Impact 731 Vent Service Manual

906-0731-04 Rev. B Sept.
2012
Page 1 of 68
Table of Contents
INTRODUCTION ............................................................................................................................................. 3
Conventions ................................................................................................................................................... 3
Terminology and Abbreviations..................................................................................................................... 3
General Warnings .......................................................................................................................................... 4
Cautionary Note ............................................................................................................................................. 4
Helpful Hints .................................................................................................................................................. 4
Limited Copyright Release ............................................................................................................................ 4
Warranty ........................................................................................................................................................ 5
Masimo Pulse Oximeter ................................................................................................................................. 5
WARNINGS AND CAUTIONS REGARDING USE....................................................................................... 6
731Series and Pulse Oximeter ....................................................................................................................... 6
Pulse Oximeter Specific Warnings And Cautions.......................................................................................... 7
MAINTENANCE .............................................................................................................................................. 9
Routine Inspections ........................................................................................................................................ 9
Cleaning ..................................................................................................................................................... 9
Storage Information ..................................................................................................................................10
Post-Contaminated Environment Cleaning ...............................................................................................10
Removable Foam Filter Replacement .......................................................................................................11
Fresh Gas/Emergency Air Intake Disk Filter Replacement ......................................................................11
Battery Capacity, Care and Recharging ....................................................................................................12
Preventive Maintenance (PM) .......................................................................................................................13
Periodic Maintenance Check (PMC) .........................................................................................................13
Troubleshooting and Repairs ............................................................................................................................15
Service Kits ...................................................................................................................................................15
Service Kit Listing ....................................................................................................................................16
Replacement Instructions ..........................................................................................................................17
Membrane Panel Kit 712-0731-01 / 712-EGL2-01...............................................................................17
SPM Kit 712-0731-02 / 712-EGL2-02 ..................................................................................................21
Battery Compartment Kit 712-0731-03 / 712-EGL2-03 .......................................................................25
Outer Air Intake Kit 712-0731-04 / 712-EGL2-04 ...............................................................................26
Bezel Assembly Kit 712-0731-05 / 712-EGL2-05 / 712-AEV1-01 ......................................................27
Power Knob Kit 712-0731-06 / 712-EGL2-06 ......................................................................................29
USB Connector Plate Kit 712-0731-07 / 712-EGL2-07 .......................................................................31
Front Case Assembly Kit 712-0731-08 / 712-EGL2-08 / 712-AEV1-02 ..............................................34
Battery Case Bottom Cover Kit 712-0731-09 / 712-EGL2-09..............................................................36
EMV Chassis Kit 712-0731-10 / 712-EGL2-10 ....................................................................................37
Connector Panel Kit 712-0731-11 / 712-EGL2-11 ...............................................................................41
Back Case Kit 712-0731-12 / 712-EGL2-12 .........................................................................................45
PIM Board Kit 702-0731-02 .................................................................................................................46
CPU/UIM & SPO2 Stack Kit 712-0731-14 ..........................................................................................49
USB Connector Kit 712-0731-15 ..........................................................................................................52
Gas Output Kit 712-0731-16 .................................................................................................................54
Power Input Kit 712-0731-17 ...............................................................................................................55
Oxygen Inlet Fitting Kit 712-0731-18...................................................................................................59
Selector Knob Kit 712-0731-19 / 392-0066-00.....................................................................................60
Troubleshooting ............................................................................................................................................62
Alarm Category .........................................................................................................................................62
Service Codes ............................................................................................................................................63
HiPot Testing ....................................................................................................................................................68
906-0731-04 Rev. B Sept. 2012
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INTRODUCTION
Conventions
WARNING!
A WARNING statement identifies conditions or information that could have an adverse effect upon the
patient or operator which if not avoided, could result in death or serious injury.
CAUTION!
A CAUTION statement provides important information about a potentially hazardous situation which if not
avoided may result in minor or moderate injury to the patient, operator or damage to the equipment or
other property.
NOTE:
A NOTE provides additional information intended to avoid inconvenience during operation.
Terminology and Abbreviations

A/C- Assist/Control
ACLS- Advanced Cardiac Life Support
ALS- Advanced Life Support
ATLS- Advanced Trauma Life Support
ACV- Assist-Control Ventilation
ATPD - Atmospheric Temperature and Pressure, Dry
BPM - Breaths per Minute
B/V - Bacterial/Viral Filter
cm H2O - Centimeters of Water
CPR - Cardiopulmonary Resuscitation
DISS - Diameter Index Safety System
FIO2 - Fraction of Inspired Oxygen
HME - Heat and Moisture Exchanger
HME/BV - Heat and Moisture Exchanger/Bacterial
Viral filter combined
Hz Hertz (as in frequency, cycles per second)
ID - Internal Diameter
L - Liters
906-0731-04 Rev. B Sept. 2012
LED - Light Emitting Diode

LPM - Liters per Minute
ml - Milliliters
mm - Millimeter
NPPV Noninvasive Positive Pressure
Ventilation
O2 - Oxygen
Paw - Airway Pressure
PEEP - Positive End Expiratory Pressure
PIP - Peak Inspiratory Pressure
psig - Pounds per Square Inch Gage
USP - United States Pharmacopeia
VAC - Volts AC
VDC - Volts DC
VT - Tidal Volume
WOB Work of Breathing
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General Warnings
The design and intended use of 731 series ventilators requires that the operation of the product be
restricted to trained medical professionals. US federal law restricts this device for sale by or on the order of
a physician.
The information contained herein is restricted for use by personnel certified by Impact Instrumentation, Inc.
in the care and servicing of this product. Impact does not authorize or assume any obligations resulting
from unauthorized servicing of its products nor will it be held liable for any injuries or damages incurred
therefrom.
This device has been classified "life supporting" and "life sustaining" by the United States Food & Drug
Administration. If you have not been trained and certified by Impact Instrumentation, Inc in the care and
servicing of this product, DO NOT attempt to service this device. Should factory based servicing become
necessary, or technical assistance is required, please have the devices Model and Serial Number available
and contact the Impact service team. All service requests, including requests to schedule service training,
may be addressed to the Service Manager, Impact Instrumentation, Inc., 19 Fairfield Place, West Caldwell,
New Jersey 07006, 973/882-1212 or email: [email protected] .
Cautionary Note
Prior to servicing this device, be aware of the presence of potentially dangerous operating voltages.
Disconnect power supply and the internal battery prior to performing any service.
Internal components are susceptible to damage from static discharge. All servicing operations MUST be done
in an ESD controlled environment.
Please review all warnings and cautions in this manual, the devices Operation manual and the RCS
Operation manual prior to servicing the 731 series ventilator.
Helpful Hints
Before attempting to service this instrument, please take a few moments to ensure that the problem is not
accessory-related. Always check the integrity of all tubing and fittings and verify that tubing is not crimped
or cracked.
Always safeguard your personal well being when troubleshooting electronic circuitry. Keep jewelry and
liquids from the vicinity of active circuitry.
Limited Copyright Release

Permission is hereby granted to any United States Military or Governmental agency to reproduce all
materials furnished herein for use in a United States Military or Governmental service training program. No
other individual, company or agency are granted the permission to copy or reproduce any materials
furnished herein without the written permission of Impact.
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Warranty
Impact Instrumentation, Inc. warrants 731 series devices and their replacement service
part kits to be free from all defects in material and workmanship for a period of one (1)
year from the date of delivery to the final purchaser
During the warranty period, Impact will repair or replace the device or any part which
upon examination is shown to be defective. At its sole discretion, Impact may choose
to supply a new or equivalent replacement product or refund the amount of the
purchase price. To qualify for such repair, replacement, or refund, the defective device
must be returned to Impact or Impacts authorized service provider within thirty (30)
days from the date that the defect is discovered. This warranty does not apply if the
device has been repaired or modified without the authorization of Impact or if the
damage was caused by incorrect storage, failure to perform recommended
maintenance, use of the product in applications not described in the intended use
statement, negligence or an accident.
Batteries, which by their nature are consumable and subjected to environmental
extremes, will be warranted for a period of ninety (90) days. Accessories, also
consumable in usage, such as connecting hose and breathing circuits, are not
warranted.
DISCLAIMER OF IMPLIED & OTHER WARRANTIES:
THE PRECEDING WARRANTY IS THE EXCLUSIVE WARRANTY AND IMPACT
INTRUMENTATION, INC. MAKES NO OTHER WARRANTY OR
REPRESENTATION OF ANY KIND WHATSOEVER, EXPRESSED OR IMPLIED,
WITH RESPECT TO MERCHANTABILITY, FITNESS FOR A PARTICULAR
PURPOSE OR ANY OTHER MATTER. THE REMEDIES STATED IN THIS
DOCUMENT WILL BE THE EXCLUSIVE REMEDIES AVAILABLE FOR ANY
DEFECTS OR FOR DAMAGES RESULTING FROM ANY CAUSE WHATSOEVER
AND WIHOUT LIMITATION.
IMPACT INSTRUMENTATION, INC. WILL NOT IN ANY EVENT BE LIABLE FOR
CONSEQUENTIAL OR INCEDENTAL DAMAGES OF ANY KIND, WHETHER
FROM DEFECTIVE OR NONCONFORMING PRODUCTS, BREACH OR
REPUDIATION OF ANY TERM OR CONTTION OF THE DOCUMENT,
NEGLIGENCE, OR ANY OTHER REASON
THE WARRANTIES SET FORTH ABOVE ARE IN LIEU OF ALL OTHER
WARRANTIES, EXPRESSED OR IMPLIED, WHICH ARE HEREBY DISCLAIMED
AND EXCLUDED BY SELLER, INCLUDING WITHOUT LIMITATION ANY
WARRANY OF MERCHANTABILITY OF FITNESS FOR A PARTICULAR PURPOSE
OR USE.
Masimo Pulse Oximeter

This device uses Masimo SET technology to provide continuous pulse oximeter and heart rate monitoring
and is covered under one or more of the following U.S.A. patents: 5,758,644, 5,823,950, 6,011,986,
6,157,850, 6,263,222, 6,501,975 and other applicable patents listed at www.masimo.com/patents.htm.
906-0731-04 Rev. B Sept. 2012
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WARNINGS AND CAUTIONS REGARDING USE

