Richard Wolf ENDOCAM 552510 Series User manual

GA-A282 /en /2018-04 V10.0 / PK17-9038
Logic HD Camera Controller
ENDOCAM
552510x
Instruction Manual
Logic 4K Camera Controller
ENDOCAM
5525301

0
GA-A282
Important general instructions and notes for use
Make sure that the product is only used as intended by adequately trained and qualified medical personnel following
the instruction manual Maintenance and repair must be carried out by authorized experts.
Use the product only in the combinations and with the accessories and spare parts specified in this instruction manual.
Use other combinations, accessories and replacement parts only if they are expressly intended for the planned appli
cation and if the performance characteristics and safety requirements are met. The product must not be altered in any
way.
Reprocess the product in accordance with the manual before every use and before return shipment to protect the pa
tient, user and third parties.
This manual is an integral part of the product and must be stored in such a way that it is accessible at any time during
its entire life cycle. This manual must be passed on to any subsequent owner or user.
Immediately on receipt, check the product and its accessories for completeness and possible damage. Should the
shipment give rise to complaints, please inform the manufacturer or supplier immediately.
Subject to technical changes!
Due to ongoing developments the illustrations and technical data may deviate slightly.
Safety instructions and levels of danger
Symbols Level of danger
WARNING!
Failure to observe can result in death or serious injury.
CAUTION!
Failure to observe can result in slight injury or damage to the product.
.
IMPORTANT!
Failure to observe can result in damage to the product or surroundings.
.
NOTE!
Tips for optimum use and other useful information.
GERMANY
RICHARD WOLF GmbH
75438 Knittlingen
Pforzheimerstr. 32
Telephone: [phone]
Telefax: [phone]
MANUFACTURER
[e-mail]
www.richard-wolf.com
USA
RICHARD WOLF
Medical Instruments Corporation
353 Corporate Woods Parkway
Vernon Hills, Illinois 60061
Toll Free: 001 (800) 323 - 9653
Phone: [phone] - 1113
Fax: [phone] - 1488
[email protected]
www.richardwolfusa.com
UK
RICHARD WOLF UK Ltd.
Waterside Way
Wimbledon
SW17 0HB
Telephone: + 44 20 89 44 74 47
Telefax: [phone]
[email protected]
www.richardwolf.uk.com
BELGIUM / NETHERLANDS
N.V. Endoscopie
RICHARD WOLF Belgium S.A.
Industriezone Drongen
Landegemstraat 6
9031 Gent Drongen
Telephone: [phone]
Telefax: [phone]
[email protected]
www.richard-wolf.be
FRANCE
RICHARD WOLF France S.A.R.L.
Rue Daniel Berger
Z.A.C. La Neuvillette
F-51100 Reims
Telephone: [phone]
Telefax: [phone]
[e-mail]
AUSTRIA
RICHARD WOLF Austria
Ges.m.b.H.
Wilhelminenstraße 93 a
A-1160 Vienna
Telephone: [phone]
Telefax: [phone]
[email protected]
www.richard-wolf.com
Marketing Office
U.A.E
RICHARD WOLF Middle East
P.O. Box 500283
AL Thuraya Tower 1
9th Floor,
Room 904, Dubai
Telephone: + 9 71 43 68 19 20
Telefax: + 9 71 43 68 61 12
[email protected]
www.richard-wolf.com
INDIA
RICHARD WOLF India Private Ltd.
JMD Pacific Square
No. 211 A, Second Floor
Behind 32nd Milestone
Gurgaon - 122 001
National Capitol Region
Telephone: + 91 12 44 31 57 00
Telefax: [phone]
[email protected]
www.richard-wolf.com

