Planning Mammomat Fusion

Mammomat Systems
Planning Guide
System
Mammomat Systems
MAMMOMAT Revelation
MAMMOMAT Inspiration
Mammomat Fusion
2 Document Version / Disclaimer / Copyright
Document Version
Siemens Healthcare GmbH reserves the right to change its products and services at any
time.
In addition, manuals are subject to change without notice. The hardcopy documents cor‐
respond to the version at the time of system delivery and/or printout. Versions to hard‐
copy documentation are not automatically distributed.
Please contact your local Siemens Healthineers office to order a current version or refer to
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Disclaimer
Siemens Healthcare GmbH provides this documentation “as is” without the assumption of
any liability under any theory of law.
The content described herein shall be used by qualified personnel who are employed by
Siemens Healthcare GmbH or one of its affiliates or who are otherwise authorized by Sie‐
mens Healthcare GmbH or its affiliates to use such documents.
Assemblers and other persons who are not employed by or otherwise directly affiliated
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Copyright
“© Siemens Healthineers, 2017” refers to the copyright of a Siemens Healthineers entity
such as:
Siemens Healthcare GmbH - Germany
Siemens Shenzhen Magnetic Resonance Ltd. - China
Siemens Shanghai Medical Equipment Ltd. - China
Siemens Healthcare Private Ltd. - India
Siemens Medical Solutions USA Inc. - USA
Siemens Healthcare Diagnostics Inc. - USA and/or
Siemens Healthcare Diagnostics Products GmbH - Germany
Mammomat Systems XPW7-000.891.01.02.02 Page 2 of 71 © Siemens Healthineers, 2017

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Table of Contents 3
1 Introduction 5
1.1 Abbreviations and terms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

1.2 Safety Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
1.2.1 General information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
1.2.2 Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
1.2.3 Hazard keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
1.3 System configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
1.4 Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
1.4.1 Planning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
1.4.2 Actions regarding winter deliveries. . . . . . . . . . . . . . . . . . . . . . . . 13
1.5 Product-specific information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
1.5.1 Network. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
1.5.2 Network Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
1.5.3 Virus Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
1.5.4 Workflow . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
1.5.5 DICOM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
1.5.6 Option: DicomProxy (for MAMMOMAT Inspiration only) . . . . . . . 16
1.5.7 Siemens Remote Service connection . . . . . . . . . . . . . . . . . . . . . . 18
1.5.8 Recommended viewing stations (Siemens Viewing Stations) . . . 18
1.5.9 Scope of delivery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
2 Room Planning 24
2.1 General information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24

2.1.1 Information regarding dimensions and orientation points. . . . . . 24
2.1.2 Safety information for the Single Touch function . . . . . . . . . . . . 24
2.1.3 Requirement for room light per DIN V 6868-157 . . . . . . . . . . . . . 25
2.2 Room size . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
2.2.1 System dimension including . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
2.2.2 With separate control room . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
2.3 Component Dimensions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
2.3.1 Stand dimension and center of gravity . . . . . . . . . . . . . . . . . . . . . 29
2.3.2 Unit base . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
2.3.3 Control console with radiation shield . . . . . . . . . . . . . . . . . . . . . . 32
2.3.4 Acquisition workstation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
2.3.5 Control box . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
2.4 Radiation protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
2.5 Notice concerning electromagnetic compatibility (EMC) . . . . . . . . . . . . . . . 36
2.5.1 Guidelines and manufacturer’s declaration . . . . . . . . . . . . . . . . . 36
2.5.2 Recommended separation distances between portable and mo‐ 39
bile RF telecommunication devices and the system . . . . . . . . . . .
3 Preparation for Installation 41
3.1 Information regarding expansion bolts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41

3.2 Floor installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
3.2.1 Stand . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
3.2.2 Control console . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
© Siemens Healthineers, 2017 XPW7-000.891.01.02.02 Page 3 of 71 Mammomat Systems

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3.3 Potential Equalization Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45

3.4 On-site Electrical Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
3.4.1 Safety Shutdowns . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
3.4.2 Power connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
3.4.3 External indicator for X-ray or door contact (blocking radiation) 47
3.4.4 Example for on-site Power Distributor (1-phase, 2-phase) ac‐ 48
cording to DIN VDE 0100-710 or National Regulations, and tak‐
ing into account the use of SIRIUS . . . . . . . . . . . . . . . . . . . . . . . .
3.5 Siemens remote services (SRS) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
4 System Connections 54
4.1 General information on wiring . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54

4.1.1 Power Line Voltage and Ground Wire Connections . . . . . . . . . . . 54
4.1.2 Signal and Data Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
4.2 Wiring fixed points . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
4.3 Cable Inlets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
4.3.1 MammoUnit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
4.3.2 Control console . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
4.4 Cable Conduits and Cable Ducts, Minimum Size. . . . . . . . . . . . . . . . . . . . . . 58
5 Technical data 59
5.1 Dimensions and weights . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59

5.2 Heat dissipation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
5.3 Climatic Conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
5.3.1 Temperature, relative humidity, and barometric pressure . . . . . . 61
5.4 Electrical data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
5.4.1 Mammomat systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
5.4.2 Workstation and monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
5.4.3 Option DicomProxy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
5.5 Paint colors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65
6 Transport and Storage Conditions 66
6.1 Climatic Conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66

6.2 Transport Dimensions and Weights . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67
7 Changes to previous version 68
8 List of Hazard IDs 69

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Introduction 1 5
1.1 Abbreviations and terms

Tab. 1 Abbreviations and terms
Abbreviations and terms Definitions

AEC Automatic Exposure Control (exposure technique)
AET Application entity titles
CBA Control board arm (part of the MammoUnit)
CBS Control Board Stand (part of the MammoUnit)
CNU Compression Unit (part of the MammoUnit)
DICOM Digital Imaging and Communication in Medicine
HIS/RIS Hospital information system / radiology information system
MammoUnit Mammomat stand
MammoUnit Web server Application software for the MammoUnit
PMMA Polymethyl Methacrylate
PSU Power Supply Unit (part of the MammoUnit)
QA Quality Assurance (test procedure)
QC Quality Control (test procedure)
RoW Rest of world - all countries except USA
STU Single Tank Unit (part of the MammoUnit)
TCP/IP Transmission Control Protocol/Internet Protocol
TiCEM Titanium Contrast Enhanced Mammography (Dual Energy)
WH AWS Women’s Health Acquisition Workstation of the Mammomat
W/Rh Tungsten/Rhodium (Target/Filter combination)
syngo Application software on the WH AWS

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6 1 Introduction
1.2 Safety Information
1.2.1 General information

n The system may be used only in rooms intended and prepared for medical purposes.
n In accordance with national radiation safety measures, the room must be prepared for
the purpose of performing medical radiographic examinations.
n National radiation safety measures must be observed.
n The national regulations in effect primarily apply. However, we strongly recommend
adherence to the standards described herein, provided they do not contradict national
regulations in effect, to ensure the safety of operators, patients, and third parties.
n The rooms intended for this medical device must meet the ordinances of the respec‐
tive national fire safety measures.
n The device was developed for the protection class against electric shock: Class I, type
B according to IEC 60601-1
n Comply with the recommendations for prevention of electromagnetic discharges and
overvoltages as defined in IEC 1024, DIN 48810, VDE 0675, and DEMVT. See also the
"Room Planning" chapter in this document.
n Minimum data (e.g., room height, safety distances) are identified in the Planning
Guide as "min."
n Refer to the Operator Manual for more information.
n The equipment does not overbalance when tilted through an angle of 5° from the hor‐
izontal in any position of normal use (IEC 60101-ff) or is subjected to a force of 220 N
applied 1.50 m above floor level (UL 187).
The device may only be transported in horizontal position, or in vertical position if the
tube arm is in its lowest position.
1.2.2 Symbols
C Caution! General hazard warning.
V Dangerous electrical voltage > 25 V AC or > 60 V DC.
X Warning about ionizing radiation or radioactive substances. Tests and adjustments that
must be performed with the radiation switched on are indicated by this radiation warning
icon.
U Certain tasks can also be performed by other technical personnel (e.g., the customer's
hospital technicians).
P Report icon. Used to indicate entries in certificates.

