Storz OR1 FUSION User manual

Instructions for use
KARL STORZ OR1 FUSION, Rel. 1.4.3
en

Copyright ©
All product illustrations, product descriptions, and texts are the intellectual property of
KARLSTORZSE&Co.KG.
Their use and reproduction by third parties require the express approval of KARLSTORZSE&Co.KG.
All rights reserved.
09-2022

Table of contents
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 3
Table of contents
1 General information............................................................................................................................ 6
1.1 Read the instructions for use ..................................................................................................... 6
1.2 Read the instructions for use of compatible products............................................................... 6
1.3 Scope......................................................................................................................................... 6
1.4 General signs and symbols........................................................................................................ 6
1.5 Description of warning messages.............................................................................................. 7
2 Normal use ......................................................................................................................................... 8
2.1 Intended use .............................................................................................................................. 8
2.2 Indications.................................................................................................................................. 8
2.3 Contraindications ....................................................................................................................... 8
2.4 Patient population ...................................................................................................................... 8
2.5 Target user populations ............................................................................................................. 8
3 Safety and warning ............................................................................................................................ 9
3.1 Serious incidents........................................................................................................................ 9
3.2 Correct handling and product testing ........................................................................................ 9
3.3 Unsterile product ....................................................................................................................... 9
3.4 Combination with other components......................................................................................... 9
3.5 Dangers from electrical current.................................................................................................. 10
3.6 Damage due to ingress of liquid in electrical components........................................................ 11
3.7 Risk of explosion and fire........................................................................................................... 11
3.8 Observing ambient conditions ................................................................................................... 11
3.9 Failure of products ..................................................................................................................... 11
3.10 Electromagnetic interference ..................................................................................................... 12
3.11 High temperature ....................................................................................................................... 12
3.12 Image display and transmission ................................................................................................ 12
3.13 Data loss .................................................................................................................................... 13
4 Product description............................................................................................................................ 14
4.1 Description of function............................................................................................................... 14
4.2 Product overview ....................................................................................................................... 14
4.3 Possible combinations ............................................................................................................... 15
4.4 Technical data............................................................................................................................ 15
4.5 Symbols employed .................................................................................................................... 16
4.5.1 Symbols on the packaging ........................................................................................... 16
4.5.2 Symbols on the product ............................................................................................... 17
4.5.3 Symbols on the type plate ............................................................................................ 18
4.6 Ambient conditions .................................................................................................................... 18
5 Preparation......................................................................................................................................... 19
5.1 Unpacking the product .............................................................................................................. 19
5.2 Setting up the device ................................................................................................................. 19
5.3 Connecting the product ............................................................................................................. 19
6 Operation ........................................................................................................................................... 20
6.1 Switching on the product........................................................................................................... 20
6.2 User interface............................................................................................................................. 20
6.2.1 Symbols on the user interface ...................................................................................... 21
6.3 Onscreen keyboard.................................................................................................................... 22

