Zeiss Cirrus Photo 600 Manual

CIRRUS photo
(CIRRUS photo 600 and CIRRUS photo 800)
Documentation set
© 2016, Carl Zeiss Meditec AG, Jena
All rights reserved in the event of granting of patents or registration as a utility

patent.
All names of companies and products cited in this documentation set may be
trademarks or registered trademarks. References to products of other manufacturers
are for information purposes only. Such references are intended neither as an
approval nor a recommendation of these products. Carl Zeiss Meditec AG accepts
no liability for the performance or use of such products.
Microsoft Windows® is a registered trademark of Microsoft Corporation, Inc.

CIRRUS photo® is a trademark of Carl Zeiss Meditec AG.
Other brand names, software and hardware names used in this documentation set
are generally subject to trademark or patent protection. The quoting of products is
for informational purposes only and does not represent a trademark misuse.
The weblinks are dynamic hyperlinks. Before incorporating any links, Carl Zeiss
Meditec AG checks their content to ensure that it is not likely to result in civil or
criminal liability. It does not, however, continuously check for any changes which
could form the basis for liability. If Carl Zeiss Meditec AG determines that a link
which it has incorporated could result in civil or criminal liability, or is alerted to the
fact by a third party, the link will be removed.
This documentation set is protected by copyright. Unless expressly authorized in

writing, dissemination, duplication or other commercial exploitation of this docu-
ment or communication of its contents or parts of it is not permitted. In case of
infringement, the violator may be liable to pay compensation for damages.
Specifications due to technical developments are subject to change. This documen-

tation set is not subject to the revision service. Please contact the manufacturer or
authorized dealer to request the latest edition of the documentation set.
Contents
User manual
1
[000000-2121-813-GA-GB-050416]
Addendum to the documentation set

Remote maintenance tool
2
[000000-2121-813-AddGA01-GB-210915]
MICROSOFT SOFTWARE LICENSE TERMS

WINDOWS EMBEDDED STANDARD 7
3
[WINDOWS EMBEDDED STANDARD 7 GB, 21.06.2012]
Appendix
CIRRUS photo 600/CIRRUS photo 800 - Settings

[000000-2121-813-AddGA02-GB-280815]
CIRRUS photo 600/800 - Internal fixation targets

[000000-2121-813-AddGA03-GB-030915]
CIRRUS photo scan acquisition - Quick instructions Models 600 and 800
[000000-2121-813-KurzGA01-GB-280815]
CIRRUS photo 600/800 quick instructions - User-defined workflow

[000000-2121-813-KurzGA02-GB-040915]
Fundus Photography - Advice and Tips

[000000-2133-713-KurzGA02-GB-190815]
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Contents
User manual
1
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CIRRUS photo
User manual
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Contents 1
Contents
Contents .....................................................................................1
Notes on the user manual ..........................................................3

Purpose and availability of documentation .................................................... 3
Questions and comments................................................................................ 3
Explanation of symbols used .......................................................................... 4
Package check list ......................................................................5
Country-specific information and labels .....................................6

Classification/Manufacturer's declaration ...................................................... 6
Intended use ................................................................................................... 7
Intended user profile....................................................................................... 9
Disposal of the product ................................................................................ 10
External labels ............................................................................................... 11
Performance specifications ......................................................15

Functional description................................................................................... 15
Service life ..................................................................................................... 16
Description of the device..........................................................17

Connection panel of main unit...................................................................... 21
Connection panel of OCT engine .................................................................. 22
Power module ............................................................................................... 23
Installation ...............................................................................25
Notes on installation and use ....................................................................... 25
Daily use ...................................................................................27

Switching on ................................................................................................. 28
Operation of the device............................................................29

General .......................................................................................................... 30
Operation using the control panel on the instrument base .......................... 31
Coaxial overlap check ................................................................................... 33
Test tool ................................................................................................................................ 33
Installation of the test tool ..................................................................................................... 33
Shutting down..........................................................................35
Switching off the device ............................................................................... 35
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2 Contents
Notes on angiography ............................................................. 36

Angiography using the CIRRUS photo 800 .................................................. 36
Maintenance and care ............................................................. 37

Fault remedy ................................................................................................ 37
Replacing the flashing diode of the external fixation lamp ......................... 38
Maintenance ................................................................................................. 39
Care and cleaning .................................................................................................................. 39
Data backup ................................................................................................. 45
Data backup using FORUM Archive ........................................................................................ 45
Data backup via DICOM export/import .................................................................................. 45
CIRRUS photo backup function .............................................................................................. 45
Further notes on data backup ................................................................................................ 46
Inspection of electrical safety....................................................................... 46
Optional accessories ................................................................ 48

Demonstration eye ....................................................................................... 49
USB flash drive ............................................................................................. 49
Printer .......................................................................................................... 50
Installation of a network printer ............................................................................................. 51
Technical data .......................................................................... 54
Electromagnetic compatibility ................................................. 56
Abbreviations/Glossary ............................................................ 61
Figures ..................................................................................... 62
Index ........................................................................................ 63
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Notes on the user manual 3
Notes on the user manual

Purpose and availability of documentation
This user manual and software description of this instrument explain the
safety precautions, functions, usage, performance parameters and measures
for care and maintenance of the CIRRUS photo.
Correct operation of the system is imperative for its safe and successful
function. You should therefore ensure that you are thoroughly familiar with
this user manual before setting up and using the CIRRUS photo the first
time. Please also observe the operating instructions for other device
components.
The user manuals and other documentation enclosed with the CIRRUS photo
should be kept accessible to users at all times to ensure that the information
required for use of the CIRRUS photo is readily available.
Questions and comments

If you have any questions or comments concerning this user manual or the
CIRRUS photo, please contact ZEISS service or your local dealer. (Contact
details see reverse.)
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4 Notes on the user manual
Explanation of symbols used

The symbols used in this user manual refer to important safety information
which warn against possible health risks or fatal injuries and contain useful
notes. Whenever you see these symbols, read the accompanying information
carefully and observe all safety notes and information in this user manual
and on device labels.
WARNING
Indicates a hazardous situation which may result in death or serious injury if
the appropriate safety precautions are not heeded.
CAUTION
Indicates a hazardous situation which may result in minor or moderate
injury if the appropriate safety precautions are not heeded.
CAUTION - PROPERTY DAMAGE

Indicates possible device damage if the appropriate safety precautions are
not heeded.
 Information, hints and advice for better understanding of the

instructions to be observed in the operation of the device.
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Package check list 5
Package check list

The following components are included in the CIRRUS photo delivery
package:
• Documentation set
• Basic device, consisting of:
– Main unit
– OCT engine
• Power module with power isolation transformer
• Instrument table
• Table mounting for power module and OCT engine
• External fixation lamp
• TFT display
• Monitor holder
• Keyboard
• Mouse
• Test equipment (coalignment tool)
• LensPen cleaning pen
• Power cable
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6 Country-specific information and labels
Country-specific information and

labels
Classification/Manufacturer's declaration
WARNING - GENERAL HAZARDS

This device may only be set up, operated and used for the specified purpose
and according to national regulations, consistent with the applicable
industry standards and occupational safety and accident prevention
regulations. Further notes on classification are to be found in section
Technical data, page 54 and following.
This device complies with EC Directive 93/42/EEC (MDD).

Device group (overall system): 2 in accordance with
ISO 15004-2:2007
Device class according to the MDD: IIa
Light emitting diodes: Class 1 according to IEC 60825-1
EMC: See section Electromagnetic

compatibility, page 56 and following.
UMDNS No.: 12-815 (fundus camera),

18-191 (optical tomography)
This declaration shall be rendered invalid if changes are made to the product
without the manufacturer’s authorization.
The product is RoHS-compliant according to Directive 2011/65/EU.
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Country-specific information and labels 7
Intended use
The CIRRUS photo is a non-contact, high-resolution tomographic and
biomicroscopic imaging device that incorporates a digital camera which is
suitable for photographing, displaying and storing the data of the retina and
surrounding parts of the eye to be examined under mydriatic and non-
mydriatic conditions.
These photographs support the diagnosis and subsequent observation of eye
diseases which can be visually monitored and photographically documented.
The CIRRUS photo is indicated for in-vivo viewing, axial cross sectional, and
three-dimensional imaging and measurement of anterior and posterior
ocular structures, including cornea, retina, retinal nerve fiber layer, macula,
and optic disc.
It also includes a Retinal Nerve Fiber Layer (RNFL), Optic Nerve Head (ONH),
and Macular Normative Database which is a quantitative tool for the
comparison of retinal nerve fiber layer, optic nerve head, and the macula in
the human retina to a database of known normal subjects. The CIRRUS
photo is intended for use as a diagnostic device to aid in the detection and
management of ocular diseases including, but not limited to, macular holes,
cystoid macular edema, diabetic retinopathy, age-related macular
degeneration, and glaucoma.
CAUTION - HAZARDS DUE TO SIDE EFFECTS

When using mydriatics observe the respective information of the
manufacturer on contraindications and side effects!
CAUTION – GENERAL HAZARDS

This device works with visual stimuli, including lights and patterns flashing
and flickering between 5 and 65 Hz. It is the responsibility of the physician
to decide whether this device is suitable for use with patients who may be
light-sensitive. This group includes epileptics.
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CAUTION - RISKS ARISING FROM OPERATING ERRORS

Do not use the instrument in patients who:
• are unable to follow the instructions of the user
• are unable to sit upright in front of the instrument
• have forehead or chin injuries that prevent the head from being
supported on the head/chin rest
Allow for serious restrictions in the use of the instrument for patient groups:
• Patients with complete or partial coverage of the cornea caused by
palpebral fissure which is closed or too small
• Patients unable to steadily fixate with the eye under examination (e.g. in
the case of nystagmus, tremor, Parkinson's disease, extremely poor
visual acuity, lack of concentration)
• Non-foreseeable influence of wearing contact lenses (remove contact
lenses before exposure)
• Patients with a small pupil
• Patients with a dense cataract
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Intended user profile

This device may only be installed, operated, used and maintained by
persons who have been properly trained or who have the required
knowledge and experience to do so. Please also adhere to the national
qualification guidelines applicable in your country.
Persons who operate the CIRRUS photo must have a basic knowledge of
ophthalmic examination and diagnosis methods. It is recommended that the
CIRRUS photo operator has the following skills:
Ophthalmic photographer, optometrist, MTA and staff who prepare

images using the CIRRUS photo
• Completed training as optician, optometrist, ophthalmo-photographer or
medical-technical assistant
• Knowledge of current ophthalmic diagnostic procedures and their
examination results
• Knowledge of the effects of incorrect or inaccurate readings on the
therapy
• Possible consistency checks against other measurement results
• Practical experience in handling ophthalmic diagnostic devices
• Experience in calming and explaining to patients, in particular older
population.
• Experience with the Microsoft Windows operating system and
applications based on it
Physicians who review images and analyze data for diagnostic

purposes with the CIRRUS photo
In addition to the above skills, the operator should have completed training
as an eye specialist in order to recognize and evaluate the different findings,
in particular:
• Diagnostically relevant findings in fundus color images or red-free
photographs
• Diagnostically relevant findings in the early, medium and late phase of
fluorescein angiograms
• Skills in the evaluation of fundus autofluorescence images and
indocyanine green angiograms
• Diagnostically relevant findings in macula and optic disc scans as well as
scans of the anterior eye segment
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Disposal of the product
CAUTION - RISK OF ENVIRONMENTAL POLLUTION

Packaging materials should be retained for future relocation or repair.
If you decide to dispose of the packaging material, submit it to a recognized
collection system for recycling.
The device contains electronic components. At the end of its lifetime, the
device and its internal batteries should be disposed of in accordance with
the relevant national regulations.
Disposal of the product within the EU

In accordance with applicable EU guidelines and national regulations at the
time at which the product was brought onto the market, the product
specified on the consignment note is not to be disposed of via the domestic
waste disposal system or communal waste disposal facilities.
For further information on disposal of this product, please contact your local
dealer or the manufacturer or its legal successor company. Please read the
latest internet information provided by the manufacturer.
Where the product or its components are resold, the seller must inform the
buyer that the product must be disposed of in accordance with the currently
applicable national regulations.
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External labels
Fig. 1 Warning and information labels on the device
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Item Label Explanation
1 CIRRUS photo type label

Manufacturer
Date of manufacture
Applied part type B
IP20 Housing protection class

(protected against solid
CIRRUS photo 800 foreign bodies of 12.5 mm in
diameter and larger, no
protection against
penetration of water)
CIRRUS photo 600
2 CIRRUS photo 800 identification label

REF Catalogue number/part number
SN Serial number
CIRRUS photo 600 identification label
3 Sign with date of manufacture
4 CE marking label and disposal advise for

EU
EU conformity symbol with
Identification number of
notified body
Disposal advise for EU
5 Not applicable Not applicable
6 Computer identification label

CIRRUS photo
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7 Sign with manufacturer's name and date