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Introduction 1 7
O Moving icon
1.2.3 Hazard keys
NOTICE
The installation of software/firmware not released or validated for the system is
strictly prohibited.
 Otherwise, patient examination, image presentation or system applications
may not function properly.
 CAUTION
Inadequate X-ray shielding
X
PATIENT AND/OR USER INJURY
 The control console shall be installed behind the radiation protection shield.
hm_DOC_F1G2U1M4 06H391224
 CAUTION
Risk of collision and crushing during movement of the swivel arm.
Injury to patients or other persons
 Ensure that there is a minimum distance of 50 cm between the swivel arm
and the surroundings.
hm_DOC_pos_injur_pinch_zones 06H462686
 CAUTION
Inadequate clearance between moving parts and fixed structure of the room
Injury to patient or operator
 The "Single Touch" is an option, which can only be activated by service, in case
of certain room dimension and in accordance with a defined safety concept.

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8 1 Introduction
 CAUTION
Swivel arm rotation without continuous operator activation “Single Touch”
 Consider the information about the room size, location of the sub components
and cabling to ensure safe installation and operation of the system.
 CAUTION
Inadequate clearance between moving parts and fixed structure of the room.
 It is recommended to mark the area where the tube head will travel to ensure
a safe operation with the Single Touch function.
 If free places to stay of the security area, also temporarily by chairs, shelves,
table or similar is not guaranteed, the function is "Single Touch" to switch off.
hm_DOC_F4G1U1M2 06H392727/ hm_DOC_F4G1U1M3 06H392728
 CAUTION
PHYSICAL INJURY
 The area of patient environment is 1.5m around the MammoUnit stand
hm_DOC_F4G1U1M10 06H392735
 CAUTION
PHYSICAL INJURY
 Install an additional grounding if the distance between the MammoUnit to
the control console is smaller than 0.75m.
hm_DOC_F4G1U1M11 06H392736

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Introduction 1 9
 CAUTION
Unintended movement because emergency stop system does not stop movement
INJURY TO PATIENT
 The installation of a emergency shut off button in the room is mandatory. The
emergency shut off button turns off the power to the system, thereby aborts
the radiation and mechanical movements.
 Consider the differences between emergency stop and emergency shut off
described in the planning guide
hm_DOC_F4G1U21M1 06H392814 / hm_DOC_F4G1U21M2 06H392815
 CAUTION
Intrusion of software virus
PROPERTY DAMAGE
 Consider the description of virus protection in the planning guide.
 CAUTION
Equipment falls over
PATIENT AND/OR USER INJURY AND/OR DAMAGE TO EQUIPMENT
 In a earthquake risk region the MammoUnit Stand and the control console ta‐
ble must be fastened to the floor!
hm_DOC_F14G5U1M2 06H394032 / hm_DOC_F14G2U4M1 06H393836
 CAUTION
Inadequate cooling of the system
PHYSICAL INJURY / SYSTEM DAMAGE
 The climatic conditions must be kept
hm_DOC_F14G3U1M4 06H393925

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10 1 Introduction
 CAUTION
Operation of the system outside specified environmental conditions
SYSTEM DAMAGE
 Check for sufficient measures (e.g. air conditioning) to keep the room condi‐
tions inside the specified ranges.
hm_DOC_inst_dam_cond_plan 06H449470
 WARNING
Leakage current too high
PHYSICAL INJURY, ELECTROCUTION
 The patient environment area according to IEC60601-1 has to be taken into
consideration.
hm_DOC_F14G8U2M4 06H394106
 CAUTION
Electrical shock due to static discharge
PHYSICAL INJURY
 Avoid highly insulated floor covering
hm_DOC_F14G8U4M1 06H394112
 WARNING
Emergency stop switch does not break the power to the system
PHYSICAL INJURY
 Consider the correct installation of the emergency shut off circuit in the plan‐
ning guide.
hm_DOC_F14G8U7M1 06H394118
 WARNING
Emergency shut off circuit is not designed error safe
PHYSICAL INJURY
 Consider the described design of the emergency shut off circuit in the plan‐
ning guide.
hm_DOC_F14G8U8M1 06H394122

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Introduction 1 11
 CAUTION
In case the TiCEM (Dual Energy) option is installed, the responsible organisation
shall install a warning lamp
UNNECESSARY RADIATION
 In case Dual Energy is installed, the responsible organization shall install a
warning lamp connected to potential-free output of the MammoUnit.
hm_DOC_duen_rad_abort_pg 06H527161

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12 1 Introduction
1.3 System configuration

The Mammomat system is a radiography system with digital image processing developer
for mammography.
The system is comprised of the following components:
n Stand (MammoUnit) with single tank (X-ray tube assembly), high-voltage generator,
detector (digital image generation), and collimator to limit the beam.
n Workstation (computer) with monitor(s) integrated into the control console
n Control box (on/off as well as radiation release) in the control console
n Control console (height adjustable) with radiation shield
Image data are exchanged between the workstation and DICOM PACS stations using the
hospital network.

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Introduction 1 13
1.4 Notes
1.4.1 Planning
All construction plans produced by the Planning Departments must be provided with a
note referring to the applicable installation and delivery conditions. The installation and
delivery conditions must be enclosed with the project plans when shipped.
1.4.2 Actions regarding winter deliveries

During winter or when temperatures are < 10°C during transport, plan at least 12 hours
during which the delivered components adapt to the climatic conditions in the examina‐
tion rooms prior to being switched on. Any installation team wait time is charged to the
local project.

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14 1 Introduction
1.5 Product-specific information
1.5.1 Network
The syngo®reg WH AWS supports the TCP/IP protocol. Based on the required data
throughput, we recommend a network of 100 MB/s. All network cables and network con‐
nectors be present on site.
If needed, an outside service provider must be present on-site. A DSL/VPN broadband con‐
nection is recommended for Siemens Remote Service. Further information can be found
in the "Siemens Remote Service" section.
 To avoid problems during startup, check for and resolve any conflict in network address‐
es with the hospital network before installation.
The WH AWS is equipped with two network adapters:

n The standard network adapter (first adapter) will be connected to and configured for
the hospital network (DICOM connectivity). The factory defaults must be checked and
modified in accordance with hospital requirements.
n The second network adapter (possibly equipped with two ports) is connected primari‐
ly to the MammoUnit and secondarily to the detector.
1.5.1.1 Additional IT Requirements for MAMMOMAT Revelation and MAMMOMAT Inspira‐

tion
With the tomo option, the following notes must be observed:
The IT environment must be set up for data transfer of up to 1.2 GB per tomo scan with‐
out the network components that are configured for local network transfer being affec‐
ted.
In addition, the archive and configured diagnostic stations must be set up for the given
data volume. More than 2 GB data memory capacity can be required per patient for a to‐
mo application.
The following topics must also be observed:
n Hospital network in capacity / capability / data transfer
n Sufficient free storage space for the archive or PACS systems
n Diagnostic stations must be prepared for the increase data volume, as well as for
speed to display the tomo reconstructions.
n The customer workflow must be discussed.

