic unit with swivelling overtable X-ray tube
assembly, oblique projection and tomography in all table positions and gently
starting and braking system movements.
Two-stage setting of the source-image distance.
Table tilt + 90° to - 17° with soft start and braking.
Motor-driven longitudinally and transversely moving tabletop.
Fully automatic spotfilm device with extensive subdivision program and 33 cm or
40 cm image intensifier or I.I. image receptor with 40 cm image intensifier, each
with a large axial travel range.
Fluoroscopy and imaging system with ergonomic remote control.
Integrated system movement control on the spotfilm device.
AXIOM Iconos R200AXD3-340.620.13.01.025 / 44
System Overview
System Description
System configuration
The label with MODEL NO.: 59 02 767 bears the CE 0123 marking for the entire
ICONOS R200 system and is attached to the back of the table frame.
Standard version
❏ ICONOS R200 system
❏ Cassette spotfilm device with image intensifier with SIRECON 33 cm or 40
cm image intensifier or I.I. image receptor with SIRECON 40 cm image intensifier
❏ VIDEOMED DH TV system (with DSA) or DHC (without DSA)
❏ OPTITOP X-ray tube assembly
❏ POLYDOROS SX X-ray generator
❏ Primary collimator
❏ Monitor trolley or ceiling suspension system
❏ 44 cm or 54 cm monitor(s)
❏ FLUOROSPOT Compact with DICOM Send and Storage Commitment
❏ Footswitch for fluoroscopy and radiography
Options
❏ DICOM functions:
–Get Worklist and MPPS
– Query/Retrieve
–Print
❏ Reference image monitor(s)
❏ VERTIX PRO/TOP Bucky wall unit
❏ 2nd X-ray tube assembly on the 3D-TOP ceiling-mounted support
❏ PACS/SIENET connection
❏ High-pressure contrast medium injector
❏ Measuring device for area dose product
❏ Mobile tableside console
6 / 44AXD3-340.620.13.01.02Operator Manual
(2)
System Overview
System Description
System overview
(1)
(3)
AXIOM
(4)
(5)
(6)
(7)
(8)
(9)
(1) ICONOS R200 examination unit
(2) Generator ON/OFF console
(3) Monitor trolley (optional)
(4) System remote control console
(5) FLUOROSPOT Compact keyboard
(6) Foot switch for fluoroscopy and radiography
(7) Desk (optional) for operating consoles
(8) Tableside control console with foot switch for fluoroscopy and radiography
(optional)
(9) Bucky wall unit (optional)
AXIOM Iconos R200AXD3-340.620.13.01.027 / 44
System Overview
System Description
(9)
Unit overview
(8)
(7)
(6)
(5)
(4)
(3)
(2)
(1)
(10)
(11)
AXIOM
(12)
(13)
(14)
(15)
(16)
(1) Image intensifier TV system with safety shut-off device
(2) Handgrip (at the front), adjustable
(3) Cassette spotfilm device or I.I. receptor unit with tableside control panel and
removable scattered radiation grid
(4) Grip protection strip (head end), detachable
(5) Handgrip strip (located on back), adjustable, secure in all patient positions
(6) Compression device (optional)
for inserting a compression cone, continuously adjustable compression force
(7) Collimator with automatic format collimation and numerical format indication,
with integrated motor-driven additional Cu filters, motor-driven adjustable
semi-transparent filters (optional)
(8) X-ray tube assembly
air-cooled, partly enclosed, can be swivelled
(9) Handle for swivelling the tube assembly
(10) Tube assembly stand on the longitudinal carriage
coupled with the spotfilm device by centering rod, axially swivelling, telescopic (SID 115cm and 150cm)
(11) Longitudinal carriage with attached tube assembly stand
(12) Tomographic height display (option) with laser line light localizer
(13) Tabletop with flat accessory rails
motor-driven longitudinal and transverse travel
(14) Footboard
adjustable for use as seat,
with attachment points for foot restraints,
can be changed over from foot end to head end.
