Bexen REANIBEX 300 User manual

AED/Manual Defibrillator
REANIBEX 300
USER MANUAL
DIH 0300 B – REV: C / 2014.FEB

REANIBEX 300
USER GUIDE
Review Date Approved by Signature
C February 2014
Gorka Landaburu
R&D Manager

Blank page

Review C February 2014
All rights are reserved for this publication.
This manual may not be totally or partially reproduced, in any way or by any
means, without prior written authorization from of OSATU S. Coop.
The information contained in this manual may be modified by the manufacturer
without requiring prior notice. If the information in this User Guide does not
correspond to the operation of the device, please contact an authorised
representative of OSATU S. Coop.
REANIBEX 300
This is a product of:
OSATU S.Coop
Edificio Zearrekobuelta
Subida de Areitio Nº 5
48260 Ermua (Bizkaia) – SPAIN
Tel.: [phone]
Fax: [phone]
E-mail: [email protected]
www.bexencardio.com

Blank page

DECLARACIÓN DE CONFORMIDAD
DECLARATION OF CONFORMITY
Directiva del Consejo con la que se declara conformidad:
Council Directive to which conformity is declared:
Annex II, section 3 of CD 93/42/EEC concerning medical devices
Aplicación de las Normas / Application of the Standards:
EN 60601-1:2005+A1:2012, EN 60601-1-2:2007+AC:2010, EN 60601-1-6:2010,
EN 60601-1-8:2006+ A1:2012, EN 60601-2-4:2010, EN 60601-2-49:2011,
EN 62304:2006, EN 1789:2007+ A1:2010
Fabricante / Manufacturer´s name: Osatu S. Coop.
Dirección del fabricante /
Manufacturer’s address:
Edificio Zearrekobuelta
Subida de Areitio Nº 5
48260-Ermua
Bizkaia (SPAIN)
Tipo de equipo / Type of equipment: Desfibrilador Manual/AED
Defibrillator Manual/AED
Marca / Trade mark: BEXEN CARDIO
Modelo / Model no.: REANIBEX 300
Clasificación / Classification: Clase IIb
Organismo notificado / Notified body: UL International (UK) Ltd (CE-0843)
Nosotros, los abajo firmantes, declaramos que el equipo antes especificado
cumple con las Directivas y las Normas mencionadas
We, the undersigned, hereby declare that equipment specified above conforms to
the above Directives and Standards
Ermua, 25 – February – 2014
Félix Ajuria
Director. Gerente
Managing Directo

Blank page

DIH 0300 B – USER GUIDE REANIBEX 300 i
TABLE OF CONTENTS

1INTRODUCTION ................................................................................................................................. 1
1.1OVERVIEW................................................................................................................................. 1
1.2INTENDED USE ......................................................................................................................... 2
1.3SAFETY CONSIDERATIONS..................................................................................................... 3
2DESCRIPTION OF THE EQUIPMENT ............................................................................................... 8
2.1BASIC ORIENTATION................................................................................................................ 8
2.1.1FRONT VIEW ...................................................................................................................... 8
2.1.2BACK VIEW.......................................................................................................................... 9
2.1.3SIDE VIEWS....................................................................................................................... 10
2.2SCREEN ................................................................................................................................... 11
2.3PROGRAMMABLE BUTTONS ................................................................................................. 13
2.4MENU OPTIONS ...................................................................................................................... 14
2.5STATUS INDICATOR ............................................................................................................... 15
2.6BATTERIES .............................................................................................................................. 15
2.6.1BATTERY CAPACITY ........................................................................................................ 15
2.6.2BATTERY DURATION ....................................................................................................... 16
2.7ELECTRODES AND CABLES.................................................................................................. 17
3INSTALLATION OF THE EQUIPMENT............................................................................................ 18
3.1CONNECTING THE ECG CABLE ............................................................................................ 18
3.2CONNECTING THE THERAPY CABLE................................................................................... 19
3.3INSTALLING THE BATTERY ................................................................................................... 20
3.4CONNECTIONS FOR THE TRANSFER OF INTERNAL EQUIPMENT DATA ........................ 20
3.4.1CONNECTING THE USB MEMORY TO THE EQUIPMENT............................................. 21
4AUTOMATED EXTERNAL DEFIBRILLATION ................................................................................ 22
4.1INTENDED USE ....................................................................................................................... 22
4.2WARNINGS AND PRECAUTIONS........................................................................................... 23
4.3PREPARING FOR AUTOMATED EXTERNAL DEFIBRILLATION .......................................... 23
4.4AUTOMATED EXTERNAL DEFIBRILLATION PROCEDURE................................................. 24
4.5TROUBLESHOOTING .............................................................................................................. 26
5MANUAL DEFIBRILLATION (OPTIONAL) ...................................................................................... 27
5.1INTENDED USE ....................................................................................................................... 27
5.2WARNINGS AND PRECAUTIONS........................................................................................... 28
5.3PREPARING FOR MANUAL DEFIBRILLATION...................................................................... 29
5.4ASYNCHRONOUS MANUAL DEFIBRILLATION PROCEDURE............................................. 31
5.5TROUBLESHOOTING .............................................................................................................. 33
6ECG MODE. NON-DIAGNOSTIC ECG MONITORING (OPTIONAL).............................................. 34
6.1INTENDED USE ....................................................................................................................... 34
6.2WARNINGS AND PRECAUTIONS........................................................................................... 34
6.3PREPARATION FOR ECG MODE ........................................................................................... 35
6.4NO DIAGNOSTIC MONITORING PROCEDURE..................................................................... 37
6.5TROUBLESHOOTING .............................................................................................................. 37
7AUTO-TRAINING .............................................................................................................................. 38

