M1310-9000B
Printed in Germany February 2002
Edition 1, A.00.01
Notice
Philips makes no warranty of any kind with regar d 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 con sequential damages in connection with the fu rnishing,
performance o r use of this material.
The information contained in this document is subject to change without
notice.
Philips assumes no responsibility for the use or reliability of its software on
equipment that is not furnished by Philips.
Responsibility of the Manufacturer
Philips only considers itself responsible for any effects on safety, reliability and
performance of the equipment if:
• assembly operations, extensions, re-adjustments, modifications or repairs
are carried out by persons authorized by Philips, and
• the electrical installation of the relevant room complies with national
standards, and
• the instrument is used in accordance with the Instructions for Use or User’s Guide.
Important
United States federal law restricts this device to sale by or on the order of a
physician.
This device is not intended for home use.
Warning
Failure on the part of the responsible individual hospital or institution
employing the use of this equipment to implement a satisfactory
maintenance schedule may cause und ue equipment failure and possible
health hazards.
Printing History
M1310-9000AApril 1994
M1310-9000BFebruary 2002
About this Manual
The manual is intended for personnel involved in the service and repair of the
M1310 Telemetry System.It enables you to diagnose and repair problems with the
minimum of inconvenience to the customer.
The philosophy for on-site diagnosis and repair of the M1310A Telemetry System
can be summarized as follows:
• General Repair Strategy
The recommended repair method is replacement of assemblies.
Every 12 months, you must carry out a series of preventive maintenance tasks and
performance assurance tests. Details can be found in Chapter 10, “Preventive
Maintenance, Care and Cleaning”.
• On-site repair for standard assemblies.
• Bench repair for RF-repair.
For an overview of the system, and how to set it up, please re fer to the Instructions for
Use.
Conventional current technical terms are used throughout the manual, and
familiarity with these terms is assumed.
The following conventions for cautions and warnings are used in this guide:
Note—A note calls attention to an important point in the text.
Warning
A warning calls attention to a condition or possible situation that could cause
injury to the user and/or patient.
Caution
A caution calls attention to a condition or possible situation that could damage
or destroy the product or the user’s work.
2002 Philips Medizinsysteme GmbH
All rights are reserved. Reproduction in whole or in part is prohibited without the
prior written consent of the copyright holder.
Read this information before setting up, using or servicing your Series 50 T
Telemetry System.
FCC WARNING
This equipment generates, uses and radiates radio-frequency energy, and
if it is not installed and used in accordance with this manual, may cause
interference to radio communications.
Operation of this equipment in a residential area may cause interference,
in which case the users, at their own expense, must take whatever
measures may be required to correct the interference.
This symbol indicates that you should consult the
Ins tructions For Use, and particularly any warning
messages.
Equipotential Terminal
This symbol identifies terminals which 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.
Prot ective Earth Terminal
This symbol identifies the terminal for connection to
an external protective earth system.
Battery
This symbol identifies the transmitter battery holder.
It takes three 1.5 V batteries (AA size, LR6 type).
Three types of battery can be used in the transmitter:
•Alkaline
•NiCd (rechargeable)
•NiMH (rechargeable).
Caution
Remove the batteries if you do not intend to use the Transmitter for a
long period of time, to avoid damage from leakage.
[9
Chapter 1 - Safety
Patient Safety
Patient Safety
Environment
The Telemetry System should only be used by, or under the direct supervision of, a
licensed physician or other health care parctitioner who is trained in the use of fetal
heart rate monitors and in th e 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, Type B instrument. It is
designed to fulfill safety requirements according to IEC 60601-1, UL 544 and CSA-
C22.2 No.601.1-M90.
The telemetry transmitter is a battery operated device, applied parts (patient
connectors) are Type CF .
Use the system in an environment which is reasonably free from vibration, dust,
corrosive or explosive ga ses, extremes o f temperatur e and humidity. 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.
1
The system (not including transducers
) can be stored at ambient temperatures
between -40°C and +75°C.
The blue Toco and Ultrasound transducers are water-tight to a depth of 50 cm (19.7
inches).
Warning
Do not use brown transducers to monitor patients under water. Ultrasound and
Toco transducers that are colored blue are watertight and comply with IEC 529
(IP68).
You can immerse the BLUE Ultrasound and Toco tranducers in water ONLY
when connected to the telemetry transmitter. NEVER connect blue transducers
directly to the fetal monitor when they are immersed in water, or likely to come
in contact with water.
NEVER immerse the telemetry transmitter in water or other liquids such as
cleaning solutions.
