Who Should Read This Guide1
What to Do Next1
Repair Strategy2
Pre-Installation Considerations2
Warnings, Cautions and Important Information2
Symbols on the System3
Patient Safety4
Protective Earth4
Environment5
General Description5
Mounting Solutions5
Applying the Velcro Fixing Tape6
Antenna Extension Mounting Kit7
Mounting on Philips Carts7
Mounting on Wooden Carts and Other Flat Surfaces7
Considerations for Choice of Configuration8
Frequency Bands8
Normal Delivery Configuration8
When is a Different Configuration Needed?8
When the Area of Reach is Not Sufficient9
When the Normal Delivery Configuration is Unsuitable9
Frequency Planning9
Setting Expectations9
Antenna System Guidelines10
2 Theory of Operation11
Receiver Board12
Human Interface Board12
Power Supply12
Slot Control and Monitor Interface Board Hardware12
Transducer Hardware Overview13
Fetal Monitor Interface15
Service Interface16
Compatible Fetal Monitors 17
4 Disassembly/Reassembly19
Introduction19
Removing the Top Cover Assembly 20
Replacing the Top Cover Assembly 21
Changing Fuses22
Changing the Power Supply/Metal Chassis Assembly25
5 Spare Parts31
Exchange Parts31
Non-Exchange Parts32
Supplies and Accessories32
Antenna and Base Station Part Numbers By Country33
6 Preventive Maintenance and Safety35
Care and Cleaning35
Recommended Frequency of Testing35
Performance Assurance Tests36
Self Test36
Parameter Test36
Safety Tests37
Safety Test Procedures38
When to Perform Safety Tests38
How to Carry Out the Test Blocks38
Description of Applicable Safety Tests40
S(1): Protective Earth Test40
S(2): Enclosure Leakage Current Test
- Normal Condition (NC)
S(3): Enclosure Leakage Current Test
- Single Fault Condition (SFC) Open Supply
S(4): Enclosure Leakage Current
- SFC Open Earth (Ground)
Instrument Safety Test41
System Test42
Regular Preventive Maintenance42
Mechanical Inspection42
Visual Check42
Toco Ventilation/Belt Button42
40
41
41
iv
Testing the Ventilation Membrane42
Battery Check43
Starting the Battery Check44
Stopping the Battery Test44
Stages of the Battery Check44
Reading Battery Check Data Using the Service Support Tool45
Battery Exchange45
7 Troubleshooting47
System is Completely Inoperative47
Common Problems47
Troubleshooting a Cordless System: an Overview49
System Reset49
Checking Contacts49
Checking the Fetal Monitor50
RF Problems50
Carrier to Noise Ratio50
Gathering Data50
Observe System Performance51
Question the User51
Area of Reach51
Range Definition52
Using the Base Station52
Using the Service Support Tool52
RF Interference 53
One-Channel or Narrowband Interference53
Broadband Interference53
Guidelines for Channel/Frequency Configuration54
Scanning the Available Frequency Range54
Excluding Frequencies 54
Base Station with Fixed Frequency54
Transducers with Fixed Frequency55
Transducers for Japan55
Testing Transducers56
Ultrasound Transducer Electrical Check 56
TOCO Transducer Electrical Check 57
ECG Transducer Electrical Check58
In DECG Mode58
In MECG Mode59
Troubleshooting the Top Cover60
Function Buttons60
Display/Window 60
LEDs60
Magnets61
v
Factory Information Code Log 61
8 Changing Settings63
Configuration Settings63
Key Click, Transducer Insertion/Take Out Confirmation Volume63
Acoustical Alarm Default64
Function Settings65
Bed Label Appearance65
Enabling/Disabling Fixed Frequency65
Selecting the Channel Frequency Spacing66
Action Settings67
Displaying the Software Revision67
Clearing the Factory Information Code (FIC) Log 67
9 Upgrades69
10 Specifications71
General71
Base Station71
Tr a n s d u c e r s72
Frequency Bands73
Frontends73
Cables74
A Removing and Replacing the Transducer Battery75
B Removing and Replacing the Transducer Belt Button77
C Avalon CTS Frequency Table79
vi
1
1General Information
This guide tells you how to service and repair the base station (M2720A) and transducers (M2725A,
M2726A, and M2727A) of the Avalon CTS Cordless Fetal Transducer System. It describes the system
hardware and software, tells you how to diagnose operating and servicing problems, and how to test the
system.