731Series and Pulse Oximeter
WARNING! Electric shock hazard: Do not remove equipment covers except to replace batteries! An
operator may only perform maintenance procedures specifically described in this manual. Refer servicing
to Impact or an authorized Impact Service Center in the repair of this equipment.
WARNING! The device is intended for use by qualified personnel only! The operator should read this
manual, all precautionary information, and specifications before using the device!
WARNING! Possible explosion hazard if used in the presence of flammable anesthetics or other flammable
substances in combination with air, oxygen-enriched environments or nitrous oxide!
WARNING! During operation the device should not be stacked on top of or under other medical equipment
due to the possibility of electromagnetic interference between the device and other equipment. (The
device was subjected to EMC testing in accordance with Military Mil-STD-461F and Commercial IEC 606011-2 and FDA Reviewers Guidance specifications.)
WARNING! Grounding:
Connect the device only to a three-wire, grounded, hospital-grade receptacle! The three-conductor
plug must be inserted into a properly wired three-wire receptacle; if a three-wire receptacle is not
available, a qualified electrician must install one in accordance with the governing electrical code.
Do not under any circumstances remove the grounding conductor from the power plug!
Do not use extension cords or adapters of any type! The power cord and plug must be intact and
undamaged.
If there is any doubt about the integrity of the protective earth conductor arrangement, operate the
oximeter on internal battery power until the AC power supply protective conductor is fully functional!
WARNING! To ensure patient electrical isolation, connect only to other equipment with electronically
isolated circuits!
WARNING! Do not use antistatic or conductive hoses or tubing with this device!
WARNING! Do not connect to an electrical outlet controlled by a wall switch or dimmer!
WARNING! As with all medical equipment, carefully route the ventilator circuit hose and tubing, patient
cabling, and external power cables to reduce the possibility of patient entanglement or strangulation!
WARNING! Do not place the device or external power supply in any position that might cause it to fall on
the patient! Do not lift the device by the power supply cord, ventilator circuit or pulse oximeter patient
cable!
WARNING! Do not use the device, its pulse oximeter or pulse oximetry sensors during magnetic resonance
imaging (MRI) scanning! Induced current could potentially cause burns. The device and/or its pulse
oximeter may affect the MRI image and the MRI unit may affect device operation or the accuracy of the
oximetry measurements.
WARNING! The device must be connected to a grounded AC power supply when connected to AC power.
The device and its integrated pulse oximeter are referred to as an IEC 601/F device in the summary situation
table contained in IEC-601-1-1.
WARNING! USB Interconnection: Do not operate the device on a patient when the USB is connected to any
other device.
NOTE: The USB interconnection does not support automatic record keeping.
WARNING! The Impact supplied ventilator circuits labeling provides the resistance and compliance values
for the circuits under normal operating conditions. If added accessories are used (e.g. humidification, filters
etc.), the operator should assure they do not degrade the performance of the device. If non-Impact circuits
are used, the operator should assure these circuits do not affect the performance of the device.
CAUTION! Federal law restricts this device to sale by or on the order of a physician.
CAUTION! Service is to be performed by qualified biomedical equipment technicians only.
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CAUTION! Internal components are susceptible to damage from static discharge. Do not remove device
covers.
NOTE: This Operation Manual is not meant to supersede any controlling standard operating procedure
regarding the safe use of assisted ventilation.
NOTE: Follow all governing regulations regarding the disposal of any part of this medical device.
NOTE: Follow all governing regulations regarding the handling of materials contaminated by body fluids.
NOTE: Follow all governing regulations regarding shipment of the Li batteries.
Pulse Oximeter Specific Warnings And Cautions

WARNING! A pulse oximeter should not be used as an apnea monitor.
WARNING! A pulse oximeter should be considered an early warning device. As a trend towards patient
deoxygenation is indicated, blood samples should be analyzed by a laboratory co-oximeter to completely
understand the patients condition.
WARNING! MEASUREMENTS
If the accuracy of any measurement does not seem reasonable, first check the patients vital signs by
alternate means and then check the pulse oximeter for proper functioning.
Inaccurate measurements may be caused by:
Incorrect sensor application or use
Significant levels of dysfunctional hemoglobin (e.g., carboxyhemoglobin or methemoglobin)
Intravascular dyes such as indocyanine green or methylene blue
Exposure to excessive illumination, such as surgical lamps (especially ones with a xenon light source),
bilirubin lamps, fluorescent lights, infrared heating lamps, or direct sunlight (exposure to excessive
illumination can be corrected by covering the sensor with a dark or opaque material)
Excessive patient movement
Venous pulsations
Placement of a sensor on an extremity with a blood pressure cuff, arterial catheter, or intravascular
line
The pulse oximeter can be used during defibrillation, but the readings may be inaccurate for a short
time.
WARNING! Interfering Substances: Carboxyhemoglobin may erroneously increase readings. The level of
increase is approximately equal to the amount of carboxyhemoglobin present. Dyes, or any substance
containing dyes, that change usual arterial pigmentation may cause erroneous readings.
WARNING! ALARMS Check alarm limits each time the pulse oximeter is used to ensure that they are
appropriate for the patient being monitored.
WARNING! Loss of pulse signal can occur in any of the following situations:
The sensor is too tight
There is excessive illumination from light sources such as a surgical lamp, a bilirubin lamp, or sunlight
A blood pressure cuff is inflated on the same extremity as the one with a SpO 2 sensor attached
The patient has hypotension, severe vasoconstriction, severe anemia, or hypothermia
There is arterial occlusion proximal to the sensor
The patient is in cardiac arrest or is in shock
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WARNING! Sensors:
Before use, carefully read the LNCS sensor directions for use.
Use only Masimo oximetry sensors for SpO2 measurements. Other oxygen transducers (sensors)
may cause improper performance.
Tissue damage can be caused by incorrect application or use of an LNCS sensor, for example by
wrapping the sensor too tightly. Inspect the sensor site as directed in the sensor Directions for Use
to ensure skin integrity and correct positioning and adhesion of the sensor.
Do not damage LNCS sensors. Do not use an LNCS sensor with exposed optical components. Do
not immerse the sensor in water, solvents, or cleaning solutions (the sensors and connectors are not
waterproof). Do not sterilize by irradiation, steam or ethylene oxide. See the cleaning instructions
in the directions for reusable Masimo LNCS sensors.

Do not use damaged patient cables. Do not immerse the patient cables in water, solvents or
cleaning solutions (the patient cables are not waterproof). Do not sterilize by irradiation, steam or
ethylene oxide. See the cleaning instructions in the directions for reusable Masimo patient cables.
CAUTION! Possession or purchase of this device does not convey any expressed or implied license to use
the device with unauthorized sensors or cables which would, alone, or in combination with this device fall
within the scope of one or more of the patents relating to this device. Impact cannot assure the proper
functioning of this device if it is used with unauthorized sensors or cables.
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MAINTENANCE
This device should be incorporated into a regular maintenance program to ensure safe and effective
operation. Electro-mechanical and pneumatic components are subject to wear and fatigue over time and
components will deteriorate more quickly when used continuously. To maintain safe operation, it is the
user's responsibility to ensure that periodic inspections and maintenance is performed and that
recommended maintenance is performed by Impact or a certified Impact trained technician.
Routine Inspections
Routine inspections should be performed on this ventilator at regular intervals and prior to its being placed
into service. Routine inspections consist of the following:
Operational inspection after every 1,000 hours of use or more
frequently if the ventilator has been used in austere environments,
confirm that that device functions properly by power cycling the
ventilator while it is connected to a ventilator circuit and test lung.
Operate the ventilator at its default settings and exercise the
membrane buttons and the rotary optical encoder to ensure they
operate as intended.
Accessory inspection replace power supply if there is damaged or
cracked casing, plugs, or cut/frayed or exposed wiring.
Filter inspection check the foam and disk filter for dust/dirt build up
and/or physical damage. Replace if dirt is visible or filter is damaged.
Battery inspection check the battery icon to ensure battery is
charging and that the ventilator operates correctly.
Breathing circuit inspection check on a daily basis the breathing
circuit for damage or wear including but not limited to cracking,
discoloration or disfigurement. If there is any sign of physical
degradation or the unit is indicating breathing circuit problems,
replace with a new breathing circuit.
High Pressure Hoses inspection: Examine hoses for cracking,
discoloration and disfigurement. Wipe the exterior wall with a damp,
soapy cloth. Dry with a lint-free cloth. Examine end connection
fittings for damaged threads and sharp edges. Replace if defective,
DO NOT attempt to repair.
Cleaning
1.
The ventilators outer case should be cleaned with a damp soapy cloth and thoroughly dried with a
lint-free cloth. Make sure that all exposed surfaces are cleaned and dried.
2.
For general decontamination/cleaning situations, a 10% bleach solution applied with a damp cloth
is an effective decontaminant that can be used. Since the potential amount of contaminants that
our ventilators might be exposed to is so large, it is difficult to provide an appropriate cleaning
method for each type of exposure. An effective cleaning agent for one type of exposure may not be
effective with another and cleaning and sterilizing practices may vary between institutions. Impact
Instrumentation, Inc. suggests that each facility have in place a procedure for the cleaning and
disinfection of its medical equipment and that these procedures be consulted for further guidance.
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3.
Care must be taken to prevent liquids from entering the ventilator. Never submerge the ventilator
and avoid using excessive amounts of water that might enter the unit.
4.
Never use abrasives or chlorinated hydrocarbon based cleansers when cleaning the ventilator, they
will damage the plastic and interface lens.
WARNING! Never use oil or grease of any kind with O2 or compressed gas equipment.
Storage Information
For optimal prolonged storage periods, the device should be stored indoors. The environment should be
clean and out of direct sunlight. Storage in non-controlled environments is permissible if batteries are
removed.
For long-term storage, the optimum storage temperature range is -15 C to 21 C (5 F to 71 F). Battery life is
diminished at temperatures above 35 C (95 F). It is recommended that batteries be discharged to 50%
capacity if long term storage above 35 C (95 F) is expected. DO NOT store batteries in a discharged
condition. Short-term, less than 10 days, storage temperatures should range between -15 C to 49 C (5 F
and 120 F) with no degradation to the device.
CAUTION! DO NOT store batteries in a discharged condition.
When batteries are in extended storage, it is recommended that they receive a refresh charge at
recommended intervals when not continuously connected to an external power source:
STORAGE AMBIENT
Below 68 F (20 C)
68 F to 86 F (20 C to 30 C)
86 F to 104 F (30 C to 40 C)
RECHARGE INTERVAL
12-months
6-months
3-months
Following periods of extended storage in non-controlled environments, allow the device sufficient time to
stabilize to a temperature within its specified operating range (see section entitled BATTERY CARE AND
RECHARGING).
If the device is subject to 6-months of continuous storage/non-use, or longer, this device should be powered
on to initiate the devices self test routine. The user should confirm that the batteries are sufficiently
charged before patient-use is attempted.
Post-Contaminated Environment Cleaning