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Introduction 1 15
1.5.2 Network Overview

Fig. 1: Mammomat Inspiration Network Connection example

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16 1 Introduction
1.5.3 Virus Protection

The Siemens Healthcare GmbH offers a security solution to guard the mammography sys‐
tem against viruses.
System Security, an advanced and comprehensive security technology powered by McA‐
fee™ Application Control, has been integrated directly into the mammography system
platform since version VB60. It provides protection from unwanted applications, blocking
both known and unknown threats by controlling dynamic whitelisting. It protects against
threats from both the network and infected local USB drives.
1.5.4 Workflow
The hospital IT workflow (data exchange to other DICOM modalities in the hospital) has
to be discussed with the customer prior to start-up of the Mammomat system and de‐
fined for system configuration.
1.5.5 DICOM
The international DICOM protocol is used for image data transfer to and from the Mam‐
momat system.
To ensure the interoperability of DICOM components communicating to exchange data in
complex hospital networks, the required DICOM partners should be listed and compared
with the DICOM Interoperability Database:
1.5.6 Option: DicomProxy (for MAMMOMAT Inspiration only)

The option DicomProxy enables the Mammomat Inspiration to convert their Tomosynthe‐
sis reconstructions (CT slices, SOP class 1.2.840.10008.5.1.4.1.1.2) to the standard DI‐
COM object format (SOP class 1.2.840.10008.5.1.4.1.1.13.1.3). This enable the use of
enhanced post processing functionality on the reporting or viewing workstations.
The DicomProxy option is delivered as a mini desktop “Fujitsu Esprimo” PC, with an inte‐
grated service user interface tailored to DicomProxy requirements, as well as an easy self-
explanatory configuration interface.
It will convert Mammomat Inspiration tomosynthesis reconstructions (slices) from DICOM
object CT/ MG to BTO (Breast Tomosysthesis Object) and route them to defined destina‐
tion network nodes.
For this reason the DicomProxy hardware is connected via Ethernet between the WH AWS
and the hospital network.
The DicomProxy should be placed on top of the Inspiration WH AWS (default Mammomat
Inspiration desk with integrated WH AWS housing).
Network
n The DicomProxy needs his own IP address within the hospital network environment (1
m Ethernet cable is part of the delivery)
Power supply
n The DicomProxy power supply is delivered with standard power plug type C (CEE 7/16
"Europlug"). This plug fits into the multi-outlet power strip located in the foot tray of

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Introduction 1 17
the Mammomat Inspiration control unit. In addition, a power socket extension is part
of the delivery to expand the multi-outlet power strip when all three plugs are occu‐
pied by monitors and the workstation.
 For deliveries to Argentina the power cable with the Europlug is removed.
IT workflow
n The DicomProxy first collects all slices of an BTO series before it will start to sending
the converted DICOM data to the destination node.
 Inform the hospital network administrator regarding the increased network load during
transfer of data when an examination is finished.
Delivery
n Esprimo Desktop with power supply
n Ethernet cable, 1 m
n Power socket extension
Fig. 2: DicomProxy

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18 1 Introduction
1.5.7 Siemens Remote Service connection

Establish the connection to Siemens Remote Service. A DSL/VPN broadband connection is
recommended for Siemens Remote Service. Further information can be found in the "Sie‐
mens Remote Service" section.
1.5.8 Recommended viewing stations (Siemens Viewing Stations)

The recommended viewing stations for the Mammomat system are:
n syngo Breast Care Workstation
n syngo Via Server with Breast Care Clients
1.5.9 Scope of delivery

The base version of the mammography system contains the following components:
1.5.9.1 System Overview
 The following images show the components of a MAMMOMAT Inspiration as an exam‐

ple.

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Introduction 1 19
Fig. 3: Mammomat Inspiration
5 3
4
10
1
9 9
(1) Control console with radiation shield

(2) WH AWS
(3) Monitor(s)
(4) Control box
(5) MammoUnit Stand
(6) Swivel arm (generator, single tank unit, and collimator)
(7) Compression unit
(8) Detector with detector cover
(9) Foot switch, right and left
(10) Stand parameter display

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20 1 Introduction
1.5.9.2 System options

Optional accessories can be ordered.
Tab. 2 System options
n Biopsy Fig. 4: Biopsy MAMMOMAT Revelation
n Laser cross Fig. 5: Laser cross

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Introduction 1 21
n Tomosynthesis Fig. 6: HD Breast Tomosynthesis

(not available for
the Mammomat
Fusion)

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22 1 Introduction
n MoodLight Fig. 7: MAMMOMAT Revelation MoodLight
n DicomProxy (for Fig. 8: DicomProxy

MAMMOMAT In‐
spiration only)
The complete shipment with order numbers and optionally available components can be
found in the price book.
1.5.9.3 Items included in the shipment
Tab. 3 Items included in the shipment
Item Material Number

Three 2 cm plexi (PMMA) 6561232
One 2 cm plexi (PMMA) 6561224

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Introduction 1 23
Item Material Number

Calibration phantom (collimator 6638527
mounted, 40 mm PMMA)
Steel plate, 30 mm x 100 mm 6655844
Emergency stop (service aid equip‐ 10643097
ment)

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24 2 Room Planning
2.1 General information
2.1.1 Information regarding dimensions and orientation points

n Unless otherwise stated, all dimensions are in "mm".
n Orientation points are:
- Points belonging to system components to which reference is made when system
parts are positioned to one another or in the room.
n Fixed points are:
- Clearly designated points on system components, walls or floors at which cable out‐
lets are located.
- The illustrations in the drawings are: Octagon with letter / number combination.
- The cable lengths define the maximum fixed-point distances, and thus the maxi‐
mum distances between the individual system components.
n Room height
- The room height is the clear space measured from the top edge of the finished floor
to the bottom edge of the ceiling substructure (bottom edge of the finished ceil‐
ing).
2.1.2 Safety information for the Single Touch function
 CAUTION
 The "Single Touch" is an option, which can only be activated by service, in case
of certain room dimension and in accordance with a defined safety concept.
 CAUTION
Swivel arm rotation without continuous operator activation “Single Touch”

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Room Planning 2 25
 CAUTION
Inadequate clearance between moving parts and fixed structure of the room.
 It is recommended to mark the area where the tube head will travel to ensure
a safe operation with the Single Touch function.
 If free places to stay of the security area, also temporarily by chairs, shelves,
table or similar is not guaranteed, the function is "Single Touch" to switch off.
hm_DOC_F4G1U1M2 06H392727/ hm_DOC_F4G1U1M3 06H392728
2.1.3 Requirement for room light per DIN V 6868-157

The lighting in rooms in which medical images are displayed on video display units (moni‐
tors) has to be adjusted following the room classification described in the DIN V 6868-157
(international standard in preparation). Please refer to DIN V 6868-157 for room lighting
planning and measurements

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26 2 Room Planning
2.2 Room size
2.2.1 System dimension including