DIH 0300 B – USER GUIDE REANIBEX 300 ii
TABLE OF CONTENTS
7.1DESCRIPTION.......................................................................................................................... 38
7.2PROGRAMMABLE BUTTON DURING THE AUTO-TRAINING .............................................. 38
7.3AUTO-TRAINING CONFIGURATION ...................................................................................... 39
7.4SCENARIOS ............................................................................................................................. 39
8CONFIGURATION ............................................................................................................................ 41
8.1ACCESS TO CONFIGURATION MODE .................................................................................. 41
8.2CONFIGURABLE PARAMETERS............................................................................................ 42
8.3SETTING DATE AND TIME...................................................................................................... 45
8.4CONFIGURATION MANAGEMENT ......................................................................................... 46
8.4.1EQUIPMENT IDENTIFIER ................................................................................................. 46
8.4.2DEFAULT SETTINGS ........................................................................................................ 47
8.4.3CONFIGURATION PASSWORD ....................................................................................... 48
8.5EQUIPMENT INFORMATION................................................................................................... 48
8.5.1EQUIPMENT INFORMATION ............................................................................................ 48
8.5.2LATEST TEST RESULTS .................................................................................................. 49
8.5.3LATEST EPISODE RESULTS ........................................................................................... 50
8.5.4EPISODE DELETION......................................................................................................... 50
8.6USB TRANSFER ...................................................................................................................... 51
8.6.1TRANSFER TO USB MEMORY......................................................................................... 51
8.6.2TRANSFER TO A PC VIA A USB CABLE ......................................................................... 52
8.7TESTS....................................................................................................................................... 52
8.7.1HARDWARE TEST ............................................................................................................ 53
8.7.2ACCESSORIES TEST ....................................................................................................... 54
8.7.3USER INTERFACE TEST .................................................................................................. 54
8.7.4AUTO- TESTS.................................................................................................................... 55
9DATA MANAGEMENT...................................................................................................................... 56
9.1DESCRIPTION.......................................................................................................................... 56
9.2STORED EVENTS.................................................................................................................... 56
10MAINTENANCE ................................................................................................................................ 58
10.1OVERVIEW............................................................................................................................... 58
10.2MAINTENANCE ROUTINE....................................................................................................... 58
10.2.1CHECK LIST....................................................................................................................... 59
10.3CLEANING INSTRUCTIONS.................................................................................................... 59
10.3.1GENERAL........................................................................................................................... 59
10.3.2ECG CABLE ....................................................................................................................... 60
10.4STORAGE................................................................................................................................. 60
10.5BATTERY MAINTENANCE ...................................................................................................... 61
10.6SERVICE AND REPAIR ........................................................................................................... 62
10.7PRODUCT RECYCLING INFORMATION ................................................................................ 63
10.8WARRANTY.............................................................................................................................. 63
10.9ACCESSORIES ........................................................................................................................ 64
11TROUBLESHOOTING ...................................................................................................................... 65
11.1GENERAL PROBLEMS............................................................................................................ 65

