Datex Ohmeda Aespire View - User Manual PDF

Aespire View
User’s Reference Manual

Software Revision 6.X
Datex-Ohmeda, Inc., a General Electric Company, doing business as GE Healthcare.
User Responsibility
This Product will perform in conformity with the description thereof
contained in this User’s Reference manual and accompanying labels
and/or inserts, when assembled, operated, maintained, and repaired
in accordance with the instructions provided. This Product must be
checked periodically. A defective Product should not be used. Parts
that are broken, missing, plainly worn, distorted, or contaminated
should be replaced immediately. Should repair or replacement
become necessary, Datex-Ohmeda recommends that a telephonic or
written request for service advice be made to the nearest
Datex-Ohmeda Customer Service Center. This Product or any of its
parts should not be repaired other than in accordance with written
instructions provided by Datex-Ohmeda and by Datex-Ohmeda
trained personnel. The Product must not be altered without the prior
written approval of Datex-Ohmeda. The user of this Product shall
have the sole responsibility for any malfunction which results from
improper use, faulty maintenance, improper repair, damage, or
alteration by anyone other than Datex-Ohmeda.
CAUTION U.S. Federal law restricts this device to sale by or on the

order of a licensed medical practitioner. Outside the
U.S.A., check local laws for any restriction that may apply.
Datex-Ohmeda products have unit serial numbers with coded logic
which indicates a product group code, the year of manufacture, and a
sequential unit number for identification. The serial number can be in
one of two formats.
AAAX11111 AAAXX111111AA
The X represents an alpha The XX represents a number
character indicating the year indicating the year the product
the product was manufactured; was manufactured; 04 = 2004,
H = 2004, J = 2005, etc. I and 05 = 2005, etc.
O are not used.
Aespire, 7900 Ventilator, Advanced Breathing System, Link-25,

ComWheel, Disposable Multi Absorber, EZchange, Reusable
Multi Absorber, PSVPro, SmartVent, Tec 6, and Tec 7 are
registered trademarks of Datex-Ohmeda, Inc.
Other brand names or product names used in this manual are
trademarks or registered trademarks of their respective holders.
Table of Contents
1 Introduction
Intended use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2

Symbols used in the manual or on the equipment . . . . . . . . 1-3
Typeface conventions used . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
2 System Controls and Menus
Anesthesia system controls . . . . . . . . . . . . . . . . . . . . . . . . . 2-2

Advanced breathing system (ABS) components . . . . . . . . . 2-5
Optional ABS components . . . . . . . . . . . . . . . . . . . . . . . 2-7
Vaporizer controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
ACGO . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10
Scavenging the ACGO sample flow . . . . . . . . . . . . . . . 2-11
Scavenging from an auxiliary manual breathing circuit 2-11
Scavenging a gas monitor sample flow . . . . . . . . . . . . 2-11
Ventilator controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
Ventilator screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
Using menus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
3 Operation
Turning on the system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2

Start mechanical ventilation . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Start manual ventilation . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Ventilator setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
Using quick keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
Changing ventilator modes and settings . . . . . . . . . . . . 3-4
Alarm Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Setting volume alarms . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Alarm limit setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Setup/Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
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Screen and audio setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7

Cardiac Bypass . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-8
Measure circuit compliance . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
Pressure waveform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
EZchange canister (optional) . . . . . . . . . . . . . . . . . . . . . . . 3-10
Condenser (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-11
Passive AGSS (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . 3-12
Connecting passive AGSS . . . . . . . . . . . . . . . . . . . . . . 3-12
Active AGSS (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13
Connecting active AGSS with a flow indicator . . . . . . . 3-14
Connecting active adjustable AGSS . . . . . . . . . . . . . . 3-15
Total flow sensing (optional) . . . . . . . . . . . . . . . . . . . . . . . 3-15
4 Preoperative Checkout
Every day before your first patient . . . . . . . . . . . . . . . . . . . . 4-2

Before every patient . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
5 Preoperative Tests
Inspect the system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2

Power failure alarm test . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Pipeline test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Total flow sensing test (if equipped) . . . . . . . . . . . . . . . . . . 5-3
Cylinder test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
Flow control test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
Vaporizer installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-7
Vaporizer back pressure test . . . . . . . . . . . . . . . . . . . . . . . . 5-8
Low-pressure leak test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9
Negative low-pressure leak test . . . . . . . . . . . . . . . . . . . 5-9
Positive low-pressure leak test . . . . . . . . . . . . . . . . . . 5-10
Alarm tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-11
Breathing system tests . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-13
Bellows test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-13
Breathing circuit test . . . . . . . . . . . . . . . . . . . . . . . . . . 5-14
APL valve test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-14
Monitor and ventilator tests . . . . . . . . . . . . . . . . . . . . . . . . 5-15
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Table of Contents
6 Alarms and Troubleshooting
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
Audio . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
Latching alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3
List of alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4
Minimum system shutdown and monitoring alarms . . . . 6-9
Alarm ranges . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Alarm tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Breathing system problems . . . . . . . . . . . . . . . . . . . . . . . . 6-12
Electrical problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-13
Pneumatic problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-14
7 User Maintenance
Repair policy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2

Maintenance summary and schedule . . . . . . . . . . . . . . . . . 7-2
User maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-3
Datex-Ohmeda approved service . . . . . . . . . . . . . . . . . 7-3
Breathing system maintenance . . . . . . . . . . . . . . . . . . . . . . 7-3
O2 cell replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
O2 cell calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-5
21% O2 cell calibration . . . . . . . . . . . . . . . . . . . . . . . . . 7-5
100% O2 cell calibration . . . . . . . . . . . . . . . . . . . . . . . . 7-6
Zeroing flow sensor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-6
Prevent water buildup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-7
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8 Setup and Connections
Canister setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4

When to change the absorbent . . . . . . . . . . . . . . . . . . . 8-6
Removing a canister . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-6
Removing an EZchange canister . . . . . . . . . . . . . . . . . . 8-7
Reusable Multi Absorber canister filling . . . . . . . . . . . . . 8-7
Electrical connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9
Outlets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9
Mains inlet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-10
Serial port . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-10
Pneumatic connections . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-10
Pipeline Inlets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-10
Scavenging . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-11
Sample gas return port . . . . . . . . . . . . . . . . . . . . . . . . 8-11
Suction regulator (optional) . . . . . . . . . . . . . . . . . . . . . 8-12
Auxiliary O2 flowmeter (optional) . . . . . . . . . . . . . . . . . 8-12
How to install gas cylinders . . . . . . . . . . . . . . . . . . . . . . . . 8-13
Pin indexed cylinder yokes . . . . . . . . . . . . . . . . . . . . . 8-13
DIN cylinder connections . . . . . . . . . . . . . . . . . . . . . . . 8-13
High-pressure leak test . . . . . . . . . . . . . . . . . . . . . . . . 8-14
How to attach equipment to the top of the machine . . . . . . 8-14
9 Parts
Flow sensor module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2

Exhalation valve assembly . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2
Breathing circuit module . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-3
Bellows assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-4
Absorber canister . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-5
AGSS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-6
EZchange canister system . . . . . . . . . . . . . . . . . . . . . . . . . . 9-7
Condenser . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-8
Test tools and system parts . . . . . . . . . . . . . . . . . . . . . . . . . 9-9
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Table of Contents
10 Specifications and Theory of Operation
System pneumatic circuits . . . . . . . . . . . . . . . . . . . . . . . . . 10-2

Gas supplies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-4
O2 flow . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-4
N2O flow . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-4
Air flow . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-4
Mixed gas . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-5
EZchange canister . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-5
Condenser . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-5
Pneumatic specifications . . . . . . . . . . . . . . . . . . . . . . . . . . 10-5
Gas supplies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-5
ACGO Port relief . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-5
Electrical block diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-6
Electrical power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-7
Power cord . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-8
Battery information . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-8
Flow specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-9
Pneumatic flow . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-9
Breathing system specifications . . . . . . . . . . . . . . . . . . . . 10-10
Gas scavenging . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-11
Physical specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-12
Environmental requirements . . . . . . . . . . . . . . . . . . . . . . 10-12
Suction regulators (optional) . . . . . . . . . . . . . . . . . . . . . . 10-13
Auxiliary O2 flowmeter (optional) . . . . . . . . . . . . . . . . . . . 10-13
Ventilator theory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-14
O2 monitoring theory of operation . . . . . . . . . . . . . . . 10-15
Modes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-15
Ventilator operating specifications . . . . . . . . . . . . . . . . . . 10-23
Pneumatics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-23
Fresh gas compensation . . . . . . . . . . . . . . . . . . . . . . 10-23
Pressure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-23
Volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-23
Oxygen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-23
Ventilator accuracy data . . . . . . . . . . . . . . . . . . . . . . . . . 10-24
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Electromagnetic compatibility (EMC) . . . . . . . . . . . . . . . . 10-26

Guidance and manufacturer’s declaration -
electromagnetic emissions . . . . . . . . . . . . . . . . . . . . . 10-26
Guidance and manufacturer’s declaration -
electromagnetic immunity . . . . . . . . . . . . . . . . . . . . . 10-27
Recommended separation distances . . . . . . . . . . . . . 10-29
Electrical safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-30
IEC 60601-1 Classification . . . . . . . . . . . . . . . . . . . . . . . . 10-31
Standards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-31
System components . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-32
Integral . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-32
Not integral . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-32
Index
Warranty
vi M1132382
1 Introduction
In this section Intended use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2

Symbols used in the manual or on the equipment . . . . . . . . 1-3
Typeface conventions used . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
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Intended use
The Aespire anesthesia system is a compact, integrated, and intuitive
anesthesia delivery system. The 7900 Ventilator provides mechanical
ventilation for patients during surgery as well as monitoring and
displaying various patient parameters.
The 7900 Ventilator uses a microprocessor-controlled ventilator with
internal monitors, electronic PEEP, Volume Mode, and other optional
features. A serial interface permits communication to external
monitoring.
This anesthesia system is not suitable for use in an MRI environment.
This system must only be operated by medical personnel authorized
and trained to use this product. It must be operated according to the
instructions in this User’s Reference manual.
Note Configurations available for this product depend on local market and
standards requirements. Illustrations in this manual may not
represent all configurations of the product. This manual does not
cover the operation of every accessory. Refer to the accessory
documentation for further information.
1-2 M1132382
1 Introduction
Symbols used in the manual or on the equipment

Symbols replace words on the equipment, on the display, or in
manuals.
Warnings and Cautions tell about the dangerous conditions that can
occur if the instructions in the manual are not followed.
Warnings tell about a condition that can cause injury to the operator
or the patient.
Cautions tell about a condition that can cause damage to the
equipment. Read and follow all warnings and cautions.
On (power) Off (power)
Standby
O2+ O2 flush button
Type BF equipment Type B equipment
Dangerous voltage Frame or chassis ground
Direct current Alternating current
Caution Attention, refer to product instructions
Refer to product instructions Exhaust
Electrical input Electrical output
Electrical input/output Sample gas inlet to scavenging
Pneumatic inlet Pneumatic outlet
SN Serial number
REF Stock number
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Equipotential Lamp, lighting, illumination
Protective earth ground Earth ground
Variability Variability in steps
Suction bottle outlet Vacuum inlet
Max Vacuum
+ Plus, positive polarity

- Minus, negative polarity
Bag position/manual ventilation Mechanical ventilation
Inspiratory flow Expiratory flow
Movement in one direction Movement in two directions
Lock Unlock
Isolation transformer Low pressure leak test
134°C Autoclavable Not autoclavable
Bellows volumes are approximate

O2% O2 cell connection
APL settings are approximate Anesthetic Gas Scavenging System
1-4 M1132382
1 Introduction
Pinch hazard Read to top of float
EZchange Canister (CO2 bypass) Caution: federal law prohibits dispensing

without prescription
Open drain (remove liquid) Close drain
Alarm silence touch key Menu touch key
Silence alarm touch key (Tec 6) Volume alarms On/Off touch key
End case touch key Cylinder
Systems with this mark agree with the Authorized representative in the European
European Council Directive (93/42/EEC) for Community
Medical Devices when they are used as
specified in their User’s Reference manuals.
The xxxx is the certification number of the
Notified Body used by GE Healthcare’s
Quality Systems.
Manufacturer Date of manufacture
Indicates that the waste of electrical and GOST R Russian certification

electronic equipment must not be disposed
as unsorted municipal waste and must be
collected separately. Please contact an
authorized representative of Datex-Ohmeda
for information concerning the
decommissioning of equipment.
This way up USB port
Ethernet connection This product consists of devices that

may contain mercury, which must be
recycled or disposed of in accordance
with local, state, or country laws. (Within
this system, the backlight lamps in the
monitor display contain mercury.
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Typeface conventions used

Menu items are written in bold italic typeface; for example, Main
Menu.
Messages that are displayed on the screen are enclosed in single
quotes: for example, ‘Total pressure exceeds Pmax.’
When referring to different sections and other documents, the names
are written in italic typeface and enclosed in double quotes; for
example, “System Controls and Menus.”
Abbreviations
Abbreviation Definition
ABS Advanced breathing system
ACGO Auxiliary common gas outlet
AGSS Anesthetic gas scavenging system
APL Adjustable pressure-limiting valve
CO2 Carbon dioxide
DAC Digital to analog converter
EMC Electromagnetic compatibility
ESD Electrostatic discharge
I:E Inspiratory-expiratory ratio
FiO2 Fraction of inspired oxygen
MIN Minimum
MV Minute volume
MVexp Expired minute volume
O2 Oxygen
1-6 M1132382
1 Introduction
Paw Patient airway pressure
PCV Pressure controlled ventilation
PCV-VG Pressure controlled ventilation - volume guaranteed
PEEP Positive end expiratory pressure
Pmax Maximum pressure
Pmean Average pressure calculated over the patient breath
Pinsp Target airway pressure
Ppause Positive airway pressure measured at the end of

Tpause
Ppeak Maximum airway pressure measured during patient

breath
Psupport Pressure support
PSVPro Pressure supported ventilation with apnea backup
RR Respiratory rate
SIMV-PC Synchronized intermittent mandatory ventilation -

pressure controlled
SIMV/PSV Synchronized intermittent mandatory ventilation /

pressure supported ventilation
TFS Total flow sensing
Tpause Pause time
Tinsp Inspired tidal volume
TV Tidal volume
TVexp Expired tidal volume
VCV Volume controlled ventilation
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1-8 M1132382
WARNING Explosion Hazard. Do not use this system with flammable

anesthetic agents.
w Do not use antistatic or electrically-conductive breathing

tubes or masks. They can cause burns if used near high
frequency surgical equipment.
In this section Anesthesia system controls . . . . . . . . . . . . . . . . . . . . . . . . . 2-2

Advanced breathing system (ABS) components . . . . . . . . . 2-5
Vaporizer controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
ACGO . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10
Ventilator controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
Ventilator screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
Using menus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
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Anesthesia system controls
13
2
12 3
4
11 5
6
10
7
9
AC.20.002
8
1. Light switch 8. Brake

2. Dovetail rails 9. O2 flush button
3. Vaporizer 10. Auxiliary O2 flow control (optional)
4. Pipeline pressure gauge(s) (upper row) 11. Breathing system
5. Cylinder pressure gauge(s) (lower row) 12. Flow controls
6. System switch 13. Ventilator display
7. Integrated suction (optional)
Figure 2-1 • Front view
2-2 M1132382
Item, Figure 2-1 Description

6 System switch Set the switch to the On (|) position to permit gas flow and to turn on the system.
7 Integrated suction Turn the switch to MAX for full vacuum. Turn the switch to Off (0) for no vacuum. Turn
(optional) the switch to On (|) for adjustable vacuum. When in adjustable vacuum, turn the knob
clockwise to increase the vacuum and counterclockwise to decrease the vacuum.
8 Brake Push down to lock. Lift to release.
9 O2 flush button Push the O2 flush button to supply high flows of O2 to the breathing system.
10 Auxiliary O2 flow Turn the knob counterclockwise to increase the flow. Turn the knob clockwise to
control (optional) decrease the flow.
12 Flow controls Turn the knob counterclockwise to increase the flow. Turn the knob clockwise to
decrease the flow. The System switch must be On for gas to flow.
M1132382 2-3
Aespire View
AC.20.012
1. Outlet circuit breaker 5. Mains inlet

2. Electrical outlet 6. System circuit breaker
3. Suction items (optional) 7. Cylinder
4. Equipotential stud 8. Pipeline connections
Figure 2-2 • Rear view
2-4 M1132382
Advanced breathing system (ABS) components
17
16
15
14
1
13
2
12
3
11
4
10
5
9
6
7
AC.20.013
1. Expiratory check valve 10. Breathing system release

2. Inspiratory check valve 11. Manual bag port
3. Auxiliary common gas outlet (ACGO) switch 12. Adjustable pressure-limiting (APL) valve
4. ACGO 13. Bag/Vent switch
5. Inspiratory flow sensor 14. Bellows assembly
6. Expiratory flow sensor 15. Sample gas return port
7. Absorber canister 16. Scavenger flow indicator (optional)
8. Absorber canister release 17. Airway pressure gauge
9. Leak test plug
Figure 2-3 • Advanced breathing system
M1132382 2-5
Aespire View

3 Auxiliary common gas outlet Sends fresh gas to the ACGO when the switch is activated. The ACGO
(ACGO) switch provides fresh gas to an external manual breathing circuit.
5,6 Inspiratory flow sensor and Flow sensors provide volume measurements for some monitoring
Expiratory flow sensor functions and tidal volume delivery.
8 Absorber canister release Push to remove the canister. This causes the breathing system to vent to
the room (unless the EZchange canister option is installed). Be sure to hold
the canister by the handle before releasing the canister.
12 Adjustable pressure-limiting Adjusts breathing system pressure limit during manual ventilation. The
(APL) valve scale shows approximate pressures. Above 30 cmH2O, the knob will click
as it turns.
20
30
N
MI
70
13 Bag/Vent switch Selects between manual ventilation (bag) or mechanical ventilation

(ventilator).
2-6 M1132382
Optional ABS
components
AB.74.120
AB.82.043
4
1. Bag support arm

2. EZchange canister system (CO2 bypass)
3. EZchange canister release
4. Condenser drain button
5. Condenser
Figure 2-4 • Breathing system options

1 Bag support arm Squeeze the button to raise or lower the arm.
3 EZchange canister Push to drop the canister to EZchange position. This seals the breathing circuit,
release permitting continued ventilation and rebreathing of exhaled gases. Be sure to
hold the canister by the handle before releasing the canister.
4 Condenser drain button Push to drain water out of the condenser.
M1132382 2-7
Aespire View
Vaporizer controls
Refer to the vaporizer User’s Reference manual for more detailed
information on the vaporizer.
3 3
4 4
AB.80.009
5
AA43051
1 2
1. Tec 6 series
2. Tec 7
3. Lock lever
4. Concentration control and release
5. Indicators (Tec 6 series)
6. Silence alarm touch key (Tec 6 series)
Figure 2-5 • Vaporizer controls
2-8 M1132382

3 Lock Lever Turn the lever fully clockwise to lock the vaporizer in position.
4 Concentration control and Push the release and turn the concentration control to set the agent
release concentration. The Tec 6 series concentration control does not turn as long
as the warm-up indicator is on.
n
Åbe
5 Indicators (Tec 6 series) All indictors come on briefly at the start. The warm-up indicator goes off
after approximately 10 minutes and the operational indicator comes on.
Other indicators come on to advise the user of required action.
6 Silence alarm touch key Push to silence alarms. Hold for 4 seconds to sound the speaker and light
(Tec 6 series) all indicators (alarm test).
M1132382 2-9
Aespire View
ACGO
Fresh gas flow with anesthetic agent is directed through the Auxiliary
Common Gas Outlet (ACGO) on the front of the system when the
ACGO switch is in the ACGO position. Mechanical ventilation is not
available when operating an auxiliary manual breathing circuit with
fresh gas from the ACGO. The Bag/Vent switch, APL valve, and bag
arm are not part of the external circuit. Volume and pressure
monitoring are not available.
O2 monitoring of fresh gas is available automatically when the ACGO
is selected. A sample of the fresh gas is diverted to the O2 cell in the
breathing system. The sample flow to the O2 cell is dependent on the
pressure in the external circuit. The sample flow reduces the fresh
gas flow rate to the auxiliary breathing circuit equal to the amount
delivered to the O2 cell.
Fresh gas oxygen concentration is displayed on the screen. Set the
alarm limits appropriately. Note that fresh gas oxygen concentration
may not reflect FiO2 during spontaneous breathing or in rebreathing
circuits.
Important Use an external O2 monitor if using a rebreathing circuit on ACGO.
Do not use an external ventilator on the ACGO. Do not use the ACGO
to drive external ventilators or for jet ventilation.
See “Scavenging” in the “Setup and Connections” section for more
information on connections.
WARNING The maximum pressure at the ACGO can be up to 55 kPa

