SOMATOM go.
Sim
Basic Planning Information
© Siemens Healthcare GmbH
SOMATOM go.Sim | Basic Planning Information
Table of contents
Planning Example 3
Room Dimensioning 5
Statics and Transport 5
Environment 7
Electrical Installation 8
General Information 9
Legend
Motion area / Swivelling range / Minimal room size / Safety distance
Service area Wall mounted
Floor mounted Additional equipment
Ceiling mounted Demolition
Dimensioning
All installation measurements apply to finished wall/floor/ceiling and are to be checked prior to assembling the unit.
cm mm
Orientation point = reference point of the Siemens unit for planning and installation
Please note: The drawing parts in this document are not to scale!
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SOMATOM go.Sim | Basic Planning Information
Planning Example
Preparation
Control room
1.05 1.03
1.04
Pat. toilet
1.02
min. 587 (Vario RT)
min. 632 (Vario 2)
Examination room
645
1.01
Changing
Changing
510
min. 301
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SOMATOM go.Sim | Basic Planning Information
SOMATOM go.Sim - Equipment Legend
Weight (kg), Heat dissipation to the air (W)
Pos. Description kg W Remark
1.01 Gantry with tablet, remote control, computer, UPS and direct 1719 6800 #1, #2, gantry not tiltable
laser
1.02 227 kg Patient table Vario RT (1600 mm scannable range) 338 300
1.03 Control unit with TFT monitor, control box, keyboard 9 75
1.04 Wireless Access Point 3
1.05 Power Distributor by customer
#1 2250 W in stand-by mode, isocentre at 1020 mm
#2 Protective regulations for dealing with laser light indicators
must be observerd
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SOMATOM go.Sim | Basic Planning Information
Room Dimensioning
Room dimensioning
The indicated room dimensions have to be checked on site. The planning department has to be informed about
possible deviations. Otherwise we cannot assume any guarantee for the accurate implementation of the dimensions
indicated in the planning documents.
Room height
Technically required minimum room height 2200 mm (with injector arm: 2400 mm, with 3D camera: 2300 mm).
Measured from the highest point of the finished floor (with covering) to the lowest point of the ceiling.
On-site LAN network
Poor network bandwidth impairs the performance of image transmission significantly. The ICSi-1d (11362303) can’t
communicate with an Ethernet slower than Gigabit.The other ICSi- types can still connect to a 100 MBit network.
If the ICSi-1d is ordered and the customer can only provide a 100 MBit/s network, a switch must be connected to
adapt the speed of 1 GBit/s to the hospital’s 100 MBit/s network. Either the switch 10547105 can be ordered, or the
customer’s IT may provide their own switch.
Statics and Transport
Transport not to scale
The transport route (doors and hallways) needs sufficient dimensions for the following parts!
Gantry with transport device
Transport rollers swiveled out Transport rollers swiveled in
ca. 2883 x 1627 x 1952* mm ( L x W x H ) ca. 3576 x 1037 x 1952* mm ( L x W x H )
2883
2499 3576
3192 982**
1438
1114
1882
* Thetransportdevicewiththegantrycanbeloweredtoagroundclearanceof7mm.
** The Gantry can be moved through the entrance < 1000 mm, when the transport adapter is partially removed.
TIPPING HAZARD ! Transport with the rollers swivelled in is permissible only in narrow passages!
As soon as the system has passed through narrow passages, the transport rollers
have to be swivelled out again.
Gantry with transport device 1825 kg, transport device 220 kg.
The maximum possible floor load (2-point load) per roller may be reached during gantry transport.
If necessary, cover the transport route with metal sheets to distribute the load.
The door must have a final clearance of 1250 mm if bed entrance to the CT examination room is requested.
PHS Vario RT Weight 570 kg 2574 x 824 x 1517 mm ( L x W x H )
PHS Vario2 Weight 592 kg 2574 x 824 x 1517 mm ( L x W x H )
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SOMATOM go.Sim | Basic Planning Information
Statics not to scale
4 The floor construction has to be performed solid and free of vibration,
3
e.g. concrete flooring C20/25 to C50/60 corresponding to DIN EN 206-1,
according to the maximum values as specified in the textblock
“Floor and building vibrations”.
It is recommended to test the weight capacity of the concrete or composite
flooring by a stress analyst.
Fastening the gantry on the floor is possible but only necessary in
1 2 countries prone to earthquakes or according to local regulations.