Manufacturer
Date of manufacture
EU conformity symbol with

Identification number of
notified body
8 OCT engine type label
9 Sign with date of manufacture
10 Information label
"Disconnect device from the power
supply before opening"
11 Information label
"Observe user manual"
12 Power supply unit type label
EU conformity symbol
UL approval for USA and Canada
AC voltage
DC voltage
"Electricity" warning label
Information label on polarity of

the 24 V output
"Danger zone" warning label
Applied part type B
EU disposal sign
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13 Power module identification label

P/N Product number
S/N Serial number
14 "24 V output" information label
15 "230 V output" information label
16 Not applicable Not applicable
17 CIRRUS photo 800 main unit

identification label
REF Catalogue number/part number
SN Serial number
CIRRUS photo 600 main unit

identification label
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Performance specifications 15
Performance specifications
Functional description
The CIRRUS photo allows the fundus of the eye to be viewed and
documented as well as the anterior segment of the eye in plain view (classic
image capture) or as an optical section (OCT scan), with the pupil in a
naturally or medicinally-induced dilated state. Easy-to-use operation of
CIRRUS photo ensures quick results. The device is particularly suitable for
routine use. The fundus is evaluated on the basis of a flash photograph or
the OCT scan image. Image capture and display is fully digital.
The CIRRUS photo employs the ophthalmoscope principle of the modern
fundus camera. Cross-sectional images of a retinal area measuring
6 mm x 6 mm are generated as a cube scan or as a 5 line raster pattern
using the high resolution "spectral domain" optical coherence tomography
(SD-OCT) technique. A flash lamp is used for the image documentation.
Images of the fundus of the eye are taken at angles of 45° or 30°. The
device operates in non-contact mode.
Positioning and focusing of CIRRUS photo using infrared light is the basis for
its non-mydriatic mode of operation. This means that the use of pupil-
dilating drops is not necessarily required. Medicinally-induced dilation of the
pupil is required for image series such as angiography. Infrared diodes are
used as a light source for setting up CIRRUS photo. The working distance is
set up using two working distance dots and the fundus brought into focus
using a focusing aid.
The CIRRUS photo supports fundus image capture modes Color, G (green),
R (red), B (blue) and FA (fluorescein angiography), FAF (autofluorescence)
and ICGA (indocyanine green angiography), and OCT scan modes Macular
Cube 512x128, Macular Cube 200x200, Optic Disc 200x200,
HD 5 Line Raster , Anterior segment 5 Line Raster and Anterior
Segment Cube 512x128. The availability of the modes depends on the
model concerned. Some of the modes can only be enabled with an
appropriate license.
The CIRRUS photo includes an intuitive software interface for database-
supported patient and image data administration. Images and scans can be
displayed, printed and exported and patient data created and adapted with
no difficulty at any time. There are special analysis modules which can be
used to aid rapid interpretation of OCT scan data. The normative databases
and algorithms provided by Carl Zeiss Meditec represent the basis for these
modules.
As with many medical devices, the CIRRUS photo only offers data storage for
a limited period of time. Images should be stored long term using an
external archiving system (e.g. FORUM system). General export of the image
data can be carried out in DICOM, BMP, JPEG, PNG or TIFF format via a
network or using standard USB media.
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16 Performance specifications
Service life

The development, production and maintenance of this device, together
with associated risks, are based on an expected service life of eight years,
assuming that the device is serviced at the specified intervals (see section
Inspection of electrical safety, page 46).
Modifications to the product or failure to follow the manufacturer’s
instructions may substantially reduce the expected service life and
significantly increase the risks associated with the use of this device.
It is the responsibility of the institution operating this product to follow the
manufacturer’s instructions and to decide on the risk/benefit ratio upon
expiration of the expected service life or maintenance and inspection
intervals specified by the manufacturer.
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Description of the device 17
Description of the device

The CIRRUS photo device consists of a fundus camera main unit (9, Fig. 2),
an OCT engine (6, Fig. 2), and the power module (7, Fig. 2), all being
installed onto an instrument table.
It is operated via computer mouse (2, Fig. 3), keyboard (3, Fig. 3), and
joystick as part of the main unit. The monitor is mounted on top of the
instrument table.
The main unit comprises the electrical and optical components to illuminate
and image the ocular structures.
A CCD camera is used for the live observation of the fundus using infrared
LEDs for illumination of the fundus. A Xenon flash lamp is used to capture
fundus images.
The OCT engine provides all means to control, obtain and reconstruct OCT
scan data. A super luminescence diode is used as light source.
To obtain three dimensional OCT data sets the light beam has to be scanned
across the ocular structure of interest. The beam is therefore guided by a
pair of perpendicular galvanometer mirrors. This XY-scan module is part of
the main unit.
The power module provides operating voltage for the main unit and the OCT
engine (3, Fig. 8). An appliance connection allows the operation of the
monitor (5, Fig. 8) via a power isolation transformer.
The computer is part of the main unit and controls both fundus camera and
OCT engine.
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18 Description of the device
1 Cap for external fixation lamp

2 External fixation lamp, freely (3D) movable (optional for CIRRUS photo 600)
3 Headrest with vertically adjustable chin rest, forehead support and mount for external fixation lamp
4 Display to control the device, monitor the adjustment process, display of examination results and other device
information
5 Instrument table
6 OCT engine
7 Power module with power isolation transformer
8 Keyboard and mouse for the entry of patient data and operation of the device
9 Main unit
Fig. 2 Basic design of the CIRRUS photo
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1Monitor
2Mouse
3Keyboard
4Connector panel (see Fig. 5)
5Rotary knob for adjusting the brightness of the observation light
6Rotary knob for locking the instrument base
7Joystick for 3D adjustment of instrument base (X/Y-axis: tilting; Z-axis: rotating),
when carrying out coarse adjustment in the X/Y axes, the instrument base is pushed in the desired direction
8 Release button
9 Control panel with quick-select buttons (see Fig. 10)
10 Knurled focusing knob
Fig. 3 Controls of main unit, right hand view
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1 Sleeve nut for external fixation lamp

2 Red eye level marks (suitable patient eye level for optimum photography)
3 Patient forehead support
4 Front lens with protective cap (exit aperture)
5 Patient chin rest
6 Fastening pins for paper pads
7 Knurled knob for vertical adjustment of chin rest
Fig. 4 Controls of main unit, left hand view
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Connection panel of main unit
1 4x USB 2.0 ports

2 Connector for additional monitor (DisplayPort)
3 Serial port (not in use)
4 Monitor port (DVI)
5 Connection for external network
6 2x USB 3.0 ports
7 Connector for communication cable
8 2x USB 2.0 ports
9 Connector for data transfer cable
10 Power supply input
11 Socket for optical fiber
12 Connector for scanner control
Fig. 5 Connection panel of main unit
 To remove the cover cap press on the indicated point on the cover
cap and remove the cap.
 The instrument supports USB version 2.0.
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Connection panel of OCT engine
1 Connector for data transfer cable

2 Socket for optical fiber
3 Connector for communication cable
4 Connector for scanner control
5 Power supply input
Fig. 6 Connection panel of OCT engine
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Power module
WARNING - RISK OF ELECTRIC SHOCK

Connect the monitor only via the power module and the integrated power
isolation transformer (medical power isolation transformer in accordance
with IEC 60601-1:2005 with "two MOPP") to the power supply grid. If
these instructions are not complied with, there is a risk of electric shock or
elimination of the required protective separation between medical devices
and non-medical equipment.
The power supply unit must only be used for supplying power to the system
components described. Use of the unit as a multiple socket is prohibited.
No components other than the system components described should be
connected.
When connecting other system components than that described in this
manual to the power module or the instrument table, a non-medical-rated
system is created in accordance with IEC 60601-1:2005 and thus the
degree of safety reduced. This also gives rise to the risk of electric shock or
elimination of the required protective separation between medical devices
and non-medical equipment.
Do not place the power module on the floor.
The CIRRUS photo and monitor are connected to the power supply via the
power module (Fig. 7 and Fig. 8) and its integrated power isolation
transformer (max. power 80 W).
The power module provides 24 V DC voltage (3, Fig. 8) for the main unit and
OCT engine.
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1 Power switch
2 Power control lamp (green)
3 Control lamp for protective conductor (orange)
(lights up continuously: phases have been changed; please turn the plug in the
power outlet to switch the phases and turn off the control lamp; flashes: protective
conductor not connected)
Fig. 7 Power module, front view
1 Power input connector

2 Fuses
3 24 V output for main unit and OCT engine
4 Grounding contact socket (230 V)
5 Appliance outlet for monitor
Fig. 8 Power module, rear view
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Installation 25
Installation
Notes on installation and use

First-time operation, installation and relocation of the device are to be
carried out by Carl Zeiss Meditec authorized specialists only.
The device may not be stored or operated in ambient conditions other than
those prescribed (see section Technical data on page 54 and following).
The device must be set up so that the power cable can be disconnected
from the power supply quickly and without any supplementary means.

Do not use additional extension cables or portable multiple sockets.
The electrical installation must conform to IEC 60364-7-710 or the
applicable national regulations. This includes the integration of a ground
fault circuit interrupter (GFCI).
To avert the risk of an electric shock, this device may only be connected to
a power supply with a protective ground conductor. To completely
disconnect from the power supply the device must be unplugged.
Ensure that the power supply plug is suitable and certified for the local
connection. Only power cables of the same type should be used if the cable
supplied needs to be replaced.
WARNING - FIRE HAZARD

The device is not suitable for operation in explosion risk areas (e.g.
combustible mixture of anesthetic, cleaning or disinfecting agents with air,
oxygen or nitrous oxide).
The electrical installation must conform to IEC 60364-7-710.
The data concerning power consumption on the type plate must be taken
into account in the selection of overcurrent protection.
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26 Installation

Do not store or use this device in damp rooms. Do not expose the device to
water splashes, dripping water or sprayed water.

Handle with care; the instrument should not be lifted or carried!
 Read the user manual of the instrument table and follow its
warning instructions.
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Daily use 27
Daily use

Prior to using the device, the user must ensure that it is in good condition
and fully functioning. Furthermore, the user must follow the instructions in
the user manual.
The following inspections must be carried out each working day prior to
use:
• Visual inspection of the housing, labels, user manual, accessories and
power cable to ensure that they are present and intact. If parts are
missing or damage is visible, the device should not be used and should
be taken out of service.
• The ventilation slits should not be covered or otherwise obstructed!

Please ensure that the following operational requirements are met each
time before using the instrument and are maintained throughout further
operation:
• Use the power cable supplied with the device. If the device is mounted
on an instrument table, it will be powered through this table.
Observe the warning instructions in the user manual of the instrument
table.
If using a table not approved by Carl Zeiss Meditec AG, the user is solely
responsible for ensuring the electrical safety of the instrument.
• The power plug must be inserted into a power outlet with an intact
protective ground connection.
• Cables and plugs may only be used if they are in perfect condition.
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28 Daily use
Switching on
• Switch on the CIRRUS photo using the power switch (1, Fig. 7) on the
power module.
When the device is turned on at the power switch, it will run through an
internal test. Once this has been successfully completed, the Patient
dialog is displayed and the device is ready for operation.
Fig. 9 Patient dialog
• Ensure that all external devices (display, printer) are switched on.

To restart the system after it has been inadvertently switched off at the
power switch (1, Fig. 7) during operation or after a system crash, switch the
device back on at the power switch. Note any error messages displayed.
After restarting, run a function test in the Acquire data user interface.
 Notes on carrying out a function test via the Acquire data user
interface can be found in the software description file.
 Some of the operating parameters are set to factory defaults and

can be changed in the CIRRUS photo software’s Settings menu
(see software description file).
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Operation of the device 29
Operation of the device
WARNING - RISK OF OPTICAL RADIATION

The light emitted by this device may be harmful. The risk of eye damage
increases with the number of pulses. Exposure at maximum intensity for
more than 1933 pulses will exceed the hazard reference value.
Do not scan patients who have received treatment which causes increased
light sensitivity, e.g. photodynamic therapy (PDT), within the previous 48
hours. If this warning is not heeded, this can result in unintended stress for
the patient and uncontrolled treatment of neovascular vessels.
Because prolonged intense light exposure can damage the retina, the use of
the device for ocular examination should not be unnecessarily prolonged,
and the brightness settings should not exceed what is needed to provide
clear visualization of the target structures.
CAUTION - GENERAL HAZARDS

The patient should not touch the instrument with his/her hands. In
particular, the device should not be used as a support or an aid when
standing up.
CAUTION - RISK OF FALSE DIAGNOSIS

The use of the HD 5 Line/1 Line Raster scans in MultiMode navigation is
additional clinical information which can be considered during diagnosis by
the physician. However, information based only on these scans is not
sufficient for diagnostic decisions.
Please note: It is the task of a physician to make a diagnosis. The diagnosis
should always be established based on various parameters and
examinations.