Contents
I
GA-A282
1 General information 1.........................................................
1.1 Symbols 1..................................................................
1.2 Symbols on handheld remote control (option) 2..................................
1.3 Intended use 3..............................................................
1.3.1 Performance characteristics 3.................................................
1.4 Indications and field of use 3..................................................
1.5 Contraindications and side effects 4............................................
1.5.1 Contraindications 4...........................................................
1.5.2 Side effects 4................................................................
1.6 License agreements 4........................................................
1.6.1 AVC Patent Portfolio License 4................................................
1.7 Combinations 5..............................................................
1.7.1 Equipotentality 6.............................................................
1.7.2 Requirements for the products / components of a combination 7....................
1.8 Electromagnetic compatibility (EMC) - IEC 60601-1-2 : 2007 8.....................
1.9 Electromagnetic compatibility (EMC) - IEC 60601-1-2 : 2014 10.....................
1.10 Connection diagram - Camera Controller in video mode 12.........................
2 Illustration 13.................................................................
2.1 Front view - Camera Controller for all models 13..................................
2.2 Rear view - Logic HD Camera Controller 552510x 14..............................
2.3 Rear view - Logic 4K Camera Controller 5525301 15...............................
2.4 Illustration of handheld remote control unit (option) 16..............................
3 Setup 17.....................................................................
3.1 Connection to the core nova system 19..........................................
3.2 Preparation 19................................................................
3.3 Selecting the menu language 20................................................
3.4 Setting the keyboard layout 20..................................................
3.5 Setting date and time 20.......................................................
3.6 Color bar test chart 21.........................................................
3.7 Adjusting LCD monitors 21.....................................................
4 Checks 22...................................................................
4.1 Visual check 22...............................................................
4.2 Function check 22.............................................................
5 Application 23................................................................
5.1 Operation 23.................................................................
5.2 Control elements and operating modes 24........................................
5.2.1 "Dialog" function 24...........................................................
5.2.2 Special Imaging Mode (SIM) 24.................................................
5.2.3 Automatic brightness control (ELC) 27...........................................
5.2.4 Temperature protection circuit 27................................................
5.2.5 Menu control via touchscreen 28................................................
5.2.6 Menu control via monitor with handheld remote control (option) 28...................
5.2.7 Menu control via monitor with PC keyboard (option) 28.............................
5.3 Menu levels 29...............................................................
5.4 Menu control via monitor with handheld remote control or PC keyboard 29............

II GA-A282
5.4.1 Overview - menu structure - "operation" main menu 29.............................
5.4.2 Overview - menu structure - "Settings" main menu 30.............................
5.4.3 Overview - menu structure - "Image archive" menu 31.............................
5.4.4 Description of the "Settings" submenus 32........................................
5.4.5 Patient Data Input 33..........................................................
5.4.6 Status display for camera head button actions 33..................................
5.4.7 Symbols and display in the status line at the lower edge of the sceen. 34.............
5.4.8 On-screen display of blue light mode 35..........................................
5.4.9 Display of function key assignment 35...........................................
5.5 Archiving with PIP camera controller (Option) 36..................................
5.6 Menu control via touchscreen functions on device 37..............................
5.6.1 Overview - menu structure 37...................................................
5.6.2 Touchscreen menus 38........................................................
5.6.3 Description of "Menu" on touchscreen 40.........................................
5.7 Operation of camera controller 41...............................................
5.7.1 General notes on the operation within the core nova system 41.....................
5.7.2 Automatic white balance (AWB) 42..............................................
5.7.3 Displaying and editing 43.......................................................
5.7.4 Image brightness 43...........................................................
5.7.5 Detail 43.....................................................................
5.7.6 Electronic zoom 43............................................................
5.7.7 Measurement window (endoscopic image adaptation) 43...........................
5.7.8 Image flip (mirror image) 44....................................................
5.7.9 Connecting the USB storage medium 44.........................................
5.7.10 USB printer 44................................................................
5.7.11 Taking out of service 44........................................................
5.8 Overview of system messages 45...............................................
5.8.1 Structure of system messages 45...............................................
5.8.2 Message types 45.............................................................
5.8.3 Functionality of control elements 45.............................................
5.8.4 Operating messages (green) 46.................................................
6 Operation in the core nova system 49............................................
6.1 Operation in the core nova system 49............................................
6.2 Combining and controlling the device 49.........................................
6.3 Connection to the core nova system 50..........................................
7 Reprocessing and maintenance 51..............................................
7.1 Reprocessing of device 51.....................................................
7.2 Reprocessing of camera head 51...............................................
7.3 Maintenance 51...............................................................
7.3.1 Maintenance intervals 51.......................................................
8 Technical description 52.......................................................
8.1 Troubleshooting 52............................................................
8.1.1 Device error 52...............................................................
8.1.2 Fault in video mode 53.........................................................
8.1.3 Error in the core nova system 54
................................................
8.1.4 Displays on the monitor 55.....................................................
8.2 Technical Data 56.............................................................