1. Transducers can be stored at temperatures between -40°C and +60°C (-40°F to +140°F).
Chapter 1 - Safety
Protective Earth
Protective Earth
To protect hospital personnel and the patient, the cabinet must be grounded.
Accordingly, the receiver 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 a dapter with the receiver. 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 impair ed, the receiver must be made
inoperative and be secured against any unintended operation.
Warning
Check each time before use that the Telemetry System is in perfect working
order and the receiver is properly grounded.
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 receiver 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.
Warning
Possible explosion hazard if used in the presence of flammable anesthetics.
Chapter 1 - Safety
Maximum Input/Output Voltages
Maximum Input/Output Voltages
Receiver (Rear View)
1. Service Socket
Maximum voltage of ±12V.
2. Socket to Fetal Monitor
Maximum voltage of ±12V.
3. Power Input Socket
100-120V ~ or 220-240V ~
4. Event Marker/Service Socket
Maximum Voltage of +5V.
5. Toco Socket
Maximum Voltage of +5V.
6. Cardio Socket
Maximum Voltage of +5V.
Transmitter
Chapter 1 - Safety
Telemetry System (Receiver and Transmitter)
Power Requirements
The Telemetry System is set for the correct voltage at the factory, but before
you connect power, ensure that the voltage swit ch is in the correct positi on
for your country.
Operating Voltage :100V - 120V~ or 220V - 240V (±10%).
Line Frequency:50 to 60Hz.
Power Consumption:19VA max.
Battery Type:3 x 1.5V (AA size).
Environment
The Telemetry System should be used in an environment which is reasonably
free from vibration, dust, corrosive or explosive gases, extremes of
temperature and humidity. It operates within specifications at ambient
temperatures between 0 and 45°C . Ambient temperatures which exceed
these limits can affect the accuracy of the Telemetry System, the Transmitter
radio frequency transmission, and cause damage to the components and
circuits.
1. Excludes transducers. T ransducers can be stored at temperatures between -40 °C
and +60°C (-40°F to +140°F).
Chapter 2 - Technical Spec ifications
Telemetry System (Receiver and Transmitter)
Controls and Indicators
Power On/Off SwitchPush Button
Pow e r On LightLEDGreen
Nurse Call Acknowledge/Volume ButtonPush Button
Nurse Call LightLEDYellow
Transmission INOP LightLEDYellow
Battery Low Light LEDYellow
Error LightLEDRed
Receiver - Controls and Indicators
DescriptionTypeColor
Power On/Off SwitchSlide Switch
Pow e r On LightLEDGreen
Nurse CallPush Butt on
Error LightLEDRed
Channels and Frequencies
Over 160 different channels in the UHF Band (430- 470 MHz) with 25 kHz/
12.5 kHz channel spacing avail able. (S ee Ch apter11 for a list of the channels
and frequencies available.)
AntennaReceiver
BNC Female input connector (standard 50 Ohms input). For standalone or
connection to an antenna system.
Transmitter
Built-in Antenn a in US and DECG transducer cables.
Transmitter - Controls and Indicators
DescriptionTypeColor
InputsReceiver
•Equipotential Grounding Point.
•Service Socket.
Chapter 2 - Technical Specifications
Transmitter
•Cardio socket for M1356A ultrasound transducer or the M1357A/
M1364A DECG transducer.
•Toco socket for the M1355A Toco transducer or an IUP Transducer
(CPJ840J5).
•Remote Event Marker and Service Socket.
OutputsReceiver
•25 pin RS232 Socket for connecting the Fetal Monitor.
Input Sensitivity-118dBM
Output PowerTransmitter
4 mW (USA)
2 mW (Europe)
1 mW (Japan)
Telemetry System (Receiver and Transmitter)
Image Rejection>80 dB
Self-Test FacilitiesSelf-test facilities include:
•Receiver Self Test: Tests the Receiver LF Part.
•Transmitter Self Test: Tests the Transmitter LF Part.
•Parameter Test: With the appropriate transducer connected to the
Transmitter, the monitoring mode (ultra sound/ DECG or Toco/IUP) is
tested from the Transmitter via Receiver to the connected Fetal
Monitor.
Chapter 2 - Technical Spec ifications
Transducers and Cables
Transducers and Cables
There are two types of Toco, Ultrasound and DECG Transducers, the
Standard Series 50 and Telemetry Transducers. The Standard Transducers
have a 2.5m/8ft 2in ventilated cable and the Telemetry Transducers have a
70cm/28in ventilated cable.
