This device is intended for use only by qualified medical personnel.
Use only Nihon Kohden approved products with this device. Use of non-approved products or in
a non-approved manner may affect the performance specifications of the device. This includes,
but is not limited to, batteries, recording paper, pens, extension cables, electrode leads, input
boxes and AC power.
Please read these precautions thoroughly before attempting to operate the instrument.
1. To safely and effectively use the instrument, its operation must be fully understood.
2. When installing or storing the instrument, take the following precautions:
(1) Avoid moisture or contact with water, extreme atmospheric pressure, excessive humidity and temperatures, poorly
ventilated areas, and dust, saline or sulphuric air.
(2) Place the instrument on an even, level floor. Avoid vibration and mechanical shock, even during transport.
(3) Avoid placing in an area where chemicals are stored or where there is danger of gas leakage.
(4) The power line source to be applied to the instrument must correspond in frequency and voltage to product
specifications, and have sufficient current capacity.
(5) Choose a room where a proper grounding facility is available.
3. Before Operation
(1) Check that the instrument is in perfect operating order.
(2) Check that the instrument is grounded properly.
(3) Check that all cords are connected properly.
(4) Pay extra attention when the instrument is in combination with other instruments to avoid misdiagnosis or other
problems.
(5) All circuitry used for direct patient connection must be doubly checked.
(6) Check that battery level is acceptable and battery condition is good when using battery-operated models.
4. During Operation
(1) Both the instrument and the patient must receive continual, careful attention.
(2) Turn power off or remove electrodes and/or transducers when necessary to assure the patient’s safety.
(3) Avoid direct contact between the instrument housing and the patient.
5. To Shutdown After Use
(1) Turn power off with all controls returned to their original positions.
(2) Remove the cords gently; do not use force to remove them.
(3) Clean the instrument together with all accessories for their next use.
6. The instrument must receive expert, professional attention for maintenance and repairs. When the instrument is
not functioning properly, it should be clearly marked to avoid operation while it is out of order.
7. The instrument must not be altered or modified in any way.
8. Maintenance and Inspection:
(1) The instrument and parts must undergo regular maintenance inspection at least every 6 months.
(2) If stored for extended periods without being used, make sure prior to operation that the instrument is in perfect
operating condition.
Service Manual TEC-7600/7700i
(3) Technical information such as parts list, descriptions, calibration instructions or other information is available for
qualified user technical personnel upon request from your Nihon Kohden distributor.
9. When the instrument is used with an electrosurgical instrument, pay careful attention to the application and/or
location of electrodes and/or transducers to avoid possible burn to the patient.
WARRANTY POLICY
Nihon Kohden Corporation (NKC) shall warrant its products against all defects in materials and workmanship for one year
from the date of delivery. However, consumable materials such as recording paper, ink, stylus and battery are excluded from
the warranty.
NKC or its authorized agents will repair or replace any products which prove to be defective during the warranty period,
provided these products are used as prescribed by the operating instructions given in the operator’s and service manuals.
No other party is authorized to make any warranty or assume liability for NKC’s products. NKC will not recognize any other
warranty, either implied or in writing. In addition, service, technical modification or any other product change performed by
someone other than NKC or its authorized agents without prior consent of NKC may be cause for voiding this warranty.
Defective products or parts must be returned to NKC or its authorized agents, along with an explanation of the failure.
Shipping costs must be pre-paid.
This warranty does not apply to products that have been modified, disassembled, reinstalled or repaired without Nihon
Kohden approval or which have been subjected to neglect or accident, damage due to accident, fire, lightning, vandalism,
water or other casualty, improper installation or application, or on which the original identification marks have been
removed.
In the USA and Canada other warranty policies may apply.
CAUTION
United States law restricts this device to sale by or on the order of a physician.
iiService Manual TEC-7600/7700
EMC RELATED CAUTION
This equipment and/or system complies with the International Standard IEC 60601-1-2 for electromagnetic
compatibility for medical electrical equipment and/or system. However, an electromagnetic environment that
exceeds the limits or levels stipulated in the IEC 60601-1-2, can cause harmful interference to the equipment and/or
system or cause the equipment and/or system to fail to perform its intended function or degrade its intended
performance. Therefore, during the operation of the equipment and/or system, if there is any undesired deviation
from its intended operational performance, you must avoid, identify and resolve the adverse electromagnetic effect
before continuing to use the equipment and/or system.