Contents
III
GA-A282
8.2.1 Camera controller extension options 57..........................................
8.2.2 Input interfaces 57............................................................
8.2.3 Output interfaces 58...........................................................
8.3 Operating, storage, transport and shipping conditions 59...........................
8.4 Spare parts and accessories 60.................................................
8.5 Replacing parts 61............................................................
8.5.1 Device fuses 61...............................................................
8.5.2 Disposal of product, packaging material and accessories 61........................

1GA-A282
1 General information
1.1 Symbols
Symbols Designation
Attention, Caution
Follow the instruction manual
OFF (no power supply, separation from mains)
On (power: connection to the power/mains)
Equipotentality
Fuse
μAlternating current (AC)
TYPE CF APPLIED PART
Camera head connector
USB interface
Data input
Data output
Network, LAN (Ethernet) interface
Manufacturer
Manufacturing date
-25_C+50_CMaximum temperature range for shipment, transport and storage
XX°
XX°
Permissible temperature range
XXhPa
XXhPa
Permissible atmospheric pressure range
XX%
XX%
Permissible humidity range
Recycle the product separately. Do not discard together with other waste.
A Registered Trademark of a Recognized Testing Laboratory, confirm the compliance to the standard
of Medical Electrical Equipment CAN/CSA C22.2 No.6011 (c) and UL606011 (us)

2
GA-A282
Designation
Symbols
A Registered Trademark of a Recognized Testing Laboratory, confirm the compliance to the standard
of Medical Electrical Equipment CAN/CSA C22.2 No.60601-1 (c) and ANSI/AAMI ES60601-1 (us)
Identification in conformity with medical devices directive 93/42/EEC only valid if the product and/or
packaging is marked with this symbol. Products of category IIa and above, as well as sterile products
or products with measuring function of category I, are additionally identified with the code no. of the
notified body (0124).
1.2 Symbols on handheld remote control (option)
Symbols Designation
"Escape" or "back"
“Up"
"left" or "minus"
"right" or "plus"
"down"
OK button for confirmation
Function key I
Function key II

3GA-A282
1.3 Intended use
The products Logic HD Camera Controller 552510x and Logic 4K Cam
era Controller 5525301 are used for visualizing natural or artificially cre
ated hollow spaces through images generated by a rigid or flexible endo
scope via natural or surgically created passages within the scope of
diagnostic or therapeutic medical endoscopy.
The Camera Controller is equipped with different output connectors
(USB, video, S-video, etc.) to which USB storage media, image storage
devices and other video devices for recording and storing video images
and video sequences can be connected.
This product is designed exclusively for use by specialized medical per
sonnel and may only be applied by medically qualified and adequately
trained persons.
1.3.1 Performance characteristics
- Image recording.
- Signal processing of the image data.
1.4 Indications and field of use
This product is used for diagnosis and therapy in conjunction with endo
scopic accessories.
On the basis of the patient’s general condition, the user in charge must
decide whether the planned use is possible or not. For further notes and
instructions please refer to the latest medical literature.
CAUTION!
The device may fail!
For therapeutic applications, a second camera with the same specifica
tions should be available.
. NOTE!
We recommend reading relevant literature for the planned application.