(15) Table frame
motor-driven adjustable in height, can be tilted + 90°/-17°
(16) Unit base with tilting drive on installation plate
AXIOM Iconos R200AXD3-340.620.13.01.029 / 44
System Overview
System Description
10 / 44AXD3-340.620.13.01.02Operator Manual
System Overview
Protective Measures
Emergency Procedures
Warning
Due to the complexity of the system, the loss of X-ray imaging or other system
functions during an examination or procedure can not be completely excluded.
Risk of failure during interventions
◆ Consider therefore the need to establish emergency procedures in such cases.
Cleaning and disinfection
Caution
Use of harsh cleaning agents, liquids or sprays.
Risk of electrical hazard or damage to the system
◆ Use only substances for cleaning and disinfection, which are recommended.
◆ Do not let cleaning liquids seep into the openings of the system
(e.g. air openings, gaps between covers).
◆ Observe the following cleaning and disinfection instructions.
AXIOM Iconos R200AXD3-340.620.13.01.0211 / 44
System Overview
Protective Measures
Radiation protection zones
Position and size of the main operating area
Horizontal patient table:
x
107
200
90
60
Main operating area
Dimensions in cm
60
12 / 44AXD3-340.620.13.01.02Operator Manual
Vertical patient table:
System Overview
Protective Measures
x
200
140
40
60
60
Main operating area
Dimensions in cm
x
107
AXIOM Iconos R200AXD3-340.620.13.01.0213 / 44
System Overview
Protective Measures
Patient table horizontal
Stray radiation in the main operating area
according to DIN EN 60601-1-3
Tolerance of the air kerma measurements ± 5%
Characteristic A and C: continuous fluoroscopy 63kV, 0.8mA (antiisowatt)
Characteristic B and D: continuous fluoroscopy 110kV, 3mA
Height above floor
cm
200
Patient table vertical
150
100
50
0
0123456
Height above floor
cm
200
150
A
B
C
Air kerma
mGy/h
100
50
0
012
14 / 44AXD3-340.620.13.01.02Operator Manual
D
Air kerma
mGy/h
System Overview
Protective Measures
Mechanical safety
Danger zones with unit in horizontal position
The places marked in the illustrations show possible danger zones at which the
patient or operator can be injured.
AXIOM Iconos R200AXD3-340.620.13.01.0215 / 44
System Overview
Protective Measures
Danger zones with unit in vertical position
The places marked in the illustration indicate possible danger points where the
patient or operating personnel can be injured.
x
Danger zone
If the patient is located in the danger zone, it must always be ensured that the
operating personnel are in the room and within reach of an emergency stop.
If the operating personnel leaves the room and/or moves out of reach of an
emergency stop, then the patient has to be moved out of the danger zone.
1
Warning signs
Special danger zones are marked on the unit with a warning sign.
This warning sign is a reference to a possible risk of injury by crushing for the patient and/or examiner.
This warning sign shows the position of the patient table in cardiopulmonary reanimation (CPR) with pressure compression up to 500N (50kg).
1
Between -90° and +90°, depending on the system version
16 / 44AXD3-340.620.13.01.02Operator Manual
System Overview
Protective Measures
Grip locations
Warning
When handling the system correctly as well as when positioning the patient,
operators and patients should use only the grip locations
provided for this purpose.
The following grip locations are provided:
❏ 1 handgrip (front)
❏ Grip protection strip (head end)
❏ Handgrip strip (back)
◆ Ensure that the handgrip strip, the grip protection strip and the handgrip are
always attached.
If these grip locations cannot be used:
◆ Pay special attention to the stated possibilities of crushing between moving
parts and their guide openings.
◆ Ensure during the examination that the patient under no circumstances holds
on to the edges of the patient table.
Not intended as gripping point:
The handle for turning the tube assembly must not be used as grip location or
hold for the patient.
Danger zones
The dotted areas mark the danger zone, where no objects must be located during
tilting.
