PAUSCH Medical GmbH

Uroview® 8K Table Uroview® 8K System

01169043 right hand version 01169043-S right hand version
01169044 left hand version 01169044-S left hand version

Site Planning Guide

English © PAUSCH Medical GmbH, Graf-Zeppelin-Str. 1, D-91056 Erlangen 01167367

Site Planning Guide
Pausch Medical GmbH

Uroview® is registered in the U.S. Patent and Trademark Office.

The Uroview® 8K is licensed under the name Uroview® FD II.

Copyright
The copyright for this Site Planning Guide remains with PAUSCH Medical GmbH.
This Site Planning Guide is intended for the owner of the equipment and the suppliers.
This manual contains requirements and notes that must not be
 reproduced
 disseminated or
 disclosed in any other manner, either in part or in full.
Any misuse is liable to criminal prosecution.
All rights reserved.

The original edition of this Site Planning Guide is the English edition.
We reserve the right to make changes pursuant to advanced technical developments.

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 Site Planning Guide
Pausch Medical GmbH Table of Contents

Table of Contents

1 Identification ........................................................................................................ 5
2 About the documentation ................................................................................... 5
2.1 Confirmation ............................................................................................................ 6
3 Configuration ....................................................................................................... 7
4 Definition of Planning Tools ............................................................................... 8
4.1 Initial Visit & Site Preparation ..................................................................................10
4.2 Uroview® 8K Site Planning Sequence of Events .....................................................11
4.3 Pre-installation Meeting and Inspection ..................................................................12
4.4 Spatial Requirements .............................................................................................15
4.5 Ambient conditions for transport and storage ..........................................................17
4.6 Ambient conditions for operation.............................................................................17
4.7 Radiation Shielding and General Safety .................................................................17
4.7.1 Scatter radiation ..........................................................................................18
4.8 Definition of System Components ...........................................................................20
5 Structural and Construction Configuration..................................................... 22
6 Electrical Configuration .................................................................................... 29
6.1 Conduit and Cabling ...............................................................................................29
6.2 System Electrical Requirements .............................................................................31
6.2.1 BOSS..........................................................................................................32
6.2.2 Generator CPI INDICO IQ® 65 / 80 kW ......................................................32
6.2.2.1 Optional circuit breaker for 3p controlled by BOSS .....................................33
6.2.3 Apparent Resistance of the Supply Mains ...................................................34
6.2.4 X-Ray On Lamp .........................................................................................34
6.2.5 Networking ..................................................................................................34
6.2.6 Door Interlock Switches (if applicable) ........................................................35
7 System Component Thermal H.V.A.C. Considerations .................................. 36
8 System Component Weight Measurements .................................................... 36
9 Uroview® Installation Information .................................................................... 37
10 Uroview® 8K Shipping Crate Information ........................................................ 37
11 System integration of the Uroview® 8K ........................................................... 41
11.1 Floor laying of the cables ........................................................................................41
11.2 Ceiling (Wall) mounted Junction Box ......................................................................42
11.3 Room example – Uroview® 8K system ....................................................................43
11.4 Uroview® System - Power Supply ...........................................................................44
12 Drawings ............................................................................................................ 45
12.1 Uroview® 8K Table ..................................................................................................45
12.2 Generator CPI INDICO IQ® 65 / 80 kW ...................................................................48
12.3 Workstation HIRIS RF43/FL with MAVEN ...............................................................51

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Table of Contents

12.4 Monitor support arm................................................................................................52

12.5 Uroshelf ..................................................................................................................54
12.6 Ceiling (Wall) mounting of the junction box .............................................................55
12.7 X-ray in Use Sign ....................................................................................................56
12.8 BOSS .....................................................................................................................57
12.9 EXECUTOR (option)...............................................................................................58
13 Index ................................................................................................................... 59

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 Site Planning Guide
Pausch Medical GmbH About the documentation

1 Identification
Manufacturer
Address PAUSCH Medical GmbH
Graf-Zeppelin-Str. 1
91056 Erlangen
Germany
Telephone number +49 (0)9131 / 99 92-0
E-mail [email protected]
Homepage www.pauschmedical.com

2 About the documentation

This guide is provided to assist in planning an installation site for a Uroview® 8K urology sys-
tem. It is necessary to have as much information as can be furnished for each unique site in
order to plan the installation successfully.

The information provided herein is a recommendation only and should be modified to meet
actual circumstances. However, the work and resource requirements specified here in repre-
sent all general requirements for an installation and should be addressed. The Customer
must specify, in writing, its inability to meet any requirement specified herein, and the alter-
native route to be taken.

After reviewing this guide, please complete the Site Evaluation Form and return with scaled
blueprints, and/or the Site Survey Sketch to GE Healthcare at the following address:
GE Healthcare
Attn: Site Planning Department
384 Wright Brothers Drive
Salt Lake City, Utah 84116
~HEALTH Uroview Site Planning <[email protected]>

If you have questions, please call 1-800-874-7378, option 1, option 3, option 3 and ask for
Uroview® Technical Support.

CAUTION
Federal law restricts the sale of this device by or on the order
of a Physician.

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About the documentation

2.1 Confirmation

GE Healthcare
384 Wright Brothers Dr.
Salt Lake City UT, 84116
PH: 1-800-874-7378

It is understood that (the customer) will read and implement all aspects of the Uroview® 8K
Site Planning Guide (01167367).

GE Healthcare guarantees installation of the Uroview® 8K system in a correctly prepped

room, as per the Site Planning Guide (01167367).

Customer Signature GE Representative

Title Title

Date Date

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 Site Planning Guide
Pausch Medical GmbH Configuration

3 Configuration

The Uroview® 8K may be ordered

in left-hand (Fig. 3-1) or right hand
(Fig. 3-2) configurations.

Left hand/right hand designation

refers to the patient's position in
relation to the table. Fig. 3-1

Example:
On a left hand table, the table is
on the left side of the patient (with
patient supine). Consideration
must be given to both space and
table movements in relation to the
orientation of the patient table.

Fig. 3-2

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Definition of Planning Tools

4 Definition of Planning Tools

A blank Site Evaluation form and Site Survey scaled graph paper are provided at the back of
this guide. These tools and the information throughout the remainder of this document are
provided to assist you identify all the critical components for completing an installation site
evaluation and survey.

Site Evaluation Form

The Site Evaluation Form helps determine site compatibility and identifies the modifications
required. This tool should be used to identify any obstacles before the installation process.
Attach notes specifying special explanation of the circumstances existing at the site and an
inability to meet the requirement specified herein and the alternative method of meeting the
requirement.

Blueprint
Whenever possible, the current blueprint of the installation site should be used to indicate lo-
cation of components and construction modifications. The Blueprint should provide details
such as windows, lighting, plumbing, floor drains, ventilation ducts, ceiling, existing power
and isolation panels, and wall recesses, built in and overhead cabinets, and counter tops,
and protrusions, notes, and any other information relevant to planning the installation. If a
current blueprint is not available, all information should be provided in the Site Survey
Sketch.

