Schiller FRED easyport plus User manual

FRED®easyport® plus
Automated external defibrillator (AED)
CPR OK Depth 5.0 cm
Rate 101 /min
CPR
00:59
User Guide
Art. no.: 2.511279 Rev. d *2.511279*

Sales and service information
The SCHILLER sales and service centre network is world-wide. For the address of your
local distributor, contact your nearest SCHILLER subsidiary.
In case of difficulty, a complete list of all distributors and subsidiaries is provided on our
internet site:
http://www.schiller.ch
Sales information can also be obtained from:
[e-mail]
Manufacturer
SCHILLER AG Phone: [phone]
Altgasse 68 Fax: [phone]
CH-6341 Baar, Switzerland E-mail: [email protected]
Web:www.schiller.ch
Schiller Medizintechnik GmbH
Otto-Lilienthal-Ring 4
85622 Feldkirchen
Germany
FRED® easyport® plus bears the CE-0123 mark (Notified Body TÜV-SÜD Produkte Ser-
vice GmbH, Ridlerstr. 65, 80339 Munich, Germany), indicating its compliance with the essential re-
quirements of the Annex I of the Medical Device Directive 93/42/EE regarding safety, functionality
and labelling. The requirements apply to patients, users and third persons who come into contact
with this device within the scope of its intended use. Date of first declaration of conformity CE
marking 12.2019
Article no.: 2.511279 Rev. d
Issue date: 15.03.22
Corresponds to: original
Software: 1.2.2

Page 3
User Guide
FRED®easyport®plus
Art. no.: 2.511279 Rev. d
Table of Contents
1 Safety Notes .............................................. 7
1.1 User profiles.......................................................................... 7
1.2 Intended Use ......................................................................... 7
1.3 Indication for use.................................................................. 7
1.4 Contraindication for use ...................................................... 8
1.5 Responsibility of the User ................................................... 8
1.6 Organisational Measures..................................................... 9
1.7 Safety-Conscious Operation ............................................... 9
1.8 Operation with other Devices .............................................. 9
1.9 Maintenance and Cleaning ................................................ 10
1.10 Side Effects ......................................................................... 10
1.11 General Notes Regarding the Unit .................................... 10
1.12 Networks and Internet........................................................ 10
1.13 Additional Terms ................................................................ 11
1.13.1 Implied authorisation........................................................................ 11
1.13.2 Terms of Warranty ........................................................................... 11
1.14 Symbols/Indicators ............................................................ 12
1.14.1 Symbols used in this user guide ...................................................... 12
1.14.2 Symbols used on the device ............................................................ 13
1.14.3 Symbols used on the batteries......................................................... 14
1.14.4 Symbols used on the CS-2 charger ................................................. 14
1.14.5 Symbols used on the electrode packaging ...................................... 15
2 Components and Operation .................. 16
2.1 General Information ........................................................... 16
2.2 Design.................................................................................. 17
2.2.1 Available versions ............................................................................ 18
2.2.2 Overview of the configurable settings .............................................. 18
2.3 Operating and Display Elements ...................................... 19
2.3.1 Overview FRED easyport plus......................................................... 19
2.3.2 FRED easyport plus with bag........................................................... 20
2.4 Display................................................................................. 21
2.5 Functions ............................................................................ 22
2.5.1 Automatic Self-test........................................................................... 22
2.5.2 Performing manual self-test ............................................................. 22
2.5.3 Defibrillation procedure .................................................................... 23

