Arjo HUNTLEIGH Sonicaid Team3 User manual

FTS-3 Fetal Telemetry System
(Wireless Transducer System)
INSTRUCTIONS FOR USE
Sonicaid®Team3
777866-2 06/2022

2
Instructions For Use
EN
About this Manual
P/N: 777866
Version 2
Release Date: June 2022
© Copyright EDAN INSTRUMENTS, INC. 2020. All rights reserved.
About this Manual
This manual will help you understand the operation and maintenance of the product
better. It is reminded that the product shall be used strictly complying with this manual.
User’s operation failing to comply with this manual may result in malfunction or
accident for which the manufacturer can not be held liable.
The manufacturer owns the copyrights of this manual. Without prior written consent
of the manufacturer, any materials contained in this manual shall not be photocopied,
reproduced or translated into other languages.
Materials protected by the copyright law, including but not limited to condential
information such as technical information and patent information are contained in this
manual, the user shall not disclose such information to any irrelevant third party.
The user shall understand that nothing in this manual grants him, expressly or implicitly,
any right or license to use any of the intellectual properties of the manufacturer.
The manufacturer holds the rights to modify, update, and ultimately explain this
manual.
Responsibility of the Manufacturer
The manufacturer only considers itself responsible for any e󰀨ect on safety, reliability
and performance of the equipment if:
Assembly operations, extensions, re-adjustments, modications or repairs are carried
out by persons authorised by the manufacturer.
The electrical installation of the relevant room complies with national standards, and
The instrument is used in accordance with the instructions for use.

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Instructions For Use
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Terms Used in this Manual
This guide is designed to give key concepts on safety precautions.
WARNING
A WARNING label advises against certain actions or situations that
could result in personal injury or death
CAUTION
A CAUTION label advises against actions or situations that could damage
equipment, produce inaccurate data, or invalidate a procedure.
NOTE
A NOTE provides useful information regarding a function or a procedure.
Regulatory Approval Remarks
MECG and DECG function ARE NOT available in the USA and Canada at the time of
release of this user manual. Consult your local representatives for the availability of the
functions.

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Instructions For Use
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Contents
1. Safety Guide ........................................................................................6
1.1 Intended Use/Indications for Use......................................................... 6
1.2 Instruction for Safe Operation.............................................................. 6
1.3 Ultrasound Safety Guide....................................................................... 7
1.4 Safety Precautions................................................................................. 8
1.4.1 Warnings ................................................................................................................ 8
1.4.2 Cautions ................................................................................................................ 13
1.5 DenitionsandSymbols....................................................................... 15
2. Introducing the FTS-3 Fetal Telemetry System ................................17
2.1 Brief Introduction................................................................................... 17
2.1.1 Base Station........................................................................................................... 18
2.1.2 The Transducers .................................................................................................... 21
2.1.3 Accessories............................................................................................................ 22
2.2 Installation Guide .................................................................................. 23
2.2.1 Opening the Package and Checking...................................................................... 23
2.2.2 Installing the Battery............................................................................................... 23
2.2.3 Installing the System .............................................................................................. 25
2.2.4 Connecting the Power Cable..................................................................................25
2.2.5 Conguration.......................................................................................................... 25
2.2.6 Connecting to the Monitor ...................................................................................... 26
2.2.7 Adjusting the Working Channel.............................................................................. 26
2.3 Basic Operation ..................................................................................... 26
2.3.1 Charging the Transducers...................................................................................... 26
2.3.2 Charge the Battery ................................................................................................. 26
2.3.3 General Application ................................................................................................ 28
2.3.4 Relocation of the Transducers................................................................................ 29
2.3.5 Ambulatory Monitoring ........................................................................................... 30
2.3.6 Underwater Monitoring........................................................................................... 31
2.3.7 Basic Function Test ................................................................................................ 31
2.3.8 Performance Test ................................................................................................... 32
2.4 EndingMonitoring/SwitchingO󰀨 ....................................................... 33
3. Maintenance and Cleaning ................................................................34
3.1 Maintenance ........................................................................................... 34
3.1.1 Maintaining Inspection............................................................................................ 34
3.1.2 Base Station Maintenance ..................................................................................... 35
3.1.3 Transducer Maintenance........................................................................................ 35
3.1.4 Battery Maintenance ............................................................................................. 35
3.2 Cleaning and Disinfecting..................................................................... 36
3.2.1 Cleaning the Base Station...................................................................................... 37
3.2.2 Cleaning the Transducers and Leads..................................................................... 37
3.3 Sterilising................................................................................................ 38
3.4 Before Use.............................................................................................. 38
4. Warranty & Service..............................................................................39
5. Manufacturers Information.................................................................39

