Storz AIDA C WD310 User manual

Instructions for use
AIDA C WD310
Release 1.1
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.
12-2021

Table of contents
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_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 Other applicable documents ........................................................................................... 6
1.5 Description of warning messages ................................................................................... 6
2 Normal use ............................................................................................................................... 8
2.1 Intended use.................................................................................................................... 8
2.2 Indications ....................................................................................................................... 8
2.3 Contraindications ............................................................................................................ 8
2.4 Target user populations................................................................................................... 8
2.5 Patient groups ................................................................................................................. 8
3 Safety ....................................................................................................................................... 9
3.1 Serious incidents ............................................................................................................. 9
3.2 Correct handling and product testing ............................................................................. 9
3.3 Unsterile product ............................................................................................................. 9
3.4 Contaminated products................................................................................................... 9
3.5 Combination with other components .............................................................................. 9
3.6 Damaged products.......................................................................................................... 10
3.7 Dangers from electrical current ....................................................................................... 10
3.8 Electromagnetic interference........................................................................................... 11
3.9 Damage due to ingress of liquid in electrical components ............................................. 11
3.10 Risk of explosion and fire ................................................................................................ 11
3.11 Observing ambient conditions......................................................................................... 12
3.12 Failure of products........................................................................................................... 12
3.13 Image display and transmission ...................................................................................... 12
3.14 Data loss.......................................................................................................................... 13
4 Product description.................................................................................................................. 14
4.1 Description of operation .................................................................................................. 14
4.2 Product overview............................................................................................................. 14
4.3 Technical data ................................................................................................................. 15
4.4 Possible combinations .................................................................................................... 16
4.5 Symbols employed .......................................................................................................... 18
4.5.1 Symbols on the packaging ................................................................................. 18
4.5.2 Symbols on the product ..................................................................................... 19
4.5.3 Symbols on the rating plate................................................................................ 19
4.5.4 Symbols on the user interface ............................................................................ 20
4.6 Ambient conditions.......................................................................................................... 21
5 Preparation ............................................................................................................................... 22
5.1 Unpacking the product.................................................................................................... 22
5.2 Inspecting the device ...................................................................................................... 22
5.3 Setting up the device....................................................................................................... 22
5.4 Connecting the product................................................................................................... 23
6 Installation and commissioning ................................................................................................ 24
6.1 Overview of configuration area........................................................................................ 24

Table of contents
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 4
6.1.1 Opening the configuration area .......................................................................... 24
6.1.2 General ............................................................................................................... 25
6.1.3 Capture ............................................................................................................... 32
6.1.4 Finish................................................................................................................... 38
6.1.5 Data entry ........................................................................................................... 43
6.1.6 Browser............................................................................................................... 48
6.1.7 User management .............................................................................................. 49
6.1.8 Remote service ................................................................................................... 52
6.1.9 Routing ............................................................................................................... 53
6.2 Start configuration ........................................................................................................... 54
6.3 User roles and access rights ........................................................................................... 54
6.3.1 Default profile...................................................................................................... 55
6.3.2 Profile management............................................................................................ 55
6.3.3 User accounts..................................................................................................... 55
6.3.4 Creating user accounts....................................................................................... 56
6.3.5 Settings as system administrator ....................................................................... 59
6.3.6 Settings as application administrator ................................................................. 60
6.3.7 Settings as configuration users .......................................................................... 62
6.3.8 Group profile and default profile......................................................................... 63
6.4 Additional installations..................................................................................................... 63
6.4.1 KARL STORZ AIDA Secure................................................................................. 64
6.4.2 Installing and approving hardware and software components .......................... 64
7 Operation.................................................................................................................................. 71
7.1 Switching on the product ................................................................................................ 71
7.2 User interface .................................................................................................................. 71
7.2.1 Home screen....................................................................................................... 72
7.3 Current procedures ......................................................................................................... 73
7.3.1 Patient................................................................................................................. 73
7.3.2 Capture ............................................................................................................... 77
7.3.3 Edit...................................................................................................................... 83
7.3.4 Finish................................................................................................................... 86
7.4 Previous procedures........................................................................................................ 88
7.4.1 Filing Cabinet ...................................................................................................... 88
7.4.2 Open tasks.......................................................................................................... 90
7.5 Control and communication ............................................................................................ 91
7.6 Switching off the product ................................................................................................ 91
8 Maintenance, servicing, repairs, and disposal ......................................................................... 92
8.1 Maintaining the product................................................................................................... 92
8.1.1 Maintenance ....................................................................................................... 92
8.2 Safety inspection in accordance with IEC 62353............................................................ 92
8.2.1 Visual inspection................................................................................................. 92
8.2.2 Electric measurements ....................................................................................... 92
8.2.3 Functional test .................................................................................................... 92
8.3 Repairing the product...................................................................................................... 93
8.4 Disposing of the product ................................................................................................. 93
9 Accessories and spare parts.................................................................................................... 94
9.1 Accessories ..................................................................................................................... 94
10 Electromagnetic compatibility.................................................................................................. 95
10.1 General information on the operating environment......................................................... 95