Danger zone
Movement range of the positioning table
◆ Prior to activating any movements of the unit, especially tilting of the unit,
make sure that there are no objects such as stairs, steps, stands, waste containers, instrument tables, beds, gurneys, monitor support systems, operating consoles or the like in its movement range.
AXIOM Iconos R200AXD3-340.620.13.01.0217 / 44
System Overview
Protective Measures
These objects are not detected by the collision monitoring of the unit. Avoiding
collisions of the unit with these objects is subject to the operator’s duty to take
care.
If a collision of the unit with a rigid obstacle (e.g. step) has occurred,
◆ press one of the red emergency stop buttons,
◆ rescue the patient,
Warning
Under no circumstances must the unit be tilted down further or tilted up, since
externally invisible, but safety-relevant damage to the tilting drive may occur.
Severe consequential damage including personal damage cannot be excluded
in this case.
◆ immediately notify the SIEMENS Uptime Service.
❏ Avoid standing or sitting immediately adjacent to the system and especially
do not sit next to the system with your legs or knees under the cross-beam at
the head or foot end of the table.
❏ Take care that during system movements no one is in the area between the
unit base and table.
❏ Take care that with the footboard attached there is a risk of collision with the
extended cone (optional) when the tabletop and / or the longitudinal carriage
are moving.
❏ Do not grasp in the loading shaft of the spotfilm device because of the risk of
crushing.
Patient positioning
❏ All safety-related equipment must be installed and operable. In particular the
handgrip strips (head end and lateral), handgrip, footboard, foot restraints,
compression belt and shoulder supports.
❏ The patient’s hands, arms, legs, head and hair must not extend unsecured be-
yond the edge of the tabletop.
❏ Observe the patient while moving the tabletop and in system movements and
take care that any catheter is correctly located.
❏ In examinations with the table tilted up vertically, the footboard serves as an
adjustable step or seat.
– Ensure that the footboard is locked together with the tabletop on both
sides.
– Check the firm location of the footboard.
18 / 44AXD3-340.620.13.01.02Operator Manual
System Overview
Protective Measures
Patient positioning with unit in vertical position
During examinations with the unit in the upright position there is a risk of crush
injuries to the patient if the X-ray system (stand with tube unit/receptor unit with
image intensifier) is moved in the longitudinal direction.
◆ Position the X-ray system approximately in the acquisition position.
◆ Move the patient into the acquisition position.
◆ Set the X-ray system to object height. Always watch the patient when initiat-
ing this movement.
Remote compression (optional)
❏ The motor-driven compression device requires special care on the part of the
examiner for the applied compression forces, especially in the case of frail
(e.g. infants), sick and elderly patients.
❏ Observe especially that both an increased risk of crushing for the patient with
consequential injury and considerable mechanical shearing forces with risk of
damage can occur between the compression cone and attached accessories,
e.g. shoulder supports, lateral support (optional) or motor-driven infant cradle
holder (optional) by collision during the motor-driven tabletop movement.
❏ When moving the compression carriage into the lowest position, the carriage
may collide with the patient’s hand on the grip protection strip.
– Use extreme caution when actuating the cone movement.
Safety devices
(1)
(3)(3)(2)
(1) Switch rail between tabletop and stand
(2)(3)
(2) Switch rails in each case at the end of the travel of the spotfilm unit
(3) Safety switching sensors on the image intensifier TV device (2 sensors))
AXIOM Iconos R200AXD3-340.620.13.01.0219 / 44
System Overview
Protective Measures
On activation of one of the safety devices (shutdown devices) all system movements stop and are blocked.
This means that one cannot move out from the blockage oneself.
If it is not possible to remove the obstruction causing the problem, call in the Siemens Uptime Services.
Movements are possible again only after one of the safety devices has be deactivated.
Possible collisions of the system with a
ceiling-mounted support
❏ System movements are possible only if the ceiling-mounted support is in its
park position or if the bypass switch is activated if necessary.
❏ Prior to actuating system movements with the bypass switch activated, verify
that no collision can take place with the ceiling-mounted support, the X-ray
tube assembly or the collimator. (No collision monitoring.)