4
GA-A282
1.5 Contraindications and side effects
1.5.1 Contraindications
Contraindications directly related to the product are presently unknown.
On the basis of the patient's general condition the doctor in charge must
decide whether the planned use is possible or not.
For further notes and instructions please refer to the latest medical litera
ture.
1.5.2 Side effects
Side effects directly related to the product are currently unknown.
1.6 License agreements
This product contains open-source software from other suppliers which
are subject to the GNU license agreements GPL (GNU General Public
License), LGPL (GNU Library/Lesser General Public License) and/or
Apache license agreements.
The license texts of the GPL, LGPL and Apache license as well as the
source code of the corresponding software components are available on
the storage medium accompanying the device.
Please read the precise wording to be informed about your rights relating
to the aforementioned licenses.
1.6.1 AVC Patent Portfolio License
THIS PRODUCT IS LICENSED UNDER THE AVC PATENT PORTFO
LIO LICENSE FOR THE PERSONAL USE OF A CONSUMER OR
OTHER USES IN WHICH IT DOES NOT RECEIVE REMUNERATION
TO (i) ENCODE VIDEO IN COMPLIANCE WITH THE AVC STANDARD
("AVC VIDEO") AND/OR (ii) DECODE AVC VIDEO THAT WAS EN
CODED BY A CONSUMER ENGAGED IN A PERSONAL ACTIVITY
AND/OR WAS OBTAINED FROM A VIDEO PROVIDER LICENSED TO
PROVIDE AVC VIDEO. NO LICENSE IS GRANTED OR SHALL BE IM
PLIED FOR ANY OTHER USE. ADDITIONAL INFORMATION MAY BE
OBTAINED FROM MPEG LA, L.L.C.
SEE HTTP://WWW.MPEGLA.COM

5GA-A282
1.7 Combinations
Logic HD Camera Controller 552510x and Logic 4K Camera Controller
5525301 must only be used in combination with the camera heads and
sensor endoscopes approved by Richard Wolf and following the corre
sponding instruction manual.
From software version R19 (>1.3.x), Logic HD Camera Controller
552510X and Logic 4K Camera Controller 5525301 feature white light,
blue light and special modes in Special Imaging Mode SIM.
In blue light mode, blue light applications are possible in combination with
system components suitable for PDD fluorescence diagnostics.
In white light mode, the white light special modes (e.g. HDR) are only
possible in combination with suitable system components.
The device automatically detects whether suitable system components
for the corresponding application are connected and only if so, the corre
sponding mode can be activated.
. IMPORTANT!
For operation in blue light mode please observe instruction manual GA-
A324 for the blue system.
. IMPORTANT!
Connect only USB accessories tested and approved by Richard Wolf to
the USB interfaces. Otherwise interference or malfunction cannot be ex
cluded.
. IMPORTANT!
The installation of the entire product including the configuration setting via
the core nova system must be carried out by an authorized and trained
expert.
. IMPORTANT!
Do not connect the device to other networks, such as the hospital in-
house network via the LAN (Ethernet) interface.
The device may only be connected within the core nova system via the
LAN (Ethernet) interface.
. IMPORTANT!
In addition to this manual follow the latest manuals of the products used
in combination with this product.
Only components approved for the core nova system may be connected.
For further information please contact Richard Wolf or your representa
tive.
. IMPORTANT!
The OR network must be galvanically isolated from the hospital network,
e.g. by:
- optical network cables with the corresponding optical transceiver for
the network switch.
- a network isolator for medical devices.
. IMPORTANT!
Close any LAN (Ethernet) sockets in the network switch that are not used
with the corresponding plastic caps.

6
GA-A282
1.7.1 Equipotentality
The potential equalization cable represents a direct connection between
a medical electrical device and a potential equlization rail.
It serves to equalize differences in potential between enclosures of elec
trical equipment and firmly installed conductive parts in the patient envi
ronment.