As this system is intended to be installed by the customer, refer to the Instructions for Use for details of how to
install the system.
The Avalon CTS Cordless Fetal Monitoring System Service Guide supplements the maintenance and
troubleshooting procedures, carried out by the operator, that are described in the Instructions for Use. Refer to
the Instructions for Use for maintenance and troubleshooting procedures that may be performed during
normal operation.
Only qualified service personnel should attempt to disassemble the base station, remove or replace any
internal assemblies, or replace the transducer batteries or belt buttons.
Who Should Read This Guide
This guide is for any qualified technical personnel servicing and repairing the Avalon CTS Cordless Fetal
Transducer System.
You must:
•understand English
• be familiar with standard medical equipment installation procedures
• be familiar with current conventional technical terms as used throughout this guide
What to Do Next
Familiarize yourself with the contents of this guide before attempting to service or repair the system.
1
1 General InformationRepair Strategy
Repair Strategy
The Service Support Tool software helps you to determine whether a fault is a hardware, software or RFrelated problem. Any maintenance and repair procedures beyond the level covered in the Instructions for Use are limited to:
• unit exchange for
–the base station
–the transducers
•replacement of
– the top cover assembly, including human interface board
– the power supply, including metal chassis
– two fuses in the power supply
– the transducer battery
– the transducer ventilation knob
Repair or replacement of individual components on the boards is not supported, and should never be
attempted.
For any problem related to connecting the base station to an antenna system, refer to the M2600A
Telemetry System’s Service Training and Reference Guide.
For tests that you are required to perform after repairs, refer to “When to Perform Safety Tests” on
page 38.
Pre-Installation Considerations
The Avalon CTS is intended to be customer installable under the following conditions:
• The system is an “out-of-the-box” stand-alone system.
• There are less than ten stand-alone systems in the institution.
• Connection to an antenna system is not planned.
• No other telemetry devices are used in the institution that can influence, or be influenced by, the
Avalon CTS.
• There are no other known or unknown sources of RF interference that influence the operation of the
Avalon CTS.
• There are no local regulations requiring special configuration.
If one or more of these conditions are not met, a special configuration of the Avalon CTS is needed. Refer
to “Considerations for Choice of Configuration” on page 8, and/or contact Philips Support to order the
appropriate services.
Warnings, Cautions and Important Information
WARNINGA warning alerts you to a potential serious outcome, adverse event or safety hazard. Failure to observe a
warning may result in death or serious injury to the user or patient.
2
Symbols on the System1 General Information
CAUTION
A caution alerts you to circumstances where special care is necessary for the safe and effective use of the
product. Failure to observe a caution may result in minor or moderate personal injury, damage to the
product or other property, and possibly in a remote risk of more serious injury.
In this book, graphical symbols (indicators or elements of the base station or transducer
displays) depicted in this way indicate that they are blinking.
Philips makes no warranty of any kind with regard to this material, including, but not limited to, the
implied warranties of merchantability and fitness for a particular purpose. Philips shall not be liable for
errors contained herein or for incidental or consequential damages in connection with the furnishing,
performance or use of this material.
All rights are reserved. Reproduction in whole or in part is prohibited without the prior written consent of
the copyright holder.
Symbols on the System
This attention symbol indicates that you should consult this book and the Instructions for Use, and
particularly any warning messages.
Power-On/Stand-by Switch.
Power-On/Stand-by Indicator.
Equipotential Terminal.
This symbol identifies terminals that are connected together, bringing various equipment or parts
of a system to the same potential. This is not necessarily earth potential. The value of potentials of
earth may be indicated adjacent to the symbol.
Protective Earth Terminal.
This symbol identifies the terminal for connection to an external protective earth system.
Antenna input symbol.
Service socket symbol.
This symbol appears on the device adjacent to the CE mark and defines Class 2 radio equipment
per Radio and telecommunications Terminal Equipment Directive 1995/5/EC.
3
1 General InformationPatient Safety
IPX1
IP68
Ingress Protection code according to IEC 60529. Base station is rated IP X1 (protection against
vertical water drops only).
Ingress Protection code according to IEC 60529. All transducers are rated IP 68 (protection
against dust, access to hazardous parts, and the effects of continuous immersion in water to a
depth of 0.5 meter for five hours).
Type CF equipment.
Patient Safety
The Telemetry System should only be used by, or under the direct supervision of, a licensed physician or
other health care practitioner who is trained in the use of fetal heart rate monitors and in the
interpretation of fetal heart rate traces. US federal law restricts this device to sale by, or on the order of, a
physician.