Page 4
FRED®easyport®plus
Art. no.: 2.511279 Rev. d
3 Initial operation .......................................24
3.1 Batteries .............................................................................. 24
3.1.1 General information and safety notes .............................................. 24
3.1.2 Battery replacement......................................................................... 25
3.1.3 Switching device On and Off............................................................ 25
3.2 Battery monitoring.............................................................. 26
3.2.1 Sufficient battery capacity indication while the device is
switched off...................................................................................... 26
3.2.2 Low battery capacity indication while the device is switched off...... 26
3.2.3 Battery depleted during use, limited mode (CPR)............................ 27
3.2.4 Pads expired .................................................................................... 27
3.2.5 Ensuring Operational Readiness ..................................................... 28
3.2.6 Display of technical notifications ...................................................... 28
4 Defibrillation ............................................29
4.1 Instructions and Safety Notes ........................................... 29
4.1.1 Instructions ...................................................................................... 29
4.1.2 Safety notes for defibrillation use..................................................... 29
4.1.3 Defibrillating children........................................................................ 31
4.2 Applying the adhesive electrodes..................................... 32
4.2.1 General information ......................................................................... 32
4.2.2 Unpacking and applying electrodes ................................................. 33
4.2.3 Applying the electrodes to the patient’s chest.................................. 34
4.2.4 Checking the electrodes .................................................................. 35
4.3 Semi-automatic defibrillation ............................................ 36
4.4 Automatic defibrillation...................................................... 38
4.4.1 Functional description of automatic AEDs ....................................... 38
4.4.2 Safety notes for automatic defibrillation........................................... 38
4.4.3 Automatic defibrillation procedure.................................................... 39
4.5 Defibrillation in manual mode ........................................... 41
4.5.1 Switching over to manual mode....................................................... 41
4.5.2 Shock delivery in manual mode....................................................... 42
4.6 Monitoring mode................................................................. 43
4.6.1 With Defi-Pads................................................................................. 43
4.7 Finishing the therapy ......................................................... 44
4.8 ARGUS LifePoint ................................................................ 45
4.8.1 ARGUS LifePoint ............................................................................. 45
4.8.2 Setup of the sensor.......................................................................... 46
5 Communication .......................................47
5.1 Transmission menu............................................................ 47
5.1.1 Retrieving intervention data via USB ............................................... 48
5.1.2 Retrieving intervention data via Bluetooth bridge ............................ 48
5.1.3 Automatic transmission of intervention data via Bluetooth bridge ... 48
6 Charging Unit CS-2 .................................49
6.1 Overview battery charger................................................... 49
6.1.1 LED Status display of the charger ................................................... 50
6.1.2 LED Status display of the rechargeable Lithium Ion battery............ 50

Page 5
User Guide
FRED®easyport®plus
Art. no.: 2.511279 Rev. d
7 Maintenance ............................................ 51
7.1 Maintenance Intervals ........................................................ 51
7.1.1 Service/Shelf life .............................................................................. 52
7.1.2 Visual inspection of the device and accessories.............................. 53
7.1.3 Functional check .............................................................................. 54
7.1.4 Maintenance of the rechargeable Li-Ion battery............................... 54
7.1.5 Maintenance of the non rechargeable Lithium/MnO2 battery .......... 55
7.2 Cleaning .............................................................................. 56
7.2.1 Detergents........................................................................................ 56
7.3 Disinfection ......................................................................... 57
7.3.1 Disinfectant ...................................................................................... 57
7.3.2 Cleaning and disinfecting the device, cable and sensor .................. 58
7.4 Accessories and disposables ........................................... 59
7.4.1 Order Information............................................................................. 59
7.4.2 Required accessories....................................................................... 59
7.5 Disposal information.......................................................... 60
7.5.1 Battery Disposal............................................................................... 60
7.5.2 Disposal of accessories that come into contact with the patient ...... 60
7.5.3 Disposal at the end of its useful life.................................................. 60
7.6 Troubleshooting ................................................................. 61
7.6.1 Error notification............................................................................... 61
7.6.2 General errors & troubleshooting..................................................... 61
7.6.3 Technical notification........................................................................ 62
7.7 Preventing electromagnetic interferences....................... 63
7.7.1 Measures to prevent electromagnetic interferences ........................ 64
8 Technical Data ........................................ 65
8.1 System Specifications ....................................................... 65
8.2 Classification and safety standards ................................. 67
8.3 Defibrillation pulse ............................................................. 68
8.3.1 Shock Advisory System ................................................................... 71
8.4 Bluetooth standard............................................................. 72
8.5 Charging unit ...................................................................... 72
8.6 ARGUS LifePoint sensor ................................................... 73
8.7 Literature ............................................................................. 74
8.8 Glossary .............................................................................. 74
8.9 Inspection report ................................................................ 75
8.10 Overview menus ................................................................. 76
8.11 Device Settings................................................................... 77
8.11.1 Shock setting.................................................................................... 77
8.11.2 CPR setting...................................................................................... 77
8.11.3 CPR Feedback................................................................................. 78
8.11.4 Communication ................................................................................ 78
8.11.5 Transmission mode.......................................................................... 79
8.11.6 Parameter in the Device Settings menu........................................... 79
8.12 System Settings.................................................................. 80
8.12.1 Local Settings................................................................................... 80
8.12.2 Base Settings................................................................................... 81
8.12.3 Self-test Settings.............................................................................. 81

