If you have any comments or suggestions
on this manual, please contact us at:
www.nihonkohden.com
0614-007205B
Page 2
Copyright Notice
The entire contents of this manual are copyrighted by Nihon Kohden. All rights are
reserved. No part of this document may be reproduced, stored, or transmitted in any
form or by any means (electronic, mechanical, photocopied, recorded, or otherwise)
without the prior written permission of Nihon Kohden.
Page 3
GENERAL HANDLING PRECAUTIONS
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.
(3) Avoid placing in an area where chemicals are stored or where there is
danger of gas leakage.
(4) Pay extra attention when the instrument is in combination with other
instruments to avoid misdiagnosis or other problems.
(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.
Operator’s Manual ZM-920PA/921PA/930PA/931PA i
Page 4
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.
personnel upon request from your Nihon Kohden representative.
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.
patient cables and/or transducers from the instrument to avoid possible
damage.
ii Operator’s Manual ZM-910PA/921PA/930PA/931PA
Page 5
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.
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 prepaid.
water or other casualty, improper installation or application, or on which the
originalidenticationmarkshavebeenremoved.
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.
Equipment Authorization Requirement
Operation of this equipment requires the prior coordination with a frequency
coordinator designated by the FCC for the Wireless Medical Telemetry Service.
Operator’s Manual ZM-920PA/921PA/930PA/931PA iii
Page 6
EMC RELATED CAUTION
This equipment and/or system complies with IEC 60601-2 International
Standard for electromagnetic compatibility for medical electrical equipment
and/or system. However, an electromagnetic environment that exceeds the
limits or levels stipulated in 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. Keep the emitter
source such as cellular phone away from the equipment and/or system, or
turn off the cellular phone.
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.
iv Operator’s Manual ZM-910PA/921PA/930PA/931PA
Page 7
5. Interference of lightning:
When lightning occurs near the location where the equipment and/or
system is installed, it may induce an excessive voltage in the equipment
and/or system.
In such a case, disconnect the AC power cord from the equipment and/or
system and operate the equipment and/or system by battery power, or use
an uninterruptible power supply.
6. Use with other equipment:
When the equipment and/or system is adjacent to or stacked with other
equipment, the equipment and/or system may affect the other equipment.
Before use, check that the equipment and/or system operates normally
with the other equipment.
7. Use of unspecified accessory, transducer and/or cable:
When an unspecified accessory, transducer and/or cable is connected to
this equipment and/or system, it may cause increased electromagnetic
emission or decreased electromagnetic immunity. The specified
configuration of this equipment and/or system complies with the
electromagnetic requirements with the specified configuration. Only use
this equipment and/or system with the specified configuration.
8. Use of unspecified configuration:
When the equipment and/or system is used with the unspecified system
configuration different than the configuration of EMC testing, it may
cause increased electromagnetic emission or decreased electromagnetic
immunity.
Only use this equipment and/or system with the specified configuration.
9. Measurement with excessive sensitivity:
The equipment and/or system is designed to measure bioelectrical signals
with a specified sensitivity. If the equipment and/or system is used with
excessive sensitivity, artifact may appear by electromagnetic interference
and this may cause mis-diagnosis. When unexpected artifact appears,
inspect the surrounding electromagnetic conditions and remove this artifact
source.
If the above suggested remedial actions do not solve the problem, consult
your Nihon Kohden representative for additional suggestions.
Operator’s Manual ZM-920PA/921PA/930PA/931PA v
Page 8
Conventions Used in this Manual and Instrument
Warnings, Cautions and Notes
Warnings, cautions and notes are used in this manual to alert or signal the reader
tospecicinformation.
WARNING
A warning alerts the user to the possible injury or death associated
with the use or misuse of the instrument.
CAUTION
A caution alerts the user to possible injury or problems with the
instrument associated with its use or misuse such as instrument
malfunction, instrument failure, damage to the instrument, or damage
to other property.
NOTE
A note provides specific information, in the form of recommendations,
prerequirements, alternative methods or supplemental information.
vi Operator’s Manual ZM-910PA/921PA/930PA/931PA
Page 9
Explanations of the Symbols in this Manual and Instrument
The following symbols found in this manual/instrument bear the respective
descriptions as given.
SymbolDescriptionSymbolDescription
Power On
Attention, consult
operator’s manual
Power OffNurse call
Debrillationprooftype
BF applied part
Debrillationprooftype
CF applied part
Direct current
Replace battery
Check electrode
Operator’s Manual ZM-920PA/921PA/930PA/931PA vii
Page 10
Introduction
The ZM-920PA/ZM-921PA/ZM-930PA/ZM-931PA transmitter transmits ECG and
other data from a patient to a Nihon Kohden monitor for continuous monitoring.
Available parameters and functions vary between the models. Read the operator’s
manual for the monitor before operation.
Model
ZM-920PA
ZM-921PA
ZM-930PA
ZM-931PA
The transmission frequency range is as follows.
ZM-920PA/930PA: 608.0250 MHz (channel number 9002) to 613.9750 MHz
ZM-921PA/931PA: 1395.0250 MHz (channel number E002) to 1399.9750 MHz
1427.0250 MHz (channel number E502) to 1431.9750 MHz
The transmitter channel can be changed by the QI-901PK Channel Writer. To
change the channel number, refer to the channel writer manual.
ParametersFunctions
The following information is indicated
• ECG
• Impedance respiration
• ECG
• Impedance respiration
• SpO
2
(channel number 9478)
(channel number E398)
(channel number E898)
by LED.
• Check ECG electrodes
• Replace batteries
The following information is indicated
on LCD.
• SpO2 value
• Pulse wave amplitude
• Replace batteries
The following information is indicated
by LED.
• Check ECG electrodes
Operator’s Manual ZM-920PA/921PA/930PA/931PA 1
Page 11
WARNING
The following actions must be taken to properly receive the
transmitter signal of the correct patient on the receiving instrument.
Otherwise, there may be signal loss or signals may mix causing a
serious accident, such as monitoring a different patient.
• Assign a channel administrator in the hospital and only he or she
should manage channel assignment.
• The channel administrator must manage the channels in the facility
so that there is no signal interference.
• When the transmitter channel is changed, the channel
administrator must check that the channel on the receiving monitor
is also changed and the signal is properly received.
• The channel administrator must replace the channel number label
on the transmitter with the new one after changing the channel.
WARNING
Do not use the same transmitter on more than one patient at the
same time. Do not connect different sensors on different patients to
the same transmitter.
CAUTION
• Do not use the same channel for different patients. If the same
channel is used for two patients, the two patients’ data will be lost
due to mutual modulation interference, or another patient’s data
may appear on the receiving monitor screen.
• Do not use transmitters of adjacent channels in a hospital. If a
transmitter of an adjacent channel is used, radio waves from one
transmitter affect the receiver of the adjacent channel’s transmitter
and there may be interference.
2 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 12
NOTE
• To prevent interference between channels, assign a channel
administrator in the hospital and only he or she should manage channel
assignment.
• Use Nihon Kohden parts and accessories to assure maximum
performance from your instrument.
• For stable signal reception, it is recommended to use a diversity
antenna system on the receiving monitor. Otherwise, spike noise from
transient fading of electric field strength (for example, people moving)
may interfere with the transmitter signal and may be mistaken as an
arrhythmia on the receiving monitor.
• Do not diagnose a patient based on only part of the monitoring data on
the transmitter or only on the data acquired by the transmitter. Overall
judgement must be performed by a physician who understands the
features, limitations and characteristics of the transmitter by reading
this operator’s manual thoroughly and by reading the biomedical signals
acquired by other instruments.
• For details on the receiving monitor and upgrade information, contact
your Nihon Kohden representative.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 3
Page 13
Panel Description
Top Panel
For attaching a strap
Refer to the warnings below
Refer to the symbol page
ECG/RESP socket
Connects to the electrode lead for measuring ECG
and/or respiration by the impedance method.
ZM-930PA/931PA only
SpO2 socket
Connects to the SpO2 probe.
Refer to the symbol page
Refer to the warnings below
WARNING
When performing defibrillation, discharge as far as possible from
electrodes, patches and any gel, cream or medicine on the chest of
the patient. If there is a possibility that the defibrillator paddle could
touch these materials, remove them from the patient. If the
defibrillator paddle directly contacts these materials, the discharged
energy may cause skin burn to the patient.
WARNING
Before defibrillation, all persons must keep clear of the bed and must
not touch the patient or any equipment or cord connected to the
patient. Failure to follow this warning may cause electrical shock or
injury.
4 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 14
Front Panel
RALALL
Va Vb
USAch
E002
1395.025 MHz
ZM-920PA/921PA
Power switch
Turns transmitter power on or off.