Both types of Toco and Ultrasound Transducers are colored blue and are
watertight complying with IEC 529 (IP68)
External Blue Toco Transducers (M1355A) or (M1355A Opt. C03)
System:Passive Straingauge.
Dynamic Range:0 to 12N (overlo ad protected).
Weight:180g (6.3oz).
Cable Length:2.5m (8ft 2in) or 70cm (28in) for Option C03.
Water-tight:To a depth of 0.5 meters.
Blue Ultrasound Transducer (M1356A) or (M1356 Opt. C03)
System:Pulsed Dopple r.
Oscillator Frequency:998.4kHz.
Weight:185g (6.5oz).
Cable Length:2.5m (8ft 2in) or 70cm (28in) for Option C03.
Size:75mm (2.95in) diameter.
Water-tight:To a depth of 0.5 meters.
Warning
Under no circumstances should the transducer be immersed in water
when connected to the Fetal Monitor.
Caution
Blue Toco Transducers have a ventilated cable. As liquid can enter this
cable through capillary action, extra care should be taken not to get the
connector wet.
Chapter 2 - Technical Specifications
DECG Transducer (M1357A)
Input Impedance:>10M (di_erential, dc to 50/60Hz).
CMRR: >110dB (with patient cable, 51.5k/0.047_F
Noise:<4_Vp (referred to input with 25k).
Contact Potential Tolerance:_500mV.
Input Voltage Range:20_Vp to 3mVp.
Patient Leakage Current:<10_Arms @ 120V/60Hz.
Patient Auxiliary Current:<0.1_A (dc).
Dielectric Strength :2000Vrms (spark-gap protected).
Weight:185g (6.5oz).
Cable Length:2.5m (8ft 2in) or 70cm (28in) for Option C03.
DECG/MECG Patient Module (M1364A)
The patient module has a7-pin ECG connector into which you can plug
either DECG cable (M1362A or M1362B) or MECG cable.
IUP Quartz Transducer (1290C #J05)
imbalance atline frequency).
Overall length:2706mm (+30, -100mm)
Length of free cable:2618mm (+30, -100mm)
Weight:120 grams
Size:88x42x30mm
Socket:DECG or MECG connection
A short cable version of the M1364A patient module with a 70 cm (28 inch)
cable is orderable as part number M1364-60003.
IUP Quartz Transducer (1290C #J05)
Dynamic Range:-50 to 300mmHg.
Sensitivity:5_V/V/mmHg.
Non-linearity:whichever is greater:
Height:21.7mm (0.9in).
Operating Te mp:15 to 40_C.
Chapter 2 - Technical Spec ifications
IUP Quartz Transducer (1290C #J05)
IUP Pressure Transducer (CPJ840J5)
Pressure range:-20 to + 300 mm Hg
Max. overpressure:10,000 mm Hg
Sensitivity:50
Resonance frequency:300 Hz typical (transducer and dome)
Max. electrical excitation:15 V DC or AC
Bridge resistance:1000 Ohms (input and output)
Non-linearity and hysteresis: max. 0.5% of full scale
Zero balance :max. 0.15 mm Hg/°C
Operating temperature range:+10 to +50°C
Storage temperature range:-20 to +70°C
Isolation resistance:min. 1000 MOhms
Leakage current:max.1.5
Weight:24 grams (without cable)
Connector:Equipment specified
Remote Event Marker (15249A)
Length:2.8m (9ft 2in).
Weight:75g (2.65oz).
µV/V/mm Hg
µA at 250V, 50 Hz
Chapter 2 - Technical Specifications
Testing the Receiver
Tests and Error Messages
To ru n the receiver self test:
1. Switch on the fetal monitor and its recorder.
2. Press the Power O n /Off button to switch the re ceiver on.
3. When you switch on:
• The receiver On light (A) comes on.
• The nurse call light (B) and the battery low light (D) are lit for one
second.
• The transmission INOP light (C) lights and stays lit until the transmitter
is switched on.
• The telemetry lamp indicator on the fetal monitor lights, in dicating
telemetry monitoring mode.
•
TELE is annotated on the fetal trace.
Chapter 3 - Tests and Error Messages
Testing the Transmitt er
Testing the Transmitter
1. Slide back the battery cover.
2. Switch on the transmitter. The green On/Off light (A) comes on
showing the transmitter is on.
3. Check the red light (B) situated behind the middle batt ery. If:
• the red light is lit for a few seconds and th en goes out, the self test is
successfully complete.