(8 psi). Use a breathing circuit with pressure relief.
2-10 M1132382
Scavenging the A sample of the fresh gas is diverted to the O2 cell in the breathing
ACGO sample flow system to show the O2 numerics on the monitor display. This sample
flow should be scavenged when an auxiliary manual breathing circuit
is used with N2O or volatile anesthetics.
If scavenging is not connected, the sample flow is emptied into the
room.
To connect the scavenging:
1. Attach a circle breathing circuit to the inspiratory and expiratory
ports.
2. Occlude the circle circuit by connecting the Y-piece to the plug
located to the rear of the expiratory port.
3. Check for clinically correct settings.
4. Check the position of the Bag/Vent switch:
• If the Bag/Vent switch is set to mechanical ventilation mode,
the bellows fills slowly with the sample flow. When the
bellows is full, the sample flow goes to the AGSS
(Mechanical ventilation does not start when ACGO switch is
set to ACGO).
• If the Bag/Vent switch is set to bag mode, set the APL valve
to MIN and attach a bag. The bag fills slowly with the sample
flow. When the bag is full, the sample flow goes to the AGSS.
Scavenging from an Scavenge the exhaust if an auxiliary manual breathing circuit is used
auxiliary manual with N2O or volatile anesthetics.
breathing circuit An auxiliary inlet is available for active and passive AGSS units. It
provides a female connection with 30 mm male - 30 mm male
connector (or a 30 mm male - 19 mm male connector) into the
auxiliary port under the breathing system.
Important Do not use these connectors as an outlet for exhaust flow.
The auxiliary inlet is a convenience inlet to the air brake of active
AGSS units. There is a reservoir to capture exhaust flows higher than
the extract flow.
A separate exhaust hose is needed from the auxiliary manual
breathing circuit to the disposal point for all AGSS units.
Scavenging a gas Sample gas from a gas monitor can be scavenged using the sample
monitor sample flow gas return port or the AGSS. To scavenge from a gas monitor using
the sample gas return port, connect the tubing from the monitor to the
sample gas return port. To scavenge from a gas monitor using the
AGSS, connect tubing from the monitor to the male luer inlet on the
bottom of the AGSS underneath the breathing system.
M1132382 2-11
Aespire View
Ventilator controls
The ventilator controls include touch keys, menu screens, and a
control knob (ComWheel). The System switch provides power
functions to the ventilator display. The Bag/Vent switch starts and
stops mechanical ventilation.
1
2
14 3
6
13
AC.20.003
12 11 10 9 8 7
1. High priority alarm indicator 8. PEEP quick key

2. Low or medium priority alarm indicator 9. Pmax or Psupport quick key
3. Alarm silence key 10. I:E or Tinsp quick key
4. Menu key 11. Respiratory rate (RR) quick key
5. End case key 12. Tidal volume (TV) or Pinsp quick key
6. ComWheel 13. Mains power indicator
7. More settings quick key 14. Volume alarms On/Off key
Figure 2-6 • Ventilator controls
2-12 M1132382
Ventilator screen
1 2 4
3
O2% low
TVexp low
Ppeak cmH2O
Paw
Pmean
Ppause
O2 %
5
TVexp ml
Time (sec) MV l/min RR /min
11 Push the knob to confirm the change. Turn the

knob to change the setting.
10 6
9 Vent On VCV - Volume Control Circle Fresh Gas Flow l/min
TV RR I:E Pmax PEEP 7
O2
More Air
Settings N2O Total
AC.20.004
ml /min cmH2O cmH2O
1. Alarm silence indicator and countdown clock 7. Total flow sensing (optional)
2. Alarm message areas 8. Ventilator settings
3. Waveform area 9. Mechanical ventilation status
4. Alarm limit settings 10. Ventilation mode
5. Measured values area 11. User message area
6. Circuit type
Figure 2-7 • Normal view
M1132382 2-13
Aespire View
Using menus
Main Menu Ppeak cmH2O
Ventilation Mode VCV Pmean

Alarm Setup PCV Ppause
Setup/Calibration SIMV/PSV
O2 %
Screen and Audio Setup PSVPro
Cardiac Bypass SIMV-PC
TVexp ml
Normal Screen
Time (sec) MV l/min RR /min
Vent On VCV - Volume Control Circle

TV RR I:E Pmax PEEP
More
AC.20.009
ml /min cmH2O cmH2O
Settings
Figure 2-8 • Menu example
1. Push the Menu key to show the Main Menu.

2. Turn the ComWheel counterclockwise to highlight the next menu
item. Turn the ComWheel clockwise to highlight the previous
menu item.
3. Push the ComWheel to enter the highlighted window or a sub
menu.
4. Turn the ComWheel clockwise or counterclockwise to highlight
the desired selection.
5. Push the ComWheel to confirm the selection.
6. Push the Menu key to exit the menu and return to the normal
monitoring screen.
2-14 M1132382
3 Operation
WARNING Maintain sufficient fresh gas flow when using sevoflurane.
In this section Turning on the system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2

Start mechanical ventilation . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Start manual ventilation . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Ventilator setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
Alarm Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Setup/Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
Screen and audio setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
Cardiac Bypass. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-8
Measure circuit compliance . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
Pressure waveform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
EZchange canister (optional) . . . . . . . . . . . . . . . . . . . . . . . 3-10
Condenser (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-11
Passive AGSS (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . 3-12
Active AGSS (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13
Total flow sensing (optional) . . . . . . . . . . . . . . . . . . . . . . . . 3-15
M1132382 3-1
Aespire View
Turning on the system

1. Plug the power cord into an electrical outlet. Make sure the
system circuit breaker is on.
• The mains indicator comes on when AC power is connected.
• The battery is charging if not already fully charged.
2. Check that the breathing system is properly connected.
CAUTION Do not turn on the system with the right-hand (inspiratory)

port plugged.
3. Turn the System switch to On.
• The display shows the power-up screen.
• The system does a series of automated self tests.
• A status bar is provided to show progress.
Start mechanical ventilation
WARNING Make sure that the patient circuit is correctly assembled

and that the ventilator settings are clinically appropriate
before starting ventilation.
1. Set the ACGO switch to the circle system position.
2. Set the Bag/Vent switch.
• If Bag/Vent switch is set to Vent, move Bag/Vent switch to
Bag and then back to Vent to start mechanical ventilation.
• If Bag/Vent switch is set to Bag, move Bag/Vent switch to
Vent to start mechanical ventilation.
3. Push the O2 flush button to inflate the bellows if needed.
Start manual ventilation

1. Connect a manual breathing circuit.
2. Make sure that the APL valve is set to a clinically appropriate
setting.
3. Set the Bag/Vent switch to Bag.
3-2 M1132382
3 Operation
Ventilator setup
The system has the following mechanical ventilation modes:
• Volume Control Ventilation (VCV).
The ventilator delivers the tidal volume to the patient at the set
respiratory rate (RR).
• Pressure Control Ventilation (PCV) (optional).
The airway pressure is controlled to the value of Pinsp in every
breath.
• Synchronized Intermittent Mandatory Ventilation with Pressure
Support Ventilation (SIMV/PSV) (optional).
Sets a minimum number of mechanical breaths using volume
control to be delivered to the patient, but allows the patient to
have spontaneous breaths which can be pressure supported.
• Pressure Support Ventilation (PSVPro) (optional).
This is a spontaneous mode that provides the set amount of
pressure to the patient during each triggered breath or, if the
patient does not have any spontaneous breaths in a set period of
time, the ventilator transitions to SIMV-PC where it delivers a
minimum number of mechanically controlled breaths.
Control (SIMV-PC) (optional).
Sets a minimum number of mechanical breaths using pressure
control to be delivered to the patient, but allows the patient to
have spontaneous breaths which can be pressure supported.
• Pressure Control Ventilation-Volume Guaranteed (PCV-VG)
(optional).
A tidal volume is set and the ventilator delivers that volume using
a decelerating flow and a constant pressure. The ventilator
adjusts the inspiratory pressure needed to deliver the set tidal
volume breath-by-breath so that the lowest pressure is used.
Note See the “Specifications and Theory of Operation” section for more
information on ventilation modes.
Using quick keys The ventilator settings for each mode can be easily changed using
the ventilator quick keys.
1. Push a ventilator quick key to select the corresponding ventilator
setting.
2. Turn the ComWheel to make a change.
3. Push the ComWheel or quick key to activate (confirm) the
change.
M1132382 3-3
Aespire View
Changing ventilator 1. Push the Menu key.

modes and settings 2. Select Ventilation Mode from the Main Menu.
Main Menu
Ventilation Mode VCV
Alarm Setup PCV
Setup/Calibration SIMV/PSV
Screen and Audio Setup PSVPro
Cardiac Bypass Off SIMV-PC
PCV-VG
Normal Screen
3. Use the ComWheel to highlight the desired setting (PSVPro

shown), and push the ComWheel to confirm the change.
4. Set the values for the selected ventilation mode.
• The value is highlighted while being set.
5. Push the ComWheel or the quick key to activate the change.
• The system returns to the normal monitoring screen.
• The ventilation mode shows on the screen.
3-4 M1132382
3 Operation
Alarm Setup
Setting volume Use the volume alarms key to turn the volume alarms on and off.
alarms When the alarms are off, an X covers the alarm limits. Use this control
during manual ventilation when constant attention is on the patient.
Use the End case key to minimize alarms between cases. The alarms
will reactivate when two or more breaths are detected within 30
seconds.
WARNING Do not turn off volume alarms for a spontaneously

breathing patient. The system will not alarm for low
volume.
Alarm limit setup To set or change alarm limits:

1. Push the Menu key.
2. Select Alarm Setup from the Main Menu.
Alarm Setup
O2 21 99
MV 3.0 7.0
TVexp 200 600
Leak Audio On
Go to Main Menu
3. To set an alarm limit, use the ComWheel to scroll to the desired

alarm limit. Push the ComWheel to select the limit. The following
alarm limits can be set or changed:
• O2, MV, and TVexp - Alarm limits for both high and low can
be set. The low limit is the left numeric field, and the high limit
is the right numeric field.
• Leak Audio - The patient circuit leak alarm activates during
mechanical ventilation if less than half of the inspired volume
returns through the expiratory flow sensor. Prevent expected
alarms from known circuit leaks by setting the Leak Audio to
Off.
4. Change the value with the ComWheel.
5. Select Go to Main Menu to return to the Main Menu, or push the
Menu key to return to the normal monitoring screen.
M1132382 3-5
Aespire View
Setup/Calibration
To change or enter Setup and Calibration information:
2. Select Setup/Calibration from the Main Menu.
Setup/Calibration
More Vent Settings
O2 Sensor Calibration
About Ventilator...
Go to Main Menu
3. Use the ComWheel to scroll to the desired submenu. Push the

ComWheel to confirm the selection. Select More Vent Settings
to set the following ventilator values:
• Pmax.
• Trig Window.
• Trigger.
• End of Breath.
• Backup Mode Active.
• Tpause.
• Rise Rate.
information on individual settings.
4. After selecting a ventilator setting, set it to the desired value by
turning the ComWheel. Confirm the value is correct by pushing
the ComWheel.
5. Select Go to Setup/Calibration Menu to return to the
Setup/Calibration, or push the Menu key to return to the normal
monitoring screen.
3-6 M1132382
3 Operation
Screen and audio setup

To change the audio and visual appearance of the screen:
2. Select Screen and Audio Setup from the Main Menu.
Screen and Audio Setup
Brightness 5
Alarm Volume 4
Alarm Limits Show
Units of Measure Show
Go to Main Menu
3. Use the ComWheel to select the desired setting and push the
ComWheel to confirm the change. The following settings are
available:
• Brightness - Sets the brightness of the screen.
• Alarm Volume - Sets the volume, or loudness of audible
alarms.
• Alarm Limits - Simplifies the screen by hiding the alarm limits.
To do this, select Hide for this option. If the screen is set to
hide the alarm limits, the limits automatically show when the
corresponding alarm occurs.
• Units of Measure - Simplifies the screen by hiding the units of
measure. To do this, select Hide for this option.
M1132382 3-7
Aespire View
Cardiac Bypass
Cardiac Bypass suspends alarms for patients on cardiac bypass
when the ventilator is not mechanically ventilating. Mechanical
ventilation must be off. When mechanical ventilation is turned on,
Cardiac Bypass is automatically turned off, the alarms are enabled,
and monitoring is available.
WARNING Cardiac Bypass mode should only be used when the

patient is receiving extra-corporeal oxygenation by means
of a heart-lung machine. This mode of ventilation is not
intended to provide metabolic levels of ventilation to the
patient.
3. Select Cardiac Bypass.
4. Set Cardiac Bypass to On.
5. Push the ComWheel to activate the change.
• The screens shows ‘Cardiac bypass’ and ‘Apnea alarm off’ in
the alarm area.
3-8 M1132382
3 Operation
Measure circuit compliance

Exhaled tidal volume (TVexp) measures the gas needed to fill the
patient circuit at the measured pressure. The compliance factor can
be used to calculate the approximate gas which goes into expanding
the compliant patient tubing and not delivered into the patient.
1. Set the ventilator to volume control ventilation (VCV) mode.
2. Set the ventilator parameters.
• TV = 25 ml.
• RR = 20.
• I:E = 1:1.
• Pmax = 100 cmH2O.
• PEEP = Off.
3. Occlude the patient Y.
4. Turn on mechanical ventilation.
5. Monitor the exhaled tidal volume (TVexp) and the measured peak
airway pressure (Ppeak).
6. Calculate the tubing compliance factor.
• TVexp/(Ppeak - 2.5* cmH2O) = Compliance factor in
ml/cmH2O.
• Example:
— Ppeak = 30 cmH2O.
— TVexp = 25 ml.
— 25/(30 - 2.5) = 0.9 ml/cmH2O.
*Pressure created by the force of the bellows.
Pressure waveform
The pressure waveform shows the measured value of the airway
pressure. The waveform automatically adjusts the time and pressure
scales. The time scale changes with the respiratory rate. The
pressure scale changes with the pressure limit.
waveform information on the ventilation modes.
Respiratory Rate (breaths per minute) Time scale (seconds)

0 to 25 0 to 16
26 to 75 0 to 8
76 to 100 0 to 4
M1132382 3-9
Aespire View
EZchange canister (optional)

Push the absorber canister release to activate the EZchange canister
mode. The canister will swing down to the EZchange position. The
EZchange canister mode seals the breathing circuit when the canister
holder is down. This permits continued ventilation and rebreathing of
exhaled gases while replacing the absorber canister.
Systems with EZchange canister have the following label on the
canister holder. When the system is in EZchange position, the
message ‘No CO2 absorption’ shows on the ventilator display.
AB.82.042
To return to absorber mode, reinsert the canister into the holder, push
the canister back up and snap it into absorber position. When the
canister is in the absorber position, the exhaled gas flows through the
absorber, removing CO2.
Note Check the absorber canister to ensure it has side rails. If the canister
does not have side rails, it will not work on the EZchange canister
holder.
AB.74p.043
3-10 M1132382
3 Operation
Condenser (optional)
Visually check the condenser reservoir daily. Drain the reservoir daily.
1. Place a container under the reservoir.
2. Push the drain button to empty any water in the condenser.
AB.75p080
2 1
1. Drain button
2. Reservoir
3. Condenser
Figure 3-1 • Condenser
M1132382 3-11
Aespire View
Passive AGSS (optional)
WARNING Always verify the proper operation of any gas scavenging

system; ensure the scavenging system is not occluded.
The passive AGSS (Anesthesia Gas Scavenging System) contains
both positive and negative pressure relief valves to protect the
breathing system and the patient. The outlet is a 30-mm connector on
the bottom of the receiver.
There is also a connector that may be used for scavenging the
sample from a gas monitor. The male luer inlet connection is located
near the 30-mm connector.
Passive AGSS is intended primarily for use in operating room
environments which have no active gas extraction system for waste
gas disposal. The disposal system generally consists of large
diameter tubing directly linking the passive AGSS with the building
exterior. The tubing should be as large in diameter and as short as
possible for the particular application.
Passive AGSS may also be used with a non-recirculating facility
ventilation system for waste gas disposal. The tubing connection from
passive AGSS to the non-recirculating facility ventilation system
should be an open connection, essentially at atmospheric pressure,
such as to an exhaust grill.
Note See “Setup and Connections” for additional scavenging connection
information.
Connecting passive To use the optional passive AGSS installed on the system, connect it
AGSS as follows:
1. Connect the proper large diameter tubing to the AGSS 30 mm
outlet connector on the bottom of the AGSS underneath the
breathing system.
Note The tubing connection from the passive AGSS to the non-circulating
facility ventilation system should be an open connection, essentially
an atmospheric pressure, such as to an exhaust grill.
2. Connect the free end of the tubing to the building exterior or
outside ventilation system.
3. The passive scavenging system relies on slight positive pressure
of gases, or on slight negative pressure caused by an exhaust
fan, to move gases through the system. For this reason, all
unused ports must be capped to prevent gas from leaking into the
room and to maintain the expected pressures.
Note In the event that excess gas accumulates in the scavenging system
and cannot exit the machine properly, pressure could build. If this
pressure reaches 10cmH20, the brass weight of the positive relief
valve will be lifted up allowing the gas to escape into the room. This
prevents the pressure from backing up into the patient circuit.
3-12 M1132382
3 Operation
Active AGSS (optional)
WARNING Always verify the proper operation of any gas scavenging

system; ensure the scavenging system is not occluded.
There are several versions of the optional active AGSS (Anesthesia
Gas Scavenging System) available depending on the hospital’s type
of waste gas disposal system.
Each version has a two-liter reservoir to capture peak exhaust flows
that briefly exceed the extract flow. Active scavenging systems
contain two relief valves to protect the patient from excess gas
pressure, or from the opposite situation, gas being drawn from the
breathing circuit.
The positive relief valve for the scavenging system is mounted on the
exhalation valve assembly. In the event that excess gas accumulates
in the scavenging system and cannot exit the machine properly,
pressure could build. If this pressure reaches 10 cmH2O, the positive
relief valve will be lifted up, allowing gas to escape into the room. This
prevents the pressure from backing up into the patient circuit.
The negative relief valve (which is located in the same place on all
scavenging receivers) serves to protect the patient in the event that
the extract flow exceeds system input flow. That is, it prevents gas
from being pulled out of the breathing circuit. If more than a small
amount of negative pressure (-0.3 cmH2O) is applied to the
scavenging system, the negative relief valve opens, allowing room air
to be drawn into the scavenging system instead of pulling gas from
the patient circuit. Its effectiveness is limited by the extract flow of the
particular active AGSS device:
• The active low flow system is for use with high vacuum disposal
systems. It requires a vacuum system capable of a continuous
nominal flow of 36 l/min and 300 mmHg (12 inHg) or greater
vacuum pressure. A flow indicator on the system indicates when
the unit is in operation.
• The active high flow system is for use with low vacuum (blower
type) disposal systems. This requires a system capable of
providing 50 to 80 l/min extract flow. A flow indicator on the
system indicates when the unit is in operation.
• Another version is the active adjustable flow. It provides the
capability to adjust the flow with a needle valve (located in a
receiver beneath the breathing system) and a visual indicator bag
which should be properly inflated. It requires a vacuum system
capable of a continuous nominal flow of 36 l/min and 300 mmHg
(12 inHg) or greater vacuum pressure. The extract flow is limited
to 36 l/min and 300 mmHg (12 inHg) vacuum.
• The active low flow system with a 12.7 mm hose barb connector
is for use with a low vacuum disposal system. It requires an
external venturi/ejector system with a flowmeter and a minimum
36 l/min extract flow.
M1132382 3-13
Aespire View
• The active low flow system with a 25 mm barb connector is for

use with low vacuum disposal systems. It requires an external
venturi/ejector system with a 40 to 50 l/min extract flow. A flow
indicator on the system indicates when the unit is in operation.
• The active low flow system with 30-mm ISO taper is for use with
low vacuum disposal systems. It requires an external venturi/
ejector system with a 40 to 50 l/min extract flow. A flow indicator
on the system indicates when the unit is in operation.
See “Setup and Connections” for additional scavenging connection
information.
Connecting active To use the optional active AGSS on a system that has a flow
AGSS with a flow indicator, connect it as follows:
indicator 1. Connect the proper hose to the AGSS outlet connector on the
bottom of the AGSS, beneath the breathing system. Attach the
other end to the hospital disposal system.
2. With the AGSS operating, verify that the flow indicator ball on the
flow indicator rises to the green zone, indicating adequate flow.
Note The ball in the upper red zone indicates excessively high extraction
flow. The ball in the lower red zone indicates extraction flow rate is
too low or the filter is blocked.
3. Complete the tests in the “Preoperative Tests” section of this
manual.
3-14 M1132382
3 Operation
Connecting active The active adjustable AGSS option flow rate is limited to 30 l/min with
adjustable AGSS this option.
To use the optional active AGSS installed on the system which uses
the three-liter bag as a visual indicator, connect it as follows:
1. Connect a disposal hose to the DISS connector on the needle
valve on the bottom of the AGSS (beneath). The hose should be
flexible and reinforced to help prevent kinking and crushing.
2. Attach the other end of the hose to the hospital disposal system.
3. Attach the three-liter bag to the 30-mm auxiliary 1 port on the
bottom of the AGSS.
4. Use the needle valve to adjust the flow rate to match the amount
of gas being scavenged. Use the visual indicator bag when
adjusting the flow rate. The bag should remain partially inflated.
AB.75p.110
5. Complete the tests in the “Preoperative Tests” section of this
manual.
Total flow sensing (optional)

The total flow sensing (TFS) option electronically measures the fresh
gas flow at the mechanical flow tubes. The total fresh gas flow
measurement displays on the bottom right corner of the screen. The
measurement specifies:
• Total gas flow.
• O2 gas flow.
• Air gas flow.
• N2O gas flow.
M1132382 3-15
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3-16 M1132382
WARNING Read each component’s User’s Reference manual and

understand the following before using this system:
• All system connections.
• All warnings and cautions.
• How to use each system component.
• How to test each system component.
w Before using this system:

• Complete the preoperative checkout.
• For in-depth test instructions, see the “Preoperative
Tests” section.
• Test all other system components.
w If a test fails, do not use the equipment.