When operating radio devices or components for radio transmission,
observe the distances recommended in section Electromagnetic
compatibility (EMC), page 56 and following. If the distance is not observed,
electro-magnetic disturbances may result in artifacts in the images.
Medical electrical devices are subject to special EMC safety regulations and
should be installed and operated in conformity with the EMC information
contained in the accompanying documentation.
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30 Operation of the device
CAUTION - HAZARD DUE TO MOVING PARTS

When lowering the instrument table always ensure that no objects or body
parts are within the movement range of the table top.
 Read the user manual of the instrument table and follow its
warning instructions.
 Users should not rely solely on images made using the device in
making decisions regarding diagnosis or other therapeutic
procedures, but should rely on their own expertise and judgement.
General
The CIRRUS photo computer uses the Windows Embedded Standard 7, 64-
Bit operating system. For safety reasons, the operating system is not
accessible to the user.
The CIRRUS photo user interface is used in the same way as Microsoft
Windows. This includes working with a mouse, using buttons, dialogs and
menus, confirmation by double-click, etc.
The software uses only a few automatic processes.
The user can switch as desired between the four user interfaces Patient,
Acquire data , Review image and Analyze.
In rare cases, Microsoft Windows error messages may be displayed on the
monitor. This may occur if, for example, the program operation is affected
(mostly by external problems).
The CIRRUS photo has been developed and tested in accordance with
national and international standards and regulations. A high degree of
device safety is thus ensured.
The CIRRUS photo may be controlled:
• by using the release button on the joystick
• by operating buttons or menus of the software with the mouse
• by operating the keys on the control panel of the instrument base
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Operation using the control panel on the instrument

base
Internal fixation target/external Switch between internal fixation target
fixation lamp (1, Fig. 10) and external fixation lamp
Position of the internal fixation Fundus images:
target (2 and 5, Fig. 10) Move the fixation target for the patient
when using the multiple fields method
(see software description file): select
previous/next fixation target positions to
correct the image sequence or to repeat
an image capture
OCT and combination mode:
Switch between fundus alignment image
and OCT alignment image
Correction value for automatic • Increment with +
flash or adjustment of flash light • Decrement with -
level with no automatic flash (see
software description file)
(3 and 4, Fig. 10)
Attention mode  (6, Fig. 10) Fundus images:
Causes the internal fixation target to
flash three times, aiding the patient to
locate it quickly
OCT and combination mode:
Starts OCT signal optimization
(analogous to Optimize button)
1 Switch between internal fixation

target and external fixation lamp
2 Move internal fixation target to next
position/Change to another mode
3 Increase flash light level
4 Reduce flash light level
5 Move internal fixation target to
previous position/Change to another
mode
6 Attention mode/OCT signal
optimization
Fig. 10 Control panel on instrument base
Coarse and fine adjustment of the device in front of the patient's eye can be
achieved by shifting the instrument base using the joystick.
For further information on software operation and positioning of the device
please see the software description file in online help, accessible via menu
item Help topics in the Help menu.
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In particular, the following warnings for activation of user management and

use of the service and administrator password must be observed.

Activate the user administration (administrator rights required) in order to
prevent access to the instrument and data by unauthorized persons. Assign
the appropriate access rights to the persons authorized to use the
instrument.
Ensure that the assigned passwords are protected from unauthorized
access.
Configuration and network settings may only be changed by an
experienced network administrator.

A forgotten administrator password can only be recovered by
ZEISS Service!
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Coaxial overlap check

Using the test tool (coalignment tool), check whether the center of the
fundus image coincides with the center of the OCT scan image within given
tolerances. In practical terms this means checking that the scan, based on
the fundus image, is actually positioned where it should be. Repeat the test
if the system does not pass it. If a test has been failed, the data recorded
since the last successful test may be unreliable.

The test must be carried out at the start of the week in which new scans
are to be obtained. It takes approximately 2 minutes to complete the test.
Test tool
The tool is included in the scope of delivery of the instrument. It contains
sensitive parts which must remain in their original position in order to ensure
precise measurements. The tool should be handled carefully and should not
be dropped. A damaged test tool can impair the test results. If the tool is
dropped, it should no longer be used for the coalignment test. In this case
contact ZEISS Service.
Installation of the test tool

The test tool (5, Fig. 11) has two adjusting pins (3, Fig. 11), one in the upper
right corner and one bottom left. There are knurled screws in the upper left
and lower right corners (2, Fig. 11). The corresponding holes are in the
protective funnel (4, Fig. 11) which is fixed to the mount of the front lens of
the instrument.
Apply the test tool to the protective funnel. Rough orientation is provided by
the four plastic pins (1, Fig. 11) around the perimeter of the test tool. The
part of the test tool labeled "Top" should face upwards. Tighten the knurled
screws on the upper and lower side by hand.
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1 Plastic pins
2 Knurled screws
3 Adjusting pins
4 Protective funnel
5 Test tool
Fig. 11 Installation of the test tool
For further information on carrying out the test please see the software
description file in online help, accessible via menu item Help topics in the
Help menu.
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Shutting down 35
Shutting down
Switching off the device

If one of the following events should occur, switch the instrument off
immediately at the power switch, disconnect the cable from the power
supply, label the instrument clearly as being out of service and report the
problem to the ZEISS service:
• Defective sensor for right/left detection
(right/left labeling may be incorrect)
• Electric shock
• Penetration of substances
• Faults that cannot be remedied according to the descriptions in this user
manual.
• To switch off the device, click on the Shut down button in the
navigation bar or in the File menu.
• Wait until the message "You can now switch off the device" appears on
the screen, then turn off the device at the power switch of the power
supply unit (1, Fig. 7).
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36 Notes on angiography
Notes on angiography
CAUTION - HAZARDS DUE TO SIDE EFFECTS

The information of the manufacturer of the injected dye relating to
contraindications and side effects must be heeded to prevent incidents
during angiography.
Angiography using the CIRRUS photo 800

In FA/ICGA capture mode, monochrome images of a patient's eye are
generated. The patient's eye is illuminated with light in different
wavelengths which stimulates the injected solution (fluorescein-sodium (F)
or indocyanine green (ICG) ) to fluoresce. The emitted light (green) is filtered
out in the camera beam path.
Image capture is triggered by pressing the release button on the joystick
(8, Fig. 3).
 Angiography is a diagnostic procedure conducted over a longer

period. It is therefore documented with a series of images, i.e. each
exposure is assigned to a particular FA running time.
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Maintenance and care 37
Maintenance and care

Further maintenance procedures above and beyond those specified in this
section (maintenance, safety inspections and repairs) may only be carried
out by persons authorized by Carl Zeiss Meditec and solely according to the
service instructions issued by Carl Zeiss Meditec. For planning and
implementing these maintenance and care procedures please contact ZEISS
service or your local dealer.
Fault remedy
Fault Possible cause Remedy

No electric function Power switch not switched on Switch power switch to ON
Basic unit power cable not Connect cables to power supply
connected
No image on monitor Monitor power cable not connected Connect cables to power module
(5, Fig. 8)
Monitor displays message Monitor signal cable not connected Connect monitor signal cable to
"Cable not connected" to basic unit basic unit
No observation light Rotary knob for brightness control Turn rotary knob to the right until
adjusted to minimum image is sufficiently visible
Observation brightness is not Brightness control is defective Contact service department
continuously adjustable
External fixation lamp is dark Flashing diode defective Replace flashing diode as described
in section Replacing the flashing
diode of the external fixation lamp
on page 38
Image is too dark, despite Flash bulb defective Contact service department
high flash light level
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38 Maintenance and care
Replacing the flashing diode of the external fixation

lamp
1 Flashing diode
2 Flashing diode holder
Fig. 12 Replacing the flashing diode
Unscrew the defective flashing diode (1, Fig. 12) from the holder (2, Fig. 12)
and replace it with a new diode.
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Maintenance
Care and cleaning

Prevent moisture from penetrating the instrument or keyboard. Disconnect
the power cable from the power supply before cleaning or disinfecting the
device.
CAUTION - RISK DUE TO CROSS-CONTAMINATION

Parts with which the patient has come into contact during the examination
(chin rest, forehead rest) should be cleaned with a disinfectant approved for
the purpose. These parts are resistant to cleaning agents categorized as
"low" (e.g. suds, quaternary ammonium compounds) and "intermediate"
(e.g. alcohol, Javel water, iodine); classification pursuant to: Disinfectants
and activity spectrum according to the Center for Disease Control and
Prevention, Atlanta, USA.

Use the supplied cover to protect the device and the cap to protect the
front lens from dust when not in use.

The national disinfecting regulations must be observed in the choice of
disinfectants and methods. Please note that some cleaning agents and
disinfectants may have an adverse effect on plastic components. Damage
caused by such disinfectants is not covered by our warranty. The surfaces of
the instrument have been tested to withstand frequent and long-term
treatment with alcoholic disinfectants and cleaning agents.
Never use aggressive or abrasive cleaning agents.
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General information
Do not use acetone and acetone-based cleaning agents to clean the device,
as they could damage the surfaces.
Use spray or wipe disinfectants for cleaning and disinfecting the instrument
casing, chinrest and forehead strap.
Heavily soiled painted surfaces should be cleaned with a cloth moistened
with a weak soap solution.
When cleaning the monitor, use only denatured alcohol or commercially
available cleaning cloths. Use commercially available cleaning cloths for the
mouse and keyboard.
To clean the printer, please observe the information given in the
manufacturer’s operating instructions.
Replacing the paper pads
• Remove the two pins for securing the paper pads (6, Fig. 4) on the
headrest.
• Place the paper pads on the chin rest (5, Fig. 4) of the headrest.
• Re-insert the two holding pins through the holes in the paper pads and
into the holes provided in the headrest.
• Tear off the top paper liner after each treatment.
Cleaning the front lens
The cleanliness of the front lens has a crucial influence on the quality of the
captured images.
Please ensure that the front lens is protected at all times from contamination
due to skin contact, body fluids and dust. Use the protective cover supplied
for the purpose.
Observe the following instructions when using the CIRRUS photo and for
cleaning the front lens:
• Pull the CIRRUS photo towards the operator when not in use and lock it
to ensure the greatest possible clearance between patient and
instrument.
• Do not remove the protective cover from the lens until all preparations
for capturing images have been completed and replace it immediately
after completing the examination.
• Never remove the lens from its casing for cleaning.
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• Use cleaning utensils only once according to the given or indicated

instructions. If the result is not satisfactory, please use a new surface or
cleaning set.
Use the following utensils for cleaning the front lens:

• Volk LensPen® cleaning pen (available from optical retailers or directly
supplied by ZEISS, order number 000000-0483-896)
• Optical cleaning set (ZEISS, order number 000000-1216-071) or  

cotton ball sticks or Safebuds from AF International (order number
SBU000)
Frequent causes of lens contamination
• The main cause of simple and uncritical lens contamination is airborne

dirt particles (e.g. dust).
• More serious contamination is caused by small drops of the patient’s tear
fluid sprayed on the front lens when blinking.
• It is important to avoid serious contamination caused by the patient
sneezing or touching the lens surface with the finger or nose. Fatty
residue of this kind results in distinct bright areas on the image and can
only be removed by moist cleaning.
Dust removal
• Dust or other loose particles on the lens surface can be quickly be

removed with the LensPen (brush side) or the brush provided in the
cleaning set.
• If necessary, the entire surface may be wiped with the special felt of the
LensPen. Apply gentle pressure to the entire lens surface with circular
movements. Start in the center of the lens surface and wipe in circles
outwards towards the edge.