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Appendix1ProductSpecications .......................................................40
A1.1EnvironmentalSpecications............................................................... 40
A1.2PhysicalSpecications .......................................................................... 40
A1.3PerformanceSpecications................................................................... 41
A1.4 Rechargeable Lithium-ion Battery ........................................................ 43
A1.5 Low Output Summary Table................................................................... 44
Appendix 2 Troubleshooting .................................................................45
Appendix 3 Ultrasound Intensity and Safety .........................................46
A3.1 Ultrasound in Medicine........................................................................... 46
A3.2 Ultrasound Safety and the ALARA Principle ........................................ 46
A3.3 Explanation of MI/TI ................................................................................ 46
A3.4 Prudent Use Statement........................................................................... 48
A3.5 References for Acoustic Output and Safety ......................................... 48
A3.6 Transducer Acoustic Output Parameters List...................................... 48
A3.6.1 Test of Wireless Transducer (FTS-3)........................................................................ 48
Appendix 4 Abbreviations ....................................................................51
Appendix 5 Ordering Information ...........................................................52
Appendix 6 EMC Information ..................................................................53
A6.1 Electromagnetic Emissions ................................................................... 53
A6.2 Recommended Separation Distances................................................... 53
A6.3 Electromagnetic Immunity ..................................................................... 54
Appendix 7 Limitations of Ultrasonic Monitoring ...............................57
A7.1 How Does Ultrasound Work................................................................... 57
A7.2 Artifacts in Fetal Heart Monitoring ........................................................ 57

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Instructions For Use
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1. Safety Guide
Caution: Federal (U.S.) Law restricts this device to sale by or on the order of a
physician.
NOTE: In order to ensure the operator and patient’s safety, read through this
chapter before using this system.
NOTE: Thisusermanualiswrittentocoverthemaximumconguration.
Therefore, your model may not have some of the parameters and functions
described, depending on what you have ordered.
1.1 Intended Use/Indications for Use
The FTS-3 wireless telemetry system is a wireless system that is compatible with
fetal & maternal monitors. It is intended for invasive or noninvasive monitoring
of fetal/maternal physiological parameters, including fetal heart rate (FHR),
fetal movement (FM), uterine activity , direct ECG (DECG) and maternal ECG
(MECG) for pregnant women >28 weeks gestation. It is intended for monitoring
inabathorshowerandonlybytrainedandqualiedpersonnelinantepartum
examination rooms, labour and delivery rooms.
1.2 Instruction for Safe Operation
NOTE: In this manual, System refers to FTS-3
• The system is designed to comply with the international safety requirements IEC/
EN 60601-1 for medical electrical equipment. It is class I equipment.
• The system operates within specications at ambient temperatures between +5
ºC (+41 ºF) and +40 ºC (+104 ºF). Ambient temperatures that exceed these limits
could a󰀨ect the accuracy of the instrument and cause damage to the modules and
circuits. Allow at least 2 inches (5 cm) clearance around the instrument for proper
air circulation
• You must check that the equipment, cables and transducers do not have visible
evidence of damage that may a󰀨ect patient safety or monitoring capability before
use. If damage is evident, replacement is recommended before use.
• The system must be serviced only by authorised and qualied personnel. The
manufacturer does not accept responsibility for safety compliance, reliability and
performance if modications or repairs are carried out by unauthorised personnel.
Identical replacement parts must be used.
• The typical operator's position is in front of the system. Please position the device in
a location where the operator can easily access the operating controls.

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Instructions For Use
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• The protective degree against electric shock of the patient connections is :
Ultrasound (FHR1, FHR2)
External TOCO
Type BF
Direct Electrocardiography (DECG) Type CF
Maternal Electrocardiography (MECG) Type CF with
debrillation protection
The monitor described in this user manual is not protected against:
a) The e󰀨ects of high frequency currents
b) The interference of electrosurgery equipment
1.3 Ultrasound Safety Guide
Fetal Use
The monitor is designed for continuous fetal heart rate monitoring during pregnancy
and labour. Clinical interpretation of fetal heart rate traces can diagnose fetal and/or
maternal problems and complications.
Instructions for Use in Minimizing Patient Exposure
The acoustic output of the monitor is internally controlled and can not be varied by the
operator in the course of the examination. The duration of exposure is, however, fully
under the control of the operator. Expertise in the examination techniques described in
the User Manual will facilitate obtaining the maximum amount of diagnostic information
with the minimum amount of exposure. The exercising of clinical judgment in the
monitoring of low risk patients will avoid unnecessary insonation.