• the red light blinks, or remains on after three seconds, change the
batteries. If the fault continues, there is a hardware error. See
troubleshooting flowcharts in Chapter4.
Chapter 3 - Tests and Error Messages
Testing the Parameter Signals
The parameter test ch ecks th e signal path to and f rom the tr ansducer so cket s,
but not the transducers themselves.
1. Switch on the monitor, the recorder and the telemetry receiver.
2. Connect the appropriate transducer to each socket on the transmitter.
3. Standing within view of the monitor, press the Nurse Call Button on
the transmitter and switch on th e transmitter simul taneously. The test
runs while the Nurse Call is pressed.
Testing the Parameter Signals
SignalCorrect Monitor Response
US
125 is displa yed and printed.
Signal Quality Indicator is green.
Fetal heartbeat is heard from the loudspeaker.
TocoA triangle signal with an amplitude of
40 units is
displayed and printed.
Each cycle lasts for 12 seconds.
DECG
150 is displa yed and printed
Signal Quality Indicator is green.
Fetal heartbeat is heard from the loudspeaker.
If the response is different, see troubleshooting flowcharts, Chapter 4.
Chapter 3 - Tests and Error Messages
Error Messages
Error Messages
The following error messages are directly related to telemetry and appear on
the fetal monitor. Refer to the Instructions for U se prov ided with your mo nitor
for error messages not related to teleme try monitoring.
Series 50 Family
MessageDisplayCauseSolution
Err 9US TocoInvalid telemetry mode.Check the cable from the telemetry
receiver and, if necessary, replace it.
Err 14US TocoIncorrect transducer
connected to transmit ter.
Check that the transducer is
compatible with Series 50T Fetal
Telemetry System.
Err 16US TocoTransducers are
connected to the front
panel of the monitor.
8040A
*
Disconnect the transducers from
the monitor or switch off the
telemetry receiver.
MessageDisplayCauseSolution
Err 16US TocoTransducers are
connected to the front
Disconnect th e transducer s from the mo nitor or
switch off the telemetry receiver.
panel of the monitor.
*. No longer available.
Chapter 3 - Tests and Error Messages
Error Messages
8041A
*
MessageDisplayCauseSolution
Signal
indicator
Indicator
Panel
Invalid telemetry mode.
Check the cable from the telemetry receiver and,
if necessary, replace it.
lamps
flashing
Incorrect transducer
connected into
Check that the transducer is compatible with
Series 50T Fetal Telemetry System.
transmitter. (Only
Ultrasound and Toco
transducers can be used).
Transducers are
connected to the front
Disconnect th e transducer s from the mo nitor or
switch off the telemetry receiver.
panel of the monitor.
*. No longer available
Chapter 3 - Tests and Error Messages
Error Messages
Chapter 3 - Tests and Error Messages
Solving General Problems
Troubleshooting is based on the interpretation of the Receiver LED’s. This
chapter describes common problems and their causes, and provides
troubleshooting flowcharts and guidance for their solution.
ProblemPossible CausesSolutions
4
Troubleshooting
All the lights on the
receiver stay on when
the receiver is turned
on.
The Telemetry
Indicator Lamp on the
fetal monito r does not
light when th e monitor
and the receiver are
switched on.
Receiver Power On
Light does not light
when the receiver is
switched on.
Transmission INOP
light on the receiver is
still lit when the
transmitter is switched
on.
Battery Low Light lit on
receiver.
Fetal monitor is switched off.
Possible defect in the receiver, interface
cable or fetal monitor.
Incorrect interface connection between
the monitor and the receiver.
Faulty interface c able.
Po wer cable not p lugged into th e power
supply.
Fuses need replacing.
Receiver and transmitter do not have
the same channel or serial number.
Batteries in the transmitter are
exhausted.
Power in batteries is low.Change batteries.
Switch on fetal monitor.
Carry out the tests described in “Testing the
Receiver” on page 11.
Follow the in structions in Instructions for Use for
details on how to connect the monitor to the
receiver.
Replace interface cable.
Plug in and switch on.
Replace fuses.
Check channel number and the serial numbers
are the same on the receiver and the transmitter.
Change the batteries in the transmitter (refer to
the Instructions for Use for details.)
INOP transmission
lamp is lit after the
patient has moved a
short distance away
form the receiver .
Local Antenna:
Antenna not connected correctly.
Remote Antenna System:
Antenna cable not connected correctly
to receiver.
Check antenna is connecting correctly.
Test the antenna system by bringing the
transmitter close to the receiver. If the
transmission is good , then the antenn a system is
not functioning properly.