The Telemetry Receiver is a Protection Class 1 instrument.
The device complies with the following safety standards:
• EN 60601-1:1990+A1:1993+A2:1995
(IEC 60601-1:1988+ A1:1991+A2:1995)
• EN 60601-1-1:2001 (IEC 60601-1-1:2000)
• UL2601-1 2nd Ed.
• CAN/CSA C22.2 No. 601.1-M90 and No. 601.1-S1-94
• JIS T 1001-1992
• JIS T 1002-1992
• AS 3200.1.0-1998
The cordless transducers are battery operated devices, applied parts (patient connectors) are Type CF
.
Protective Earth
WARNINGCheck each time before use that the system is in perfect working order and the base station is properly
grounded.
To protect hospital personnel and the patient, the cabinet must be grounded. Accordingly, the base
station is equipped with a 3-wire power cable which grounds it to the power line ground when plugged
into an appropriate 3-wire receptacle. Do not use a 3-wire to 2-wire adapter with the base station. Any
interruption of the protective earth grounding will cause a potential shock hazard that could result in
serious personal injury.
Whenever it is likely that the protection has been impaired, the base station must be made inoperative and
be secured against any unintended operation.
The patient cable must be positioned so that it does not come into contact with any other electrical
equipment.
Before operation, make sure that the base station is free from condensation. This can form when
equipment is moved from one building to another, and is exposed to moisture and differences in
temperature.
4
Environment1 General Information
Environment
Before operation, make sure that the base station is free from condensation. This can form when
equipment is moved from one building to another, and is exposed to moisture and differences in
temperature.
Use the system in an environment which is reasonably free from vibration, dust, corrosive or explosive
gases, extremes of temperature, humidity, and so forth. It operates within specifications at ambient
temperatures between 0 and +45°C. Ambient temperatures that exceed these limits can affect the accuracy
of the system, the transmitter radio frequency transmission, and can damage the components and circuits.
The system can be stored at ambient temperatures between -20°C and +60°C.
The transducers are watertight to a depth of 1.0 meter, and comply with IEC 60529 (IP 68). The base
station is rated IP X1 according to IEC 60529.
General Description
Refer to the Instructions for Use for operating information of the base station and the transducers. It
includes descriptions of the installation and setup of the system and modes of operation.
Mounting Solutions
You can mount the Avalon CTS:
• In a standard cart drawer. The base station with docked transducers fits into Philips Carts CL, CX and
CM. Use the lower drawer, and secure the base station using the Velcro fixing tape supplied.
• On a cart shelf (for example that of the Philips Cart CP, M1326A), using either the Velcro fixing tape or
the mounting brackets supplied.
• On top of carts, desks or other flat surfaces using the mounting brackets supplied.
• In a wide variety of situations using the GCX mounting adapter for mounting the base station (order
directly from GCX, part number PH-0042-80).
• On top of Series 50 IX/XM/XMO fetal monitors using the mounting brackets supplied.
Mounting Brackets
Refer also to the fitting instructions that come with the relevant solution.
5
1 General InformationApplying the Velcro Fixing Tape
Applying the Velcro Fixing Tape
Two self-adhesive Velcro fixing tape sets are supplied, each set consisting of two halves.
1 Strip off the paper backing on one half of the Velcro set and attach to one side of the underneath of the
base station. Repeat for the other side.
2 Strip off the paper backing on the other half of the Velcro set and attach to the fixing surface so that the
two halves of the Velcro set mate up when the base station is correctly positioned.
Apply one
half of
Velcro
tape in
position
shown
Apply other half of
Velcro tape to appropriate
place on fixing surface
6
Antenna Extension Mounting Kit1 General Information
Antenna Extension Mounting Kit
If the base station is installed in a cart or other mounting solution where the standard antenna cannot be
attached directly to the base station, or does not provide sufficient transmission range, use the antenna
extension mounting kit (M1361A Option 1AA).
The kit contains:
• Antenna extension cable with BNC connectors (1.0m approx.)
• Mounting bracket, including fixings, for mounting onto Philips Carts.
The mounting bracket can also be fitted on walls, wooden carts, or other flat surfaces using fixings (not
supplied) appropriate for the surface material.