Replace batteries LED
Lights when the batteries
need replacement.
CALL key
When this key is pressed,
a “peep” sounds at the
transmitter, and “CALL”
message appears at the
Check electrodes LED
Lights when the
electrode is detached
from the patient.
monitor. Depending
on the settings on
the monitor, an ECG
waveform is recorded
when this key is pressed.
Refer to the warning below.Battery case
Contains two 1.5 V dry cell batteries (AA).
WARNING
Close the battery case cover during operation. If the transmitter is
used with the battery case cover open, anyone who touches the
opened battery case may receive an electrical shock when
defibrillation is performed. Touching the opened battery case may
cause electrostatic discharge and intermittently interfere with the
waveform or data.
Only use your finger to press the CALL key. Do not press the key with
a sharp object. Otherwise the key may be damaged.
CAUTION
Operator’s Manual ZM-920PA/921PA/930PA/931PA 5
Page 15
ZM-930PA/931PA
RALALL
Va Vb
USAch
E002
1395.025 MHz
RALALL
Va Vb
USAch
E002
1395.025 MHz
Battery replacement mark:
Appears when the batteries
are weak. Immediately
replace the batteries when
this appears.
For the descriptions except for the
LCD, refer to the “ZM-920PA/921PA”
section on the previous page.
LCD
LCD
%SpO2:
Displayed when the power is
turned on. This indication is not
displayed when SpO2 display is
turned off.
Pulse level bar graph:
Displays pulse level in
SpO2 data:
7 steps.
Displays SpO2 data.
When SpO2 is 41 to 100%, the value is displayed. (ex. )
When SpO2 is under 40%, “ ” is displayed.
When the detected pulse is too small to measure, “” is
displayed.
6 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 16
Important Safety Information
General
WARNING
Never use the transmitter in the presence of any flammable
anesthetic gas or high concentration oxygen atmosphere. Failure to
follow this warning may cause explosion or fire.
WARNING
Never use the transmitter in a hyperbaric oxygen chamber. Failure to
follow this warning may cause explosion or fire.
WARNING
Do not take this transmitter into the MRI test room. This transmitter is
not designed to be used during MRI tests.
WARNING
When performing MRI test, remove all electrodes from the patient
which are connected to this transmitter. Failure to follow this warning
may cause skin burn on the patient. For details, refer to the MRI
manual.
WARNING
When performing defibrillation, discharge as far as possible from
electrodes, patches and any gel, cream or medicine on the chest of
the patient. If there is a possibility that the defibrillator paddle could
touch these materials, remove them from the patient. If the
defibrillator paddle directly contacts these materials, the discharged
energy may cause skin burn to the patient.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 7
Page 17
WARNING
Before defibrillation, all persons must keep clear of the bed and must
not touch the patient or any equipment or cord connected to the
patient. Failure to follow this warning may cause electrical shock or
injury.
WARNING
When the transmitter is used with an electrosurgical unit (ESU),
firmly attach the entire area of the ESU return plate. Otherwise, the
current from the ESU flows into the electrodes of the transmitter,
causing electrical burn where the electrodes are attached. For
details, refer to the ESU manual.
WARNING
Close the battery case cover during operation. If the transmitter is
used with the battery case cover open, anyone who touches the
opened battery case may receive an electrical shock when
defibrillation is performed. Touching the opened battery case may
cause electrostatic discharge and intermittently interfere with the
waveform or data.
WARNING
If detergent or liquid spills into the transmitter, clean it and dry it
completely before use. If a wet transmitter is used, the patient or
operator may receive an electrical shock or injury.
WARNING
Do not use the same transmitter on more than one patient at the
same time. Do not connect different sensors on different patients to
the same transmitter.
8 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 18
CAUTION
Only use Nihon Kohden specified electrodes, electrode leads and
SpO2 probes. Otherwise, the maximum performance from the
transmitter cannot be guaranteed.
CAUTION
Do not reuse disposable parts and accessories.
CAUTION
Do not shake or swing the transmitter while holding the leads or
cables connected to the transmitter. The transmitter may come off
and injure someone or damage surrounding instruments.
CAUTION
Attach a strap to the transmitter to prevent the transmtiter from falling.
CAUTION
Turn off the power of mobile phones, small wireless devices and
other devices which produce strong electromagnetic interference
around a patient (except for devices allowed by the hospital
administrator). Radio waves from devices such as mobile phones or
small wireless devices may be mistaken as pulse waves and the
displayed data may be incorrect.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 9
Page 19
CAUTION
• Do not use the same channel for different patients. If the same
channel is used for two patients, the two patients’ data will be lost
due to mutual modulation interference, or another patient’s data
may appear on the receiving monitor screen.
• Do not use transmitters of adjacent channels in a hospital. If a
transmitter of an adjacent channel is used, radio waves from one
transmitter affect the receiver of the adjacent channel’s transmitter
and there may be interference.
Battery
WARNING
• Keep the batteries away from fire. They may explode.
• Keep the batteries away from patients.
• Never short-circuit the + and – terminals on the battery. It may
cause overheating and fire.
• Do not damage, disassemble, drop or give impact to the battery.
WARNING
If the battery is damaged and the substance inside the battery
contacts the eyes or skin, wash immediately and thoroughly with
water and see a physician. Never rub your eyes, because you may
lose your eyesight.
CAUTION
Battery replacement must be performed by the operator. When
replacing batteries of the transmitter currently used for a patient,
disconnect electrode leads from the transmitter before replacing
batteries or do not touch the patient during replacement.
10 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 20
CAUTION
The battery charger must be used outside the patient environment.
CAUTION
Refer to the battery and battery charger manuals for details on
handling the batteries.
Transmitter Channel Management
WARNING
The following actions must be taken to properly receive the
transmitter signal of the correct patient on the receiving instrument.
Otherwise, there may be signal loss or signals may mix causing a
serious accident, such as monitoring a different patient.
• Assign a channel administrator in the hospital and only he or she
should manage channel assignment.
• The channel administrator must manage the channels in the facility
so that there is no signal interference.
• When the transmitter channel is changed, the channel
administrator must check that the channel on the receiving monitor
is also changed and the signal is properly received.
• The channel administrator must replace the channel number label
on the transmitter with the new one after changing the channel.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 11
Page 21
For Patients Using Implantable Pacemaker
WARNING
Interaction Between Minute Ventilation Rate-Adaptive Pacemakers
and Cardiac Monitoring and Diagnostic Equipment
The bioelectric impedance measurement sensor of a minute
ventilation rate-adaptive implantable pacemaker may be affected by
transmitter which is connected to the same patient. If this occurs, the
pacemaker may pace at its maximum rate and the transmitter may
give incorrect data to the monitor. If this occurs, disconnect the
electrode leads from the patient or change the setting on the
pacemaker by referring to the pacemaker’s manual. For more details,
contact your pacemaker representative or Nihon Kohden
representative.
Output Signal
WARNING
Do not use the output signal from the receiving monitor as the
synchronization signal for other equipment such as IABP, MRI,
echocardiography or defibrillator. There may be time delay between
the monitor and the other equipment caused by waveform
transmission delay and spike noise may interfere on the output signal
and be mistaken as a trigger.
12 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 22
ECG Monitoring
CAUTION
Only use Nihon Kohden specified electrodes and electrode leads.
When other type of electrodes or electrode leads are used, the
“CHECK ELECTRODES” message may be displayed and monitoring
may stop.
CAUTION
When the “ELECTRODE OFF” or “CHECK ELECTRODE” message
is displayed on the receiving monitor, ECG is not monitored properly
and the ECG alarm does not function. Check the electrode, electrode
leads, and if necessary, replace with new ones.
SpO2 Monitoring
WARNING
SpO2 measurement may be incorrect in the following cases.
• When the patient’s carboxyhemoglobin or methemoglobin
increases abnormally.
• When dye is injected in the blood.
• When using an electrosurgical unit.
• During CPR.
• When measuring at a site with venous pulse.
• When there is body movement.
• When the pulse wave is small (insufficient peripheral circulation).
Operator’s Manual ZM-920PA/921PA/930PA/931PA 13
Page 23
WARNING
Check the circulation condition by observing the skin color at the
measurement site and pulse waveform. Change the measurement
site every 8 hours for disposable probes and every 4 hours for
reusable probes (every 8 hours for TL-630T/TL-631T series probe).
The skin temperature may increase at the attached site by 2 or 3°C
(4 or 5°F) and cause a burn or pressure necrosis. When using the
probe on the following patients, take extreme care and change the
measurement site more frequently according to symptoms and
degree.