DIH 0300 B – USER GUIDE REANIBEX 300 iii
TABLE OF CONTENTS
11.2ECG MODE PROBLEMS.......................................................................................................... 67
11.3MANUAL DEFIBRILLATION PROBLEMS................................................................................ 69
11.4AUTOMATED DEFIBRILLATION PROBLEMS ........................................................................ 70
A.1SYMBOLS..................................................................................................................................... 71
A.2SCREEN MESSAGES .................................................................................................................. 75
A.3SPECIFICATIONS AND CHARACTERISTICS........................................................................... 77
A.4DEFIBRILLATION WAVE............................................................................................................ 82
A.5RHYTHM DETECTION SYSTEM ................................................................................................ 84
A.6ELECTROMAGNETIC COMPATIBILITY GUIDE ....................................................................... 85
A.7ACCESSORIES ........................................................................................................................... 88

DIH 0300 B – USER GUIDE REANIBEX 300 iv
TABLE OF CONTENTS

DIH 0300 B – USER GUIDE REANIBEX 300 i
TABLE OF ILLUSTRATIONS
Illustrations
Figure 1 Front View ...................................................................................................................................... 8
Figure 2: Rear views................................................................................................................................... 10
Figure 3: Left side view............................................................................................................................... 10
Figure 4: Right side view ............................................................................................................................ 10
Figure 5: Distribution of the information on the display screen .................................................................. 11
Figure 6: Programmable buttons to change the operating mode............................................................... 13
Figure 7: Manual Defibrillator programmable buttons ................................................................................ 13
Figure 8: Automated Defibrillator programmable buttons .......................................................................... 14
Figure 9: Manual Defibrillator mode menu options .................................................................................... 14
Figure 10: Automated Defibrillator mode menu options............................................................................. 14
Figure 11: ECG mode menu options.......................................................................................................... 14
Figure 12: 3-lead patient cable................................................................................................................... 17
Figure 13: ECG cable connection .............................................................................................................. 19
Figure 14: Therapy cable connection......................................................................................................... 19
Figure 15: Battery installation..................................................................................................................... 20
Figure 16: Battery removal ......................................................................................................................... 20
Figure 17: USB memory connection .......................................................................................................... 21
Figure 19: “Apply electrodes” display in Automated Defibrillator mode ..................................................... 24
Figure 20: CPR time display in Automated Defibrillator mode................................................................... 25
Figure 21: Energy charge display in Automated Defibrillator mode........................................................... 25
Figure 22: Placing the electrode pads in the antero-lateral position (adult and paediatric) ....................... 30
Figure 23: Placing the electrode pads in the antero-posterior position (adult and paediatric)................... 31
Figure 24: Placing the monitoring electrode pads...................................................................................... 36
Figure 25: Heart Rate monitoring value ..................................................................................................... 37
Figure 26: Configuration mode access screen........................................................................................... 41
Figure 27: Module Menu screen................................................................................................................. 42
Figure 28: General Options modification screen........................................................................................ 44
Figure 29: “User Interface” options screen................................................................................................. 45
Figure 30: Date / Time adjustment screen ................................................................................................. 46
Figure 31: Equipment ID Code modification screen................................................................................... 47
Figure 32: Changing the CONFIGURATION mode access password....................................................... 48
Figure 33: Equipment information screen .................................................................................................. 49
Figure 34: Screen with the information to transfer to the USB memory..................................................... 52
Figure 35: Hardware Test screen............................................................................................................... 53

DIH 0300 B – USER GUIDE REANIBEX 300 ii
TABLE OF ILLUSTRATIONS
Figure 36: Confirmation request during the Hardware Test....................................................................... 54
Figure 37: Defibrillation wave ..................................................................................................................... 82