Page 6
FRED®easyport®plus
Art. no.: 2.511279 Rev. d
9 Index ........................................................82
10 Appendix - Symbols ...............................83

Page 7
Safety Notes 1
User Guide User profiles 1.1
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
1 Safety Notes
1.1 User profiles
The following persons may use the FRED® easyport® plus:
• Layperson trained in Basic Life Support and/or on the device
• Healthcare provider trained in Basic Life Support and/or on the device
• Physicians or other healthcare provider trained in Advanced Life Support may use
the FRED easyport plus with manual override or in monitoring mode.
1.2 Intended Use
1.3 Indication for use
The FRED easyport plus is a defibrillator with the possibility to deliver a shock
either in semi-automatic, fully-automatic or manual mode.
FRED easyport plus® is intended to be used to terminate cardiac arrhythmia
such as Ventricular Fibrillation or Ventricular Tachycardia with a defibrillation
shock.
The intended patient population are adults >25 kg and children weighing less
than 25 kg (younger than 8 years of age).
The portable device is intended to be used in following environmental:
– Primarily in pre-hospital care and transport applications (including ambulances,
fixed and rotary wing aircraft) patient’s homes or work places.
FRED easyport plus is intended to be used to terminate cardiac arrhythmia
such as Ventricular Fibrillation or Ventricular Tachycardia with a defibrillation
shock.

1 Safety Notes
1.4 Contraindication for use
Page 8
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
1.4 Contraindication for use
1.5 Responsibility of the User
AED mode
The defibrillator must not be used when the person:
– is responsive
– is breathing normally
– has pulse
Manual defibrillation mode
– Defibrillation is contraindicated in the treatment of Pulseless Electrical Activity
(PEA), such as idioventricular or ventricular escape rhythms, and in the treat-
ment of asystole.
CPR feedback
The CPR feedback option is contraindicated for use on neonatal and pediatric
patients under 8 years and < 25 kg.
CPR feedback option is contraindicated when manual CPR is contraindicated.
Other contraindications
Do not use the device in or near magnetic resonance imaging equipment (MRI).
Danger of explosion! — The device must not be used in areas where there is
any danger of explosion. There might be a danger of explosion in areas where
flammable products (petrol), flammable anaesthetic agents or products for skin
cleaning/disinfection are in use, or where the ambient air's oxygen concentration
is higher than 25 %.
The device is not designed for sterile use.
The device is not for use in or near magnetic resonance imaging equipment.
.
Regulations on who is allowed to use devices like the
FRED easyport plus and which training is required, are country-specific. In any
case, legal regulations have to be observed.
Before using the device, a SCHILLER representative must perform a
presentation on the device's operation and safety measures, if it is required by
the local regulations.
Interpretation suggested by the device must be examined with respect to the
patient's overall clinical condition and the quality of the recorded data.
Damaged or missing components must be replaced immediately.
The device must be stored in a place inaccessible to children.
Properly dispose of the packaging material and make sure it is out of children's
reach.
The FRED easyport plus is an emergency device and must be ready for
operation at any time and in all situations. Make sure that:
– the device is always equipped with a sufficiently charged battery
– you always keep a new spare battery on hand
– an empty battery must not be reused and must be disposed of immediately
– a set of adult electrodes is pre-connected and a spare set of electrodes must be
stored with the device
– the maintenance intervals are observed see 7 Maintenance.
If any serious incident has occurred in relation to the device it should be reported
to the manufacturer and the competent authority of the Member State in which
the user and/or patient is established.