The following describes some common interference sources and remedial actions:
1. Strong electromagnetic interference from a nearby emitter source such as an authorized radio station or cellular
phone:
Install the equipment and/or system at another location if it is interfered with by an emitter source such as an
authorized radio station. Keep the emitter source such as cellular phone away from the equipment and/or
system.
2. Radio-frequency interference from other equipment through the AC power supply of the equipment and/or
system:
Identify the cause of this interference and if possible remove this interference source. If this is not possible, use
a different power supply.
3. Effect of direct or indirect electrostatic discharge:
Make sure all users and patients in contact with the equipment and/or system are free from direct or indirect
electrostatic energy before using it. A humid room can help lessen this problem.
4. Electromagnetic interference with any radio wave receiver such as radio or television:
If the equipment and/or system interferes with any radio wave receiver, locate the equipment and/or system as
far as possible from the radio wave receiver.
If the above suggested remedial actions do not solve the problem, consult your Nihon Kohden Corporation
subsidiary or distributor for additional suggestions.
In IEC 60601-1-2 Medical Electronic Equipment, Part 1: General Requirements for Safety, 2. Collateral Standard:
The ECG lead key error is detected.Faulty key board.
Faulty main board.
The ECG sensitivity key error is
detected.
The ECG silence alarm key error is
detected.
The alarm setting key error is detected.Faulty key board.
The record key error is detected.Faulty key board.
The event key error is detected.Faulty key board.
The SYSNC button error (front panel) is
detected.
The CHARGE button error (front panel)
is detected.
The right DISCHARGE button error
(front panel) is detected.
The left DISCHARGE button error
(front panel) is detected.
The CHARGE button error (apex
external paddle) is detected.
The DISCHARGE button error (apex
external paddle) is detected.
The DISCHARGE button error
(sternum external paddle) is detected.
When the NIBP unit is connected, the
NIBP START/STOP key error is
detected.
The PACING START/STOP key error
is detected.
Faulty key board.
Faulty main board.
Faulty key board.
Faulty main board.
Faulty main board.
Faulty main board.
Faulty main board.
Faulty main key board.
Faulty main board.
Faulty main key board.
Faulty main board.
Faulty main key board.
Faulty main board.
Faulty main key board.
Faulty main board.
Faulty external paddles.
Faulty main board.
Faulty external paddles.
Faulty main board.
Faulty external paddles.
Faulty main board.
Faulty NIBP unit.
Faulty pacer board.
Faulty main board.
NOTE
Replace the key board.
Replace the main board.
Replace the key board.
Replace the main board.
Replace the key board.
Replace the main board.
Replace the key board.
Replace the main board.
Replace the key board.
Replace the main board.
Replace the key board.
Replace the main board.
Replace the main key board.K507
Replace the main board.
Replace the main key board.K508
Replace the main board.
Replace the main key board.K509
Replace the main board.
Replace the main key board.K510
Replace the main board.
Replace the external paddles.K511
Replace the main board.
Replace the external paddles.K512
Replace the main board.
Replace the external paddles.K513
Replace the main board.
Replace the NIBP unit.
Replace the pacer board.K516
Replace the main board.
Service Manual TEC-7600/77002.5
2. TROUBLESHOOTING
Communication
Error CodeMeaningPossible CauseAction
C501
C502
C504
C505
C507
C508
C511
When the CO2sensor kit is connected,
CO2data is not received.
When the SpO2adapter is connected,
SpO2data is not received.
When the NIBP unit is connected, the
communication between the NIBP unit
and sub-CPU is not performed correctly.
When the ZB interface unit and
transmitter are connected, the
communication between the transmitter
and main-CPU is not performed
correctly.
The battery CPU does not transfer the
battery data to the main CPU for more
than 10 seconds.
When the power is turned on, the
communication error between the RTC
(real time clock) and main CPU is
detected for one second.
When the 12 lead ECG unit is
connected, the communication between
the 12 lead ECG unit and main-CPU is
not performed correctly.
The sub CPU does not update the data
in the DPRAM for one second.
Faulty CO2sensor kit.
Faulty DSI interface board.