Site Survey Sketch

The Site Survey Sketch should be a scaled ¼ inch (.65 cm) or ½ inch (1,3 cm) representa-
tion of the room indicating proposed locations for major Uroview® 8K components. The Site
Survey Sketch or blueprint should provide details such as windows, lighting, plumbing, floor
drains, ventilation ducts, ceiling and wall recesses, built in and over head cabinets, counter
tops, and protrusions, notes, and any other information relevant to the installation.

Site Plan
The Site Plan is the first formalized drawing of the installation site. Site Plan drawings will be
based on unique room layouts and Customer preference. The Site Plan is drawn by GE
Healthcare and controlled by the customer.
By request, GE can provide examples of site design and specification requirements. See
also chap 11.3 for a room example.
GE drawings represent only the proposed layout of the urology room after considera-
tion of the Site Evaluation, Blueprint and/or Site Survey Sketch submitted by the Cus-
tomer.

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Note
GE Healthcare is not an architectural firm. Any site plan draw-
ings supplied by GE Healthcare or its representatives are not
to be used for construction purposes. The approved Site Plan
drawing is to be used by our Customers or their appointed rep-
resentatives only to compile actual construction drawings. The
Customer is responsible for all construction drawings, con-
struction and preparation costs, permits, inspection, and fees,
and conformance to all local and national building and electri-
cal codes.

The Site Plan will recommend the following:

 Optimal location for the table in the room
 Method of anchorage
 Left hand or right hand
 Optimal location of an added or proposed floor drain (if applicable)
 Electrical conduit schematic of the Uroview®8K equipment
 System cable lengths and minimum wire gauges to maintain a <2% voltage drop
 Special instructions or requirements
 Other recommended modifications to the room

The Site Plan will be submitted to the Customer for approval signatures. Approval signatures
represent approval for GE Healthcare to install the configuration selected and outlined on the
approved Site Plan. Changes will be made as required until the Site Plan correctly reflects
the planned site and the final plan contains approval signatures.

Refer to Uroview® 8K Urology / Cystology Room Example chapter 11.3

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4.1 Initial Visit & Site Preparation

(Please Review chapter 4.4 Spatial Requirements)
Site planning for the installation of a Uroview® 8K Urology system is a mutual effort between
the Customer and GE Healthcare.
GE Healthcare must have accurate information describing the installation site in order to
plan its part of the installation, and to ensure ease of installation. To begin a successful en-
deavor, GE will provide the Customer with system requirements for evaluation, which the
Customer and members of the GE sales team will use to generate a site plan. The Customer
will provide a copy of the latest scaled blueprint of the proposed site. If the blueprint is not
available, the Site Survey Sketch (in back of Site Planning Guide) will contain the all blue-
print information.
Clear indication on the Site Evaluation Form or attached notes of any special Customer,
Specific Country, State and Local requirements, including any special circumstances or
obstacles (i.e. surgical lights, view boxes, medical gas drops, floor drains, etc). Special sys-
tem requirements typically include the necessity for door interlock switches applicable by
federal, state, and local codes.
If quality of input power is not known, GE Healthcare can perform a power and grounding au-
dit to examine condition of facility power.
Using the information provided by the Customer, GE Healthcare will give a proposed site
plan to the Customer. Contact GE Healthcare for specifics regarding cost and availablity. The
Customer will review, make corrections or changes that approve the site plan. Once the plan
is accepted by both the Customer and GE, the Customer will complete construction at the
proposed site, and GE installs the Uroview® 8K urology system.
Refer to the Sequence of Events for the Uroview® 8K site planning process (shown in flow
chart form).
Site Preparation and supervision is the sole responsibility of the Customer. GE Healthcare
will offer advice when requested. For site preparation, it may be necessary for the following
personnel to attend: Bio-Medical Engineer or Plant Engineer, Project Manager, Contractor (if
applicable) Surgical Staff, Urologist and/or Radiologic Technologists.
Customer will determine the best delivery route from the receiving area to the installation site
to determine whether all system pieces fit around corners, through doors, under lights, and
access to elevators etc.

Note
Once final equipment location has been decided, the Customer
must sign! the site plan, and return to the site planning depart-
ment before the equipment is shipped. This customer signature
is required in order to ensure proper table configuration, gener-
ator size, cable lengths.

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4.2 Uroview® 8K Site Planning Sequence of Events

The collaborative effort between GE OEC and the Customer should flow similar to following.

Fig. 4-1

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4.3 Pre-installation Meeting and Inspection

When Customer’s preparations are complete, the major responsibility shifts to the GE Sales
and/or Field Service Team and is defined by the following:
GE Healthcare
The sales representatives and/or the local field service engineer will schedule a pre-installa-
tion meeting to be held. The purpose of this meeting will be to introduce installation person-
nel, inspect the installation site discuss and coordinate the installation schedule, answer
questions, and correct any last minute problem solving to ensure ease of installation.

The following Customer representative should plan to attend Urologist, Operating Room Su-
pervisor or representative from the urology department, representative from Anesthesiology,
the Administrative Director of Radiology or his/her representative.

GE Healthcare will be represented by the Sales Representative, and an installation engineer

and/or field service engineer.

During the pre-installation process, the Customer will be asked to provide the site planning
and field service departments with the following:
 An individual to coordinate the efforts of contractors, architects, physicists, and the
installation engineer.
 The most current and accurate representation of the proposed site by redlined Blue-
print complete with all inner dimensions, along with any information pertaining to the
site modifications.
 The site inspected and approved for X-ray shielding and safety devices as required
by federal, state and local regulations. Inspections and approvals must be obtained
and documented before GE representatives will begin installation. Documented ap-
provals include electrical and construction code, radiation health and safety inspec-
tions, and other medical permits or licenses.
 It is the responsibility of the Customer to have the site evaluated by a radiation health
physicist to determine the adequacy of the shielding and compliance to state and lo-
cal codes.
 It is highly recommended to have a power and grounding audit completed by a GE
Healthcare Power and Grounding Auditor to ensure cleanest power possible can be
provided.
 If ceiling mounted monitor suspension is desired, the Customer is responsible to coor-
dinate with a Unistrut representative to determine location of Unistrut mounting and is
responsible for all costs incurred with materials, preparation, and installation of ceiling
suspension. Note: careful consideration must be taken in placement of ceiling
suspensions in relation to Uroview® 8K Table position. This must be coordinated
prior to equipment sale to ensure it will work with the Uroview® 8K.
 Customer assumes all responsibility for any construction costs, whether or not related
to installation of GE Healthcare equipment. No work may be performed or materials
furnished at GE Healthcare expense unless authorized by a signed purchase order.

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GE Healthcare warranty, express or implied, shall be contingent upon compliance by Cus-

tomer and Customer’s Contractors with the installation requirements specified in this docu-
ment.
Prior to installation, the following must be completed by the customer
 Customer shall have completed all aspects of actual construction including modifica-
tions to lighting, air conditioning, fire protection, plumbing, structure (wall, floor, or
ceiling reinforcement), radiation shielding,
 Auxiliary base plates, electrical rigid conduit, electrical junction boxes and cover
plates, bushings, wire, and cable duct.
 Customer shall have completed the install for all accessory items including, X-ray
warning lights, door interlocks, apron hangers, and any other product not sold by GE
Healthcare at time of installation.