Have a Datex-Ohmeda trained service representative
repair the equipment.
In this section Every day before your first patient . . . . . . . . . . . . . . . . . . . . 4-2

Before every patient . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
M1132382 4-1
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Every day before your first patient
Check that necessary emergency equipment is available and in good

condition.
Check that the equipment is not damaged and that components are
correctly attached.
Check that pipeline gas supplies are connected and cylinders are
installed and adequately filled.
Check the system suction connections.
Check the vaporizer installation:

• The top of each vaporizer is horizontal (not on crooked).
• Each vaporizer is locked and cannot be removed.
• The alarms and indicators operate correctly (Tec 6 series
vaporizers).
• More than one vaporizer cannot be turned on at the same time.
• All vaporizers are full.
Check that the breathing circuit is correctly connected, not damaged,

and the breathing system contains sufficient absorbent.
Turn the System switch to On.
Connect the scavenging and verify proper operation.
Do the Pipeline test and Cylinders test.
Do the Flow control tests.
Do the Vaporizer back pressure tests.
Do a Low-pressure leak test.
Do the Alarm tests.
Do the Breathing system tests.
Set the appropriate controls and alarm limits for the case.
4-2 M1132382
Before every patient

Note This check does not need to be done before the first case of the day if
the “Every day before your first patient” check was done.
Check that necessary emergency equipment is available and in good

condition.
Check the vaporizer installation:

• The top of each vaporizer is horizontal (not on crooked).
• Each vaporizer is locked and cannot be removed.
• The alarms and indicators operate correctly (Tec 6 series
vaporizers).
• More than one vaporizer cannot be turned on at the same time.
• All vaporizers are full.
Do the Breathing system tests.
Set the appropriate controls and alarm limits for the case.
M1132382 4-3
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4-4 M1132382
In this section Inspect the system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2

Power failure alarm test . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Pipeline test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Total flow sensing test (if equipped) . . . . . . . . . . . . . . . . . . . 5-3
Cylinder test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
Flow control test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
Vaporizer installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-7
Vaporizer back pressure test . . . . . . . . . . . . . . . . . . . . . . . . 5-8
Low-pressure leak test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9
Alarm tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-11
Breathing system tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-13
Monitor and ventilator tests. . . . . . . . . . . . . . . . . . . . . . . . . 5-15
M1132382 5-1
Aespire View
Inspect the system
WARNING Do not exceed the top shelf weight limit of 34 kg (75 lb).
w Make sure that the breathing circuit is correctly connected

and not damaged. Replace the breathing circuit if it is
damaged.
w Do not leave gas cylinder valves open if the pipeline

supply is in use. Cylinder supplies could be depleted,
leaving an insufficient reserve supply in case of pipeline
failure.
Before using the system, make sure that:
• The equipment is not damaged.
• Components are correctly attached.
• The breathing circuit is correctly connected, not damaged, and
the breathing system contains sufficient absorbent.
• The vaporizers are locked in position and contain sufficient agent.
• Pipeline gas supplies are connected and the pressures are
correct.
• Cylinder valves are closed on models with cylinder supplies.
• Models with cylinder supplies have a cylinder wrench attached to
the system.
• Models with cylinder supplies have a reserve supply of O2
connected to the machine during system checkout.
• The necessary emergency equipment is available and in good
condition.
• Equipment for airway maintenance, manual ventilation, tracheal
intubation, and IV administration is available and in good
condition.
• Applicable anesthetic and emergency drugs are available.
• If an auxiliary O2 flowmeter is present, ensure there is adequate
flow.
• If an optional suction regulator is present, ensure proper
connections and that there is adequate suction.
• The brakes are set and prevent movement.
• The power cord is connected to a wall outlet. The mains indicator
comes on when AC power is connected. If the indicator is not on,
the system does not have mains (electrical) power. Use a
different outlet, close the circuit breaker, or replace or connect the
power cable.
• The O2 flush button is in working condition.
5-2 M1132382
Power failure alarm test

1. With the System switch set to On, unplug the power cord.
2. Make sure that the power failure alarm sounds.
3. Connect the power cord to the electrical outlet.
4. Verify that the alarm tone stops.
Pipeline test
1. Disconnect the pipeline supplies and close all cylinder valves.
2. If the pipeline and cylinder pressure gauges are not at zero.
• Connect an O2 supply.
• Set the System switch to On.
• Set the flow controls to mid range.
• Make sure that all of the gauges except for O2 go to zero.
• Disconnect the O2 supply.
• Make sure that the O2 gauge goes to zero. As the pressure
decreases, the alarms for O2 supply failure should occur.
3. Connect the pipeline supplies.
4. Verify the pipeline pressure is between 280-600 kPa (41-87 psi).
Total flow sensing test (if equipped)

1. Connect the pipeline supplies to the anesthesia system.
2. Set the System switch to On.
4. Set each gas flow to 0.80 l/min using flow tubes. Refer to “Flow
controls” for more information.
5. Verify that the flow readings on the display for each gas read
between 0.60 l/min and 1.0 l/min.
M1132382 5-3
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Cylinder test
CAUTION To prevent damage to the system, open the cylinder

valves slowly and do not force the flow controls.
WARNING Do not leave gas cylinder valves open if the pipeline

failure.
1. Disconnect the pipeline supplies and close all cylinder valves.
2. If the pipeline and cylinder pressure gauges are not at zero:
• Connect an O2 supply.
• Set the flow controls to mid range.
• Make sure that all of the gauges except for O2 go to zero.
• Disconnect the O2 supply.
• Make sure that the O2 gauge goes to zero. As the pressure
decreases, the alarms for O2 supply failure should occur.
3. Make sure that the cylinders are full.
• Open each cylinder valve.
• Make sure that each cylinder has sufficient pressure.
• If the cylinder does not have sufficient pressure, close the
cylinder valve and install a full cylinder.
4. Set the System switch to Standby.
5. Turn off the auxiliary O2 flowmeter (if equipped).
6. Turn off the suction (if equipped).
7. Test one cylinder at a time for high-pressure leaks.
• Open the cylinder.
• Note the cylinder pressure.
• Close the cylinder valve.
• Wait for one minute and record the cylinder pressure again.
• If the cylinder pressure for Air or O2 decreases more than
690 kPa (100 psi), there is a leak.
• If the cylinder pressure for N2O decreases more than
690 kPa (100 psi), there is a leak.
5-4 M1132382
Flow control test
WARNING The Link-25 system cannot replace an O2 monitor.

Sufficient O2 in the fresh gas may not prevent hypoxic
mixtures in the breathing circuit.
w Nitrous oxide (N2O), if available, flows through the system

during this test. Use a safe and approved procedure to
collect and remove the N2O.
w Incorrect gas mixtures can cause patient injury. If the

Link-25 system does not supply O2 and N2O in the
correct proportions, do not use the system.
w This procedure tests for significant malfunction of the

Link-25 system. It does not confirm the proper calibration
of the Link-25 system. Perform periodic calibrations using
an accurate and properly calibrated O2 monitor as
recommended in the “User Maintenance” section.
1. Connect the pipeline supplies or slowly open the cylinder valves.
2. Turn all flow controls fully clockwise for minimal flow.
3. Set the ACGO switch to ABS.
Note Do not use the system if the Low battery or any ventilator failures
occur.
5. Make sure that the O2 flow tube shows approximately 0.025 to
0.075 l/min.
WARNING Keep the Link-25 system engaged. Adjust only the test
control for the following steps.
• Test N2O first and then O2.
• The O2 cell must be correctly calibrated.
M1132382 5-5
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6. Test the Link-25 system by increasing the N2O flow.

• Slowly turn the N2O flow control counterclockwise.
• Increase the N2O flow as specified in the following table and
make sure the O2 flow is as specified.
N2O flow l/min O2 flow greater than l/min

0.8 0.2
2 0.5
4 1.0
10 2.5
7. Test the Link-25 system with O2 flow decreasing.

• Set the N2O flow to 9 l/min.
• Set the O2 flow to 3 l/min or higher.
• Slowly turn the O2 flow control clockwise. Set the N2O flow to
the rates shown in the following table.
N2O flow l/min O2 flow greater than l/min

8 2
4 1
0.8 0.2
8. Adjust the flow of all gases through the full range and make sure
that the flow tube floats move smoothly.
9. Disconnect the O2 pipeline supply or close the O2 cylinder valve.
10. Make sure that:
• The low O2 supply alarm occurs.
• The N2O and the O2 flows stop. The O2 flow should stop
last.
• The air flow continues (if equipped).
• The gas supply alarms occur on the ventilator if the ventilator
uses O2 as the drive gas.
11. Turn all the flow controls fully clockwise for minimum flow.
12. Reconnect the O2 pipeline supply.
5-6 M1132382
Vaporizer installation
WARNING Use only Datex-Ohmeda, Inc. Selectatec series

vaporizers Tec 4 or greater.
w Do not use a vaporizer if it lifts off the manifold when the

lock lever is in the locked position.
w Do not use the system if more than one vaporizer can be

turned on at the same time.
w Tec 6 series vaporizers need the power cable to go

through the channel on the bottom of the vaporizer for
proper alignment. Do not put the power cable on the top
of the manifold or between the vaporizers.
1. Place the vaporizer straight on the manifold.
2. Make sure that the top of each vaporizer is horizontal.
• If a vaporizer is not horizontal, remove it and reinstall it.
3. Set each vaporizer lock lever to the locked position.
4. Try to lift each vaporizer straight up off the manifold.
• Do not pull forward on the vaporizer.
• Do not rotate the vaporizer on the manifold.
5. If the vaporizer lifts off of the manifold, install it again and repeat
this “Vaporizer installation” procedure. If the vaporizer lifts off a
second time, do not use the system.
6. For a Tec 6 series vaporizer:
• Connect the vaporizer to an electrical outlet.
• Hold the Silence alarm touch key (minimum of 4 seconds).
• Make sure all indicators turn on and that the alarm tone
occurs.
• Release the Silence alarm touch key.
7. Try to turn on more than one vaporizer at the same time.
• Test each possible vaporizer combination.
• If more than one vaporizer turns on at the same time, remove
the vaporizers, install them again, and repeat the “Vaporizer
installation” procedure. If the test continues to fail, contact a
Datex-Ohmeda trained service representative.
M1132382 5-7
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Vaporizer back pressure test
WARNING Anesthetic agent comes out of the common gas outlet

during this test. Use a safe, approved procedure to
remove and collect the agent.
CAUTION To prevent damage to the vaporizer, turn the flow controls

fully clockwise (minimum flow or off) before turning on the
system.
1. Set the System switch to On. Alarms may occur.
2. Set the O2 flow to 6 l/min.
3. Make sure that the O2 flow stays constant and the float moves
freely.
4. Adjust the vaporizer concentration from 0 to 1%. The O2 flow
must not decrease more than 1 l/min through the full range.
• If the O2 flow decreases more than 1 l/min, install a different
vaporizer and repeat the steps 1 through 4.
• If the O2 flow decreases less than 1 l/min when testing a
different vaporizer, the malfunction is in the vaporizer that
failed the test.
• If the O2 flow decreases more than 1 l/min with the different
vaporizer, the malfunction is most likely in the system. Do not
use the system.
5. Repeat steps 1 through 4 for each vaporizer.
5-8 M1132382
Low-pressure leak test
WARNING Do not use a system that has a low-pressure leak.

Anesthetic agent will go into the atmosphere instead of
into the breathing circuit.
Perform either the “Negative low-pressure leak test” or the “Positive
low-pressure leak test” depending on local requirements. It is not
necessary to perform both tests.
Negative low- 1. Make sure the System switch is set to Standby.

pressure leak test 2. Turn off all vaporizers.
3. Turn the ACGO switch to the ACGO position.
4. Compress and release the bulb until all air is removed from the
bulb.
• Occlude the inlet of the test device. Make sure it is a tight
seal.
• If the bulb of the test device inflates in less than 60 seconds,
use a different test device.
5. Test the system for low-pressure leaks.
• Turn the flow controls one and a half turns counterclockwise.
• Connect the test device to the auxiliary gas outlet.
• Compress and release the bulb until all air is removed from
the bulb.
• The floats will move. If the bulb inflates in 30 seconds or less,
there is a leak in the low-pressure circuit. See “Pneumatic
problems” in the “Alarms and Troubleshooting” section.
• Disconnect the test device.
6. Test each vaporizer for low-pressure leaks.
• Turn on one vaporizer.
• Set the vaporizer to 1%.
• Perform step 5.
• Repeat this test with each vaporizer.
• If a low-pressure leak occurs while testing any of the
vaporizers, see “Pneumatic problems” in the “Alarms and
Troubleshooting” section.
• Turn off all vaporizers.
7. Turn all flow controls fully clockwise for minimum flow. Do not
overtighten.
M1132382 5-9
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WARNING Agent mixtures from the low-pressure leak test stay in the
system. Clear the system by flowing O2 at 1 l/min for one
minute.
8. Clear the system of agent.
• Set the O2 flow to 1 l/min.
• Flow O2 for one minute.
• Turn the O2 flow control fully clockwise for minimum flow.
Positive low- 1. Connect the test device to the ACGO port with the positive-
pressure leak test pressure leak test adapter.
Note Push the positive-pressure leak test adapter into the ACGO port
throughout the test to maintain a tight seal.
CAUTION Do a positive low-pressure leak test at the ACGO port

only.
2. Turn the ACGO switch to the ACGO position.
3. Turn all flow controls fully clockwise for minimum flow.
4. Turn all vaporizers off.
5. Fully open the needle valve on the test device.
Note Keep the test device flow tube vertical for accurate results.
CAUTION If the needle valve is not fully open, this test can damage
the pressure gauge on the test device.
6. Open the O2 flow control and set for a total flow on the test
device of 0.4 l/min.
7. Make sure that the pressure gauge on the test device is at zero,
and make sure that all other flow controls are fully closed.
8. Close the needle valve on the test device until the gauge reads
20 kPa (3 psi) for (BSI) or 3 kPa (.4 psi) for ISO.
9. If the flow through the test device is less than 0.35 l/min ISO or
0.3 l/min (BSI), there is a low pressure leak in the system. See
“Pneumatic problems” in the “Alarms and Troubleshooting”
section.
10. Test each vaporizer.
• Turn on the vaporizer being tested, and set it to 1%.
• Perform steps 5 through 9 of this test for each vaporizer.
11. Make sure all vaporizers are turned off.
5-10 M1132382
WARNING Agent mixtures from the low-pressure leak test stay in the
system. Clear the system by flowing O2 at 1 l/min for one
minute.
12. Clear the system of agent.
• Set the O2 flow to 1 l/min.
• Flow O2 for one minute.
• Turn the O2 flow control fully clockwise for minimum flow.
Alarm tests
1. Connect a test lung to the patient connection.
2. Set the Bag/Vent switch to Vent.
5. Select Ventilation Mode - VCV.
• TV 400 ml.
• Rate 12.
• I:E 1:2.
• Pmax 40 cmH2O.
• PEEP Off.
7. Set the O2 flow to the minimum flow.
8. Turn off all other gases.
9. Push the O2 flush button to fill the bellows.
10. Set the Bag/Vent switch to Bag and then to Vent. Make sure that:
• Mechanical ventilation starts.
• A subatmospheric pressure alarm does not occur.
• The ventilator shows the correct data based on settings.
• The bellows inflate and deflate during mechanical ventilation.
11. Set the O2 flow control to 5 l/min. Make sure that:
• The pressure at the end of the breath is approximately
2 cmH2O. This can be seen on the pressure waveform
displayed below.

M1132382 5-11
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12. Test the O2 monitor and alarms (alarms other than Low O2 and
High O2 may occur).
• Remove the O2 cell, and make sure that the cell measures
approximately 21% O2 in room air.
• Push the Menu key.
• Select Alarm Setup from the Main Menu.
• Set the Low O2 alarm to 50%, and make sure that a Low O2
alarm occurs.
• Set the Low O2 alarm to 21%, and make sure that the Low
O2 alarm stops. This will create a latched alarm,
acknowledge this by pushing the Alarm silence key.
• Put the O2 cell back into the circuit.
• Set the High O2 alarm to 50%.
• Push the O2 flush button to fill the breathing system, and
make sure that the High O2 alarm occurs.
• Set the High O2 alarm to Off, and make sure that the alarm
stops.
• Flow 100% O2 for 2 minutes, and make sure that the O2 cell
measures 100% O2.
13. Test the low minute volume alarm.
• Push the Menu key.
• Select Alarm Setup from the Main Menu.
• Set the alarm limit for low minute volume to 6 l/min.
• Make sure that the low minute volume alarm occurs.
• Set the low minute volume alarm to Off.
14. Test the low airway pressure alarm.
• Remove the test lung from the patient connection.
• Make sure that the low airway pressure alarm occurs (other
alarms may occur).
15. Test the sustained airway pressure alarm.
• Set the APL valve to 70 cmH2O.
• Set the Bag/Vent switch to Bag.
• Occlude the patient connection and push the O2 flush button.
• Make sure that the Ppeak high. Blockage? (sustained airway
pressure) alarm occurs after approximately 15 seconds at the
sustained pressure limit.
5-12 M1132382
Breathing system tests

1. Make sure that the auxiliary equipment is functioning correctly.
2. Verify that AGSS is functioning correctly.
• Some breathing systems with active AGSS have a flow
indicator on the side. Make sure that the flow indicator shows
a flow in the green range.
3. Make sure that the check valves on the breathing circuit module
work correctly.
• The expiratory check valve rises during expiration and falls at
the start of inspiration.
• The inspiratory check valve rises during inspiration and falls
at the start of expiration.
WARNING Objects in the breathing system can stop gas flow to the
patient, causing injury or death. Use a test plug that is the
appropriate size so that it will not fall into the breathing
system.
After performing the breathing system tests, make sure

that there are no test plugs or other objects caught in the
breathing system.
Bellows test 1. Set the System switch to Standby.

3. Set all flow controls to minimum flow.
4. Occlude the patient connection.
5. Push the O2 flush button to fill the bellows. Release the O2 flush
button.
6. Make sure that the pressure does not increase to more than
15 cmH2O on the pressure gauge.
7. If the bellows falls lower than the top of the indicator, there is a
leak. See “Breathing system problems” in the “Alarms and
Troubleshooting” section.
M1132382 5-13
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Breathing circuit test 1. Set the System switch to On.

3. Occlude the bag port.
4. Set the APL valve to 70 cmH2O.
5. Set the O2 flow to 250 ml/min.
7. Push the O2 flush button and pressurize the bag to approximately
30 cmH2O.
8. Release the O2 flush button. The pressure must not decrease.
Any pressure decrease shown on the pressure gauge indicates a
leak. Repair any leaks in the breathing circuit.
APL valve test 1. Set the System switch to On.

3. Occlude the bag port.
4. Set the APL valve to 70 cmH2O.
5. Set the O2 flow to 3 l/min. Make sure that the value on the
inspiratory pressure gauge does not exceed 85 cmH2O. Some
pressure fluctuation is normal.
6. Set the APL valve to MIN.
7. Make sure that the value on the inspiratory pressure gauge is
less than approximately 5 cmH2O.
8. Push the O2 flush button. Make sure that the value on the
inspiratory pressure gauge stays near zero.
9. Set the O2 flow to minimum and make sure that the value on the
inspiratory pressure gauge does not decrease below 0 cmH2O.
5-14 M1132382
Monitor and ventilator tests

5. Select Ventilation Mode - VCV.
• TV 400 ml.
• Rate 12.
• I:E 1:2.
• Pmax 40 cmH2O.
• PEEP Off.
8. Push the O2 flush button to fill the bellows.
9. Make sure that:
• Mechanical ventilation starts.
• A subatmospheric pressure alarm does not occur.
10. Set the O2 flow control to 5 l/min.
11. Make sure that:
• The end expiratory pressure is approximately 2 cmH2O.
Positive end expiratory pressure that occurs when PEEP is
Off may indicate that the scavenging system is not removing
enough gas.

M1132382 5-15
Aespire View
12. Set the ventilator controls and alarm limits to clinically appropriate
levels.
13. Prepare the system.
• Turn all vaporizers off.
• Set the APL valve to MIN.
• Set the Bag/Vent switch to Bag.
• Set all flow controls to minimum.
• Set sufficient patient suction.
• Make sure that the breathing system is correctly connected
and not damaged.
WARNING Flush the system with 5 l/min of O2 for at least one minute
to remove any gas mixtures or by-products from the
system.
5-16 M1132382
WARNING Set alarm levels appropriately before starting ventilation

(manual or mechanical).
w If an alarm occurs, safeguard the patient first before

performing troubleshooting or doing repair procedures.
w Do not use malfunctioning equipment. Contact a

Datex-Ohmeda trained representative for service.
w No repair should ever be attempted by anyone not having

experience in the repair of devices of this nature. See the
“Repair policy” in the “User Maintenance” section.
In this section Alarms. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2

List of alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4
Alarm ranges . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Alarm tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Breathing system problems . . . . . . . . . . . . . . . . . . . . . . . . 6-12
Electrical problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-13
Pneumatic problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-14
M1132382 6-1
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Alarms
When an alarm occurs during a case, an alarm tone sounds and the
alarm message is displayed in the alarm message field. The alarm
message area has room for four alarms to be shown at one time. If
more than four alarms occur, the alarms cycle every two seconds.
Alarms have three general causes:
• Malfunctions - Result in reduced system function or prevent
mechanical ventilation.
• Patient monitoring - Are caused by high and low limit settings that
are adjusted by the user.
• Informational - Are caused by control settings or system
conditions that may change system operation.
Audio Alarm priority is dependent on the level of risk to the patient.

A high-priority alarm tone sounds in two bursts of five tones, a 10
second pause, and then repeats. Some high-priority alarms can be
silenced for 120 seconds.
Medium-priority alarm tones sound in three tones with a 25 second
pause, then repeats. Medium priority alarms can be silenced for 120
seconds.
Informational alarms have a single alarm tone and the tone does not
repeat.
Silencing an alarm stops the audible tone for 120 seconds. Pushing
the Alarm silence key when no medium or high-priority alarms are
active suspends audible alarm tones for 90 seconds.
Display Messages for alarms are displayed as follows:

• High-priority alarms show in white text on a red background.
• Medium priority alarms show in yellow text on a dark gray
background.
• Informational messages show in white text on a dark gray
background.
6-2 M1132382
Latching alarms Some patient parameter alarms continue to be displayed (latch) when
the alarm condition is corrected. When an alarm is latched, the alarm
messages show in white text on a black background.
Latching alarm Flashing parameter

O2% low O2
No O2 pressure None
Ppeak high Ppeak
PEEP high. Blockage? Ppeak
Negative airway pressure None
Apnea > 120 s TVexp
Inspiration stopped None
The alarm remains in this condition until it is acknowledged by

pushing the Alarm silence key or until the alarm reoccurs. When the
alarm is acknowledged, it is removed from the screen. If an alarm has
latched and the alarm reoccurs before it is acknowledged, the alarm
will revert to an active state.
M1132382 6-3
Aespire View
List of alarms
If corrective action does not resolve the alarm, contact a
Message Priority Cause Action

+15V Analog out- Minimum shutdown Ventilator malfunction. Ventilate manually. Monitoring is not reliable.
of-range (High) Contact a Datex-Ohmeda trained service
representative.
+6V Analog out-of- Minimum shutdown Ventilator malfunction. Ventilate manually. Monitoring is not reliable.
range (High) Contact a Datex-Ohmeda trained service
representative.
-6V Analog out-of- Minimum shutdown Ventilator malfunction. Ventilate manually. Monitoring is not reliable.
representative.
5V Ref out-of-range Minimum shutdown Ventilator malfunction. Ventilate manually. Monitoring is not reliable.
(High) Contact a Datex-Ohmeda trained service
representative.
1.225 V Ref out-of- Minimum shutdown Ventilator malfunction. Ventilate manually. Monitoring is not reliable.
representative.
12 hour test Informational System is in use for more than 12 At end of the case, move the System switch
recommended hours without a power-up self test. from On to Standby to On.
A/D converter Minimum shutdown Ventilator malfunction. Ventilate manually. Monitoring is not reliable.
failure (High) Contact a Datex-Ohmeda trained service
representative.
Absorber panel Medium The breathing system is not fully Fully latch the breathing system.
open latched.
ACGO on Medium The outlet selection switch is set to Connect the patient circuit to the auxiliary outlet.
(Informational after the auxiliary common gas outlet. For mechanical ventilation or ventilation with
acknowledge) monitoring, select the circle system setting.
Apnea > 120 s High No mechanical breaths or Check the patient. Bag as needed. Check for
spontaneous breaths greater than 5 disconnects. If the patient is on a heart lung
ml in last 120 seconds. machine, select Cardiac Bypass from the Main
menu.
Apnea Medium No mechanical breaths or Check the patient. Bag as needed. Check for
spontaneous breaths greater than 5 disconnects. If the patient is on a heart lung
ml in last 30 seconds. machine, select Cardiac Bypass on the Main
Menu.
Apnea alarm off Informational The Cardiac Bypass option is set to Set Cardiac Bypass to Off in the Main Menu.
On in the Main Menu.
Apnea alarm Informational Normal condition after End Case, Monitoring resumes after first breath
standby power-up, or ACGO change from On (mechanical) or two breaths within 30 seconds
to Off. (non-mechanical).
Backup mode Informational No spontaneous breaths in set period Select a new ventilation mode or switch to
active of time and 30 seconds have elapsed manual ventilation.
since starting PSVPro mode.
Battery charger fail Informational The current in the battery charging System is operational, but may fail on battery if
circuit is too high. mains power is lost. Contact a Datex-Ohmeda
trained service representative.
Battery charging Informational Battery is not fully charged. Leave the system plugged in to charge the
battery.
Battery circuit Informational Battery measures less than 7 V or System is operational, but may fail on battery if
failure higher than 16.5 V. mains power is lost. Contact a Datex-Ohmeda
Battery current high Informational Battery current greater than 6 amps System is operational, but may fail on battery if
for 10 seconds. mains power is lost. Contact a Datex-Ohmeda
6-4 M1132382

Battery failure high Informational Battery voltage greater than 16 V for System is operational, but may fail on battery if
10 seconds. mains power is lost. Contact a Datex-Ohmeda
Battery failure low Informational The battery voltage is too low (less System is operational, but will fail on battery if
than 7 V) to supply the system if mains power is lost. Leave the system plugged
power fails. in to charge the battery. If the battery does not
charge in 24 hours, contact a Datex-Ohmeda
Calibrate flow Informational The last flow sensor calibration failed. Zero the flow sensors. Look for water in the flow
sensors sensor tubes and dry if necessary. Replace
sensor if necessary. Contact a Datex-Ohmeda
trained service representative if calibrating or
replacing the sensor does not correct the
problem.
Calibrate O2 Informational Calibration failure or O2% > 110%. Calibrate the O2 sensor. Replace the sensor if
sensor calibration is unsuccessful. Contact a Datex-
Ohmeda trained service representative if
calibrating or replacing the sensor does not
correct problem.
Cardiac bypass Informational The Cardiac Bypass option is set to Set Cardiac Bypass to Off in the Main Menu.
On. Apnea alarms are off.
Check flow sensors Medium System has detected an improper flow Check if the flow sensors are correctly installed.
(Informational after pattern in the breathing circuit. Check for water buildup in the flow sensor
acknowledge) tubes. Inspect one way valves (breathing circuit
module.) Check the condition of the flow sensor
and its tubing.
Circuit leak Medium Exhaled volume less than 50% of Check breathing circuit and flow sensor
inspired volume for at least 30 connections. Patient circuit leak audio can be
seconds (mechanical ventilation). turned off in the Alarm Setup menu.
Circuit leak audio Informational Leak Audio is set to Off on the Alarm Turn Leak Audio to On on the Alarm Setup
off Setup menu. menu.
Connect O2 sensor Medium O2 cell is not installed in the breathing Install or replace the O2 cell.
system. The O2 cell is not measuring
gas in the breathing circuit.
CPU failure Minimum shutdown Ventilator malfunction. Ventilate manually. Monitoring is not reliable.
(High) Contact a Datex-Ohmeda trained service
representative.
Display failure Medium Backlight input supply is less than Continue to use the system normally. Contact a
9.35V or greater than 13.65V. This Datex-Ohmeda trained service representative.
alarm message may not always be
viewable.
Dry or replace flow Medium Expired volume is greater than Check patient condition. Check that the flow
sensors (Informational after inspired volume for six breaths with a sensors are installed correctly. Check that there
acknowledge) circle module. is no water buildup in the flow sensor tubes.
Verify proper check valve operation. Inspect one
way valves (breathing circuit module). Replace
flow sensors.
Gas inlet valve Minimum shutdown Ventilator pressure sensor Ventilate manually. Monitoring is not available.
failure (High) malfunction. Contact a Datex-Ohmeda trained service
representative.
Increase low MV Medium The low MV limit is set to Off. Turn on the MV low setting.
limit
Inspiration stopped High Drive gas safety switch activated (high Adjust the controls. Check the system for
pressure). blockages. Contact a Datex-Ohmeda trained
service representative if problem continues.
Internal ventilator Minimum shutdown Ventilator malfunction. Ventilate manually. Monitoring is not reliable.
clock too fast (High) Contact a Datex-Ohmeda trained service
representative.
Internal ventilator Minimum shutdown Ventilator malfunction. Ventilate manually. Monitoring is not reliable.
clock too slow (High) Contact a Datex-Ohmeda trained service
representative.
M1132382 6-5
Aespire View

Invalid circuit Informational Absorber switches do not detect a Make sure the breathing system is correctly
module valid breathing circuit module. installed. Continue to use normally. Contact a
Limit task light use Informational The system is operating on battery Manually ventilate the patient to save power.
power. Make sure power is connected and circuit
breakers are closed.
Loss of backup Medium Alarm audio malfunction. Continue to use normally. Contact a Datex-
audio (Informational after Ohmeda trained service representative.
acknowledge)
Low battery voltage Medium Voltage is less than 11.65V while Manually ventilate the patient to save power.
using battery power. Make sure power is connected and circuit
breakers are closed.
Memory Informational The system cannot access some Default settings are used. Ventilation is still
(EEPROM) failure stored values. possible but service is necessary. Contact a
Memory (flash) Minimum shutdown Ventilator malfunction. Ventilate manually. Monitoring is not reliable.
failure (High) Contact a Datex-Ohmeda trained service
representative.
Memory (redundant Minimum shutdown Ventilator malfunction. Ventilate manually. Monitoring is still available.
storage) fail (High) Contact a Datex-Ohmeda trained service
representative.
Monitoring only Medium A severe malfunction prevents Ventilate manually. Cycle system power (On-
mechanical ventilation. Other alarms Standby-On). If the alarm clears, restart
may also occur. mechanical ventilation. Contact a Datex-
Ohmeda trained service representative.
MVexp high Medium Exhaled minute volume is greater Check patient for spontaneous breathing. Adjust
than the high limit setting. This alarm control settings.
is suspended for nine breaths or one
minute (whichever is greater) after the
ventilator settings are changed.
MVexp low Medium Exhaled minute volume less than the Check patient condition. Check tubing
low limit alarm setting. This alarm is connections. Check alarm settings.
suspended for nine breaths or one
minute (whichever is greater) after the
ventilator settings are changed.
Negative airway High Subatmospheric pressure (less than Check the patient condition for spontaneous
pressure -10 cmH2O). activity. Increase fresh gas flow. Look for high
flow through gas scavenging. Calibrate the flow
sensors. With active scavenging, check the
negative relief valve on the receiver.
No CO2 absorption Medium Absorber canister is not latched when Check that the absorber canister is properly
(Informational after CO2 bypass is in place. latched. Continue to use the system normally.
acknowledged) Contact a Datex-Ohmeda trained service
representative.
No exp flow sensor Medium Electrical signals show the flow Connect the flow sensors. Make sure the flow
(Informational after sensor is not connected. sensor module is on all the way.
acknowledge)
No insp flow sensor Medium Electrical signals show the flow Connect the flow sensors. Make sure the flow
(Informational after sensor is not connected. sensor module is on all the way.
acknowledge)
No O2 pressure High (cannot be The O2 supply has failed for 10 Air flow will continue. Ventilate manually if
silenced) seconds. necessary. Connect a pipeline supply or install
an O2 cylinder.
O2 flush stuck on? Informational O2 flush flow is detected for greater Stop pressing the O2 flush button. If this alarm
than or equal to 30 seconds. occurs when flush is not in use, contact a Datex-
O2% high Medium O2% is greater than the alarm high Verify that the limit it set correctly. Check that
limit setting. the O2 flow is adequate. Calibrate the O2
sensor. If calibration fails, replace the O2
sensor.
6-6 M1132382

O2% low High O2% is less than the alarm low limit Verify that the limit it set correctly. Check that
setting. the O2 flow is adequate. Calibrate the O2
sensor. If calibration fails, replace the O2
sensor. As the cell wears out, the measured %
of O2 decreases.
PEEP high. Minimum shutdown Paw greater than 100 cmH2O for 10 Check the tubing and breathing system for
Blockage? (High) seconds. blockages. Ventilate manually. Contact a Datex-
PEEP high. High Paw greater than or equal to Check tubing for kinks, blockages, disconnects.
Blockage? sustained pressure limit for 15 Calibrate the flow sensors.
seconds1.
Plug in power Medium The mains supply is not connected or Ventilate manually to save power. At full charge,
cable. On battery. (Informational after has failed and the system is using the battery permits approximately 90 minutes of
acknowledge) battery power. mechanical ventilation. Make sure power is
connected and circuit breakers are closed.
Positive SIB Vref Minimum shutdown Ventilator malfunction. Ventilate manually. Monitoring is still available.
out-of-range (High) Contact a Datex-Ohmeda trained service
representative.
Ppeak high High Ppeak is greater than Pmax. The Verify Pmax and other controls are set correctly.
ventilator cycles to expiration. Look for blockages. Check patient connection.
Ppeak low. Leak? Medium Ppeak is less than 4 cm above Pmin Verify circuit connections are okay. Look at the
for 20 seconds when RR is greater Paw gauge on the absorber. Look for circuit
than or equal to four. disconnection.
Ppeak is less than 4 cm above Pmin
for 35 seconds when RR is less than
four.
Pressure/volume Medium The outlet selection switch is set to Connect the patient circuit to the auxiliary outlet.
monitor inactive (Informational after the ACGO. For mechanical ventilation or ventilation with
acknowledge) monitoring, select the circle system setting.
Replace exp flow Informational The system cannot read the Operation continues with reduced accuracy.
sensor calibration data stored in the sensor. Replace the flow sensor.
Replace insp flow Informational The system cannot read the Operation continues with reduced accuracy.
sensor calibration data stored in the sensor. Replace the flow sensor.
Replace O2 sensor Informational O2% is less than 5%. Make sure the patient receives O2. Use a
different monitor. Calibrate the O2 sensor.
Replace the O2 cell.
Reverse exp flow Medium Flow through the expiratory sensor Look at the check valves. Check for water
(Informational after during inspiration (for six breaths in a buildup in the flow sensor tubes. Check the flow
acknowledge) row). sensor condition. Replace the expiratory check
valve.
Reverse insp flow Medium Flow through the inspiratory sensor Look at the check valves. Check for water
(Informational after during expiration (for six breaths in a buildup in the flow sensor tubes. Check the flow
acknowledge) row). sensor condition. Replace the expiratory check
valve.
Select gas outlet Medium With ACGO On, the flow sensors Turn the ACGO off or connect the non-circle
have detected three breaths in patient patient circuit to the ACGO. Note: The bag arm
circuit during the last 30 seconds. will not ventilate a patient at the auxiliary outlet.
Service calibration Informational Corrupt or invalid calibration data for The system is operational. Contact a Datex-
the flow valve. Ohmeda trained service representative.
Software error Minimum Indicates that a software error has Ventilate manually. Monitoring is not reliable.
Shutdown (High) occurred. Contact a Datex-Ohmeda trained service
representative.
Software/Hardware Minimum Compatibility error between the Ventilate manually. Contact a Datex-Ohmeda
Incompatibility Shutdown (High) software and the hardware. trained service representative.
System leak? Medium Leak detected between ventilator and Look for leaks in the absorber system. Check
(Informational after patient circuit. the integrity of the flow sensors. Zero the flow
acknowledge) sensors. Inspect for leaks (repair). Inspect or
replace flow sensors.
TFS module error Informational TFS module connected but not System is operational, but TFS is not
operating correctly. functioning correctly. Contact a Datex-Ohmeda
M1132382 6-7
Aespire View

TFS module error - Informational TFS module connected but the Air System is operational, but the Air flow sensor is
Air sensor sensor is reporting an error. not functioning correctly. Contact a Datex-
TFS module error - Informational TFS module connected but N2O fresh System is operational, but N2O sensor is not
N2O sensor gas sensor is reporting an error. functioning correctly. Contact a Datex-Ohmeda
TFS module error - Informational TFS module connected but O2 fresh System is operational, but the O2 flow sensor is
O2 sensor gas sensor is reporting an error. not functioning correctly. Contact a Datex-
TVexp high Medium Exhaled tidal volume is greater than Check patient for spontaneous breathing.
the high alarm limit. This alarm is Check ventilator and alarm settings.
suspended for nine breaths after a
change in the ventilator settings.
TVexp low Medium Exhaled tidal volume is less than the Check patient condition. Check tubing
low alarm limit. This alarm is connections. Check alarm settings.
suspended for nine breaths after a
change in the ventilator settings.
TV not achieved Informational Tidal volume measured by inspiratory Adjust controls to supply adequate tidal
flow sensor is less than the set value volumes. Check I:E, Pmax, and volume
for six breaths in a row after the first settings. Possible leak. Modify settings or check
minute of mechanical ventilation. for system leaks.
Unable to drive Informational Manifold pressure is greater than Check the drive gas. Increase fresh gas flow (or
bellows Paw. push the O2 flush button) to fill the bellows.
Ventilator has no Medium The ventilator does not detect supply Manually ventilate the patient. Make sure that
drive gas (Informational after pressure. the appropriate gas supplies (O2 or Air) are
acknowledge) connected and pressurized.
Vol vent only. No Medium Manifold pressure error. Pressure Continue to use volume control ventilation or
PEEP or PSV. control unavailable. ventilate manually. Shut down system as soon
as possible. Contact a Datex-Ohmeda trained
service representative.
1The sustained pressure threshold is calculated from the pressure limit setting. The sustained limit is
calculated as follows:
Mechanical For Pmax less than or equal to 30 cmH2O, the sustained pressure limit is 6 cmH2O.
ventilation with For Pmax between 30 and 60 cmH2O, the sustained pressure limit is 20% of Pmax.
PEEP Off For Pmax greater than or equal to 60 cmH2O, the sustained pressure limit is 12 cmH2O.
Mechanical For Pmax less than or equal to 30 cmH2O, the sustained pressure limit is 6 cmH2O plus
ventilation with “set PEEP” minus 2 cmH2O.
PEEP On For Pmax between 30 and 60 cmH2O, the sustained pressure limit is 20% of Pmax plus
“set PEEP” minus 2 cmH2O.
For Pmax greater than 60 cmH2O, the sustained pressure max is 12 cmH2O plus “set
PEEP” minus 2 cmH2O.
Mechanical For Pmax between 12 and 60 cmH2O, the sustained pressure limit is 50% of Pmax.
Ventilation Off For Pmax greater than 60 cmH2O, the sustained pressure limit is 30 cmH2O.
6-8 M1132382
Minimum system There are two special alarm types:

shutdown and • Minimum system monitoring alarms stop mechanical ventilation.
monitoring alarms • Minimum system shutdown alarms stop mechanical ventilation
and monitoring.
The software goes to minimum system monitoring when a non-
recoverable error occurs during bootup or normal operation. The
ventilator shows data and mechanical ventilation stops. ‘Monitoring
only’ appears in the Alarm message area and a specific failure
message appears in the User message area.
The following are minimum system monitoring alarms:
• Manifold pressure sensor failure.
• Pressure limit switch failure.
• Flow valve (DAC) failure.
• Flow valve (current) failure.
• Valve power failure.
A severe malfunction causes minimum system shutdown alarms.
This condition prevents mechanical ventilation and monitoring. If this
condition occurs:
• Ventilate manually.
• Use a stand-alone monitor.
• Cycle system power (On-Standby-On).
If the alarm clears, restart mechanical ventilation. If the alarm does
not clear, contact a Datex-Ohmeda trained service representative.
M1132382 6-9
Aespire View
Alarm ranges
Alarm Range Increment Default

O2% high Off, 21-99% 1% Off
O2% low 18-99% 1% 21%
MVexp high Off, 0.5-30 l/min 0.5 l/min 10.0 l/min
MVexp low Off, 0.1-10 l/min 0.1 l/min 2.0 l/min
TVexp high 20-1600 ml 20 ml 1000 ml
TVexp low Off, 5-1500 ml 5 ml for less than Off
20 ml,
otherwise 20 ml
Leak Audio On, Off N/A On
Alarm tests
Test the system to verify that alarms are functioning:
2. Start a case.
4. Set the controls.
• Ventilation mode: Volume Control (VC).
• Ventilator.
— Tidal Vol: 400 ml
— Rate: 12
— I:E Ratio: 1:2
— Plimit: 40 cmH2O
— PEEP: Off
• Anesthesia machine.
— O2 flow: minimum flow (25-75 ml/min).
— All other gases: Off
— Push O2 flush button to fill bellows.
5. Set the O2 concentration to 30% and allow the O2 reading to
stabilize.
6-10 M1132382
6. Test the O2 alarms.

• Remove the O2 cell from the breathing circuit and make sure
it measures approximately 21% O2 in room air.
• Set the O2 low alarm limit to 50%. Make sure the O2% low
alarm occurs.
• Set the O2 low alarm limit back to 21% and make sure that
the O2% low alarm cancels.
• Install the O2 cell in the breathing circuit.
• Set the O2 high alarm limit to 50%.
• Push the O2 flush button to fill the breathing system.
• Make sure the O2% high alarm occurs.
• Set the O2 high alarm limit back to Off. Make sure that the
O2% high alarm cancels.
• After two minutes in pure O2, the O2 cell measures
approximately 100% O2.
7. Test the MVexp low alarm.
• Go to the Alarm Setup menu.
• Set the MV low alarm limit to 6.0 l/min
• Make sure the MVexp low alarm occurs.
• Set the MV low alarm limit to Off.
8. Test the Ppeak high alarm.
• Set Pmax to less than the peak airway pressure.
• Make sure the Ppeak high alarm occurs.
• Set Pmax to the desired level.
9. Test the PEEP high. Blockage? alarm.
• Close the APL valve.
• Set the Bag/Vent switch to Bag. Mechanical ventilation stops.
• Block the patient connection and push the O2 flush button.
• Make sure the PEEP high. Blockage? alarm occurs after
approximately 15 seconds.
10. Test the Ppeak low. Leak? alarm.
• Unblock the patient connection.
• Set the Bag/Vent switch to Vent.
• Set the tidal volume and total flow to minimum.
• Other alarms such as MVexp low can occur.
• Make sure that the Ppeak low. Leak? alarm occurs.
11. Set all alarm limits to approved clinical values.
M1132382 6-11
Aespire View
Breathing system problems
System Problem Solution

Gas scavenging flow is Scavenging extract flow Use a different scavenging
too low or too high. problem. extraction system. Verify flow is
within specification.
Filter blockage. Active systems Replace the filter. See
have a flow indicator. “Remove the AGSS Receiver
Filter” in the “ABS Cleaning
and Sterilization” manual.
The bellows fills when the Leak through the Bag/Vent Contact a Datex-Ohmeda
Bag/Vent switch is set to switch. trained service representative
Bag or the bag fills when to repair the system.
the switch is set to Vent.
The ventilator does not Ventilator or absorber Ventilate manually. Contact a
read the position of the malfunction. Datex-Ohmeda trained service
Bag/Vent switch. representative to repair the
system.
APL valve does not APL valve problem. Replace APL valve seal and
operate correctly. diaphragm.
Large breathing system Bag hose not connected Ensure that the bag hose is
leak not quickly located. properly. connected to the bag port
(below the APL valve).
Absorber canister not installed Reinstall the absorber canister,
correctly. ensure both pins are engaged.
Bellows falls below top of Leak in the breathing system. Check, clean or reposition the
indicator during “Bellows pressure relief valve. If the
test.” problem persists, replace the
pressure relief valve, bellows
base, or bellows assembly.
6-12 M1132382
Electrical problems
WARNING If a circuit breaker opens frequently, do not use the

system. Have a Datex-Ohmeda trained service
representative repair the system.

Mains indicator is not on. The electrical power cable is not Connect the power cable.
connected.
The inlet circuit breaker (switch) Turn the circuit breaker on.
is off.
The power cable is damaged. Replace the power cable.
The electrical socket the power Use a different electrical
cable connects to had no power. socket.
An internal fuse is open. Have a Datex-Ohmeda trained
service representative repair
the system.
One electrical outlet does The outlet circuit breaker is off. Turn the circuit breaker on.
not have power.
A circuit breaker opens Equipment connected to the Use a different power supply
frequently. outlet uses more current than for some of the equipment.
the circuit breaker rating.
The equipment connected to the Have a Datex-Ohmeda trained
outlet has a short. service representative repair
the system.
Tec 6 series vaporizer Not plugged into outlet. Connect power cable.
has no power. The outlet circuit breaker is off Turn the circuit breaker on.
M1132382 6-13
Aespire View
Pneumatic problems

High-pressure leak test Controls are not set correctly. Make sure that no gas is
fails. flowing, turn off the auxiliary
flowmeter, and repeat the test.
Incorrect cylinder connection. Make sure that there is only
one cylinder gasket, the gasket
is in good condition, and the
connection is tight.
Low-pressure leak test The vaporizer is not correctly Correctly install the vaporizer.
fails with a vaporizer on. installed.
The vaporizer filler is loose Tighten the filler.
(funnel fill type vaporizer).
Vaporizer port o-rings (external) Install new o-rings.
are damaged or not installed.
A vaporizer malfunction (the leak Send the vaporizer to an
stops if a different vaporizer is approved service center for
used in the same manifold repair.
position).
A port valve malfunction (the Contact a Datex-Ohmeda
leak continues if a different trained service representative
vaporizer in the same manifold to repair the vaporizer
position). manifold.
Low-pressure leak with a Anesthesia machine problem. Contact a Datex-Ohmeda
vaporizer off. trained service representative.
6-14 M1132382
7 User Maintenance
WARNING To help prevent fires:

• Only use lubricants approved for anesthesia or O2
equipment, such as Krytox.
• Do not use lubricants that contain oil or grease. They
may burn or explode in high O2 concentrations.
• All materials used to cover the system must be made
from antistatic (conductive) materials. Static electricity
can cause fires.
• Desiccated (dehydrated) absorbent material may
produce dangerous chemical reactions when exposed
to inhalation anesthetics. Adequate precautions
should be taken to ensure that absorbent does not dry
out. Turn off all gases when finished using the system.
w Obey infection control and safety procedures. Used

equipment may contain blood and body fluids.
w Moveable parts and removable components may present

a pinch or a crush hazard. Use care when moving or
replacing system parts and components.
In this section Repair policy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2

Maintenance summary and schedule . . . . . . . . . . . . . . . . . . 7-2
Breathing system maintenance. . . . . . . . . . . . . . . . . . . . . . . 7-3
O2 cell replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
O2 cell calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-5
Zeroing flow sensor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-6
Prevent water buildup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-7
M1132382 7-1
Aespire View
Repair policy
Do not use malfunctioning equipment. Make all necessary repairs or
have the equipment serviced by a Datex-Ohmeda trained service
representative. After repair, test the equipment to ensure that it is
functioning properly in accordance with Datex-Ohmeda’s published
specifications.
To ensure full reliability, have all repairs and service done by a
No repair should ever be attempted by anyone not having training
and experience in the repair of devices of this nature.
Replace damaged parts with components manufactured or sold by
Datex-Ohmeda. Then test the unit to ascertain that it complies with
Datex-Ohmeda’s published specifications.
Contact a Datex-Ohmeda Field-Service Representative for service
assistance.
Maintenance summary and schedule

These schedules indicate the minimum frequency of maintenance
based on typical usage of 2000 hours per year. Equipment should be
serviced more frequently if it is used more than the typical yearly
usage.
For detailed cleaning instructions, refer to the Advanced Breathing
System Cleaning and Sterilization manual which accompanies the
machine.
Note Local policies or regulations may require that maintenance be
performed more frequently than stated here.
7-2 M1132382
7 User Maintenance
User maintenance
Minimum Frequency Maintenance
Daily • Clean the external surfaces.
• Perform 21% O2 calibration.
• Check the condenser reservoir (if equipped). Drain if
needed.
• Zero the flow sensors.
Two weeks Drain the vaporizers and discard the agent. This is not
necessary for the Tec 6 series vaporizers.
Monthly • Perform 100% O2 calibration.
• Lubricate all cylinder supply tee handle threads with
Krytox or a lubricant approved for use with 100% O2.
During cleaning and Inspect the parts for damage. Replace or repair as
setup necessary.
Annually Replace the external o-rings on the vaporizer ports.
As necessary • Install new cylinder gaskets on cylinder yokes.
• Empty the water reservoir and replace the absorbent in
the canister.
• Empty the overflow trap on the optional suction
regulator (if equipped).
• Replace the circuit O2 cell (under typical use the cell
meets specifications for 1 year).
• Replace the disposable (plastic) flow sensors (under
typical use the non-offset flow sensors meet
specifications for a minimum of three months and the
offset flow sensors meet specifications for a minimum
of six months).
• Replace the autoclavable (metal) flow sensors (under
typical use the sensors meet specifications for a
minimum of one year).
• Replace the receiver filter (if equipped - active gas
scavenging only).
Datex-Ohmeda This is the minimum level of maintenance recommended by

approved service Datex-Ohmeda. Local regulations may contain additional
maintenance requirements. Datex-Ohmeda advocates compliance
with local regulations which meet or exceed this minimum level of
maintenance.
Minimum Frequency Maintenance

12 months Have a Datex-Ohmeda trained service representative
complete the scheduled service maintenance checks, tests,
calibrations, and parts replacement as defined in the
Technical Reference manual.
Breathing system maintenance

Replace any parts that are visibly cracked, chipped, distorted, or worn
when cleaning the breathing system.
M1132382 7-3
Aespire View
O2 cell replacement
WARNING Handle and dispose of O2 cells according to site

biohazard policies. Do not incinerate.
1. Pull the latch to unlock the flow sensor module.
AB.74p.052
2. Pull the flow sensor module out of the breathing system.
3. Remove the cable connector from the O2 cell, and unscrew the
cell counterclockwise.
AB.74p.065
Important Make sure that the o-ring is on the replacement O2 cell before
installation.
AB.74p.083
4. Install the replacement O2 cell and reconnect the O2 cell cable.

5. Put the flow sensor module back into the system and push the
latch closed to secure the flow sensor module.
6. Perform “O2 cell calibration” after O2 cell replacement.
7-4 M1132382
7 User Maintenance
O2 cell calibration
WARNING Do not perform O2 cell calibration while the system is

connected to a patient.
w The O2 cell must be calibrated at the same environment

pressure at which it will be used to monitor oxygen
delivery in the patient circuit.
w Operation at pressures other than the pressures present

during calibration may result in readings outside of the
stated monitoring accuracy.
Important It may take a new O2 cell 90 minutes to stabilize. If the O2 cell
calibration fails after a new O2 cell has been installed, wait 90
minutes and repeat the calibration.
21% O2 cell Complete a 21% O2 cell calibration before performing the 100% O2
calibration cell calibration.
2. Select Setup/Calibration.
3. Select O2 Sensor Calibration.
4. Select 21% O2.
5. Remove the O2 cell from the circuit.
• Pull the latch to unlock the flow sensor module.
• Pull the flow sensor module out of the breathing system.
• Remove the O2 cell by unscrewing the cell counterclockwise.
This exposes the O2 cell to room air.
6. Select Start Calibration. ‘Calibrating . . .’ shows on the screen
while the O2 cell is being calibrated to the room air.
7. ‘Complete’ shows on the screen upon successful calibration:
• Reinstall the O2 cell.
• Select Go to Setup/Calibration Menu.
8. If the screen shows ‘Failure,’ repeat the 21% O2 cell calibration.
9. If the calibration fails after another attempt, perform a 100% O2
cell calibration. Then try the 21% O2 cell calibration again.
10. Replace the O2 cell if repeated failures occur.
M1132382 7-5
Aespire View
100% O2 cell Complete a 21% O2 cell calibration before performing a 100% O2 cell
calibration calibration.
1. Make sure that the O2 cell is in the circuit.
2. After performing a 21% calibration, select 100% O2.
3. Push the O2 flush button for 5 seconds and set the O2 flow to
5 l/min and set other gases to minimal flow.
4. Select Start Calibration.
5. ‘Complete’ shows on the screen upon successful calibration.
6. If ‘Failure’ shows on the screen, repeat the 100% O2 cell
calibration.
• If the calibration fails after another attempt, decrease the
airway pressure and try the 100% O2 cell calibration again.
• If calibration fails after repeated attempts, perform a 21% O2
cell calibration. Then try a 100% O2 cell calibration again.
• If the 100% O2 cell calibration does not pass, replace the O2
cell.
7. Perform the “Breathing system tests” in the “Preoperative Tests”
section before using the system.
Zeroing flow sensor
WARNING Do not perform calibration while system is connected to a

patient.
Note The system automatically corrects for zero offset when the flow
sensor connectors are unplugged and the system power is on.
2. Remove the flow sensor module.
• Pull the latch to unlock the flow sensor module from the
breathing system.
• Pull the flow sensor module out of the breathing system.
3. ‘No insp flow sensor’ and ‘No exp flow sensor’ show on the
display when the zeroing is complete.
4. Reinstall the flow sensor module.
5. Perform the “Breathing system tests” in the “Preoperative Tests”
section before using the system.”
7-6 M1132382
7 User Maintenance
Prevent water buildup

Water is created from exhaled gas and a chemical reaction between
CO2 and the absorbent. Water buildup increases when the system is
used at low fresh gas flows. At low flows, more CO2 stays in the
absorber producing water and more moist exhaled gas remains in the
absorber.
Note Pooled water in the flow sensor or water in the sensing lines can
cause inaccurate alarms. Small beads of water or a foggy
appearance in the flow sensors is acceptable.
To manage excess water:
• Empty the water reservoir in the absorbent canister when
changing the absorbent.
• Make sure that any water condensing in the breathing circuit
tubes is not allowed to drain into the flow sensors.
• Water condensation in the breathing circuit tubing might be
lessened by using a Heat and Moisture Exchange (HME) filter at
the airway connection.
• Install the condenser or EZchange canister option.
M1132382 7-7
Aespire View
7-8 M1132382
In this section Canister setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4

Electrical connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9
Pneumatic connections. . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-10
How to install gas cylinders. . . . . . . . . . . . . . . . . . . . . . . . . 8-13
How to attach equipment to the top of the machine . . . . . . 8-14
M1132382 8-1
Aespire View
WARNING Datex-Ohmeda strongly recommends the use of O2

monitoring with this equipment. Refer to local standards
for mandatory monitoring.
w European, international, and national standards require

the following monitoring be used with this system:
• Exhaled volume monitoring.
• O2 monitoring.
• CO2 monitoring.
• Anesthetic agent monitoring be used when anesthetic
vaporizers are in use.
w Always make sure that the pipeline supply hoses and the
breathing circuit components are not toxic and will not:
• Cause an allergic reaction in the patient.
• React with the anesthetic gases or agent to produce
dangerous by-products.
w To prevent incorrect values or equipment malfunction,

use only cables, hoses, and tubing approved by
Datex-Ohmeda.
w This system operates correctly at the electrical

interference levels of IEC 60601-1-2. Higher levels can
cause nuisance alarms that may stop mechanical
ventilation.
w To help prevent false alarms from devices with high-

intensity electrical fields:
• Keep the electrosurgical leads away from the
breathing system, flow sensors, and O2 cell.
• Do not allow the electrosurgical leads to contact any
part of the anesthesia system.
• Do not use cell phones near the anesthesia system.
8-2 M1132382
w To protect the patient when electrosurgical equipment is

used:
• Monitor the correct operation of all life support and
monitoring equipment.
• Keep backup manual ventilation available in case the
electrosurgical equipment prevents safe use of the
ventilator.
w Do not use antistatic or electrically-conductive breathing

tubes or masks. They can cause burns if used near high
frequency surgical equipment.
w Use only reservoir bags that comply with EN1820 on this

system.
w Use only breathing tubes that comply with EN12342 on

this system.
w A malfunction of the medical gas central supply system

may cause all connected devices to stop.
M1132382 8-3
Aespire View
Canister setup
1
6
5
2
AB.74p042
AB.74p043
1. Canister support pin
2. Canister handle
3. Disposable Multi Absorber canister
4. Absorbent
5. Expiratory water reservoir
6. Canister release latch
7. Reusable Multi Absorber canister
Figure 8-1 • Canister
8-4 M1132382
WARNING Obey applicable safety precautions:

• Do not use the absorber with chloroform or
trichloroethylene.
• The Disposable Multi Absorber is a sealed unit which
should not be opened or refilled.
• The Disposable Multi Absorber cannot be disinfected
and is not autoclavable. Be aware that cross-
contamination is possible.
• Avoid skin or eye contact with the contents of the
absorber. In the event of skin or eye contact,
immediately rinse the affected area with water and
seek medical assistance.
• Do not change the absorber during ventilation unless
the EZchange canister system is installed.
• Change absorbent often to prevent the buildup of
non-metabolic gases when the system is not in use.
• Inspect absorbent color at the end of a case. During
non-use, absorbent can go back to the original color.
Refer to the absorbent labeling for more information
about color changes.
• If the absorbent completely dries out, it may give off
carbon monoxide (CO) when exposed to anesthetic
agents. For safety, replace the absorbent.
• Desiccated (dehydrated) absorbent material may
produce dangerous chemical reactions when exposed
to inhalation anesthetics. Adequate precautions
should be taken to ensure that absorbent does not dry
out. Turn off all gases when finished using the system.
The absorber canister is available in two versions:
• Disposable Multi Absorber.
• Reusable Multi Absorber.
Both versions are removed and installed on the breathing system in
the same way.
Each canister holds 800 grams of loose absorbent. Datex-Ohmeda
recommends MedisorbTM absorbent.
Both absorber versions should only be used with mixtures of air,
oxygen, nitrous oxide, halothane, enflurane, isoflurane, desflurane
and sevoflurane.
M1132382 8-5
Aespire View
When to change the A gradual color change of the absorbent in the canister indicates
absorbent absorption of carbon dioxide. The color change of the absorbent is
only a rough indicator. Use carbon dioxide monitoring to determine
when to change the canister.
Discard the absorbent when it has changed color. If left standing for
several hours, absorbent may regain its original color giving a
misleading indication of activity.
Important Read the canister instructions completely before using the product.
Removing a canister 1. Hold the canister by the handle and push on the release latch to
unlock the canister.
AB.74p058
2. Remove the canister by tilting it downward and off the two
support pins.
8-6 M1132382
Removing an 1. Hold the canister by the handle and push the canister cradle
EZchange canister release latch to unlock the canister cradle.
AB.75p088
2. Slide the canister up and out of the cradle.
AB.75p089
Reusable Multi 1. Turn the canister upside down and, using your thumbs, turn the
Absorber canister cover locking ring counterclockwise to unlock it.
filling
AC.20p003
2. Push up to release the seal.
M1132382 8-7
Aespire View
3. Lift off the cover to remove it.
AC.20p003
4. Remove and properly discard the foam filters, the absorbent, and
any water in the reservoir.
WARNING Be careful when draining condensate from the absorber.

The liquid is caustic and may burn skin.
AC.20p0004
5. To clean and disinfect the canister, see “Absorber canister” in the
“Cleaning and Sterilization” manual.
6. Assemble canister.
• Place a new filter in the bottom of the canister.
• Pour absorbent into the canister.
• Place a new filter over the absorbent.
• Align the cover slots with the canister locking tabs and press
the cover down into place.
• Turn the cover locking ring clockwise to lock the cover in
place.
• Ensure cover is properly sealed to prevent leaks and spillage.
• Wipe off any absorbent dust.
Note Alignment of the arrows helps to indicate correct assembly.
8-8 M1132382
AB.82p001
WARNING The filters must be in place to help prevent dust and
particles from entering the breathing circuit.
7. When replacing the canister, make sure that it is seated properly
on the support pins or in the EZchange canister module before
latching it into place.
Electrical connections
Outlets Labels show outlet voltage ratings and circuit breaker amp ratings.
These are isolated outlets. Regularly test the leakage current.
WARNING Equipment connected to electrical outlets that are not

isolated outlets can increase the leakage current.
Regularly test the leakage current.
AB.74p049
M1132382 8-9
Aespire View
Mains inlet Arrow shows the mains power inlet and cord.
AB.74p048
Serial port The system has an RS-232C electrical interface. The RS-232C
connector allows serial input/output of commands and data. The 15-
pin connector is located on the back of the display unit.
The 15-pin female D connector - Data Communications Equipment
(DCE) configuration:
• Pin 1 - Monitor On/Standby.
• Pin 5 - Signal ground.
• Pin 6 - Receive data.
• Pin 9 - Monitor On/Standby Return.
• Pin 13 - Transmit data.
Pneumatic connections
CAUTION Use only medical grade gas supplies. Other types of gas
supplies may contain water, oil, or other contaminants
which could affect the operation of the pneumatic system.
The gas supplies provide gas to these optional devices through
internal connections:
• Venturi suction regulator (optional).
• Auxiliary O2 flowmeter (optional).
Pipeline Inlets
AB.91p040
8-10 M1132382
Scavenging The scavenging assembly is located below the bellows on the

breathing system. Adapters may be necessary to interface to the
scavenging connector.
See the “Operation” section for more scavenging information.
AB.91p045
Sample gas return Connect the sample gas exhaust tube from the airway module to the
port gas return port. Exhaust gas will be directed to the scavenging
system.
AC.82p001
M1132382 8-11
Aespire View
Suction regulator Venturi regulators use the system air or O2 supply. Vacuum
(optional) regulators must be connected to an external vacuum supply.
2
1
3
4
5
AB.74p189
AB.74p032
1. External vacuum (non-venturi) connection
2. Venturi muffler
3. Collection bottle connection
4. Splash guard
5. Overflow safety trap
Auxiliary O2
flowmeter (optional)
2
AB.91p039
1. Auxiliary O2 outlet
2. Auxiliary O2 flow control
8-12 M1132382
How to install gas cylinders
CAUTION Do not leave gas cylinder valves open if the pipeline

failure.
Pin indexed cylinder 1. Locate the cylinder wrench.

yokes 2. Close the cylinder valve on the cylinder to be replaced.
3. Loosen the tee handle.
4. Open the cylinder yoke.
5. Remove the used cylinder and the used gasket.
6. Remove the cap (if equipped) from the cylinder valve on the new
cylinder.
WARNING Make sure there is only one gasket on the cylinder

connection. No gasket or more than one gasket can
cause a leak.
7. Install a new gasket.
8. Align the cylinder post with the index pins.
9. Close the yoke gate and tighten the tee handle.
10. Make sure there is a cylinder plug and gasket in any empty
cylinder yokes.
11. Perform a “High-pressure leak test.”
DIN cylinder 1. Close the cylinder valve on the cylinder to be replaced.

connections 2. Loosen the adapter and remove the cylinder.
3. Remove the cap from the cylinder valve on the new cylinder.
4. Install the cylinder.
5. Perform a “High-pressure leak test.”
M1132382 8-13
Aespire View
High-pressure leak
test
Note Datex-Ohmeda recommends testing one cylinder at a time.
1. Turn on the system.
2. Disconnect pipeline supplies.
3. Turn off the auxiliary O2 flowmeter and the venturi suction (if
equipped).
4. Open the cylinder.
5. Record the cylinder pressure.
6. Close the cylinder.
• If the cylinder pressure decreases more than 690 kPa
(100 psi) in one minute there is a significant leak.
7. To repair a leak, install a new cylinder gasket and tighten the tee
handle.
8. Repeat the leak test. If the leak continues, do not use the system.
How to attach equipment to the top of the machine
WARNING Do not exceed the top shelf weight limit of 34 kg (75 lb).
Check the stability of the system in its final configuration.

Make sure that the weight is evenly distributed throughout
the system.
1. Locate the clips or slots.
2. Install the straps.
3. Fully tighten the straps.
4. Make sure the straps hold the equipment in position.
WARNING Fully tighten the straps. If straps are not fully tightened,
equipment can fall off the top of the machine.
8-14 M1132382
9 Parts
This section lists user-replaceable parts only. For other components,

refer to the Technical Reference manual.
In this section Flow sensor module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2

Exhalation valve assembly . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2
Breathing circuit module . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-3
Bellows assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-4
Absorber canister . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-5
AGSS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-6
EZchange canister system . . . . . . . . . . . . . . . . . . . . . . . . . . 9-7
Condenser . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-8
Test tools and system parts . . . . . . . . . . . . . . . . . . . . . . . . . 9-9
M1132382 9-1
Aespire View
Flow sensor module
AB.82.019
Item Description Stock number
Flow sensor module (does not include flow sensors) 1407-7001-000
1 Flow sensor cover 1407-3000-000
2 Flow sensor cuff 1407-3004-000
3 Flow sensor, disposable (plastic) non-offset 1503-3858-000
Flow sensor, disposable (plastic) offset 1503-3856-000
Flow sensor, autoclavable (metal) 1503-3244-000
Exhalation valve assembly
Description Stock number

Exhalation valve assembly 1407-7005-000
9-2 M1132382
9 Parts
Breathing circuit module
AB.82.021
5

Breathing circuit module (does not include O2 cell, 1407-7002-000
o-ring, or cable)
1 Check valves circuit lens 1407-3101-000
2 Check valve assembly 1406-8219-000
3 O-ring for O2 cell or plug 1406-3466-000
4 O2 cell (includes o-ring) 6050-0004-110
5 Cable, O2 cell 1009-5570-000
M1132382 9-3
Aespire View
Bellows assembly
4
8
11
10 5
9 7
AC.20.016
AB.82.018
6

1 Bellows housing 1500-3117-000
2 Bellows 1500-3378-000
3 Rim 1500-3351-000
4 Pressure relief valve assembly 1500-3377-000
5 Latch, rim 1500-3352-000
6 Manifold, bellows base 1407-3702-000
7 Bellows base with latch 1407-7006-000
8 Seal, base 1500-3359-000
9 Diaphragm, APL 1406-3331-000
10 Cage, APL 1406-3333-000
11 Poppet, APL valve 1406-3332-000
9-4 M1132382
9 Parts
Absorber canister
3
1
AB.82.017
1 Multi absorber, reusable (includes 40 pack of foam) 1407-7004-000
(does not include absorbent)
2 Cover assembly, CO2 canister 1009-8240-000
3 Foam, CO2 canister (pack of 40) 1407-3201-000
4 O-ring 1407-3204-000
5 Canister, CO2 with handle 1407-3200-000
- Multi absorber, disposable, white to violet, (pack of 6) 8003138
- Multi absorber, disposable, pink to white (pack of 6) 8003963
M1132382 9-5
Aespire View
AGSS

Common
Cap 3.18 barb silicone 1406-3524-000
Connector, inlet 30 mm male to 9 mm male M1003134
Connector, inlet 30 mm male to 30 mm male M1003947
O-ring for connector, 21.95 ID 1406-3558-000
O-ring for receiver, 22 ID 1407-3104-000
O-ring for thumbscrews, 4.47 ID 1407-3923-000
Reservoir scavenger 1407-3903-000
Seal, down tube scavenger 1407-3904-000
Seal, receiver scavenger 1407-3901-000
Thumbscrew M6 X 28.5 1406-3305-000
Thumbscrew, M6 X 43 1406-3304-000
Valve, unidirectional (complete assembly) 1406-8219-000
Passive AGSS
Adapter, outlet 30 mm female to 19 mm male (pack of 5) 1500-3376-000
Exhaust hose 8004461
Plug assembly 30 mm ISO 1407-3909-000
Screw, shoulder 4 diameter X 4 L M3 X 0.5 sst 1407-3915-000
Active AGSS, adjustable flow
Bag with 30 mm male connector 8004460
Plug assembly 30 mm ISO 1407-3909-000
Active AGSS, high flow
Filter, 225 micrometer nylon screen AGSS 1406-3521-000
Seal, filter scavenger 1407-3902-000
Active AGSS, low flow
Filter, 225 micrometer nylon screen AGSS 1406-3521-000
Seal, filter scavenger 1407-3902-000
9-6 M1132382
9 Parts
EZchange canister system
3 1
AB.82.044
2
4
AB.82.057
1 EZchange canister module, includes valve and cap 1407-7021-000
2 Valve 1407-3126-000
3 Cap 1407-3130-000
4 Condenser 1407-7024-000
- EZchange canister module with condenser 1407-7027-000
M1132382 9-7
Aespire View
Condenser
AB.82.045
Condenser assembly (includes module and 1407-7026-000
condenser)
1 Condenser module 1407-7025-000
2 Condenser 1407-7024-000
9-8 M1132382
9 Parts
Test tools and system parts

Cylinder gasket (pin indexed cylinders only) 0210-5022-300
Cylinder wrench (DIN 477 and high-pressure hose) 1202-3651-000
Cylinder wrench for pin-indexed cylinder 0219-3415-800
DIN O2 plug (cylinder connection) 1202-7146-000
Handle for yoke tee 0219-3372-600
Negative low pressure leak test device 0309-1319-800
Positive low pressure leak test device (BSI) 1001-8975-000
Positive low pressure leak test device (ISO) 1001-8976-000
Positive pressure leak test adapter 1009-3119-000
Ring, sealing gasket (for DIN 477 and O2 high-pressure hose) 1009-3356-000
Ring, sealing gasket (for N2O high-pressure hose) 1202-3641-000
Test lung 0219-7210-300
Test plug 2900-0001-000
Touch-up paint, Neutral Gray N7 (Medium Dark), 18 ml 1006-4198-000
Touch-up paint, Neutral Gray N8 (Medium), 18 ml 1006-4199-000
Touch-up paint, Neutral Gray N9 (Light), 18 ml 1006-4200-000
Vaporizer port o-rings, external (6 pack) 1102-3016-000
Yoke plug 0206-3040-542
M1132382 9-9
Aespire View
9-10 M1132382
10 Specifications and Theory of
Operation
Important All specifications are nominal and subject to change without notice.
Note All displayed values are shown at ambient temperature and pressure
dry.
In this section System pneumatic circuits . . . . . . . . . . . . . . . . . . . . . . . . . 10-2

Pneumatic specifications . . . . . . . . . . . . . . . . . . . . . . . . . . 10-5
Electrical block diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-6
Electrical power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-7
Flow specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-9
Breathing system specifications . . . . . . . . . . . . . . . . . . . . 10-10
Physical specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-12
Environmental requirements . . . . . . . . . . . . . . . . . . . . . . . 10-12
Suction regulators (optional) . . . . . . . . . . . . . . . . . . . . . . . 10-13
Auxiliary O2 flowmeter (optional) . . . . . . . . . . . . . . . . . . . 10-13
Ventilator theory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-14
Ventilator operating specifications . . . . . . . . . . . . . . . . . . 10-23
Ventilator accuracy data . . . . . . . . . . . . . . . . . . . . . . . . . . 10-24
Electromagnetic compatibility (EMC) . . . . . . . . . . . . . . . . 10-26
Electrical safety. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-30
IEC 60601-1 Classification . . . . . . . . . . . . . . . . . . . . . . . . 10-31
Standards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-31
System components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-32
M1132382 10-1
Aespire View
System pneumatic circuits
AC.20.001
Figure 10-1 • Pneumatic circuit diagram
10-2 M1132382
1. Auxiliary O2, 0-10 l/min (optional) 36. Scavenging pressure relief valve, 1.0 kPa
2. O2 flush (10 cmH2O)
3. 241 kPa (35 psi) second O2 regulator 37. Gas to scavenging: 0-10 l/min drive gas, 0-10 l/min
4. Paw Gauge patient and fresh gas, 0-20 l/min total typical flow
5. O2 P-Line 38. 200 mL reservoir
6. O2 cylinder (optional) 39. Control bleed approximately 1.0 l/min at 0.29 kPa
7. Air P-Line (optional) (3.0 cmH2O) if continuous (rate dependent)
8. Total flow sensor (optional) 40. O2 Flush pressure switch
9. Air cylinder (optional) 41. ACGO selector valve
10. N2O P-Line (optional, standard U.S. variant) 42. 22 mm port (ACGO)
11. 758 kPa (110 psi) relief 43. O2 sensor
12. N2O cylinder (optional) 44. Inspiratory flow sensor
13. Cylinder supply and Pipeline supply 45. Absorber
14. Ventilator drive gas select 46. Drain
15. Venturi (optional) 47. Negative pressure relief valve (-14 cmH2O)
16. System switch 48. Sample gas return connection
17. O2 secondary regulator 207 kPa (30 psi) 49. Bag/Vent switch
18. Link-25 50. Bag
19. Flowmeter module (single flow tubes optional) 51. APL valve
20. Gas inlet valve assembly 52. Gas monitor (optional external gas monitor)
21. Air flow meter assembly (optional) 53. Expiratory flow sensor
22. Selectatec manifold 54. Inspiratory flow transducer
23. 37.9 kPa (5.5 psi) pressure relief valve 55. Expiratory flow transducer
24. Vaporizer 56. Sensor interface board
25. N2O balance regulator (required with N2O) 57. Scavenger flow indicator (optional)
26. O2 Flush regulator 172 kPa (25 psi) at 58. Patient
15 l/min 59. 30 mm male - to disposal system
27. Inspiratory flow control valve 60. 0.05 kPa (0.5 cmH2O) entrainment
28. Drive gas check valve (3 cm H2O) 61. Passive gas scavenging interface
29. To disposal system 62. Adjustable scavenging system (optional)
30. Active gas scavenging interface (optional) 63. Filter
31. Mechanical overpressure valve, 10.8 kPa 64. High or low flow restrictor
(110 cmH2O) 65. Bellows
32. Free breathing check valve 66. Scavenging reservoir
33. Room Air 67. Scavenging over pressure relief valve
34. Popoff valve (4 cmH2O) 68. Scavenging reservoir bag with 30 mm male connector
35. Exhalation valve 0.20 kPa (2.0 cmH2O bias) 69. Needle valve assembly (with DISS EVAC connector)
M1132382 10-3
Aespire View
Gas supplies Pressurized gas supplies enter the system through a pipeline or
cylinder connection. All connections have indexed fittings, filters, and
check valves. Gauges show the cylinder and pipeline pressures.
A regulator decreases the cylinder pressures to the appropriate
system pressure. A pressure relief valve helps protect the system
from high pressures.
To help prevent problems with the gas supplies:
• Install yoke plugs on all empty cylinder connections.
• When a pipeline supply is connected, keep the cylinder valve
closed.
• Disconnect the pipeline supplies when the system is not in use.
WARNING Do not leave gas cylinder valves open if the pipeline

failure.
O2 flow Pipeline or regulated cylinder pressure supplies O2 directly to the

ventilator (O2 Ventilator). A secondary regulator decreases the
pressure for the flush valve and the auxiliary flowmeter.
The flush valve supplies high flows of O2 to the fresh gas outlet when
you push the flush button. The flush switch uses pressure changes to
monitor the position of the flush valve.
When the System switch is ON, O2 flows to the rest of the system
and there is a minimum flow through the O2 flowmeter.
A secondary regulator supplies a constant O2 pressure to the flow
control valve.
An electrical switch monitors the O2 supply pressure. If the pressure
is too low, an alarm appears on the ventilator.
N2O flow A balance regulator controls the flow of N2O to the flow control valve.
Oxygen pressure at a control port adjusts the output of the regulator.
This stops flow during an O2 supply failure and ensures that the
hypoxic gas pressures decrease with the O2 supply pressure.
Changes in O2 pressure do not affect Air.
A chain linkage (Link-25) on the N2O and O2 flow controls helps keep
the O2 concentration higher than approximately 21% at the fresh gas
outlet.
Air flow Pipeline or regulated cylinder pressure directly supply Air to the
ventilator (Air Ventilators). When the System switch is On, air flows to
the rest of the system. Because there is no balance regulator, air flow
continues at the set rate during an O2 supply failure.
10-4 M1132382
Mixed gas The mixed gas goes from the flowmeter outlet through the vaporizer
that is ON, to the fresh gas outlet, and into the breathing system. A
pressure relief valve sets the maximum outlet pressure.
EZchange canister When activated, this module permits continued ventilation and
rebreathing of exhaled gases without any gas passing through the
absorbent.
Condenser The condenser removes water in the system that is produced from
the reaction of CO2 gas with the absorbent during low flow
anesthesia (fresh gas flows less than 1.5 l/min). The condenser is
connected between the outlet of the absorber canister and the inlet of
the circuit module. Moisture in the gas is condensed into water
droplets, which run into the condenser’s reservoir.
Pneumatic specifications
CAUTION All gases supplied to the system must be medical grade.
Gas supplies
Pipeline gases O2, Air, N2O
Cylinder gases • O2, Air, N2O (maximum: 2 cylinders of
each gas) with 3 cylinders total.
• 1 cylinder maximum on pendant model
Cylinder connections • Pin indexed (all gases).
• Nut and gland DIN-477 (O2, N2O, Air)
• Large cylinder kit available for O2 and
N2O
Primary regulator output • Pin indexed: The primary regulator is set
pressure to pressure less than 345 kPa (50 psi).
• DIN-477: The primary regulator is set to
pressure less than 414kPa (60 psi).
Pressure-relief valve Approximately 758 kPa (110 psi)
Pipeline connections • DISS - Male; DISS-Female; AS 4059
(filtered) (Australian).
• S90-116 (French Air Liquide)
• BSPP 3/8 (Scandinavian) or NIST (ISO
5359).
• All fittings available for O2, Air, and N2O.
Pressure displays Color coded gauges
Pipeline inlet pressure 280-600 kPa (41-87 psi)
O2 supply failure alarm 193 to 221 kPa (28 to 32 psi)
N2O shutoff 3.5 kPa (0.5 psi)
ACGO Port relief Valve limits fresh gas pressure to 138 kPa (20 psi) at the flush flow.
M1132382 10-5
Aespire View
Electrical block diagram
Figure 10-2 • Electrical block diagram AC.20.008
10-6 M1132382
1. Anesthesia system 23. Breathing system

2. Power cord 24. Bag/Ventilator switch
3. AC inlet with breaker and line filter 25. ABS on switch
4. Isolation transformer 26. Canister switch
5. Inrush board 27. CO2 bypass switch
6. Fuses 28. Bulkhead connector
7. Line filter 29. Expiratory flow sensor
8. Outlet box 30. Inspiratory flow sensor
9. Universal power supply 31. O2 sensor
10. Battery, 12 V 32. Enhanced sensor interface board
11. DAQ board 33. ACGO select
12. On/Standby switch 34. O2 flush switch
13. O2 supply switch 35. AC power in/communication to system
14. Task light switch 36. LCD backlight 1
15. Task light 37. LCD backlight 2
16. Total flow sensor board (optional) 38. Left membrane switch
17. CPU board 39. Bottom membrane switch
18. LCD 40. Right membrane switch
19. ComWheel 41. USB I/O port
20. Ventilator engine board 42. Network I/O port (Ethernet)
21. Gas inlet valve 43. Patient monitoring port (Ohmeda Com)
22. Flow control valve 44. Serial I/O port
Electrical power
Supply voltage 100-120 or 220-240 Vac ±10% at 50 or 60 Hz

Average power less than 50 VA
consumption
Note: Measured through the power cord when operated at the ventilation setting
VCV, TV = 1500 l/min, RR = 26, I:E = 1:2, and PEEP is Off; three gas TFS
option installed, LCD backlights at level 5, task light on maximum, and following
15 minutes of system running on battery power.
Inlet circuit 100-120 Vac 220-240 Vac
breakers 15 A 8A
Outlet circuit 110-120 Vac Japan 220-240 Vac
breakers (3) 2 A (2) 2A (3) 1 A
(1) 3 A (1) 4A (1) 2 A
System leakage UL and CSA rated systems (U.S.A. and Canada): less than
current limit - do 300 μamps for the system and all systems connected to
not exceed: electrical outlets.
IEC rated systems (Not U.S.A. and Canada): less than 500
μamps for the system and all systems connected to
electrical outlets.
Resistance to less than 0.2 Ω
ground
WARNING The connection of equipment to the auxiliary mains

electrical outlets may increase the patient leakage
currents to values exceeding the allowable limits in the
event of a defective earth conductor.
M1132382 10-7
Aespire View
Power cord
Length 5 meters (Danish: 3m)
Voltage rating 100 to 240 Vac
Current capacity • 10 A for 220-240 Vac
• 15 A for 100-120 Vac
Type Three conductor power supply cord (medical grade where
required).
WARNING Unplug the system power cord to run the system on the
battery power if the integrity of the protective earth
conductor is in doubt.
Battery information The system is not a portable unit; a sealed lead acid battery supplies
backup power in the event of a power failure:
• Capacity to operate for 90 minutes under typical operating
conditions.
• The system functions to specifications through the transition to
battery power.
CAUTION Contact a Datex-Ohmeda trained service representative to replace or

disconnect the battery if the equipment is not likely to be used for an
extended time.
Important Batteries must be disposed of in accordance with applicable
regulatory requirements in effect at the time and place of disposal.
10-8 M1132382
Flow specifications
Pneumatic flow
Parameter Range
Flush flow 35 to 75 l/min
Flow range Minimum O2 flow 50 ml/min
O2 • 0.05 to 0.95 l/min
• 1 to 15 l/min
N2O • 0.05 to 0.95 l/min
• 1 to 10 l/min
Note: The Link-25 system sets the nominal O2 flow to 25%

of the total of O2 and N2O flow.
Air • 0.05 to 0.95 l/min
• 1 to 15 l/min
Accuracy • At 20°C with gas supply pressures at 345 kPa (50 psi)
and an outlet pressure of 101.3 kPa (absolute) (14.7
psi) flowmeter accuracy agrees with VDE 3513 Part 3,
Accuracy Class 2.5 or better.
• Different breathing circuit pressures, barometric
pressures or temperatures change the accuracy. With
some conditions, these changes can be larger than
the tolerances.
Total flow sensing
Flow Range
O2 0, 0.05 to 15.0 l/min
Air 0, 0.05 to 15.0 l/min
N2O 0, 0.05 to 10.0 l/min
Total 0 to 40.0 l/min
Accuracy • Greater of ± 25 ml/min or ± 6% of measured value at 20-25°C
with gas supply pressures at 480.5 kPa (69.7 psi) and an
outlet pressure of 101.3 kPa (absolute) (14.7 psi).
• Different breathing circuit pressures, barometric pressures or
temperatures change the accuracy. With some conditions,
these changes can be larger than the tolerances.
M1132382 10-9
Aespire View
Breathing system specifications
Volume Ventilator side 2730 ml; bag side 1215 ml

With EZchange canister system and condenser:
• Ventilator side 3445 ml
• Bag side 1930 ml
Absorbent 950 ml canister
Connections Auxiliary Common Gas Outlet: ISO 5356 type connector
on the front of the system (standard 22 mm OD or
15 mm ID conical friction fit connectors).
System leakage Less than or equal to 150 ml/min total at 3 kPa (30
cmH2O) with EZchange canister system and condenser
(both in absorber mode and with canister removed).
System compliance Volume of gas lost due to internal compliance
(bag mode only):
• 1.82 ml/0.098 kPa (1 cmH2O)
• 55 ml/3 kPa (30 cmH2O)
With EZchange canister system and condenser:
• 2.67 ml/0.98 kPa (1 cmH2O)
• 80 ml/3 kPa (30 cmH2O)
Pressure required to • Dry: 0.49 cmH2O
open Inspiratory or • Wet: 0.91 cmH2O
expiratory valves
Pressure generated by a 0.81 cmH2O
wet unidirectional valve
APL valve Approximately 0 to 70 cmH2O
Breathing system resistance in bag mode*

l/min kPa cmH2O
5 0.06 0.6
30 0.22 2.2
60 0.52 5.3
EZchange canister system and condenser, absorber mode
5 0.06 0.6
30 0.24 2.4
60 0.57 5.8
EZchange canister system and condenser, canister removed
5 0.06 0.6
30 0.24 2.4
60 0.49 5.0
*Values include patient circuit tubing and Y-piece 0.15 kPa (0.20 psi) expiratory
resistance at 1 l/s. Patient circuit tubing and breathing system configurations
may affect resistance.
10-10 M1132382
Pressure flow data (APL valve completely open)

Flow (l/min) Flow (l/s) APL pressure cmH2O
3 0.05 0.78
10 0.17 1.14
30 0.51 1.43
60 1.0 2.61
70 1.17 3.21
Gas scavenging
All scavenging
Positive pressure relief 10 cmH2O
Passive scavenging
Negative pressure relief 0.3 cmH2O
Outlet connector 30 mm male taper ISO
Active scavenging
Hospital waste gas disposal
Disposal system type Outlet connector*
system requirements
Adjustable flow, high DISS EVAC 305 mmHg (12 inHg) minimum at
vacuum 36 l/min flow
High flow, low vacuum BSI 30 mm threaded 50 to 80 l/min flow
(BS6834)
Low flow, high vacuum DISS EVAC 305 mmHg (12 inHg) minimum at
36 l/min flow
Low flow, low vacuum 12.7 mm barb 36 l/min flow
Low flow, low vacuum 25 mm barb 40 to 50 l/min flow
Low flow, low vacuum 30 mm ISO taper 40 to 50 l/min flow
male
*Other market-specific connectors may be available.
Particle filter at the outlet has a pore size of 225 microns. All flow data uses a new
filter.
M1132382 10-11
Aespire View
Physical specifications
All specifications are approximate values and can change without
notice.
CAUTION Do not subject the system to excessive shock and

vibration.
w Do not place excessive weight on flat surfaces or

drawers.
System Height 136 cm (53.5 in)

Width 75 cm (29.5 in)
Depth 74 cm (29.1 in)
Weight 136 kg (300 lb)
Top of machine 34 kg (75 lb)
weight limit
Casters 12.5 cm (4.9 in) with brakes on the
front casters
Drawers 17.5 cm x 33 cm x 26.5 cm
(6.9 in x 13 in x 10.4 in)
Ventilator display 30.7 cm (12.1 in) color SVGA LCD
Environmental requirements
Operation Storage
Temperature 10 to 40°C -25 to 60°C
O2 cell operates to O2 cell storage is -15 to 50°C
specifications at 10 to 40°C
Humidity 15 to 95% RH, non-condensing 10 to 95%, non-condensing
Altitude 500 to 800 mmHg 375 to 800 mmHg
(3565 to -440 meters) (5860 to -440 meters)
10-12 M1132382
Suction regulators (optional)
Venturi Suction Regulator

Performance Category Pharyngeal Suction
Supply Air or O2 from system gas supply
Drive Gas Consumption* 28 l/min with pipeline drive gas at 280 kPa (41 psi)
52 l/min with pipeline drive gas at 600 kPa (87 psi)
Maximum Vacuum** 600 mmHg with pipeline drive gas at 280 kPa (41 psi)
550 mmHg with pipeline drive gas at 600 kPa (87 psi)
Maximum Flow* 29 l/min with pipeline drive gas at 280 kPa (41 psi)
32 l/min with pipeline drive gas at 600 kPa (87 psi)
Vacuum Gauge Accuracy ±5% of full scale
*Values are approximate.
**Approximate values are at sea level. Performance is reduced at higher elevations.
Continuous Suction Regulator

Performance Category Pharyngeal Suction
Supply External vacuum
Maximum Vacuum* 540 mmHg with external vacuum applied of
540 mmHg and 40 l/min free flow
Maximum Flow* 39 l/min with external vacuum applied of 540 mmHg
and 40 l/min free flow
Vacuum Gauge Accuracy ±5% of full scale
*Values are approximate.
Auxiliary O2 flowmeter (optional)
Supply O2 from system gas supply

Flow rate 0 to 10 l/min
Accuracy ±5% of full scale; not pressure compensated
M1132382 10-13
Aespire View
Ventilator theory
The ventilator pneumatics are located in the rear of the breathing
system. A precision flow valve controls gas flow to the patient. During
inspiration, this gas flow closes the exhalation valve and pushes the
bellows down. During expiration, a small flow pressurizes the
exhalation diaphragm to supply PEEP pressure.
Volume measurements come from flow sensors in the flow sensor
module. Two tubes from each sensor connect to a transducer. The
transducer measures the pressure change across each sensor,
which changes with the flow. A third pressure transducer measures
airway pressures at the inspiratory flow sensor.
The ventilator uses data from the flow sensors for volume-related
numerics and alarms. The ventilator also uses the flow sensors to
adjust its output for changes in fresh gas flow and small leaks in the
breathing system.
In volume ventilation modes, certain alarm conditions prevent the
automatic adjustment of ventilator delivery based on measured flow
values. In these cases, the ventilator may not be able to deliver within
the accuracy range specified. If compensation stops for a number of
breaths, the condition causing the hold shows as an alarm. Automatic
volume compensation resumes when alarm conditions are resolved.
For better precision a small quantity of gas bleeds through a resistor
to help keep the pressure on the exhalation valve constant. At high
airway pressures, this can cause a slight hiss during inspiration.
WARNING Do not try to silence the pneumatic resistor. If it is

blocked, the ventilator can malfunction and cause patient
injury.
10-14 M1132382
O2 monitoring theory O2 monitoring measures O2 concentration in the patient circuit. The

of operation O2 concentration measured from the O2 cell is shown on the
ventilator display.
The O2 sensor is an electrochemical device (galvanic cell). Oxygen
diffuses through a membrane into the cell and oxidizes a base metal
electrode. This oxidation produces an electrical current proportional
to the partial pressure of the oxygen at the electrode’s sensing
surface. The base metal electrode gradually wears out from the
oxidation process.
The voltage from the cell cartridge is affected by the temperature of
the monitored gas mixture. A thermistor in the cell’s housing
automatically compensates for temperature changes in the cell.
O2 monitoring uses signal processing and analyzing circuitry to
convert the cell signal into a corresponding % oxygen value. The
system displays this value and compares it to saved alarm limits. If
the value falls outside the limits, the monitor produces the appropriate
alarms.
Modes The system has the following modes of mechanical ventilation:

• Volume Control Ventilation (VCV).
• Pressure Control Ventilation (PCV) (optional).
Support Ventilation (SIMV/PSV) (optional).
• Pressure Support Ventilation (PSVPro) (optional).
Control (SIMV-PC) (optional).
• Pressure Control Ventilation-Volume Guaranteed (PCV-VG)
(optional).
M1132382 10-15
Aespire View
VCV
1
2
AB.91.038
3
4
1. Paw
2. Pmax
3. PEEP
4. Time
Figure 10-3 • Volume control diagram
Volume control supplies a set tidal volume. The ventilator calculates a

flow based on the set tidal volume and the length of the inspiratory
time from the I:E and respiratory rate settings. An optional inspiratory
pause can be set to improve gas distribution in the lungs.
A typical volume-controlled pressure waveform increases throughout
the entire inspiratory period and rapidly decreases at the start of
expiration.
The ventilator adjusts gas flow to the bellows based on measured
inspiratory volumes. This is called tidal volume compensation.
Volume control settings include:
• TV - sets the amount of tidal volume.
• RR - sets the rate of mechanically driven breaths.
• I:E - sets the amount of inspiration to expiration ratio.
• Pmax - sets the maximum airway pressure.
• Tpause - sets the inspiratory pause time.
10-16 M1132382
PCV
1
2
AB.91.039
4
5
1. Paw
2. Pmax
3. Pinsp
4. PEEP
5. Time
Figure 10-4 • Pressure control diagram
Pressure control supplies a constant set pressure during inspiration.

The ventilator calculates the inspiratory time from the respiratory rate
and I:E ratio settings. A high initial flow pressurizes the circuit to the
set inspiratory pressure. The flow then decreases to maintain the set
pressure (Pinsp).
Pressure sensors in the ventilator measure patient airway pressure.
The ventilator automatically adjusts the flow to maintain the set
inspiratory pressure.
Pressure control settings include:
• Pinsp - sets the target airway pressure.
• PEEP - sets the positive end expiratory pressure.
• Rise Rate - sets the amount of time to attain Pinsp.
M1132382 10-17
Aespire View
SIMV/PSV
3
AB.90.040
4
5 2
TI
1. Mandatory SIMV breath

2. Spontaneous pressure supported breath
3. Paw
4. Psupport
5. PEEP
Figure 10-5 • SIMV/PSV diagram
Synchronized Intermittent Mandatory Ventilation with Pressure
Support (SIMV/PSV) is a mode in which periodic volume breaths are
delivered to the patient at preset intervals (time-triggered). Between
the machine delivered breaths, the patient can breathe
spontaneously at the rate, tidal volume, and timing that the patient
desires.
At the specified time interval, the ventilator will wait for the next
inspiratory effort from the patient. The sensitivity of this effort is
adjusted using the flow trigger level. When the ventilator senses the
beginning of inspiration it synchronously delivers a volume breath
using the set tidal volume, and inspiratory time that is set on the
ventilator. If the patient fails to make an inspiratory effort during the
trigger window time interval, the ventilator will deliver a machine
breath to the patient. The ventilator will always deliver the specific
number of breaths per minute that the clinician has set.
In SIMV/PSV, the spontaneous breaths can be pressure supported to
assist the patient in overcoming the resistance of the patient circuit
and the artificial airway. When the Psupport level is set, the ventilator
will deliver the pressure support level to the patient during inspiration.
PEEP can also be used in combination with this mode.
SIMV/PSV settings include:
• TV - sets the amount of tidal volume.
• Tinsp - sets the inspiration time for a mechanical breath.
• Psupport - sets the pressure support level.
• Tpause - sets the inspiratory pause time.
• End of Breath - the drop in inspiratory flow from the peak
inspiratory flow level where the ventilator stops pressure support
mechanical inspiration and begins exhalation.
• Trigger - sets the flow trigger level.
• Trig Window - sets the range in percent of the exhalation phase
where a patient may trigger a mechanical breath.
10-18 M1132382
PSVPro
1
AB.91.041
2
TI
3
1. Paw
2. PEEP
3. Time
Figure 10-6 • PSVPro diagram
PSVPro is pressure supported ventilation with apnea backup.

PSVPro is a spontaneous mode of ventilation that provides a
constant pressure once the ventilator senses that the patient has
made an inspiratory effort. In this mode, the clinician sets the
Pressure Support (Psupport) and PEEP levels. The patient
establishes the rate, inspiratory flow, and inspiratory time. The tidal
volume is determined by the pressure, lung characteristics, and
patient effort.
PSVPro uses an inspiration termination level that establishes when
the ventilator will stop the pressure supported breath and cycle to the
expiratory phase. The inspiration termination level is user adjustable
from 5% to 50%. This parameter sets the percent of the peak
inspiratory flow that the ventilator uses to end the inspiratory phase of
the breath and to cycle into the expiratory phase. If the inspiration
termination is set to 30% then the ventilator will stop inspiration when
the flow decelerates to a level equal to 30% of the measured peak
inspiratory flow. The lower the setting the longer the inspiratory time
and conversely, the higher the setting the shorter the inspiratory
phase.
An apnea backup mode is provided in the event the patient stops
breathing. When setting this mode the clinician adjusts the inspiratory
pressure (Pinsp), respiratory rate, and the inspiratory time (Tinsp). As
long as the patient is triggering the ventilator and the apnea alarm
does not activate, the patient will get pressure-supported breaths and
the ventilator will not deliver machine breaths.
If the patient stops triggering the ventilator for the set apnea delay
time, the apnea alarm will activate and the ventilator will automatically
switch to the backup mode that is SIMV-PC mode. See “SIMV-PC” for
operation details for this mode.
M1132382 10-19
Aespire View
When the ventilator switches to the backup mode, the alarm text
“Backup Mode active’ displays and remains in the low priority
message site until PSVPro is reinstated or until another mode is
selected. To reactivate the PSVPro mode the user must go into the
Ventilation Mode menu and select PSVPro. Upon selecting PSVPro
the ventilator will immediately begin providing pressure supported
breaths to the patient using the established settings.
PSVPro settings include:
• Backup mode active - sets the time for backup mode to activate.
10-20 M1132382
SIMV-PC
3
1
4
AB.91.042
5 2
TI
6
1. Mandatory pressure control breath

2. Spontaneous pressure supported breath
3. Paw
4. Psupport
5. PEEP
6. Time
Figure 10-7 • SIMV-PC diagram
Synchronized Intermittent Mandatory Ventilation with Pressure