Faulty DSI/AUX OUT
interface board.
Faulty main board.
Faulty SpO2adapter.
Faulty DSI interface board.
Faulty DSI/AUX OUT
interface board.
Faulty main board.
Faulty NIBP unit.
Faulty main board.
Faulty ZB interface unit.
Faulty transmitter.
Faulty main board.
Faulty main board.
Faulty main board.
Faulty ECG 12L board.
Faulty ECG-COM board.
Faulty main board.
Faulty main board.
Replace the
Replace the
Replace the
interface board.
Replace the main board.
Replace the Sp
Replace the
Replace the
interface board.
Replace the main board.
Replace the NIBP unit.C503
Replace the main board.
Replace the ZB interface unit.
Replace the transmitter.
Replace the main board.
Replace the main board.
Replace the main board.
Replace the ECG 12L board.
Replace the ECG-COM board.
Replace the main board.
Replace the main board.
CO2sensor kit.
DSI interface board.
DSI/AUX OUT
DSI interface board.
DSI/AUX OUT
O2adapter.
2.6Service Manual TEC-7600/7700
2. TROUBLESHOOTING
Data Error
Error CodeMeaningPossible CauseAction
D501
D511
D512
Data in the DRAM or flash memory is
not read out correctly (summation
error).
When the power is turned on, settings in
the System Maintenance screen do not
match the backup data in the flash
memory.
When the power is turned on, damaged
waveform report data in the flash
memory is detected.
Faulty DRAM or flash
memory.
After settings in the System
Maintenance screen are
changed, the “Flash Save”
procedure is not performed.
During power off sequence,
power down occurs.
Faulty main board.
During power off sequence,
power down occurs.
Faulty main board.
Replace the main board.
Perform the “Flash Save”
procedure in the System
Maintenance screen.
Delete the report data in the
System Setup screen.
Replace the main board.
Delete the report data in the
System Setup screen.
Replace the main board.
Pacing (TEC-7631/7731 Series Only)
Error CodeMeaningPossible CauseAction
P501Pacing output rate does not match the
selected rate.
P502Pulse width of the pacing output pulse is
larger or smaller than the selected width.
P503Current intensity of the pacing output
pulse is larger than the selected value.
P504Current intensity of the pacing output
pulse is smaller than the selected value.
P505Pacing output that is not requested by the
CPU is detected.
P506Pacing output voltage exceeds the upper
limit.
P507Reference voltage exceeds the specified
value.
P511Error was detected in the short-mode of
the transistor.
Faulty pacer board.
Faulty main board.Replace the main board.
Faulty pacer board.
Faulty main board.Replace the main board.
Faulty pacer board.
Faulty main board.Replace the main board.
Faulty pacer board.
Faulty main board.Replace the main board.
Faulty pacer board.
Faulty main board.Replace the main board.
Faulty pacer board.
Faulty main board.Replace the main board.
Faulty pacer board.
Faulty main board.Replace the main board.
Faulty pacer board.
Replace the pacer board.
Replace the pacer board.
Replace the pacer board.
Replace the pacer board.
Replace the pacer board.
Replace the pacer board.
Replace the pacer board.
Replace the pacer board.
Service Manual TEC-7600/77002.7
2. TROUBLESHOOTING
12 Lead ECG Measurement
Error CodeMeaningPossible CauseAction
T501Serial communication error between
the input CPU and host CPU on the
ECG 12L board.
T502Command communication error
between the input CPU and host CPU
on the ECG 12L board.
T503Data from the input CPU on the ECG
12L board is out of range.
T507Timer error of the host CPU on the
ECG 12L board.
T511Bus error of the host CPU on the ECG
12L board.
T512Address error of the host CPU on the
ECG 12L board.
T513Invalid command error of the host CPU
on the ECG 12L board.
T514Division error of the host CPU on the
ECG 12L board.
T516Check sum error of the EEPROM on
the ECG 12L board.
T517Writeerroroftheflashmemoryonthe
ECG 12L board.
T522Time out of the 12 lead ECG analysis.Faulty ECG 12L board.
T523The sensitivity and time constant data
differ between the EEPROM and flash
memory on the ECG 12L board.
Faulty ECG 12L board.
Faulty ECG 12L board.
Faulty ECG 12L board.
Faulty ECG 12L board.