7GA-A282
1.7.2 Requirements for the products / components of a combination
1.5m
IEC 60601-1, 3. Ed.
1.5m
1.5m
The general requirements depend on whether the products / com
ponents are inside or outside the patient environment.
Medically used room Non-medically
used room
Requirements / measures
inside the
patient environment
outside the
patient environment
Leakage currents to section 16.6
IEC 60601-1:2005 / EN 60601-1:2006 *
MP MP
~~- - Verification of the total patient leakage current
MP MP
~**
-
-
Verification of leakage currents
a) additional protective earth connection
(consult the corresponding manufacturer),
or
b) additional isolating transformer for medical applications **
MP
~
NMP
~*
*
MP NMP
~**
NMP
~
MP
MP NMP
~
MP MP / NMP
~**
MP
~
NMP
~-
Verification of leakage currents
a) no plugs with metal housing, or
b) additional isolation device (to avoid voltage differentials)
MP
~
MP / NMP
~
Verification of leakage currents
a) common protective earth connection, or
b) additional protective earth connection at MP (clarify with the corre
ponding manufacturer), or
c) additional isolation device (to avoid voltage differentials), or
d) no plugs with metal housing in the patient environment
additional "isolating transformer" to IEC/ EN60601-1
**
additional isolating device to IEC/
EN 60601-1 Multiple socket strip
Functional connection ~Power supply grid
MP =medical electrical device to IEC/ EN 60601-1, ANSI/AAMI es60601-1, CSA C22.2 No. 60601-1
NMP =non-medical electrical device in accordance with product-specific IEC/EN/UL standards
*When connected via the same multiple socket strip under standard conditions, the earth leakage current of the socket strip must not exceed 5 mA.
** e.g. Richard Wolf video cart with "isolating transformer"
Only connect devices with a safety extra-low voltage of no more than 60 V DC / 42.4 V AC peak to the connectors for electrical connections, i.e. the signal
inputs and outputs.

8
GA-A282
. IMPORTANT!
Persons combining products to form a system are responsible for not impairing the system's compliance with perfor
mance and safety requirements, and that the technical data and the intended use are adequately fulfilled.
Possible electromagnetic or other interference that may occur between the product and other products can cause
faults or malfunctions.
When selecting the system components, make sure that they meet the necessary requirements of the medical envi
ronment they are used in, in particular IEC/ EN 60601-1
. In case of doubt contact the manufacturer(s) of the system
components.
Do not touch connectors for electrical connections between various components (such as signal input connectors
and signal output connectors for video signals, data exchange, controls etc.) and the patient at the same time.
1.8 Electromagnetic compatibility (EMC) - IEC 60601-1-2 : 2007
Please observe the following:
The device/system, in the following referred to as product, always relates to Logic HD Camera Controller 552510x and Logic 4K
Camera Controller 5525301.
Guidelines and manufacturer's declaration - Electromagnetic emissions
The product is intended for use in the environment specified below. The user must assure that the product is used in such an environment.
Emissions measurement / test Compliance Electromagnetic environment - Guidelines
HF emissions to CISPR 11 Group 1
The product uses HF energy for its internal function.
The HF emission level is extremely low and is not likely to cause any
interference in nearby electronic equipment.
HF emissions to CISPR 11 Class A The product is suitable for use in buildings other than residential buildings
and buildings that are immediately connected to the public power supply
network that also supplies buildings used for residential purposes pro
vided the following warning is observed:
Warning: The product is only intended for use by specialized medical
staff. This product can cause radio interference which may make it neces
sary to take suitable remedial measures such as new alignment, new
positioning or screening of the product or a filter in the connection to the
installation site.
Harmonic emissions
to IEC 61000-3-2 Class A
In conformity with IEC 61000-3-3 “Emission of voltage fluctuations
/flicker"
Guidelines and manufacturer's declaration - Electromagnetic immunity
The product is intended for use in the environment specified below. The user must assure that the product is used in such an environment.
Immunity tests IEC 60601 test level Compliance Electromagnetic environment - Guidelines
Electrostatic discharge (ESD)
to IEC 61000-4-2
6 KV contact discharge
8 KV air discharge Yes
Floors should be wood, concrete or ceramic tile. If
floors are covered with synthetic material, the rela
tive humidity should be at least 30%.
Electrical fast transience, bursts
to IEC 61000-4-4
2 KV for power supply lines
1 KV for input and output
lines
Yes Mains/line power quality should be that of a typical
commercial or hospital environment.
Surge voltage (surges)
to IEC 61000-4-5
1KVlinetoline
voltage
2 KV line to ground
voltage
Yes Mains/line power quality should be that of a typical
commercial or hospital environment.
Voltage dips, short interruptions and sup
ply voltage variations
to IEC 61000-4-11
Voltage dip for 0.5 cycle
> 95% UT*
Voltage dip for 5 cycles
60% UT*
Voltage dip for 25 cycles
30% UT*
Voltage dip for 5 sec
> 95% UT*
Yes
Mains/line power quality should be that of a typical
commercial or hospital environment. If the user of
the product requires continued operation during
power mains/line interruptions it is recommended
that the product be powered from an uninterrupt
ible power supply or battery.
Power frequency (50/60 Hz) magnetic
field,
to IEC 61000-4-8
3A/m Yes
Power frequency magnetic fields should be at lev
els characteristic of a typical location in a commer
cial or hospital environment.
*NOTE! UTis the line / mains voltage prior to application of the test level.