• Patient with a fever
• Patient with peripheral circulation insufficiency
• Neonate or low birth weight infant with delicate skin
• Patient who is receiving photodynamic therapy*
* Photodynamic therapy is a treatment to remove the affected tissue by using a
photosensitizing agent and exposing the tissue to light. This treatment has a side
a burn. This probe uses two light wavelengths in the range from 650 to 950 nm.
The maximum light intensity is less than 5.5 mW/sr.
WARNING
When not monitoring SpO2, disconnect the SpO2 cable from the
transmitter. Otherwise, noise from the probe sensor may interfere and
incorrect data is displayed on the screen.
14 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 24
WARNING
• When using the TL-201T finger probe, do not fasten the probe and
cable to the finger by wrapping with tape. This may cause burn,
congestion or pressure necrosis from poor blood circulation.
• When using probes other than the TL-201T finger probe, to avoid
poor circulation, do not wrap the tape too tight. Check the blood
circulation condition by observing the skin color and congestion at
the skin peripheral to the probe attachment site. Even for shortterm monitoring, there may be burn or pressure necrosis from
poor blood circulation, especially on neonates or low birth weight
infants whose skin is delicate. Accurate measurement cannot be
performed on a site with poor peripheral circulation.
CAUTION
While a patient is on medication which causes vasodilation, the pulse
waveform may change and in rare cases the SpO2 value might not be
displayed.
CAUTION
Normal external light does not affect monitoring but strong light such
as a surgical light or sunlight may affect monitoring. If affected, cover
the measuring site with a blanket.
CAUTION
If the attachment site is dirty with blood or bodily fluids, clean the
attachment site before attaching the probe. If there is nail polish on
the attachment site, remove the polish. Otherwise, the amount of
transmitted light decreases, and measured value may be incorrect or
measurement cannot be performed.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 15
Page 25
CAUTION
Do not use a probe which is deteriorated by aging. Accurate
measurement cannot be performed.
CAUTION
Do not use a damaged or disassembled probe. It causes incorrect
measurement and may injure the patient.
CAUTION
The disposable probe is not sterilized. Use the disposable probe only
for a single patient. Never reuse the disposable probe for another
patient because it causes cross infection.
CAUTION
If the skin gets irritated or redness appears on the skin from the
probe, change the attachment site or stop using the probe. Take
extreme care for the patients with delicate skin.
CAUTION
Do not pull or bend the probe cable, and do not put caster feet on the
probe cable. Do not immerse the probe cable in chemical solutions or
water. Failure to follow these instructions may cause cable
discontinuity, short circuit, skin burn on the patient and incorrect
measurement data. Replace any broken probe with a new one.
CAUTION
When the probe is attached on an appropriate site with sufficient
circulation and the error message confirming the probe attachment
repeatedly appears, the probe may be deteriorated. Replace it with a
new one.
16 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 26
CAUTION
When a message indicates a faulty probe, stop monitoring and
replace the probe with a new one.
CAUTION
When any of the following conditions occurs, the probe may be
broken. Replace it with a new one.
• The transmitter generates “pip” sounds.
• SpO
data is 85% and blinking.
2
CAUTION
Neonatal skin is delicate. Remove the probe and tape carefully and
slowly.
CAUTION
When removing a probe that is taped to the skin, do not pull the
probe cable because this can damage the cable.
CAUTION
When removing the probe from the attachment tape, do not pull the
sensor cable because this can damage the cable.
CAUTION
Do not immerse the disposable probe in detergents or water. If the
probe adhesive surface gets wet, adhesiveness becomes weak and
the probe cannot be attached to the skin.
CAUTION
Refer to the probe instruction manual for details.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 17
Page 27
Maintenance
CAUTION
If detergent or liquid spills into the transmitter, clean it and dry it
completely before use. If a wet transmitter is used, the transmitter
may malfunction or get damaged.
CAUTION
Never disassemble or repair the transmitter. Disassembly and repair
must be performed by qualified service personnel.
CAUTION
Before cleaning or disinfection, remove the batteries from the
transmitter. Failure to follow this instruction may result in electrical
shock or transmitter malfunction.
CAUTION
The transmitter cannot be sterilized. Sterilizing the transmitter may
damage it.
18 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 28
Preparation
Installing (Replacing) Batteries
Use two AA(R6) type alkaline dry cell batteries, manganese dry cell batteries,
NiCd rechargeable batteries or NiMH batteries.
Battery Lifetime
With new alkaline batteries, the transmitter can continuously measure for the
following number of days. Operation time depends on the thickness of the SpO2
probe attachment site.
Transmitter
ZM-920PA/930PA3 days4 days
ZM-921PA/931PA2.5 days3.5 days
The capacity of manganese, NiCd and NiMH batteries is less than that of
alkaline batteries, therefore the lifetime of the battery is shorter.
TypeLifetime
ManganeseAbout 1/2 of alkaline batteries
NiCdAbout 1/3 of alkaline batteries (when fully charged)
NiMHAbout 1/2 of alkaline batteries (when fully charged)
Recommended Batteries
Alkaline primary: Nihon Kohden Medipower (equivalent to Panasonic LR6 (G))
Operating time (Measuring parameters)
ECG, Resp, SpO
NOTE
2
ECG, Resp
CAUTION
Battery replacement must be performed by the operator. When
replacing batteries of the transmitter currently used for a patient,
disconnect electrode leads from the transmitter before replacing
batteries or do not touch the patient during replacement.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 19
Page 29
If electrode leads are attached to the patient and the person replacing the batteries
touches the patient, the patient leakage current over the amount allowed may
occur.
CAUTION
• Replace all batteries at the same time.
• Do not use different types of batteries together.
NOTE
Insert the batteries with the correct polarity (+ and −).
Procedure
1. Open the battery case cover.
1
1
3
3
2
2
2. Insert two dry cell batteries (LR6) into
the battery case observing the correct
polarity.
3. Close the cover and press it gently
until it clicks.
WARNING and CAUTION for Battery Handling
WARNING
• Keep the batteries away from fire. They may explode.
• Keep the batteries away from patients.
• Never short-circuit the + and – terminals on the battery. It may
cause overheating and fire.
• Do not damage, disassemble, drop or give impact to the battery.
20 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 30
WARNING
If the battery is damaged and the substance inside the battery
contacts the eyes or skin, wash immediately and thoroughly with
water and see a physician. Never rub your eyes, because you may
lose your eyesight.
CAUTION
Do not handle the batteries with wet hands.
CAUTION
When the transmitter is not in use, remove batteries. When batteries
are installed, battery power is consumed even if measurement is not
performed. Especially, when NiMH batteries remain in the transmitter
when the transmitter is not in use, the battery may become unusable
from overdischarge and leak liquid which will damage the transmitter.
CAUTION
Refer to the battery and battery charger manuals for details on
handling the batteries.
CAUTION
The battery charger must be used outside the patient environment.
NOTE
• When using rechargeable NiCd batteries or NiMH batteries, shallow
charging/discharging shortens battery capacity. For details, refer to the
battery operator’s manual.
• Remove the batteries from the transmitter before disposing of the
transmitter.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 21
Page 31
Situations Requiring Battery Replacement
Replace the batteries when any of the following occurs.
• The “” LED lights (ZM-920PA/921PA) or the “” mark is displayed on
the LCD (ZM-930PA/931PA) on the transmitter.
• The transmitter generates a constant alarm (continuous “peep” sound).
• The monitor displays the battery replacement message on the screen.
• When the power of the LCD transmitter is turned on, no message or icon is
displayed. (Only the ZM-930PA/931PA).
CAUTION
When using batteries other than alkaline, the interval between the
battery replacement indication and battery discharge may be shorter.
Replace the batteries immediately upon battery replacement
indication.
Attaching a Strap to the Transmitter
To open the clip, firmly pull out the
tab in direction of the arrow.
CAUTION
Attach a strap to the transmitter to prevent the transmtiter from falling.
NOTE
Do not attach the clip to hard objects such as thick cloth or zippers, or the
clip may break.
Attach a strap to the transmitter and fasten the clip to the patients’ clothes or bed
sheets.
22 Operator’s Manual ZM-920PA/921PA/930PA/931PA
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If the transmitter falls off, the battery cover may be opened. If the patient touches
ON
OFFONOFF
the terminals of the batteries, patient leakage current over the allowable amount
can occur.
Turning On/Off the Transmitter
Check Items Before Turning On the Power
To use the instrument in a safe and optimum condition, before turning on the
transmitter power switch, check the following.
Appearance
• There is no damage or dirt on the outside of the transmitter. (Power switch,
LED, LCD, CALL key, junction, battery case cover, battery case, etc.)