Table of contents
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 5
10.2 Cables.............................................................................................................................. 95
10.3 Table 1 – Compliance level for immunity tests................................................................ 97
10.4 Table 2 – Test levels for proximity fields from HF wireless communications equipment 98
10.5 Table 3 – Test levels for radiated and conducted immunity tests................................... 99
10.6 Table 4 – Emission class and group................................................................................ 100
10.7 Table 5 – Recommended separation distances between portable and mobile HF
communications equipment and the product ................................................................. 101
11 Errors and messages................................................................................................................102
11.1 Formatting the hard disk ................................................................................................. 102
11.2 System recovery.............................................................................................................. 103
11.2.1 Backing up data from the (D:) drive ....................................................................103
11.2.2 Complete system recovery .................................................................................103
11.2.3 Operating system recovery.................................................................................105
11.2.4 Performing system recovery...............................................................................107
12 Subsidiaries ..............................................................................................................................111

General information
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_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
AIDA C WD310
1.4 Other applicable documents
The following documents must also be observed:
– AIDA C System Security Plan
– AIDA C installation instructions
– Regulatory information on Intel Corporation radio receiver
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.

General information
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 7
NOTICE
NOTICE
Designates a possibly harmful situation. If this is not avoided, the products could be damaged.

Normal use
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 8
2 Normal use
2.1 Intended use
The KARLSTORZAIDA C is intended for use by qualified personnel in the doctor's office and
operation rooms. The KARLSTORZAIDA C is an appliance (comprising hardware and
software) for the documentation of audiovisual data and patient data during diagnostic and
therapeutic procedures. It allows the operation to be recorded and described for
documentation purposes. The audiovisual data which is recorded and forwarded using the
KARLSTORZAIDA C 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
Receiving audio and video signals from signal sources and sending them 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 Target user populations
The medical device may only be used by doctors and medical assistants with a relevant
specialist qualification.
2.5 Patient groups
There are no restrictions in terms of patient groups for this product.

Safety
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 9
3 Safety
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.
Check the product for the following properties, for example, before and after every use:
– Functionality
– Damage
– Changes to the surface
– In the case of several components: completeness and correct assembly
Do not continue to use damaged products.
Dispose of the product properly.
Do not leave broken-off components inside the patient.
Do not overload the product with mechanical stress.
Do not bend bent products back to their original position.
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 Contaminated products
Contaminated products pose a risk of infection for users, patients, and third parties.
Comply with national laws and regulations.
Observe the guidelines of the Employer’s Liability Insurance Association and equivalent
organizations.
3.5 Combination with other components
The use of unauthorized devices and components or unauthorized changes to the product can
result in injuries.

Safety
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 10
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).
Only combine the product with devices and components that are approved for combined
use by the manufacturer.
The product should not be used immediately adjacent to or stacked with other equipment.
If adjacent or stacked use is necessary, the product should be observed to verify normal
operation in the configuration in which it will be used.
Observe the instruction manuals and interface specifications of the devices and
components used in combination.
Only use devices with display capability that are identified as "display".
Comply with national and local regulations.
Only make changes to the product if these changes are approved by KARLSTORZ.
3.6 Damaged products
Damaged products can result in injury to patients, users, and third parties.
Before every use, check all components of the product for damage.
Do not use damaged products.
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.
3.7 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 operating 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.
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.
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.