Note
Customer is responsible to drill mounting holes in the floor and walls.

The Customer Representative will coordinate all installation activities including verifi-
cation that:
 All construction, modifications, and preparations are completed and conform to all ap-
plicable federal, local and state codes by the time the GE installation team arrives to
install the Uroview® 8K urology system.
 Hospital personnel has reviewed placement of system components before any com-
ponents are mounted to the walls, floor, or ceiling. Room sign off should be com-
pleted by this point.
 Ongoing assistance by an electrician as required by the GE installation engineer for
cutting connector holes in junction box cover plates and installing connectors as out-
lined by GE Sales or Field Service Representative in accordance to room site plan
drawing.
 At least a week prior to the installation, provide GE Healthcare with the actual internal
conduit lengths (maximum conduit length is 34 ft). If this is not provided in advance or
is not accurate it will cause significant delays with the installation.

PRE-INSTALL WALKTHROUGH:
One week prior to the installation, the GE Installation team will:
 Inspect the room to ensure that all wiring (i.e. - incoming electrical circuits, x-ray in
use light, door switches, etc.), conduit, and junction boxes are installed according to
the Site Plan. Ensure customer/contractor has left 10-foot pigtails at all junction points
(per site plan, reference Junction Point Notes on page E1).
 Review architectural drawings and Site Plan to verify all details.
 Review the needs of the installation team including availability of customer/contractor
tools and ladders, access hours, and noise or dust restrictions.
 Determine whether the installation team must be warned of any hazards near the
area in which they will be working, such as exposed wiring, radiation, or hazardous
chemicals.

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 Discuss any conduit, wire, connectors, crimping tools, grommet materials, clamps or
special parts required for this installation. The customer’s electrician will provide such
parts. Modifications to the initial Site Plan can be made at this time. Changes shall be
noted and accepted by the customers signature on the initial Site Plan. The hospital
representatives and GE representative must each sign the approved plan. (Should be
at pre-installation meeting)
 Attain documentation from customer with verification of actual measurements of the
diameter and length of all conduit runs and the depth of concrete.
 The actual measurement of the floor depth needs to be provided at least one week in
advance. If this is not provided in advance or is not accurate it will cause significant
delays with the installation.

Note
GE Healthcare does not accept or assume any liability for problems
that may arise when the actual construction or modifications to the site
if site does not meet the approved plans and specifications. If local
codes conflicts with any recommendation in this guide or in the Site
Plan, the local codes will take precedence. GE Healthcare should be
notified and approve changes to plans or drawings during site plan-
ning or at pre-installation meeting.
Note: GE Healthcare Field service representative must have a copy of
proposed order from customer to allow for all installation configura-
tions.

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4.4 Spatial Requirements

It is important that the Customer recognize the physical requirements of the system for ade-
quate floor support and thickness, ceiling height, and spatial freedom of movement.

Ceiling Height
By default, the Uroview® 8K urology system is designed for a minimum height of 8.53 ft
(102.362 inches / 260 cm). See chapter 12.1
Deviating from the recommended minimum-room height a customized option for a reduced
room height of 8 ft (2.44 m) is possible. The standard movement range is then restricted.
This must be specified when ordering the system.
Proximity to Drain

The floor drain (FD) location that is

recommended by GE Healthcare
can be seen on Fig. 4-2. This is
optimum location for utilization of
the floor drain in conjunction with
Uroview® 8K collapsible drain pan
assembly and extendable drain-
age tube. It is not advisable to lo-
cate the drain directly at the foot of
the table. It is better placed a little
out of the way to prevent interfer-
ence with physicians and techni-
cians.
Refer to Fig. 12-3 for optimum
floor drain location.
 All plumbing modifications
shall conform to the re-
quirements of the National
Plumbing Code, OSHA,
and any applicable local
codes and ordinances. Any
and all costs of plumbing
modifications shall be the
responsibility of the Cus-
tomer.

Fig. 4-2

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X-ray Head Travel

No obstructions (sprinkler heads, ceiling lights, monitor suspensions, etc.) shall be in the
path of the X-ray head through the full range of travel.

Uroview® 8K monitor support arm

The Uroview® 8K Table includes a monitor support arm with two 27” monitor. If not planned
properly damage can occur to the monitors, monitor support arm or wall.
For the recommended minimum distance to the wall on the rear side of the device see di-
mension drawings in chapter 12. If the distance is smaller, the accessibility is restricted for
the service.
The optimal distance to the wall from the head end of the table should be 118.11 in (300 cm).
The cables for the monitors are laid inside the monitor support arm.
ATTENTION
Collision with the wall
It is possible to pivot the monitors around the rear side of the
Uroview® 8K Table.
(See chapter 12.1 und 12.4)

Uroview® 8K support arm with X-ray protective shield / lamp / monitor(option)

In addition to the monitor support arm it is possible to install another support arm.
You can choose between:
 support arm with lamp
 support arm with X-ray protective shield
 support arm with X-ray protective shield and lamp
 support arm with monitor 24”

Table Location Limitations

It is necessary to have a minimum distance of 68.90 in (175 cm) on the foot end of the table
to the wall for the Uroview® 8K Table. The distances for the rear side and head end of the ta-
ble of the Uroview® 8K Table are obtained from chapters 12.1 and 12.4.
ATTENTION
Collision with objects or electrical components
No objects or electrical components should be placed within
the minimum distance to the ceiling, rear wall and side walls.
Particular consideration should be given to the travel range
of the longitudinal and lateral directions of the table, as well
as the pivot range of the table/tube support arm.

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4.5 Ambient conditions for transport and storage

Permissible ambient temperature range -25 °C to 70 °C
Permissible relative humidity range 5 % to 95 %
Permissible air pressure range 700 hPa to 1100 hPa
Tab. 4-1

4.6 Ambient conditions for operation

Maximum operating height 2000 m
Permissible ambient temperature range 10 °C to 40 °C
Permissible relative humidity range 20 % to 80 %
Permissible air pressure range 700 hPa to 1100 hPa
Tab. 4-2

4.7 Radiation Shielding and General Safety

Radiation protection requirements are not included in this plan and shall be specified by a
qualified radiation physicist employed by the Customer. The Customer is responsible for
providing adequate room and operator shielding and any additional radiation warning or
monitoring devices (if applicable).

Note
It is the responsibility of the customer to conduct or have a ra-
diation scatter survey of the site room by a qualified Radiologi-
cal Physicist to determine if lead shielding is required.