Fig. 9: System dimension
A X-ray tube assembly focus

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Room Planning 2 27
*1 Distance of at least 150 mm from the wall if the stand is not anchored to the floor (service
can performed at the back by sliding the stand out).
Distance of at least 500 mm from the wall if the stand is anchored to the floor (necessary for
service at the back of the stand).
*2 2 cable conduits (each 2 m) are included in the shipment for laying cables "on the floor".
If needed, additional cable conduits, Part No. 64 38 795 X041E, can be ordered for the con‐
nection between the stand and the radiation shield.
*3 For safety reasons (electrical components that can be touched by the patient), the acquisi‐
tion workstation (installed in the control console as standard) as well as any evaluation sta‐
tions in the room, should be set up outside of a radius of 1.5 m from the stand in accordance
with IEC 60601-1, 3rd Edition.
Note: If for construction reasons the distance from the MammoUnit to the control unit has to
be reduced, the control console (including workstation) must be connected to the MammoU‐
nit potential equalization.
The 50 cm safety distance to movable parts must always be maintained.
The local radiation safety regulations relative to the reduced distance must be observed.
Monitors and Monitor Support Arm:
One or two monitors can be attached to the control console. The monitor can be installed to
the right (default) or left. A longer DVI cable (3 m) is required for left installation (see the
notes in the System Cabling section). A swivel; range of +/- 90° with a tolerance of +/- 1° can
be set for the lower monitor support arm. An inward swivel range of 90° (tolerance +/- 1°)
and an outward swivel range of 125° (tolerance +/- 1°) can be set for the upper monitor sup‐
port arm.
2.2.2 With separate control room

The following figure shows an example of a room with separate control room

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28 2 Room Planning
Fig. 10: Example for separate control room
 If the control room is separate, audio-visual communication with the patient has to be
ensured, for example, through a window to the patient room and an intercom system.

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Room Planning 2 29
2.3 Component Dimensions
2.3.1 Stand dimension and center of gravity
 By adjusting the end switch, you can reduce the maximum stand height by about 32 cm
if necessary.
Fig. 11: Stand dimensioning

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30 2 Room Planning
Fig. 12: Stand center of gravity

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Room Planning 2 31
2.3.2 Unit base

Fig. 13: Stand base dimensioning

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32 2 Room Planning
2.3.3 Control console with radiation shield

Fig. 14: Control console dimensioning
The cables can be routed from the sides (left and right) or from below
A foot switch for triggering radiation is available as an option.
 The foot switch must be installed in a fixed location behind the radiation protection
screen, and the connection cable must be routed to allow for safe operation and use.

The glass and the console structure have a shielding equivalent to 0.5 mm lead.
In case additional shielding structures are needed please consider the value ≥0.5 mm Pb.

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Room Planning 2 33
2.3.4 Acquisition workstation
Fig. 15: e.g. WH AWS M740 n 186 x 481 x 430 mm

(W x D x H)
n 7.32 x 18.9 x 16.9 inches
(W x D x H)

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34 2 Room Planning
2.3.5 Control box
Fig. 16: Control box
n height approx. 55 mm
n diameter approx. 200 mm

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Room Planning 2 35
2.4 Radiation protection

The on-site radiation shield depends on the setup location of the medical device in the
room and on the function of the adjacent rooms. Follow and comply with this informa‐
tion

The glass and the console structure have a shielding equivalent to 0.5 mm lead.
In case additional shielding structures are needed please consider the value ≥0.5 mm Pb.

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36 2 Room Planning
2.5 Notice concerning electromagnetic compatibility (EMC)

Medical electrical equipment is subject to special precautions regarding EMC. These sys‐
tems must be installed and put into service in accordance with the EMC guidelines provi‐
ded in the accompanying documents.
Portable and mobile RF communications equipment can affect medical electrical equip‐
ment
When using the unit or system in close proximity to or stacking with other units: Proper
operation is not guaranteed! -> When operation near or stacked on other devices is re‐
 quired. If necessary, monitor the device or system to ensure proper operation in the ar‐
rangement used. This could be the case for example in the vicinity of MRI systems, retail
checkout scanners, or subways.
Fixed equipment cabling or system cabling that cannot be removed by the user is not
 listed. This cabling is part of the system and was accounted for in all EMC measure‐
ments. Without this cabling, the equipment or system would not function.
 WARNING
Note regarding accessories, converters, and cables that differ from the ones
specified:
Increased emission and reduced interference immunity of the unit or system are
possible when such items are used!
 Only use converters and cables that are sold by the manufacturer of the unit
or system as replacement parts for internal components.
2.5.1 Guidelines and manufacturer’s declaration

The system is intended for use in an electromagnetic environment as specified below.
The customer or the user of the system should ensure that it is operated in such an envi‐
ronment.
2.5.1.1 Electromagnetic emissions
Tab. 4
Interference emission Compliance Electromagnetic environment – Guidelines

measurements
RF emissions according Group 1 The system uses RF energy exclusively for its internal
to CISPR 11 function. Therefore, its RF emissions are very low and
not likely to cause any interference in nearby electron‐
ic equipment.

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Room Planning 2 37
Interference emission Compliance Electromagnetic environment – Guidelines

measurements
RF emissions according Class B
to CISPR 11
The system is intended for use in all facilities, except
Harmonic current emis‐ Not applicable for housing facilities and facilities directly connected
sions according to IEC to a public low-voltage power supply network that al‐
61000-3-2 so supplies buildings used for housing.
Emissions of voltage Not applicable The system has a nominal input current of more than
fluctuations and flicker‐ 16 A per phase.
ing acc. to IEC
61000-3-3
NOTICE
Using the unit or system in close proximity to other units, or stacking with other
units:
Proper operation is not guaranteed!
 If it is necessary to operate this equipment or system near other devices or af‐
ter stacking it with other devices, then it is necessary to observe the equip‐
ment or system in order to monitor its proper operation in this arrangement.
2.5.1.2 Electromagnetic interference immunity
Tab. 5
Immunity tests IEC 60601 Test Compliance level Electromagnetic environ‐

level ment – Guidelines
Electrostatic discharge ± 6 kV ± 6 kV Floors should be made of
(ESD) IEC 61000-4-2 Contact discharge Contact discharge wood, concrete, or ceramic
tiles. If the floor is covered
or or with synthetic materials, the
± 8 kV ± 8 kV relative humidity must be at
least 30 %.
Air discharge Air discharge
Electrical fast transient / ± 2 kV ± 2 kV The line power quality should
bursts according to IEC for power supply for power supply correspond to that of a typical
61000-4-4 lines lines commercial or hospital envi‐
ronment.
or or
± 1 kV ± 1 kV
for input/output for input/output
lines lines

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38 2 Room Planning
Immunity tests IEC 60601 Test Compliance level Electromagnetic environ‐

level ment – Guidelines
Surges according to IEC ± 1 kV ± 1 kV The line power quality should
61000-4-5 Differential mode Differential mode correspond to that of a typical
voltage voltage commercial or hospital envi‐
ronment.
or or
± 2 kV ± 2 kV
Common mode Common mode
voltage voltage
Voltage dips, short in‐ < 5% VT1 (> 95% Not applicable
The line power quality should
terruptions, and fluctua‐ dip in VT) for 0.5 correspond to that of a typical
tions of the power sup‐ cycles commercial or hospital envi‐
ply voltage according to ronment. If the user of the
IEC 61000-4-11 < 5% VT1 (> 95% Not applicable system requires continued op‐
dip in VT) for 0.5 eration during line power dis‐
cycles ruptions, it is recommended
1
70% VT (30% dip in Not applicable that the system be powered
VT) for 25 cycles from an uninterruptible pow‐
er supply. The system has a
< 5% VT1 (> 95% < 5% VT1(> 95% dip nominal input current of more
dip in VT ) for 0.5 in VT1) for 5 sec‐
1 than 16 A per phase.
cycles onds
Power frequency (50/60 3 A/m 3 A/m Power frequency magnetic
Hz) magnetic field ac‐ fields should be at levels char‐
cording to IEC acteristic of a typical location
61000-4-8 in a commercial or hospital
environment.
1. VT is the AC supply voltage prior to application of the test level.
NOTICE
Using the unit or system in close proximity to other units, or stacking with other
units:
Proper operation is not guaranteed!
 If it is necessary to operate this equipment or system near other devices or af‐
ter stacking it with other devices, then it is necessary to observe the equip‐
ment or system in order to monitor its proper operation in this arrangement.
This could be the case in the vicinity of MR systems, retail checkout scanners,
or subways.