Table of contents
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 4
6.4 Volume control ........................................................................................................................... 22
6.5 Presets ....................................................................................................................................... 23
6.5.1 Creating a preset .......................................................................................................... 23
6.5.2 Using the preset............................................................................................................ 25
6.5.3 Searching for a preset .................................................................................................. 26
6.6 "Current procedure" application area ........................................................................................ 27
6.6.1 Patient........................................................................................................................... 28
6.6.2 Checklist ....................................................................................................................... 33
6.6.3 Capture ......................................................................................................................... 35
6.6.4 Edit................................................................................................................................ 40
6.6.5 Finish............................................................................................................................. 42
6.7 "Control" application area.......................................................................................................... 44
6.7.1 Anesthesia Safety ......................................................................................................... 45
6.7.2 Routing ......................................................................................................................... 45
6.7.3 Controlling the room camera ........................................................................................ 57
6.7.4 Medical Device Control – SCB ..................................................................................... 57
6.7.5 Entertainment................................................................................................................ 58
6.7.6 Light .............................................................................................................................. 59
6.7.7 Room Control ............................................................................................................... 60
6.8 "Previous procedures" application area .................................................................................... 61
6.8.1 Filing cabinet................................................................................................................. 61
6.8.2 Open tasks.................................................................................................................... 64
6.9 "Communication" application area ............................................................................................ 65
6.9.1 Access status ............................................................................................................... 66
6.9.2 Streaming...................................................................................................................... 68
6.9.3 Phone............................................................................................................................ 68
6.9.4 Unified Communication ................................................................................................ 70
6.9.5 Video conference.......................................................................................................... 78
6.9.6 Room connection ......................................................................................................... 83
6.10 Switching off the product........................................................................................................... 91
7 Maintenance, servicing, repairs, and disposal................................................................................... 92
7.1 Maintaining the product ............................................................................................................. 92
7.1.1 Maintenance ................................................................................................................. 92
7.2 Repairing devices....................................................................................................................... 92
7.3 Disposing of the product ........................................................................................................... 92
8 Accessories and spare parts.............................................................................................................. 93
8.1 Accessories................................................................................................................................ 93
9 Electromagnetic compatibility............................................................................................................ 94
9.1 General information on the operating environment ................................................................... 94
9.2 Cables ........................................................................................................................................ 94
9.3 Table 1 – Compliance level for immunity tests .......................................................................... 95
9.4 Table 2 – Test levels for near fields from HF wireless communications equipment .................. 96
9.5 Table 3 – Test levels for radiated and conducted immunity tests ............................................. 97
9.6 Table 4 – Emission class and group .......................................................................................... 98
9.7 Table 5 – Recommended separation distances between portable and mobile HF
communications equipment and the product............................................................................ 99
9.8 Regulatory information on telecommunications ........................................................................ 99
9.8.1 USA............................................................................................................................... 99
9.8.2 Canada ......................................................................................................................... 99

Table of contents
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 5
9.8.3 European Union ............................................................................................................100
10 Subsidiaries........................................................................................................................................101

General information
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 6
1 General information
1.1 Read the instructions for use
If the instructions for use are not followed, patients, users, and third parties may be injured or the
product may be damaged.
Read the instructions for use carefully and follow all the safety notes and warnings.
Read the reprocessing instructions carefully and follow all the safety notes and warnings. The
reprocessing instructions can be downloaded from www.karlstorz.com/ifu by entering the item
number.
Keep the instructions for use and reprocessing instructions in a safe place.
1.2 Read the instructions for use of compatible products
If the instructions for use of compatible products are not followed, patients, users, and third parties
may be injured or the product may be damaged.
Read the instructions for use of the compatible products carefully and follow all the safety notes
and warnings.
Read the reprocessing instructions of the compatible products carefully and follow all the safety
notes and warnings.
1.3 Scope
This instruction manual is valid for:
Product name Item number
KARLSTORZ OR1 FUSION CONTROL WO300
1.4 General signs and symbols
The signs and symbols used in this document have the following meaning:
Practical tip
This sign refers to useful and important information.
Actions to be performed
Action to be carried out by several steps:
üPrerequisite that must be met before carrying out an action.
1. Step 1
ðInterim result of an action
2. Step 2
ðResult of a completed action
Actions in safety notes or in the case of a single step:
Step 1
Lists
1. Numbered list
– Unnumbered list, 1st level

General information
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 7
– Unnumbered list, 2nd level
1.5 Description of warning messages
To prevent any injury to persons or damage to property, the warnings and safety notes in the
instructions for use must be observed. The warnings use the following levels of danger:
WARNING
WARNING
Designates a possible imminent risk. If this is not avoided, it could lead to death or serious injuries.
CAUTION
CAUTION
Designates a possible imminent risk. If this is not avoided, it could lead to minor injuries.
NOTICE
NOTICE
Designates a possibly harmful situation. If this is not avoided, the products could be damaged.