If the ventilator is operated in an environment where it may have been exposed to contamination from a
hazardous materials accident, mass epidemic or weapon of mass destruction, Impact recommends that the
guidelines below be followed.
1.
The ventilators outer case should be cleaned with a damp soapy cloth and thoroughly dried
with a lint-free cloth. Make sure that all exposed surfaces are cleaned and dried.
2.
For general decontamination/cleaning situations, a 10% bleach solution applied with a damp
cloth is an effective decontaminant that can be used. Since the potential amount of
contaminants that our ventilators might be exposed to is so large, it is difficult to provide an
appropriate cleaning method for each type of exposure. An effective cleaning agent for one
type of exposure may not be effective with another and cleaning and sterilizing practices may
vary between institutions. Impact Instrumentation, Inc. suggests that each facility have in place
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a procedure for the cleaning and disinfection of its medical equipment and that these
procedures be consulted for further guidance.
3.
Care must be taken to prevent liquids from entering the ventilator. Never submerge the
ventilator and avoid using excessive amounts of water that might enter the unit.
4.
Never use abrasives or chlorinated hydrocarbon based cleansers when cleaning the ventilator,
they will damage the plastic and interface lens.
5.
Always follow the decontamination procedures specified by the local Incident Command Safety
Officer.
6.
Equipment should be cleaned and decontaminated as soon as possible after use. Personnel
should always wear the appropriate Personal Protective Equipment while decontaminating
equipment.
7.
The ventilators outer case should be cleaned with a damp soapy cloth and thoroughly dried
with a lint-free cloth. Make sure that all exposed surfaces are cleaned and dried.
8.
For general decontamination/cleaning situations, a 10% bleach solution applied with a damp
cloth is an effective decontaminant that can be used. Since the potential amount of
contaminants that our ventilators might be exposed to is so large, it is difficult to provide an
appropriate cleaning method for each type of exposure. An effective cleaning agent for one
type of exposure may not be effective with another and cleaning and sterilizing practices may
vary between institutions. Impact Instrumentation, Inc. suggests that each facility have in place
a procedure for the cleaning and disinfection of its medical equipment and that these
procedures be consulted for further guidance.
9.
Care must be taken to prevent liquids from entering the ventilator. Never submerge the
ventilator and avoid using excessive amounts of water that might enter the unit.
10. Never use abrasives or chlorinated hydrocarbon based cleansers when cleaning the ventilator,
they will damage the plastic and interface lens.
Removable Foam Filter Replacement

Removable Foam Filter: The Removable Foam Filter is located on the right side of the ventilator. It should
be inspected and replaced if needed every 1,000 hours of operation or more frequently if used in dusty
environments. Remove the filter using a pair of tweezers or similar tool. Examine the filter for dirt, lint, or
general wear. Replace if necessary (Part # 465-0028-00). DO NOT attempt to clean this filter.
CAUTION! Do not operate the compressor without a filter in place.
Fresh Gas/Emergency Air Intake Disk Filter Replacement

Fresh Gas/Emergency Air Intake Disk Filter: The Fresh Gas/Emergency Air Intake Disk Filter (Part #4650027-00) is located behind the Removable Foam Filter. This filter provides a second level of filtration to the
ambient air that is delivered to the patient. This filter must be checked periodically and replaced when
necessary. The device triggers an alarm when the combination of Removable Foam Filter and Fresh
Gas/Emergency Air Intake Disk Filter become dirty. This alarm signifies that the device is still able to deliver
the correct tidal volume but one or more of its filters need replacement. The Fresh Gas/Emergency Air
Intake Disk Filter can be visually inspected after the Removable Foam Filter is removed. If the filter appears
discolored it must be replaced. See Appendix 5 in the Operation Manual: Internal Filter Change/Insertion.
CAUTION! There are no user serviceable parts except the filter components described above.
CAUTION! When used in dusty/dirty environments the foam and disk filters should be checked, and
replaced as needed. This will prevent particle build up on the transducer screen and the need to take the
unit out of service for maintenance by a biomedical technician.
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CAUTION! If filters have been exposed to biological matter dispose of them following Universal Precaution
procedures for your facility.
NOTE: Do not attempt to clean this filter and do not operate internal compressor without filter in place.
Battery Capacity, Care and Recharging

While the unit is operating on battery power, users can best determine the relative amount of charge in the
internal battery by looking at the BATTERY Icon/Indicator. The BATTERY icon appears in outline form and is
filled with horizontal rows of lines indicating its current capacity. Each line represents approximately 5% of
battery capacity.
The device uses a rechargeable lithium-ion battery which offers a wide temperature operating range, does
not exhibit "memory" characteristics (reduced capacity) or vent hydrogen gas. The life of this battery
depends, to a great extent, upon the care it receives. Avoid exposing it to direct sunlight or heat sources
and never store the battery at temperatures above 76 C (170 F) for more than 2 hours. Following these
simple guidelines will prevent premature charge depletion and reduction of battery life.
If the unit was supplied without the battery installed or battery replacement is required see Appendix 4:
Internal Battery Change/Insertion.
CAUTION! Only use the Power Supply provided with the unit. Use of any other power supply could cause
damage or create a fire and/or destroy the battery and unit.
CAUTION! If you witness a battery or the battery compartment starting to balloon, swell up, smoke or feel
excessively hot, turn off the unit, disconnect external power and observe it in a safe place for
approximately 15 minutes and send the unit for service. Never puncture or disassemble the battery packs
or cells.
CAUTION! Never attempt to completely discharge the battery by shorting or some other method and
never ship the battery in a completely discharged state.
CAUTION! During continuous, uninterrupted use (>100 hours) it is recommended that the ventilator be
disconnected from AC power for 30 seconds to allow the battery to run diagnostics while the battery is
discharging.
NOTE: The ventilator continuously monitors the available power sources; occasionally a false low priority
power alarm can be triggered for ~1 second. These false alarms immediately clear themselves.
1.
2.
3.
4.
Battery charging is controlled by ventilator in the temperature range of 0 C to 45 C (32F to 113 F)

to provide the best life time for the battery
The battery has a discharge (operational) temperature range of -25 to 49 C (-13 F to 120 F) (as
validated by Impact Instrumentation).
DO NOT store the ventilator with the batteries discharged. Always store with the battery fully
charged.
For long-term storage, the optimum storage temperature range is -15 C to 21 C (5 F to 71 F).
Lithium-ion batteries exhibit excellent charge retention characteristics. Prolonged periods of disuse will not
substantially reduce operating capability. If long-term storage/non-use is common, recharge the unit every
six months; this will insure that battery charge is maintained at 80% capacity or better. The 731 series
devices battery rapidly recharges to 90% of its capacity in approximately 2 hours. It will take approximately
another 2 hours of trickle-charging to top off the battery to 100% of its capacity. Continuous charging is
permissible with the supplied 12 VDC Power Cable or AC/DC Power Supply.
Operating power will always default to the external power source to preserve the internal battery charge.
This assures that power is available for transport use or emergency back-up. If the EXTERNAL POWER LOW/ FAIL
alarm occurs, the device will automatically revert to its internal batteries for operating power.
The BATTERY Icon/Indicator indicates (1) the presence of a functional battery, (2) when the battery is
charging and (3) what its current capacity is. The BATTERY icon appears in outline form and is filled with
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horizontal rows of lines indicating its current capacity. When the battery is charging, these horizontal rows
of lines cyclically scroll vertically, one row at a time, from the bottom row to the top. When the battery is
fully charged, the icon is completely filled with lines and scrolling stops. Each line represents approximately
5% of battery capacity. During internal battery operation a horizontal line disappears as battery capacity
is reduced by a 5% increment. The BATTERY icon will flash off/on when a BATTERY POWER LOW alarm occurs.
The icon will flash off/on and present with a diagonal line when no battery is connected.
Preventive Maintenance (PM)

Scheduled replacement of filters, batteries, seals and mechanical/pneumatic moving parts will ensure the
device is always operating at peak performance. The table below describes the scheduled interval for
routine parts replacement, calibration and functional testing. Ventilators used in extreme environments
may warrant earlier or more frequent maintenance scheduling.
Maintenance Activity
Replace inlet oxygen and compressor foam
and disk filters
Perform a Periodic Maintenance Check
(PMC)
Year after initial purchase of ventilator

1
*
*
*
*
*
*
Replace the main battery

Replace the real time clock battery (RTC)
Inspect and replace if needed any internal
tubing, gaskets, or O-Rings that show signs of
wear
Inspect internal pneumatic & electromechanical components
Table 1 Maintenance Schedule.
Periodic Maintenance Check (PMC)