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4.7.1 Scatter radiation

Measurement plane 150cm height above the floor
20 cm Distance: 470 nGy/s (without filtering)
Isokerma- diagram (32/16/8/4/2) [ µGy/Gy cm2 ]

Fig. 4-3

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Measurement plane 100cm height above the floor

20 cm Distance: 727 nGy/s 50
Isokerma-diagram (50/25/12.5/6.25/3.125/1.5625) [ µGy/Gy cm2 ]

Fig. 4-4

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4.8 Definition of System Components

Uroview® 8K Table
The Uroview® 8K Table can be configured in one of two ways and both positions refer to pa-
tient position.
 Left Hand Configuration-- This configuration refers to the position of the patient. (i.e. if
the patient is laying on the table with the tower off to his/her left hand, it is a “Left”
hand configuration.)
 Right Hand Configuration—This configuration refers to the position of the patient (i.e.
if the patient is lying on the table with the tower off to his/her right hand, it is a “Right”
hand configuration.)
 The Uroview® 8K Table can be tilted 88 degrees with the head end up, or can be
tilted 20 degrees with the head end down. The patient table can move laterally or lon-
gitudinally.
 The X-ray head can travel towards the back of the tower
(See chapter 12.1 for dimensions)

Generator (CPI INDICO IQ® 65 / 80 kW)

The standard configuration of the Uroview® 8K System is a three-phase generator with a
power output of 65 kW.
The generator is optionally available with 80 KW.

Workstation (HIRIS RF43/FL)

 The Workstation contains all the imaging functions. Many options are available to in-
tegrate into the workstation If using the DICOM or a P.A.C.S. or other network de-
vices, the HiRis cabinet comes with an RJ45 connector for network connections. If
connection to network is desired, it is highly recommended that the final location of
HiRis cabinet be decided before the facility network connections are installed. It is
highly recommended that category 5 (CAT 5 UTP) 100BaseT cable be used for con-
nection of workstation to network demark.

Remote Generator Membrane R&F Console

 The Remote Generator Membrane R&F Console controls technique settings for radi-
ographic functions. Field Service personnel can also access system diagnostics.

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Uninterrupted Power Supply (UPS)

The Back-UPS device offers guaranteed power protection for the HIRIS with its standby bat-
tery supply. The management software of the UPS allows to optimize the use of the UPS.
Premium features of this device may include Automatic Voltage Regulation (AVR) and a LCD
display.
The battery cartridge typically lasts 3 to 6 years. Environmental factors impact on the battery
life. High temperatures, poor quality A/C power, and frequent, short duration discharges will
shorten the battery life.
The Uninterrupted Power Supply is a part of the MAVEN. (See page 26)

BOSS
For information to BOSS see page 27

Uroshelf Option
The Uroshelf assembly attaches to the Uroview® 8K Table for use as a 4-leveled, support for
accessories or peripherals. It is also equipped with a 6 plug power strip for 120V AC power
sources (i.e. Storz Video equipment, etc.) The shelves are non-adjustable. The Uroshelf
power strip must have its own dedicated AC power source. It cannot be connected to the
Uroview® 8K Table for its power.
(See Fig. 5-4 for Uroshelf placement)
(See chapter 12.5 for Uroshelf dimensions)

Accompanying Documents
The Installation Manual from each individual system component is to be observed during the
installation of the Uroview®8K. The Manuals from each individual system component are
listed in Overview Accompanying Documents 01167336 and are supplied with the delivery of
the Uroview® 8K system.

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Structural and Construction Configuration

5 Structural and Construction Configuration

Refer to chapter 7 for heat outputs and to chapter 8 for component weights of the
Uroview®8K.
Anchorage
With the help of the supporting feet (2), the workstation is secured to prevent any uninten-
tional movement.

All shipped components will be on pallets and some will have casters for ease of transporta-
tion. When the components are in their permanent locations, they can be held stationary as
follows:
 The Workstation has castors and supporting feets. (see page 26)
 The table base plate or auxiliary base plate (if applicable) is always anchored to the
floor.
 For the generator see page 27.
Table
1. The floor must be rated to support a concentrated load of 353 pounds per square
ft / 1723 kg per square meter.
2. The anchor bolts are included in the scope of supply. The quality of concrete must at
least comply with C20/25 according to EN 206:2000-12 for broken and unbroken
floors.
3. The floor must be level (non-corrugated) concrete with a minimum thickness “H” (Fig.
5-1) to accept the standard Uroview®Systems method of anchorage.

Default fastening kit

The floor mounting of the Uroview® 8K ta-
ble/tower takes place at 5 attachment points.
By default, the Uroview® 8K table is used as
fixing bolt Safety bolt S M8-12/55/40.
D = Ø0.47 in (Ø12 mm)
T = min. 4.13 in (min.105 mm)
max. - do not exited concrete thickness
L = 4.53 in (115 mm)
SW = 0.51 in (13 mm)
H = min. 4.72 in (120 mm) - depending on the
load capacity of the floor
tinst = 20 Nm
Ba = Base of the device
Fig. 5-1

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Optional fastening kit

Optionally the fischer heavy-duty fastening system “Superbond FSB” for
fastening the device on the floor is available. The Fastening system consists of:
threaded rod RG M resin capsule RSB mini
X=M10; Y=4.33 in (110 mm)

Other tools of the kit are:

Cleaning brush BS Hexagon nut M10 (as lock nut)
SDS-Adapter for cleaning brush Hand pump great AB G
To drill the mounting hole, a concrete drill Ø0.47 in (Ø12 mm) is required. (not in
the delivery)
Drill appropriate sized hole.
Drill hole diameter=Ø0.47 in (Ø12 mm); Drill hole depth = 2.95 in (75 mm)

 Refer to Fig. 12-3 for Uroview® 8K Table foot print.

 Refer to chapter 7 for System Component Thermal H.V.A.C. Considerations
 Refer to chapter 8 for System Component Weight Measurements

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ATTENTION
The column of the Uroview® 8K should always be screwed
directly onto the concrete or tiled floor at the place of installa-
tion (No floorings like PVC etc. in the area occupied by the
base of the equipment).
Customer can be given the option to mount directly on the
existing floor, but must be informed that this can reduce ef-
fectiveness of disinfection and table vibration behavior.
Please document acceptance by customer.

4. The anchorage system is designed to withstand 2500 pounds/1134 kg per anchor

working load. If the mounting surface will not withstand a concentrated load of
353 pounds per square ft./1723 kg per square meter, an auxiliary base plate with a
larger area may be required. If this is necessary, the auxiliary base plate must be large
enough to accommodate the Uroview® 8K. Detailed engineering data and calculations
regarding weight distribution, center of gravity, etc. is available from GE Healthcare
upon request.
5. The Customer’s structural engineer must determine the necessity for additional floor
support.
If an auxiliary base plate is needed, careful consideration of Uroview® 8K Table must
be taken in order to ensure proper mounting once the holes have been drilled into the
base plate.
For the supplied safety bolts, 5 bores are required. dimensions see Fig. 5-1 and Fig.
12-3

CAUTION
The Uroview® is designed for a maximum table load of
628 lbs / 285 kg.
If any approved accessories are attached to the Uroview® ,
the maximum patient load may get restricted correspond-
ingly.