Page 9
Safety Notes 1
User Guide Organisational Measures 1.6
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
1.6 Organisational Measures
1.7 Safety-Conscious Operation
1.8 Operation with other Devices
Before using the unit, ensure that an introduction regarding the unit functions
and the safety precautions has been provided and understood.
Keep these operating instructions in an accessible place for reference when
required. Make sure that they are always complete and legible.
Danger of electric shock! - Danger for user, rescuer and patient.
The energy applied to the patient can be conducted through the patient to other
persons, who may suffer a lethal electric shock. Therefore:
– do not touch the patient, the electrodes or other conducting objects during defi-
brillation.
– do not defibrillate the patient in a puddle of water or on other conducting surfac-
es,
– switch the device off when it is no longer used.
Danger of explosion! — The device must not be used in areas where there is
any danger of explosion. There might be a danger of explosion in areas where
flammable products (petrol), flammable anaesthetic agents or products for skin
cleaning/disinfection are in use, or where the ambient air's oxygen concentration
is higher than 25 %.
Immediately report any changes that impair safety (including operating
behaviour) to the responsible person.
Only use original SCHILLER electrodes and accessories.
Check that the unit's casing and electrode connections are not damaged.
Check expired date of the defibrillation electrodes.
After use, refer to the chapter 7 Maintenance.
Immediately replace a damaged unit, or damaged cables and connections.
Operating the device with a defective casing or damaged cables constitutes a
danger to life.
Only operate the device in accordance with the specified technical data
8 Technical Data.
Magnetic and electrical fields from X-ray or tomographic devices, portable radio
equipment, HF radios and devices labelled with the symbol can affect the
operation of this device (see section 8.7). Avoid using such devices or keep a
sufficient distance from them.
FRED easyport plus is not intended to be operated while using high-frequency
surgical devices.
Interference with other devices - The charging of energy and the release of the
defibrillation impulse can disturb other devices. Check these devices before their
further use.
Other medical equipment applied to patient which has no defibrillation proof
applied part must be disconnected from the patient.
The patient can be endangered by too high leakage currents (summation of
leakage currents) if several devices are connected to the patient. For this
reason, devices that are not required should be disconnected from the patient,
and only equipment approved by SCHILLER may be connected to the device.

1 Safety Notes
1.9 Maintenance and Cleaning
Page 10
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
1.9 Maintenance and Cleaning
1.10 Side Effects
1.11 General Notes Regarding the Unit
1.12 Networks and Internet
Danger of electric shock! Do not open the device. No serviceable parts inside.
Refer servicing to qualified personnel only.
Do not service, maintain or clean the device while in use with a patient.
Before cleaning, switch the unit off and remove the battery.
Do not use high-temperature sterilisation processes (such as autoclaving). Do
not use E-beam or gamma radiation sterilisation.
Do not use aggressive or abrasive cleaners.
Do not, under any circumstances, immerse the device or cable assemblies in
liquid.
To ensure patient safety, only use original SCHILLER accessories. The user is
responsible for the use of third-party accessories. The warranty does not cover
damage resulting from the use of accessories or consumables other than those
marketed by SCHILLER.
Defibrillating a patient can cause:
– skin irritations or burns
– malfunction or damage of implanted pacemaker
A defibrillation can fail with certain disease patterns.
When the unit is part of a network, (LAN, WLAN, HIS, etc.), or any other
transmission/reception medium, or if exposed to the Internet or other insecure
networks, appropriate security measures must be taken to protect the stored
patient data.
Patient data security and security of the network is the sole responsibility of the
user.
In order to guarantee the security of the network, Schiller recommends the
following:
– isolating the FRED easyport plus network from other networks
– defining access authorisation for the configuration of the host system, incl.
FRED easyport plus, so that no unauthorised alterations of the system are
possible.