Faulty ECG 12L board.
Faulty ECG 12L board.
Faulty ECG 12L board.
Faulty ECG 12L board.
Faulty ECG 12L board.
The power is turned off
during shutdown.
Faulty ECG 12L board.
Faulty ECG 12L board.
Replace the ECG 12L board.
Replace the ECG 12L board.
Replace the ECG 12L board.
Replace the ECG 12L board.
Replace the ECG 12L board.
Replace the ECG 12L board.
Replace the ECG 12L board.
Replace the ECG 12L board.
Replace the ECG 12L board.
Turn the power off after the
system shutdowns correctly.
Replace the ECG 12L board.
Turn the power off, then retry the
12 lead ECG analysis. If the error
code appears again, replace the
ECG 12L board.
Replace the ECG 12L board.
2.8Service Manual TEC-7600/7700
2. TROUBLESHOOTING
Message
Instrument and SpO2/CO2 Measurement
MessageMeaningPossible CauseAction
Battery charge
timed out
Battery charging
error
Battery discharge
timed out
Capacitor test fail
CO2module not
working
CO2module
disconnected
ERROR AXXX
ERROR CXXX
ERROR DXXX
ERROR KXXX
ERROR PXXX
ERROR TXXX
FET error
High voltage
monitor error
During battery test
The battery was not fully
charged 5 hours after battery
charging started.
During battery test
An error occurred in battery
charging
During battery test
The voltage did not decrease to
the specified level 4 hours after
battery discharging started.
Capacitor test failed.Faulty HV capacitor.
CO2module is faulty.
CO2cable is disconnected from
the instrument.
Faulty HV
Communication error
Faulty ROM/RAM
Faulty keys
Faulty pacing unit
Faulty 12 lead ECG unit
The circuit to measure remaining
battery charge is faulty.
Faulty high voltage monitor circuit.Faulty relay unit, biphasic HV unit
Faulty battery pack.
Faulty main board.
Faulty battery pack.
Faulty main board.
Faulty battery pack.
Faulty main board.
Faulty CO2sensor kit.
Faulty the QI-762V DSI
Interface Unit or QI-763V
DSI/AUX OUT Interface Unit.
CO2cable is disconnected from
the QI-762V DSI Interface Unit
or QI-763V DSI/AUX OUT
Interface Unit.
Faulty DSI interface unit or
DSI/AUX OUT interface unit
—
Faulty main board.
or main board.
Replace the battery pack.
Replace the main board.
Replace the battery pack.
Replace the main board.
Replace the battery pack.
Replace the main board.
Replace the HV capacitor.
Replace the
Replace the DSI Interface Unit
or DSI/AUX OUT Interface
Unit.
Press the Silence alarm key to
turn off the message. If the
message still appears, the
interface unit or DSI/AUX
interface unit is faulty. Replace
the DSI interface unit or
DSI/AUX interface unit.
Turn off the instrument, then turn
on and do the same operation. If the
message still appears, refer to the
table for each error code.
Replace the main board.
Turn off the instrument, then turn
on and do the same operation. If the
message still appears, the relay unit,
biphasic HV unit or main board is
faulty. Replace the relay unit,
biphasic HV unit or main board.
CO2sensor kit.
DSI
Service Manual TEC-7600/77002.9
2. TROUBLESHOOTING
MessageMeaningPossible CauseAction
OverheatingThe high voltage charge circuit
heats up.
Power abnormalityInput power voltage is too high.Not specified battery is used.Only use the NKB-301V battery.
Relay drive errorFaulty relay drive circuit
Replace batteryBattery test result is 0 to 49%.
The
working
SpO2 module
disconnected
instrument
battery should be replaced with a
new one.
SpO2 module is faulty.
SpO2 cable is disconnected from
the instrument.
judged that the
The
instrument
frequently
Faulty relay unit, biphasic HV unit
or main board.
Faulty relay unit or biphasic HV
unit.
Faulty main board.Replace main board.
Faulty battery pack.Replace the battery.
Faulty the SpO2 adapter.Replace the SpO2 adapter.SpO2 module not
Faulty the QI-762V DSI
Interface Unit or QI-763V
DSI/AUX OUT Interface Unit.