• The transmitter is completely dry.
• The electrode lead is not broken.
• There is no damage or dirt on the SpO2 probe or on the disposable electrodes.
• The transmitter channel corresponds to those of the receiving monitor.
• The same channel is not being used on a different transmitter in the surrounding
area.
Turning On/Off the Power
To turn on the power, turn the power switch to the right.
After a “peep” sound for about one second, the power is
turned on.
(There is no “peep” sound when the “” LED light or
the “” are blinking on the LCD).
To turn off the power, turn the power switch to the left.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 23
Page 33
Check Items After Turning On the Power
After turning on the power, check the following items.
Power On
• The power switch is not damaged.
• The transmitter generates a “peep” sound for about one second.
• All LEDs light and values are displayed on the LCD for about one second.
• The transmitter does not generate a continuous “pip” sound.
• The transmitter does not liberate excessive heat.
• The “” LED does not light or the “” mark is not displayed on the LCD.
• The transmitter does not interfere with the operation of medical instruments
used near it.
Basic Operation
• The “signal loss” message is not displayed on the monitor when the transmitter
is inside the receiving range of the monitor.
• A “peep” sounds at the transmitter and “CALL” message appears at the
receiving monitor when the CALL key is pressed and the transmitter is inside
the receiving range of the monitor.
• The battery replacement message is not displayed on the monitor.
Check Items After the Power Off
• ECG electrode leads and SpO2 probe are cleaned and disinfected.
• When the transmitter gets wet, liquid is wiped off and the transmitter is
thoroughly dried.
• There are enough consumables, such as disposable electrodes.
• The power is turned off.
• The batteries are removed from the transmitter when it will not be used for a
long time.
• Dead batteries are disposed of properly.
24 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 34
ECG Monitoring
When 6 leads are used on this transmitter, up to 8 lead (I, II, III, aVR, aVL, aVF,
Va and Vb) of ECG waveforms can be displayed on the receiving monitor. The
heart rate is also measured. When 3 leads are used, one channel ECG waveform of
lead II can be displayed on the receiving monitor. Refer to the operator’s manual
of the monitor for details.
WARNING
Interaction Between Minute Ventilation Rate-Adaptive Pacemakers
and Cardiac Monitoring and Diagnostic Equipment*
The bioelectric impedance measurement sensor of a minute
ventilation rate-adaptive implantable pacemaker may be affected by
transmitter which is connected to the same patient. If this occurs, the
pacemaker may pace at its maximum rate and the transmitter may
give incorrect data to the monitor. If this occurs, disconnect the
electrode leads from the patient or change the setting on the
pacemaker by referring to the pacemaker’s manual. For more details,
contact your pacemaker representative or Nihon Kohden
representative.
* Minute ventilation is sensed in rate-adaptive pacemakers by a technology
known as bioelectric impedance measurement (BIM). Many medical devices in
addition to pacemakers use this technology. When one of these devices is used
on a patient with an active, minute ventilation rate-adaptive pacemaker, the
pacemaker may erroneously interpret the mixture of BIM signals created in the
patient, resulting in an elevated pacing rate.
For more information, see the FDA web site.
http://www.fda.gov/cdrh/safety.html
Operator’s Manual ZM-920PA/921PA/930PA/931PA 25
Page 35
WARNING
When the transmitter is used with an electrosurgical unit (ESU),
firmly attach the entire area of the ESU return plate. Otherwise, the
current from the ESU flows into the electrodes of the transmitter,
causing electrical burn where the electrodes are attached. For
details, refer to the ESU manual.
NOTE
• This transmitter is not protected against noise generated from an
electrosurgical unit.
• If an electric blanket is used and incorrect heart rate is displayed on the
monitor, turn off the pacing pulse detection on the monitor.
ECG Measurement Procedure
1. Select the type of electrode lead and disposable electrode according to the
purpose.
2. Connect the electrode lead to the ECG/RESP socket.
3. Connect disposable electrodes to the electrode lead and attach electrodes to
Only use Nihon Kohden specified electrodes and electrode leads.
When other type of electrodes or electrode leads are used, the
“CHECK ELECTRODES” message may be displayed and monitoring
may stop.
Option
Electrode lead
BR-916PA
BR-906PA
6 electrodes, snap type
BR-913PA
3 electrodes, snap type
Operator’s Manual ZM-920PA/921PA/930PA/931PA 27
6 electrodes, clip type
BR-903PA
3 electrodes, clip type
Page 37
Connecting the Electrode Lead to the Transmitter
Connect the electrode lead to the ECG/RESP socket on the transmitter.
CAUTION
Do not shake or swing the transmitter while holding the leads or
cables connected to the transmitter. The transmitter may come off
and injure someone or damage surrounding instruments.
CAUTION
Hold the connector of the electrode lead when connecting/
disconnecting the electrode lead. If you disconnect the electrode lead
by pulling the lead, it damages the electrode lead.
Selecting the Electrode Position
Follow the physician’s instructions for electrode placement when available.
For ECG monitoring, electrodes are attached only on the chest to allow patient
movement and obtain continuous stable ECG. Following leads are examples.
When also monitoring respiration, refer to the “Electrode Position for Respiration
Monitoring” section.
NOTE
The optimum electrode positions for ECG measurement of a patient
are not always optimum for respiration measurement of the patient.
Select positions suitable for both ECG and respiration measurements, or
positions which have priority for one measurement.
28 Operator’s Manual ZM-920PA/921PA/930PA/931PA
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Six Electrodes
RA
LA
N (RL)
LL
Va
Vb
Electrode Position
The 6-electrode method with lead II and lead V5 is effective for monitoring
myocardial ischemia. You can improve monitoring accuracy considerably by
adding lead V4 to this combination. Va and Vb can be at any position of the
standard 12 leads V1 to V6, but V4 and V5 are most appropriate for myocardial
ischemic monitoring.
SymbolLead Color (Clip Color)Electrode Position
RAWhite (White)Right infraclavicular fossa
LABlack (Black)Left infraclavicular fossa
Lowest rib on the left anterior
axillary line
Right anterior axillary line at the
same level as LL
Fifth intercostal space on the left
midclavicular line. (V4 position of
standard 12 leads)
Left anterior axillary line at the
same level as Va. (V5 position of
standard 12 leads)
LLRed (Red)
N (RL)Green (Green)
Va
Vb
Brown (Brown) (BR-906PA)
Brown-blue (BR-916PA)
Brown (Brown) (BR-906PA)
Brown-orange (BR-916PA)
Operator’s Manual ZM-920PA/921PA/930PA/931PA 29
Page 39
Lead Position
Standard limb leads
Monopolar limb leads
Monopolar chest leads
Lead I
Lead I
Lead IILead III
aVR leadaVL leadaVF lead
V1 to V6 leads
V1 to V6 leads
to
RA
RA
RA
RA
RA
RA
RA
LA
LA
LA
LA
LA
LA
LA
LL
LL
LL
LL
LL
LL
LL
N (RL)
N (RL)
N (RL)
N (RL)
N (RL)
N (RL)
N (RL)
ON
RALALL
Va
Vb
USAch
E002
1395.0250 MHz
ON
RALALL
Va
Vb
USAch
E002
1395.0250 MHz
When Using 4 to 6 DIN Type Leads to Monitor 6 Lead ECG
When the BR-906PA/916PA electrode
leadsarenotused,thetransmitterisxed
to 3 lead ECG monitoring. To monitor 6
lead ECG using 4 to 6 DIN type leads,
power, press and hold the CALL key and
turn on the transmitter power.
When the transmitter power is turned off
and on again, the monitoring mode returns
to the original mode.
30 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 40
Three Electrodes
By using the optional BR-913PA/903PA electrode lead, 3 lead ECG monitoring is
available.
Electrode Position
• Lead MII, which is similar to standard lead II, used when ECG measurement
has priority
Electrode PositionSymbol Lead Color
Left infraclavicular fossaLA (N)Black
Right infraclavicular fossa
Below lowest rib on the
left anterior axillary line
RA (−)
LL (+)Red
White
• Lead MI, which is similar to standard
lead I
Change LL and LA of the lead MII.
• Lead MIII, which is similar to
standard lead III
Change RA and LA of the lead MII.
If the electrode position shown above is not available due to chest surgery, attach
the electrodes to the root of the limbs or below the clavicles for stable ECG
monitoring.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 31
Page 41
Connecting the Electrode Lead and Disposable
Electrodes
Preparing the Patient Skin
Shave off excessive body hair.
To reduce skin impedance, clean the electrode site with cream or with a cotton pad
moistened with the electrode site with cream or with a cotton pad moistened with
alcohol. Thoroughly dry the skin with a clean cotton pad.