1
Warning
If system movements are possible even though the ceiling-mounted support is
not in the park position and the bypass switch is not activated,
immediately press the emergency shutdown button and notify the
SIEMENS Uptime Service.
Measures for avoiding equipment damage
◆ Before activating system movements, especially tilting the table, make sure
that the movement range is free of obstructions.
◆ Move especially monitor support systems, operating consoles, gurneys, beds
and instrument tables out from the tilting range of the table and remove
chairs, steps, stands, waste containers and similar objects from the movement area. (No collision monitoring.)
◆ Do not place any objects or consumable material on the cover of the table support, on the spotfilm device and on the longitudinal guides of the stand carriage.
– Considerable forces which can damage these objects in the area of move-
ment of the systems arise during movements of the spotfilm device or of
the tabletop.
◆ Do not place any loose objects anywhere on the table.
– These objects could fall down when the table is tilted, causing injury or
damage.
1
optional
20 / 44AXD3-340.620.13.01.02Operator Manual
System Overview
Protective Measures
◆ Do not stand at any place on the spotfilm device or on the covers of the table
support outside the marked areas provided for this.
– The covers can be deformed.
Components located underneath them are damaged and thus lead to operating disturbances.
◆ Place no objects on the operating areas of the control consoles and the tableside control.
Caution
Unintentional activation of control elements for movements
Collision with patient, operator or equipment
◆ Do not load the remote console with any objects, accessories, folders or
documents.
To avoid unintentional activation of control elements for movements concerning
bed exposure, please adhere to the following workflow:
◆ Select aquisition mode Bed exposure at the generator control console.
◆ Tilt the system and move it to the correct SID.
◆ Rotate the tube assembly accordingly.
◆ Position the patient.
◆ Control patient and system.
◆ Don’t let patient stay in system area during absence of operator.
◆ In vertical table positions do not use the stand column, the tube assembly sup-
port arm, the tube assembly cover or the primary collimator as seat or support.
– This unallowed loading can lead to material breakage and damage to bear-
ings.
◆ Never put contrast medium cups or open containers with liquid or pasty contents on the unit, on the remote console or on the control cabinets.
– Contrast medium can spill, leak or overflow into system parts and lead to
operational disturbances of the unit or to misinterpretation of exposures.
◆ When storing contrast medium in the cup holder on the compression carriage,
use only cups with a maximum volume of 0.25 liter made of unbreakable materials, i.e. under no circumstances glass or porcelain.
– Remove contrast medium traces immediately!
Measures for avoiding unwanted radiation
◆ Before starting system movements make sure that the foot switch for fluoroscopy and radiography (optional) in the examination room is not in the travel
range of the image intensifier light distribution system.
AXIOM Iconos R200AXD3-340.620.13.01.0221 / 44
System Overview
Protective Measures
Safety-relevant parts subject to wear
This system contains no safety-relevant parts subject to wear.
Maintenance intervals
Maintenance must be performed annually in order to ensure the safety and functioning ability of the system.
If you have not concluded a maintenance contract, please notify the Siemens Uptime Service on time.
CAREWATCH
Display data
At the start of fluoroscopy/acquisition the following system parameters are displayed in the lower right area of the live monitor:
1st line
– Display of the prefilter in fluoroscopy
2nd line
– Display of the prefilter in radiography
With the area dose product meter (optional)
3rd line
– Area dose product in cGycm²
4th line
During fluoroscopy
– Display of the patient entrance dose
In the radiation pauses
– the percentage of the patient entrance dose reached related to a config-
1
urable limit
– the accumulated patient entrance dose in mGy is displayed.
of 0.5 to 5 Gy or
1
2
in mGy/min
The measuring device must be calibrated at regular intervals. This is done within
the scope of a maintenance contract. If no maintenance contract have been concluded, the measuring device can be calibrated by the Siemens Uptime Service
of the manufacturer.
1
can be configured by the SIEMENS Uptime Service
2
standardized to 30 cm above the tabletop
22 / 44AXD3-340.620.13.01.02Operator Manual
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