At start up, the device performs a self check that includes a check for pre-existing alarm conditions.
Following start up, the presence of alarm conditions is checked continuously. When in operation the
ventilator circuit connects to a pressure transducer in the ventilator. Periodically, the transducer
recalibrates itself using the ambient air pressure as a reference. This process maintains a consistent
transducer baseline over a wide temperature and altitude range to assure display, monitoring and triggering
accuracy.
The ventilator also automatically performs an AUTO CAL procedure that affects 3 transducer systems:
Compressor Flow, Oxygen Flow and Airway Pressure. The purpose of AUTO CAL is to compensate for small
temperature related drifts in the transducer offset (zeroing). The AUTO CAL is performed at start up during
o
the self check and then every 5 minutes thereafter. However, if a temperature change emceeing +/-1.5 C is
sensed, the AUTO CAL time interval is reduced automatically to assure a stable pressure measurement
baseline. This continuous correction for variations in ambient temperature and pressure enable the
ventilator to deliver targeted volumes and pressure over the entire operating altitude and temperature
ranges described in the operations manual.
The automated self check at start up and the AUTO CAL tests confirm that the device is operating within its
specifications when in use. If the start up or AUTO CAL tests fail, the unit will not operate. Because the
automated tests do not confirm that flow and pressure outputs from the device are verified against a
controlled external pressure, flow and temperature measurement device, the PMC procedure should be
done every 12 months or after 1,500 hours of use, or to reset the performance maintenance check low
906-0731-04 Rev. B Sept. 2012
Page 13 of 68
priority alarm, to document that the ventilator has been maintained and is operating properly. The PMC
should also be performed whenever the operator suspects that the device is not functioning properly or
following mass deployment and before the device is returned to storage. If the device fails the PMC it
should be maintained by a certified Impact service technician in the field or at Impact authorized service
locations. A secure record of PMC results should be maintained for devices not returned to Impact for
maintenance.
Impacts 731 series service tool the RCS is needed to perform the PMC and reset the performance
maintenance check low priority alarm. This tool includes can be purchased from Impact for use by Impact
trained and certified biomedical technicians. Alternatively, 731 series can be sent to an Impact authorized
service center for PMC or other service requirements.
In addition to automating and documenting the PMC process, the RCS is also capable of calibrating the
device and installing and verifying software upgrades and updates to the 731 series of devices.
If you would like to return the ventilator to Impact for service please contact Impact prior to returning this
instrument. (Telephone 973.882.1212, email [email protected]). A Returned-Goods-Authorization
number (RGA #) will be issued. The RGA # must appear on both the packing slip and address label. This will
facilitate better tracking of the returned item and result in improved scheduling and handling.
Annual and 4-Year PM Kits are available to trained personnel and service centers.
Picture
Description
Kit #
Annual Preventive Maintenance Kit
712-0731-20
4-Year Preventive Maintenance Kit
712-0731-21
906-0731-04 Rev. B Sept. 2012
Page 14 of 68
Troubleshooting and Repairs

The device uses a comprehensive suite of alarms to alert the operator and guide their actions to resolve the
alarm condition and assure patient safety. At the onset of an alarm, the screen displays the alarm name and
then a series of context-sensitive help messages (see Figure 2 example). These messages serve to guide the
operator by presenting suggestions as to the cause and resolution of a particular alarm. When multiple
alarms occur they are prioritized and displayed based on the risk to the patient. Should the operator not be
able to correct the problem, the ventilator should be taken out of use and sent to an authorized Impact
repair facility.
Trained bio-med technicians are encouraged to use a systematic approach to solving issues with the
ventilator. Use the Alarm Category and Service Code matrices listed in Appendix to resolve the problem or
to identify the suggested replacement service kit. Check on-hand availability or order the kit(s) from Impact,
then follow the detailed instructions listed to replace the kit. Trained repair facilities can contact Impacts
technical service department via email: service @impactii.com or by telephone toll free: 800-969-0750 or
973-882-1212 for troubleshooting and repair recommendations.
ALARM & PLOT LIST: FIGURE 2
Service Kits
Service kits, which are preassembled and factory tested subassemblies, are available should physical
damage or problems of an unforeseen nature arise. Service kits are available only to qualified trained
biomedical personnel or authorized Impact service centers. Each kit replacement must be followed by a
HiPot test (See section titled HiPot Testing ), then either by a functional test or a calibration and functional
test using the Remote Calibration System (RCS).The following table lists the kits for each 731 series model.
906-0731-04 Rev. B Sept. 2012
Page 15 of 68
Service Kit Listing

EMVP
Description
Eagle II
Picture
Kit #
Picture
Kit#
Membrane Panel Kit
712-0731-01
712-EGL2-01
SPM/Vent Assembly Kit
712-0731-02
712-EGL2-02
Battery Compartment Kit
712-0731-03
712-EGL2-03
712-EGL2-13 (MR)
Outer Air Intake Kit
712-0731-04
712-EGL2-04
Bezel Assembly Kit
712-0731-05 (EMVP)
712-AEV1-01 (AEV)
712-EGL2-05
Power Knob Kit
712-0731-06
712-EGL2-06
USB Connector Plate Kit
712-0731-07
712-EGL2-07
Front Case Assembly Kit
712-0731-08 (EMVP)
712-AEV1-02 (AEV)
712-EGL2-08
Battery Case Bottom Cover Kit
712-0731-09
712-EGL2-08
EMV Chassis Kit
712-0731-10
712-EGL2-10
Connector Panel Kit
712-0731-11
712-EGL2-11
Back Case Kit
712-0731-12
712-EGL2-12
PIM Board Kit
702-0731-02
702-0731-02
CPU/UIM & SPO2 Stack Kit
712-0731-14
712-0731-14
USB Connector Kit
712-0731-15
712-0731-15
Gas Output Kit
712-0731-16
712-0731-16
Power Input Kit
712-0731-17
712-0731-17
Oxygen Inlet Fitting Kit
712-0731-18
712-0731-18
Selector Knob Kit
712-0731-19
392-0066-00
906-0731-04 Rev. B Sept. 2012
Page 16 of 68
Replacement Instructions
CAUTION! Internal components are susceptible to damage from static discharge. All servicing
operations MUST be done in an ESD controlled environment.
CAUTION! Disconnect external power and battery pack prior to performing any service.
Membrane Panel Kit 712-0731-01 / 712-EGL2-01

Contents:
ITEM
QTY
DESCRIPTION
Membrane Panel Assembly
Screw, Phillips, Pan Head, Zinc Plated, 4-40 X 1/4
Power Select Knob with Set screw
Selector Knob
Instructions:
STEP NO.
DIRECTIONS
Loosen but do not remove the

(4) 8-32 X 3 screws on the outer air
intake.
Loosen and remove the (2) 10-32

Keps nuts and the (4) 6-32 X 2
screws. Remove the back case by
lifting from the ventilator.
Remove the (2) 4-40 X screws on

the Dovetail Mounting Bracket and
disconnect the ribbon cable on the
PIM PCB by simultaneously applying
pressure on the two locking ears.
906-0731-04 Rev. B Sept. 2012
Page 17 of 68
Flip the ventilator over and remove

the front case assembly by lifting it
straight up away from the ventilator
module.
Remove the bezel by loosening and

removing the (7) 4-40 X screws
that hold the bezel to the front case.
Using a sharp knife, carefully cut the

RTV sealant around the USB Printed
Circuit Board and around the SPO2
Connector. Be careful not to cut
either cable.
Loosen and remove the two 4-40 X
3/16 screws holding the Mini USB
Cable Assembly to the front case.
Loosen and remove the two M2.5 X
5mm screws holding the SPO2 cable
to the front case.
Loosen and remove the two (2)

6-32 X 5/16 screws that hold the
CPU/UIM & SPO2 Stack to the front
case.
Lift the CPU/UIM & SPO2 Stack up

from the front case. Handle the
SPO2 cable with extreme care. Do
not pull on the cable.
10

5/16 screws holding the USB
Connector Plate to the front case.
906-0731-04 Rev. B Sept. 2012
Page 18 of 68
Tighten the two 4-40 X 5/16 screws

holding the USB Connector Plate to
the replacement front case. Tighten
the two (2) 6-32 X 5/16 screws that
hold the CPU/UIM & SPO2 Stack to
the front case. Make sure that all the
pins on the header mate correctly.
11
12
Make sure the SPO2 Flex Cable lays

flat against the front case and is
assembled correctly into the UIM
Bracket and SPO2 Isolation Shield.
Insert and tighten the two M2.5 X
to the front case.
13
Remove any excess RTV sealant from

the SPO2 flex cable and USB PCB.
holding the USB PCB to the front
case. Apply RTV sealant to USB PCB
and SPO2 flex cable. Allow to
dry/cure.
14
Dress the USB Connector cable along

the case and over the SPO2 flex
cable.
15
Place the included power knob on

the new membrane panel switch align with flat on switch insert the
included 6-32 X set screw and
tighten. Push the included selector
knob on the membrane panel switch
- align with flat on switch .
16
Place the front case assembly on to

the bezel and tighten the included
(7) 4-40 X screws.
906-0731-04 Rev. B Sept. 2012
Page 19 of 68
17
Place the front case assembly over

the vent module and tighten the (2)
4-40 X screws unto the dovetail
mounting bracket. Reconnect the
ribbon cable unto the PIM PCB.
Make sure the two locking ears
lock into position.
18
Attach the back case to the vent

module and align cover with handle,
air intake housing and dovetail
mounting studs. Insert and tighten
the included (2) 10-32 Keps nuts and
the (4) 6-32 X 2 screws.
19
Tighten the (4) 8-32 X 3 screws on

the outer air intake.
20
Perform HiPot Testing then perform

Calibration and Functional Test using
the RCS.
906-0731-04 Rev. B Sept. 2012
Page 20 of 68
SPM Kit 712-0731-02 / 712-EGL2-02

Contents:
ITEM
QTY
DESCRIPTION
SPM/Vent Assembly
Instructions:
STEP NO.
DIRECTIONS

intake.



module.
Remove the battery compartment

cover by unscrewing the (4) 6-32 X
5/16 screws.
Remove the battery by unscrewing

the (4) 6-32 X 2 screws and
detaching the plug from its locking
latch.
906-0731-04 Rev. B Sept. 2012
Page 21 of 68
Unscrew the (4) 6-32 X 5/16 Phillips

screws to remove the damaged battery
compartment case.
Loosen and remove the (2) 4-40 X 1

Screws and nylon spacers supporting the
Power Input assembly unto the chassis.
Loosen and remove the (2) 6-32 X

screws holding the chassis to the dovetail
mounting bracket and remove the SPO2
insulator. Loosen and remove the (2) 832 X screws holding the chassis to the
vent module.
10
Insert screwdriver through the holes on

the chassis to loosen and remove the (2)
6-32 x 5/16 screws holding the chassis to
the vent module.
11
Lift the damaged chassis from the

ventilator module.
Disconnect the Power Input cable from

the PIM PCB by pressing on the locking
latch and pulling the cable straight up
from the connector.
12
Remove the PIM PCB by loosening the (5)