NOTE
• For a patient with frequent body movement, rub the sites with Skinpure
skin preparation gel. However, do not use Skinpure skin preparation gel
for sensitive skin.
• Do not place electrodes on a wound or on an inflamed, wrinkled or
uneven skin surface.
Attaching Electrodes to the Patient
CAUTION
Do not reuse disposable parts and accessories.
NOTE
• To maintain good contact between the electrode and skin, check that the
paste of the disposable electrode is not dry.
• When contact between the disposable electrode and skin becomes
poor, replace electrodes with new ones immediately. Otherwise, contact
impedance between the skin and the electrode increases and the
correct ECG cannot be obtained.
Refer to the electrode operator’s manual for details.
1. Connect the electrode lead to the electrode.
32 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 42
2. Carefully remove the backing paper from
the electrode. Avoid touching the adhesive
surface.
3. Place the electrode on the previously
cleaned skin. Pay attention to the electrode
lead color and symbol.
4. Fasten the electrode lead wire with surgical
tape with an extra length of wire between
the tape and the electrode. This lessens
the movement of electrode leads by body
movement and helps stable monitoring.
Detection and Display of Measurement Condition
Electrode Detachment
The “ ” LED lights on the transmitter or the “CHECK ELECTRODE” message
is displayed on the screen of the monitor in the following cases.
• Electrode is detached from skin.
• Electrode lead is disconnected from the electrode.
• Polarization voltage between the electrode and skin is excessively high.
In these cases, check the cause and if necessary, replace electrodes with new ones.
CAUTION
When the “ELECTRODE OFF” or “CHECK ELECTRODE” message
is displayed on the receiving monitor, ECG is not monitored properly
and the ECG alarm does not function. Check the electrode, electrode
leads, and if necessary, replace with new ones.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 33
Page 43
Respiration Monitoring
Respiration is monitored by measuring changes in impedance between the RA
and LL ECG electrodes. This transmitter sends the changes in impedance to the
monitor as a respiration waveform. The monitor displays the respiration waveform
and calculates respiration rate. Refer to the operator’s manual of the monitor for
details.
WARNING
Interaction Between Minute Ventilation Rate-Adaptive Pacemakers
and Cardiac Monitoring and Diagnostic Equipment*
The bioelectric impedance measurement sensor of a minute
ventilation rate-adaptive implantable pacemaker may be affected by
transmitter which is connected to the same patient. If this occurs, the
pacemaker may pace at its maximum rate and the transmitter may
give incorrect data to the monitor. If this occurs, disconnect the
electrode leads from the patient or change the setting on the
pacemaker by referring to the pacemaker’s manual. For more details,
contact your pacemaker representative or Nihon Kohden
representative.
* Minute ventilation is sensed in rate-adaptive pacemakers by a technology
known as bioelectric impedance measurement (BIM). Many medical devices
in addition to pacemakers use this technology. When one of these devices is
used on a patient with an active, minute ventilation rate-adaptive pacemaker,
thepacemaker may erroneously interpret the mixture of BIM signals created in
the patient, resulting in an elevated pacing rate.
For more information, see the FDA web site.
http://www.fda.gov/cdrh/safety.html
34 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 44
Respiration Measurement Procedure
1. Select the electrode lead and disposable electrodes.
2. Connect the electrode lead to the ECG/RESP socket.
3. Connect disposable electrodes to the electrode lead and attach electrodes to
the patient.
Place the RA and LL electrodes so that the lungs are between the electrodes.
NOTE
The optimum electrode positions for ECG measurement of a patient
are not always optimum for respiration measurement of the patient.
Select positions suitable for both ECG and respiration measurements, or
positions which have priority for one measurement.
Electrode Position Examples
NOTE
The following examples are when monitoring with 3 electrodes. ECG
cannot be monitored correctly when electrodes are attached as the
following examples when monitoring with 6 electrodes.
Position 1
In this position, respiration measurement is available; however, there is a
difference in amplitude between different patients.
RALL
Right infraclavicular
fossa
Operator’s Manual ZM-920PA/921PA/930PA/931PA 35
Fifth intercostal space on the
left midclavicular line, V4
Page 45
Position 2
In this position, the waveform amplitude is usually large and the ECG lead is
similar to Lead MII. This position can be generally recommended.
RALL
Right infraclavicular
fossa
Fifth intercostal space on the
left midaxillary line, V6
Position 3
In this position, the respiration waveform is optimum, but the ECG lead is
unusual.
RALL
Right midaxillary at the
horizontal level of V4
Fifth intercostal space on the
left midaxillary line, V6
variation of the abdomen, so the cardiac pulse wave included in the respiration
wave is reduced. Note that the waveform is inverted in phase compared with the
The SpO2 monitoring is only available on the ZM-930PA/931PA transmitter.
This transmitter sends SpO2 and pulse waveform to the monitor and displays SpO2
data and pulse level bar graph on the LCD.
Refer to the operator’s manual of the monitor for details.
WARNING
SpO2 measurement may be incorrect in the following cases.
• When the patient’s carboxyhemoglobin or methemoglobin
increases abnormally.
• When dye is injected in the blood.
• When using an electrosurgical unit.
• During CPR.
• When measuring at a site with venous pulse.
• When there is body movement.
• When the pulse wave is small (insufficient peripheral circulation).
WARNING
When not monitoring SpO2, disconnect the SpO2 cable from the
transmitter. Otherwise, noise from the probe sensor may interfere and
incorrect data is displayed on the screen.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 37
Page 47
WARNING
Check the circulation condition by observing the skin color at the
measurement site and pulse waveform. Change the measurement
site every 8 hours for disposable probes and every 4 hours for
reusable probes (every 8 hours for TL-630T/TL-631T series probe).
The skin temperature may increase at the attached site by 2 or 3°C
(4 or 5°F) and cause a burn or pressure necrosis. When using the
probe on the following patients, take extreme care and change the
measurement site more frequently according to symptoms and
degree.
• Patient with a fever
• Patient with peripheral circulation insufficiency
• Neonate or low birth weight infant with delicate skin
• Patient who is receiving photodynamic therapy*
* Photodynamic therapy is a treatment to remove the affected tissue by using a
photosensitizing agent and exposing the tissue to light. This treatment has a side
a burn. This probe uses two light wavelengths in the range from 650 to 950 nm.
The maximum light intensity is less than 5.5 mW/sr.
CAUTION
Turn off the power of mobile phones, small wireless devices and
other devices which produce strong electromagnetic interference
around a patient (except for devices allowed by the hospital
administrator). Radio waves from devices such as mobile phones or
small wireless devices may be mistaken as pulse waves and the
displayed data may be incorrect.
CAUTION
Normal external light does not affect monitoring but strong light such
as a surgical light or sunlight may affect monitoring. If affected, cover
the measuring site with a blanket.
38 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 48
CAUTION
Do not pull or bend the probe cable, and do not put caster feet on the
probe cable. Do not immerse the probe cable in chemical solutions or
water. Failure to follow these instructions may cause cable
discontinuity, short circuit, skin burn on the patient and incorrect
measurement data. Replace any broken probe with a new one.
CAUTION
When the probe is attached on an appropriate site with sufficient
circulation and the error message confirming the probe attachment
repeatedly appears, the probe may be deteriorated. Replace it with a
new one.
CAUTION
While a patient is on medication which causes vasodilation, the pulse
waveform may change and in rare cases the SpO2 value might not be
displayed.
NOTE
ZM-930PA only
When monitoring SpO2, monitor ECG at the same time. The ECG
electrode lead works as an antenna for transmitting data from the
transmitter to the receiving monitor. If ECG is not measured, the telemetry
signal may not be received.
Only use Nihon Kohden specified electrodes, electrode leads and
SpO2 probes. Otherwise, the maximum performance from the
transmitter cannot be guaranteed.
CAUTION
Do not use a damaged or disassembled probe. It causes incorrect
measurement and may injure the patient.
Cable length:
TL-630T1/631T1: 60 cm
TL-630T3/631T3: 160 cm
Operator’s Manual ZM-920PA/921PA/930PA/931PA 41
Page 51
Disposable Probes
CAUTION
The disposable probe is not sterilized. Use the disposable probe only
for a single patient. Never reuse the disposable probe for another
patient because it causes cross infection.