Mounting on Philips Carts
A
C
B
1 Remove the plastic cover (A).
2 Slide the fixings for the mounting bracket (C) into the groove (B) in the cart.
3 Replace the plastic cover (A) before sliding the mounting bracket fully down.
4 Slide the mounting bracket downwards in the groove (B) in the cart until the antenna holder part of the
bracket rests on the plastic cover.
5 Tighten the fixing screws to secure the mounting bracket.
Mounting on Wooden Carts and Other Flat Surfaces
7
1 General InformationConsiderations for Choice of Configuration
Considerations for Choice of Configuration
There are a number of factors that can influence how you finally configure the Avalon CTS.
Frequency Bands
Depending on the country of use, the system uses radio frequencies within one of two bands, the Wireless
Medical Telemetry Systems (WMTS) band, or the Industrial, Scientific and Medical (ISM) band. The
actual approved frequencies used depend on country-specific regulations. The following diagram gives an
example overview of the system’s frequency band configuration.
5
4
3
2
1
1 = The full (hardware) frequency range (10 MHz wide).
2 = The country-specific frequency range governed and approved by local regulatory bodies.
3 = The available frequency range: shows the real, current frequency range available within the country
range. This will differ from the country range due to:
– excluded frequency ranges
– frequency ranges already allocated to other Avalon CTS systems in the same establishment.
4 = Excluded frequency ranges (ranges occupied by other telemetry systems, or other RF interferers).
5 = Fixed frequency ranges.
Normal Delivery Configuration
The Avalon CTS is normally delivered with:
• Automatic channel search.
• A standard antenna.
Using the standard antenna, the potential operating range is up to 100 meters. The actual effective area of
reach will vary according to the geographical and physical characteristics of the building where the system
is installed, and is also influenced by the presence of other radio frequency (RF) devices or interference.
We recommend that you define effective operating range prior to putting the system into operation.
If the area of reach is adequate for the intended monitoring area, and the system’s operation is not
influenced by other RF sources, then the normal delivery configuration is sufficient.
When is a Different Configuration Needed?
This section deals with possible reasons why the normal delivery configuration may not be adequate.
8
Setting Expectations1 General Information
When the Area of Reach is Not Sufficient
If the area of reach is not sufficient using the standard antenna supplied with the system, there are a few
things to consider:
– The placement of the antenna has an effect on the operating range. If it is located inside a metal cart
or other RF-absorbing material, then place the antenna externally by using the Antenna Extension
Mounting Kit (M1361A Option 1AA) to increase the range.
– Check the orientation of the antenna. In general, the antenna provides the greatest range when it is
positioned vertically.
– If the area of reach is still insufficient, consider installing an antenna system.
When the Normal Delivery Configuration is Unsuitable
The normal delivery configuration, with free base station channel search, may be unsuitable if:
• There are other telemetry systems installed in the hospital.
• There are multiple (more than ten) stand-alone Avalon CTS systems.
• There are other sources of RF interference.
• The Avalon CTS system causes interference on other telemetry or RF systems.
• If you connect the Avalon CTS to an antenna system.
Frequency Planning
For multiple cordless/telemetry installations in the same hospital, an RF frequency plan should be
implemented. Document all frequencies or frequency ranges occupied by:
• Other telemetry systems (adult and fetal).
• Multiple Avalon CTS systems (operating on fixed frequencies). Remember that the Avalon CTS is also a
potential interference source for other RF systems.
• Other sources of RF interference (other electrical equipment, broadcasting stations, or paging systems,
for instance).
Once you have identified all the occupied frequencies or frequency ranges (for example, by using the
Service Support Tool software) you can change the system’s configuration by following the guidelines for
RF channel/frequency configuration.
• Exclude frequency ranges already occupied by other telemetry systems or that are subject to interference
from other RF sources (see page 54).
• Use fixed frequencies for the base station, possibly in conjunction with altering the channel spacing (see
page 66).
• Use fixed frequencies for the transducers (see page 55).
Setting Expectations
No matter how good a telemetry system design is, it will always experience occasional loss of radio
communications, resulting in US/Toco/ECG dropouts. A telemetry system will never be as reliable as a
hard-wired monitor that transmits its signal through a wire. If occasional loss of US/Toco/ECG
monitoring is not acceptable for certain patients, they should be connected to a hard-wired bedside
monitor.
9
1 General InformationAntenna System Guidelines
WARNINGTelemetry should not be used for primary monitoring in applications where the momentary loss of the
US/Toco/ECG signal is unacceptable.