DIH 0300 B – USER GUIDE REANIBEX 300 1
1 INTRODUCTION
1 INTRODUCTION
The REANIBEX 300 is a portable, lightweight Defibrillator designed to carry out advanced monitoring and
resuscitation functions. It offers three operating modes: Manual Defibrillator, Automated Defibrillator and
ECG Mode.
This guide contains the instructions necessary for safe and appropriate use of the equipment, as well as
information on its configuration and maintenance. The guide includes the information and procedures for
all the features of the REANIBEX 300. The device you have purchased may not have all the features
contained in this manual.
Ensure that you are familiar with the features and operation of the REANIBEX 300 before using the
device.
WARNING
Some accessories of the REANIBEX 300 are not interchangeable with the accessories used in other
REANIBEX equipment. Incompatibilities between accessories are included in this manual.
1.1 OVERVIEW
The REANIBEX 300 offers several operating modes:
xManual Defibrillator Mode - Recommended for manual defibrillation and monitoring of vital
signs.
xAutomated Defibrillator Mode - Recommended for analysis of the ECG signal and defibrillation,
if required. It guides the user through the operating protocol.
xECG Mode - Available if the equipment has the patient cable connected to the equipment and
always from Manual mode (with electrodes no connected to the equipment). This mode provides
a no diagnostic ECG display from the lead II. When in ECG mode the discharge capacity is
disable.
xConfiguration Mode - This mode may be used to carry out manual tests, to configure the
various operation modes, to access the information stored on the internal memory and to carry
out maintenance functions.
xDemo Mode - This mode is used to demonstrate the equipment operation displaying simulated
waveforms. This operating mode can only be accessed through the maintenance options of the
Configuration mode.
xAuto-training mode – This mode allows work education and training in the use of the equipment
by simulating predefined usage scenarios (for more information see “REANIBEX 300/500 User
manual – Training options”). This operating mode is only accesible if you have installed the
training battery (DIS 3200 A).
If required, the Manual Defibrillator mode may be used to apply a defibrillation discharge following three
easy steps:
1. Charge
2. Apply the discharge.
The selection of the energy to be applied during the Manual mode should be done from Configuration
mode. During Manual mode the user can not select the value of the energy.

DIH 0300 B – USER GUIDE REANIBEX 300 2
1 INTRODUCTION
In the Manual Defibrillator mode, the defibrillation discharge may be applied using multifunction
disposable electrodes. Access to this operating mode may be restricted via the configuration options.
When operating in Automated Defibrillator mode, the REANIBEX 300 analyses the patient’s
electrocardiogram (ECG) and decides whether the rhythm analysed can be shockable. If so, the user
must take action to administer the discharge. Throughout the process, the equipment guides the user
through all operations by means of text messages displayed on the screen and audible instructions
provided by a loudspeaker located on the right side of the device. In AED mode, the REANIBEX 300 can
also be configured to record the audio generated during the incident.
The REANIBEX 300 can operate with rechargeable Li-ion batteries or with disposable LiSO2batteries.
Remaining battery power is shown at all times at the top of the device screen. Rechargeable batteries are
charged using an external charger with the battery removed from the device.
The REANIBEX 300 has an internal memory that stores the data from the last 10 patient interventions
performed by the equipment. These data include patient ECG signals and the events that occurred during
the intervention. Optionally, they can include audio of the equipment and ambient noise if the equipments
operating in Automated Defibrillator mode. In addition to these data, the equipment stores the last 100
tests performed at the request of the user or during an Auto Test. All this information can be downloaded,
viewed and stored using the “REANIBEX DATA MANAGER” PC application.
In addition to the patient-related operating modes described above, the REANIBEX 300 has a special
switch-on function that accesses the Configuration mode. This mode is used to configure and adjust the
parameters that control the operation of the equipment to the requirements of the various users and to
perform various Manual Tests at user request.
During start-up and operation, the REANIBEX 300 performs a series of Auto Tests to detect any failures
or anomalous conditions in the equipment that may compromise safe operation. Errors are indicated
through a status indicator located at the front of the device. This indicator is active whether the device is
switched on or off and shows error messages on the screen when the equipment is switched on.
Lastly, the REANIBEX 300 performs automatic daily, weekly and monthly tests, as well as Auto Tests
each time it detects a new battery. Therefore, apart from the tests performed during operation and when
the device is switched on, the device performs the following Auto Tests.
xBattery Insertion Auto Test
xDaily Auto Test; this test is performed every day between the time programmed in the
Configuration mode and the following hour.
xWeekly Auto Test; this test is performed once a week and includes the Auto Test of the day in
question.
xMonthly Auto Test; this verification is carried out once a month and includes the weekly and daily
Auto Tests.
1.2 INTENDED USE
The REANIBEX 300 is recommended for use by personnel trained in the use of the equipment and
qualified in basic life support, advanced life support or defibrillation in hospital and out-of- hospital
environments that meet the environmental conditions indicated in this guide.
When used in Manual Defibrillator or ECG modes, the REANIBEX 300 should be used by medical
personnel trained in advanced life support.