ModelSubject (Weight)Attachment Site
TL-251TAdult
(30 kg or more)
Finger or toe
TL-252TChild
(3 to 40 kg)
TL-253T
TL-051S/052S
Cable length TL-051S: 80 cm
TL-052S: 160 cm
42 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Neonate
(3 kg or less)
Adult
(50 kg or more)
Neonate
(3 kg or less)
Finger or toe
Instep and sole
Finger
Instep and sole
Page 52
TL-061S/062S
ModelSubject (Weight)Attachment Site
Adult, child
Finger
(15 to 50 kg)
Cable length TL-061S: 80 cm
TL-062S: 160 cm
TL-271T/271T3
Cable length TL-271T: 80 cm
TL-271T3: 160 cm
TL-272T/272T3
Cable length TL-272T: 80 cm
TL-272T3: 160 cm
TL-273T/273T3
Child, infant
(3 to 15 kg)
Adult
(30 kg or more)
Child
(10 to 50 kg)
Neonate
(3 kg or less)
Toe
Finger or toe
Instep and sole
Adult
Finger or toe
(40 kg or more)
Cable length TL-273T: 80 cm
TL-273T3: 160 cm
Operator’s Manual ZM-920PA/921PA/930PA/931PA 43
Page 53
ModelSubject (Weight)Attachment Site
TL-274T/274T3
Cable length TL-274T: 80 m
TL-274T3: 160 cm
Infant
(3 to 20 kg)
Finger or toe
Connecting SpO2 Probe to the Transmitter
Connect the probe to the SpO2 socket on the transmitter.
CAUTION
Do not shake or swing the transmitter while holding the leads or
cables connected to the transmitter. The transmitter may come off
and injure someone or damage surrounding instruments.
CAUTION
Hold the connector when connecting/disconnecting the SpO2 probe.
If you disconnect the SpO2 probe by pulling the cable, it damages the
cable.
44 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 54
Attaching the Probe to the Patient
For details, refer to the operator’s manual of each probe.
WARNING
• When using the TL-201T finger probe, do not fasten the probe and
cable to the finger by wrapping with tape. This may cause burn,
congestion or pressure necrosis from poor blood circulation.
• When using probes other than the TL-201T finger probe, to avoid
poor circulation, do not wrap the tape too tight. Check the blood
circulation condition by observing the skin color and congestion at
the skin peripheral to the probe attachment site. Even for shortterm monitoring, there may be burn or pressure necrosis from
poor blood circulation, especially on neonates or low birth weight
infants whose skin is delicate. Accurate measurement cannot be
performed on a site with poor peripheral circulation.
WARNING
Check the circulation condition by observing the skin color at the
measurement site and pulse waveform. Change the measurement
site every 8 hours for disposable probes and every 4 hours for
reusable probes (every 8 hours for TL-630T/TL-631T series probe).
The skin temperature may increase at the attached site by 2 or 3°C
(4 or 5°F) and cause a burn or pressure necrosis. When using the
probe on the following patients, take extreme care and change the
measurement site more frequently according to symptoms and
degree.
• Patient with a fever
• Patient with peripheral circulation insufficiency
• Neonate or low birth weight infant with delicate skin
• Patient who is receiving photodynamic therapy*
* Photodynamic therapy is a treatment to remove the affected tissue by using a
photosensitizing agent and exposing the tissue to light. This treatment has a side effect of
uses two light wavelengths in the range from 650 to 950 nm. The maximum light intensity
is less than 5.5 mW/sr.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 45
Page 55
CAUTION
If the attachment site is dirty with blood or bodily fluids, clean the
attachment site before attaching the probe. If there is nail polish on
the attachment site, remove the polish. Otherwise, the amount of
transmitted light decreases, and measured value may be incorrect or
measurement cannot be performed.
CAUTION
If the skin gets irritated or redness appears on the skin from the
probe, change the attachment site or stop using the probe. Take
extreme care for the patients with delicate skin.
CAUTION
When the probe is attached on an appropriate site with sufficient
circulation and the error message confirming the probe attachment
repeatedly appears, the probe may be deteriorated. Replace it with a
new one.
CAUTION
Do not use a probe which is deteriorated by aging. Accurate
measurement cannot be performed.
CAUTION
Neonatal skin is delicate. Remove the probe and tape carefully and
slowly.
CAUTION
When removing a probe that is taped to the skin, do not pull the
probe cable because this can damage the cable.
46 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 56
CAUTION
When removing the probe from the attachment tape, do not pull the
sensor cable because this can damage the cable.
CAUTION
Do not immerse the disposable probe in detergents or water. If the
probe adhesive surface gets wet, adhesiveness becomes weak and
the probe cannot be attached to the skin.
CAUTION
Refer to the probe instruction manual for details.
Starting Measurement
When monitoring starts, SpO2 and pulse waveform are sent to the monitors and
SpO2 data and pulse level bar graph are displayed on the transmitter LCD.
You can turn off the display of SpO2 data and pulse level bar graph on the LCD.
Refer to the “Turning SpO2 Data and Pulse Level Bar Graph Display On/Off”
section.
CAUTION
When the probe is attached on an appropriate site with sufficient
circulation and the error message confirming the probe attachment
repeatedly appears, the probe may be deteriorated. Replace it with a
new one.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 47
Page 57
Turning SpO2 Data and Pulse Level Bar Graph
RALALL
Va
Vb
USAch
E002
1395.025 MHz
RALALL
Va
Vb
USAch
E002
1395.025 MHz
Display On/Off
You can turn off the display of SpO2 data and pulse level bar graph on the LCD.
SpO2 display off
SpO2 display off
CALL key
CALL key
Press the CALL key for more than 3
seconds within 10 seconds after turning
transmitter power on (after a “peep”
sound).
“%SpO2” is not displayed. When SpO2
monitoring starts, SpO2 data and pulse
level bar graph are not displayed on the
LCD.
To turn SpO2 display on, turn the
transmitter power off and turn the power
on again.
48 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 58
Detecting and Displaying Measurement Condition
External Light Noise Alarm
CAUTION
Normal external light does not affect monitoring but strong light such
as a surgical light or sunlight may affect monitoring. If affected, cover
the measuring site with a blanket.
affect SpO2 monitoring. When external light is too strong to correctly measure
SpO2, the transmitter generates an alarm tone (“pip” sound every 0.5 seconds).
Cover the probe attachment site with blanket or cloth.
transmitter generates the following sound and indication.
(4)
(4)
(1) “peep” sound (every 1 second)
(2) pulse level bar graph is maximum
(all bars are lit.)
(3) SpO2 data is displayed as “”
(4) %SpO2 is blinking.
In this case, change the attachment site to the appropriate site. Refer to the
operator’s manual of the SpO2 probe.
Probe Malfunction Alarm
(3)
(3)
(2)
(2)
CAUTION
When any of the following conditions occurs, the probe may be
broken. Replace it with a new one.
• The transmitter generates “pip” sounds.
• SpO
data is 85% and blinking.
2
Operator’s Manual ZM-920PA/921PA/930PA/931PA 49
Page 59
When Measurement Condition is Unstable
SpO2 data blinks every 1 second when SpO2 signal stability decreases and
the transmitter cannot detect correct pulse waveform because of patient body
movement, poor attachment condition or poor circulation condition at the probe
attachment site.
CAUTION
SpO2 data blinking every second indicates an unstable pulse
waveform and displayed SpO2 value may be inaccurate. The
displayed data might not reflect sudden SpO2 changes.
50 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 60
Alarm List
RA
LA
LL
Va
Vb
(1)
Displayed as LED on
ZM-920PA/921PA
%SpO2 indication
(5)
pulse level bar graph
(4)
(2)
SpO2 data
(3)
SoundDisplayCauseCountermeasure
Single “peep”
sound
---The CALL key is pressed. The sound lasts while
the key is pressed.
for 4 s
---(1)The battery voltage
decreases and battery
Replace the batteries
with new ones.
charge is almost zero.
Continuous
“peep” sound
All lights are offBattery is completely
discharged.
Replace the batteries
with new ones. To
stop the sound, turn
off the power.
---(2)Electrode lead is
disconnected from the
electrode.
Electrode lead is
disconnected from the
transmitter.
Electrode lead
discontinuity
Electrodeisnotrmly
attached to the skin.
Firmly connect the
electrode lead to the
electrode.
Firmly connect the
electrode lead to the
transmitter.
Replace the electrode
lead with a new one.
Replace the electrode
with a new one.
Polarization voltage is
abnormally high.
Intermittent
“pip” sound
every 0.5 s
---SpO2 measurement site
isunderuorescent
light, surgical light,
sunlight, etc.
Cover the
measurement site
with a blanket or
cloth.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 51
Page 61
SoundDisplayCauseCountermeasure
Intermittent
“peep” sound
every 1 s
(3)
(4) all lit
(5) blinking
Cannot receive
sufcientlightfromthe
probe photo emitter.
Attach probe to a
site with 6 to 14
mm thickness where
sufcientlightcanbe
received.