Page 11
Safety Notes 1
User Guide Additional Terms 1.13
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
1.13 Additional Terms
1.13.1 Implied authorisation
Possession or purchase of this device does not convey any express or implied license
to use the device with replacement parts which would alone, or in combination with
this device, fall within the scope of one or more patents relating to this device.
1.13.2 Terms of Warranty
Your SCHILLER FRED easyport plus is warranted against defects in material and
manufacture according the general terms of condition. Excluded from this warranty is
damage caused by an accident or as a result of improper handling. The warranty
entitles to free replacement of the defective part. Any liability for subsequent damage
is excluded. The warranty is void if unauthorised or unqualified persons attempt to
make repairs.
In case of a defect, send the device to your dealer or directly to the manufacturer. The
manufacturer can only be held responsible for the safety, reliability, and performance
of the apparatus, and assume the warranty, if:
• assembly operations, extensions, readjustments, modifications, or repairs are
carried out by persons authorised by him,
• spare parts used for assembly operations, extensions, readjustments, modifica-
tions or repairs are recommended or supplied by SCHILLER, and,
• the SCHILLER FRED easyport plus and approved attached equipment is used
in accordance with the manufacturer's instructions.
There are no express or implied warranties which extend beyond the warranties
hereinabove set forth. SCHILLER makes no warranty of merchantability or fitness for
a particular purpose with respect to the product or parts thereof.

1 Safety Notes
1.14 Symbols/Indicators
Page 12
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
1.14 Symbols/Indicators
1.14.1 Symbols used in this user guide
The safety levels are classified according to ANSI Z535.6. The following overview
shows the safety symbols and pictograms used in this user guide.
The terms Danger, Warning, and Caution are used in this User Guide to point out
potential dangers and to indicate risk levels. Familiarise yourself with their definitions and
significance.
For a direct danger which could lead to severe personal injury or death.
For a possibly dangerous situation which could lead to severe personal injury or to
death.
For a possibly dangerous situation which could lead to personal injury. This symbol is
also used to indicate possible damage to property.
For general safety notes as listed in this section.
For electrical hazards, warnings or precautionary measures when dealing with
electricity.
Important or helpful user information.
Do not use the device in or near magnetic resonance imaging equipment (MRI).

Page 13
Safety Notes 1
User Guide Symbols/Indicators 1.14
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
1.14.2 Symbols used on the device
General used symbols see 10 Appendix - Symbols.
Reading the instruction for use is mandatory before using the device!
Caution: Consult the warning and safety information in the instructions for use!
BF symbol. The device's signal input is defibrillation-protected.
Dangerous voltage! Used for electrical dangers during defibrillation.
IP44
The device rated IP44 meaning protection against solid objects over 1 mm diameter,
e.g. persons fingers, and splash water protected (no harmful effect from vertically
splashing water from all direction.
Battery replacement instruction
Bluetooth inside
Attention: non ionising electromagnetic radiation. Some of the devices contain an HF
transmitter (Bluetooth).
The FRED easyport plus radiates high-frequency electromagnetic energy and can
disturb other devices if not installed and operated in accordance with the user guide.
However, there is no guarantee that no interference can occur in certain installations.
If the FRED easyport plus causes interferences, these can be determined by
switching the device off/on or by transmitting/not transmitting ECG data. The user
can take the following measures to prevent electromagnetic interferences:
• Increase the distance between the disturbed device and the FRED easyport plus.
A minimum distance of 20 cm must be kept between the device and a pacemaker.
• Turn the device to change the angle of radiation.
For more details, see page 63.