SpO2 cable is disconnected from
the QI-762V DSI Interface Unit
or QI-763V DSI/AUX OUT
Interface Unit.
Faulty DSI interface unit or
DSI/AUX OUT interface unit.
discharged too
Turn off the instrument and leave
the instrument for 10 minutes, then
turn on.
Turn off the instrument and leave
the instrument for 10 minutes, then
turn on. If the message appears, the
relay unit, biphasic HV unit or
main board is faulty. Replace the
relay unit, biphasic HV unit or
main board.
Replace the relay unit or biphasic
HV unit.
Replace the DSI Interface Unit
or DSI/AUX OUT Interface
Unit.
Press the Silence alarm key to
turn off the message. If the
message still appears, the
interface unit or DSI/AUX
interface unit is faulty. Replace
the DSI interface unit or
DSI/AUX interface unit.
DSI
2.10Service Manual TEC-7600/7700
NIBP Measurement
MessagePossible CauseAction
NIBP air hose disconnected
NIBP air leak
NIBP cuff occlusionThe cuff pressure does not decrease
Cuff pressure abnormalExcessive pressure was applied by the
NIBP module not working
NIBP measurement time outThe measuring time exceeded the
The air hose is disconnected from the
NIBP socket.
The air hose is damaged.Replace the air hose with a new one.
Faulty NIBP unit.Replace the NIBP unit.
The cuff pressure does not change after
inflation even after a certain period of
time.
The cuff or air hose is damaged.Replace the cuff or air hose with a new
Faulty NIBP unit.Replace the NIBP unit.
after measurement has completed.
Faulty NIBP unit.Replace the NIBP unit.
cuff.
Faulty NIBP unit.Replace the NIBP unit.
Faulty NIBP unit.Replace the NIBP unit.
specified time due to arrhythmia or
noise.
Faulty NIBP unit.Replace the NIBP unit.
2. TROUBLESHOOTING
Connect the air hose properly. When
NIBP monitoring is not necessary, press
the SILENCE ALARM key to silence
the alarm. The NIBP display can be
cleared.
Connect the cuff to the air hose
properly.
Connect the air hose to the socket
properly.
one.
Check that the air hose is not bent or
squeezed.
When measuring an adult, ask the
patient not to move too much.
If the cause is arrhythmia, measure by
invasive blood pressure measurement.
Removethecauseifduetonoise.
12 Lead ECG Measurement
MessagePossible causeAction
Check XX electrodeThe displayed is detached. (XX:
electrode name)
Faulty electrode lead or patient cable.Replace the electrode lead or patient
Check chest electrodeTwo or more chest electrodes are
detached.
Faulty electrode lead or patient cable.Replace the electrode lead or patient
A 5 lead electrode is used.Use the specified electrode lead and
Check limb electrodeTwo or more limb electrodes from the
R(RA), L(LA) or F(LL) electrode are
detached.
The RF electrode is detached.
No electrode is attached to the patient.
Faulty electrode lead or patient cable.Replace the electrode lead or patient
A 3 lead electrode is used.Use the specified electrode lead and
Not enough free memoryThere is no space to save new ECG
data file in the memory card.
Insert memory cardA memory card is not inserted.Insert the memory card into the
Check memory cardAn unspecified memory card is
inserted.
Faulty memory card.Replace the memory card.
Check the electrode attachment of the
indicated position.
cable.
Check the chest electrode attachment.
cable.
patient cable.
Check the limb electrode attachment.
cable.
patient cable.
Replace the memory card with a new
one.
memory card slot.
Insert the specified memory card.
Service Manual TEC-7600/77002.11
2. TROUBLESHOOTING
Troubleshooting
General
ProblemPossible CauseAction
The instrument heats up.The instrument is used for many hours.There is no abnormality in the
instrument. Turn the Energy/Mode
select control to OFF position and
disconnect the power cord.
No operation when the instrument is
turned on.
characters are not seen.
The printed data is JAN/01/80.
The report data are not saved.On the Setup screen, the report data
The power cord is disconnected.
The battery is not installed.Install the specified battery.
Faulty battery
Remaining battery charge is low.Charge the battery.
Faulty main key board.Replace the main key board.
Faulty main board.Replace the main board.
Faulty AC/DC unit.Replace the AC/DC unit.