Intermittent
“pip” sound
(3) 85%, blinking Broken probeReplace the probe
with a new one.
every 0.25 s
---(3) blinkingPatient body movement Remove the cause
by checking the
patient condition
and changing the
attachment site.
Probe is not attached
securely.
Securely attach the
probe.
52 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 62
Troubleshooting
If the problem still remains after checking the following, contact your Nihon
Kohden representative.
ProblemCauseCountermeasure
The power cannot be
turned on.
Nothing is displayed on
the LCD after turning the
power on. (ZM-930PA/
931PA only)
Nothing is displayed on
the monitor after turning
the transmitter power on.
Signal receiving condition
is poor.
Batteries are not
installed correctly.
The battery polarity is
wrong.
Batteries are
completely
discharged.
SpO2 display is turned
off.
The channel of the
transmitter and
monitor does not
match.
Electrode lead is
not connected to the
transmitter.
Another transmitter
of the same channel is
used near by.
Signals are mixing.Follow the instruction of your
The transmitter is
damaged.
Install the batteries correctly.
Replace the batteries with new ones.
Turn off the power, and turn on the
power again.
Set the correct channel on the
monitor.
Connect the electrode lead to the
transmitter. ECG electrode lead works
as an antenna for transmitting data
to the receiving monitor. If ECG is
not measured, the signal may not be
received.
Turn the transmitter power off. If the
monitor still receives a signal, there
is a high probability that another
transmitter of the same channel is
used nearby.
Follow the instruction of your
channel administrator and use another
transmitter of a different channel.
channel administrator and use another
transmitter of a different channel.
Contact your Nihon Kohden
representative.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 53
Page 63
ProblemCauseCountermeasure
3 electrode leads are
properly attached to the
patient but LEDs light.
Heart rate of the rate of the
patient who is using an
electric blanket cannot
be monitored on the
receiving monitor.
ECG baseline is thick.
(Hum is overlapping)
Respiration waveform
measurement is unstable.
SpO2 data is unstable and
not reliable.
The transmitter
isxedto6lead
monitoring.
Pacing pulse detection
is set to ON on the
monitor.
The gel on the
electrode is dried out.
The gel on the
electrode is coming
off.
Electric blanket is
used.
Humlterissetto
OFF on the monitor
The gel on the
electrode is dried out.
The gel on the
electrode is coming
off.
The probe size is not
appropriate for the
patient.
Probe is attached to
the same limb that
is used for NIBP
measurement.
Probe attachment
condition is poor.
Probe is about to
detach from the skin.
External light gets in.
Measurement site
is dirty. Patient is
wearing nail polish.
Turn off and on the transmitter power.
Turn off the pacing pulse detection.
Replace the electrode with a new one.
Cover the blanket with a shield cover.
SettheltertoON.
Replace the electrode with a new one.
Use the appropriate probe for the
patient.
Attach the probe to the opposite limb.
Avoid a site where blood circulation
condition changes greatly.
Firmly attach the probe according to
the procedure in the probe operator’s’ss
manual.
Remove dirt and nail polish.
54 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 64
Changing the Transmitter Channel
The transmitter channel can be changed by the QI-901PK Channel Writer. To
change the channel number, refer to the channel writer manual.
WARNING
The following actions must be taken to properly receive the
transmitter signal of the correct patient on the receiving instrument.
Otherwise, there may be signal loss or signals may mix causing a
serious accident, such as monitoring a different patient.
• Assign a channel administrator in the hospital and only he or she
should manage channel assignment.
• The channel administrator must manage the channels in the facility
so that there is no signal interference.
• When the transmitter channel is changed, the channel
administrator must check that the channel on the receiving monitor
is also changed and the signal is properly received.
• The channel administrator must replace the channel number label
on the transmitter with the new one after changing the channel.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 55
Page 65
Lifetime and Disposal
Disposing of Used Batteries
Replacement
When the “” LED is lit or the “” is displayed on the LCD during operation,
the batteries are running out.
Replace the batteries with new ones. When using rechargeable batteries, recharge
them.
for details in your area for proper disposal. It may be illegal to dispose of these
batteries in the municipal waste stream.
Disposing of Electrodes and SpO2 Probes
Refer to the manual of each item.
56 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 66
Cleaning, Disinfection and Sterilization
Transmitter and Electrode Lead
CAUTION
If detergent or liquid spills into the transmitter, clean it and dry it
completely before use. If a wet transmitter is used, the transmitter
may malfunction or get damaged.
CAUTION
Before cleaning or disinfection, remove the batteries from the
transmitter. Failure to follow this instruction may result in electrical
shock or transmitter malfunction.
CAUTION
The transmitter cannot be sterilized. Sterilizing the transmitter may
damage it.
CAUTION
Dispose of the transmitter, options and accessories as specified by
Nihon Kohden. Otherwise, it causes infection or environmental
contamination.
Before cleaning or disinfecting, remove the batteries from the transmitter. Be
careful not to let any liquid get inside the transmitter.
Cleaning
Wipe the transmitter and electrode leads with a soft cloth moistened with
disinfecting alcohol or neutral detergent diluted with water. After cleaning, dry
them completely.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 57
Page 67
Disinfection
CAUTION
• Do not immerse the electrode lead connector in liquid.
• Do not disinfect with hypochlorous acid.
• Use the recommended concentration.
Wipe the outside surface of the transmitter and electrode lead with a non-abrasive
cloth moistened with any of the disinfectants listed on the next page. Use the
recommended concentration.
When the battery case cover is damaged, replace it with a new one.
Battery case cover, code no. 6113-046365C.
Other than the battery case cover, there are no serviceable parts for the transmitter.
Repair Parts Availability Policy
Nihon Kohden Corporation (NKC) shall stock repair parts (parts necessary
to maintain the performance of the instrument) for a period of 6 years after
NKC announces discontinuation of the instrument. In that period, NKC or its
distributors will repair the instrument. This period may be shorter than 6 years if
the necessary board or part is not available. For discontinuation announcements,
contact your Nihon Kohden distributor or representative.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 59
Page 69
Specifications
ZM-920PA/930PA
ECG measurement
Channels: 4
Input range: ±5 mV or more
DC offset: ±500 mV or more
Inputimpedance:5MΩormore(5Hz)
Pacing pulse detection: ANSI/AAMI EC13
Based upon Pacemaker pulse rejection Capability
Respiration measurement
Measuring method: Impedance method
Impedancerange:0to2kΩ
SpO2 measurement
Measuring range: 0 to 100%, in 1% steps
Measuring accuracy
When the measuring accuracy of the SpO2 probe is not considered:
Antenna: ECG electrode lead
Transmission channel: Indicated on the transmitter
Transmission frequency range: 608.0250 to 613.9750 MHz
Channel spacing: 50 kHz or 37.5 kHz (12.5 kHz when interleaved)
Modulation scheme: FSK (Frequency Shift Keying)
Occupied bandwidth: <20 kHz
Effective radiated power: 1.0 mW (conducted)
Safety standards
Safety standard: CSA C22.2 No. 601-1 M90: 1994
IEC 60601-1: 1988
IEC 60601-1 Amendment 1: 1991
IEC 60601-1 Amendment 2: 1995
IEC 60601-1-2: 1993
IEC 60601-2-27: 1994
According to the type of protection against electrical shock:
INTERNALLY POWERED EQUIPMENT
According to the degree of protection against electrical shock:
ECG/impedance method respiration: DEFIBRILLATION-PROOF
TYPE CF APPLIED PART
SpO2: DEFIBRILLATION-PROOF
TYPE BF APPLIED PART
According to the degree of protection against harmful ingress of water:
IPX0 (Ordinary equipment)
According to the degree of safety of application in the presence of a
FLAMMABLE ANAESTHETIC MIXTURE WITH AIR, OR WITH OXYGEN
OR NITROUS OXIDE: Equipment not suitable for use in the presence of
FLAMMABLE ANAESTHETIC MIXTURE
WITH AIR, OR WITH OXYGEN OR NITROUS
OXIDE