4-40 X 5/16 screws.
13
906-0731-04 Rev. B Sept. 2012
Page 22 of 68
14
Remove the Dovetail stabilizer bracket by

loosening and removing the (2) 6-32 x
and the (2) 4-40 X screws.
15
Install the dovetail stabilizer bracket onto

the new SPM assembly by tightening the
(2) 6-32 X and (2) 4-40 X screws.
16
Secure the PIM Board to the new SPM

with the (5) 4-40 x 5/16 screws.
17
Secure the chassis to the vent module

using the (2) 6-32 X screws with SPO2
insulator, the (2) 8-32 X and the (2) 632 x 5/16 screws.
18
Secure the Power Input assembly to the

Chassis using the (2) spacers and (2) 4-40
X 1 screws. Do not over-tighten the
screws.
906-0731-04 Rev. B Sept. 2012
Page 23 of 68
19
Rotate battery compartment to mate

with upper and lower case cutouts and
press firmly into place. Secure with (4) 632 X 5/16 screws provided.
20
Re-assemble the battery by connecting

its cable to the connector (pull on cable
to insure it is locked in place) then
tightening the (4) 6-32 X 2 screws.
21
Re-assemble the battery compartment

cover by tightening the (4) 6-32 X 5/16
screws.
22
Place the front case assembly over the

vent module and tighten the (2) 4-40 X
screws unto the dovetail mounting
bracket. Reconnect the ribbon cable unto
the PIM PCB. Make sure the two locking
ears lock into position.
23
Attach the back case to the vent module

and align cover with handle, air intake
housing and dovetail mounting studs.
Insert and tighten the included (2) 10-32
Keps nuts and the (4) 6-32 X 2 screws.
24
Tighten the (4) 8-32 X 3 screws on the

outer air intake.
25

Calibration and Functional Test using the
RCS.
906-0731-04 Rev. B Sept. 2012
Page 24 of 68
Battery Compartment Kit 712-0731-03 / 712-EGL2-03

Contents:
ITEM
QTY
DESCRIPTION
Battery Compartment Case with Gaskets
Screw, Phillips, Pan Head, SS, 6-32 X 5/16
Instructions:
Step No.
Directions
Remove the battery

compartment cover by
unscrewing the (4) 6-32 X 5/16
screws.
Remove the battery by

unscrewing the (4) 6-32 X 2
screws and detaching the plug
from its locking latch.
Unscrew the (4) 6-32 X 5/16

Phillips screws to remove the
damaged battery compartment
case.
Rotate battery compartment to

mate with upper and lower case
cutouts and press firmly into
place. Secure with (4) 6-32 X
5/16 screws provided.
Re-assemble the battery by
connecting its cable to the
connector (pull on cable to
insure it is locked in place) then
tightening the (4) 6-32 X 2
screws.
Re-assemble the battery
compartment cover by tightening
the (4) 6-32 X 5/16 screws.
Perform HiPot Testing then

perform Functional Test using
the RCS.
906-0731-04 Rev. B Sept. 2012
Page 25 of 68
Outer Air Intake Kit 712-0731-04 / 712-EGL2-04

Contents:
ITEM
QTY
DESCRIPTION
Plate, Intake
Screw, PFH, SS, 8-32 X 3
Adapter, 40mm with O-Ring
O-Ring, Buna, 2-3/8X2.5X1/16" (Pre-installed into 40mm adapter)
Instructions:
STEP NO.
DIRECTIONS
Remove the damaged Outer Air Intake by
unscrewing the (4) 8-32 X 3 screws.
The O-Ring is pre-installed into the groove on

40mm Adapter. Verify it is inserted correctly.
Place Intake Plate over 40mm Adapter and the 4

8-32 X 3 screws through Intake Plate and 40mm
Adapter.
Rotate assembly such that the alignment pin on

the BV Filter Holder mates with the alignment
hole on the 40mm Adapter.
Place entire assembly into BV Filter Holder and

tighten the included (4) 8-32 X 3 screws.
Perform HiPot Testing then perform Calibration

and Functional Test using the RCS.
906-0731-04 Rev. B Sept. 2012
Page 26 of 68
Bezel Assembly Kit 712-0731-05 / 712-EGL2-05 / 712-AEV1-01

Contents:
ITEM
QTY
DESCRIPTION
Bezel Assembly
EMV Label
EMVP Label
Instructions:
STEP NO.
DIRECTIONS

(4) 8-32 X 3 screws on the outer air intake.
Loosen and remove the (2) 10-32 Keps nuts

and the (4) 6-32 X 2 screws. Remove the
back case by lifting from the ventilator.
Remove the (2) 4-40 X screws on the

Dovetail Mounting Bracket and disconnect
the ribbon cable on the PIM PCB by
simultaneously applying pressure on the
two locking ears.
Flip the ventilator over and remove the

front case assembly by lifting it straight up
away from the ventilator module.
906-0731-04 Rev. B Sept. 2012
Page 27 of 68

removing the (7) 4-40 X screws that hold
the bezel to the front case.
Select the correct label for your device,

peel the backing off and affix to the front
bezel.
Install the new bezel by tightening the

included (7) 4-40 X screws.
Place the front case assembly over the vent

module and tighten the (2) 4-40 X screws
unto the dovetail mounting bracket.
Reconnect the ribbon cable unto the PIM
PCB. Make sure the two locking ears lock
into position.

10

outer air intake.
11

Functional Test using the RCS.
906-0731-04 Rev. B Sept. 2012
Page 28 of 68
Power Knob Kit 712-0731-06 / 712-EGL2-06

Contents:
ITEM
QTY
DESCRIPTION
Power Knob
Screw, Socket, Cup Point, Set, 6-32 X 1/4 (installed into knob)
Instructions:
STEP NO.
DIRECTIONS



two locking ears.


removing the (7) 4-40 X screws that hold
the bezel to the front case.
906-0731-04 Rev. B Sept. 2012
Page 29 of 68
On the membrane panel assembly, loosen

the 6-32 X set screw using a 1/16 Ball Hex
Driver (located in the power knob) and lift
the damaged knob from the membrane
panel.
Place the replacement knob on the

membrane panel switch - align with flat on
switch insert the included 6-32 X set
screw and tighten.


into position.
10

11

outer air intake.
12

RCS.
906-0731-04 Rev. B Sept. 2012
Page 30 of 68
USB Connector Plate Kit 712-0731-07 / 712-EGL2-07

Contents:
ITEM
QTY
DESCRIPTION
USB Connector Plate Assembly
Instructions:
STEP NO.
DIRECTIONS

intake.
Loosen and remove the (2) 10-32 Keps

nuts and the (4) 6-32 X 2 screws.
Remove the back case by lifting from
the ventilator.


module.

removing the (7) 4-40 X screws that
hold the bezel to the front case.
906-0731-04 Rev. B Sept. 2012
Page 31 of 68

Circuit Board and around the SPO2
Connector. Be careful not to cut either
cable.

to the front case.

case.

from the front case. Handle the SPO2
cable with extreme care. Do not pull
on the cable.
10

5/16 screws holding the damaged USB
Connector Plate to the front case.
11
Insert and tighten the two included 440 X 5/16 screws holding the
replacement USB Connector Plate to
the front case.
Tighten the two (2) 6-32 X 5/16 screws

that hold the CPU/UIM & SPO2 Stack
to the front case. Make sure that all
the pins on the header mate correctly.
12
906-0731-04 Rev. B Sept. 2012
Page 32 of 68
13

to the front case.
14
Remove any excess RTV sealant from

the SPO2 flex cable and USB PCB.
holding the USB PCB to the front case.
Apply RTV sealant to USB PCB and
SPO2 flex cable. Allow to dry/cure.
15
Place the included power knob on the

new membrane panel switch - align
with flat on switch insert the
included 6-32 X set screw and
tighten. Push the included selector
knob on the membrane panel switch align with flat on switch .
16
Place the front case assembly on to

the bezel and tighten the included (7)
4-40 X screws.
17

vent module and tighten the (2) 4-40
X screws unto the dovetail
ribbon cable unto the PIM PCB. Make
sure the two locking ears lock into
position.
18

mounting studs. Insert and tighten the
included (2) 10-32 Keps nuts and the
(4) 6-32 X 2 screws.
19

outer air intake.
20

the RCS.
906-0731-04 Rev. B Sept. 2012
Page 33 of 68
Front Case Assembly Kit 712-0731-08 / 712-EGL2-08 / 712-AEV1-02

Contents:
ITEM
QTY
DESCRIPTION
Front Case Assembly
EMV Label
EMVP Label
Instructions:
WARNING: Disconnect external power and battery pack prior to performing service.
STEP NO.
DIRECTIONS

intake.

the ventilator.


the damaged front case assembly by
lifting it straight up away from the
ventilator module.
906-0731-04 Rev. B Sept. 2012
Page 34 of 68
Place the replacement front case

assembly over the vent module and
tighten the (2) 4-40 X screws unto
the dovetail mounting bracket.
Reconnect the ribbon cable unto the
PIM PCB. Make sure the two locking

(4) 6-32 X 2 screws.

outer air intake.
Select the correct label for your

device, peel the backing off and affix
to the front bezel.
a.
9
b.
Update serial numbers using

the RCS:
Use the C:\program
files\impact\EMV\bin\
EmvDLGui.exe to change
the serial numbers.
Use the RCS FD app to reflash the firmware.

the RCS.
10
906-0731-04 Rev. B Sept. 2012
Page 35 of 68
Battery Case Bottom Cover Kit 712-0731-09 / 712-EGL2-09

Contents:
ITEM
QTY
DESCRIPTION
Battery case bottom cover
Bumper, Rubber, Foot, P/S, Round, 1/2" Dia. X 1/8", Blk
Instructions:
STEP NO.
DIRECTIONS
Remove the damaged cover by unscrewing

the (4) 6-32 X 5/16 screws.
Remove backing from Bumper feet and place

one at each corner of Battery case bottom
cover.
Rotate cover to align with battery

compartment then insert and tighten the (4)
6-32 X 5/16 screws.