Normal use
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 8
2 Normal use
2.1 Intended use
The OR1 FUSION CONTROL is designed for use in operation rooms by qualified personnel. The OR1
FUSION CONTROL is an appliance (comprising hardware and software) for the documentation of
audiovisual data and patient data during diagnostic or therapeutic procedures. It allows the operation
to be recorded and described for documentation purposes. The audiovisual data that is recorded and
forwarded using the OR1 FUSION CONTROL is for examination and information purposes, and not
primarily for making diagnoses. The recorded audiovisual data is not intended to be shown
intraoperatively on the operation monitor.
2.2 Indications
Routing of audio, video, and control signals from signal sources to signal destinations in the case of
medical procedures.
2.3 Contraindications
Use is contraindicated if, in the opinion of the responsible physician, the device is not compatible with
successful completion of the planned procedure due to its technical design.
2.4 Patient population
There are no restrictions in terms of patient groups for this product.
The product does not come into direct contact with the patient.The product does not come into direct
contact with the patient.
2.5 Target user populations
The medical device may only be used by doctors and medical assistants with a relevant specialist
qualification.

Safety and warning
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 9
3 Safety and warning
WARNING
Danger due to non-observance of warnings and safety notes
This chapter contains warnings and safety notes structured according to hazards and risks.
1. Carefully read and observe all warnings and safety notes.
2. Follow the instructions.
3.1 Serious incidents
A ‘serious incident’ includes incidents which, directly or indirectly, had, could have had or could have
any of the following consequences:
– Death of a patient, user, or another person
– Temporary or permanent serious deterioration in the medical condition of a patient, user, or
another person
– A serious threat to public health
The manufacturer and appropriate authority must be notified of all serious incidents.
3.2 Correct handling and product testing
If the product is not handled correctly, patients, users, and third parties may be injured.
Only persons with the necessary medical qualification and who are acquainted with the
application of the product may work with it.
Check that the product is suitable for the procedure prior to use.
Do not convert or modify the product.
Check the product for the following properties, for example, before and after every use:
– Functionality
– Damage
Do not continue to use damaged products.
Dispose of the product properly.
Have defective products checked by KARLSTORZ or by companies authorized by KARLSTORZ.
Have regular safety inspections performed by KARLSTORZ or by companies authorized by
KARLSTORZ.
3.3 Unsterile product
The product is not sterile when delivered. The use of non-sterile products poses a risk of infection for
patients, users, and third parties.
Reprocess the product in line with the reprocessing instructions before initial use and every
subsequent use.
3.4 Combination with other components
The use of unauthorized devices and components or unauthorized changes to the product can lead to
malfunctions and injuries.
Additional devices connected to electrical medical equipment must comply with the relevant IEC or
ISO standards. Furthermore, all configurations must comply with the requirements for medical
electrical systems (see IEC 60601-1-1 or clause 16 of the 3rd edition of IEC 60601-1). Any person who

Safety and warning
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 10
connects additional devices or components to the product changes the medical electrical system and
is therefore responsible for ensuring that it complies with the requirements for medical electrical
systems.
Only combine the product with devices and components that are approved for combined use by
the manufacturer.
Only use approved accessories.
Observe the instruction manuals and interface specifications of the devices and components
used in combination.
Only use devices and components that have standardized interfaces and do not breach the
normal use of the product.
Only use devices that can be displayed in the monitor as a "playback device."
Perform an equipment test before use.
Comply with national and local regulations.
Only make changes to the product if these changes are approved by KARLSTORZ.
3.5 Dangers from electrical current
An improper power supply may cause an electric shock and injure patients, users, or third parties. All
electrical installations of the operation room in which the product is connected and used must meet
the applicable IEC standards. Input and output equipment connected to the product must comply
with IEC60601-1.
Have the device installed and put into service by authorized and trained electricians of
KARLSTORZSE&Co.KG or by companies authorized by KARLSTORZ.
Use either the power cord supplied by KARLSTORZ or a power cord which has the same
properties and which bears a national mark of conformity.
The product may only be operated with the line voltage stated on the rating plate.
Position the product appropriately so that the power cord can be unplugged at any time. The
product is only voltage-free when the mains plug has been disconnected.
Ensure potential equalization according to the applicable national rules and regulations.
To ensure reliable protective earth grounding, connect the product to a properly installed socket
that is approved for use in the operation room. Routinely inspect the electrical plug and cord and
do not use if the inspection reveals damage.
Connect the product to a power supply with protective conductor.
If several devices are connected to the product, note the maximum leakage current.
Do not use any additional multiple socket outlets or extension cables.
Do not use freely accessible multiple socket outlets.
Multiple socket outlets must not be placed on the floor.
In the case of electrical products, individual components or the product itself may be live. Live parts
can cause electric shocks in the event of contact and injure patients, users, and third parties.
Do not open the product.
Have servicing carried out by KARLSTORZ or a company authorized by KARLSTORZ. Failure to
do so will void the guarantee.
Do not touch the output jacks of the product and the patient at the same time during use
Always pull out the mains plug before carrying out any cleaning and maintenance work.
Disconnect the power plug before opening the housing.