Safety
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 11
Disconnect the power plug before opening the housing.
3.8 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.
Observe the information on electromagnetic compatibility, see chapter Electromagnetic
compatibility [p.95].
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.
3.9 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.
3.10 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.

Safety
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 12
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.
3.11 Observing ambient conditions
If the device is stored, transported, operated or reprocessed under unsuitable conditions,
patients, users or third parties may be injured and the device can be damaged.
Observe the ambient conditions listed in the instructions for use and reprocessing.
3.12 Failure of products
The product may fail during use.
Have a replacement product ready for each application or plan for an alternative surgical
technique.
3.13 Image display and transmission
The video signals and recordings shown may display artifacts as a result of compression and/
or scaling. The image preview on the touch screen is not intended to be used for diagnostic or
therapeutic purposes. Always use the monitor of the connected device for diagnostic images.
Signals in 3D are only correctly displayed on suitable display equipment.
The following data may only be used for documentation purposes:
– Image information in printed form.
– Image information which was compressed or recorded in non-native resolution.
– Image information which originates from or was recorded by a device which was not
manufactured by KARLSTORZ.
Image data may be lost if the product 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 operation room can cause
image interference and malfunctioning.
Only connect permitted signal types.
Perform equipment tests before use.

Safety
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 13
3.14 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 • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 14
4 Product description
4.1 Description of operation
The device enables diagnostic and therapeutic interventions to be recorded as still images,
video and audio sequences.
The recorded data can be saved, edited and annotated, forwarded and printed for
documentation purposes.
4.2 Product overview
4
123 5
Front
1ON/OFF rocker switch
Standby and operating state
4 Access to hard disk LED, red
2 Standby LED, yellow 5 USB 3.0
3 ON LED, green
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.
4
123568
15 12 13
1416
17 910
11
7
Rear
1 Power connection 10 Phoenix 2-pin (On Air Lamp)
2 Potential equalization connector 11 Serial interface (SmartScreen)
3 Serial interface (D-Sub DE 9) 12 Audio output
4 ACC connections (camera head but-
tons)
13 4x USB 3.0
5 Foot pedal connection (Lemo 5-pin) 14 Monitor (DVI)
6 2x LAN (RJ-45) 15 2x monitor (digital port)

Product description
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 15
7 Audio input 16 4x USB 2.0
8 HDMI port (video input) 17 Mouse/keyboard (PS/2)
9 Remote switch (Phoenix 4-pin)
4.3 Technical data
Description Value
Power supply
Operating voltage 100–240V
Operating frequency 50–60Hz
Power input 5–2A
Electrical protection class I
Degree of protection acc. to IEC 60259 IP20
Housing
Dimensions (LxHxW) 355x74.5x305mm
Weight 6.0kg
System
WLAN adaptor In accordance with IEEE 802.11ac
Channel width (bidirectional) 20MHz / 40MHz / 80MHz
Preferred frequencies (bidirectional) Channel used is determined by external infra-
structure (access point).
Bandwidth (receiver) 2.4GHz / 5GHz
Frequencies and frequency bands (receiver) 2.4GHz
2.399–2.4845GHz (channel 1 to 13)
5GHz
5.15–5.35GHz (channel 36 to 64)
5.47–5.725GHz (channel 100 to 140)
Frequencies and frequency bands (transmit-
ter)
2.4GHz
2.399–2.4845GHz (channel 1 to 13)
5GHz
5.15–5.35GHz (channel 36 to 64)
5.47–5.725GHz (channel 100 to 140)
Modulation characteristics In accordance with IEEE 802.11ac
Transmission power (effective) 2.4GHz
100mW
5.15–5.35GHz
200mW
5.47–5.725
200mW
Hard disk capacity 1TB