According to the mode of operation: CONTINUOUS OPERATION
Water resistance
Water does not get inside the transmitter except for the battery case when
immersed in water up to 30 cm deep for 3 minutes.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 61
Page 71
Power requirements
Battery type: two AA type alkaline dry cell batteries,
manganese dry cell batteries, NiCd rechargeable
batteries, NiMH batteries
Battery lifetime:
ZM-930PA: approximately 3 days
(with alkaline batteries, measuring ECG,
respiration and SpO2 of approximately 60 kg
weightadultmalepatientatthepointingnger)
approximately 4 days
(with alkaline batteries, measuring ECG and
respiration only)
ZM-920PA: approximately 4 days
Environment
Operating environment
Operating temperature: 5 to 40°C, 41 to 104°F
Operating humidity: 30 to 85% (non-condensing)
Operating atmospheric pressure: 70 to 106 kPa
Operating voltage: 1.6 to 3.2 V
Storage environment
Storagetemperature:−20to65°C,−4to149°F
Storage humidity: 15 to 95%
Storage atmospheric pressure: 70 to 106 kPa
Dimension and Weight
Dimension: 78 W × 122 H × 26 D (mm)
Weight (without batteries): ZM-930PA: about 180 g
ZM-920PA: about 165 g
62 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 72
ZM-921PA/931PA
ECG Measurement
Channels: 4
Input range: ±5 mV or more
DC offset: ±500 mV or more
Inputimpedance:5MΩormore(5Hz)
Pacing pulse detection: ANSI/AAMI EC13
Based upon Pacemaker pulse rejection Capability
Respiration Measurement
Measuring method: Impedance method
Impedancerange:0to2kΩ
SpO2 Measurement
Measuring range: 0 to 100%, in 1% steps
Measuring accuracy
When the measuring accuracy of the SpO2 probe is not considered:
Antenna: Internal
Transmission channel: indicated on the transmitter
Transmission frequency range: 1395.0250 to 1399.9750 MHz
1427.0250 to 1431.9750 MHz
Operator’s Manual ZM-920PA/921PA/930PA/931PA 63
Page 73
Channel spacing: 50 kHz or 37.5 kHz (12.5 kHz when interleaved)
Modulation scheme: FSK (Frequency Shift Keying)
Occupied bandwidth: <20 kHz
Effective radiated power: 5.0 mW (factory default setting)
Can be changed to 1.0 mW if required
Safety Standards
Safety standard: CAN/CSA-C22.2 No. 601-1 M90: 1990
CAN/CSA-C22.2 No. 601-1. 1S1-94: 1994
CAN/CSA-C22.2 No. 601-1. 1B-90: R2002
CAN/CSA-C22.2 No. 60601-2-49-04: 2004
CAN/CSA-C22.2 No. 601.2.27-98: 1998
IEC 60601-1: 1988
IEC 60601-1 Amendment 1: 1991
IEC 60601-1 Amendment 2: 1995
IEC 60601-1-2: 2001
IEC 60601-1-2 Amendment 1: 2004
IEC 60601-2-27: 2005
IEC 60601-2-49: 2001
ISO 9919: 2005
According to the type of protection against electrical shock:
INTERNALLY POWERED EQUIPMENT
According to the degree of protection against electrical shock:
ECG/impedance method respiration: DEFIBRILLATION-PROOF
TYPE CF APPLIED PART
SpO2: DEFIBRILLATION-PROOF
TYPE BF APPLIED PART
According to the degree of protection against harmful ingress of water:
IPX0 (Ordinary equipment)
According to the degree of safety of application in the presence of a
FLAMMABLE ANAESTHETIC MIXTURE WITH AIR, OR WITH OXYGEN
OR NITROUS OXIDE: Equipment not suitable for use in the presence of
FLAMMABLE ANAESTHETIC MIXTURE
WITH AIR, OR WITH OXYGEN OR NITROUS
OXIDE
According to the mode of operation: CONTINUOUS OPERATION
64 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 74
Water Resistance
Water does not get inside the transmitter except for the battery case when
immersed in water up to 30 cm deep for 3 minutes.
Power Requirements
Battery type: two AA type alkaline dry cell batteries,
manganese dry cell batteries, NiCd rechargeable
batteries, NiMH batteries
Battery lifetime:
ZM-931PA: approximately 2.5 days
(with alkaline batteries, measuring ECG,
respiration and SpO2 of approximately 60 kg
weightadultmalepatientatthepointingnger)
approximately 3.5 days
(with alkaline batteries, measuring ECG and
respiration only)
ZM-921PA: approximately 3.5 days
Environment
Operating environment
Operating temperature: 5 to 40°C, 41 to 104°F
Operating humidity: 30 to 85% (non-condensing)
Operating atmospheric pressure: 70 to 106 kPa
Operating voltage: 1.6 to 3.2 V
Storage environment
Storagetemperature:−20to65°C,−4to149°F
Storage humidity: 15 to 95%
Storage atmospheric pressure: 70 to 106 kPa
Dimension and Weight
Dimension: 78 W × 122 H × 26 D (mm)
Weight (without batteries): ZM-931PA: about 190 g
ZM-921PA: about 170 g
Group 1roup 1oup 1The ZM-921PA/931PA uses RF energy onlyZM-921PA/931PA uses RF energy only uses RF energy only
Class Blass BThe ZM-921PA/931PA is suitable for usee ZM-921PA/931PA is suitable for use ZM-921PA/931PA is suitable for useZM-921PA/931PA is suitable for use is suitable for usele for usee for use
Not
applicable
Not
applicable
for its internal function. Therefore, its RF internal function. Therefore, its RFinternal function. Therefore, its RF Therefore, its RFTherefore, its RF
emissions are very low and are not likely to low and are not likely tolow and are not likely to and are not likely toand are not likely to
cause any interference in nearby electronicnterference in nearby electronicterference in nearby electronicference in nearby electronicerence in nearby electronicn nearby electronic nearby electronicroniconic
equipment..
in all establishments, including domesticll establishments, including domesticl establishments, including domestic establishments, including domesticestablishments, including domesticts, including domestics, including domestic including domesticincluding domestic
establishments.
Electromagnetic Immunity
This Model ZM-921PA/931PA is intended for use in the electromagnetic
electrically radiating equipment near the impedance respiration measurements.
Operator’s Manual ZM-920PA/921PA/930PA/931PA 67
Page 77
Immunity
test
IEC 60601
test level
Compliance
level
Electromagnetic environment
- guidance
Portable and mobile RF
communications equipment should be
used no closer to any part of the ZM921PA/931PA, including cables, than
the recommended separation distance
calculated from the equation applicable
to the frequency of the transmitter.
Recommended separation
distance
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
3 Vrms
3 V/m
80 MHz to
2.5 GHz
3 Vrms
3 V/m 80 MHz
to 2.5 GHz
(1 V/m 80 MHz
to 2.5 GHz for
respiration)
d = 1.2√P
d = 1.2√P 80 MHz to 800 MHz
d = 2.3√P 800 MHz to 2.5 GHz
(d = 3.5√P 80 MHz to 800 MHz for
respiration
d = 7.0√P 800 MHz to 2.5 GHz for
respiration)
where P is the maximum output
power rating of the transmitter in
watts (W) according to the transmitter
manufacturer and d is the recommended
separation distance in meters (m).
FieldstrengthsfromxedRF
transmitters, as deter mined by an
electromagnetic site survey*1, should be
less than the compliance level in each
frequency range*2.
Interference may occur in the vicinity of
equipment marked with the following
symbol:
68 Operator’s Manual ZM-920PA/921PA/930PA/931PA
Page 78
Immunity
test
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation
cordless) telephones and land mobile radios, amateur radio, AM and FM radio
broadcast and TV broadcast cannot be predicted theoretically with accuracy.
in the location in which the ZM-921PA/931PA is used exceeds the applicable RF
compliance level above, the ZM-921PA/931PA should be observed to verify normal
operation. If abnormal performance is observed, additional measures may be
necessary, such as re-orienting or relocating the ZM-921PA/931PA.
V/m for respiration and 3 V/m for all other functions.
IEC 60601
test level
Compliance
level
Electromagnetic environment
- guidance
Operator’s Manual ZM-920PA/921PA/930PA/931PA 69
Page 79
Recommended Separation Distances between Portable and Mobile
RF Communications Equipment
The ZM-921PA/931PA is intended for use in an electromagnetic environment in
which radiated RF disturbances are controlled. The customer or the user of the
ZM-921PA/931PA can help prevent electromagnetic interference by maintaining
a minimum distance between portable and mobile RF communications equipment
(transmitters) and the ZM-921PA/931PA as recommended below, according to the
maximum output power of the communications.
Rated
maximum
output power
of transmitter
(W)
0.010.120.12 (0.35*)0.23 (0.7*)
0.10.380.38 (1.1*)0.73 (2.2*)
11.21.2 (3.5*)2.3 (7.0*)
103.83.8 (11*)7.3 (22*)
1001212 (35*)23 (70*)
For transmitters rated at a maximum output power not listed above, the recommended
separation distance d in meters (m) can be estimated using the equation applicable to
the frequency of the transmitter, where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.
(* For respiration)
NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation
Separation distance according to frequency of transmitter (m)