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6. If the customer installs a base plate under the tower of the Uroview®8K, it must be pro-
vided with five (5) 5/8 in /1.6 cm UNC hole. dimension see Fig. 12-3
The thickness of the baseplate must not exceed 1.18 in / 30 mm when the supplied
safety bolts will be used.
The baseplate of the UroView® 2800 can be used.

Note
This calculation is determined by using the following: 2225 lbs.
(1009 kg) + 346 lbs. (157 kg) = total system weight divided by
the 7.28 square foot area (6763.3 sq cm) of the Uroview® 8K
baseplate. Using this formula, weight distribution will be signifi-
cantly lower per square foot due to larger plate area.

(a) Fig. 12-3 shows the Uroview® 8K Table foot print.

(b) Fig. 5-2 shows the Uroview® 8K through Bolted.

Fig. 5-2

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Note
Customer is responsible to drill mounting holes in the floor and
walls.
It is absolutely essential that floor thickness be determined be-
fore installation!
Corrugated concrete floors may not be sufficient for standard
anchoring and should be evaluated by the facility's structural
engineer. If core samples are necessary, it is the Customer’s
responsibility for all costs involved in determining floor thick-
ness. For any deviation from the recommended anchorage
methods discussed in this manual, the customer must write,
sign and distribute an informal waiver to the field technician,
the regional sales manager in the customer's area.
Any auxiliary base plate will be the sole responsibility of the
Customer. GE Healthcare does not fabricate or provide auxil-
iary base plates.

Workstation (HIRIS)
The workstation is pushed into its installation site with its castors (1). With the help of the
supporting feet (2), the workstation is secured to prevent any unintentional movement.

Fig. 5-3

Upon positioning the workstation, the following should be observed:

 you keep the cabinet away from heat sources,
 the cabinet is not placed against walls or other structures that limit proper ventilation,
 you regularly check the efficiency of the cabinet cooling system (fans work, air grilles
not obstructed).
MAVEN Cabinet
This Medical Adjustment Voltage ENclosure will be located on top of the Workstation and is
protected against lateral movement as well as tilting.
The MAVEN includes:
 Pre Transformer (115 V to 230 V)
 Uninterrupted Power Supply (UPS)

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BOSS
The Box On Steady Structure is determined to be mounted on a wall.
This Box includes:
 Emergency Stop
 ON – OFF switch
Turning on the ON-Switch, the table, generator smf HiRis will start up. Switching to OFF-
Position the table and generator will shut down immediately amd HiRis will shut down after
5 minutes.
The lockable emergency stop will shut down the whole system in case of emergency.

Generator Main Cabinet

Place the generator cabinet in a location that will allow the following:
 Easy access for service and sufficient clearance at the rear for room interface cables.
 Air circulation: The main cabinet is fan cooled; therefore room-temperature air must
be free to circulate around the cabinet (3 inch wall clearance). The cooling slots in the
cabinet must be unobstructed at all times.
 A stable footing.
 Close proximity to service-disconnect boxes. Cables should be a maximum of 15ft/5m
in length and located away from traffic areas.
 Adjust the leveling feet to the desired height, making sure that the generator is lev-
eled. Then raise the locking nut for each leveling foot up against the bottom of the
generator cabinet and tighten the locking nuts to firmly secure the leveling feet.
Anchoring the Generator to the Floor:
Mounting holes have been provided in the base of the generator to secure the generator to
the floor, if required. Refer to chapter 12.2
The customer has to provide the hardware required to secure the generator to the floor.
The generator should be secured to the floor via 1/2 in (13mm) diameter clearance holes that
are located in base of the cabinet. (see also Fig. 12-5)

Membrane R&F Console

The Uroview® 8K Membrane R&F Console for the generator is placed on a table.

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Operation from the control room (optional)

There is the option of integrating a second hand-held operating unit and the foot switch for
exposure / fluoroscopy into the system.
The kit includes controls for the control room
 EXECUTOR (1) including Emergency stop switch
 Hand-held operating unit
 Foot switch exposure - fluoroscopy
With the additional hand-held operating unit and the foot switch exposure - fluoroscopy, the
same functions can be carried out from a control room as with those directly on the device.

Uroshelf Option
The Uroshelf is an option that will be mounted on the side of the Uroview® 8K Table at the
“FOOT” end of the table.
It can be seen in Fig. 5-4 (Uroview® 8K left-hand version) how the Uroshelf (U) is to be posi-
tioned on the equipment column.

Fig. 5-4

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6 Electrical Configuration
ATTENTION
®
The Uroview 8K system is only to be installed and operated
off electrical power networks which satisfy a device protec-
tion according to EN 60601-1, protection class 1.

Note
The site mains connection for the Uroview® 8K system should
be near to the device. (Maximum distance to the mains con-
nection of the Uroview® 8K system 16.4 ft / 5 m)

6.1 Conduit and Cabling

The Uroview® 8K will have the capability of using overhead ceiling conduit or below floor
connection using divided raceway or conduit. Because of the monitors, careful consideration
must be taken for ceiling cabling to avoid collision of monitor carriage (Refer to Fig. 11-4).
All wires and cables, whether installed by GE Healthcare or by the Customer must be
contained in troughing or raceway and shall conform to regulations and requirements of the
National Electrical Code, OSHA, specific country, state, and/or local code. The Customer is
responsible for installing the complete electrical system indicated in the site plan including all
junction boxes & cover plates, circuit switches, emergency off switches and power
transformers and/or power distribution unit. (if dictated by NEC or local code), outlets,
conduits, input power wires, door interlock switches (if required) and power for x-ray in use
lamps or any external monitors. If existing conduit, junction boxes, circuit switches or
raceway is to be used, specific details on conduit routing, junction box size and locations,
amp ratings for circuit switches must be given to GE Healthcare for development of the site
plan. It is important that conduits be properly terminated at their wall or ceiling entrance and
exit at junctions boxes. The depth of the junction box depends upon the number of cables
being terminated at the box.
In order to install the components, a maximum length of 49 ft 2.55 in (15 m) of cable is
provided from the table to the HiRis/Generator cabinets. Taking into account ceiling height,
service loop, etc, this allows for a maximum conduit run of 34 ft. It is recommended that the
Customer determines the actual path and conduit length with a cable snake to ensure that
the conduit or raceway length does not exceed the maximum allowed.

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The GE Site Plan recommends the conduit or raceway routing for the installation. If the rout-
ing is changed from the Site Plan recommendation, make a change on the site plan, initial it,
and return a copy to GE Site Planning Department before beginning construction

Note
It is very important that the Customer’s building engineer is di-
rectly involved in planning cable, conduit and raceway routing
for the electrical connections to be made to the room and be-
tween the Uroview® 8K urology system components.

Note
The Uroview® 8K is in compliance with the National Electric
Code (NEC) 1999 Edition, Published by the National Fire Pro-
tection Agency (NFPA) and Canadian Electric Code (CEC),
C22.1-1998.
Installation at Health Care Facility shall comply with local and
state laws. Please consult your local Jurisdiction of Authority in
your area.