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Instructions For Use
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1.4 Safety Precautions
WARNING and CAUTION messages must be observed. To avoid the
possibility of injury, observe the following precautions during the
operation of the instrument.
1.4.1 Warnings
For using safely:
FTS-3isprovidedfortheuseofqualiedphysiciansorpersonnel
professionally trained.
FTS-3 is not intended for use in intensive care units (ICU), operating
rooms or for home use
Nomodicationofthissystemisallowed.
Do not switch on FTS-3 until all cables have been properly connected
andveried.
EXPLOSIONHAZARD-DonotuseFTS-3inthepresenceofammable
anesthetics or other materials.
SHOCK HAZARD - The power receptacle must be a three-wire grounded
outlet.Nevertrytoadaptthethree-prongplugtotatwo-slotoutlet.
A hospital grade outlet is required. If the outlet has only two slots,
make sure that it is replaced with a three-slot grounded outlet before
attempting to operate FTS-3.
The protective earth conductor is required for EMC purposes. It has no
protective function against electric shock. Double and/or reinforced
insulation protects this device against electric shock
Multipleportablesocket-outletsshallnotbeplacedontheoor.
Additional multiple socket-outlet or extension cord must not be
connected to the system.
The multiple portable socket-outlet provided with the system shall
be only used for supplying power to equipment which is intended to
form part of the system. If an electrical device that does not belong to
the system is plugged into the socket, the total power may exceed the
maximum load of the separating transformer causing high temperature
andre.Enclosureleakagecurrentwithinthesystemmayexceedthe
standard limit, which may lead to an electrical risk

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Instructions For Use
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SHOCK HAZARD - Do not attempt to connect or disconnect a power
cord with wet hands. Make certain that your hands are clean and dry
before touching a power cord.
SHOCK HAZARD-To avoid the risk of electric shock, this equipment
must only be connected to a mains supply with protective earth.
Do not touch accessible parts of non-medical electrical equipment and
the patient simultaneously
Do not touch the signal input or output connector and the patient
simultaneously.
Equipment connected to the analog and digital interfaces must be
certiedaccordingtotherespectiveIEC/ENstandards(e.g.IEC/EN
60950 for data processing equipment and IEC/EN 60601-1 for medical
equipment).Furthermoreallcongurationsshallcomplywiththevalid
version of the system standard IEC/EN 60601-1. Anybody who connects
additional equipment to the signal input connector or signal output
connectortocongureamedicalsystemmustensurethatthesystem
complies with the requirements of the valid version of the system
standard IEC/EN 60601-1. If in doubt, consult our technical service
department or your local distributor
Connecting any accessory (such as external printer) or other device
(such as the computer) to this system makes a medical system. In that
case, additional safety measures should be taken during installation of
the system, and the system shall provide:
a) Within the patient environment, a level of safety comparable to
that provided by medical electrical equipment complying with
IEC/EN 60601-1, and
b) Outside the patient environment, the level of safety appropriate
for non-medical electrical equipment complying with other IEC
or ISO safety standards
Usingaccessoriesotherthanthosespeciedbythemanufacturer
may result in increased electromagnetic emissions or decreased
electromagnetic immunity of the device.
The device should not be used adjacent to or stacked with other
equipment and that if adjacent or stacked use is necessary, the device
shouldbeobservedtoverifynormaloperationinthecongurationin
which it will be used.
All the accessories connected to system must be installed outside the
patient vicinity, if they do not meet the requirement of IEC/EN 60601-1.
Do not exceed the maximum permitted load when using multiple
portable socket-outlets to supply the system