Following are guidelines to set proper expectations of hospital staff and to improve system performance:
• Clinicians will tend to see more motion related artifact on the US/Toco/ECG measurements of
ambulatory patients than on patients that are restricted to a bed.
• Patients should be restricted to the designated coverage area. Monitoring performance will degrade if
patients go outside the radius of coverage of the receiving antenna.
• Keep the size of the antenna system as small as possible. Telemetry system performance will degrade as
the system size increases. The larger a system is, the greater the potential for receiving interfering
signals. In addition, as more devices are added to the antenna system, the noise generated by the
antenna system itself increases.
• A patient location protocol is critical to a telemetry system. If a life-threatening event occurs, the
clinician must be able to locate the patient quickly. The importance of this increases as the antenna
system size increases.
• Philips Medical Systems has no control over the RF environment in the hospital. If interference exists at
the operating frequencies, telemetry system performance will be affected. Careful selection of
frequencies for all wireless devices used within a facility (telemetry transmitters, walkie-talkies,
ambulance radios, other wireless medical devices, etc.) is important to prevent interference between
them. Frequency management is the responsibility of the hospital.
Antenna System Guidelines
The Avalon CTS (M2720A) is compatible with the dual band antenna system components as used with
the M2600A adult telemetry system. Antenna systems must be designed according to adult telemetry
system rules, and presales activities and site preparation must be done according to the existing M2600A
series antenna systems rules. These activities are not bundled into the product price and have to be
ordered separately at the PSS or HPS organization.
Additional to the M2600A antenna system design rules, the following antenna specifications apply to the
Avalon CTS:
• Only original M2600A antenna system components will be supported.
• The antenna spacing must not exceed a radius of 10m (32ft).
• Any mixture of Avalon CTS and other telemetry devices (for example, M1310A or M2600A Adult
Telemetry Transmitter/Receiver) on the same antenna system is not supported.
• Contact Philips Support regarding antenna system design.
10
2
2Theory of Operation
This chapter describes the functional operation of the system, including the base station and transducers. It
incorporates features of the mechanical design, indicating the physical relationship of the assemblies and
components.
Base Station Hardware Overview
Figure 1 Base Station Boards
The Base Station consists of four functional components:
11
2 Theory of Operation
Receiver Board
The receiver is a double superheterodyne narrowband frequency modulation (FM) receiver, with two
mixers and two intermediate frequencies (IFs). Three radio frequency (RF) signals can be received
independently with three identical receiver channels.
for frequency shift key (FSK) detection, analog-to-digital conversion of the low frequency (LF signal),
signal filtering, and radio frequency (RF) channel management.
transducers.
and each docking slot.
While charge power is on, a serial communication link is established between the base station
The digital section of the main CPU is responsible
The main CPU communicates with the
Human Interface Board
The Human Interface (HIF) board provides the user interface, and the display, indicators, keys and the
slot charging contacts are all located on this board.
Power Supply
The power supply is a wide-range input swtching unit, with an output of +48V. It is located on the chassis
assembly.
Slot Control and Monitor Interface Board Hardware
The Monitor Interface (MIF) board provides the interface to the fetal monitor as well as the
communication interface to the transducer slots. Power conversion is performed by a DC-DC converter.
The digital (active) parts of the human interface also reside on this board.
The MIF board consists of the following functional blocks:
• DC-DC Converter - the 48V DC input for the DC-DC converter comes from the primary AC-DC
converter. Since the 48V DC voltage is sufficiently stabilized, two fixed pulse width step down
transformers are used to transform the high voltage down to the required 3V, 5V and 12V (postregulated for accuracy).
The +12V supply is mainly used for battery charging and you can access this voltage at the charge
contacts. The fuse on the MIF board are not replaceable, and if it blows, the board must be replaced. If
there is a short to ground, unlimited current will blow the fuse. To avoid this, a current limiter is used
to limit the output current.
• Monitor interface - three major blocks make up the monitor interface:
– PWM Toco digital-to-analog (D/A) converter
– Two PWM wave D/A converters for FHR low frequency (LF) 1, and FHR LF 2.
– Digital status ports
• Transducer slot interface - this block is responsible for transducer detection, safety features of the
charge power switch, serial communication between base station and transducers and synchronization
clock generation for the power supply.
contacts when there is no transducer docked in a slot, charge power in each slot is only applied after a
transducer has been detected.