Faulty LCD inverter board.Replace the LCD inverter board.Screen is dim. Waveform and
Faulty LCD unit.Replace the LCD unit.
Faulty main board.Replace the main board.
The backup battery is almost
discharged.
were deleted.
Firmly connect the power cord to the
AC outlet and the defibrillator.
Replace the battery with a new one
(NKB-301V).
Replace the main board. (Under normal
use condition, the backup battery
lifetime is about 6 years.)
Deleted data cannot be recovered.
When the power is tuned off, the AC
power cord is disconnected while the
"Shutdown" message is displayed.
Faulty main board.Replace the main board.
All settings set in the Setup screen and
System Setup screen return to the
default settings.
2.12Service Manual TEC-7600/7700
When the power is tuned off, the AC
power cord is disconnected while the
"Shutdown" message is displayed.
Faulty main board.Replace the main board.
Do not disconnect the AC power cord
while the "Shutdown" message is
displayed.
Do not disconnect the AC power cord
while the "Shutdown" message is
displayed.
2. TROUBLESHOOTING
ProblemPossible CauseAction
When the battery is installed, the
instrument suddenly changes to battery
operation.
When the battery is not installed, the
instrument power suddenly drops.
Thedateandtimeprintedonthe
recording paper is incorrect.—
Power voltage changed.Check that the AC power cord is
The backup battery for the clock is
discharged.
Faulty main board.Replace the main board.
Defibrillation
connected to the instrument. If the
trouble is not solved, the AC/DC unit or
AC power cord faulty. Replace the
AC/DCunitorACpowercord.
Set the date and time on the
Date/Volume screen. Refer to Section 3
of the Operator's manual
Replace the backup battery.
ProblemPossible CauseAction
The defibrillator self-discharges the
energy during charging.
Cannot switch to synchronized mode.
In battery operation, the battery is
almost discharged.
Faulty high voltage unit.
(Error code appears on the screen.)
Appropriate lead is not selected.Change to the appropriate lead.
You tried to perform synchronized
cardioversion with the PADDLE lead
but synchronized cardioversion with
the PADDLE lead is set to OFF on the
Paddle Setup screen.
Faulty main key board.Replace the main key board.
Faulty main board.Replace the main board.
Operate the defibrillator on AC power
and recharge the battery. The battery
is automatically charged when the
defibrillator is connected to AC power.
When an error code appears on the
screen, refer to the Defibrillation table
in the Error Code section.
On the Paddle Setup screen, set the
“syncbypaddlelead”toON.
“0 J” is printed on the defibrillation
report recording.
TTR is 15 Ω or less
TTR is 255 Ω or more.
Check that the paddles do not touch
each other.
Press the paddles on the patient firmly.
Service Manual TEC-7600/77002.13
2. TROUBLESHOOTING
Monitoring
ECG
ProblemPossible CauseAction
Dotted lines appear instead of the ECG
waveforms.
An ECG electrode is detached.
An electrode lead is disconnected from
the electrode.
Remove the cause of the trouble. If the
trouble is not solved, the main board is
fault. Replace the main board.
The ECG connection cable is
disconnected from the defibrillator.
An electrode lead is faulty.
Faulty main board.
No sync soundFaulty main board.Replace the main board.
No alarm is generated
The SILENCE ALARMS key is
pressed.
On the Setup screen, alarm is set to
OFF.
Press the SILENCE ALARMS key
again.
On the Setup screen, set the
upper/lower limit of each vital alarm.
Faulty main board.Replace the main board.
Faulty speaker or speaker cable.Replace the speakerNo sound
Faulty main board.Replace the main board.
SpO
2
ProblemPossible CauseAction
SpO2 value is not displayed on the
screen.
The SpO2 adapter cable is
disconnected from the SpO2/CO2
connector.
The SpO2 probe is disconnected from
the SpO2 adapter.
Cable discontinuity in SpO2 adapter or
probe
SpO2 probe attachment to the patient is
loose.
Dotted lines appear instead of the pulse
Faulty SpO2 probe.Replace the SpO2 probe.
waveforms.
Faulty SpO2 adapter.Replace the SpO2 adapter.
Faulty QI-762V DSI Interface Unit.Replace the DSI interface unit.
Faulty QI-763V DSI/AUX OUT
Interface Unit.