Please note that upon replacement after cleaning or repeat wiping,
the protective cap of the special felt tip must be rotated three or
four times.
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Fig. 13 Remove dust from front lens
Removing splashes of tear fluid
Tear fluid drops are usually discernible in the images as light spots.
• Apply circular movements with the LensPen (as described in Dust
removal, page 41).
• If the desired result is still not achieved after repeated wiping, e.g. the
bright spots remain visible, the lens surface must be moist cleaned (see
Removing severe dirt accumulation).
Removing severe dirt accumulation
A typical cause of severe contamination is accidental contact between the

front lens and the patient’s nose when the instrument is not positioned far
enough away from the patient.
• Use the cleaning fluid and microfiber cloth or the moist disposable cloths
provided in the cleaning set, cotton ball sticks or Safebuds.
• If a microfiber cloth is used, spray a small amount of cleaning fluid onto
the tightly folded cloth and shake off any surplus fluid.
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 Never allow your fingers to touch the part of the utensil used for
cleaning.
Hold the cloth between your fingers so they cannot touch the
surface of the lens accidentally.
Fig. 14 Cleaning with microfiber cloth
• Similar to the LensPen, start in the center and make circular movements
over the lens surface.
• Repeat this procedure several times, each time with a clean side of the
cloth.
• Check the result by breathing on the lens and inspecting it for smudges
and streaks as described under Checking on the progress of cleaning in
the following.
• For fine cleaning, apply the cleaning disc of the LensPen (as described in
Dust removal, page 41).
Checking on the progress of cleaning
In the absence of a patient, instant information on cleaning progress can be

obtained by taking a photograph in the darkened room.
Before doing this, with the focusing aid switched on, turn the focusing knob
until the displayed focusing bar extends to the left edge.
Besides the typical spatial structures, no significant bright spots should be
visible in the resulting flash image. The pictures below (Fig. 15) show
examples of the image center (brighter due to post-treatment).
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Contamination Cleaning not yet optimal Acceptable result

due to a fingerprint
Fig. 15 Progress of cleaning
The following pictures (Fig. 16) represent how contamination will appear in
patient images.
The extremely bright spot was caused by An image following moist cleaning.
contact with the finger or nose. Fine cleaning with the LensPen removes the
residual light patches.
Fig. 16 Example for dirt and cleaning
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Data backup
Storing your image data on the hard disk is no substitute for archiving. We
strongly recommend exporting image data daily for backup purposes.
Data backup using FORUM Archive

Our preferred data archiving solution is the FORUM Archive which stores all
data from CIRRUS photo (for configuration see online help file).
If the FORUM software is connected to CIRRUS photo, an automatic data

exchange between both systems will ensure that all data will be saved in
FORRUM and that all examination data will be available in CIRRUS photo
when selecting a patient.
In this case, CIRRUS photo will save data only temporarily. When exiting
CIRRUS photo software, all data saved in FORUM will be deleted from
CIRRUS photo.
Data backup via DICOM export/import

If FORUM is not available, a backup copy can be created via DICOM data
export whereby data is archived on an external storage device (e.g. a
network server or a NAS drive) using the mass export function (see online
help). As with FORUM data storage, the data will be saved independently of
the CIRRUS photo hardware. If necessary (e.g. in case of a hard disk failure),
all data can be restored via a DICOM import. The advantage of this data
export is that it is not required to import all data and that data can be
expanded.
CIRRUS photo backup function

As a further backup function, a database backup can be generated with
CIRRUS (see online help). The backup function allows to restore the database
in its last backup status, however, all data recorded after the backup is lost.
 Please note that data export with Asian characters is not

supported.
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Further notes on data backup

The device’s software can be used to export medical and administrative
data. The transfer of exported data via networks or the import of such data
into third party application software may result in the loss of or unintended
modification of medical information or unintended disclosure of confidential
data. The manufacturer accepts no liability for the correct transfer and
import of data and will not pay compensation for any damage incurred.
No attempt should be made to tamper with the operating system! In

particular, deactivation of the Windows firewall is not permitted!
The user should ensure that, where external data communication takes
place, the system is protected from viruses.
Inspection of electrical safety

To ensure safety, please obtain information on the relevant regulations in
your country regarding electrical equipment inspections. These must be
adhered to!
Unless legal requirements dictate otherwise, the operator is advised to carry
out an annual inspection in which the electrical safety is tested in
accordance with IEC 62353:2014.
When performing the inspection, observe the following instructions or the
service instructions issued by Carl Zeiss Meditec.
If you wish Carl Zeiss Meditec to perform the inspection, please contact
ZEISS Service or your local dealer.
Perform the following steps in the given order to perform an electrical safety
inspection of the device:
• Perform a visual inspection of all components and cables to ensure
orderly condition.
• Check the protective earth conductor resistance. To do this, connect the
device to the measuring instrument using the power cable. To perform a
measurement, press the measuring tip to the measurement points 1, 2
and 3 shown in Fig. 17. The measured value may not exceed 0.3 Ω.
• If there are doubts as to the effectiveness of the insulation (e.g. frequent
triggering of the ground fault circuit interrupter or of other protective
devices in the clinic or practice, or traces of liquid on the device indicating
that liquid has entered into the device), measure the insulation resistance
using a test voltage of 500 V. The measured value may not fall below
2 MΩ.
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1 Measurement point at head rest (screw)

2 Measurement point at instrument base (metallic connector panel)
3 Measurement point at power supply unit (screw)
Fig. 17 Testing electrical safety
• After successful measurement, the device leakage current must be

measured. Preferably, the differential current method should be used. The
device is in its operating state. Press the measuring tip onto the
measurement points again (1, 2, 3, Fig. 17). The measured value may not
exceed 0.5 mA.
• The inspection will be concluded by a function check. This should be
performed by a person who is familiar with the application.
• Note down the measured values.
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48 Optional accessories
Optional accessories
WARNING - RISK OF OPTICAL RADIATION

Use only accessories and spare parts approved by Carl Zeiss Meditec.

If connecting external components to the interfaces of the device, the
operator must ensure to meet the safety requirements as per
IEC 60601-1:2005, chapter 16 (medical electrical systems)!
For connection to a LAN, a network isolator must be installed (cut-off
voltage at least 4 kV). To ensure electromagnetic immunity, only network
isolators supplied by Carl Zeiss Meditec may be used. Network isolators and
network cables must be installed in accordance with Fig. 18.
A USB isolator (cut-off voltage at least 4 kV) with USB cable must be used
for data exchanged via external USB devices with separate power supply.
The USB isolator may not be powered by a separate power supply.
CAUTION - RISK OF OPERATING ERRORS

Only software authorized by Carl Zeiss Meditec may be used in this
instrument.
The device may only be connected to private networks which are protected
from public networks (Internet) by firewalls conforming to the latest
technical standards!
The following may be purchased as optional accessories for CIRRUS photo:

• Demonstration eye
• USB flash drive
• Printer
• Network isolator and network cable
• USB isolator and USB cable
A complete up-to-date list of accessories can be obtained from your dealer.
000000-2121-813-GA-GB-050416
Optional accessories 49
Demonstration eye
The demonstration eye is designed for practicing operation of the CIRRUS
photo.
When required, the holder with the demonstration eye is inserted into the
fastening pin holes for the paper pads (6, Fig. 4) on the head rest. By moving
the unit longitudinally, an ametropia of ±5 D can be adjusted.
USB flash drive

The USB flash drive can be used for fast data transfer. It is connected to a
vacant USB port on the CIRRUS photo connection panel.
 The USB flash drive should not be inserted or removed while the
system is switching on or off. It should not be removed from the
system, when the LED on the USB flash drive is lit.
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Printer

The printer must be set up outside the patient environment (1.5 m from the
patient's seat at the instrument), operated with a network isolator and
plugged into a separate socket. The user may not touch the printer and
patient simultaneously.
CAUTION - RISK DUE TO FAULTY DATA

Only a PostScript-capable network printer may be used.
The printer is used for printing capture images. It can be connected to the
CIRRUS photo via the network as a network printer (see Fig. 18) or directly
(peer-to-peer), see the following description.
1 CIRRUS photo
2 Network cable with ferrite core
3 Ferrite core
4 Network isolator
5 Network cable
6 Network printer
Fig. 18 Connection to a printer via a network
 The purpose of the network isolator is to provide a galvanic

separation of the network supply (network cable) between the
CIRRUS photo and a network or network printer.
Risks arising from the printer or network for patiants and users are
thereby excluded.
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Installation of a network printer

The CIRRUS photo supports only PostScript® network printers. These can be
connected to the CIRRUS photo via Ethernet or via a printer server in an
existing network, or directly (peer-to-peer).
 Keep the user manual for your printer or printer server at hand. The
printer must be configured according to the instructions contained
in the user manual for the printer or printer server.
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Printer outside the patient environment
CIRRUS photo and printer are connected via a network
Fig. 19 Variations for printer installation
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Peer-to-peer connection of printer with CIRRUS photo
• Connect the network printer or printer server to the CIRRUS photo using
a so-called crossover cable or a non-crossover cable with a crossover
adapter.
 Select the length of the network cable such that the printer can be
positioned outside the patient environment (at least 1.5 m from
the patient to be examined).
• Switch on the CIRRUS photo and printer or printer server.

• Configure the network printer or printer server with the aid of the user
manual provided with the device as follows:
IP address: 192.168.100.6
Subnet mask: 255.255.255.0
Connection of printer via an existing network
 The administrator responsible for your local network must first of

all set up a network printer or printer server in the network. The
procedure for printer configuration is described in the user manual
for the network printer or printer server. The IP address and subnet
mask to be used will be assigned by the administrator of the
network.
• Connect the CIRRUS photo to the network with a network cable.

• Switch on the CIRRUS photo and printer or printer server.
• Click on the Print setup entry in the File menu.
• In the following dialog click to Add new printer and install the network
printer using the installation wizard.
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54 Technical data
Technical data
Essential performance of the CIRRUS photo
The essential performance features of the device are imaging and displaying measurements of the anterior
and posterior eye segment or in case of error no imaging or displaying of information.
Device data
Rated voltage; frequency 230 V AC (±10 %); 50/60 Hz
Total power consumption max. 2.0 A at 230 V
Protection mode IP 20 (conforming to EN 60529)
Protection class I (according to IEC/AAMI/ANSI 60601-1:2005)
Application class (device type) B (according to IEC/AAMI/ANSI 60601-1:2005)
Observation illumination IR-LEDs - light emitting diodes, 830 nm
Fuses 2 x T6.3 A/H 250 V 5 mm x 20 mm
Battery of the PC motherboard
Type CR 2032
Manufacturer Varta
Dimensions
Utility space of instrument table (W x D) 1060 mm x 420 mm (different dimensions may apply
depending on the instrument table used)
Footprint of table-top unit 469 mm x 466 mm (including lateral cable covers)
Total height (including head rest) 1390 mm (plus 300 mm lift)
Weights
Instrument table 48 kg
Table-top unit 33 kg
Under-desk unit 28 kg
Monitor 6 kg
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Technical data 55
Imaging
Fundus camera image capture
Field angle 45° and 30°
Ametropia compensation +35 D to -35 D continuous
Filter Blue/IR cut filter (UV and IR protection)
Fluorescein and ICG angiography filter
Fundus autofluorescence filter
Max. image sequence 1 image every 2 s
Magnification 0.5x on image sensor (image diameter on sensor 7.4 mm),
independent of focusing state
Light source Xenon flash bulb
HD-OCT imaging
Axial resolution 5 µm (in tissue)
Transversal resolution 15 µm (in tissue)
Scan rate 27,000 A-scans per seconds
A-scan depth 2.0 mm (in tissue); 1024 pixels
Radiation source Superluminescence diode (SLD), 840 nm
Optical power < 725 µW on the cornea
Ambient conditions for intended use

Temperature +10 °C to +35 °C
Relative humidity 30 % to 90 %
Altitude up to 3,000 m above sea level
Environmental conditions for storage and transport (unpacked)

Temperature -10 °C to +55 °C
Ambient conditions for storage and transport in original packaging

Temperature -40 °C to +70 °C
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56 Electromagnetic compatibility
Electromagnetic compatibility
CAUTION - RISK OF ELECTROMAGNETIC RADIATION

The CIRRUS photo may not be placed next to or stacked together with
other equipment, except in the device configurations described in this user
manual. If it is necessary to stack the device near to or together with other
devices, monitor the performance of the CIRRUS photo to check that it is
operating correctly in this configuration.
CAUTION - RISK OF MEASURING ERRORS

It is not possible to predict the precise effect that the field strength of
portable and mobile RF communication equipment and fixed transmitters
will theoretically have on the CIRRUS photo. Observe the recommended
distances in section Electromagnetic compatibility when operating radio
devices or radio transmission components in the direct vicinity of the
CIRRUS photo. Monitor the CIRRUS photo during use to ensure that it is
being used as specified in the particular environment. Users should not rely
solely on measuring results made using CIRRUS photo in making decisions,
but should rely on their own expertise and judgment.
Replacement cables should only be purchased from Carl Zeiss Meditec itself
or dealers authorized by Carl Zeiss Meditec.
The use of accessories, any converters or cables which are not specified in
this user manual or have not been purchased as spare parts from
Carl Zeiss Meditec can result in increased emissions or reduced immunity of
the device.
Relevant accessories, leads and converters:
• Power supply cable (2.5 m)
• Appliance extension: Table  power supply (0.4 m)
• Appliance extension: Power supply  monitor (0.75 m)
• Keyboard and cable (1.75 m)
• Mouse and cable (1.80 m)
• DVI cable (1.80 m)
• Cable 24 V (0.65 m/0.90 m)
• CC Galvo cable external (1.20 m)
• Patch cable CAT6 (1 m)
• PCIe cable AWG28 (1 m)
000000-2121-813-GA-GB-050416
Electromagnetic compatibility 57
The information below only applies for the accessories specified and
supplied by Carl Zeiss Meditec for the device.
Guidance and manufacturer’s declaration - electromagnetic emissions

The CIRRUS photo is intended for use in the electromagnetic environment specified below. The customer or
the user of the CIRRUS photo should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
RF emissions CISPR 11 Group 1 The CIRRUS photo uses RF energy only for its
internal function. Therefore, its RF emissions
are very low and are not likely to cause any
interference in nearby electronic equipment.
RF emissions CISPR 11 Class B The CIRRUS photo is suitable for use in all
establishments, including domestic
Harmonic emissions IEC 61000-3-2 Class A
establishments and those directly connected
Voltage fluctuations/flicker emissions Complies to the public low-voltage power supply
IEC 61000-3-3 network that supplies buildings used for
domestic purposes.
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Guidance and manufacturer’s declaration - electromagnetic immunity

Immunity test IEC 60601 test level Compliance level Electromagnetic environment -
guidance
Electrostatic ±6 kV contact ±6 kV contact Floors should be wood, concrete
discharge (ESD) ±8 kV air ±8 kV air or ceramic tile. If floors are
IEC 61000-4-2 covered with synthetic material,
the relative humidity should be at
least 30 %.
Fast electrical ±2 kV for power supply ±2 kV for power supply Mains power quality should be
transient/burst lines lines that of typical commercial or
IEC 61000-4-4 ±1 kV for input/output ±1 kV for input/output hospital environments.
lines lines
Surge IEC 61000-4-5 ±1 kV line(s) to line(s) ±1 kV line(s) to line(s) Mains power quality should be
±2 kV line(s) to ground ±2 kV line(s) to ground that of typical commercial or
hospital environments.
Voltage dips, short < 5 % UT < 5 % UT Mains power quality should be
interruptions and (> 95 % dip in UT) (> 95 % dip in UT) that of typical commercial or
voltage variations on for 0.5 cycle for 0.5 cycle hospital environments. If the user
power supply input 40 % UT 40 % UT of the CIRRUS photo requires
lines IEC 61000-4-11 (60 % dip in UT) (60 % dip in UT) continued operation during
for 5 cycles for 5 cycles power mains interruptions, it is
recommended that the
70 % UT 70 % UT
CIRRUS photo be powered from
(30 % dip in UT) (30 % dip in UT)
an uninterruptible power supply
for 25 cycles for 25 cycles
or a battery.
< 5 % UT < 5 % UT
(> 95 % dip in UT) (> 95 % dip in UT)
for 5 s for 5 s
Power frequency 3 A/m 3 A/m Power frequency magnetic fields
(50/60 Hz) magnetic should be at levels characteristic
field IEC 61000-4-8 of a typical location in a typical
commercial or hospital
environment.
Note: UT is the a.c. mains voltage prior to application of the test level.
000000-2121-813-GA-GB-050416
Electromagnetic compatibility 59
Guidance and manufacturer’s declaration - electromagnetic immunity

Immunity test IEC 60601 test Compliance level Electromagnetic environment -
level guidance
Portable and mobile RF communications
equipment should be used no closer to any
part of the CIRRUS photo, including cables,
than the recommended separation distance
calculated from the equation applicable to
the frequency of the transmitter.
Recommended separation distance

Conducted RF 3 Vrms 3V d = 1.2 P
IEC 61000-4-6 150 kHz to
80 MHz
Radiated RF 3 V/m 3 V/m d = 1.2 P 80 MHz to 800 MHz
IEC 61000-4-3 80 MHz to
2.5 GHz d = 2.3 P 800 MHz to 2.5 GHz
where P is the maximum output power

rating of the transmitter in watts (W)
according to the transmitter manufacturer
and d is the recommended separation
distance in meters (m).
Field strengths from fixed RF transmittersa
should be less than the compliance levelb in
each frequency range.
Interference may occur in the vicinity of
equipment marked with the following
symbol:
Note 1: At 80 and 800 MHz, the separation distance of the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile
radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To
assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be
considered. If the measured field strength in the location in which the CIRRUS photo is used exceeds the applicable RF
compliance Level above, the CIRRUS photo should be observed to verify normal operation. If abnormal performance is
observed, additional measures may be necessary, such as re-orienting or relocating the CIRRUS photo.
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m
000000-2121-813-GA-GB-050416
Recommended separation distances between portable and mobile RF communications equipment

and the CIRRUS photo
The CIRRUS photo is intended for use in an electromagnetic environment in which radiated RF disturbances
are controlled. The customer or the user of the CIRRUS photo can help prevent electromagnetic interference
by maintaining a minimum distance between portable and mobile RF communications equipment
(transmitters) and the CIRRUS photo as recommended below, according to the maximum output power of the
communications equipment.
Rated maximum Separation distance according to frequency of transmitter
output power of m
transmitter
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
W
d = 1.2 P d = 1.2 P d = 2,3 P
0.01 0.12 0.12 0.23
0.1 0.37 0.37 0.74
1 1.2 1.2 2.3
10 3.7 3.7 7.4
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d
in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is
the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
Note 1: At 80 and 800 MHz, the separation distance of the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
000000-2121-813-GA-GB-050416
Abbreviations/Glossary 61
Abbreviations/Glossary
B Blue (capture mode)
D Diopters
(unit of measurement for refractive power)
DICOM Digital Imaging and Communications in Medicine
(Open standard for the exchange of digital images and
corresponding patient data in the medical sector)
DIN Deutsches Institut für Normung
(German standards institution)
DVI Digital visual interface
(interface for the digital transfer of video data)
EMR system Electronical medical record system
(practice management system)
EN European standard
FA Fluorescein angiography (capture mode)
FAF Fundus autofluorescence (capture mode)
Fig. Figure
FTP File transfer protocol
(network protocol for data transfer)
G Green (capture mode)
HD High definition
ICGA Indocyanine green angiography (capture mode)
IEC International electrotechnical commission
IR Infrared
LED Light emitting diode
MTA Medical technology assistant
OCT Optical coherence tomography
PC Personal computer
PDT Photodynamic therapy
R Red (capture mode)
SD-OCT Spectral domain optical coherence tomography
SLD Superluminescent diode
USB Universal serial bus
(standard interface for PC peripherals)
UV Ultraviolet
VGA Video graphics array (video signal output standard for PC)
000000-2121-813-GA-GB-050416
62 Figures
Figures
Fig. 1 Warning and information labels on the device ............................ 11
Fig. 2 Basic design of the CIRRUS photo ............................................... 18
Fig. 3 Controls of main unit, right hand view ........................................ 19
Fig. 4 Controls of main unit, left hand view .......................................... 20
Fig. 5 Connection panel of main unit .................................................... 21
Fig. 6 Connection panel of OCT engine ................................................ 22
Fig. 7 Power module, front view .......................................................... 24
Fig. 8 Power module, rear view ............................................................ 24
Fig. 9 Patient dialog ............................................................................ 28
Fig. 10 Control panel on instrument base ............................................... 31
Fig. 11 Installation of the test tool .......................................................... 34
Fig. 12 Replacing the flashing diode ....................................................... 38
Fig. 13 Remove dust from front lens....................................................... 42
Fig. 14 Cleaning with microfiber cloth .................................................... 43
Fig. 15 Progress of cleaning ................................................................... 44
Fig. 16 Example for dirt and cleaning ..................................................... 44
Fig. 17 Testing electrical safety ............................................................... 47
Fig. 18 Connection to a printer via a network ......................................... 50
Fig. 19 Variations for printer installation ................................................. 52
000000-2121-813-GA-GB-050416
Index 63
Index
A
Abbreviations ............................................................................................ 61
Accessories, optional ................................................................................. 48
Angiography ............................................................................................. 36
C
Care .......................................................................................................... 39
Cleaning .................................................................................................... 39
Control ...................................................................................................... 30
Control panel ............................................................................................ 31
D
Daily use.................................................................................................... 27
Data backup ........................................................................................ 39, 45
Demonstration eye .................................................................................... 49
Description of the device ........................................................................... 17
Device classification ..................................................................................... 6
Disposal..................................................................................................... 10
E
Electrical connection .................................................................................. 21
Electromagnetic compatibility .................................................................... 56
F
Fault remedy ............................................................................................. 37
Figures ...................................................................................................... 62
Flashing diode, replacing ........................................................................... 38
Fluorescein angiography ............................................................................ 36
Functional description ............................................................................... 15
G
Glossary .................................................................................................... 61
I
ICG angiography ....................................................................................... 36
Installation ................................................................................................ 25
Intended use ............................................................................................... 7
L
Labels ........................................................................................................ 11
M
Maintenance ............................................................................................. 39
Maintenance and care ............................................................................... 37
Manufacturer’s declaration .......................................................................... 6
000000-2121-813-GA-GB-050416
64 Index
O
Operation of the device ............................................................................ 29
P
Package check list ....................................................................................... 5
Paper pads................................................................................................ 40
Performance specifications........................................................................ 15
Printer installation ..................................................................................... 51
S
Safety inspections ..................................................................................... 46
Service life ................................................................................................ 16
Shutting down .......................................................................................... 35
Switch off ................................................................................................. 35
Switching on............................................................................................. 28
Symbols ...................................................................................................... 4
T
Technical data .......................................................................................... 54
U
USB-flash drive.......................................................................................... 49
User interface ........................................................................................... 30
User profile ................................................................................................. 9
000000-2121-813-GA-GB-050416
Carl Zeiss Meditec AG
Goeschwitzer Str. 51-52
07745 Jena
Germany
Phone: +49 3641 220 333
Fax: +49 3641 220 112 000000-2121-813-GA-GB-050416
Email: info.meditec@zeiss.com CIRRUS photo
Internet: www.zeiss.com/med Specifications subject to change
Contents

2
[000000-2121-813-AddGA01-GB-210915]
000000-2121-813-Inhalt2-GB

000000-2121-813-AddGA01-GB-210915
Online remote maintenance tool 1
Online remote maintenance tool

The device is equipped with an online remote maintenance module, which
enables you to contact Carl Zeiss Meditec Service for troubleshooting and
remedy via the Internet.
The online remote maintenance module offers two problem resolution

options:
• The software user interface is made visible to a service technician. The
operator carries out actions himself under instruction from the service
technician.
• The user interface is visible to a service technician, who is able to operate
or configure the software directly using the remote control function.
To use the remote maintenance tool, proceed as follows:

• Ensure that the device is connected to the Internet.
• Start the online remote maintenance tool as described in the software
description of the device. A dialog will be displayed asking you to confirm
the terms and conditions.
Fig. 1 Dialog box for confirmation of the conditions of use
• If you do not accept the conditions of use, terminate the procedure by

clicking on Cancel.
• If you accept the conditions of use, select Yes, I agree and click on
Next. The login window for remote maintenance will be displayed.
000000-2121-813-AddGA-GB-210915
2 Online remote maintenance tool
Fig. 2 Login window for remote maintenance
• Call the Carl Zeiss Meditec service team who will provide you with a
6-digit session number.
• Enter the session number in the Session ID and click on Finish.
Fig. 3 Dialog for confirmation of screen content transfer
• Confirm the transfer in the netviewer dialog by clicking on Yes.

• A connection will be established and the remote maintenance module
control window will be displayed on your screen.
• Allow the service technician to remotely control your PC by clicking on
Yes in the following dialog.
000000-2121-813-AddGA01-GB-210915
Offline remote maintenance tool 3
Fig. 4 Dialog for remote control confirmation
• The control window for remote control will be displayed on your screen.
The service technican is now able to control the user interface of your in-
strument and resolve the problem.
• Closing the control window will terminate the remote maintenance
session.
Offline remote maintenance tool

If the device does not have a network connection, the offline remote
maintenance module can be used.
In the event of problems, the user can create an archive with information
and screenshots of the occurring problem, export them to an external net-
work drive or USB flash drive and send them by e-mail to Carl Zeiss Meditec
Service.
Fig. 5 Dialog box for generating an archive for offline remote maintenance
000000-2121-813-AddGA-GB-210915
4 Offline remote maintenance tool
To start offline remote maintenance, proceed as follows:

• Enter a description of the problem in the Problem description text box
of the dialog window.
• Screenshots which serve to illustrate the problem may be added by press-
ing the Add screenshot button.
• If you consent to the image export, click on Yes in the following dialog
box.
Fig. 6 Request for consent to export a screenshot
• In the next window specify the quality of the exported image and click on
the Screenshot button to generate a screenshot of your screen.
• Once you have created all the necessary screenshots, click on Continue
in the offline remote maintenance dialog box (see Fig. 5).
• In the next step select the external drive (network drive or USB flash drive)
to which the file package is to be exported and click on Continue.
If the creation of the archive was successful, a confirmation will be dis-
played. The file ServicePackage.svp will now be found on the drive speci-
fied in the last step. Send this file via e-mail to Carl Zeiss Meditec Service.
Carl Zeiss Meditec Service will evaluate the file and issue instructions to solve
the problem or arrange a service appointment with you.
000000-2121-813-AddGA01-GB-210915
Notes on and conditions of use for the remote maintenance tool 5
Notes on and conditions of use for the remote

maintenance tool
1. Use of the remote maintenance tool requires that the
Carl Zeiss Meditec AG service team or a company authorized by them
be contacted beforehand.
2. The remote maintenance function can be activated by the user only.

This requires the entry of an activation code. The user can then switch
between observation mode and remote control mode. The user can
abort the selected remote maintenance mode at any time by closing the
remote maintenance dialog box. It is not possible for the service techni-
cian to start or restart observation mode without the user's consent.
3. In observation mode, a service technician from Carl Zeiss Meditec AG or

a company authorized by them is able to continuously view a copy of
the current program interface. Service personnel may therefore be able
to view patient details if they are displayed in the visible program inter-
face. It is solely the user’s responsibility to take all necessary measures
to ensure that confidential data is protected during the remote mainte-
nance session and that all legal regulations are adhered to.
4. In remote control mode, a service technician from Carl Zeiss Meditec AG

or an authorized company is able to operate the instrument’s user
interface with the privileges of the currently logged in user. Remote
control mode can be terminated at any time by pressing <F5>. The
program will then switch to observation mode. It is solely the user’s
responsibility to take all necessary measures to ensure that confidential
data is protected during the remote maintenance session and that all
legal regulations are adhered to.
5. The user may not leave the instrument unsupervised in observation or

remote maintenance mode. Under no circumstances is the remote
maintenance tool to be used for fault diagnosis while treatment is being
carried out. The user must alert the service technician from
Carl Zeiss Meditec AG or a company authorized by them by telephone if
there are other people in the room in which the instrument is located
during a remote maintenance session.
6. The user is solely responsible for the safe operation of the instrument
during a remote maintenance session.
000000-2121-813-AddGA-GB-210915
6 Notes on and conditions of use for the remote maintenance tool
7. No guarantee is entered into for advice given during a remote mainte-

nance session. Carl Zeiss Meditec AG in particular does not guarantee
that they or a company authorized by them will be able to diagnose or
remedy a fault using remote maintenance mode. If it is not possible to
diagnose or remedy the fault in remote maintenance mode, the user
will need to request that a service technician attend the installation. This
will incur further costs.
8. The user may only permit the use of remote maintenance mode if the
currently logged on user’s privileges do not permit unauthorized access
to protected data.
9. The user may only permit the use of remote maintenance mode if no
danger can arise to patients or other persons through the operation of
the instrument in remote maintenance mode.
10. Except in cases of intent or gross negligence, Carl Zeiss Meditec AG

accepts no liability – on any legal basis – for damages arising during
fault diagnosis or maintenance in remote maintenance mode.
11. Place of jurisdiction is, for commercial customers, the registered place of
business of the Carl Zeiss Group company making use of these condi-
tions of use. We are, however, also entitled to pursue claims against
you at your official place of business.
12. The law of the Federal Republic of Germany applies, with the exclusion
of UN sales law and the referral provisions of German private interna-
tional law.
13. In addition, the currently applicable version of the general terms and
conditions for service agreements apply to all remote maintenance pro-
cedures. Users can view the current version of the general terms and
conditions for service agreements on the internet at
http://www.zeiss.com/med/terms.
14. Should any individual provisions of these conditions be in part or in full

invalid, the validity of the remaining provisions or the remaining parts of
such provisions shall not be affected.
000000-2121-813-AddGA01-GB-210915
07745 Jena
Germany
Phone: +49 3641 220 333
Fax: +49 3641 220 112 000000-2121-813-AddGA01-GB-210915
Email: info.meditec@zeiss.com Remote maintenance tool
Internet: www.zeiss.com/med Specifications subject to change
Contents

3
[WINDOWS EMBEDDED STANDARD 7 GB, 21.06.2012]
000000-2121-813-Inhalt3-GB
These license terms are an agreement between you and Carl Zeiss Meditec AG (CZM). Please read them.
They apply to the software included on this device. The software also includes any separate media on
which you received the software.
The software on this device includes software licensed from Microsoft Corporation or its affiliate.
The terms also apply to any Microsoft
• updates,
• supplements,
• Internet-based services, and
• support services
for this software, unless other terms accompany those items. If so, those terms apply.
If you obtain updates or supplements directly from Microsoft, then Microsoft, and not CZM, licenses those
to you.
As described below, using the software also operates as your consent to the transmission of
certain computer information for Internet-based services.
By using the software, you accept these terms. If you do not accept them, do not use the
software. Instead, contact CZM to determine its return policy for a refund or credit.
If you comply with these license terms, you have the rights below.
1. USE RIGHTS
Use. The software license is permanently assigned to the device with which you acquired the
software. You may use the software on the device.
2. ADDITIONAL LICENSING REQUIREMENTS AND/OR USE RIGHTS
a. Specific Use. CZM designed the device for a specific use. You may only use the software for
that use.
b. Other Software. You may use other programs with the software as long as the other programs
y directly supports the manufacturer’s specific use for the device, or
y provide system utilities, resource management, or anti-virus or similar protection.
Software that provides consumer or business tasks or processes may not be run on the
device. This includes email, word processing, spreadsheet, database, scheduling and
personal finance software. The device may use terminal services protocols to access such
software running on a server.
c. Device Connections. You may not use the software as server software. In other words, more
than one device may not access, display, run, share or use the software at the same time.
You may use terminal services protocols to connect the device to a server running
business task or processes software such as email, word processing, scheduling or
spreadsheets.
You may allow up to ten other devices to access the software to use
• File Services,
• Print Services,
WINDOWS EMBEDDED STANDARD 7 GB, 21.06.2012 1

• Internet Information Services, and
• Internet Connection Sharing and Telephony Services.
The ten connection limit applies to devices that access the software indirectly through
“multiplexing” or other software or hardware that pools connections. You may use unlimited
inbound connections at any time via TCP/IP.
d. Remote Access Technologies. You may access and use the software remotely from another
device using remote access technologies as follows.
Remote Desktop. The single primary user of the device may access a session from any other
device using Remote Desktop or similar technologies. A “session” means the experience of
interacting with the software, directly or indirectly, through any combination of input, output and
display peripherals. Other users may access a session from any device using these technologies,
if the remote device is separately licensed to run the software.
Other Access Technologies. You may use Remote Assistance or similar technologies to share an
active session.
Other Remote Uses. You may allow any number of devices to access the software for purposes
other than those described in the Device Connections and Remote Access Technologies sections
above, such as to synchronize data between devices.
e. Font Components. While the software is running, you may use its fonts to display and print
content. You may only
• embed fonts in content as permitted by the embedding restrictions in the fonts; and
• temporarily download them to a printer or other output device to print content.
f. Icons, images and sounds. While the software is running, you may use but not share its icons,
images, sounds, and media.
3. VHD BOOT. Additional copies of the software created using the software’s Virtual Hard Disk
functionality (“VHD Image”) may be pre-installed on the physical hard disk of the device. These VHD
Images may only be used for maintaining or updating the software installed on the physical hard disk
or drive. If the VHD Image is the only software on your device, it may be used as the primary
operating system but all other copies of the VHD Image may only be used for maintenance and
updating.
4. POTENTIALLY UNWANTED SOFTWARE. The software may include Windows Defender. If

Windows Defender is turned on, it will search this device for “spyware,” “adware” and other
potentially unwanted software. If it finds potentially unwanted software, the software will ask you if
you want to ignore, disable (quarantine) or remove it. Any potentially unwanted software rated
“high” or “severe,” will be automatically removed after scanning unless you change the default
setting. Removing or disabling potentially unwanted software may result in
• Other software on your device ceasing to work, or
• Your breaching a license to use other software on this device
By using this software , it is possible that you will also remove or disable software that is not
potentially unwanted software.
5. SCOPE OF LICENSE. The software is licensed, not sold. This agreement only gives you some rights
to use the software. CZM and Microsoft reserve all other rights. Unless applicable law gives you more
rights despite this limitation, you may use the software only as expressly permitted in this agreement.
In doing so, you must comply with any technical limitations in the software that allow you to use it
2 WINDOWS EMBEDDED STANDARD 7 GB, 21.06.2012

only in certain ways. For more information, see the software documentation or contact CZM. You
may not:
work around any technical limitations in the software;
reverse engineer, decompile or disassemble the software;
make more copies of the software than specified in this agreement;
publish the software for others to copy;
rent, lease or lend the software; or
use the software for commercial software hosting services.
Except as expressly provided in this agreement, rights to access the software on this device do not
give you any right to implement Microsoft patents or other Microsoft intellectual property in software
or devices that access this device.
6. INTERNET-BASED SERVICES. Microsoft provides Internet-based services with the software.
Microsoft may change or cancel them at any time.
a. Consent for Internet-Based Services. The device may contain one or more of the software
features described below. These features connect to Microsoft or service provider computer
systems over the Internet. In some cases, you will not receive a separate notice when they
connect. For more information about these features, visit
go.microsoft.com/fwlink/?linkid=104604.
By using these features, you consent to the transmission of this information. Microsoft
does not use the information to identify or contact you.
Computer Information. The following features use Internet protocols, which send to the
appropriate systems computer information, such as your Internet protocol address, the type of
operating system and browser, the name and version of the software you are using, and the
language code of the device where you installed the software. Microsoft uses this information to
make the Internet-based services available to you. CZM has elected to turn on the following
features on the device.
• Plug and Play and Plug and Play Extensions. You may connect new hardware to your device.
Your device may not have the drivers needed to communicate with that hardware. If so, the
update feature of the software can obtain the correct driver from Microsoft and install it on
your device.
• Web Content Features. Features in the software can retrieve related content from Microsoft
and provide it to you. Examples of these features are clip art, templates, online training,
online assistance and Appshelp. You may choose to switch them off or not use them.
• Digital Certificates. The software uses x.509 version 3 digital certificates. These digital
certificates confirm the identity of user sending information to each other and allow you to
encrypt the information. The software retrieves certificates and updates certificate revocation
lists over the Internet.
• Auto Root Update. The Auto Root Update feature updates the list of trusted certificate
authorities. You can switch off this feature.
• Windows Media Digital Rights Management. Content owners use Windows Media digital
rights management technology (WMDRM) to protect their intellectual property, including
copyrights. This software and third party software use WMDRM to play and copy WMDRM-
protected content. If the software fails to protect the content, content owners may ask

Microsoft to revoke the software’s ability to use WMDRM to play or copy protected content.
Revocation does not affect other content. When you download licenses for protected content,
you agree that Microsoft may include a revocation list with the licenses. Content owners may
require you to upgrade WMDRM to access their content. Microsoft software that includes
WMDRM will ask for your consent prior to the upgrade. If you decline an upgrade, you will
not be able to access content that requires the upgrade. You may switch off WMDRM
features that access the Internet. When these features are off, you can still play content for
which you have a valid license.
• Windows Media Player. When you use Windows Media Player, it checks with Microsoft for
compatible online music services in your region;
new versions of the player; and
codecs if your device does not have the correct ones for playing content.
You can switch off this feature. For more information, go to:
go.microsoft.com/fwlink/?LinkId=51331.
• Malicious Software Removal/Clean On Upgrade. Before installation of the software, the
software will check and remove certain malicious software listed at
www.support.microsoft.com/?kbid=890830 (“Malware”) from your device. When the
software checks your device for Malware, a report will be sent to Microsoft about any
Malware detected or errors that occurred while the software was checking for Malware. No
information that can be used to identify you is included in the report. You may disable the
software’s Malware reporting functionality by following the instructions found at
www.support.microsoft.com/?kbid=890830.
• Network Awareness. This feature determines whether a system is connected to a network by

either passive monitoring of network traffic or active DNS or HTTP queries. The query only
transfers standard TCP/IP or DNS information for routing purposes. You can switch off the
active query feature through a registry setting.
• Windows Time Service. This service synchronizes with www.time.windows.com once a week
to provide your l device with the correct time. The connection uses standard NTP protocol.
• Search Suggestions Service. In Internet Explorer, when you type a search query in the
Instant Search box or type a question mark (?) before your search term in the Address bar,
you will see search suggestions as you type (if supported by your search provider).
Everything you type in the Instant Search box or in the Address bar when preceded by a
question mark (?) is sent to your search provider as you type. Also, when you press Enter or
click the Search button, the text in the Instant Search box or Address bar is sent to the
search provider. If you use a Microsoft search provider, use of the information sent is subject
to the Microsoft Online Privacy Statement. This statement is available at
go.microsoft.com/fwlink/?linkid=31493. If you use a third-party search provider, use of the
information sent will be subject to the third party’s privacy practices. You can turn search
suggestions off at any time. To do so, use Manage Add-ons under the Tools button in
Internet Explorer. For more information about the search suggestions service, see
go.microsoft.com/fwlink/?linkid=128106.
• Consent to Update Infrared Emitter/Receiver. The software may contain technology to

ensure the proper functioning of the infrared emitter/receiver device shipped with certain
Media Center-based products. You agree that the software may update the firmware of this
device.

• Media Center Online Promotions. If you use Media Center features of the software to access
Internet-based content or other Internet-based services, such services may obtain the
following information from the software to enable you to receive, accept and use certain
promotional offers:
• certain device information, such as your Internet protocol address, the type of operating
system and browser you are using, and the name and version of the software you are
using,
• the requested content, and
• the language code of the device where you installed the software.
• Your use of the Media Center features to connect to those services serves as your
consent to the collection and use of such information.
• Media Playback Updates. The software on the device may include media playback features
which receives updates directly from the MSCORP Media Playback Update servers. If
activated by your manufacturer, these updates will be downloaded and installed without
further notice to you. The manufacturer is responsible for ensuring these updates work on
your device.
• Windows Update Agent. The software on the device includes Windows Update Agent
(“WUA”). This feature enables your device to access Windows Updates either directly from
MSCORP Windows Update server or from a server installed with the required server
component and from the Microsoft Windows Update server. To enable the proper functioning
of the Windows Update service in the software (if you use it) updates or downloads to the
Windows Update service will be required from time to time and downloaded and installed
without further notice to you. Without limiting any other disclaimer in these license terms or
any license terms accompanying a Windows Update, you acknowledge and agree that no
warranty is provided by Microsoft Corporation or their affiliates with respect to any Windows
Update that you install or attempt to install on your device.
b. Use of Information. Microsoft may use the device information, error reports, and Malware
reports to improve our software and services. We may also share it with others, such as
hardware and software vendors. They may use the information to improve how their
products run with Microsoft software.
c. Misuse of Internet-based Services. You may not use these services in any way that
could harm them or impair anyone else’s use of them. You may not use the services to try to
gain unauthorized access to any service, data, account or network by any means.
7. PRODUCT SUPPORT. Contact CZM for support options. Refer to the support number provided with
the device.
8. MICROSOFT .NET BENCHMARK TESTING. The software includes one or more components of the
.NET Framework (“.NET Components”). You may conduct internal benchmark testing of those
components. You may disclose the results of any benchmark test of those components, provided that
you comply with the conditions set forth at go.microsoft.com/fwlink/?LinkID=66406.
Notwithstanding any other agreement you may have with Microsoft, if you disclose such benchmark
test results, Microsoft shall have the right to disclose the results of benchmark tests it conducts of
your products that compete with the applicable .NET Component, provided it complies with the same
conditions set forth at go.microsoft.com/fwlink/?LinkID=66406.

9. BACKUP COPY. You may make one backup copy of the software. You may use it only to reinstall
the software on the device.
10. DOCUMENTATION. Any person that has valid access to your device or internal network may copy
and use the documentation for your internal, reference purposes.
11. PROOF OF LICENSE. If you acquired the software on the device, or on a disc or other media, a
genuine Certificate of Authenticity label with a genuine copy of the software identifies licensed
software. To be valid, this label must be affixed to the device, or included on or in CZM’s software
packaging. If you receive the label separately, it is not valid. You should keep the label on the device
or packaging to prove that you are licensed to use the software. To identify genuine Microsoft
software, see www.howtotell.com.
12. TRANSFER TO A THIRD PARTY. You may transfer the software only with the device, the
Certificate of Authenticity label, and these license terms directly to a third party. Before the transfer,
that party must agree that these license terms apply to the transfer and use of the software. You
may not retain any copies of the software including the backup copy.
13. NOTICE ABOUT THE H.264/AVC VISUAL STANDARD, THE VC-1 VIDEO STANDARD, THE
MPEG-4 VISUAL STANDARD AND THE MPEG-2 VIDEO STANDARD. This software may include
H.264/AVC, VC-1, MPEG-4 Part 2, and MPEG-2 visual compression technology. If the software
includes those visual compression technologies MPEG LA, L.L.C. requires this notice:
THIS PRODUCT IS LICENSED UNDER ONE OR MORE VIDEO PATENT PORTFOLIO LICENSES SUCH
AS, AND WITHOUT LIMITATION, THE AVC, THE VC-1, THE MPEG-4 PART 2 VISUAL, AND THE
MPEG-2 VIDEO PATENT PORTFOLIO LICENSES FOR THE PERSONAL AND NON-COMMERCIAL USE OF
A CONSUMER TO (i) ENCODE VIDEO IN COMPLIANCE WITH THE ABOVE STANDARDS (“VIDEO
STANDARDS”) AND/OR (ii) DECODE VIDEO THAT WAS ENCODED BY A CONSUMER ENGAGED IN A
PERSONAL AND NON-COMMERCIAL ACTIVITY OR WAS OBTAINED FROM A VIDEO PROVIDER
LICENSED TO PROVIDE VIDEO UNDER SUCH PATENT PORTFOLIO LICENSES. NONE OF THE
LICENSES EXTEND TO ANY OTHER PRODUCT REGARDLESS OF WHETHER SUCH PRODUCT IS
INCLUDED WITH THIS PRODUCT IN A SINGLE ARTICLE. NO LICENSE IS GRANTED OR SHALL BE
IMPLIED FOR ANY OTHER USE. ADDITIONAL INFORMATION MAY BE OBTAINED FROM MPEG LA,
L.L.C. SEE WWW.MPEGLA.COM.
14. NOTICE ABOUT THE MP3 AUDIO STANDARD. This software includes MP3 audio encoding and
decoding technology as defined by ISO/IEC 11172-3 and ISO/IEC 13818-3. It is not licensed for any
implementation or distribution in any commercial product or service.
15. NOT FAULT TOLERANT. The software is not fault tolerant. CZM installed the software on
the device and is responsible for how it operates on the device.
16. RESTRICTED USE. The Microsoft software was designed for systems that do not require fail-safe
performance. You may not use the Microsoft software in any device or system in which a malfunction
of the software would result in foreseeable risk of injury or death to any person. This includes
operation of nuclear facilities, aircraft navigation or communication systems and air traffic control.
17. NO WARRANTIES FOR THE SOFTWARE. The software is provided “as is”. You bear all
risks of using it. Microsoft gives no express warranties, guarantees or conditions. Any
warranties you receive regarding the device or the software do not originate from, and
are not binding on, Microsoft or its affiliates. When allowed by your local laws, CZM and
Microsoft exclude implied warranties of merchantability, fitness for a particular purpose
and non-infringement.
18. LIABILITY LIMITATIONS. You can recover from Microsoft and its affiliates only direct
damages up to two hundred fifty U.S. Dollars (U.S. $250.00). You cannot recover any
other damages, including consequential, lost profits, special, indirect or incidental
damages.

This limitation applies to:
anything related to the software, services, content (including code) on third party
internet sites, or third party programs, and
claims for breach of contract, breach of warranty, guarantee or condition, strict
liability, negligence, or other tort to the extent permitted by applicable law.
It also applies even if Microsoft should have been aware of the possibility of the
damages. The above limitation may not apply to you because your country may not allow
the exclusion or limitation of incidental, consequential or other damages.
19. EXPORT RESTRICTIONS. The software is subject to United States export laws and regulations.
You must comply with all domestic and international export laws and regulations that apply to the
software. These laws include restrictions on destinations, end users and end use. For additional
information, see www.microsoft.com/exporting.
20. ENTIRE AGREEMENT. This agreement, additional terms (including any printed-paper license terms
that accompany the software and may modify or replace some or all of these terms), and the terms
for supplements, updates, Internet-based services and support services that you use, are the entire
agreement for the software and support services.
21. APPLICABLE LAW
a. United States. If you acquired the software in the United States, Washington state law governs
the interpretation of this agreement and applies to claims for breach of it, regardless of conflict of
laws principles. The laws of the state where you live govern all other claims, including claims
under state consumer protection laws, unfair competition laws, and in tort.
b. Outside the United States. If you acquired the software in any other country, the laws of that
country apply.
22. Third Party Programs. Microsoft provides the following copyright notices for third party software
included in the software. These notices are required by the respective copyright holders and do not
change your license to use this software.
Portions of this software are based in part on the work of Spider Systems ® Limited. Because Microsoft has
included the Spider Systems Limited software in this product, Microsoft is required to include the following text that
accompanied such software:
Copyright 1987 Spider Systems Limited
Portions of this software are based in part on the work of Seagate Software.
Portions of this software are based in part on the work of ACE*COMM Corp. Because Microsoft has included the
ACE*COMM Corp. software in this product, Microsoft is required to include the following text that accompanied
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Copyright 1995-1997 ACE*COMM Corp
Portions of this software are based in part on the work of Sam Leffler and Silicon Graphics, Inc. Because Microsoft
has included the Sam Leffler and Silicon Graphics software in this product, Microsoft is required to include the
following text that accompanied such software:
Copyright © 1988-1997 Sam Leffler

Copyright © 1991-1997 Silicon Graphics, Inc.

Permission to use, copy, modify, distribute, and sell this software and
its documentation for any purpose is hereby granted without fee, provided
that (i) the above copyright notices and this permission notice appear in
all copies of the software and related documentation, and (ii) the names of
Sam Leffler and Silicon Graphics may not be used in any advertising or
publicity relating to the software without the specific, prior written
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THE SOFTWARE IS PROVIDED "AS-IS" AND WITHOUT WARRANTY OF ANY KIND,

EXPRESS, IMPLIED OR OTHERWISE, INCLUDING WITHOUT LIMITATION, ANY
WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE.
IN NO EVENT SHALL SAM LEFFLER OR SILICON GRAPHICS BE LIABLE FOR

ANY SPECIAL, INCIDENTAL, INDIRECT OR CONSEQUENTIAL DAMAGES OF ANY KIND,
OR ANY DAMAGES WHATSOEVER RESULTING FROM LOSS OF USE, DATA OR PROFITS,
WHETHER OR NOT ADVISED OF THE POSSIBILITY OF DAMAGE, AND ON ANY THEORY OF
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Portions Copyright © 1998 PictureTel Corporation
Portions of this software are based in part on the work of Highground Systems. Because Microsoft has included the
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Copyright © 1996-1999 Highground Systems
Windows 7 incorporates compression code from the Info-ZIP group. There are no extra charges or costs due to the
use of this code, and the original compression sources are freely available from www.info-zip.org/ or ftp://ftp.info-
zip.org/pub/infozip/src/ on the Internet.
Portions Copyright © 2000 SRS Labs, Inc
This product includes software from the 'zlib' general purpose compression library.
Portions of this software are based in part on the work of ScanSoft, Inc. Because Microsoft has included the
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TextBridge® OCR © by ScanSoft, Inc.
Portions of this software are based in part on the work of University of Southern California. Because Microsoft has
included the University of Southern California software in this product, Microsoft is required to include the
Copyright © 1996 by the University of Southern California

All rights reserved.
Permission to use, copy, modify, and distribute this software and its documentation in source and binary
forms for any purpose and without fee is hereby granted, provided that both the above copyright notice and

this permission notice appear in all copies, and that any documentation, advertising materials, and other
materials related to such distribution and use acknowledge that the software was developed in part by the
University of Southern California, Information Sciences Institute. The name of the University may not be
used to endorse or promote products derived from this software without specific prior written permission.
THE UNIVERSITY OF SOUTHERN CALIFORNIA makes no representations about the suitability of this
software for any purpose. THIS SOFTWARE IS PROVIDED "AS IS" AND WITHOUT ANY EXPRESS
OR IMPLIED WARRANTIES, INCLUDING, WITHOUT LIMITATION, THE IMPLIED
WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE.
Other copyrights might apply to parts of this software and are so noted when applicable.
Portions of this software are based in part on the work of James Kanze. Because Microsoft has included the James
Kanze software in this product, Microsoft is required to include the following text that accompanied such software:
COPYRIGHT AND PERMISSION NOTICE

Permission is hereby granted, free of charge, to any person obtaining a copy of this software and associated
documentation files (the "Software"), to deal in the Software without restriction, including without
limitation the rights to use, copy, publish, distribute, and/or sell copies of the Software, and to permit
persons to whom the Software is furnished to do so, provided that the above copyright notice(s) and this
permission notice appear in all copies of the Software and that both the above copyright notice(s) and this
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any extend, under the condition that, in the modified software, the prefix "GB_" is changed to something
else, and the name directories for includes files ("gb" in this distribution) is also changed.
THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR
IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY,
FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT OF THIRD PARTY RIGHTS.
IN NO EVENT SHALL THE COPYRIGHT HOLDER OR HOLDERS INCLUDED IN THIS NOTICE
BE LIABLE FOR ANY CLAIM, OR ANY SPECIAL INDIRECT OR CONSEQUENTIAL DAMAGES,
OR ANY DAMAGES WHATSOEVER RESULTING FROM LOSS OF USE, DATA OR PROFITS,
WHETHER IN AN ACTION OF CONTRACT, NEGLIGENCE OR OTHER TORTIOUS ACTION,
ARISING OUT OF OR IN CONNECTION WITH THE USE OR PERFORMANCE OF THIS
SOFTWARE.
Except as contained in this notice, the name of a copyright holder shall not be used in advertising or
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the copyright holder.
This product contains software from Cisco ISAKMP Services.
Portions of this software are based in part on the work of RSA Data Security, Inc. Because Microsoft has included
the RSA Data Security, Inc. software in this product, Microsoft is required to include the following text that
Copyright © 1990, RSA Data Security, Inc. All rights reserved.
License to copy and use this software is granted provided that it is identified as the "RSA Data Security,
Inc. MD5 Message-Digest Algorithm" in all material mentioning or referencing this software or this
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as "derived from the RSA Data Security, Inc. MD5 Message-Digest Algorithm" in all material mentioning
or referencing the derived work.