To ensure that there is no charge power applied to the charge
12
• Drivers for the HIF board interface - this block contains the multiplexing and driving components for
the function buttons, the display backlight and the seven-segment LEDs.
Transducer Hardware Overview2 Theory of Operation
Transducer Hardware Overview
The system has three transducer types:
•Toco
•US
•ECG
They all share the same modulation and digital processor circuitry, power supply, liquid crystal display, and
RF transmitter. The processor software is also the same for all transducers. The frontends, however, are
specific to each transducer type.
Functional Description of the RF/CPU Hardware
The RF/CPU section of the transducers is made up of the following functional blocks:
• CPU (micro controller)
•LCD
• Base Station communication
• EEPROM
•FLASH download port
• Clock generator
• Power supply and battery charger
• Modulator
• RF transmitter
Boards: M2725-66501,
M2726-66501,
M2727-66501
parameter
frontends
(see separate description)
power supply
and battery
charger
wave
frontend control
power management
base station
communication
Figure 2 Transducer Block Diagram
Base Station Communication
An active base station communicates with docked transducers to check the correct transducer type, serial
number, to program the RF frequency, to initiate test cycles, and to check the current battery status.
gain control
Modulator
CPU
(micro
controller)
FSK signal
modulation signal
(wave +FSK)
frequency control
Clock
generator
RF
transmitter
FLASH
download
port
LCD
EEPROM
13
2 Theory of OperationToco Frontend Hardware
Power Supply and Battery Charger
A Lithium-Ion (Li-Ion) battery powers the transducer. Batteries are charged whenever a transducer is
docked in an base station connected to AC power. Charge power is transferred by the spring-loaded, twopin charge contacts. Communication between the base station and the transducer processors is also done
using these contacts.
An intelligent Li-Ion charging circuit in the transducer controls the battery management. See page 72 for
battery charging times.
Modulator
The analog heart rate signals (ultrasound Doppler or fetal ECG) are pre-processed and band-limited by
filters. The signals are then fed into a programmable gain amplifier controlled by an automatic gain
control circuit and a digital FSK modulated subcarrier (1.6 kHz or 2.4 kHz) is added to the RF carrier
signal. The subcarrier is responsible for the digital transmission of the Toco data, along with safety and
status information, such as serial number, bed label, fetal movement data, battery information.
RF Transmitter
The RF transmitter block contains:
• a PLL synthesizer that divides the reference frequency down to 12.5 kHz, and can be tuned in steps of
12.5 kHz.
• a voltage controlled ocillator (VCO).
• a power amplifier (antenna driver).
Toco Frontend Hardware
Uterine activity is measured by evaluating the hardness of the mother’s abdomen with a pressure sensitive
resistor bridge (DMS element). The DMS element requires an excitation voltage and its differential
output signal is proportional to the pressure applied to the DMS element. An AC excitation voltage is
used, and the resulting AC output signal is amplified and converted to a pressure proportional DC voltage
by a synchronous rectifier followed by a low pass filter.
Ultrasound Frontend Hardware
The ultrasound frontend is a pulsed Doppler system with a 1.0 MHz ultrasound frequency, and a pulse
repetition rate of 3.2 kHz. Seven ultrasound crystals are used as transmitter and receiver.
ECG Frontend Hardware
Several parameter frontends are combined on the ECG frontend board. Currently supported parameters
are DECG and MECG.
A seven-pin ‘D-type’ socket carries all parameter related inputs and outputs. An external mode resistor,
connected to one of the pins, detects which ECG mode to set when an adapter cable is plugged in. The
M1362B ECG adapter cable, used with the M1364A patient module, is also used for the fetal scalp or
adult electrodes.
14
The Avalon CTS has two system interfaces:
• Fetal monitor interface
• Service Interface
Fetal Monitor Interface
The Fetal Monitor Interface on the base station allows digital and analog outputs to the Series 50 fetal
monitors. The interface is enhanced to support additional transducer combinations for future fetal monitors.
The following table lists the signals at each pin.
19Reserved. (Tele-Marker on the fetal monitor side.)
20Tele-FMP on (L) if FMP available.
21Tele-Fetal movement on (L).
22MECG Inop.
23Not connected.
24Ground.
25MECG Mode.
Service Interface
The service socket on the rear of the base station takes a stereo phone jack for RS232 connection to an
industry standard compatible PC installed with the Service Support Tool software. Use the interface cable
M1350-61675. The transducers must be docked in the base station for communication with the Service
Support Tool.