Deformed or damaged SpO2 probeProbe was disinfected in a way other
than the specified way.
SpO2 probe is repeatedly used.Replace the probe with a new one when
Connect the SpO2 adapter to the
SpO2/CO2 connector.
Firmly connect the probe to the SpO2
adapter.
Replace the SpO2 adapter or probe.
Firmly attach the probe to the patient.
Replace the DSI/AUX OUT interface
unit.
Replace the probe with a new one.
Use the specified disinfecting method.
its lifetime is over.
2.14Service Manual TEC-7600/7700
CO
2
ProblemPossible CauseAction
The measured value is not displayed on
the screen.
The red LED on the CO2 adapter
blinks.
2. TROUBLESHOOTING
The CO2 sensor kit cable is
disconnected from the SpO2/CO2
Connect the CO2 sensor kit cable to the
SpO2/ CO2 connector.
connector.
CO2 gas is in the inspiration.
With the CO2 sensor kit, measurements
are based on the assumption of no CO2
gas in the inspiration. Do not connect a
Jackson Rees respiration circuit or
Mapleson D respiration circuit to the
patient. Measurement cannot be done
correctly.
The airway adapter is dirty.
Replace the airway adapter with a new
one.
The measurement is preformed where
atmospheric pressure is low, such as at
Consider the atmospheric pressure
when making evaluations.
high altitude.
CO2 sensor or CO2 adapter is faulty.Replace the CO2 sensor or CO2
adapter with a new one.
The respiration has not been detected
for longer than 20 s.
The red LED blinks when the
respiration has not been detected for
longer than 20 s regardless of the alarm
setting on the defibrillator.
Service Manual TEC-7600/77002.15
2. TROUBLESHOOTING
NIBP
TroublePossible CauseAction
The displayed cuff type is not correct.The air hose is not connected to the
Connect the air hose to the socket
firmly.
Connect the air hose to the socket
properly.
Wrap the cuff around the upper arm.
or is wrapped too loosely.
The cuff does not inflate when the
NIBP START/STOP key is pressed.
The air hose is not connected to the
cuff socket.
The cuff hose or air hose may be folded
Connect the air hose to the socket
firmly.
Check the cuff hose and air hose.
or squeezed.
Abnormal measurement results are
displayed.
The cuff size is not correct.Select the cuff which fits the patient’s
limb circumference.
The cuff is not wrapped around the arm
correctly.
NIBP data is not correct because of
body movement.
The cuff is touched during
measurement.
The cuff is not wrapped at the correct
Wrap the cuff around the upper arm,
not too tightly or too loosely.
Prevent the patient from moving during
measurement.
Do not touch the cuff during
measurement.
Wrap the cuff at the correct position.
position.
The cuff is suddenly deflated during
inflation.
TheNIBPSTART/STOPkeyispressed
during inflation.
The energy charging for defibrillation
is started.
—
Form the start of charging to
discharging, the NIBP measurement
cannot be preformed.
In battery operation, the battery is
almost discharged.
The air hose is disconnected from the
NIBP socket (The NIBP air hose
disconnected” message is displayed).
Replace the battery or switch to AC
operation.
Connect the air hose properly. When
NIBP monitoring is not necessary, press
the SILENCE ALARM key to silence
the alarm. The NIBP display can be
cleared
Auto measurement does not start even
when the time interval has passed.
ThetimeintervalfortheNIBPauto
measurement is changed.
The measurement is stopped by the
safety circuit (The “NIBP safety circuit
operating” message is displayed).
The cuff inflation pressure is deflated
enoughorduringNIBPmeasurement
Check the time interval.
Wait for 40 seconds before
remeasurement (This measurement is
canceled).
The measurement automatically starts
after the stop interval.
stop interval (2 or 30 seconds).
The previous measurement is not
This measurement is canceled.
complete.
The cuff suddenly inflates.The measurement mode is set to auto
Check the time interval.
mode.
Cannot connect cuff to the air hose.Unspecified cuff is used.Use a cuff specified by Nihon Kohden.
If none of the actions solve the problem, replace the NIBP unit.
2.16Service Manual TEC-7600/7700
2. TROUBLESHOOTING
ProblemPossible CauseAction
Cannot measure NIBP.
Noise which disables calculation of the
blood pressure has interfered.