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Room Planning 2 39
Tab. 6
Immunity tests IEC 60601 Test Compliance Electromagnetic environment – Guide‐

level level lines
n.a. n.a. n.a. Portable and mobile RF communications
equipment should be used no closer to any
part of the system, including cables, than
the recommended separation distance cal‐
culated from the equation applicable for
the transmission frequency.
Conducted RF 3 Vrms 150 kHz 3 Vrms Recommended separation distance: d=1.2 √
disturbances ac‐ to 80 MHz P1 for 80 MHz to 800 MHz
cording to IEC
61000-4-6
Radiated RF in‐ 3 V/m 80 MHz to 3 V/m Recommended separation distance: d=1.2 √
terference ac‐ 2.5 GHz P1 for 80 MHz to 800 MHz
cording to IEC
61000-4-3
1. Where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufac‐
turer, and d is the recommended separation distance in meters (m). Field strengths from fixed RF transmitters, as deter‐
mined by an electromagnetic site survey (2), should be less than the compliance level in each frequency range (3). In‐
terference is possible in the vicinity of devices carrying the following symbol
At 80 MHz and 800 MHz, the higher frequency range applies. These guidelines may not apply in all situations. Electro‐
magnetic propagation is affected by absorption and reflection from structures, objects, and people.
2. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile
radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To
be able to assess the electromagnetic environment with regard to the stationary transmitters, an electromagnetic site
study should be considered. If the measured field strength at the location where the system is used exceeds the applica‐
ble RF compliance level specified above, the system should be observed to verify normal operation. Should unusual per‐
formance features be observed, additional measures (such as change in orientation or change of site of the system)
may be necessary.
3. Over the frequency range of 150 kHz to 80 MHz, the field strength should be less than 3 V/m.
2.5.2 Recommended separation distances between portable and mobile RF

telecommunication devices and the system
The system is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the system can help prevent
electromagnetic interference by maintaining a minimum distance between portable and
mobile RF communications equipment (transmitters) and the system as recommended
below, according to the maximum output power of the communications equipment.

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40 2 Room Planning
Tab. 7
Separation distance according to frequency of transmitter [m]

Power rating of
transmitter [W] 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
d = 1.2 √ P d = 1.2 √ P d = 2.3 √ P
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended
separation distance d in meters (m) can be determined using the equation applicable to
the frequency of the transmitter, where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.
At 80 MHz and 800 MHz, the higher frequency range applies.
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects, and people.

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Preparation for Installation 3 41
3.1 Information regarding expansion bolts

n The specifications and instructions of the manufacturer must be observed for expan‐
sion bolts.
n Cut out an opening in the floor covering when installing the device on a solid floor.
n Installation materials must be obtained on site.

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42 3 Preparation for Installation
3.2 Floor installation
3.2.1 Stand
The stand floor plate is designed to include the unit base.
The stand can be set up as follows:
1. Stand without floor anchoring:
The stand is designed such that operation without floor anchoring is possible.
2. Stand with floor anchoring (5 anchoring points are provided)
Concrete quality for solid floors, min. C20/25.
Should anchoring to the floor be required due to local regulations (e.g. in seismic
areas) or due to the quality of the floor covering, the stand can be installed with
heavy-duty expansion bolts or threaded bolts (with counter plate).
The heavy-duty anchors and threaded bolts have to be procured locally.
3.2.1.1 Information regarding floor anchoring
 Heavy-duty anchor is required for max. tensile force per mounting point of 1.5 kN

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Fig. 17: Stand base floor installation
*1 n min. distance from wall is 150 mm when the stand is not

anchored to the floor.
see
n min. distance from wall is 500 mm when the stand is anch‐
ored to the floor.
see (Access for Service Providers),
*2 Recess for laying cables
3.2.2 Control console

The control console is equipped with a radiation shield; the workstation, monitor(s) and
control box are integrated.
The control console floor plate is designed to also serve as the unit base.
The control console can be set up as follows:
1. Control console without floor anchoring.
The control console is designed such that operation without floor anchoring is possi‐
ble.

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2. Control console with floor anchoring (2 anchoring points are provided)

The heavy-duty anchors and threaded bolts have to be procured locally.
Example: HILTI HSL M8-20 heavy duty expansion bolts
3.2.2.1 Information regarding floor anchoring

n Control console installation points

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3.3 Potential Equalization Connection

To maintain the local legal regulations or if the spacing from the control console to the
stand (MammoUnit) is less than 0.75 m, lay a potential equalization cable between the
stand (line power connection terminal) and the control console. In addition, connect the
workstation to this control console potential equalization.
The control console potential equalization connection point is located at the right foot
side.
 The potential equalization cable with connection loop (cable lug d = 6 mm) is always rec‐
ommended.
Fig. 18: Control console
(E) Potential equalization connection point

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Fig. 19: WH AWS, back
(1) Potential equalization connection point

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3.4 On-site Electrical Installation
3.4.1 Safety Shutdowns

Emergency Stop function
n The MammoUnit and control console (control box) are equipped with the emergency
stop function.
n Activating the emergency stop switch (on the right and left of the stand) blocks all
motorized movements. The system remains in operation.
n After disengaging the emergency stop switches, motorized movements are again pos‐
sible.
Emergency shutdown function
n To ensure the device is de-energized in the event of an emergency, an emergency
shutdown switch has to be installed.
n One or more emergency shutdown switches have to be installed so they can be
reached in the examination room by operating personnel. Pressing the switch de-en‐
ergizes the unit (stand, workstation, and an optional MoodLight). A SIRIUS safety shut‐
down is recommended.
3.4.2 Power connection

The power connection for the Mammomat Inspiration is divided as follows:
n MammoUnit electric power connection with emergency shutdown, 1 or 2 phase with
neutral wire and protective conductor connection
n Workstation power line voltage connection, including monitor(s) on a separate socket
 The power plug of the WH AWS / control console table must be connected to a properly
grounded power outlet.
n A socket for the MoodLight should be provided as an option, with a safety shutdown
(emergency off).
3.4.3 External indicator for X-ray or door contact (blocking radiation)

The modifications indicated below can be performed for the following options.
n A control contact for the external radiation indicator is available and can be config‐
ured.
 The relay contacts are potential-free and can be used to switch extra-low voltages (24
VAC / 25 W).

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n Radiation blocking via a door contact can be configured or implemented.
 Make sure that the contact of the door switch is potential-free (no contact to any supply
voltage or ground).
 The power supply of the stand must not be used for any for external consumers.
3.4.4 Example for on-site Power Distributor (1-phase, 2-phase) according to

DIN VDE 0100-710 or National Regulations, and taking into account the
use of SIRIUS
Tab. 8 Line power information for MAMMOMAT Revelation and MAMMOMAT Inspiration, permanently connected stand
Line power: TN-S 1(2)/N/GND, AC 50/60 Hz, ± 1 Hz Connection rating 7.5 kVA
Stand connection voltage: 1~ (1P/N/GND) 208 - 277 V
or
2~ (2P/N/GND) 208 - 400 V Power consumption: Value
Internal line resistance ≤ 300 mΩ n Continuous n 0.5 kVA
Power distributor fuse rat‐ 25 A slow blow

n Short-term n 7.5 kVA
ing:
Min/max cable cross section: 4 mm2 / 6 mm2
Tab. 9 Line power information for Mammomat Fusion, permanently connected stand
Line power: TN-S 1(2)/N/GND, AC 50/60 Hz, ± 1 Hz Connection rating 7.5 kVA
Stand connection voltage: 1~ (1P/N/GND) 208, 220, 230, 240 V
or
2~ (2P/N/GND) 208, 220, 230, 240, Value
400 V Power consumption: n 0.5
n Continuous kVA
Internal line resistance ≤ 300 mΩ
n Short-term n 7.5
Power distributor fuse rat‐ 25 A slow blow kVA
ing:
Min/max cable cross section: 4 mm2
 Do not connect any external power equipment to the line power supply.

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 Electrical installation according to IEC 60364-7-710, follow national and regional regula‐
tions.
Tab. 10 Line power information for workstation and monitors, removable power connection
Line power: TN-S 1/N/GND, AC 50/60 Hz, ± 1Hz

Connection voltage for 100 - 120 V
workstation and monitors or
200 - 240 V
Power distributor fuse rat‐ Standard line power connection,
ing: 16 A slow blow
 Do not connect any external power equipment to the line power supply.
 Electrical installation according to IEC 60364-7-710, follow national and regional regula‐
tions.

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Fig. 20: Electrical installation: 1-phase

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Fig. 21: Electrical installation: 2/3 -phase
Tab. 11 Legend / on-site interfaces to system
Position Designation
P1 Stand (Mammo Unit) line power connection
ND Power distributor, on-site
RD Control cable
EAT On/Off switch with indicator light
AT Emergency shutdown switch with mechanical locking mechanism, to de-en‐
ergize
1 Potential equalization (protective conductor) to the stand has to be provided
on-site
2 Power cable, 2 mm2 / 4 mm2, obtained on-site
3 RCD ground fault circuit interrupter 25 A / 30 mA Type B,
VN = 400/415 V~
4 Fuse according to national regulations

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Position Designation
5 K2 master relay
6 SITOP voltage transformer from AC 230-500 V to DC 24 V
7 Sirius safety relay
8 Control relay
9 For the workstation (WH AWS), a separate electrical outlet (AC 230 V or
country-specific) is required within 2 m from where it is positioned.
To maintain the local legal safety measures or if the spacing from the control
console to the MammoUnit is less than 1.5 m, route a potential equalization
cable from the control console to the MammoUnit (P1). At a distance of
greater than 1.5 m, this potential equalization cable is recommended.
10 A second socket within 3 m of the stand should be provided for the Mood‐
Light option. The MoodLight itself does not have an off switch. A socket that
can be switched off is recommended.

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3.5 Siemens remote services (SRS)

Perform the technical preparations and measures to start up Siemens Remote Service for
Mammomat,. including:
n IT link to install a broadband DSL/VPN connection to the Siemens Remote Service in‐
frastructure. Detailed information on SIEMENS Remote ServicesTM (SRS) can be found
in the PG TDIT-000.891.01.xx.02
n Complete the site-specific data according to the SRS checklist in the SRS tool kit and
send to the SRS-final team.
In addition to fast reaction times in service situations, Siemens Remote Service supports
special services such as Remote Update Handling, Virus Protection, and more.

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54 4 System Connections
4.1 General information on wiring
4.1.1 Power Line Voltage and Ground Wire Connections

n The stand is hardwired to the local power line voltage. The stand has to be able to be
de-energized through an emergency off switch in the examination room.
n Connect the control console (triple power strip), including the workstation and moni‐
tor(s), to the local line power socket.
Only system-internal loads can be connected to these sockets. External devices may
not be connected here
n It is recommended to connect the stand to the control console using a 6 mm2 poten‐
tial equalization cable (provided on site).
4.1.2 Signal and Data Cables

n The following controls and data lines are delivered with the system:
- MammoUnit control line (Ethernet cable)
- Detector control line (Ethernet)
- MammoUnit / control console control line
n Hospital IT network connection is provided on site, with connection to the workstation
n Optionally, potential-free signals of system status (X-ray, door contact) can be picked
up by the stand's CBS assembly.

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System Connections 4 55
4.2 Wiring fixed points

Fig. 22: Fixed point
Fixed point Component Type of wiring fixed point

P1 Stand Floor wiring fixed point
P1a Control Console with radiation shield Floor wiring fixed point
PC Power distribution box Wall wiring fixed point
Component
A Power distribution box (on-site)
B Power On/Off switch 1
C Stand
D Control console with radiation shield and control box
E Lamp for external radiation display (optional)
F “Radiation off” door contact (optional)
G Acquisition Workstation (WH AWS) and monitor(s) 2
1. The power On/Off switch (EAT) should be near the P1a/control console fixed point so that the operating
personnel can de-energize the entire system.
2. For a monitor to be installed on the left side of the operating console, a longer DVI cable (3 m) must be
provided. If necessary, the 3 m DVI cable can be ordered using item no. 8677028.

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Tab. 12 Distances between fixed points
Wiring From To fixed point Conduit, Min. open‐ Max. fixed Remarks
Har‐ fixed Clear space ing [mm] point dis‐
ness point [inches] tance [m]
No.
1 PC P1 – – – Power cable to be ob‐
tained on-site, cross
section 6 mm2 rigid
cable or 4 mm2 flexi‐
ble cable
2 P1 P1a 3/4 ∅ 45 6.5 Control console cable
shipped length: 10 m
3 P1 P1a 2 ∅ 45 7 Ethernet cable ship‐
ped length: 10 m
4 P1a Hospital IT network 2 ∅ 45 on site with Ethernet cable
outlet restrictions
Hospital power line 2 ∅ 45 on-site within for power line voltage
voltage socket 2 m of the to the workstation
control con‐ and monitors
sole
5 P1 External "radiation", 1/2 ∅ 10 on site with Optionally, potential-
"X-ray" signal pro‐ restrictions free "X-ray" or "door
cessing * contact" signals can
be picked up at P1
6 P1 External "door con‐ 1/2 ∅ 10 on site with and used for external
tact" signal process‐ restrictions display; one control
ing ** cable each is re‐
quired, 2x1.5 mm2,
shielded, provided
7 P1 P1a – – 7 Potential equalization
cable, minimum 6
mm2, provided on-
site
 *The relay contacts are potential-free and can be used to switch extra-low voltages (24
VAC / 25 W).
 ** Make sure that the contact of the door switch is potential-free (no contact to any sup‐
ply voltage or ground).

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System Connections 4 57
4.3 Cable Inlets
4.3.1 MammoUnit
Fig. 23: MammoUnit: cable inlet
4.3.2 Control console

Fig. 24: Control console: cable inlets

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4.4 Cable Conduits and Cable Ducts, Minimum Size

Suggestions for laying cables
n Cable duct depth, 60 mm
n It may be necessary to provide for greater duct depth for cross-overs.
n Route power cables separately from control cables (provide shielding where possible)
The following points must be taken into consideration:
n Avoid cable ring formations and intersections.
n Lay in separate conduits or closed cable ducts.
n When laying in open cable channels, lay cables separately using metal dividers or a
similar device.
Fig. 25: Cable duct
(1) dividers
(2) cable duct

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Technical data 5 59
5.1 Dimensions and weights

Tab. 13 Dimensions and Weights
Component Dimensions (WxDxH) [mm] Weight [kg]

Stand with floor plate 780 x 1175 x 2352 350
Control console with radi‐ 860 x 577 x 1945 130
ation shield
Workstation (WH AWS) 215 x 520 x 446 26
Control box height approx. 55 mm 1
diameter approx. 200 mm
Wall holder (optional) 1180 x 80 x 40 –
19" color display 404 x 205 x 406-506 6.9
21" color display 368 x 209 x 516-598 (portrait 9.2
format)
DicomProxy 53 x 179 x 250 mm 1.3
(option)

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60 5 Technical data
5.2 Heat dissipation

Tab. 14 Heat dissipation
Component Heat Dissipation [W]

Stand with floor plate 500
Control console with radiation shield –
Workstation (WH AWS) –
Control box 10
19" color display 50
21" color display 110
Option DicomProxy
Power consumption: short idle (Pshort idle)
5.46
(S0, running OS, Idle mode)
Power consumption: long idle (Plong idle)
4.76
(S0, running OS, Idle mode)
Power consumption: Standby (Psleep) (ACPI
status S3*, sleep, energy saving mode, 1.03
WOL enabled)
Power consumption: Minimum (Poff) (ACPI
status S5, soft off, wake up power button) 0.33 W
2)
Typical Energy Consumption (ETEC), ENER‐
24.7 kWh/year
GY STAR 6 based, conventional mode, 3)

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Technical data 5 61
5.3 Climatic Conditions
5.3.1 Temperature, relative humidity, and barometric pressure

Tab. 15 System environmental conditions during operation
System During opera‐

tion
Recommended ambient temperature for +20° - +35° C
MAMMMOMAT Inspiration and Mammomat
Fusion1
Recommended ambient temperature for +12°- +35°
MAMMMOMAT Revelation
Relative Humidity (non-condensing) 30 - 75%
Permissible Barometric Pressure 70 kPa - 106 kPa
Max. temperature gradient 10 K/h
1. The detector temperature during operation is approx. 3 - 5° C above the ambient temperature. The per‐
missible detector temperature must be taken into consideration, see
Tab. 16 Option DicomProxy
Option DicomProxy During opera‐

tion
Ambient temperature 10 - 35 °C
Relative humidity 5 - 85%
NOTICE
The detector is calibrated manually in periodic intervals.
Based on this calibration, a working range of ± 7°deg C is available.
Optimum image quality outside of this working range without re-calibration is not
ensured.
 To ensure constant and optimal image quality, environmental conditions
must be maintained absolutely. Avoid direct sunlight!

Restricted 04.18
62 5 Technical data
5.4 Electrical data
5.4.1 Mammomat systems

Tab. 17 MAMMOMAT Revelation and MAMMOMAT Inspiration electrical specifications
Power connection 1~ 208, 230, 240, 277 V, ± 10%, 50/60 Hz

2~ 208, 230, 240, 277, 400 V, ±10%, 50/60 Hz
Input fusing: 25 A
Power cable Recommended cable cross section:
6 mm2 rigid cable
Internal line impedance RI UN [V] Rimax [Ω]
208 0.25
230 0.30
240 0.35
277 0.45
400 0.90
Fusing (internal) 25 A for 208, 230, 240, 277 and 400 V
Imax 40 A for 230 V, 35 A for 400 V (2-phase)
Power Consumption Short-term power consump‐ Continuous load approx. 0.5
tion approx. 7.5 kVA kVA
Power factor (cos ϕ) 0.6 at 230 V
Connection value 7.5 kVA at 230 V
Tab. 18 Mammomat Fusion electrical specifications
Power connection 1~ (1P/N/PE) 208, 220, 230, 240V ± 10 %, 50/60 Hz

or
2~ (2P/N/PE) 208, 220, 230, 240, 400 V ±10 % 50/60 Hz
Input fusing: 25 A
Power cable Recommended cable cross section:
6 mm2 rigid cable
4 mm2 flexible cable

04.18 Restricted
Technical data 5 63
Internal line impedance RI UN [V] Rimax [Ω]

208 0.25
220 0.28
230 0.30
240 0.35
400 0.90
Fusing (internal) 25 A for 208, 220, 230, 240, and 400 V
Imax 40 A for 230 V, 35 A for 400 V (2-phase)
Power Consumption Short-term power consump‐ Continuous load approx. 0.5
tion approx. 7.5 kVA kVA
Power factor (cos ϕ) 0.6 at 230 V
Connection value 7.5 kVA at 230 V
5.4.2 Workstation and monitor

Tab. 19 Workstation and monitor electrical data
Component Power connection values

Workstations 100 - 127 V, +/9.5 A / 50/60 Hz
or
200 - 240 V, 4.0 A, 50/60 Hz
19” standard monitor 100 - 120 V, 0.80 A, 50/60 Hz
or
200 - 240 V, 0.45 A, 50/60 Hz
3 MP monitor 100 - 120 V, 1.4 - 1.1 A, 50/60 Hz
or
200 - 240 V, 0.7 - 0.6 A, 50/60 Hz
5.4.3 Option DicomProxy

Tab. 20 Option DicomProxy electrical data
Electrical values values

Rated voltage range 100 V - 240 V (AC Input)
Rated frequency range 50 Hz - 60 Hz
Operating voltage range 100 V - 240 V (AC Input)

Restricted 04.18
64 5 Technical data
Electrical values values

Operating line frequency range 50 Hz - 60 Hz
Max. output of single power supply 40 W

04.18 Restricted
Technical data 5 65
5.5 Paint colors

Tab. 21 Paint color
Base color, surface Signal white, RAL 9003

Stripes, sides White aluminum, RAL 9006
Tab. 22 MAMMOMAT Revelation additional paint color
Additional paint colors Aero Silver

Healthy Orange
RAL 7015
RAL 9006 Black (RAL 9005)

Restricted 04.18
66 6 Transport and Storage Conditions
6.1 Climatic Conditions

Tab. 23 System
System Transport / Storage

Ambient temperature -20°C to + 70°C
Tab. 24 Workstation
Workstation Transport / Storage

Permissible ambient temperature -40°C to +70°C
Tab. 25 MAMMOMAT Revelation and MAMMOMAT Inspiration detector
Anrad detector Transport / Storage

Admissible ambient and detector temperature 5°C to + 40°C
Tab. 26 Mammomat Fusion detector
Detector Transport / Storage

Admissible ambient and detector temperature – 20°C to + 70°C

04.18 Restricted
Transport and Storage Conditions 6 67
6.2 Transport Dimensions and Weights

Largest Crate Dimensions L x W x H [mm] Weight [kg]
Stand 2260 x 930 x 1550 550
Detector 900 x 800 x 600 40
Radiation shield, workstation, and 2100 x 800 x 1320 220 - 300 1
accessories
Stand, without packaging and lift‐ 1930 x 780 x 1175 530
ing carriage
1. depends on the options ordered

Restricted 04.18
68 7 Changes to previous version
Version <02> compared to version <01>
Chapter Changes
Room planning The following sections were changed:
n Instructions for positioning an optional foot switch for
radiation release have been added in the section “Con‐
trol Console”.
Preparation for Installation The following sections were changed:

n The connection options for additional external Radia‐
tion On and door contact indicators have been upda‐
ted.
System Connections The following sections were changed:

n The connection options for additional external Radia‐
tion On and door contact indicators have been upda‐
ted.

04.18 Restricted
List of Hazard IDs 8 69
The list shows the Hazard IDs of this document.

n hm_DOC_F14G3U1M4 06H393925
-Inadequate cooling of the system (Page 9)
n hm_DOC_F3G1U2M3 06H392683
-Swivel arm rotation without continuous operator activation “Single Touch” (Page 8)
(Page 24)
n hm_DOC_F14G5U1M2 06H394032 / hm_DOC_F14G2U4M1 06H393836
-Equipment falls over (Page 9)
-Intrusion of software virus (Page 9)
n hm_DOC_F4G1U1M11 06H392736
-Inadequate clearance between moving parts and fixed structure of the room
(Page 8)
X -Inadequate X-ray shielding (Page 7)
n hm_DOC_duen_rad_abort_pg 06H527161
-In case the TiCEM (Dual Energy) option is installed, the responsible organisation
shall install a warning lamp (Page 11)
n hm_DOC_inst_dam_cond_plan 06H449470
-Operation of the system outside specified environmental conditions (Page 10)
(Page 7)(Page 24)
n hm_DOC_pos_injur_pinch_zones 06H462686
-Risk of collision and crushing during movement of the swivel arm. (Page 7)
n hm_DOC_F4G1U1M10 06H392735
(Page 8)
n hm_DOC_F4G1U1M2 06H392727/ hm_DOC_F4G1U1M3 06H392728
-Inadequate clearance between moving parts and fixed structure of the room.
(Page 8)(Page 25)
n hm_DOC_F14G8U7M1 06H394118
-Emergency stop switch does not break the power to the system (Page 10)
n hm_DOC_F4G1U21M1 06H392814 / hm_DOC_F4G1U21M2 06H392815
-Unintended movement because emergency stop system does not stop movement
(Page 9)
n hm_DOC_F14G8U4M1 06H394112
-Electrical shock due to static discharge (Page 10)
n hm_DOC_F14G8U2M4 06H394106
- Leakage current too high (Page 10)

Restricted 04.18
70 8 List of Hazard IDs
n hm_DOC_F14G8U8M1 06H394122
- Emergency shut off circuit is not designed error safe (Page 10)

04.18 Restricted
- Restricted - All documents may
only be used by authorized person‐
nel for rendering services on Sie‐
mens Healthcare Products. Any
document in electronic form may
be printed once. Copy and distribu‐
tion of electronic documents and
hardcopies is prohibited. Offenders
will be liable for damages. All other
rights are reserved.
siemens-healthineers.com
Siemens Healthineers Headquarters

Siemens Healthcare GmbH
Henkestr. 127
91052 Erlangen
Germany
Telephone: +49 9131 84-0
siemens-healthineers.com
Print No.: XPW7-000.891.01.02.02 | Replaces: XPW7-000.891.01.01.02

Doc. Gen. Date: 04.18 | Language: English
© Siemens Healthineers, 2017

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Mammomat Systems

Mammomat Systems XPW7-000.891.01.02.02 Page 2 of 71 © Siemens Healthineers, 2017

1.1 Abbreviations and terms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

2.1 General information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24

3 Preparation for Installation 41

3.1 Information regarding expansion bolts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41

© Siemens Healthineers, 2017 XPW7-000.891.01.02.02 Page 3 of 71 Mammomat Systems

3.3 Potential Equalization Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45

4.1 General information on wiring . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54

5.1 Dimensions and weights . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59

6 Transport and Storage Conditions 66

6.1 Climatic Conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66

7 Changes to previous version 68

8 List of Hazard IDs 69

Mammomat Systems XPW7-000.891.01.02.02 Page 4 of 71 © Siemens Healthineers, 2017

1.1 Abbreviations and terms

Abbreviations and terms Definitions

© Siemens Healthineers, 2017 XPW7-000.891.01.02.02 Page 5 of 71 Mammomat Systems

1.2 Safety Information

1.2.1 General information

C Caution! General hazard warning.

V Dangerous electrical voltage > 25 V AC or > 60 V DC.

P Report icon. Used to indicate entries in certificates.

Mammomat Systems XPW7-000.891.01.02.02 Page 6 of 71 © Siemens Healthineers, 2017

1.2.3 Hazard keys

© Siemens Healthineers, 2017 XPW7-000.891.01.02.02 Page 7 of 71 Mammomat Systems

Mammomat Systems XPW7-000.891.01.02.02 Page 8 of 71 © Siemens Healthineers, 2017

© Siemens Healthineers, 2017 XPW7-000.891.01.02.02 Page 9 of 71 Mammomat Systems

Mammomat Systems XPW7-000.891.01.02.02 Page 10 of 71 © Siemens Healthineers, 2017

© Siemens Healthineers, 2017 XPW7-000.891.01.02.02 Page 11 of 71 Mammomat Systems

1.3 System configuration

Mammomat Systems XPW7-000.891.01.02.02 Page 12 of 71 © Siemens Healthineers, 2017

1.4.2 Actions regarding winter deliveries

© Siemens Healthineers, 2017 XPW7-000.891.01.02.02 Page 13 of 71 Mammomat Systems

1.5 Product-specific information

The WH AWS is equipped with two network adapters:

1.5.1.1 Additional IT Requirements for MAMMOMAT Revelation and MAMMOMAT Inspira‐

Mammomat Systems XPW7-000.891.01.02.02 Page 14 of 71 © Siemens Healthineers, 2017

1.5.2 Network Overview

© Siemens Healthineers, 2017 XPW7-000.891.01.02.02 Page 15 of 71 Mammomat Systems

1.5.3 Virus Protection

1.5.6 Option: DicomProxy (for MAMMOMAT Inspiration only)

Mammomat Systems XPW7-000.891.01.02.02 Page 16 of 71 © Siemens Healthineers, 2017

© Siemens Healthineers, 2017 XPW7-000.891.01.02.02 Page 17 of 71 Mammomat Systems

1.5.7 Siemens Remote Service connection

1.5.8 Recommended viewing stations (Siemens Viewing Stations)

1.5.9 Scope of delivery

1.5.9.1 System Overview

 The following images show the components of a MAMMOMAT Inspiration as an exam‐

Mammomat Systems XPW7-000.891.01.02.02 Page 18 of 71 © Siemens Healthineers, 2017

Fig. 3: Mammomat Inspiration

(1) Control console with radiation shield

© Siemens Healthineers, 2017 XPW7-000.891.01.02.02 Page 19 of 71 Mammomat Systems

1.5.9.2 System options

n Biopsy Fig. 4: Biopsy MAMMOMAT Revelation

n Laser cross Fig. 5: Laser cross

Mammomat Systems XPW7-000.891.01.02.02 Page 20 of 71 © Siemens Healthineers, 2017

n Tomosynthesis Fig. 6: HD Breast Tomosynthesis

© Siemens Healthineers, 2017 XPW7-000.891.01.02.02 Page 21 of 71 Mammomat Systems