1 Safety Notes
1.14 Symbols/Indicators
Page 14
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
1.14.3 Symbols used on the batteries
For general used symbols see 10 Appendix - Symbols.
1.14.4 Symbols used on the CS-2 charger
For general used symbols see 10 Appendix - Symbols.
Caution: Consult the warning and safety information in the instructions for use!
Do not incinerate
Do not crush
Do not saw
Rechargeable Li-Ion battery
min/max discharging temperature for rechargeable Li-Ion battery.
Note: Fully charged batteries may only be stored up to one month at max. discharging
temperature.
Primary Lithium Manganese dioxide battery (non-rechargeable)
min/max discharging temperature for primary Lithium/MnO2battery.
Note: Storage at max. discharging temperature will increase the self discharge of the
battery.
Expiry date of the primary Lithium/MnO2battery.
-20°C
60°C
-20°C
60°C
Indoor use only
CS-2 charger is protection class III
DC voltage

Page 15
Safety Notes 1
User Guide Symbols/Indicators 1.14
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
1.14.5 Symbols used on the electrode packaging
General used symbols see 10 Appendix - Symbols.
Reading the instruction for use is mandatory before using the electrodes!
Do not bend packing
Don’t use if the packaging is damaged
Disposable item; do not reuse
• Remove the patient's clothes
• Open the electrode packaging
• Peel off the protective foil
Storage temperature for the electrodes
Expiry date of the electrodes
An open package cannot be conserved more than one day.
The product is intended to be used on patients weighing 25 kg or more.
The product is intended to be used on patients weighing less than 25 kg.

2 Components and Operation
2.1 General Information
Page 16
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
2 Components and Opera-
tion
2.1 General Information
FRED easyport plus is an automated external defibrillator (AED).
The FRED easyport plus is available as an automatic, semi-automatic or manual
defibrillator.
Professional use For the professional use, the FRED easyport plus offers an AED with ECG display,
an optional data transfer and a manual override.
Local laws and regulations regarding the use of an AED vary from country to country.
While some countries allow laypersons to use AEDs without any special training,
other countries restrict the use of AEDs to an Emergency Medical Technician or First
Responders after they have undergone special training.
Biocompatibility
The parts of the product described in this user guide, including all accessories, that
come in contact with the patient during the intended use, fulfil the biocompatibility
requirements of the applicable standards. If you have any questions on this matter,
please contact SCHILLER.

Page 17
Components and Operation 2
User Guide Design 2.2
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
2.2 Design
Defibrillator The FRED easyport plus is a defibrillator featuring biphasic pulsed defibrillation
impulse – Multipulse Biowave®. The defibrillation is done using disposable
adhesive electrodes (pads), which also acquires the ECG signal for the analysis.
Adhesive electrodes for children and adults are available. The device recognises the
connected electrodes and selects the defibrillation energy levels accordingly. Adult
electrode can be used also for children. In this case, the child mode has to be selected
with the button Adult/Child on the front panel. In the AED mode, the user will be given
visual and audible instructions (display/loudspeaker).
Languages The device can be provided with different languages.
Metronome The FRED easyport plus emits a sound pace for the cardiopulmonary resuscitation
(CPR) - rate is configurable.
CPR Feedback (option) Real time information on the chest compression frequency using the ARGUS
LifePoint feedback sensor.
Data memory The device is equipped with an internal 8 Gbit memory to store 8 hours intervention.
During the intervention, data can therefore be saved, including the analysed ECG
data. In addition, technical data (logs) will be stored.
Data transmission •TheFRED easyport plus has a USB host connection in order to
– retrieve data via USB memory stick
– perform software and configuration updates
– connect the Argus LifePoint feedback sensor
• USB device connection for service
– Bluetooth connection to host
Power supply • The device is operated with a rechargeable or non rechargeable lithium battery.
The battery capacity is sufficient for (if the device is stored/used in optimal temper-
ature conditions between 15...25 °C:
• with Lithium/MnO2
– approx. 70 shocks at max. energy with 2 minutes monitoring between shocks with a
total running time of approx. 4 h 50 minutes
– Standby with weekly selftest: approx. 1 year 6 months
– Standby with monthly selftest: approx. 2 years 6 months
• with Li-Ion (rechargeable)
– approx. 70 shocks at max. energy with 2 minutes monitoring between shocks with a
total running time of approx. 3 h
– Standby with weekly selftest approx. 1 year 1 months
– Standby with monthly selftest approx. 1 year 11 months
Note
When depletion notification is issued (battery below 10%), approx. 5 shocks can be
delivered until the battery is completely empty.
Self test RTU (Ready to use) • To ensure its readiness for use, the device performs a daily, weekly or monthly
self-test. Self-test includes the test of the charging circuit and the battery capacity.
• If this test is completed successfully, the green RTU (Ready-To-Use) LED is blink-
ing (two second interval), showing that the device has not detected an error.