The pulse wave is unstable due to
arrhythmia.
Remove the cause. Do not touch the
cuff during measurement.
Ask the patient not to move too much
and perform invasive blood pressure
measurement as required.
The air hose is bent or squeezed.Remove the cause.
Thecuffhaswornout.Useanewcuff.
Increase the measuring interval.Blood congestion occurs.Measuring over a long period of time at
intervals less than 2.5 minutes.
Do not measure NIBP over a long time.
Thrombus occurs.Measuring a sickle anemia patient.Do not perform NIBP measurement on
asickleanemiapatient.
Buzzing sounds when the NIBP
START/STOP key is pressed and NIBP
cannot be measured.
TheNIBPSTART/STOPkeyispressed
before the cuff inflation pressure has
deflated enough or during NIBP
Wait for the NIBP measurement stop
interval to elapse before
remeasurement.
measurement stop interval (2 or 30
seconds).
The energy charging for defibrillation
is started.
Form the start of charging to
discharging, the NIBP measurement
cannot be preformed.
In battery operation, the battery is
almost discharged.
The measurement is stopped by the
safety circuit (The “NIBP safety circuit
Replace the battery or switch to AC
operation.
Wait for 40 seconds before
remeasurement.
operating” message is displayed).
The air hose is disconnected from the
NIBP socket (The NIBP air hose
disconnected” message is displayed).
Connect the air hose properly. When
NIBP monitoring is not necessary, press
the SILENCE ALARM key to silence
the alarm. The NIBP display can be
cleared
Thesizeofthemeasurementdataon
the screen is small.
The size of the measurement data
changes to small 10 seconds after the
—
last measurement.
Service Manual TEC-7600/77002.17
2. TROUBLESHOOTING
Recording
ProblemPossible CauseAction
Printing is blurred. Dots are missing.The specified recording paper is not
used.
The thermal head is dirty.Clean the thermal head with the head
There is no printing.
The recording paper is not loaded.Load new recording paper.
Recording unit door is not properly
closed.
The recording paper is set with the
wrong side facing up.
Faulty key board.If the lamp does not light when you
Faulty recorder.
Faulty main board.
Use the specified recording paper.
cleaning pen. If the trouble not solved.
The recorder unit is faulty. Replace the
recorder unit.
Close the door until it clicks.
Set the recording paper correctly.
press the record key, check the key
function and recorder with the System
Maintenance screen. If the recorder
check is passed, the key board is faulty.
Replace the key board.
If the lamp lights when you press the
record key, check the recorder in the
System Maintenance screen.
Printing is light.The recording unit temperature is too
hot.
Battery
ProblemPossible CauseAction
The battery charging lamp is blinking.The instrument is too hot.
Faulty battery.Replace the battery with a new one.After starting battery charging, the
charging stops. (neither battery
charging lamp nor battery charge
complete lamp lights.)
Charging circuit is not working.Replace the main board.
Cool the instrument down in a cooler
place. If the trouble is not solved, the
recorder unit or main board is faulty.
Replace the recorder unit or main
board.
Bring the instrument to a cool place.
When the battery temperature
decreases, charging resumes.
2.18Service Manual TEC-7600/7700
Pacing (TEC-7631/7731 Series Only)
ProblemPossible CauseAction
2. TROUBLESHOOTING
Although the PULSE lamp is lit, pacing
pulse does not appear on the ECG.
Although the START/STOP lamp is lit,
pacing does not start.
Faulty pacer board.Replace the pacer board.
Faulty main board.Replace the main board.
Pacing energy is set to 0 mA.Set the appropriate pacing energy with
the PACING OUTPUT control.
In DEMAND mode, selected pacing
rate is faster than the patient heart rate.
Faulty pacer board.Replace the pacer board.
Faulty main board.Replace the main board.
Set the pacing rate appropriate for the
patient heart rate. When the patient
heart rate is slower than the selected
pacing rate, pacing pulse is output
automatically.
Service Manual TEC-7600/77002.19
2. TROUBLESHOOTING
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2.20Service Manual TEC-7600/7700
Section 3Disassembly
TEC-7621/7631 Series
Before You Begin .............................................................................................................. 3.1.1
Warnings, Cautions and Notes ............................................................................... 3.1.1