Safety and warning
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 11
3.6 Damage due to ingress of liquid in electrical components
In the case of electrical products, individual components or the product itself may be live. Liquid
ingress into an electrical product may result in a short circuit or an unintentional transfer of current.
The product is damaged as a result and patients, users and third parties may be injured.
Do not store liquids near the product or on the product.
If liquid has entered the product, pull out the plug and allow the product to dry completely.
3.7 Risk of explosion and fire
The product can generate sparks, which cause combustible or flammable gases and liquids to ignite
or explode. This may cause injuries to patients, users, and third parties.
The product must not be operated in oxygenated environments.
Do not operate the product in explosive atmospheres.
Do not operate the product in environments with combustible gases such as inhalation
anesthetics and mixtures thereof. Observe the hazard zones:
Combustible and flammable gases must be allowed to escape, be extracted, or be displaced with
CO2 before use.
Combustible and flammable liquids such as cleaning and disinfecting solutions must be allowed
to vaporize, or be wiped away or extracted before use.
Remove any swabs or cloths soaked in flammable liquid from the application area.
Only start the application when combustible or flammable gases and liquids are no longer
present.
Only connect or disconnect the power plug to or from the power supply outside explosive
atmospheres.
3.8 Observing ambient conditions
If the product is used in an unsuitable environment, patients, users, and third parties may be injured.
Always operate the product in the prescribed ambient conditions.
Position the product so that there is sufficient free space for air circulation.
Install the product and its components out of reach of patients.
3.9 Failure of products
The product may fail during use. In this case, image transmission will be interrupted. The patient may
be injured.
Always have a backup system (direct line between endoscopic camera and monitor) ready.
In case of a failure or malfunction, cease work immediately and switch to a backup system.
Prior to each operation, make sure that the personnel are familiar with the procedure for switching
over to the backup system.

Safety and warning
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 12
3.10 Electromagnetic interference
Medical electrical devices are subject to special precautions regarding electromagnetic compatibility
and must be installed and commissioned according to the tables on electromagnetic compatibility. If
other products (e.g., for MRT, CT, diathermy, electrocautery, or RFID) emit electromagnetic radiation,
the function of the product may be impaired. High-frequency communication equipment can affect
medical electrical devices and impair their performance.
Do not use the product in the vicinity of a magnetic resonance tomograph (MRT).
Do not use the product next to or together with other devices. If such use is required, monitor the
product and the other devices, and follow the relevant instructions for use in the event of
malfunctions.
Portable RF communications equipment including peripheral devices (e.g., antenna cables and
external antennas) should be used no closer than 30cm from the product, including cables
specified by the manufacturer.
During installation and operation of the product, please take note of the information on
electromagnetic compatibility, see chapter Electromagnetic compatibility.
In case of uncertainties, seek expert advice from KARLSTORZ.
Before use, a clinical/biomedical engineer or an EMC specialist should carry out an ad-hoc test of
the electromagnetic radiation.
To prevent increased electromagnetic emissions or reduced electromagnetic immunity of the
product, only use accessories, transducers, and cables recommended or supplied by the
manufacturer.
In order to avoid exposing patients, users, or third parties to harmful electromagnetic interference,
the product must not be operated outside of its intended EMC environment. Furthermore, the
product must not be operated if the housing, cable, or electromagnetic shielding equipment is
damaged.
3.11 High temperature
On in-wall installations, the temperature and ventilation of the housing are subject to constant
monitoring. The system will notify you if a certain temperature is exceeded and inform you that the
system may shut off automatically.
Always observe any error messages issued by the system.
When prompted to do so, cease work immediately and switch to a backup system ("direct line").
Prior to each operation, make sure that the personnel are familiar with the procedure for switching
over to the backup system ("direct line").
3.12 Image display and transmission
Recordings and image preview are not intended to be used for diagnostic or therapeutic purposes.
The following data may only be used for documentation purposes:
– Image information in printed and electronically recorded form.
– Image information that originates from or was recorded by equipment not manufactured by
KARLSTORZ.
Always use the monitor of the connected device for diagnostic images. Signals in 3D will only
display correctly on suitable display equipment.
Image data may be lost if the device is switched off while processing patient data.
Only switch off the product using the rocker switch.
Connecting non-compatible signal types to the patch panel in the OR can cause image interference
and malfunctioning.
Only connect permitted signal types.