906-0731-04 Rev. B Sept. 2012
Page 36 of 68
EMV Chassis Kit 712-0731-10 / 712-EGL2-10

Contents:
ITEM
QTY
DESCRIPTION
EMV Chassis Assembly
Screw, Phillips, Flat Head, 8-32 X 1/4, Undercut, ZP
Screw, Phillips, Flat Head, 6-32 X 1/4, Undercut
SPO2 Insulator
Instructions:
STEP NO.
DIRECTIONS

intake.

the ventilator.


module.
906-0731-04 Rev. B Sept. 2012
Page 37 of 68
Remove the battery compartment cover

by unscrewing the (4) 6-32 X 5/16
screws.
Remove the battery by unscrewing the

(4) 6-32 X 2 screws and detaching the
plug from its locking latch.
Unscrew the (4) 6-32 X 5/16 Phillips

screws to remove the damaged battery
compartment case.


screws holding the chassis to the dovetail
mounting bracket and remove the SPO2
insulator. Loosen and remove the (2) 832 X screws holding the chassis to the
vent module.
10
Insert screwdriver through the holes on

the chassis to loosen and remove the (2)
6-32 x 5/16 screws holding the chassis to
the vent module.
11
Lift the damaged chassis from the

ventilator module.
906-0731-04 Rev. B Sept. 2012
Page 38 of 68
12
Secure the replacement Chassis to the

vent module using the included (2) 6-32 X
screws with SPO2 insulator, the (2) 832 X and the (2) 6-32 x 5/16 screws.
13

screws.
14
Rotate battery compartment to mate

with upper and lower case cutouts and
press firmly into place. Secure with (4) 632 X 5/16 screws provided.
15
Re-assemble the battery by connecting

its cable to the connector (pull on cable
to insure it is locked in place) then
tightening the (4) 6-32 X 2 screws.
16
Re-assemble the battery compartment

cover by tightening the (4) 6-32 X 5/16
screws.
17

906-0731-04 Rev. B Sept. 2012
Page 39 of 68
18

19

outer air intake.
20

RCS.
906-0731-04 Rev. B Sept. 2012
Page 40 of 68
Connector Panel Kit 712-0731-11 / 712-EGL2-11

Contents:
ITEM
QTY
DESCRIPTION
Connector Panel Assembly
8-32 X 1/4 Screw
6-32 Keps Nut
O-Ring OD X 3/8 ID
Instructions:
STEP NO.
DIRECTIONS

intake.

the ventilator.


module.
906-0731-04 Rev. B Sept. 2012
Page 41 of 68
Remove the O2 Inlet fitting by

unscrewing the dust cap then unscrewing
the (3) 8-32 X 7/16 screws.

screws. Loosen and remove the Gas
Output fitting using a 1-inch deep-socket
wrench.
Disconnect the Power Input cable by

pressing on the locking latch and pulling
the cable straight up from the connector.


nuts using a 5/16 open-end wrench.
10
Using a needle nose pliers, carefully

remove the 3 tubing on the
Transducer, Exhaust Do not Occlude,
and Exhalation Valve fittings.
11

nuts using a 5/16 open-end wrench.
906-0731-04 Rev. B Sept. 2012
Page 42 of 68
12
Lift the damaged connector panel

assembly out from the SPM.
13
Place the included OD X 3/8 ID O-ring

onto the manifold.
14
Position the replacement Connector

Panel over the SPM and secure with the
(4) included 6-32 Keps nuts.
15

screws. Connect the Power Input cable
by inserting into connector. Insure that
locking latch engages.
16
Insert the 3 tubing unto their correct

connectors. V_BACKUP to Exhalation
Valve, V_ACAL to Transducer and
smallest tubing to Exhaust do Not
occlude
17
Secure the connector panel to the vent

module using the (3) included 8-32 X
screws.
18
Insert the included 3/8 ID O-Ring unto

the Oxygen Inlet fitting and the existing
1/2 ID O-ring unto the Gas Output
adapter.
906-0731-04 Rev. B Sept. 2012
Page 43 of 68
Place Oxygen Inlet Fitting over the

connector panel then insert and tighten
with the (3)8-32 X 7/16 screws.
19
Place fitting and O-ring unto Gas Output
and tighten with a 1 deep socket
wrench. (Do not cross thread).
20

21

22

outer air intake.
23

RCS.
906-0731-04 Rev. B Sept. 2012
Page 44 of 68
Back Case Kit 712-0731-12 / 712-EGL2-12

Contents:
ITEM
QTY
DESCRIPTION
Back Case Assembly
Screw, Phillips, Pan Head, SS, Black Oxide, 6-32 X 2
Nut, Keps, 10-32
Instructions:
STEP NO.
DIRECTIONS


case by lifting from the ventilator.
Place the replacement cover over ventilator

housing and dovetail mounting studs. Insert
and tighten the included (2) 10-32 Keps nuts
and the (4) 6-32 X 2 screws.
Tighten the (4) 8-32 X 3 screws on the outer

air intake.

906-0731-04 Rev. B Sept. 2012
Page 45 of 68
PIM Board Kit 702-0731-02

Contents:
ITEM
QTY
DESCRIPTION
PIM PCB
Instructions:
STEP NO.
DIRECTIONS

(4) 8-32 X 3 screws on the outer
air intake.
Loosen and remove the (2) 1032 Keps nuts and the (4) 6-32 X
2 screws. Remove the back case
by lifting from the ventilator.
Remove the (2) 4-40 X screws

on the Dovetail Mounting
Bracket and disconnect the
ribbon cable on the PIM PCB by
simultaneously applying
pressure on the two locking
ears.
Flip the ventilator over and

remove the front case assembly
by lifting it straight up away
from the ventilator module.
Remove the battery

unscrewing the (4) 6-32 X 5/16
screws.
Remove the battery by

unscrewing the (4) 6-32 X 2
screws and detaching the plug
from its locking latch.
Disconnect the Power Input

cable from the PIM PCB by
pressing on the locking latch and
pulling the cable straight up
from the connector.
906-0731-04 Rev. B Sept. 2012
Page 46 of 68
Loosen and remove the(5) 4-40

X 5/16 screws holding the PIM
PCB to the ventilator module.
Position SPO2 Insulator out of
the way (Do Not Fold) and insert
screwdriver through the holes
to aid in removing screws.
Lift the defective PIM Board out

of the ventilator module.
10
Place the new PIM Board

Unto the vent module (make
sure male header pins are
inserted correctly into the
mating header.
11
Secure the PIM Board with the

(5) 4-40 x 5/16 screws.
connector (pull on cable to
insure it is locked in place) then
screws.
tightening the (4) 6-32 X 5/16
screws.
12
13
Place the front case assembly

over the vent module and
tighten the (2) 4-40 X screws
unto the dovetail mounting
bracket. Reconnect the ribbon
cable unto the PIM PCB. Make
sure the two locking ears lock
into position.
14
906-0731-04 Rev. B Sept. 2012
Page 47 of 68
15

module and align cover with
handle, air intake housing and
dovetail mounting studs. Insert
and tighten the included (2) 1032 Keps nuts and the (4) 6-32 X
2 screws.
16
Tighten the (4) 8-32 X 3 screws

on the outer air intake.
17

perform Calibration and
906-0731-04 Rev. B Sept. 2012
Page 48 of 68
CPU/UIM & SPO2 Stack Kit 712-0731-14

Contents:
ITEM
QTY
DESCRIPTION
CPU/UIM & SPO2 Stack
Screw, Metric, Phillips, Flat Head, M2.5 x 5mm Stainless Steel
Instructions:
STEP NO.
DIRECTIONS

intake.

the ventilator.


module.

RTV sealant around the SPO2 Cable.
906-0731-04 Rev. B Sept. 2012
Page 49 of 68

to the front case.
Disconnect the USB cable by pressing

on locking tab and pulling cable
downwards.

case.

from the front case. Handle the SPO2
cable with extreme care. Do not pull
on the cable.
Tighten the two (2) 6-32 X 5/16 screws

that hold the CPU/UIM & SPO2 Stack
to the front case. Make sure that all
the pins on the header mate correctly.
10

to the front case.
11
906-0731-04 Rev. B Sept. 2012
Page 50 of 68
12
Apply RTV Sealant around the SPO2

Flex Cable and allow to dry.
13
Dress the USB Connector cable along

the case and over the SPO2 flex cable.
14
Attach USB Connector cable to its

mating connector on the CPU PCB.
Make sure tab locks the cable in place.
15

position.
16

(4) 6-32 X 2 screws.
17

outer air intake.
18

the RCS.
906-0731-04 Rev. B Sept. 2012
Page 51 of 68
USB Connector Kit 712-0731-15

Contents:
ITEM
QTY
DESCRIPTION
USB Connector Assembly
Instructions:
STEP NO.
DIRECTIONS

intake.

the ventilator.


module.

Circuit Board.

906-0731-04 Rev. B Sept. 2012
Page 52 of 68
Remove the damaged cable by

pressing on locking tab and pulling
cable downwards.
Remove any excess RTV from the

case. Insert and tighten the two
included 4-40 X 3/16 screws holding
the new USB Connector to the front
case. Dress the USB Connector cable
along the case and over the SPO2 flex
cable.
Attach USB Connector cable to its

mating connector on the CPU PCB.
Make sure tab locks the cable in place.
10
Apply RTV Sealant around USB PCB

and allow to dry.
11

position.
12

(4) 6-32 X 2 screws.
13

outer air intake.
14

906-0731-04 Rev. B Sept. 2012
Page 53 of 68
Gas Output Kit 712-0731-16

Contents:
ITEM
QTY
DESCRIPTION
Fitting, Patient, Outlet, SPM
O-Ring, Neoprene, 1/2" ID
Instructions:
Step No.
Directions
Remove the damaged fitting by unscrewing

with a 1-inch deep socket wrench.
Place O-ring unto underside of outlet fitting.
Place fitting and O-ring unto Gas Output and

tighten with a 1 deep socket wrench. (Do
not cross thread).

906-0731-04 Rev. B Sept. 2012
Page 54 of 68
Power Input Kit 712-0731-17

Contents:
ITEM
QTY
DESCRIPTION
Power Input Assembly
Screw, Phillips, Flat Head, Zinc Plated, 4-40 X 1/4
Screw, Phillips, Flat Head, 4-40 X 1 1/4
Spacer, Nylon, #4, x .812 Long
Instructions:
Step No.
Directions

(4) 8-32 X 3 screws on the outer
air intake.