9GA-A282
Guidelines and manufacturer's declaration - Electromagnetic immunity for products that are not life-supporting
The product is intended for use in the environment specified below. The user must assure that the product is used in such an environment.
Immunity tests IEC 60601 test level Compliance Electromagnetic environment - Guidelines
Conducted HF interference
to IEC 61000-4-6
Radiated HF interference
to IEC 61000-4-3
3V
rms
150 kHz to 80 MHz
3V/m
80MHzto2.5GHz
Yes
Portable and mobile RF communications equipment should
be used no closer to any part of the product, including ca
bles, than the recommended separation distance calculated
from the equation applicable to the frequency of the transmit
ter.
Recommended separation distance:
d=1.2pP
d=1.2pP for 80 MHz to 800 MHz
d=2.3pP for 800 MHz to 2.5 GHz
P = Nominal power output rating of the transmitter in watts
(W)
(according to the transmitter manufacturer)
d = recommended separation distance in meters (m)
Field strengths from fixed RF transmitters, as determined by
an electromagnetic site survey1, should be less than the
compliance level in each frequency range2.
Interference may occur in the vicinity of devices with the
following symbol:
REMARKS:
At 80 MHz and 800 MHz the higher frequency range applies. These guidelines may not apply in all situations. The propagation of electromag
netic waves is affected by absorption and reflexion from buildings, objects and people.
1= The field strength of stationary transmitters (e.g. base station for radio phone, earth to earth radio stations,, amateur radio stations, radio
and television transmitters) cannot be exactly predicted in theory. To assess the EMC environment due to fixed transmitters an electromagnetic
site survey should be conducted. If the measured field strength in the location in which the product is used exceeds the applicable compliance
level above, the product should be observed to verify normal operation.
If abnormal performance is observed, additional measures may be required, such as reorienting or relocating the product.
2= Over the frequency range between 150 kHz and 80 MHz the field strength should be below 3 V/m.
Recommended separation distances between portable and mobile HF telecommunication devices and devices which
are not life-supporting
The product is intended for use in an electromagnetic environment where HF disturbances are controlled.
The user can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile HF telecommunica
tions equipment and the product.
Rated nominal output power of
thetransmitter (W)
Separation distance as a function of transmitter frequency (m)
150kHzto80MHz
d=1.2pP
80 MHz to 800 MHz
d=1.2pP
800 MHz to 2.5 GHz
d=2.3pP
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
11.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a nominal output power not listed in the table above, the recommended separation distance (d) in meters (m) can be
determined using the applicable equation (observe frequency). P = nominal power of the transmitter in Watts (W).
REMARKS:
At 80 MHz and 800 MHz the higher frequency range applies. These guidelines may not apply in all situations. The propagation of electromag
netic waves is affected by absorption and reflexion from buildings, objects and people.