Safety and warning
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 13
Perform equipment tests before use.
3.13 Data loss
Data may be lost when working on the software and hardware or on the hard disk, e.g., during a
system recovery.
Back up existing data before formatting the hard disk.
Only transfer encrypted data.
Ensure that data storage is finished and only then remove an external storage medium.
Perform a system test which verifies perfect functioning after adding new software or hardware.
Shut down the software via the user interface or by briefly pressing the rocker switch.

Product description
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 14
4 Product description
4.1 Description of function
KARL STORZ OR1 FUSION is designed for use in the operating rooms of clinics and hospitals.
The product is used to aid the implementation and documentation of medical procedures aimed at
examining and treating patients.
The following can be performed from the central touchscreen:
– Control non-medical devices.
– Transfer and display video and audio signals from the integrated signal sources to the integrated
peripheral devices.
– Record, save, edit, forward, and print medical examinations and procedures in the form of stills,
video sequences, and audio sequences.
4.2 Product overview
WARNING
Electric shock!
There is a voltage of 12V/2A at the "Smart Screen" socket.
Do not touch the socket during operation.
Only connect or remove the cable when the product is switched off.
12345
OR1 FUSION CONTROL - Front view
1 ON/OFF rocker switch
Standby and operating state
4 LED, red, hard disk access
2 LED, yellow, Standby 5 USB port
3 LED, green, ON status

Product description
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 15
123568
9
10
11
121314151617
47
18
OR1 FUSION CONTROL - Rear view
1 Power connection 10 On Air Light (Phoenix 2-pin)
2 Potential equalization connection 11 Mini jack (audio IN/OUT)
3 Serial interface (DE 9) 12 4x USB 3.0
4 4x 3.5 mini jack (camera head buttons) 13 2x LAN (RJ-45)
5 Lemo 5-pin (foot pedal) 14 Monitor (DVI)
6 Serial interfaces, smart screen (D-Sub DE
9)
15 2x monitor (digital port)
7 Serial interface (DE 9) 16 4x USB 2.0
8 2x 10G fiber-optic interface 17 Keyboard (PS/2)
9 Remote switch (Phoenix 4-pin) 18 Mouse (PS/2)
4.3 Possible combinations
It is recommended that the suitability of the products for the intended procedure be checked prior to
use. Please note that the products listed here may not yet be available in all countries due to
differences in approval requirements.
The product consists of the items listed in the scope and is used exclusively in combination with
these.
4.4 Technical data
Description Value
Power supply
Operating voltage 100–240V
Operating frequency 50/60Hz
Maximum current consumption 5–2A
Electrical protection class I

Product description
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 16
Description Value
Degree of protection acc. to IEC 60259 IPX0
Housing
Dimensions (LxHxW) 355 x 74.5 x 305mm
Weight 6kg
System
Hard drive capacity 2TB
Random Access Memory (RAM) 16GB
CPU Intel® CoreTM [email protected] GHz
Operating system Windows® 10 Embedded
Operating mode Continuous operation
The KARL STORZ OR1 FUSION contains a lithium battery that needs to be checked and
replaced regularly.
4.5 Symbols employed
4.5.1 Symbols on the packaging
Symbol Meaning
Manufacturer
Date of manufacture
Medical device
Article no.
Serial number
Number of products in the product packaging
Unique Device Identifier
Consult the printed or electronic instructions for use
Fragile, handle with care