DIH 0300 B – USER GUIDE REANIBEX 300 3
1 INTRODUCTION
All of the operating modes of the device are intended to be used in both adult and paediatric patients, as
long as the applied electrodes are appropriate for each type of patient.
Thus, both the Automated and Manual defibrillator mode can be used with standard defibrillation
electrodes only in adults and in children over 8 years of age or weighing over 25 kg (55 lbs). Both the
Automated and Manual defibrillator mode can be used in children under 8 years of age or weighing less
than 25 kg (55 lbs) with specific paediatric defibrillation electrodes.
Whichever mode is used, the device will adjust the power levels, alarm limits, metronome characteristics
and all the necessary patient parameters according to the type of electrode that is connected: standard
(adult) or paediatric.
For further information on the intended use of the device, indications for use and contraindications of the
monitoring and treatment functions, please refer to the corresponding sections in this guide that explain
these functions.
WARNING
The REANIBEX 300 must be used on a single patient at a time.
1.3 SAFETY CONSIDERATIONS
HAZARD
EXPLOSION HAZARD
.Possible explosion hazard if the REANIBEX 300 is used in the presence of mixtures with
concentrations of oxygen over 25% or flammable anaesthetic products.
WARNING
Improper use of the device can cause injuries. Follow the instructions in the User Guide to ensure
proper use.
WARNING
• Avoid connecting the patient to several devices at the same time to prevent exceeding leakage
current limits.
• Avoid touching the monitoring electrodes or other measuring devices when these are placed on the
patient, as this may affect safety and results.
WARNING
Prevent conductive parts of electrodes and connectors associated with applied parts, including the
neutral electrode, from coming into contact with other conductive parts, including the earth.
WARNING
SHOCK OR FIRE HAZARD. The defibrillator can deliver up to 360 Joules of energy. If the equipment is
not used correctly, as described in these instructions for use, this energy may cause severe injuries or
death. Ensure that you are familiar with how to use the equipment before using it.

DIH 0300 B – USER GUIDE REANIBEX 300 4
1 INTRODUCTION
WARNING
SHOCK OR FIRE HAZARD. Do not disassemble the defibrillator. This equipment contains dangerous
high voltage. For repairs, please contact authorised technical service staff.
WARNING
SHOCK OR FIRE HAZARD
• Never use the REANIBEX 300 over stagnant water. Do not submerge the equipment or any part of it
in water or any other liquid. Do not spill liquid on the equipment or any of its accessories. If the
equipment gets wet, dry it with a towel.
• Do not clean the equipment with flammable agents such as acetones.
• Do not sterilise the equipment in an autoclave or by any other means.
ATTENTION
HAZARDOUS ELECTRICAL SHOCK. The REANIBEX 300 is not intended for use by personnel
without appropriate training. Use of the equipment by untrained personnel can cause injuries or death.
The equipment must be used only by medical personnel that have a specific minimum qualification in
the following areas:
- Cardio-Pulmonary Resuscitation (CPR)
- Use of a Defibrillator/Monitor according to the recommendations of the American Heart
Association - AHA or the European Resuscitation Council- ERC
- Use of the REANIBEX 300
WARNING
DANGEROUS ELECTRIC SHOCK HAZARD
• The defibrillator can deliver up to 360 Joules of energy during shock delivery. When the shock is being
discharged to the patient, do not touch the patient or the defibrillation electrodes.
• During defibrillation, make sure that different parts of the patient’s body do not come into contact (bare
skin on the head and limbs) with conducting fluids such as gel, blood or saline solution or with metal
objects such as the stretcher. These can cause undesirable branching of the defibrillation current.
WARNING
DANGEROUS ELECTRICAL SHOCK HAZARD
• Keep feet and hands away from the edge of the electrodes.
• During shock delivery, never touch the patient or any equipment connected to the patient (including
the bed or stretcher).
WARNING
• The air cavities formed between the defibrillation electrode pads and the skin of the patient can cause
burns during defibrillation. Ensure that the defibrillation electrode pads are perfectly adhered to the
patient’s skin. Once adhered, if the position of the electrodes needs to be changed, remove the
electrode pads and replace them with new ones.
• Do not allow the defibrillation electrodes to touch each other or to touch any conducting material
during defibrillation. This contact can generate an electrical arc and cause burns on the patient’s skin,
which could, in turn, divert the current away from the heart.