10
GA-A282
1.9 Electromagnetic compatibility (EMC) - IEC 60601-1-2 : 2014
Please observe the following:
The device/system, in the following referred to as product, always relates to Logic HD Camera Controller 552510x and Logic 4K
Camera Controller 5525301.
Guidelines and manufacturer's declaration - Electromagnetic emissions
The product is intended for use in the environment specified below. The user must make sure that the product is used in such an environment.
Emissions measurement / test Compliance Electromagnetic environment - Guidelines
HF emissions to CISPR 11 Group 1
The product uses HF energy for its internal function.
The HF emission level is extremely low and is not likely to cause any
interference in nearby electronic equipment.
HF emissions to CISPR 11 Class A The product is suitable for use in buildings other than residential buildings
and buildings that are immediately connected to the public power supply
network that also supplies buildings used for residential purposes pro
vided the following warning is observed:
Warning: The product is only intended for use by specialized medical
staff. This product can cause radio interference which may make it neces
sary to take suitable remedial measures such as new alignment, new
positioning or screening of the product or a filter in the connection to the
installation site.
Harmonic emissions
to IEC 61000-3-2 Class A
In conformity with IEC 61000-3-3 “Emission of voltage fluctuations
/flicker"
Guidelines and manufacturer's declaration - Electromagnetic immunity
The product is intended for use in the environment specified below. The user must assure that the product is used in such an environment.
Immunity tests IEC 60601 test level Compliance Electromagnetic environment - Guidelines
Electrostatic discharge (ESD)
to IEC 61000-4-2
8 KV contact discharge
15 KV air discharge Yes
Floors should be wood, concrete or ceramic tile.
With floors made of synthetic material, the relative
humidity of the ambient air must be at least 30%.
Electrical fast transience, bursts
to IEC 61000-4-4
2 KV for power supply lines
1 KV for input and output
lines
Yes Mains/line power quality should be that of a typical
commercial or hospital environment.
Surge voltage (surges)
to IEC 61000-4-5
1KVlinetoline
voltage
2 KV line to ground
voltage
Yes Mains/line power quality should be that of a typical
commercial or hospital environment.
Voltage dips, short interruptions and sup
ply voltage variations
to IEC 61000-4-11
0% UT*; 1/2 period at 0.45,
90, 135, 180, 225, 270 and
315 degrees
0% UT*;1Period
and
70% UT*; 25/30 Periods
single-phase: at 0 degrees
Yes
Mains/line power quality should be that of a typical
commercial or hospital environment. If the user of
the product requires continued operation during
power mains/line interruptions it is recommended
that the product be powered from an uninterrupt
ible power supply or battery.
Power frequency (50/60 Hz) magnetic
field,
to IEC 61000-4-8
30A/m Yes
Power frequency magnetic fields should be at lev
els characteristic of a typical location in a commer
cial or hospital environment.
*NOTE! UTis the line / mains voltage prior to application of the test level.