Product description
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 17
Symbol Meaning
Keep dry
Humidity limit
Air pressure limit
Federal (USA) law restricts this device to sale by or on the order of a physician.
CE marking
With this marking, the manufacturer declares the conformity of the product
with the applicable EU directives. A code number after the CE mark indicates
the responsible notified body.
The EU directives relevant to the product can be found in the EU Declaration
of Conformity, which can be requested from KARLSTORZ.
4.5.2 Symbols on the product
Symbol Meaning
Follow the instructions for use.
The color may differ on the product. The symbol is black/white on the packag-
ing label.
Ready/standby button
ON
Hard disk
USB port
Dangerous voltage
Danger of an electric shock!
The potential equalization is responsible for equalizing the potentials of differ-
ent metal parts that can be touched at the same time, or for reducing potential
differences that could occur between the body, electromedical devices, and
external live parts during use.

Product description
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 18
4.5.3 Symbols on the type plate
Symbol Meaning
Manufacturer
Date of manufacture
CE marking
With this marking, the manufacturer declares the conformity of the product
with the applicable EU directives. A code number after the CE mark indicates
the responsible notified body.
The EU directives relevant to the product can be found in the EU Declaration
of Conformity, which can be requested from KARLSTORZ.
Medical device
Federal (USA) law restricts this device to sale by or on the order of a physician.
CSA certification mark for the USA and Canada
With this mark, the manufacturer declares compliance with the certification re-
quirements.
Prevention of pollution by electronic devices
Alternating current
Separate collection of electrical and electronic devices.
Do not dispose of in household refuse.
4.6 Ambient conditions
Storage/transport conditions
Temperature -10°C...+60°C (14°F...140°F)
Relative humidity
(non-condensing)
5–95%
Air pressure 500–1,080hPa
Operating conditions
Temperature 5°C...35°C (41°F...95°F)
Relative humidity
(non-condensing)
20–80%
Air pressure 700–1,080hPa
Max. operating altitude 3,000m

Preparation
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 19
5 Preparation
5.1 Unpacking the product
1. Carefully remove the product and accessories from the packaging.
2. Check the delivery for missing items and any possible damage.
3. In the case of damage, hidden defects, and short deliveries, document their nature and extent
and contact the manufacturer or supplier immediately.
4. Keep packaging for further transport.
5.2 Setting up the device
The product can be operated free-standing, in a rack, or as a wall-mounted solution in either a vertical
or horizontal position.
1. Clean and disinfect the product thoroughly before using for the first time.
2. Ensure that the ambient conditions are observed.
3. Observe the technical data.
4. Install the product out of reach of patients.
5. Note the free area dimensions based on the graphic to guarantee that the product is sufficiently
ventilated.
85,9 85,9310
20
375
20
1 2 3
5
4
1 Air inlet (max. temperature 35°C) 4 Front
2 Housing 5 Defined free areas
3 Air outlet
Nothing may be mounted in the defined free areas.
5.3 Connecting the product
The product may only be connected to other components by KARLSTORZ service personnel or
personnel authorized by KARLSTORZ.

Operation
Instructions for use • KARL STORZ OR1 FUSION, Rel. 1.4.3 • JEB924_EN_V3.0_09-2022_IFU_CE-MDR 20
6 Operation
6.1 Switching on the product
1. Switch on the connected equipment.
2. Switch on the product via the rocker switch.
ðThe software will start up.
6.2 User interface
The following user interface appears when the KARL STORZ OR1 FUSION application is started:
4
1
2
3
5
1 Messages 4 Navigation bar
2 Patient data 5 Functions
3 Application areas
Messages
System information and notes appear in the top bar.
Patient data
The following data for the current patient appears if patient data is entered:
– Gender
– Last name
– First name
– Date of Birth
– Age
– Patient ID
Application areas
The application areas contain modules that can vary depending on the configuration: