For Technical Support and Customer Service, contact:
USA and Canada: 1-800-345-6443 (toll free) or 724-387-4000
Respironics Europe, Africa, Middle East: +33-1-47-52-30-00
Respironics Asia Pacific: +852-3194-2280
Facsimile: 724-387-5012
United States of America
Respironics California, Inc.
2271 Cosmos Court
Carlsbad, CA 92011
USA
2009 Respironics California, Inc. and its affiliates.
All rights reserved.
This work is protected under Title 17 of the United States copyright code and is the sole property of Respironics
California, Inc. No part of this document may be copied or otherwise reproduced, or stored in any electronic
information retrieval system, except as specifically permitted under United States copyright law, without the
prior written consent of Respironics California, Inc.
The V60 ventilator is a microprocessor-controlled, positive pressure ventilator
assist system. The ventilator provides noninvasive and invasive ventilatory
support for spontaneously breathing adult and pediatric patients.
The ventilator has a variety of modes and monitoring capabilities to assist in
assessing performance and patient-to-ventilator synchrony. The safety features
include in-depth alarms and a variety of integrated safety and self-diagnostic
features. Many system functions are automatically checked at startup and
during operation.
The ventilator includes a touch screen user interface (UI) and navigation ring
(nav-ring) that allows the operator to select ventilator and alarm settings and
displays of ventilator and patient data.
The ventilator is designed to be upgradeable, and features communications
capabilities and an internal battery backup option.
Read this manual thoroughly before performing service or maintenance on the
V60 ventilator. This manual includes advanced troubleshooting, calibration,
and maintenance instructions for the ventilator. All maintenance and repair
work should be performed by qualified biomedical technicians who have
appropriate training and authorization to provide maintenance, repair, and
service for the V60.
Review the operating instructions for the V60 ventilator before running tests,
checking operational readiness, or initiating patient use. These instructions
include important information about ventilator safety and operation.
For additional information about accessories or related equipment, such as
humidifiers and remote alarm systems, refer to the appropriate instruction
manual prior to operating the V60 ventilator. Review the applicable warnings
and cautions in the V60 User Manual before operating the ventilator.
1049766 Rev AV60 Ventilator Service Manual 1-1
Chapter 1
Introduction and Intended Use
1.1 Intended UseThe Respironics V60 ventilator is an assist ventilator that is intended to
augment patient breathing. It is intended for spontaneously breathing
individuals who require mechanical ventilation: patients with respiratory
failure, chronic respiratory insufficiency, or obstructive sleep apnea in a
hospital or other institutional settings under the direction of a physician.
The ventilator is intended to support pediatric patients weighing 20 kg (44 lb.)
or greater to adult patients. It is also intended for intubated patients meeting
the same selection criteria as the noninvasive applications. The ventilator is
intended to be used by qualified medical professionals such as physicians,
nurses, and respiratory therapists. The ventilator is intended to be used only
with various combinations of Respironics recommended patient circuits,
interfaces (masks), humidifiers, and other accessories.
1-2 V60 Ventilator Service Manual1049766 Rev A
Chapter 1
Introduction and Intended Use
1.2 Recommended
Test Equipment,
Tools, and Supplies
Table 1-1 lists the recommended tools, test equipment, and materials required
to service and maintain the V60 ventilator.
Table 1-1: Recommended Test Equipment, Tools, and Materials
DescriptionManufacturer and Model
Test Equipment
Digital multimeter (DMM) accurate to three decimal
places
Electrical safety analyzerDale LT 5440 or equivalent
Pneumatic calibration analyzer capable of measuring
low pressure (cmH
(liters)
Temperature/humidity monitorFisher Scientific 11661-14 or
Test lungIngMar QuickLung or equivalent
O), flow rate (LPM), and volume
2
Service Tools and Supplies
V60 Service Kit, which includes:Respironics P/N 1054291
Adapter, 22-mm OD, both endsRespironics P/N 1002505
Before servicing the Respironics V60 ventilator, read and understand this
service manual, especially safety considerations. These safety considerations
are for reference only, and are not intended to supersede your institution’s
protocol for service or safe use of noninvasive ventilation.
The instructions in this manual are primarily reserved for use by a qualified
service technician.
WARNING:Alerts the user to the possibility of injury, death, or other serious adverse
reactions associated with the use or misuse of the device.
CAUTION:Alerts the user to the possibility of a problem with the device associated
with its use or misuse, such as device malfunction, device failure,
damage to the device, or damage to other property.
NOTE:Emphasizes information of particular importance.
2.1 GeneralWARNING:An alternative means of ventilation shall be available whenever the ventilator
is in use. If a fault is detected in the ventilator, disconnect the patient from it
and immediately start ventilation with such a device. The ventilator must be
removed from clinical use and serviced by Respironics-authorized service
personnel.
WARNING:Use the Respironics V60 ventilator on spontaneously breathing patients only.
It is an assist ventilator and is intended to augment the ventilation of a
spontaneously breathing patient. It is not intended to provide the total
ventilatory requirements of the patient.
WARNING:We do not recommend you use the Respironics V60 ventilator on patients who
require ventilation at predetermined tidal volumes. The ventilator provides
continuous positive airway pressure (CPAP) and positive pressure ventilation
(S/T, PCV, and AVAPS) and is indicated for assisted ventilation only. These
modes do not provide ventilation with guaranteed tidal volume delivery.
WARNING:We do not recommend you use AVAPS on patients who require rapid and
frequent IPAP adjustments to maintain a consistent tidal volume. AVAPS, a
volume targeted mode, changes the IPAP setting in order to achieve the target
tidal volume. During AVAPS setup, there may be a period of time before the
target tidal volume is achieved. AVAPS is ideal for more stabilized patients.
1049766 Rev AV60 Ventilator Service Manual2-1
Chapter 2
Warnings and Cautions
WARNING:To reduce the risk of CO2 rebreathing, make sure EPAP pressures and
exhalation times are sufficient to clear all exhaled gas through the exhalation
port. In noninvasive ventilation continuous air flow through the port flushes
exhaled gases from the circuit. The ability to completely exhaust exhaled gas
from the circuit depends on the EPAP setting and I:E ratio. Higher tidal
volumes further increase the volume of CO
rebreathed by the patient.
2
WARNING:To reduce the risk of CO
rebreathing, monitor the patient for changes in
2
respiratory status at the start of ventilation and with each change in ventilator
settings, circuit configuration, or patient condition. Pay attention to ventilator
alarms that warn of increased CO
rebreathing risk.
2
WARNING:Be aware of the possibility of contamination from patient exhalate being
exhausted into the room through the exhalation port.
WARNING:To ensure accuracy of oxygen administration and to monitor for the presence
of contamination (incorrect gas connected), use an external oxygen monitor
to verify the oxygen concentration in the delivered gas.
WARNING:To reduce the risk of fire, use the ventilator in well-ventilated areas away from
flammable anesthetics. Do not use in a hyperbaric chamber or other similarly
oxygen-enriched environments. Do not use near an open flame.
WARNING:To reduce the risk of electric shock from liquid entering the device, do not put
a container filled with a liquid on the ventilator.
WARNING:To reduce patient risk of hypoxemia, keep free-flowing oxygen away from air
inlet of ventilator.
WARNING:Connect to the ventilator only items that are specified as part of or compatible
with the ventilator system. Additional equipment connected to medical
electrical equipment must comply with the respective IEC or ISO standards.
Furthermore, all configurations shall comply with the requirements for
medical electrical systems (see IEC 60601-1-1 or clause 16 of edition 3 of
IEC 60601-1, respectively). Anybody connecting additional equipment to
medical electrical equipment configures a medical system and is therefore
responsible for ensuring that the system complies with the requirements for
medical electrical systems. Also be aware that local laws may take priority
over the above mentioned requirements. If in doubt, consult Respironics.
WARNING:To reduce the risk of fire, explosion, leakage, or other hazard, take these
precautions with respect to the battery:
•Do not attempt to disassemble, open, drop, crush, bend or deform, insert
foreign objects into, puncture, or shred the battery pack; modify or
remanufacture it; immerse or expose it to water or other liquids; expose
it to fire, excessive heat (including soldering irons); or put it in a
microwave oven.
•Replace the battery only with another battery specified by the
manufacturer.
•Follow all instructions for proper use of the battery.
•Do not short-circuit the battery or allow metallic or conductive objects to
contact the battery connector housing.
•Use the battery with the Respironics V60 ventilator only.
2-2 V60 Ventilator Service Manual1049766 Rev A
Chapter 2
Warnings and Cautions
WARNING:The nurse call/remote alarm should be considered a backup to the ventilator’s
primary alarm system.
WARNING:To ensure that the alarm will be heard, make sure the alarm loudness is
adequate and avoid blocking the alarm speakers beneath the ventilator.
CAUTION:Federal law (USA) restricts this device to sale by or on the order of a
physician.
CAUTION:The Respironics V60 ventilator is designed to operate in the temperature
range of 5 to 40 ºC (41 to 104 ºF). To minimize the risk of overheating the
device, do not operate adjacent to heaters or other heat sources.
NOTE:The displays shown in this manual may not exactly match what you see on
your own ventilator.
NOTE:Pressures are indicated on the ventilator in cmH2O. Millibars and
hectopascals (hPa) are used by some institutions instead. Since 1
millibar equals 1 hPa, which equals 1.016 cmH
used interchangeably.
O, the units may be
2
NOTE:The ventilator is not intended for use as an ambulance transport ventilator
or as an Automatic Transport Ventilator as described by the American
Hospital Association and referenced by the FDA. It is intended to allow
the patient to be transported within the hospital setting using a cart to
move the ventilator.
NOTE:When attachments or other components or subassemblies are added to
the ventilator breathing system, the pressure gradient across the
ventilator breathing system, measured with respect to the ventilator
outlet, may increase.
NOTE:The Respironics V60 ventilator parts that have patient contact are free of
latex.
NOTE:If an alarm persists for no apparent reason, discontinue ventilator use and
contact Respironics.
NOTE:If you detect any unexplained changes in the performance or visual
displays of the ventilator, discontinue ventilator use and contact
Respironics.
NOTE:The Respironics V60 ventilator does not support automatic record
keeping.
1049766 Rev AV60 Ventilator Service Manual2-3
Chapter 2
Warnings and Cautions
2.2 Preparing for
Ventilation
WARNING:To ensure the correct performance of the ventilator and the accuracy of
patient data, we recommend you use only Respironics-approved accessories
with the ventilator.
WARNING:To prevent possible asphyxia and to reduce the risk of CO2 rebreathing, take
these precautions with respect to mask and exhalation port use:
•Use only a mask with an exhalation port or a nasal mask for noninvasive
ventilation.
•Do not occlude the exhalation port.
•Turn on the ventilator and verify that the port is operational before
application. Pressurized gas from the ventilator should cause a
continuous flow of air to exhaust from the leak port, flushing exhaled gas
from the circuit.
WARNING:Never leave the mask on the patient while the ventilator is not operating.
When the ventilator is not operating, the exhalation port does not allow
sufficient exhaust to eliminate CO
rebreathing may occur.
WARNING:To ensure normal air circulation and exchange, do not cover or block the
ports on the ventilator or ventilator circuit. Do not block the air inlet panel on
the right side of the ventilator.
WARNING:To prevent possible patient injury and possible water damage to the ventilator,
make sure the humidifier is set to appropriate temperature and humidification
settings.
from the circuit. Substantial CO2
2
WARNING:To prevent the possibility of inadequate humidification, pay close attention to
the humidifier’s functioning when operating the ventilator at an ambient
temperature > 30 ºC (86 ºF). The ventilator warms the air delivered to the
patient above ambient temperature, which may impair the humidifier’s
performance.
WARNING:To reduce the risk that the patient will aspirate condensed water from the
breathing circuit, position any humidifier lower than both the ventilator and
the patient.
WARNING:To prevent possible patient injury and equipment damage, do not turn the
humidifier on until the gas flow has started and is regulated. Starting the
heater or leaving it on without gas flow for prolonged periods may result in
heat build-up, causing a bolus of hot air to be delivered to the patient. Circuit
tubing may melt under these conditions. Turn the heater power switch off
before stopping gas flow.
WARNING:To reduce the risk of fire, use only patient circuits intended for use in oxygen-
enriched environments. Do not use antistatic or electrically conductive
tubing.
WARNING:To prevent patient or ventilator contamination, recommend you use a
Respironics-approved main flow bacteria filter on the patient gas outlet port.
Filters not approved by Respironics may degrade system performance.
2-4 V60 Ventilator Service Manual1049766 Rev A
Chapter 2
Warnings and Cautions
WARNING:To reduce the risk of bacterial contamination or damage, handle bacteria
filters with care.
WARNING:To reduce the risk of strangulation from patient tubing, use a tubing support
arm and secure the proximal pressure line with clips.
WARNING:To reduce the risk of electric shock, connect the ventilator to an AC supply
mains with protective earth only.
WARNING:Do not use extension cords, adapters, or power cords with the ventilator that
are not approved by Respironics.
WARNING:To prevent unintentional disconnection of the power cord, always use the
correct, Respironics-supplied power cord and lock it into place with the
power cord retainer before you switch the ventilator on. The retainer is
designed to hold the connector end of the Respironics-supplied cord securely
in place.
WARNING:To reduce the risk of electric shock, regularly inspect the AC power cord and
verify that it is not frayed or cracked.
WARNING:To reduce the risk of strangulation, route the power cord to avoid
entanglement.
WARNING:To reduce the risk of power failure, pay close attention to the battery’s charge
level. The battery’s operation time is approximate and is affected by ventilator
settings, discharge and recharge cycles, battery age, and ambient
temperature. Battery charge is reduced at low ambient temperatures or in
situations where the alarm is continuously sounding.
WARNING:To ensure the ventilator’s safe operation, always run the full preoperational
check described in the operator’s manual before using the ventilator on a
patient. If the ventilator fails any tests, remove it from clinical use
immediately. Do not use the ventilator until necessary repairs are completed
and all tests have passed.
WARNING:To prevent possible patient injury, disconnect the patient from the ventilator
before running the preoperational check. Make sure another source of
ventilatory support is available.
WARNING:To prevent possible patient injury due to nonannunciating alarms, verify the
operation of any remote alarm device before use.
CAUTION:To prevent possible damage to the ventilator, ensure that the connection
to the oxygen supply is clean and unlubricated, and that there is no water
in the oxygen supply gas.
CAUTION:For 120 V equipment, grounding reliability can only be achieved when it
is connected to an equivalent receptacle marked “hospital only” or
“hospital grade.”
1049766 Rev AV60 Ventilator Service Manual2-5
Chapter 2
Warnings and Cautions
2.3 OperationWARNING:To prevent possible patient injury, avoid setting alarm limits to extreme
values, which can render the alarm system useless.
2.4 Alarms and
Messages
2.5 Care and
Maintenance
WARNING:If AC power fails and the backup battery is not installed or is depleted, an
audible and visual alarm annunciates for at least 2 minutes. Immediately
discontinue ventilator use and secure an alternative means of ventilation. As
in most ventilators with passive exhalation ports, when power is lost,
sufficient air is not provided through the circuit and exhaled air may be
rebreathed.
WARNING:WARNING: To reduce the risk of electric shock, power down the ventilator and
disconnect it from AC power before cleaning or servicing it.
WARNING:WARNING: To prevent patient or ventilator contamination, inspect and replace
the main flow bacteria filter between patients and at regular intervals (or as
stated by the manufacturer).
WARNING:WARNING: To prevent possible patient injury, inspect and verify the proper
operation of the exhalation port regularly during use.
CAUTION:Do not attempt to sterilize or autoclave the ventilator.
CAUTION:To prevent possible damage to the ventilator, use only those cleaning
agents listed in this manual.
CAUTION:To prevent possible damage to the touchscreen, take care when cleaning
it. Do not drip water and/or soap solution. After cleaning and rinsing,
remove all moisture with a dry, soft cloth. Never clean the touchscreen
with an abrasive brush or device, since this will cause irreparable
damage.
CAUTION:To avoid introducing foreign matter into the ventilator and to ensure
proper system performance, change the air inlet filter at regular intervals
(or as stipulated by your institution).
CAUTION:To ensure proper system performance, use a Respironics-approved air
inlet filter.
CAUTION:Because some environments cause a quicker collection of lint and dust
than others, inspect the filters more often when needed. The air inlet
filter should be replaced; the cooling fan filter should be cleaned.
CAUTION:To prevent possible damage to the ventilator, always ship it with the
original packing material. If the original material is not available, contact
Respironics to order replacements.
2-6 V60 Ventilator Service Manual1049766 Rev A
Chapter 2
Warnings and Cautions
2.6 First-Time
Installation
2.7 Communications
Interface
WARNING:Never attempt to disconnect or reconnect the battery during operation.
CAUTION:To prevent possible damage to the ventilator, always secure it to its stand
or securely place it on a flat, stable surface that is free of dirt and debris.
Do not use the ventilator adjacent to, or stack it with, other equipment.
WARNING:Connect to the ventilator only items that are specified as part of or compatible
with the ventilator system. Additional equipment connected to medical
electrical equipment must comply with the respective IEC or ISO standards.
Furthermore, all configurations shall comply with the requirements for
medical electrical systems (see IEC 60601-1-1 or clause 16 of edition 3 of
IEC 60601-1, respectively). Anybody connecting additional equipment to
medical electrical equipment configures a medical system and is therefore
responsible for ensuring that the system complies with the requirements for
medical electrical systems. Also be aware that local laws may take priority
over the above mentioned requirements. If in doubt, consult Respironics.
WARNING:It is the responsibility of the end user to validate the compatibility and use of
information transmitted from the ventilator with the device to be connected to
the ventilator.
WARNING:The data provided through the communications interface is for reference only.
Decisions for patient care should be based on the clinician’s observations of
the patient.
WARNING:To prevent possible patient injury due to nonannunciating alarms, verify the
operation of any remote alarm device before use.
WARNING:To ensure the functionality of the remote alarm, connect only Respironics-
approved cables to the remote alarm port.
CAUTION:The remote alarm port is intended to connect only to an SELV (safety
extra-low voltage and ungrounded system with basic insulation to
ground), in accordance with IEC 60601-1. To prevent damage to the
remote alarm, make sure the signal input does not exceed the maximum
rating of 24 VAC or 36 VDC at 500 mA with a minimum current of
1 mA.
>
2.8 Diagnostic ModeWARNING:To prevent possible patient injury, do not enter the diagnostic mode while a
patient is connected to the ventilator. Verify that the patient is disconnected
before proceeding.
1049766 Rev AV60 Ventilator Service Manual2-7
Chapter 2
Warnings and Cautions
(This page is intentionally blank.)
2-8 V60 Ventilator Service Manual1049766 Rev A
Chapter 3. Theory of Operation
The V60 ventilator is a microprocessor-controlled gas flow control and
monitoring system that can deliver air and oxygen to augment or replace the
work normally performed by the patient’s respiratory system. The ventilator
uses electromechanical control circuits, flow and pressure monitors, and
software programs to deliver pressure controlled breaths.
The ventilator includes a user interface (UI), internal blower, and gas delivery
subsystem (GDS) that mixes air and oxygen. The ventilator can operate from a
40 to 87 psig (276 to 600 kPa) medical grade oxygen source for enriched
oxygen operation. The internal power supply that can operate from mains (100
to 240 V AC 50/60 Hz) or internal battery (14.4 V DC) power. The ventilator
also includes several communications interfaces.
Schematic diagrams of the V60 ventilator are available upon request.
3.1 PneumaticsThe pneumatic subsystem delivers and monitors pressurized gas to the patient
in response to commands from the CPU subsystem. The pneumatic subsystem
includes the:
•Manifold
•Blower
•Oxygen solenoid valve
•Air and oxygen flow sensors
•Pressure transducers
•Solenoid valves
•Motor controller (MC) PCBA
•Data acquisition (DA) PCBA
The ventilator uses ambient air and high-pressure oxygen. Air enters through
an inlet filter. Oxygen enters though a high-pressure inlet, and a proportional
valve provides the operator-set concentration. The system mixes the air and
oxygen, pressurizes it in the blower, and then regulates it to the user-set
pressure. To do this, the ventilator compares the proximal (patient) pressure
measurement with the ventilator outlet (machine) pressure, and adjusts the
machine pressure to compensate for the pressure drop across the inspiratory
filter, patient circuit, and humidifier. This helps ensure accurate and
responsive pressure delivery and leak compensation.
The ventilator delivers gas to the patient through a main flow (inspiratory)
bacteria filter, a single-limb patient breathing circuit, a humidification device
(optional), and a patient interface such as a mask or ET tube. A pressure tap
1049766 Rev AV60 Ventilator Service Manual 3-1
Chapter 3: Theory of Operation
Air inlet
filter
Ambient air
inlet
proximal to the patient is used to monitor patient pressure. The internal
exhalation port continually clears gas from the ventilator airway to ensure
delivery of an accurate oxygen mixture.
Figure 3-1 shows a pneumatic schematic of the V60 ventilator.
The air inlet filter is designed to filter 5-micron particles at 70% efficiency at
150 SLPM flow.
Air inlet filter
3-2 V60 Ventilator Service Manual1049766 Rev A
Manifold
Air flow sensor
Chapter 3: Theory of Operation
3.1.3Air Flow Sensor
The air flow sensor measures a subset (bypass flow) of total flow in the
pneumatic air path and interpolates the measurements according to constants
that are calculated during gas delivery subsystem (GDS) calibration. The air
flow sensor also helps provide closed-loop control of gas flow during oxygen
blending.
3.1.4Machine and Proximal Pressure Transducers
The machine and proximal pressure transducers on the DA PCBA measure the
machine and proximal pressure over a range of -20 to +65 cmH
O.
2
3.1.5Barometric Pressure Transducer
The barometric pressure transducer on the DA PCBA measures barometric
pressure over a range of 525 to 850 mmHg.
3.1.6Oxygen Pressure Transducer
The oxygen pressure transducer on the DA PCBA measures inlet pressure over
Oxygen pressure
transducer
Machine pressure
transducer
DA PCBA
a range of 0 to 87 psig. An alarm results if oxygen supply pressure is below
40 psig (276 kPa) or above 92 psig (634 kPa).
Proximal
pressure
transducer
Barometric
pressure
transducer
1049766 Rev A V60 Ventilator Service Manual3-3
Chapter 3: Theory of Operation
Oxygen
filter
element
Manifold
Oxygen
inlet
filter
Manifold
Oxygen
breather
vent
3.1.7Manifold, Oxygen Inlet Filter, Filter Element
The manifold includes a connection for the oxygen inlet, allowing countryspecific oxygen connections to be attached to the manifold. The manifold
provides the pneumatic interfaces to the air inlet, oxygen inlet, blower inlet,
and proximal and machine pressure lines.
The oxygen inlet filter removes 5-micron particles from the oxygen gas supply.
A 40-micron sintered bronze filter element acts to reduce turbulence in the
oxygen flow. The 40-micron oxygen breather vent reduces noise in the oxygen
flow.
3.1.8Oxygen Solenoid Valve
The oxygen solenoid valve and valve driver circuitry control the flow of oxygen
according to the set O
there is a loss of power or system reset.
and flow. The oxygen solenoid valve is closed when
2
Manifold
Oxygen flow
sensor
Oxygen solenoid valve
Blower
3.1.9Oxygen Flow Sensor
The oxygen flow sensor measures a subset (bypass flow) of the total flow.
These measurements are interpolated according to constants that are
calculated during GDS calibration. Together, the oxygen solenoid valve and
flow sensor provide closed-loop control for delivered oxygen flow.
3.1.10 Blower
The blower is controlled by the MC PCBA, and generates flow and pressure for
the system. The blower includes an impeller, housing, and a three-phase
brushless DC motor. The blower delivers a maximum pressure of less than 125
cmH
O in a dead-head condition, can accelerate from 10,000 to 22,500
2
revolutions per minute (RPM) in 120 msec from a nominal 5- to 25-cmH
pressure rise. Maximum motor speed is approximately 40,000 RPM. The
blower motor has internal Hall Effect sensors that are monitored by the MC
PCBA and measure impeller speed.
O
2
3-4 V60 Ventilator Service Manual1049766 Rev A
3.1.11 Solenoid Valves
Chapter 3: Theory of Operation
Manifold
Solenoid valves (x4)
Four solenoid valves are mounted on the manifold and controlled by the DA
PCBA. These three-way autozero solenoids include SOL1 (purge solenoid),
SOL2 and SOL4 (machine pressure autozero solenoids), and SOL3 and SOL4
(proximal pressure autozero solenoids).
Solenoid valves
SOL2, SOL4: Machine pressure autozero solenoids.
SOL1: Purge solenoid, uses the machine pressure
line to purge the proximal pressure line.
SOL3, SOL4: Proximal pressure autozero solenoids. SOL4:
Also connects machine pressure to the proximal pressure
transducer during autozero.
1049766 Rev A V60 Ventilator Service Manual3-5
Chapter 3: Theory of Operation
3.2 Electronics The electronics system provides software-based control and monitoring, power
management, user input, display, subsystem I/O, external communication, and
alarms. The electronics system includes a Cirrus EP9307 microcontroller for
control and monitor processing.
Control tasks include breath delivery, patient data calculation, and alarm
detection/response. Monitoring tasks include controlling the LCD, front panel
keys and indicators, inputs, and primary alarm output. An independent
watchdog control provides safety monitoring.
•Backup alarm control circuitry, including power fail detection.
•Power switch control circuitry.
•System alarm and reset management.
•Electrical interfaces between the CPU PCBA, LCD, and the user
interface (UI) PCBA.
•Includes an EEPROM for calibration data, board identification
information, and PM PCBA power-on hours.
3.2.2Power Supply
•Provides ventilator and battery recharging power from AC line voltage.
•Converts AC line voltage (100 to 240 VAC, 50 to 60 Hz) into 24 VDC
power.
•Includes input over-current, output over-voltage, and output currentlimiting protection.
Internal battery
3.2.3Internal Battery
•14.4-V, 11.5-Ah lithium-ion battery has a run-time of at least six
hours under normal conditions.
•Provides operating power when AC power is not available.
•Provides charge and temperature status to the PM PCBA.
•Internal circuitry monitors battery status, provides self-contained
fault control features, and communicates this information to the PM
PCBA.
1049766 Rev A V60 Ventilator Service Manual3-7
Chapter 3: Theory of Operation
CPU PCBA
3.2.4CPU PCBA
•Microprocessor: once in a run state, the microprocessor can only be
reset by a watchdog timeout or out-of-specification power condition.
Monitors operation of the ventilator and controls delivery of air and
oxygen to the patient. Verifies safe ventilator operation.
•Flash memory: 8 MB program storage.
•RAM: 8 MB for program execution and volatile data storage.
•EEPROM: 4 KB of storage for board-specific information (including
operating hours, time since last service, serial numbers, part
numbers, and software and hardware revisions).
•Watchdog timer: disables the blower and oxygen flow if not strobed by
software within a predefined time window that is independent of the
CPU master clock. In addition, ensures that software is operating.
•Real-time clock (RTC): a time of day clock that provides the date and
time to the ventilator, and is powered by a dedicated 3-V lithium coin
cell battery.
•LCD interface supports a display of 1024 horizontal x 768 vertical
pixels in 256 colors with a refresh rate of at least 50 Hz. The CPU
PCBA controls LCD brightness by varying a control voltage over a
range of 0 to 3.5 V (minimum to maximum brightness).
•Touch screen interface supports a five-wire type touch screen.
•Nav-ring rotary adjustment interface with a minimum resolution of 24
ticks per revolution.
•User key switches: interfaces to front panel keys.
•Alarm subsystem: includes a speaker driver circuit for the two main
speakers, a backup piezo alarm, and a three-wire relay-controlled
remote alarm interface (normal open, NO, or normal closed, NC) on
the ventilator back panel.
•Blower speed monitor measures blower speeds from 3,000 to 50,000
RPM with 2% accuracy.
•Electrical interfaces to the power management (PM) and motor
controller (MC) PCBAs.
•Two USB ports and an ethernet connection are designed for future
enhancements. Table 3-1 summarizes hospital information system
(HIS) RS-232 port pinout.
3-8 V60 Ventilator Service Manual1049766 Rev A
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