RSA Data Security, Inc. makes no representations concerning either the merchantability of this software or
the suitability of this software for any particular purpose. It is provided "as is" without express or implied
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These notices must be retained in any copies of any part of this documentation and/or software.
Portions of this software are based in part on the work of OpenVision Technologies, Inc. Because Microsoft has
included the OpenVision Technologies, Inc. software in this product, Microsoft is required to include the following
text that accompanied such software:
Copyright 1993 by OpenVision Technologies, Inc.
Permission to use, copy, modify, distribute, and sell this software and its documentation for any purpose is
hereby granted without fee, provided that the above copyright notice appears in all copies and that both that
copyright notice and this permission notice appear in supporting documentation, and that the name of
OpenVision not be used in advertising or publicity pertaining to distribution of the software without
specific, written prior permission. OpenVision makes no representations about the suitability of this
software for any purpose. It is provided "as is" without express or implied warranty.
OPENVISION DISCLAIMS ALL WARRANTIES WITH REGARD TO THIS SOFTWARE,

INCLUDING ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS, IN NO
EVENT SHALL OPENVISION BE LIABLE FOR ANY SPECIAL, INDIRECT OR CONSEQUENTIAL
DAMAGES OR ANY DAMAGES WHATSOEVER RESULTING FROM LOSS OF USE, DATA OR
PROFITS, WHETHER IN AN ACTION OF CONTRACT, NEGLIGENCE OR OTHER TORTIOUS
ACTION, ARISING OUT OF OR IN CONNECTION WITH THE USE OR PERFORMANCE OF THIS
SOFTWARE.
Portions of this software are based in part on the work of Regents of The University of Michigan. Because Microsoft
has included the Regents of The University of Michigan software in this product, Microsoft is required to include
the following text that accompanied such software:
Copyright © 1995, 1996 Regents of The University of Michigan.

All Rights Reserved.
Permission to use, copy, modify, and distribute this software and its documentation for any purpose and
without fee is hereby granted, provided that the above copyright notice appears in all copies and that both
that copyright notice and this permission notice appear in supporting documentation, and that the name of
The University of Michigan not be used in advertising or publicity pertaining to distribution of the software
without specific, written prior permission. This software is supplied as is without expressed or implied
warranties of any kind.
Copyright © 1993, 1994 Regents of the University of Michigan.

Redistribution and use in source and binary forms are permitted provided that this notice is preserved and
that due credit is given to the University of Michigan at Ann Arbor. The name of the University may not be
used to endorse or promote products derived from this software without specific prior written permission.
This software is provided ``as is'' without express or implied warranty.
Portions of this software are based in part on the work of Massachusetts Institute of Technology. Because Microsoft
has included the Massachusetts Institute of Technology software in this product, Microsoft is required to include the

Copyright 1989, 1990 by the Massachusetts Institute of Technology. All Rights Reserved.
Export of this software from the United States of America may require a specific license from the United
States Government. It is the responsibility of any person or organization contemplating export to obtain
such a license before exporting.
WITHIN THAT CONSTRAINT, permission to use, copy, modify, and distribute this software and its
documentation for any purpose and without fee is hereby granted, provided that the above copyright notice
appear in all copies and that both that copyright notice and
this permission notice appear in supporting documentation, and that the name of M.I.T. not be used in
advertising or publicity pertaining to distribution of the software without specific, written prior permission.
M.I.T. makes no representations about the suitability of this software for any purpose. It is provided "as is"
without express or implied warranty.
Under U.S. law, this software may not be exported outside the US without license from the U.S. Commerce
department.
Copyright 1994 by the Massachusetts Institute of Technology. All Rights Reserved.
Export of this software from the United States of America may require a specific license from the United
States Government. It is the responsibility of any person or organization contemplating export to obtain
such a license before exporting.
WITHIN THAT CONSTRAINT, permission to use, copy, modify, and distribute this software and its
documentation for any purpose and without fee is hereby granted, provided that the above copyright notice
appear in all copies and that both that copyright notice and this permission notice appear in supporting
documentation, and that the name of M.I.T. not be used in advertising or publicity pertaining to distribution
of the software without specific, written prior permission. M.I.T. makes no representations about the
suitability of this software for any purpose. It is provided "as is" without express or implied warranty.
This product includes software developed by the University of California, Berkeley and its contributors.
Portions of this software are based in part on the work of the "Entrust" security technology licensed from Northern
Telecom.
Portions of this software are based in part on the work of Hewlett-Packard Company. Because Microsoft has
included the Hewlett-Packard Company software in this product, Microsoft is required to include the following text
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Copyright © 1994 Hewlett-Packard Company
Permission to use, copy, modify, distribute and sell this software and its documentation for any purpose is
hereby granted without fee, provided that the above copyright notice appear in all copies and that both that
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Company and Microsoft Corporation make no representations about the suitability of this software for any
purpose. It is provided "as is" without express or implied warranty.
This product includes software from the 'libpng' PNG reference library.
Portions of this software are based in part on the work of Autodesk, Inc. Because Microsoft has included the
Autodesk, Inc. software in this product, Microsoft is required to include the following text that accompanied such
software:
© Copyright 1995 by Autodesk, Inc.

This product contains graphics filter software; this software is based in part on the work of the Independent JPEG
Group.
This product includes “True Verb” technology from KS Waves Ltd.
Portions of this software are based in part on the work of SGS-Thomson Microelectronics, Inc. Because Microsoft
has included the SGS-Thomson Microelectronics, Inc. software in this product, Microsoft is required to include the
Copyright 1996 SGS-Thomson Microelectronics, Inc. All Rights Reserved
Portions of this software are based in part on the work of Unicode, Inc. Because Microsoft has included the
Unicode, Inc. software in this product, Microsoft is required to include the following text that accompanied such
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COPYRIGHT AND PERMISSION NOTICE
Copyright © 1991-2005 Unicode, Inc. All rights reserved. Distributed under the Terms of Use in
www.unicode.org/copyright.html.
Permission is hereby granted, free of charge, to any person obtaining a copy of the Unicode data files and
any associated documentation (the "Data Files") or Unicode software and any associated documentation
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THE DATA FILES AND SOFTWARE ARE PROVIDED "AS IS", WITHOUT WARRANTY OF ANY
KIND, EXPRESS OR IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF
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THIRD PARTY RIGHTS. IN NO EVENT SHALL THE COPYRIGHT HOLDER OR HOLDERS
INCLUDED IN THIS NOTICE BE LIABLE FOR ANY CLAIM, OR ANY SPECIAL INDIRECT OR
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otherwise to promote the sale, use or other dealings in these Data Files or Software without prior written
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The Combined PostScript Driver was the result of a cooperative development process by Adobe Systems
Incorporated and Microsoft Corporation.
Portions of this software are based in part on the work of Media Cybernetics. Because Microsoft has included the
Media Cybernetics software in this product, Microsoft is required to include the following text that accompanied
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HALO Image File Format Library © 1991-1992 Media Cybernetics, Inc.
Portions of this software are based in part on the work of Luigi Rizzo. Because Microsoft has included the Luigi
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© 1997-98 Luigi Rizzo (luigi@iet.unipi.it)
Portions derived from code by Phil Karn (karn@ka9q.ampr.org), Robert Morelos-Zaragoza

(robert@spectra.eng.hawaii.edu) and Hari Thirumoorthy (harit@spectra.eng.hawaii.edu), Aug 1995
Redistribution and use in source and binary forms, with or without modification, are permitted provided
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TO, PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES; LOSS OF USE, DATA, OR
PROFITS; OR BUSINESS INTERRUPTION) HOWEVER CAUSED AND ON ANY THEORY OF
LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT (INCLUDING
NEGLIGENCE OR OTHERWISE) ARISING IN ANY WAY OUT OF THE USE OF THIS SOFTWARE,
EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.
Portions of this software are based in part on the work of W3C. Because Microsoft has included the W3C software
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W3C ® SOFTWARE NOTICE AND LICENSE

www.w3.org/Consortium/Legal/2002/copyright-software-20021231
This work (and included software, documentation such as READMEs, or other related items) is being
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3. Notice of any changes or modifications to the files, including the date changes were made. (We
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THIS SOFTWARE AND DOCUMENTATION IS PROVIDED "AS IS," AND COPYRIGHT HOLDERS
MAKE NO REPRESENTATIONS OR WARRANTIES, EXPRESS OR IMPLIED, INCLUDING BUT
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Portions of this software are based in part on the work of Sun Microsystems, Inc. Because Microsoft has included
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Sun RPC is a product of Sun Microsystems, Inc. and is provided for unrestricted use provided that this
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In no event will Sun Microsystems, Inc. be liable for any lost revenue or profits or other special, indirect
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2550 Garcia Avenue
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Manufactured under license from Dolby Laboratories. “Dolby” and the double-D symbol are trademarks of Dolby
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Portions of this software are based in part on the work of Andrei Alexandrescu. Because Microsoft has included the
Andrei Alexandrescu software in this product, Microsoft is required to include the following text that accompanied
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The Loki Library

Copyright © 2001 by Andrei Alexandrescu
This code accompanies the book:
Alexandrescu, Andrei. "Modern C++ Design: Generic Programming and Design Patterns Applied."
Copyright © 2001. Addison-Wesley.
Permission to use, copy, modify, distribute and sell this software for any purpose is hereby granted without
fee, provided that the above copyright notice appear in all copies and that both that copyright notice and
this permission notice appear in supporting documentation.

The author or Addison-Welsey Longman make no representations about the suitability of this software for
any purpose. It is provided "as is" without express or implied warranty.
Portions Copyright © 1995 by Jeffrey Richter
Portions of this software are based in part on the work of the Distributed Management Task Force, Inc. (DMTF).
Because Microsoft has included software based on DMTF specifications in this product, Microsoft is required to
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Copyright © 2007 Distributed Management Task Force, Inc. (DMTF). All rights reserved.
Portions of this work are derived from "The Draft Standard C++ Library" Copyright © 1995 by P.J. Plauger
published by Prentice-Hall and are used with permission.
Portions of this software are based in part on the work of Hewlett-Packard Company. Because Microsoft has
included the Hewlett-Packard Company software in this product, Microsoft is required to include the following text
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Copyright © 2002, 2003 Hewlett-Packard Company.
About Notice:
This software is based on software available from mpvtools.sourceforge.net.
This software processes a format called MPV. MPV is an open specification for managing collections and
multimedia playlists of photo, video, and music content and associated metadata and is available at no cost
from the Optical Storage Technology Association. More information about the MPV specification can be
found at www.osta.org/mpv.
Permission Notice:
Permission is hereby granted, free of charge, to any person obtaining a copy of this software and associated
documentation files (the "Software"), to deal in the Software without restriction, including without
limitation the rights to use, copy, modify, merge, publish, distribute, sublicense, and/or sell copies of the
Software, and to permit persons to whom the Software is furnished to do so, subject to the following
conditions:
The above copyright notice, this permission notice, and the above About Notice shall be included in all
copies or substantial portions of the Software.
THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR
IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY,
FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL THE
AUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER
LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR
OTHERWISE, ARISING FROM, OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE
USE OR OTHER DEALINGS IN THE SOFTWARE.
otherwise to promote the sale, use or other dealings in this Software without prior written authorization of
the copyright holder.
All other trademarks are property of their respective owners.

07745 Jena
Germany
Phone: +49 3641 220 333
Fax: +49 3641 220 112
Email: info.meditec@zeiss.com
Internet: www.zeiss.com/med
CIRRUS photo
000000-2121-813-DokS-GB-050416 Specifications subject to change

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Addendum to the documentation set

MICROSOFT SOFTWARE LICENSE TERMS

CIRRUS photo 600/CIRRUS photo 800 - Settings

CIRRUS photo 600/800 - Internal fixation targets

CIRRUS photo 600/800 quick instructions - User-defined workflow

Fundus Photography - Advice and Tips

Notes on the user manual ..........................................................3

Package check list ......................................................................5

Country-specific information and labels .....................................6

Performance specifications ......................................................15

Description of the device..........................................................17

Daily use ...................................................................................27

Operation of the device............................................................29

Notes on angiography ............................................................. 36

Maintenance and care ............................................................. 37

Optional accessories ................................................................ 48

Technical data .......................................................................... 54

Electromagnetic compatibility ................................................. 56

Notes on the user manual

Questions and comments

Explanation of symbols used

CAUTION - PROPERTY DAMAGE

 Information, hints and advice for better understanding of the

Package check list

Country-specific information and

WARNING - GENERAL HAZARDS

This device complies with EC Directive 93/42/EEC (MDD).

Device class according to the MDD: IIa

Light emitting diodes: Class 1 according to IEC 60825-1

EMC: See section Electromagnetic

UMDNS No.: 12-815 (fundus camera),

CAUTION - HAZARDS DUE TO SIDE EFFECTS

CAUTION – GENERAL HAZARDS

CAUTION - RISKS ARISING FROM OPERATING ERRORS

Intended user profile

CAUTION - RISKS ARISING FROM OPERATING ERRORS

Ophthalmic photographer, optometrist, MTA and staff who prepare

Physicians who review images and analyze data for diagnostic

Disposal of the product

CAUTION - RISK OF ENVIRONMENTAL POLLUTION

Disposal of the product within the EU

Fig. 1 Warning and information labels on the device

Item Label Explanation

1 CIRRUS photo type label

Applied part type B

IP20 Housing protection class

CIRRUS photo 600

2 CIRRUS photo 800 identification label

CIRRUS photo 600 identification label

3 Sign with date of manufacture

4 CE marking label and disposal advise for

5 Not applicable Not applicable

6 Computer identification label

Item Label Explanation

7 Sign with manufacturer's name and date

EU conformity symbol with

8 OCT engine type label

9 Sign with date of manufacture