Securing the patient table to the floor is mandatory.
Total weight of Gantry: 1699 kg Totalstaticload(centerofgravity) : Fstatotal =17 kN
Partial load on gantry foot number 1 2 3 4
Nominal static load after levelling Fstat nom [kN] 3.44 4.75 5.10 3.70
Maximumdynamicload(amplitude)duringgantryrotation Fdyn max [kN] ± 0.3 ± 0.3 ± 0.3 ± 0.3
Outer diameter gantry foot [mm] 54 54 54 54
Floor contact area gantry foot [cm²] 16 16 16 16
During gantry installation and leveling, the maximum possible load on one gantry foot can be 9.85 kN (the gantry is
standing on two diagonal feet). Design access floors for a weight capacity of min. 400 kg per slab/plate. During
gantry transport, the load may be higher at certain individual points (3-point load, e.g. due to uneven flooring).
When the system has tilt function, the tilt actuator will be equipped and a fifth gantry foot has to touch the floor
during system installation.
The fifth foot shouldn't share floor load from the other four feet on static mode. It will share the load from the tilt
actuator when gantry ist tilting.
Floor- and building vibrations
Floor- and building vibrations can reduce image quality!
Permissable continuous floor vibrations
Permissible acceleration rms-value [m/s²]
Sources that produce vibrations are, e.g.:
Railroad routes, subways, roads, road works and construction
1
sites, hospital power plants, mines, open-cast minings, quarries
(explosions), ferry moorings, any other sources of striking
vibrations. Any transient vibration has to be less than 0.5 m/s²
peak-to-peak in the time domain. The vibrations have to be 0.1
measured with a sampling rate of 1000 Hz.
The CT system is not sensitive to common vibrations. If the CT is
away from vibrational sources, or the CT is replacing a CT system
that to date has not shown image quality problems due to 0.01
vibrations, it is usually not necessary to execute vibrational 1 10
Frequency [Hz]
100
measurements.
It is the customer's responsibility to contract a qualified specialist.
The specialist must implement site modifications to meet the specific
limits, and to design structural solutions in case of deviations.
If there are any doubts, the following thresholds have to be verified by measurement:
Inthethreespatialdirections,accelerationinvibrationsatthemountingpointsofthecomputertomograph(Gantryand
Patient Handling System PHS) must not exceed the thresholds as described in the above shown diagram.
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SOMATOM go.Sim | Basic Planning Information
Environment
Environment
All CT components Temperature 18 to 30 °C
Relative humidity 20 to 75 %
Absolute humidity max. 30 g/m³
Barometric pressure 800 to 1060 hPa
Temperature gradient 6 K/h
Transport / storage Temperature -20 to 50 °C
Relative humidity 10 to 95 %
Absolute humidity max. 30 g/m³
Barometric pressure 700 to 1060 hPa
Temperature gradient 10° K/h
Maximum storage period 2 months
If it is not possible to maintain these ranges, an air conditioning system with or without humidifier / dehumidifier
should be installed. By intake of outside air it is recommended to install air filters (Class EU3 to EU4)
for filtering dust particles of > 10 µm (DIN EN 779).
On-site cooling requirements not to scale
Workload CT-system [%] 100 (maximum power) 0 (stand-by) 2
Heat dissapation to ambient air 6.8 kW 2.25 kW
Air temperature (air intake) 18 °C to 30 °C
1
Temperaturegradient(airintake) max.±1K/min;max.<6K/h;
max.±4K/hin24h 1
Humidity (air intake) 20 % to 75 % REAR
Airflowrate(throughtheGantry) 1800 m³/h to 2200 m³/h 1) air intake 2) exhaust air
The climatic room conditions for all air-cooled CT system components are influenced by design room conditions
(e.g. windows, large glass areas, building and room insulation, room size and volume, etc.) and must be observed
in the case of a new or existing air conditioning system in the examination room.
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SOMATOM go.Sim | Basic Planning Information
Electrical Installation
Power requirements
Power Line: TN-S 3/N/PE AC 50/60 Hz ± 3Hz Connection value 69.2 kVA
Line Voltage: 400 V ± 10 % Power consumption:
Stand-by: ≤ 3 kVA
Line impedance: ≤ 250 mΩ System off: 0 kVA
for the time up to 4 s: max. 115 kVA
Cable cross section is to be determined by country regulation and calculation.