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6.2 System Electrical Requirements

The Uroview® 8K system will require three-phase 400 VAC - 480 VAC power for the genera-
tor and 115 VAC single phase for the BOSS box.
The Uroview® 8K Table has been designed and tested to meet the requirements of
IEC 60601-2-46 with the exception of Clause 49.101, which relies on hospital back up power
to provide the means to move the table to the normal position. If it is necessary to meet the
requirements of IEC 60601-2-46 Clause 49.101 (interruption of power supply) it is the opera-
tor’s responsibility.
The mains power for Generator and BOSS must be routed via a 30 mA fault current operated
circuit breaker installed on site. Installation in a room must comply with DIN VDE 0100-710.
In all countries other than the Federal Republic of Germany, primarily the statutory national
regulations must be complied with.
Since there are many variations between domestic and international voltages, please refer to
chapters 6.2.3 Apparent Resistance of the Supply Mains, for proper mains loading and ser-
vice sizing.
The Uroview® 8K requires a common ground, common potential input power. The grounding
must be connected to a facilities common ground point at the service panel. A common po-
tential, common ground power can be achieved by the following method described below:
 Input voltages must connect to shunt trip circuit breakers. An EMO (Emergency
Off) positive lock type switch must be installed to shunt trip circuit breakers to dis-
connect all main system power.
 Optional a dedicated circuit breaker for 3p can be setup with control by the BOSS
Refer to 6.2.2.1 Optional circuit breaker for 3p controlled by BOSS.
Note
For proper Uroview® 8K operation, it is necessary to have the
cleanest power. Power and grounding issues should be re-
solved and corrected before installation of the Uroview®8K.
GE Healthcare does have power and grounding auditors avail-
able to evaluate facility power and recommend repairs (if appli-
cable) that must be made in order to ensure that the cleanest
power can be provided. All costs related to repairing and/or in-
stallation of power and grounding components shall be the sole
responsibility of the Customer. If power and grounding issues
(if applicable) are not resolved it can cause Uroview®8K relia-
bility and operational problems, leading to intermittent machine
failure.

Line Regulation
Total branch circuit regulation or voltage drop not to exceed 6 % maximum. Wiring is
calculated for a 2 % maximum voltage drop (regulation), reserving a maximum 4 % volt-
age drop (regulation) available for the transformer.

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6.2.1 BOSS
The BOSS shall be connected to the facility power.
The BOSS is wall mounted and will require a permanent, dedicated 115 VAC single phase
circuit with a L/N/G configuration. It is recommended to fuse it with 115 VAC / 20 Amp
(Type C).
An isolated 60/G/60 configuration or LIM power cannot be used.
The 1p power distribution will source the following parts of the device on separate lines:
 Uroview® 8K Table
 MAVEN
Each output line is internally fused.
The connecting cables for these system components with the BOSS are included in the
delivery. For cable length see Fig. 11-6.

6.2.2 Generator CPI INDICO IQ® 65 / 80 kW

The Generator for the Uroview® 8K urology system will require (1) high voltage source
(X-Ray generation).
Two generator sizes are available:

Standard 65 Kilowatt, Three Phase Generator (400 VAC - 480 VAC Three Phase 4
wire input)

Optional 80 Kilowatt, Three Phase Generator (400 VAC - 480 VAC Three Phase 4
wire input)
Both kinds of generator requires 3 phase legs and ground (no neutral line). The three phase
input can be connected directly to the generator.
Mains voltage

Power output 65 kW 80 kW
Mains voltage, three phases 400 V – 480 VAC 400 V – 480 VAC
AC line frequency 50/60 Hz 50/60 Hz
AC line configuration 3 N~ 3 N~
Main resistance per phase 0.13 Ω – 0.19 Ω 0.11 Ω - 0.15 Ω
Maximum deviation of line 10% 10%
135 A (400 VAC) – 168 A (400 VAC) –
Momentary current
110 A (480 VAC) 140 A (480 VAC)
Standby current1) <0,5 A <0,5 A
Tab. 6-1

1) Standby Current: This is the current that the generator draws when it is “idle”; i.e. with the
generator switched on and filaments at standby level. External or installer- supplied equipment
connected to the generator may increase the standby current beyond the values shown.

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Minimum Generator Minimum Minimum Minimum Apparent

Recomended Momentary Recomended Recommended Recom- Mains
Mains Mains Line Generator Distribution mended Resistance
Voltage Disconnect to Current Service Transformer Ground
Generator Rating Rating Wire Size
15ft/5m max.
65 kW 3 Generator
400 #6* 135 A 100 A 85 kVA #6** 0.13 Ω
VAC (13.3mm2) (13.3mm2)
480 #6* 110A 100 A 85 kVA #6** 0.19 Ω
VAC (13.3mm2) (13.3mm2)
80 kW 3 Generator
400 #6* 168 A 100 A 105 kVA #6** 0.11 Ω
VAC (13.3mm2) (13.3mm2)
480 #6* 140 A 100 A 105 kVA #6** 0.15 Ω
VAC (13.3mm2) (13.3mm2)
Tab. 6-2
 All wiring and grounding must comply with local electrical codes.
Maximum size for the ground wire is #4 AWG (21 mm2)
*Maximum wire gauge is #4 AWG (21 mm2)
 All wire must be copper

6.2.2.1 Optional circuit breaker for 3p controlled by BOSS

Optional a dedicated circuit breaker for 3p can be setup controlled by the BOSS and it’s
EMO. The control output line for the circuit breaker is internally fused with 115 VAC/0.5 Amp.
The dedicated circuit breaker shall have following characteristics:

Description Value
Utilisation category AC-3
Poles description 3P
Power pole contact composition 3 NO
Rated operational voltage > 550 V AC at 50/60 Hz
Rated operational current > 110 A (≤ 55°C) at ≤ 440 V AC-3
Control circuit voltage 115 VAC, 50/60 Hz
Overvoltage category III
Average impedance ≤ 0.6 mΩ - lth 200 A for power circuit
IEC/EN 60947
Standards UL
CSA if applicable
600 V for power circuit certification CSA / UL
Rated insulation voltage
600 V for signaling circuit certification CSA / UL
Hold-in power consumption < 50 VA at 20°C
Ambient air temperature for operation ≥ 0°C…≤ 50°C
Connections - terminals Must fit flexible cable with/without cable end
Tab. 6-3

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6.2.3 Apparent Resistance of the Supply Mains

Components

Fuse (Fuse
protection)
Frequency
Tolerance
Voltage

Current

Phases
Type

VA
Uroview® Uroview® 100 VAC 1600 VA +/- 10 % 16 A 50/60Hz L/N/PE
16/10 A
Table –
240 VAC 1600 VA 6.7 A
Generator CPI
INDICO 100 A
IQ® 400 VAC 54 - 135°A – L1, L2, * Minimum

65 kW – 52.8kVA +/- 0 % 110°A 50/60Hz L3/PE recom-

480 VAC mended

67.2 kVA 168°A – Generator

80 kW 144°A Service Rat-

ing

HIRIS HIRIS 230 VAC 700 VA +/- 10 % 3A

Detector RF43/FL 230 VAC 130 VA +/- 10 % 0,57°A

Monitor Dell 100-240 360VA +/- 10 % 1.5 A- L/N/PE 10°A via

50/60Hz
2418HT VAC BOSS

or 100-240 200 VA- +/- 10 % 2-0.4A

VAC 96 VA
FS-Y1901D
Support
Monitor 1 100 VAC
120 VA 1.2 A – 50/60 2°A via
C83W+ – +/- 10 % L/N/PE
Support max. 0.5 A Hz Table
240 VAC
Monitor 2
Tab. 6-4

6.2.4 X-Ray On Lamp

The X-Ray On Lamp is a part of the delivery. The X-Ray On Lamp is connected to the gener-
ator. Additional to the flashing light an auditive signal is provided. X-Ray On Lamp must be
installed so that they can easily be recognized from each working place.