Remove the (2) 4-40 X screws

on the Dovetail Mounting
Bracket and disconnect the
ribbon cable on the PIM PCB by
simultaneously applying pressure
on the two locking ears.
Flip the ventilator over and

remove the front case assembly
by lifting it straight up away from
the ventilator module.
906-0731-04 Rev. B Sept. 2012
Page 55 of 68
Remove the battery compartment

cover by unscrewing the (4) 6-32 X
5/16 screws.
Remove the battery by unscrewing

the (4) 6-32 X 2 screws and
detaching the plug from its locking
latch.

1 Screws and nylon spacers
supporting the Power Input
assembly unto the chassis.
Disconnect the Power Input cable

from the PIM PCB by pressing on
the locking latch and pulling the
cable straight up from the
connector.

screws holding the Power Input
to the connector panel.
10
Using two small flat blade

screwdrivers, separate the two
locking tabs on the power plug
and pull the power input assembly
away from the connector panel.
Unobstructed view
906-0731-04 Rev. B Sept. 2012
Page 56 of 68
11
Insert the new power input

assembly into the connector panel
socket and pull on the assembly to
insure the locking tabs have
engaged.
12
Secure the Power Input assembly

to the Connector Panel using the
(2) included 4-40 X screws.
13
Secure the Power Input assembly

to the Chassis using the (2)
included spacers and (2) included
4-40 X 1 screws. Do not overtighten the screws.
14

connector (pull on cable to insure
it is locked in place) then
screws.
15

compartment cover by tightening
the (4) 6-32 X 5/16 screws.
16
Place the front case assembly over

the vent module and tighten the
(2) 4-40 X screws unto the
dovetail mounting bracket.
Reconnect the ribbon cable unto
the PIM PCB. Make sure the two
locking ears lock into position.
17

module and align cover with
handle, air intake housing and
dovetail mounting studs. Insert
and tighten the included (2) 10-32
screws.
906-0731-04 Rev. B Sept. 2012
Page 57 of 68
18
Tighten the (4) 8-32 X 3 screws on

the outer air intake.
19

perform Calibration and
906-0731-04 Rev. B Sept. 2012
Page 58 of 68
Oxygen Inlet Fitting Kit 712-0731-18

Contents:
ITEM
QTY
DESCRIPTION
Oxygen Inlet Fitting with Filter, Cap and Chain
Screw, Phillips, Flat Head, 8-32 X 7/16, ZP
O-Ring, Black, Neoprene, 1/2"O.D.X 3/8"I.D. (Nominal)
Instructions:
STEP NO.
DIRECTIONS
Remove the damaged O2 Inlet fitting by

unscrewing the dust cap then unscrewing the
(3) 8-32 X 7/16 screws.
Install the included O-Ring into groove on

underside of inlet fitting.
Place Oxygen Inlet Fitting over the ventilators

connector panel then insert and tighten the 3
supplied 8-32 X 7/16 screws.

906-0731-04 Rev. B Sept. 2012
Page 59 of 68
Selector Knob Kit 712-0731-19 / 392-0066-00

Contents:
ITEM
QTY
DESCRIPTION
Selector Knob with label
Instructions:
STEP NO.
DIRECTIONS (For Eagle II go to step no. 12)



two locking ears.

Remove the bezel from the membrane

panel assembly by loosening and removing
the (7) 4-40 X screws that hold the bezel
to the front case.
906-0731-04 Rev. B Sept. 2012
Page 60 of 68
Lift the damaged selector knob from the

membrane panel assembly.
Push the replacement knob on the

membrane panel switch - align with flat on
switch .


into position.
10

11

outer air intake.
12
For Eagle II ventilators the Selector knob

can be removed by prying the knob up
from the case. Align flats on knob and shaft
and push down to install.
13

906-0731-04 Rev. B Sept. 2012
Page 61 of 68
Troubleshooting
A list of alarms by category and service codes follows with a description of each alarm and possible service
kit(s) or action to use to repair the device.
Alarm Category
Ventilator
Alarm Category
Comments
Service Kit / Resolution
CPU Failure
user interface goes blank; audible and red LED

indicators activated; backup vent; Mute/Cancel no
effect
712-0731-14
no compressor
712-0731-02
Compressor
Fault/Failure
O2 Valve
Fault/Failure
restrictions through pneumotach screen or internal

gas path detected by internal sensor; outside normal
operating conditions
no O2 Valve
restrictions through pneumotach screen or internal
gas path detected by internal sensor; outside normal
operating conditions
712-0731-02
712-0731-02
712-0731-02
O2 Supply
Pressure Low
Fault/Failure
inability to detect presence of high-pressure O2;

trigger < 35 psig, clear > 45 psig
712-0731-02
O2 Supply
Pressure High
Fault/Failure
inability to detect presence of high-pressure O2;

trigger > 80 psig, clear < 75 psig
712-0731-02
Fresh Gas Intake

Fault/Failure
obstructions of Fresh Gas / Emergency Air Intake;

internal filter dirty/clogged (pressure drop across
filter monitored)
712-0731-02
failure of internal power management system
702-0731-02
remaining operating time
703-0731-01
not able to detect internal battery

CPU does not recognize SPM; indicative of complete
unit not properly calibrated after new SPM installed
associated with internal sensors monitoring and
controlling breath delivery
702-0731-02
Power
Fault/Failure
Low Battery
Power
Missing Battery
SPM Change
Calibration
Fault/Failure
Recalibrate using RCS

712-0731-02
Exhalation System
Fault/Failure
associated with control of exhalation valve and

airway pressure; triggers (airway pressure): > 40, 75
cmH2O
712-0731-02
Airway Pressure
High
trigger (factory default) > 35 cmH2O
712-0731-02
906-0731-04 Rev. B Sept. 2012
Page 62 of 68
PEEP Leak
airway pressure
712-0731-02
Disconnect
airway pressure
712-0731-02
Calibration Due
Ambient Pressure
Fault
Ambient
Temperature
Fault
time since last calibration
Recalibrate using RCS
ambient pressure range: -2000 to +25,000 ft altitude
712-0731-02
ambient temperature range: -25 to +50C
712-0731-02
Service Codes
Service
Code
Alarm Name
Comments
1001
Compressor Failure (Compressor

Control Fault - No Backup)
compressor fails to operate or

provide enough flow
2001
Compressor Fault (Compressor Control

Fault - Backup Available)
communication between
compressor controller and SPM
fails
3001
Compressor Fault (Compressor Control

Fault - Backup Selected)
compressor fails to operate or

provide enough flow
1002
Compressor Failure (Compressor Signal

Chain Fault - No Backup)
is lost
2002
Compressor Fault (Compressor Signal

Chain Fault - Backup Available)
is lost
3002
Compressor Fault (Compressor Signal

Chain Fault - Backup Selected)
1003
1010
1011
2011
3011
1012
2012
3012
1020
Self Check Failure

O2 Valve Failure (O2 Valve Failed
Open)
O2 Valve Failure (O2 Valve Control
Fault - No Backup)
O2 Valve Fault (O2 Valve Control Fault
- Backup Available)
O2 Valve Fault (O2 Valve Fault - Backup
Selected)
O2 Valve Failure (O2 Valve Signal Chain
Fault - No Backup)
O2 Valve Fault (O2 Valve Signal Chain
Fault - Backup Available)
O2 Valve Fault (O2 Valve Signal Chain
Fault - Backup Selected)
O2 Supply Failure (O2 Tank Pressure
Low - No Backup)
906-0731-04 Rev. B Sept. 2012
Service Kit /
Resolution
712-0731-02
712-0731-02
is lost
flow error > +/- 20%
712-0731-02
O2 Valve fails in open position
712-0731-02
O2 Valve not delivering required

flow
signal to O2 Valve outside of
calibration range for given flow
signal to O2 Valve outside of
calibration range for given flow
communication between O2
Valve and SPM fails
Valve and SPM fails
Valve and SPM fails
O2 supply pressure: trigger < 35
psig, clear > 40 psig
Page 63 of 68
712-0731-02
712-0731-02
712-0731-02
2020
O2 Supply Pressure Low (O2 Tank

Pressure Low)
1030
Fresh Gas Intake Failure
2030
Fresh Gas Intake Fault (Compressor

Intake Blocked - Backup Available)
Fresh Gas / Emergency Air Inlet

blocked
3030

Intake Blocked - Backup Selected)

blocked
3031

Intake Restricted)

blocked
712-0731-02
3032
Fresh Gas Intake Fault (Intake Pressure

Signal Chain Failure)
communication between Fresh

Gas / Emergency Air Inlet
pressure sensor and SPM lost
712-0731-02
1041
O2 Supply Pressure High Failure (O2

Tank Pressure Excessive - No Backup)
O2 supply pressure > 80 psig
1051
O2 Supply Pressure High (O2 Tank

Pressure High)
Run-Time Calibration Failure
1052
Airway Pressure Sensing Failure
2053
Suspicious Triggers (False Trigger or

Bad Baseline)
3041
1060
1061
Exhalation System Failure (Exhalation

Valve Failure)
Exhalation System Failure (Excessive
Airway Pressure)
2062
Exhalation System Fault (Gas Trapped)
2070
2071
2072
2073
2074
2075
2076
Airway Pressure High

Low Airway Pressure
High Tidal Volume
Low Tidal Volume
High Breath Rate
Low Breath Rate / Apnea
Apnea
2090
PEEP Leak
3091
Incomplete Exhalation
3092
Patient Inspiratory Demand Not Met
2095
Insufficient Flow
906-0731-04 Rev. B Sept. 2012
O2 supply pressure: trigger < 35

psig, clear > 40 psig
blocked
O2 supply pressure: trigger > 75

psig, clear < 68 psig
failure of calibration system
communication between airway
pressure sensor and SPM is lost
airway pressure sensor fails to
calibrate during expiratory
phase of breath
exhalation control valve fails to
operate
triggers (airway pressure): > 40,
75 cmH2O
airway pressure at end of
expiration > 5 cmH2O above
PEEP
Paw > high limit
Paw < low limit
Vt > high limit
Vt < low limit
BPM > high limit
BPM < low limit
BPM < low limit
Paw < [PEEP - 2 cmH2O] during
expiration
exhaled flow from patient
continues throughout expiratory
period
end inspiratory Paw < -1.0
cmH2O
pressure target not reached
during inspiratory period during
pressure-targeted ventilation
Page 64 of 68
712-0731-02
Lower Oxygen
input pressure
712-0731-02
712-0731-02
712-0731-02
712-0731-02
712-0731-02
712-0731-02
712-0731-02
712-0731-02
Check
internal/exter
nal tubing
connections
2100
Patient Disconnect
Paw < [PEEP + 7 cmH2O]
3110
RTC Battery Fault (RTC Battery Low)
Vstby < 2.5V
712-0731-02
3120
Self Check Fault (Calibration Due)
> 365 days since last calibration
Recalibrate
using RCS
Ambient Pressure Fault (Excessive