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Instructions For Use
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SHOCK HAZARD – Do not connect non-medical electrical equipment
which has been supplied as a part of the system, directly to the wall
outlet when the non-medical equipment is intended to be supplied by a
multiple portable socket-outlet with an isolation transformer. If multiple
instruments are connected to a patient, the sum of the leakage currents
may exceed the limits given in the IEC/EN 60601-1 and may pose a
safety hazard. Consult your service personnel.
SHOCK HAZARD - Do not connect electrical equipment which has not
been supplied as a part of the system, to the multiple portable socket-
outlet supplying the system.
Do not connect any equipment or accessories that are not approved by
the manufacturer or that are not IEC 60601-1 approved to FTS-3. The
operation or use of non-approved equipment or accessories with FTS-
3 is not tested or supported, and system operation and safety are not
guaranteed.
Do not apply this system and other ultrasonic equipment simultaneously
on a same patient, in case of a possible hazard caused by leakage
current superposition. Do not apply this system simultaneously with
other PATIENT-connected equipment, such as, a cardiac pacemaker or
other electrical stimulators, on the same patient.
Do not place the TOCO transducer on oedematous or fragile tissue;
change the measuring site after half an hour
FTS-3 must only be used on one patient at a time.
SHOCK HAZARD - Do not remove the top panel cover during operation
or while power is connected.
Equipment and devices that connect to FTS-3 should form an
equipotentialbodytoensuree󰀨ectivegrounding.
Nomodicationofthisequipmentisallowedwithoutauthorizationofthe
manufacturer.Ifthisequipmentismodied,appropriateinspectionand
testing must be conducted to ensure continued safe operation.
Only connect accessories supplied or recommended by the
manufacturer to the device
FTS-3 should be operated by a trained healthcare professional.
Do not apply FTS-3 during electro-surgery or MRI; otherwise it might
result in harming the patient or the operator
Any non-medical equipment (such as the external printer) is not allowed
to be used within the patient vicinity (1.5m/6ft.).

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Makesurethatthepoweristurnedo󰀨andthepowercordis
disconnected from the AC socket before connecting or disconnecting
equipment. Otherwise, the patient or operator may receive electrical
shock or other injury.
Parts and accessories used must meet the requirements of the
applicable IEC 601 series safety standards, and/or the system
congurationmustmeettherequirementsoftheIEC60601-1medical
electrical systems standard.
Never reuse disposable transducers, sensors, accessories, and so forth
that are intended for single use, or single patient use only. Reuse may
compromise device functionality and system performance, and cause a
potential hazard.
Do not use a damaged transducer or one with exposed electrical
contacts.
Do not service or maintain FTS-3 or any accessory whilst in use with the
patient.
AssemblyofFTS-3andmodicationsduringactualservicelifeshallbe
evaluated based on the requirements of IEC60601-1.
The disposable ECG electrode must not be reused and must not be used
if the packaging is damaged.
The instrument is precise. Therefore, to avoid instrument damage, do
not operate the instrument violently, and avoid falling and impacting
during use.
Battery Use:
Before using the rechargeable lithium-ion battery (hereinafter called
battery), be sure to read the user manual and safety precautions
thoroughly.
Use the battery only in FTS-3.
Do not reverse the battery pole or it will cause explosion.
Do not unplug the battery when monitoring.
Donotheatorthrowthebatteryintoare
Donotuseorleavethebatteryclosetoareorotherplaceswhere
temperatures may be above +40 ºC (+104 ºF).

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Do not immerse, throw or wet the battery in water/ seawater.
Do not destroy the battery: Do not pierce battery with a sharp object
such as a needle. Do not hit with a hammer, step on or throw or drop to
cause strong shock. Do not disassemble or modify the battery.
Do not use the battery if it has been dropped or knocked against a hard
surface, or if it is visibly damaged.
Keep batteries out of the reach of children.
Do not short-circuit the battery by connecting the battery cable
connector or battery socket with metal objects or solder
If a liquid leak from the battery spills onto your skin or clothes, wash
well with fresh water immediately.
If a liquid leak from the battery gets into the eyes, do not rub the eyes.
Wash them well with clean water and see a doctor immediately.
Keepthebatteryawayfromreimmediatelywhenleakageorfoulodor
is detected.
Stop using the battery if abnormal heat, odor, discoloration, deformation
or abnormal condition is detected during use, charging, or storage.
Keep it away from FTS-3.
Remove the battery and store it at a cool and dry environment if FTS-3 is
not used for a long time.
Unplug FTS-3 before installing and removing the battery.
Do not connect the battery directly to an electric outlet or cigarette
lighter charger.
Batteries have a life cycle. If the battery operating time becomes much
shorter than usual, the battery life is at an end. Replace the battery
withanewoneofthesamespecicationastheoneprovidedor
recommended by the manufacturer.
When the battery is aged, either after 3 years from manufacturing date
or after 300 charge-discharge cycles, it is recommended to replace the
battery. If the battery is stored alone and not used for a long time, we
recommend that the battery should be charged at least once every 6
months to prevent overdischarge.