11 GA-A282
Guidelines and manufacturer's declaration - Electromagnetic immunity for products that are not life-supporting
The product is intended for use in the environment specified below. The user must assure that the product is used in such an environment.
Immunity tests IEC 60601 test level Compliance Electromagnetic environment - Guidelines
Conducted HF interference
to IEC 61000-4-6
Radiated HF interference
to IEC 61000-4-3
6V
rms
150 kHz to 80 MHz
3V/m
80MHzto2.7GHz
Yes
Yes
Portable and mobile RF communications equipment should
be used no closer to any part of the product, including ca
bles, than the recommended separation distance calculated
from the equation applicable to the frequency of the transmit
ter.
Recommended separation distance:
d=1.2pP
d=1.2pP for 80 MHz to 800 MHz
d=2.3pP for 800 MHz to 2.5 GHz
P = Nominal power output rating of the transmitter in watts
(W)
(according to the transmitter manufacturer)
d = recommended separation distance in meters (m)
Field strengths from fixed RF transmitters, as determined by
an electromagnetic site survey1, should be less than the
compliance level in each frequency range2.
Interference may occur in the vicinity of devices with the
following symbol:
REMARKS:
At 80 MHz and 800 MHz the higher frequency range applies. These guidelines may not apply in all situations. The propagation of electromag
netic waves is affected by absorption and reflexion from buildings, objects and people.
1= The field strength of stationary transmitters (e.g. base station for radio phone, earth to earth radio stations,, amateur radio stations, radio
and television transmitters) cannot be exactly predicted in theory. To assess the EMC environment due to fixed transmitters an electromagnetic
site survey should be conducted. If the measured field strength in the location in which the product is used exceeds the applicable compliance
level above, the product should be observed to verify normal operation.
If abnormal performance is observed, additional measures may be required, such as reorienting or relocating the product.
2= Over the frequency range between 150 kHz and 80 MHz the field strength should be below 3 V/m.
Recommended separation distances between portable and mobile HF telecommunication devices and devices which
are not life-supporting
The product is intended for use in an electromagnetic environment where HF disturbances are controlled.
The user can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile HF telecommunica
tions equipment and the product.
Rated nominal output power of
thetransmitter (W)
Separation distance as a function of transmitter frequency (m)
150kHzto80MHz
d=1.2pP
80 MHz to 800 MHz
d=1.2pP
800 MHz to 2.5 GHz
d=2.3pP
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
11.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a nominal output power not listed in the table above, the recommended separation distance (d) in meters (m) can be
determined using the applicable equation (observe frequency). P = nominal power of the transmitter in Watts (W).
REMARKS:
At 80 MHz and 800 MHz the higher frequency range applies. These guidelines may not apply in all situations. The propagation of electromag
netic waves is affected by absorption and reflexion from buildings, objects and people.

12
GA-A282
1.10 Connection diagram - Camera Controller in video mode
3
2
1
3
3
Legend
Direct connection
1LAN (Ethernet) connection cable (option) -
core nova System
2Video cables in accordance with the signal types of the Camera Controller used
Connection via recording devices
3Video cables in accordance with signal types of the Camera Controller and recording devices used
. IMPORTANT!
Connection of the LAN (Ethernet) connection cable (1)only inthecaseofaninteractive light source.

13 GA-A282
2 Illustration
2.1 Front view - Camera Controller for all models
11.1
2
3
4
Legend
1Power/mains switch 3Camera socket
(type CF applied part)
1.1 Power ON/OFF LED 4USB 2.0 interface (for external storage media)
2Touch-screen

14
GA-A282
2.2 Rear view - Logic HD Camera Controller 552510x
DC OUT
REMOTE
LAN
SDI
HD- SDI
3G- SDI
3G- SDI
VIDEO
S- VIDEO
FEDERAL LAW RESTRICTS THIS UNIT TO BE
USED OR SOLD, EXCEPT UNDER THE SUPER-
VISION OF A MEDICAL DOCTOR.
6
9
11
75
810
12 1413 15
16
HDMI
HD
Legend
5HDMI HD output 11 Power supply 5V DC, 12V DC
6USB 2.0 port 12 Remote output connectors
(e.g. printer remote control)
7LAN (Ethernet) network connector 13 PIP module (option)
8Equipotential connector 14 HD-SDI module (option)
9Power input connector with fuse holder 15 SD-Video module (option)
10 Fuse label 16 Identification plate

15 GA-A282
2.3 Rear view - Logic 4K Camera Controller 5525301
DC OUT
REMOTE
LAN
SDI
HD- SDI
3G- SDI
HDMI
3G- SDI 4K
FEDERAL LAW RESTRICTS THIS UNIT TO BE
USED OR SOLD, EXCEPT UNDER THE SUPER-
VISION OF A MEDICAL DOCTOR.
6
9
11
75
810
12 1413 15
16
HD
HDMI
Legend
5HDMI HD output 11 Power supply 5V DC, 12V DC
6USB 2.0 port 12 Remote output connectors
(e.g. printer remote control)
7LAN (Ethernet) network connector 13 PIP module
8Equipotential connector 14 HD-SDI module
9Power input connector with fuse holder 15 HDMI 4K module
10 Fuse label 16 Identification plate