2 Components and Operation
2.2 Design
Page 18
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
2.2.1 Available versions
2.2.2 Overview of the configurable settings
SCHILLER's service centre can configure the following password-protected
parameters:
Model Description
AED FIRST AED semi-automatic with or without ECG display (config-
urable)
AED Fully automated AED fully automatic with or without ECG display (configur-
able)
AED MANUAL AED semi-automatic and manual with ECG display
Settings are only modified if requested by the customer, or due to legal
requirements.
These modifications need to be registered in the device documentation as well
as communicated to all users.
Modification in the password-protected menus is only allowed by authorised
users.
Any unauthorized modification may endanger the patient.
Configurable device parameters Detail see Password required
• Selftest 2.5.2 Performing manual self-test No
• Bluetooth pairing see service manual No
• Device information 8.10 Overview menus No
•Device Settings >>>
– Shock settings >>> Energy level for 1st, 2nd and 3rd shock
– CPR settings >>>
– CPR feedback >>>
– Communication >>>
– Transmission mode >>>
8.11 Device Settings Yes
– System settings >>>
- Local settings >>> Language, country, Date, Time, Timezone
- Base settings >>>
- Maintenance >>>(Year month) Lenght Unit (metric/inches);
Monitor enable; Device name
- Selftest Setting >>> (daily, weekly or monthly)
- Volume settings
- ECG and HR display
- Show pacer markers
- Auto Switch off time
8.12 System Settings Yes
– Restore Factory Defaults
– Import/Export settings
8.11.6 Parameter in the Device
Settings menu
Yes
• Device update see service manual Yes
• Pads expired 3.2.4 Pads expired No
• Production
– Metronome CPR Time and number of breats
see service manual Yes
• Log Files see service manual Yes

Page 19
Components and Operation 2
User Guide Operating and Display Elements 2.3
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
2.3 Operating and Display Elements
2.3.1 Overview FRED easyport plus
The picture below shows the user interface for an AED with ECG and CPR feedback
display.
Fig. 2.1 Operating Elements
(1) Green button to switch the device on/off and RTU LED (Ready -to-use LED)
(2) Orange indicator lamp; lit as long as no electrodes are connected
(3) Electrode connector
(4) LCD screen
(5) Switching to child mode when using adult electrodes (PATIENT button)
(6) USB connector for Argus LifePoint sensor or USB memory stick
(7) Orange button: key to trigger a defibrillation impulse (SHOCK button)
(8) Battery at back
(9) Loudspeaker
(10) Microphone
(11) Data transfer (COM) button
(12) Ambient light sensor
11
34
5
9
1
7
10
6
8
2
12 30 CHEST COMPRESSIONS
THEN 2 RESCUE BREATHS
CPR OK Depth 5.0 cm
Rate 101 /min
CPR
00:59
To ensure patient safety
– only use original SCHILLER electrodes (3)
– connect only the LifePoint sensor to the USB port (6)
– connect only USB memory stick to USB port (6), when device is not in use.

2 Components and Operation
2.3 Operating and Display Elements
Page 20
Art. no.: 2.511279 Rev. d
FRED®easyport®plus
2.3.2 FRED easyport plus with bag
(1) RTU LED (Ready -to-use LED) transparent window
(2) Defibrillation electrode compartment
(3) Scissor and razor compartment
(4) Connection ARGUS LifePoint CPR feedback sensor (USB Port)
(5) ARGUS LifePoint compartment
5
9
1
8
3
2
4
1