Altitude Sensor Failure)
Altitude)
Altitude)
Operational Temperature Fault
Operational Temperature Fault
(Excessive Temperature Low)
ambient pressure transducer

has failed
ambient pressure transducer:
altitude > 25,000 ft
ambient pressure transducer:
altitude < -2,000 ft
ambient temperature > 55C
3130
3131
3132
3140
3141
3143
Self Check Fault
2170
Spontaneous Breath - PIP High
2171
Spontaneous Breath - PIP Low
1172
Run-Time Self Check Alarm
2172
Spontaneous Breath - Vt High
ambient temperature < -10C

failure of internal temperature
sensors
Paw > high limit during 2
consecutive spontaneous
breaths
Paw < low limit during 2
breaths
supply voltage to circuitry NG
Vt > high limit during 2
breaths
communication between EMV
and SPM fails
1173
Internal Comm Failure
2173
Spontaneous Breath - Vt Low
1174
Self Check Failure
1175
1176
Offset Self-check Failure
2300
3300
Pulse Ox Module Failed

Pulse Ox Module Failed
2301
Internal Comm Failed
communication between pulse

oximeter module and CPU fails
3301
Internal Comm Failed (Comm Failure

EMV-Pulse Ox - Monitor Not In Use)
communication between pulse

oximeter module and CPU fails
Pulse Ox Sensor Not Connected

Defective Pulse Ox Sensor (Defective
Sensor)
Pulse Search (Pulse Search)
Pulse Ox Signal Interference
pulse oximeter detects SpO2

sensor disconnect; no power
from either internal battery or
external source
3310
3311
3312
3313
906-0731-04 Rev. B Sept. 2012
Vt < low limit during 2

breaths
failure of PGA offset control
detected during startup
SPM DSP unable to
communicate with PGA's
calibration file fails its integrity
test
712-0731-02
Ventilator
being used
outside of
specification
limits
712-0731-02
712-0731-02
Check Cable
from PIM
board to CPU;
702-0731-02
712-0731-02
712-0731-02
712-0731-02
712-0731-14
Page 65 of 68
712-0731-14
712-0731-14
2314
3315
3316
3317
3318
2401
2410
2411
1420
2421
3421
Pulse Ox Sensor Off Patient

Pulse Ox Light Contamination
Invalid Pulse Ox Sensor
Low SpO2 Perfusion
Low SpO2 Perfusion
SpO2 Low
Heart Rate High
Heart Rate Low
Complete Power Failure
Input Protection Circuit Failed
External Power Fail/Disconnect
3422
Missing Battery
2423
Power Circuit Hardware Fault
3423
1430
Battery Charge Circuit Failed

Empty Battery
2430
Low Battery (Low Battery - No Backup)
3430
Low Battery (Low Battery - Warning)
3431
3441
3442
Low Battery (Low Battery - With

Backup)
External Power Failed (External Power
High)
External Power Failed (External Power
Low)
failure of input protection circuit

external power < 5 VDC
battery and CPU has failed
internal power circuit has failed,
external power connected but
cannot be used
< 5 min of battery operation

remaining
remaining
remaining
external power: trigger > 33
VDC, clear < 30 VDC
703-0731-01;
702-0731-02
702-0731-02
703-0731-01
703-0731-01
702-0731-02
5V < external power < 11.5V
702-0731-02
Use Impact
Power supply
Only
3444
External Power Failed
external power voltage polarity

reversed
2450
Battery Fault - No External Power

Connected (Battery Nearly Too Hot for
Discharge)
battery temperature > 70C
3450
Battery Fault - With External Power

Connected (Battery Nearly Too Hot for
Discharge)
3451

Connected (Battery Too Hot for
Discharge)
3452
Battery Fault (Battery Too Hot for

Charging)
3453

Connected (Battery Too Cold for
Charging)
battery temperature < 0C
2455
Battery Fault - No External Power

Connected (Communication Failure)
EMV not able to communicate

with internal battery
906-0731-04 Rev. B Sept. 2012
702-0731-02
Page 66 of 68
703-0731-01
703-0731-01;
702-0731-02
3455

Connected (Battery Communication
Failure)

with internal battery
3470
Internal Communication (Comm)

Failure Fault - PIM Comm

with PIM
1471

Failure
CPU unable to communicate

with UIM and interface controls
1472

Failure
CPU unable to communicate

with SPM
1473
no valid data sent from SPM
1474
CRC check between EMV and

SPM fails
1475
LCD Control Failure
1480
SPM Compatibility Failure
3480
SPM Compatibility Fault
1485
Power-On Self-Check Failure
906-0731-04 Rev. B Sept. 2012
CPU unable to control LCD

contrast
EMV and SPM software revs
incompatible
EMV software detects that it has
not been calibrated with SPM
inside unit
SPM software fails and is shut
down
Page 67 of 68
Check Cable
from PIM
board to CPU;
702-0731-02
Check Flex
cable to LCD;
712-0731-14
Check Cable
from PIM
board to CPU;
702-0731-02
Check Cable
from PIM
board to CPU;
702-0731-02
Check Cable
from PIM
board to CPU;
702-0731-02
712-0731-08
Recalibrate
using RCS
712-0731-02
HiPot Testing
(708-0731-01)
UUT
Equipment required: 1) Masimo cable (708-0731-01) with braided conductors. 2) Associated Research Hypot III Dielectric Withstand Tester Model 3765 and test leads.
1) DONT TOUCH THE UUT OR THE CONNECTIONS DURING THE TEST. HANDLE TEST CLIPS BY INSULATION ONLY, NEVER TOUCH CLIPS DIRECTLY. DO NOT WEAR AN ESD WRISTSTRAP.
Do not attempt to operate the Hipot if impaired for any reason including medication, illness, alcohol, Mental stress etc.
2) Perform continuity and AC Hipot test on the Hipot before testing a unit to ensure the hipots functionality.
3) Insure that the hipot testers POWER switch is off. Connect the line cord to the back of the hipot tester and to a grounded 120VAC outlet.
4) Connect the black then white test leads to the hipot tester as indicated
5) Connect the UUTs power supply to the UUT as indicated.
6) Connect the modified Masimo cable to the UUT as indicated.
7) Connect the black alligator clip to the UUTs Exhaust Fitting not on the holes as indicated.
8) Connect the red alligator clip to the modified Masimo cable as indicated.
9) Turn the POWER switch ON.
10) Set the HiPot tester as follows: Voltage = 5.00kV, Current = 50uA, Duration = 0.5 sec.
11) Press the green TEST button. The HIGH VOLTAGE ON indicator flashes during the test.
12) If the UUT passes the test, the tester will beep and display the results.
13) If there is a failure, the tester will alarm and the red failure indicator will light up. To stop the alarm press the red RESET button. Record the failure on the DHR and apply a
rejected tag identifying the non conformity after completing steps 13. Place UUT into the NCM area.
14) Turn the POWER switch OFF.
15) Disconnect black test lead from exhaust port and connect to power supply plug ground repeat above starting at step 8.
16) Disconnect the Masimo cable from the UUT.
17) Disconnect the black alligator clip from the power supply plug ground.
18) If there are more units to test, go to step 4.
19) If there are no more units to test, disconnect the white then black test leads from the hypot tester.
906-0731-04 Rev. B Sept. 2012
Page 68 of 68

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906-0731-04 Rev. B Sept.

906-0731-04 Rev. B Sept. 2012

Terminology and Abbreviations

906-0731-04 Rev. B Sept. 2012

LED - Light Emitting Diode

Limited Copyright Release

906-0731-04 Rev. B Sept. 2012

Masimo Pulse Oximeter

906-0731-04 Rev. B Sept. 2012

WARNINGS AND CAUTIONS REGARDING USE

906-0731-04 Rev. B Sept. 2012

Pulse Oximeter Specific Warnings And Cautions

906-0731-04 Rev. B Sept. 2012

in the directions for reusable Masimo LNCS sensors.

906-0731-04 Rev. B Sept. 2012

906-0731-04 Rev. B Sept. 2012

Post-Contaminated Environment Cleaning

906-0731-04 Rev. B Sept. 2012

Removable Foam Filter Replacement

Fresh Gas/Emergency Air Intake Disk Filter Replacement

906-0731-04 Rev. B Sept. 2012

Battery Capacity, Care and Recharging

Battery charging is controlled by ventilator in the temperature range of 0 C to 45 C (32F to 113 F)

906-0731-04 Rev. B Sept. 2012

Preventive Maintenance (PM)

Year after initial purchase of ventilator

Replace the main battery

Table 1 Maintenance Schedule.

Periodic Maintenance Check (PMC)

906-0731-04 Rev. B Sept. 2012

Annual Preventive Maintenance Kit

4-Year Preventive Maintenance Kit

906-0731-04 Rev. B Sept. 2012

Troubleshooting and Repairs

ALARM & PLOT LIST: FIGURE 2

906-0731-04 Rev. B Sept. 2012

Service Kit Listing

Membrane Panel Kit

SPM/Vent Assembly Kit

Battery Compartment Kit

Bezel Assembly Kit

Power Knob Kit

USB Connector Plate Kit

Front Case Assembly Kit

Battery Case Bottom Cover Kit

EMV Chassis Kit

Connector Panel Kit

Back Case Kit

PIM Board Kit

CPU/UIM & SPO2 Stack Kit

USB Connector Kit

Gas Output Kit

Power Input Kit

Oxygen Inlet Fitting Kit

Selector Knob Kit

906-0731-04 Rev. B Sept. 2012

Membrane Panel Kit 712-0731-01 / 712-EGL2-01

Membrane Panel Assembly

Screw, Phillips, Pan Head, Zinc Plated, 4-40 X 1/4

Power Select Knob with Set screw