Size of connector terminals in the gantry is 25 to 95 mm². N, PE adapter terminal 16 mm² available
Room lighting
Ambient lighting in rooms with diagnostics or with workstations must comply with the respective local and national
regulations.
General requirements like the needed intensity of illumination - adjustable, reproducible, flicker-free or a limitation of
dazzlings and reflections etc. have to be observed (EN 12464-1, DIN 5035-7).
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SOMATOM go.Sim | Basic Planning Information
General Information
Display screen workstations
For setting up display screen workstations, take account of the guidelines in the Display Screen Workstation
directive as well as any national regulations (e.g. EN ISO 9241-5).
Smart Remote Services (SRS)
Smart Remote Services (SRS) is used for remote diagnostics as well as remote service to provide
highest system availability.
Requirements:
- Broadband connection (minimum 4 MBit/s down- and 768 kBit/s upstream, optimum 30 MBit/s down- and
2 MBit/s upstream) without time or volume limitations
- Router (for exclusive use with SRS)
Data protection and security is defined in the Smart Remote Services security concept.
Network Integration
The Siemens components are using TCP/IP Protocol, a 100/1000 Mbit/s switched Ethernet network and
static IP addresses.
The required network cabling (min. CAT 5 TP) has to be provided on site.
Media converters, which are needed for using fibre optic cabling, are not in the scope of Siemens delivery.
To prepare the implementation of the new system into the existing network environment, the availability
of the needed network data at least two weeks before starting the installation is mandatory.
This is the only way to ensure a seamless integration of the new system into the workflow of the department.
Notes on preparations for installation
Contracts for performing and supervising on-site installation preparations should be concluded with technically
competent companies by the customer. The customer is responsible for timely and proper completion and
supervision of all preparations for installation at the construction site in observance of all applicable legal regulations
(e.g. X-ray regulations, radiation protection regulations) and all applicable general recognized rules of technology
(e.g. VDE regulations, DIN standards).
Execution and supervision of installation preparations at the construction site and later observance of the standard
operating conditions are not included in our duties. The customer is responsible for checking the static calculations
and, where applicable, the air conditioning in the building to be equipped.
Safety distances
Distances from moving parts of the medical device to walls, furniture and other equipment have to be kept to avoid
injuries by crushing in compliance with local regulations, e.g. a minimum distance of 50 cm according to EN 349.
It is the customer's responsibility to ensure the above requirements are followed.
This is to avoid the risk of injury.
If safety distances are not maintained appropriate on-site safety measures have to be put in place.
Clear visible markings according to national guidelines, e.g. crushing warning signs, hazard warning
tape, hazard area cordon, safety mats, may be required.
Radiation protection
Thestructuralradiationprotectiondependsonthelocationoftheunitandthefunctionofthesurroundingrooms.Byorder,
theplanningdepartmentsofSiemensHealthcareprepareradiationprotectioncalculationandradiationprotectionplan.
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On account of certain regional limitations of sales rights and
service availability, we cannot guarantee that all products
included in this brochure are available through the Siemens sales
organization worldwide. Availability and packaging may vary by
country and are subject to change without prior notice. Some/all
of the features and products described herein may not be available
in the United States.
The information in this document contains general technical
descriptions of specifications and options as well as standard
and optional features which do not always have to be present
in individual cases.
The statements by Siemens’ customers described herein are based
on results that were achieved in the customer’s unique setting.
Since there is no “typical” hospital and many variables exist (e.g,
hospital size, case mix, level of IT adoption), there can be
no guarantee that other customers will achieve the same results.
The customers cited are employed by an institution that might
provide Siemens product reference services, R&D collaboration
or other relationship for compensation pursuant to a written
agreement.
Siemens reserves the right to modify the design, packaging,
specifications, and options described herein without prior notice.
Please contact your local Siemens sales representative for the
most current information.
Note: Any technical data contained in this document may vary
within defined tolerances. Original images always lose a certain
amount of detail when reproduced.
Not all features shown in this brochure are necessarily standard
and available in all countries.
Published by
Siemens Healthcare GmbH
SHS ES FD
Siemens Healthineers Headquarters
Siemens Healthcare GmbH
Henkestr. 127
91052 Erlangen, Germany
Phone: 49 9131 84-0
siemens-healthineers.com
© Siemens Healthcare GmbH