Product description
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 16
Description Value
Random Access Memory (RAM) 8GB
CPU Intel® Core™ i5-9500TE
Operating system Windows10 IoT Enterprise
Operating mode Continuous operation
4.4 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.
Supported touch screen models
Use the supplied DisplayPort cable to connect touch screens. Alternatively, you can use a DVI-
D single link cable, 18+1 with a maximum length of 3m and two ferrite cores.
Use the supplied cable for WM20.
Item Order no.
KARLSTORZ touch screen, 21.5" WM100
KARLSTORZ touch screen, 21.5" 20090621
KARLSTORZ touch screen, 21.5" 20090521
KARLSTORZ touch screen, 24.5" WM101
KARLSTORZ touch screen, 24.5" 20090624
KARLSTORZ touch screen, 24.5" 20090524
OR1 SmartScreen WM200
Supported display types
Item Order no.
2D monitor 9524NB
2D monitor 9726NB
2D monitor 9626NB
2D monitor 9627NB
2D monitor 9526NBL
2D monitor 9619NB
2D monitor 9626NB-2
2D monitor 9826NB
2D monitor TM220
2D monitor TM263
2D monitor TM340

Product description
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 17
Item Order no.
2D monitor TM341
2D monitor TM342
2D monitor TM440
Supported camera types
To connect other HDMI image sources, KARLSTORZ recommends using Premium High
Speed HDMI cables with a maximum length of 2m (e.g., PureLink PS3000-020).
Item Order no.
IMAGE1 S CONNECT®TC200
IMAGE1 S CONNECT® II TC201
IMAGE1 HD 22202020x
IMAGE1 HUB HD 22201020x
TELECAM C3 TC100
Remote switch
Item Order no.
Remote switch W23174
Footswitch
Item Order no.
Footswitch 20014430
Connecting cable
Item Order no.
Connecting cable 2.5m 4802051
This accessory must be used if the product is installed in a housing, rack, or in-wall
configuration.

Product description
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 18
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
Keep dry
Temperature limit
Humidity limit

Product description
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 19
Symbol Meaning
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 prod-
uct 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 Decla-
ration of Conformity, which can be requested from KARLSTORZ.
4.5.2 Symbols on the product
Symbol Meaning
Dangerous voltage
Danger of an electric shock!
The potential equalization is responsible for equalizing the potentials of
different metal parts that can be touched at the same time, or for reduc-
ing potential differences that could occur between the body, electromed-
ical devices, and external live parts during use.
"STANDBY"
When the yellow indicator light is on, the product is in standby mode.
"ON"
When the green indicator light is on, the product is switched on.
"Access to hard disk"
When the red indicator light is on, the hard disk is being accessed.
USB
4.5.3 Symbols on the rating plate
Symbol Meaning
Manufacturer
Date of manufacture
Environmental protection use period of 10 years (China RoHS)
Separate collection of electrical and electronic devices.
Do not dispose of in household refuse.

Product description
Instructions for use • AIDA C WD310 • AAB272_EN_V2.0_12-2021_IFU_CE-MDR 20
Symbol Meaning
CSA certification mark for the USA and Canada
With this mark, the manufacturer declares compliance with the certifica-
tion requirements.
Alternating current
SN Serial number
Medical device
Non-ionizing radiation
The IC identification code refers to the internal Wi-Fi adaptor
FCCID: FCC identification number of the internal WLAN adapter
IC: IC identification number of the internal WLAN adapter
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 prod-
uct with the applicable EU directives. A code number after the CE mark
indicates the responsible notified body.
The EU legislation relevant to the product can be found in the EU Decla-
ration of Conformity, which can be requested from KARL STORZ.
4.5.4 Symbols on the user interface
Symbol Meaning
User
Call up the user login.
Filing Cabinet
Display documentation which has already been created. The symbol is only
available if the home screen has been deactivated.
Microphone
Mute the microphone. The microphone is muted as standard and must be ac-
tivated manually.
Volume
Set the output level of the active speakers or headphones.
Settings
Select the functional scope and application-specific settings. This area is
password protected.