6.2.5 Networking
If the Uroview® 8K system is integrated into a medical network, the operator must ensure the
safety / security of the network according to the current state of technology.
The standard "Common Criteria for Information Technology Security Evaluation (CC)"
(ISO / IEC 15408-1) must be observed.
Network security concerns only image software.

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6.2.6 Door Interlock Switches (if applicable)

The door interlock switches can be connected to the generator with a 18 AWG cable for each
door interlock switch. Maximum cable voltage is 30 VDC.

Use configuration A or configuration B as described below, depending on the desired mode

of operation to wire the room door interlock.

Configuration A
This configuration inhibits new exposures if the room door is open. This does not interrupt
exposures in progress when the door is opened.
The door interlock switch connects to the room door interlock inputs.

Configuration B
This configuration inhibits new exposures if the room door is open, and stops fluoro expo-
sures if the room door is opened during a fluoro exposure. A double-pole type room interlock
switch is required for this configuration.
One pole on the door interlock switch is connected to the room door interlock inputs on the
room I/O board. One side of the second pole on the door interlock switch connects to one
terminal on the remote fluoro exposure input, and one side of the fluoro footswitch connects
to the second terminal on the remote fluoro exposure input on the room I/O board. The free
side of the room interlock switch and the free side of the fluoro footswitch should be spliced
together using a suitable insulated connector. This connects the door interlock switch and the
fluoro footswitch in series across the remote fluoro exposure input on the room I/O board.

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7 System Component Thermal H.V.A.C. Considerations

SYSTEM COMPONENT HEAT OUTPUT

Uroview® 8K TABLE 1092 BTU/H ≈ 320 W

The maximum heat output of the generator is approxi-
CPI Generator mately 22 W(75BTU/h) during stand by and approxi-
mod. stand by mately 1025 W (3500BTU/h) during fluoroscopic oper-
mode fluoroscopy ation. The heat output of the Console is less than
30 W (100BTU/h)
HIRIS (without monitor) 512 BTU/H ≈ 150 W

MAVEN
290 BTU/H ≈ 85 W
(UPS and medical transformer)

Detector 110 BTU/H ≈ 30 W

Power Supply Detector 34 BTU/H ≈ 10 W

Monitor (Workstation HIRIS)
Standby Mode 70 BTU/H ≈ 20 W
Maximum 210 BTU/H ≈ 60 W
Monitor 1 / 2 (27“)
Standby Mode 20 BTU/H ≈ 6 W
Maximum 85 BTU/H ≈ 25 W
Wall box BOSS 34 BTU/H ≈ 10 W
Tab. 7-1

8 System Component Weight Measurements

SYSTEM COMPONENT Weight (lbs / kg)

Uroview® 8K TABLE
(unloaded, incl. X-ray tube, collimator, Monitor 1874 lbs / 850 kg
support arm without monitors)
Uroview® 8K TABLE
2502 lbs / 1135 kg
(with max. table load)
Generator Cabinet with HV Modul 200 lbs / 91 kg
Workstation (HIRIS) 278 lbs / 126 kg
MAVEN
115 lbs / 52 kg
(including Uninterrupted Power Supply (UPS))
BOSS (Emergency Stop + ON/OFF Switch) 5,7 lbs / 2,6 kg
Membrane R&F Console 8 lbs / 3.7 kg
Uroshelf 95 lbs / 43 kg
Tab. 8-1

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Pausch Medical GmbH Uroview® 8K Shipping Crate Information

9 Uroview® Installation Information

All Uroview® 8K urology system components must be maneuvered around corners, through
doors, under lights and into elevators, and elevator lifting capacity. The delivery path must be
taken into consideration to accommodate ease of transporting Uroview® 8K components into
proposed installation site. If facility does not have loading dock it will be necessary to ship
equipment on trucks with a lift gate. Door width must be a minimum of 42 inches (106 cm).
For complete dimensions and shipping weights of each component of the Uroview® 8K,
please see the chapter 10.

The dimensions for the transport

of the Uroview® 8K Table with the
Pausch Mounting Aid (1) are:
L= 78.35 in / 1990 mm
W= 45.28 in / 1150 mm
H= ca. 73.63 in / 1870 mm
The dimensions are valid only
when the X-ray tube support arm
was not installed after the delivery
of the device. Fig. 9-1

10 Uroview® 8K Shipping Crate Information

The dimensions shown here represent the Uroview® 8Ksystem on its shipping pallet(s).
The transport dolley (provided in jack & wheel crate) attaches to the Uroview® 8Kfor transpor-
tation throughout the facility. With the transport dolley attached, dimensions
are as follows: 34 in(W) [860 mm] x 72 in(L) [1830 mm].
Dimensions Weight
Palette (LxWxH)
Uroview® 8K 80.71 in x 39.96 in x 74.41 in
1984 lbs / 900 kg
(unloaded) 2050 mm x 1015 mm x 1890 mm

Uroview® 8K 94.09 in x 29.53 in x 23.62 in

308 lbs / 140 kg
Monitor support arm 2390 mm x 750 mm x 600 mm
Uroview® 8K 881 lbs / min. 400 kg
Generator; Workstation 80.71 in x 39.96 in x 74.41 in Depending on the ac-
(Hiris); Cabinet MAVEN; 2050 mm x 1015 mm x 1890 mm cessories which are in
Components) the delivery
Uroview® 8K 77 in X 26 in X 19 in
-------------------------
Jack & and Wheel Crate 1960 mm x 660 mm x 480 mm
Tab. 10-1

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Customer:

Address:

City: State: Zip:

Customer Contacts:

Department:

GE OEC Sales Representative:

Circle YES or NO for the following questions.

Any YES answers must be reflected in the Site Survey Sketch

1. Is there any existing equipment in the room? Yes No

2. Does the room have an existing floor drain? Yes No

3. Is the floor drain position (dimensions) labeled on the drawing? No Yes

4. Will cabling be run through the floor? Yes No

Is there existing conduit and/or cable raceways?
5. Yes No
(if answer is yes, please list ALL conduit and/or raceway sizes)
6 The quality of concrete has been validated. Yes No

7. Can architectural or electronic drawings be obtained? Yes No

8. Is there any existing casework (i.e. shelves, cupboards, sinks, etc)? Yes No

9. Is the main patient entrance noted? Yes No

Are there any anesthesia gas drops?
10. Yes No
(if answer is yes please note proper placement on drawing)
11. Are there any support structures, abutments, etc in the room? Yes No
Are there any existing AC supply boxes, switches, or breakers?
12. Yes No
(if answer is yes please note locations of each on drawing)
Are there any ceiling obstructions?
13. Yes No
(i.e. monitor suspensions, surgical lights, etc.)
Are there any wall obstructions?
14. Yes No
(i.e. view boxes, phones, lead glass, etc)

15. Is three phase power available? Yes No

16. Is equipment delivery path adequate? Yes No

17. Is emergency back up power available? Yes No

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 Site Planning Guide
Pausch Medical GmbH Uroview® 8K Shipping Crate Information

Site Survey Sketch (Scale= 1/4" = 1'0)

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Uroview® 8K Shipping Crate Information

Site Survey Sketch (Scale= 1/4" = 1'0)

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 Site Planning Guide
Pausch Medical GmbH System integration of the Uroview® 8K

11 System integration of the Uroview® 8K

11.1 Floor laying of the cables
Upon shipping the equipment, the cables for the X-ray tube, collimator, detector etc. are al-
ready laid and installed in the equipment, as shown in Fig. 11-1. The installation is suitable
for cable laying on the floor or in the floor.

When laying the cables on the floor, the

cables are guided through the opening
(Fig. 11-1/10) on the rear wall and then laid
horizontally (9) out of the equipment to the
target.

Fig. 11-1

When laying the cables in the floor, the

cables are vertically guided into the pre-
pared opening (UF) in the floor and then Fig. 11-2
laid to the target. The supplied cover is to
be assembled via the opening in the rear
wall (Fig. 11-2/10). See also Fig. 11-3.

Fig. 11-3

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System integration of the Uroview® 8K

11.2 Ceiling (Wall) mounted Junction Box

dimensions in inches (millimeters)
When laying the cables
above the ceiling, the ca-
bles are guided into the
rear wall (2) and upwards
to a junction box (1.1) in
the ceiling. It is also possi-
ble to install the junction
box on the wall below the
ceiling.
The parts for this version of
cable laying are not in-
cluded in the standard
scope of delivery and have
to be ordered extra.

1 Junction Box
1.1 Ceiling mounted
1.2 Wall mounted

2 Uroview® 8K Backpack

3 Uroshelf

4 Monitor Travel Area

Area in which the mon-

A itor support arm can
collide with the wall.

Fig. 11-4

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Pausch Medical GmbH System integration of the Uroview® 8K

11.3 Room example – Uroview® 8K system

Fig. 11-5

1 Uroview® 8K Table 7 Monitor support arm with Portegra 2

2 Detector, Grid, Measuring chamber 8 Medical Display 27”
3 X-ray tube 9 Emergency Instructions
4 Collimator 10 Uroshelf (US)
Digital imaging system 11 X-ray In Use Lamp (XL)
5 HIRIS Workstation and MAVEN (5.1); BOSS with Emergency off Switch
Monitor and keyboard (5.2) 12
(EMO) an ON / OFF switch
Generator Option: Column with radio protection
13
6 Power cabinet (6.1) shield and operatory light
Membrane R&F Console (6.2) 14 Option: EXECUTOR
Tab. 11-1

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System integration of the Uroview® 8K

11.4 Uroview® System - Power Supply

Fig. 11-6

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Pausch Medical GmbH Drawings

12 Drawings
12.1 Uroview® 8K Table
left hand verson

Fig. 12-1

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Drawings

right hand version

Fig. 12-2

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Pausch Medical GmbH Drawings

Uroview® 8K Base Plate and drilling pattern

dimensions in inches (millimeters)

Fig. 12-3

FD = recommended range for the floor outlet

UF= recommended range for the inlet with under-floor cable laying

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Drawings

12.2 Generator CPI INDICO IQ® 65 / 80 kW

Power cabinet

Fig. 12-4

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Pausch Medical GmbH Drawings

Seismic Centers and mounting hole locations

Depending on your installation requirement, the mounting holes can be used if seismic
mounting is necessary.

Fig. 12-5

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Drawings

Membrane R&F Console

dimensions in millimeters (inches)

Fig. 12-6

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Pausch Medical GmbH Drawings

12.3 Workstation HIRIS RF43/FL with MAVEN

dimensions in inches (millimeters)

Fig. 12-7

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Drawings

12.4 Monitor support arm

left hand version

Fig. 12-8
*) Depending on the distance of the device to the rear room wall

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Pausch Medical GmbH Drawings

right hand version

Fig. 12-9
*) Depending on the distance of the device to the rear room wall

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Drawings

12.5 Uroshelf
dimensions in inches (millimeters)

Fig. 12-10

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Pausch Medical GmbH Drawings

12.6 Ceiling (Wall) mounting of the junction box

dimensions in inches (millimeters)

Fig. 12-11

CM = ceiling mounting
WM = wall mounting

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Drawings

12.7 X-ray in Use Sign

Fig. 12-12

dimensions in inches (millimeters)

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Pausch Medical GmbH Drawings

12.8 BOSS
dimensions in inches (millimeters)

Dimensions for Wall Mounting

Fig. 12-13

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Drawings

12.9 EXECUTOR (option)

Name of components and dimension drawing (standard delivery hand-held operating unit
right - It is possible to remodel the assembly that the hand-held operating controll unit is on
the left side.

Fig. 12-14

1 Emergency-Stop 3 Holder for hand-held operating unit 5 Connectors for plugs

2 Cabinet 4 Mounting strip 6 Connector cable interface
Drilling pattern (standard delivery hand-held operating unit right)

Fig. 12-15

1 drilling template 2 Mounting strip of the EXECUTOR

Using the drilling template, drill the 3 holes for the dowels / screws at the desired mounting
location.

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Pausch Medical GmbH Index

13 Index

A Monitor support arm .........................16, 52

Address ................................................... 5 N
B Networking ............................................ 34
Baseplate ........................................ 24, 47 O
BOSS .............................................. 27, 57 Operating conditions ............................. 17
C P
Cable length .......................................... 44 Power cabinet ..................................20, 48
Ceiling height ........................................ 15 Power Supply........................................ 44
Console ............................... 20, 27, 36, 50 R
D Room example ...................................... 43
Dimensions ........................................... 37 S
Door Interlock Switch ............................ 35 Site Survey Sketch.............................8, 39
Door width ............................................. 37 T
Drain ............................................... 15, 47 Table Location Limitations .................... 16
G Transport .........................................17, 37
Generator ............................ 22, 27, 32, 36 U
H Uroshelf ............................... 21, 28, 36, 54
HIRIS .................................................... 51 V
I Version
Installation site ........................................ 8 left hand .............................................. 7
L right hand ............................................ 7
Lamp ............................................... 34, 56 W
Weight ....................................... 24, 36, 37
M
Manufacturer ........................................... 5 Workstation .................... 20, 22, 26, 36, 51
MAVEN ..................................... 26, 43, 51

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