Signal Details
16
Figure 3 Interface cable for connecting an industry standard compatible PC to the Avalon
base station.
Compatible Fetal Monitors3 System Interfaces
Compatible Fetal Monitors
A list of compatible fetal monitors (including interfaces) is given in the following table.
Parameter
Monitor / Interface (IF)
M1350x
with M1350-66531 IF
M1350x
with M1350-66536 IF
M1351A
with M1353-66531 IF
M1351A
with M1353-66531 E IF
M1353A
with M1353-66531 IF
M1353A
with M1353-66531 E IF
Key: ! = supported; - = not supported
HR 1-HR 1!!Only one FHR is transmitted.
HR 1
HR 1---!No ECG processing. DECG mode generates
HR 1!--!Software revision A.02.00 or greater.
HR 1-HR 1-!Only one HR transmitted.
HR 1!HR 1-!Software revision A.02.00 or greater.
!
CommentsUSFMPDECG MECG Toco
HR 1!!Software revision A.04.01 or greater.
“Err 9”.
17
3 System InterfacesCompatible Fetal Monitors
18
4Disassembly/Reassembly
WARNING• Performance verification: do not place the system into operation after repair or maintenance has been
performed, until all performance tests and safety tests listed in Chapter 6 of this service manual have been
performed. Failure to perform all tests could result in erroneous parameter readings, or patient/operator
injury.
• Energized circuits are accessible with the covers open. Do not work on the base station with the covers open
and AC power connected. Only qualified service personnel should open or disassemble the base station.
• Before attempting to open or disassemble the base station, disconnect it from the AC mains supply.
CAUTIONObserve ESD (electrostatic discharge) precautions when working within the unit.
4
Introduction
Remember to store all screws and parts in a safe place for later refitting.
How to Use this Chapter
The disassembly sections detail the step-by-step procedures you use to access replaceable parts of the base
station.
All the transducers are sealed at the factory and are not repairable. Replacement transducers are supplied
complete with both battery and belt button fitted.
The Avalon base station consists of two major assemblies:
• The top cover assembly
• The chassis assembly
The top cover assembly contains the human interface (HIF) board, the keypad inlay, and the battery charge
contacts and wiring. The top cover assembly is only available as a complete assembly, and a repair to any part
of the top cover assembly is effected by replacement of the whole assembly.
The chassis assembly contains the metal chassis and power supply, the receiver board and the monitor
interface (MIF) board. The power supply always comes complete with the chassis (without boards), and a
repair to either the power supply or the chassis is effected by replacement of this chassis/power supply
assembly.
There are no boards available individually as replacement parts. In the case of a defective receiver board or
MIF board, a repair is effected by exchanging the whole base station assembly (unit exchange).
19
4 Disassembly/ReassemblyRemoving the Top Cover Assembly
All part numbers of spare parts are listed in Chapter 5.
Tools Required
CAUTIONWhen replacing the front cover, do not over-torque the screws. Excessive torque may damage the plastic
screw mountings.
You need the following tools:
•Torx-head screwdriver, size T-10
or
•Torx bit, for suitable driver, size T-10
Removing the Top Cover Assembly
6 Carefully place the base station upside down. To avoid scratches, place the unit on some cloth or other
soft surface.
Screw locations
7 Remove the six screws securing the top cover assembly to the chassis, using a T-10 Torx driver.
8 Holding both top cover and chassis assemblies together, place the base station upright again.
9 Lift the front edge of the top cover and disconnect the spade connector for the ESD ground wire from
the terminal on the metal chassis.
20
ESD ground
spade connector
Replacing the Top Cover Assembly4 Disassembly/Reassembly
Now raise the cover a little more, and disconnect the multipin connector of the ribbon cable from the
10
MIF board. Pull straight up to avoid bending the pins. The top cover assembly is now free of the chassis
assembly.
Top
cover
assembly
Chassis
assembly
Ribbon cable
connector
Replacing the Top Cover Assembly
The serial number appears initially in two places on the base station - on the rear of the top cover
assembly, and on the bottom of the metal chassis. A replacement top cover does not carry a serial
number.
1 Ensure all items are replaced in the top cover assembly.
2 Reconnect the multipin ribbon cable connector to the socket on the MIF board.
Reconnect ribbon cable connector
3 Important! Reconnect the ESD ground wire spade connector to the terminal on the chassis.
4 Place the front cover back to its normal position.
ESD ground
spade connector
21
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