DIH 0300 B – USER GUIDE REANIBEX 300 5
1 INTRODUCTION
WARNING
• Carefully follow the instructions indicated on the labels of the defibrillation and the monitoring
electrode pads.
• The defibrillation and monitoring electrode pads must be used before the expiry date indicated on their
labels. If the electrode pads are dried out or damaged, they can generate electrical arcs and burns
during their use.
• Do not open the defibrillation electrode pad packaging until just prior to use.
• Do not reuse the defibrillation or monitoring electrode pads. Dispose of all defibrillation or monitoring
electrode pads after use.
WARNING
• Keep careful watch over the patient during defibrillation. A delay in delivering the shock can involve a
spontaneous change from a rhythm analysed as shockable to a rhythm that is not shockable, giving
rise to inadequate shock delivery.
ATTENTION
POSSIBLE DAMAGE TO THE EQUIPMENT. Before using the defibrillator, disconnect the patient from
all the equipments that are not protected against defibrillation.
WARNING
POSSIBLE ELECTRICAL INTERFERENCE
• The presence of radio frequency (RF) sources near the REANIBEX 300 can cause incorrect operation
of the equipment. The electromagnetic compatibility of adjacent equipment must be verified before
using the REANIBEX 300.
• Avoid using the REANIBEX 300 placed next to or on other equipment. If the equipment must be used
next to or on other equipment, make sure that the equipment works properly before using it on a
patient.
• The REANIBEX 300 is intended to be used exclusively by medical personnel. The equipment can
cause radio interferences or interfere with the operation of adjacent equipment. It may be necessary to
mitigate these effects by reorienting or moving the REANIBEX 300 equipment or shielding the location.
• The use of cables, electrodes or accessories not specified in this manual for use with the REANIBEX
300 can give rise to an increase in emissions or lower immunity versus electromagnetic or radio
interferences. These interferences can affect operation of the defibrillator or of equipment in the
immediate surroundings.
• The REANIBEX 300 must be installed and started up according to the information dealing with
Electromagnetic Compatibility (EMC) in Section “A.6 - Electromagnetic Compatibility Guide”.
WARNING
• The REANIBEX 300 and its accessories may be sensitive to interferences from other sources of
emissions.
ATTENTION
RESTRICTIONS FOR USE. ECG and monitored parameter waveform artefacts caused by
electromagnetic interference should be evaluated by a physician or staff authorised by a physician to
determine whether they could adversely affect patient diagnosis or treatment.

DIH 0300 B – USER GUIDE REANIBEX 300 6
1 INTRODUCTION
ATTENTION
POSSIBLE EQUIPMENT MALFUNCTION
• The use of cables, electrodes or batteries from other manufacturers may affect proper operation of the
equipment and invalidate the safety certification. Use only the accessories specified in this GUIDE.
• Using the REANIBEX 300 or its accessories in environmental conditions other than those specified
in this manual may affect proper operation of the equipment or the accessories. Before using the
REANIBEX 300, make sure the equipment is stabilised at the operating temperature range.
WARNING
POSSIBLE EQUIPMENT MALFUNCTION. Changing the configuration of the equipment’s factory
default values will affect the operation of the equipment. Changes to the default configuration must be
performed only by authorised personnel.
PRECAUTION
POSSIBLE DAMAGE TO THE EQUIPMENT
• Handle the patient cables and the ECG monitoring equipment carefully when using the equipment
with high frequency surgical equipment.
• The equipment can be damaged by mechanical or physical maltreatment, such as immersion in water
or falls over 0.75 m.
• The components of the equipment can undergo damage if it is placed near sources of vibration.
HAZARD
FIRE OR ELECTRICAL SHOCK HAZARD: Make sure that the accessories and all the components are
properly connected. Components or accessories that are not properly connected can cause fire or
electrical shock.
PRECAUTION
The REANIBEX 300 is intended for use in the presence of high frequency surgical equipment. After the
interferences caused by the electric scalpel, the equipment returns to its previous operating mode in 10
seconds, without losing any of the data stored. Accuracy in the measurements may be affected
temporarily during surgery with electrical equipment or defibrillation. This will not affect the safety of the
patient or the equipment. Please refer to the Instructions for Use of the electric scalpel to minimise risk
of burns in the event of a defect in the equipment.
WARNING
The REANIBEX 300 does not have the capacity to reject the pulses of internal pacemakers in all cases.
The equipment may detect pulses from internal pacemakers as QRS complexes and therefore indicate
an incorrect heart rate. Therefore, the heart rate indicated by the equipment for patients with internal
pacemakers should not be trusted.
Patients with internal pacemakers must be carefully monitored. See the “Internal pacemaker pulse
rejection” section in the Appendix of this manual. This section indicates the capacity of the equipment to
reject internal pacemaker pulses.
WARNING
The REANIBEX 300 has been designed for the treatment of cardiac arrest in adult and paediatric
patients. To apply the therapy, the REANIBEX 300 must be used with the specific electrodes indicated