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If the battery is stored inside FTS-3 for a long time without AC power
connection, it will discharge over time and the battery indicator for
"remaining capacity" will become less accurate.
High internal temperature may prevent the battery from charging. Keep
FTS-3 at room temperature and move it away from heat sources or out of
direct sunlight. The battery will resume charging when the temperature
is within range again
Only the battery supplied or recommended by the manufacturer can be
used.Useofadi󰀨erentbatterymaypresentariskofreorexplosion.
Please arrange a function test periodically for the system.
Do not move the system when it is powered on and do not soak it in any
liquid.
Please check the transducer, cable and base station periodically. If the
transducers are damaged, do not use them.
The battery in the wireless transducer should be replaced by service
personnel authorised by the manufacturer.
If the transducer has been dropped or knocked, please check whether
the cover is airproof or damaged. If you have any doubt, please contact
the manufacturer or local agent.
If the battery is removed from the base station and not used for a long
time, we recommend that the battery should be charged at least once
every 6 months to prevent over discharge.
1.4.2 Cautions
The device is designed for continuous operation. Avoid liquid splashing on the
device.
Servicing should be performed only by Huntleigh Healthcare Ltd or their
appointedserviceagent.Ifyouhavedi󰀩cultyobtainingserviceforFTS-3,
contact Huntleigh Healthcare Ltd.
Keep the environment clean. Avoid vibration. Keep it far from corrosive
medicine, dusty areas, high-temperature and humid environments.
Do not operate the unit if it is damp or wet because of condensation or
spills. Avoid using the equipment immediately after moving it from a cold
environment to a warm, humid location.
Do not sterilize FTS-3 or any accessory with autoclave or gas.

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Switcho󰀨thesystempowerbeforecleaning.Cleaningconsistsofremovingall
dust from the exterior surface of the equipment with a soft brush or cloth.
Only the sensor and cable of US/TOCO transducers are watertight. Pay
attention not let any liquid enter the transducer plug.
The materials with which the patient or any other person can come into contact
conform to the standard of EN ISO 10993-1.
Electromagnetic Interference - Ensure that the environment in which FTS-3 is
installed is not subject to any source of strong electromagnetic interference,
such as CT, radio transmitters, mobile phone base stations, etc. Even though
other devices are in accordance with national standard radiation requirements,
FTS-3maysu󰀨erinterference.
Electromagnetic Interference - Do not use in close proximity to mobile phones.
Electromagnetic Interference - Fetal parameters, especially ultrasound and
ECG, are sensitive measurements involving small signals, and the monitoring
equipmentcontainsverysensitivehighgainfront-endampliers.Immunity
levelsforradiatedRFelectromagneticeldsandconducteddisturbances
inducedbyRFeldsaresubjecttotechnologicallimitations.Toensurethat
externalelectromagneticeldsdonotcauseerroneousmeasurements,itis
recommended to avoid the use of electrically radiating equipment in close
proximity to these measurements.
Electromagnetic Interference - FTS-3 should not be used adjacent to or
stacked with other equipment, refer to section A6.2 Recommended Separation
Distances
Electromagnetic interference is not unique to this system but is characteristic
of fetal patient monitoring equipment in use today. This performance is due
toverysensitivehighgainfront-endampliersrequiredtoprocessthesmall
physiological signals from the patient. Among the various monitoring systems
already in clinical use, interference from electromagnetic sources is rarely a
problem
The medical electrical equipment needs to be installed and put into service
according to Appendix 6 EMC Information.
PortableandmobileRFcommunicationsequipmentcana󰀨ectmedical
electrical equipment, refer to section A6.2 Recommended Separation
Distances.
If the terminals of the battery become dirty, wipe with a dry cloth before using
the battery
Accessories and consumables are subject to the WEEE (Waste Electrical and
Electronic Equipment) regulations and should be disposed of responsibly in
accordance with local procedures.

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The wireless transducers are IPX8 waterproof, but the base station should be
kept non-soaked and non-condensing. The system may be condensing during
transportation in high humidity or low temperature.
Theuseofaccessoriesandcablesotherthanthosespeciedmayresultin
increased electromagnetic emissions or decreased electromagnetic immunity
of the system.
This equipment generates, uses and radiates radio-frequency energy, and if it
is not installed and used in accordance with its accompanying documentation,
it may cause interference to radio communications.
When the battery is charged, used or stored, keep it away from objects or
materials with static electric charges.
The recommended charging temperature for the battery is between 0° ~ +40°
(+32 ºF ~ +104 ºF). Please do not exceed the temperature range.
1.5 DenitionsandSymbols
Rx
Only
Federal (U.S.) Law restricts this device to sale by or on the order of
a physician
IPX1 Protected against vertically falling water drops
IPX8 Protected against the e󰀨ects of continuous immersion in water
This product, including its accessories and consumables, is subject to the
WEEE (Waste Electrical and Electronic Equipment) regulations and should
be disposed of responsibly in accordance with local procedures.
AUTHORISED REPRESENTATIVE IN THE EUROPEAN COMMUNITY
CE Mark Date of Manufacture
YYYY-MM
Manufacturer Applied parts type BF
Applied parts type CF Applied parts type CF with
debrillator protection
Follow Instructions for Use Refer to Instructions for Use
General Warning or
Caution.
Caution, consult Accompanying
Documents
SN Serial Number P/N Part Number

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Instructions For Use
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Fragile , handle with care General symbol for recovery/
recyclable
Keep Dry This way up
HANDLE WITH CARE DO NOT STEP ON
STACKING LIMIT BY
NUMBER Channel Adjustment
Non-ionizing
electromagnetic radiation USB Connection (Reserved)
Ethernet Port (Reserved) Wireless Transducer Working
Indicator
Importer Distributor

17
Instructions For Use
EN
2. Introducing the FTS-3 Fetal Telemetry
System
2.1 Brief Introduction
FTS-3 Fetal Telemetry System (hereinafter called FTS-3) provides monitoring for FHR,
DECG MHR, AFM and TOCO for pregnant women. When connected to a compatible
fetal monitor, FTS-3 provides wireless patient monitoring in the antepartum period and
during labor and delivery.
It is intended to be used only by trained and qualied personnel in antepartum
examination rooms, labor and delivery rooms. It is not intended for use in intensive
care units, operating rooms or for home use.
FTS-3 is used with fetal/maternal monitor and connects to the monitor by an interface
cable supplied with the product. The wireless transducers monitor the FHR, and TOCO
parameters up to 110 Metres line of sight, and then the base station transfers the data
to the monitor via the interface cable. The monitor can display, alarm, print or review
the parameters.
FTS-3 consists of the wireless US transducers (US-T transducers), the wireless TOCO
transducer (TOCO-T transducer or TOCO-E transducer) and the base station.
The wireless signal is transmitted in the Industrial Scientic Medical Band (ISM)
according to the local regulations. The transmission range depends on where the
system is used. It is recommended to use in hospital for better transmission. The
transmission range is shorter in water than that in the air.
Battery Check

18
Instructions For Use
EN
2.1.1 Base Station
Top Panel
1
2
3
4
6
5
Item Description
1Docking Slot Locate and charge the transducer.
2Power Indicator When you turn the power supply, the indicator is on.
3AC Indicator When AC power is supplied, the indicator is on.
4Battery Indicator When the base station battery is charging, the indicator
is on. When the battery level is low, it is ashing.
5Wireless Connection
Indicator
When the transducer connects to the base station
successfully, the green light is on.
6Charging Point When you place the transducer in the docking slot, you
can charge the transducer by these contacts.
WARNING.
Thechargingcontactsarespecicallyforchargingthetransducers.
Do not touch the charging point and the patient at the same time.

19
Instructions For Use
EN
Rear Panel
1 2 3
5
6
4
Item Description
1AC Outlet Mains supply
2Cooling Fan Air ventilation
3Channel Adjustment Button Adjust the base station channel
4USB port Reserved
5Ethernet port Reserved
6Communication Socket Fetal monitor interface
Right Panel
1
Item Description
1Power Switch Turn the base station on or o󰀨.
CAUTION. This system is a normal medical device.
Donotswitchtheunitonando󰀨repeatedlyasdamagecouldoccur.
CAUTION.Donotswitchtheunito󰀨whenthetransducersareinuse.

20
Instructions For Use
EN
Base Panel
1
Item Description
1Battery Compartment Battery location