Controlled Ventilation is a mode in which a relatively slow mandatory
breathing rate is set with pressure-controlled breathing. This mode
combines mandatory breaths with spontaneous breath support. If a
trigger event occurs within the synchronization window, a new
pressure-controlled breath is initiated. If a trigger event occurs
elsewhere during the expiratory phase, a support for a spontaneous
breath is provided with pressure support added as set by the clinician.
SIMV-PC settings include:
M1132382 10-21
Aespire View
PCV-VG
2 3
1
5
7
6
AB.98.034
1. Paw waveform
2. Tinsp
3. Texp
4. Variable pressure to deliver desired TV
5. PEEP
6. Flow waveform
7. TV
Figure 10-8 • PCV-VG waveforms
In PCV-VG, a tidal volume is set and the ventilator delivers that

volume using a decelerating flow and a constant pressure. The
ventilator will adjust the inspiratory pressure needed to deliver the set
tidal volume breath-by-breath so that the lowest pressure is used.
The pressure range that the ventilator will use is between the PEEP +
2 cmH2O level on the low end and 5 cmH2O below Pmax on the high
end. The inspiratory pressure change between breaths is a maximum
of ±3 cmH2O.
This mode will deliver breaths with the efficiency of pressure
controlled ventilation, yet still compensate for changes in the patient’s
lung characteristics. PCV-VG begins by first delivering a volume
breath at the set tidal volume. The patient’s compliance is determined
from this volume breath and the inspiratory pressure level is then
established for the next PCV-VG breath.
PCV-VG settings include:
10-22 M1132382
Ventilator operating specifications
Pneumatics
Gas source Anesthesia system
Gas composition Medical air or O2
Nominal supply pressure 350 kPa (51 psi)
Pressure range at inlet 240 to 700 kPa (35 to 102 psi)
Flow valve range 1 to 120 l/min at 240 kPa (35 psi)
Fresh gas
compensation
Flow compensation range 200 ml/min to 15 l/min
Gas composition O2, N2O, Air, anesthetic agents
Pressure
Patient airway pressure range -20 to +120 cmH2O
Patient airway display range -20 to +120 cmH2O
Pinsp setting range 5 to 60 cmH2O
PEEP setting range Off, 4 to 30 cmH2O
High pressure alarm set range 12 to 100 cmH2O, 1 cm increment
Sustained pressure alarm range (when • 6 to 42 cmH2O, 1 cm increment
‘PEEP high. Blockage?’ alarm occurs) (mechanical ventilation)
• 6 to 30 cmH2O, 1 cm increment
(manual ventilation)
Volume
Tidal volume display range 5 to 9999 ml, 1 ml resolution
Setting range 20 to 1500 ml
Minute volume display range 0.0 to 99.9 liters
Breath rate settings • For VCV, PCV, PCV-VG:
4 to 100 bpm, 1 bpm resolution
• For SIMV-PC, SIMV/PSV:
2 to 60 bpm, 1 bpm resolution
Flow sensor type Variable flow orifice
Oxygen
Display range 5 to 110% O2
Display resolution 1% increments
Sensor type Galvanic fuel cell
Measurement range 0 to 100% O2
Measurement accuracy ± 3% of full scale
Cell response time 35 seconds, 10 to 90%. Response time
of cell and adapters is measured using
the test method described in ISO 7767
(1997)
Low O2 alarm range 18% to 99%
High O2 alarm setting 21% to 99%, Off
Low O2 limit may not be set above
High O2 limit. High O2 limit may not be
set below the Low O2 limit.
M1132382 10-23
Aespire View
Expected cell life Four months of shelf life (23°C room

air) and one year of normal operation.
Ventilator accuracy data

The following accuracy data are based on patient conditions and
settings described in ASTM F1101. The ventilator is assumed to be
operating in volume mode. For the following to be true, the ventilator
is operating with 100 percent oxygen in the breathing system. Errors
may occur as described in the gas composition chart.
The minimum detectable breath size is 5.0 ml.
Delivery accuracy
Volume control mode Greater than 210 ml tidal volume -
accuracy of ±7% of set TV
60 to 210 ml tidal volume - accuracy of
±15 ml
Less than 60 ml tidal volume -
accuracy of ±10 ml
Pressure mode Inspiratory pressure - accuracy of ±3.0
cmH2O or 10% of delivered pressure
PEEP - accuracy of ±1.5 cmH2O
Monitoring accuracy
Volume control Greater than 210 ml tidal volume -
accuracy of ±9% of TV
60 to 210 ml tidal volume - accuracy of
±18 ml
Less than 60 ml tidal volume -
accuracy of ±10 ml
Pressure mode Accuracy of ±2.0 cmH2O or ±5% of
reading whichever is greater.
Note: Gas composition errors may be in addition to the above normalized
accuracy. When adding errors, positive errors can have the effect of nulling out
negative errors.
Note: Use of anesthetic agent could affect the errors by approximately -0.95% /
% volume agent.
Oxygen monitor accuracy
• When subjected to gas mixtures containing the following concentrations of
gases, the oxygen monitor has been tested to be within ±5% of the actual
gas concentration.
• Gas mixtures other than the ones listed below may result in an accuracy of
the oxygen monitor outside of the ±5% V/V.
Gas: At concentration:
Helium 50%
Carbon dioxide 5%
Nitrous oxide 80%
Halothane 4%
Enflurane 5%
Isoflurane 5%
Sevoflurane 5%
Desflurane 15%
10-24 M1132382
AB.74.027
Figure 10-9 • Gas composition related errors
M1132382 10-25
Aespire View
Electromagnetic compatibility (EMC)
WARNING Changes or modifications to this equipment not expressly

approved by the manufacturer could cause EMC issues
with this or other equipment. Contact the manufacturer for
assistance. This device is designed and tested to comply
with applicable regulations regarding EMC as follows.
w Use of portable phones or other radio frequency (RF)

emitting equipment (that exceed electromagnetic
interference levels specified in IEC 60601-1-2) near the
system may cause unexpected or adverse operation.
Monitor operation when RF emitters are in the vicinity.
w Use of other electrical equipment on or near this system

may cause interference. Verify normal operation of
equipment in the system before use on patients.
Guidance and The system is suitable for use in the specified electromagnetic
manufacturer’s environment. The customer and/or the user of the system should
assure that is used in an electromagnetic environment as described
declaration - below.
electromagnetic
emissions
Emissions test Compliance Electromagnetic environment guidance
RF emissions Group 1 The system uses RF energy only for its internal function. Therefore, its RF emissions are
CISPR 11 very low and are not likely to cause any interference in nearby electronic equipment.
RF emissions Class B The system is suitable for use in all establishments, including domestic establishments
CISPR 11 and those directly connected to the public low-voltage power supply network that supplies
Harmonic Class A buildings used for domestic purposes.
emissions
IEC 61000-3-2
Voltage Complies
fluctuations/flicker
emissions
IEC 61000-3-3
10-26 M1132382
Guidance and The system is suitable for use in the specified electromagnetic
manufacturer’s environment. The customer and/or the user of the system should
assure that it is used in an electromagnetic environment as described
declaration - below.
electromagnetic
immunity
Power immunity
Immunity test IEC 60601-1-2 test Level Compliance level Electromagnetic environment guidance
Electrostatic ± 6 kV contact ± 6 kV contact Floors should be wood, concrete, or
discharge (ESD) IEC ± 8 kV air ± 8 kV air ceramic tile. If floors are covered with
61000-4-2 synthetic material, the relative humidity
should be at least 30%.
Electrical fast ± 2 kV for power supply ± 2 kV for power supply Mains power quality should be that of a
transient/burst IEC lines lines typical commercial and/or hospital
61000-4-4 ± 1 kV for input/output ± 1 kV for input/output environment.
lines lines
Surge IEC 61000-4-5 ± 1 kV differential mode ± 1 kV differential mode Mains power quality should be that of a
± 2 kV common mode ± 2 kV common mode typical commercial and/or hospital
environment.
Voltage dips, short <5% UT (>95% dip in <5% UT (>95% dip in Mains power quality should be that of a
interruptions and UT) for 0.5 cycle UT) for 0.5 cycle) typical commercial and/or hospital
voltage variations on 40% UT (60% dip in UT) 40% UT (60% dip in UT) environment. If the user of the system
power supply input for 5 cycles for 5 cycles requires continued operation during
lines IEC 61000-4-11 70% UT (30% dip in UT) 70% UT (30% dip in UT) power mains interruptions, it is
for 25 cycles for 25 cycles recommended that the system be
<5% UT(>95% dip in UT) <5% UT(>95% dip in powered from an uninterruptible power
for 5 sec. U ) for 5 sec. supply or a battery.
T
Power frequency (50/ 3 A/m 3 A/m If display distortion or other abnormalities
60 Hz) magnetic field occur, it may be necessary to position
IEC 61000-4-8 3 the Anesthetic System further from
sources of power frequency magnetic
fields or to install magnetic shielding. The
power frequency magnetic field should
be immersed in the intended installation
location to assure that it is sufficiently
low.
Note: UT is the AC mains voltage before application of the test level.
M1132382 10-27
Aespire View
Radiated immunity
Electromagnetic
environment guidance
Immunity test IEC 60601-1-2 test Level Compliance level
Recommended separation
distance
Portable and mobile RF
communications equipment
should be used no closer to
any part of the system,
including cables, than the
recommended separation
distance calculated from the
equation appropriate for the
frequency of the transmitter.
Conducted RF 3 Vrms 3 Vrms (V1) D=3.5√P
IEC 61000-4-6 150 kHz to 80 MHz outside
ISM bands
10 Vrms 10 Vrms (V2) D=12√P
150 kHz to 80 MHz in ISM
bands
Radiated RF 10 V/m 10 V/m (E1) D=1.2√P 80 mHz to 800 mHz
IEC 61000-4-6
80 MHz to 2.5 GHz D=3.5√P 800 mHz to 2.5 GHz
Where P is the maximum
output power rating of the
transmitter in watts (W)
according to the transmitter
manufacturer and D is the
recommended separation
distance in meters (m).
Field strengths from fixed RF
transmitters, as determined by
an electromagnetic site survey,
should be less than the
compliance level in each
frequency range.
• The ISM (industrial, scientific and medical) bands between 150 kHz and 80 MHz are 6.765 MHz to 6.795 MHz; 13.553 MHz
to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz.
• The compliance levels in the ISM frequency bands between 150 kHz and 80 MHz and in the frequency range 80 MHz to 2.5
GHz are intended to decrease the likelihood that a portable communications device could cause interference if it is
inadvertently brought into patient areas. For this reason, an additional factor of 10/3 is used in calculating the recommended
separation distance for transmitters in these frequency ranges.
• Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios,
amateur radio, AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To assess
the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the
measured field strength in the location in which the system is used exceeds the applicable RF compliance level above, the
system should be observed to verify normal operation. If abnormal performance is observed, additional measures may be
necessary, such as re-orienting or relocating the system.
• Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 1 V/m.
Note: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects, and people.
10-28 M1132382
Recommended The system is intended for use in the electromagnetic environment in

separation distances which radiated RF disturbances are controlled. The customer or the
user of the system can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF
communications equipment (transmitters) and the system as
recommended below, according tho the maximum power of the
communications equipment.
Separation distance in meters (m) according to frequency of the transmitter

Rated maximum 150 kHz to 80 MHz 150 kHz to 80 MHz In 80 MHz to 800 MHz 800 MHz to 2.5 GHz
output power of Outside ISM bands ISM bands
transmitter watts (W)
0.01 0.35 1.2 0.12 0.23

0.1 1.1 3.8 0.38 0.73
1 3.5 12 1.2 2.3
10 11 38 3.8 7.3
100 35 120 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation distance D in meters (m) can be
determined using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.
Note 1: At 80 MHz to 800 MHz the separation distance for the higher frequency range applies.
Note 2: The ISM (Industrial, Scientific and Medical) bands between 150 kHz and 80 MHz are 6.765 MHz to 6.795 MHz; 13.553 MHz
to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz.
Note 3: An additional factor of 10/3 is used in calculating the recommended separation distance for transmitters in the ISM
frequency bands between 150 kHz and 80 MHz and in the frequency range 80 MHz to 2.5 GHz to decrease the likelihood that
mobile/portable communications equipment could cause interference if it is inadvertently brought into patient areas.
Note 4: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from
structures, objects, and people.
M1132382 10-29
Aespire View
Electrical safety
WARNING The system provides connections for items such as

printers, visual displays and hospital information networks
(only connect items that are intended to be part of the
system). When these items (non-medical equipment) are
combined with the system, these precautions must be
followed:
• Do not place items not approved to IEC 60601-1
closer than 1.5 m to the patient.
• All items (medical electrical equipment or non-medical
electrical equipment) connected to the system by a
signal input/signal output cable must be supplied from
an AC power source which uses a separating
transformer (in accordance with IEC 60989) or be
provided with an additional protective earth conductor.
• If a portable multiple socket outlet assembly is used as
an AC power source, it must comply with IEC 60601-1.
The assembly must not be placed on the floor. Using
more than one portable multiple socket outlet
assembly is not recommended. Using an extension
cord is not recommended. After connecting anything
to these outlets, conduct a complete system leakage
current test (according to IEC 60601-1).
• Do not connect non-medical electrical equipment
directly to the AC outlet at the wall instead of an AC
power source which uses a separating transformer.
Doing so may increase enclosure leakage current
above levels allowed by IEC 60601-1 in normal
conditions and under single-fault conditions. This may
cause an unsafe electrical shock to the patient or
operator.
w An operator of the medical electrical system must not

touch non-medical electrical equipment and the patient
simultaneously. This may cause an unsafe electrical
shock to the patient.
10-30 M1132382
IEC 60601-1 Classification

This system is classified as follows:
• Class I Equipment.
• Type B Equipment.
• Ordinary Equipment.
• Not for use with flammable anesthetics.
• Continuous operation.
Standards
Devices used with this anesthesia system shall comply with the
following standards where applicable:
• Breathing systems and breathing system components
ISO 8835-2.
• Anesthetic vapor delivery devices ISO 8835-4.
• Anesthetic agent monitors ISO 11196.
• Oxygen monitors ISO 7767.
• Carbon dioxide monitors ISO 9918.
• Exhaled volume monitors IEC 60601-2-13.
M1132382 10-31
Aespire View
System components
Integral This anesthesia system contains the following integral components,

monitoring devices, alarm systems, and protection devices that
comply with European, international, and national standards:
• Breathing system pressure-measuring device.
• Airway pressure-limitation device.
• Exhaled-volume monitor.
• Breathing system integrity alarm.
• Breathing system continuing-pressure alarm.
• O2 monitor.
• Anesthesia ventilator.
• Breathing system.
Not integral These devices are not integral to this anesthesia system:
• CO2 monitor.
• Anesthetic agent monitor.
WARNING European, international, and national standards require

the following monitoring be used with this system:
• Exhaled volume monitoring.
• O2 monitoring.
• CO2 monitoring.
• Anesthetic agent monitoring be used when anesthetic
vaporizers are in use.
When adding devices to the anesthesia systems, follow the
installation instructions provided by the device manufacturer.
Whoever adds individual devices to the anesthesia system shall
provide instructions on how to enable the individual devices (for
example, a preoperative checklist).
10-32 M1132382
Index
A Controls
anesthesia system 2-2
Absorber canister vaporizer 2-8
filling 8-7 ventilator 2-12
parts 9-5 Cylinder
removing 8-6 installation 8-13
setup 8-4
ACGO 2-10
E
positive low-pressure leak test 5-10
scavenging the ACGO sample flow 2-11 Electrical safety 10-30
Advanced breathing system 2-5 Electromagnetic compatibility 10-26
optional components 2-7 EZchange canister
AGSS removal 8-7
active 3-13 system parts 9-7
connecting active adjustable 3-15
connecting active with a flow indicator 3-14 F
passive 3-12
Alarms 6-2 Flow controls 2-3
display 6-2
latching 6-3 G
list of 6-4 Gas scavenging
minimum system monitoring 6-9 specifications 10-11
minimum system shutdown 6-9
power failure test 5-3 I
tests 5-11
Auxiliary O2 flow control 2-3 Integrated suction 2-3
B L
Battery information 10-8 Low-pressure leak test 5-9
Bellows assembly
parts 9-4 M
test 5-13
Mains inlet 8-10
Breathing system
Maintenance schedule 7-2
maintenance 7-3
Menus
troubleshooting 6-12
using 2-14
C N
Calibration
Negative low-pressure leak test 5-9
flow sensor (zeroing) 7-6
Condenser
operation 3-11
Connections
electrical 8-9
pneumatic 8-10
M1132382 I-1
Aespire View
O S
O2 cell Scavenging 8-11
calibration 7-5 a gas monitor sample flow 2-11
replacement 7-4 ACGO sample flow 2-11
O2 flush button 2-3 from an auxiliary manual breathing circuit
2-11
P specifications 10-11
Serial port 8-10
Parts Specifications
absorber canister 9-5 breathing system 10-10
AGSS 9-6 flow 10-9
breathing circuit module 9-3 gas scavenging 10-11
condenser 9-8 physical 10-12
exhalation valve assembly 9-2 pneumatic 10-5
EZchange canister system 9-7 ventilator operating 10-23
flow sensor module 9-2 Suction regulator 8-12
test tools and system parts 9-9 Sustained limit 6-8
Pneumatic Sustained pressure threshold 6-8
connections 8-10 System
specifications 10-5 switch 2-3
system pneumatic circuits 10-2 turn on 3-2
Positive low-pressure leak test 5-10
Preoperative Checkout 4-1
T
Preoperative Tests 5-1
Preoperative tests Troubleshooting
alarm 5-11 breathing system 6-12
APL valve 5-14 electrical 6-13
bellows assembly 5-13 pneumatic 6-14
breathing circuit 5-14 Turning on the system 3-2
breathing system 5-13
cylinder 5-4 U
flow control 5-5
monitor and ventilator 5-15 Using menus 2-14
negative low-pressure leak 5-9
pipeline 5-3 V
positive low-pressure leak 5-10 Vaporizer
power failure alarm 5-3 controls 2-8
total flow sensing (optional) 5-3 Ventilation modes
vaporizer back pressure test 5-8 PCV 10-17
Problems PCV-VG 10-22
breathing system 6-12 PSVPro 10-19
electrical 6-13 SIMV/PSV 10-18
pneumatic 6-14 SIMV-PC 10-21
VCV 10-16
R
Repair policy 7-2
I-2 M1132382
Ventilator
accuracy data 10-24
modes 10-15
operating specifications 10-23
setup 3-3
theory 10-14
Ventilator screen 2-13
W
Water buildup
prevent 7-7
Z
Zeroing flow sensor 7-6
M1132382 I-3
Aespire View
I-4 M1132382
Warranty
This Product is sold by Datex-Ohmeda under the warranties set forth
in the following paragraphs. Such warranties are extended only with
respect to the purchase of this Product directly from Datex-Ohmeda
or Datex-Ohmeda’s Authorized Dealers as new merchandise and are
extended to the Buyer thereof, other than for the purpose of resale.
For a period of twelve (12) months from the date of original delivery to
Buyer or to Buyer’s order, but in no event for a period of more than
two years from the date of original delivery by Datex-Ohmeda to a
Datex-Ohmeda Authorized Dealer, this Product, other than its
expendable parts, is warranted against functional defects in materials
and workmanship and to conform to the description of the Product
contained in this User’s Reference manual and accompanying labels
and/or inserts, provided that the same is properly operated under the
conditions of normal use, that regular periodic maintenance and
service is performed and that replacements and repairs are made in
accordance with the instructions provided. This same warranty is
made for a period of thirty (30) days with respect to expendable parts.
The foregoing warranties shall not apply if the Product has been
repaired other than by Datex-Ohmeda or in accordance with written
instructions provided by Datex-Ohmeda, or altered by anyone other
than Datex-Ohmeda, or if the Product has been subject to abuse,
misuse, negligence, or accident.
Datex-Ohmeda’s sole and exclusive obligation and Buyer’s sole and
exclusive remedy under the above warranties is limited to repairing or
replacing, free of charge, at Datex-Ohmeda’s option, a Product,
which is telephonically reported to the nearest Datex-Ohmeda
Customer Service Center and which, if so advised by Datex-Ohmeda,
is thereafter returned with a statement of the observed deficiency, not
later than seven (7) days after the expiration date of the applicable
warranty, to the Datex-Ohmeda Customer Service and Distribution
Center during normal business hours, transportation charges prepaid,
and which, upon Datex-Ohmeda’s examination, is found not to
conform with above warranties. Datex-Ohmeda shall not be
otherwise liable for any damages including but not limited to
incidental damages, consequential damages, or special damages.
There are no express or implied warranties which extend beyond the
warranties hereinabove set forth. Datex-Ohmeda makes no warranty
of merchantability or fitness for a particular purpose with respect to
the product or parts thereof.
Aespire View
User’s Reference Manual
English
M1132382
02 09 002 18 05 02
Printed in USA
©Datex-Ohmeda, Inc.
All rights reserved

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What is the intended use of the product?

What is the intended use of the product?

What are the user's responsibilities regarding the product?

What are the user's responsibilities regarding the product?

Aespire View

User’s Reference Manual

CAUTION U.S. Federal law restricts this device to sale by or on the

Aespire, 7900 Ventilator, Advanced Breathing System, Link-25,

Intended use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2

Anesthesia system controls . . . . . . . . . . . . . . . . . . . . . . . . . 2-2

Turning on the system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2

Screen and audio setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7

Every day before your first patient . . . . . . . . . . . . . . . . . . . . 4-2

Inspect the system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2

6 Alarms and Troubleshooting

Repair policy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2

8 Setup and Connections

Canister setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4

Flow sensor module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2

10 Specifications and Theory of Operation

System pneumatic circuits . . . . . . . . . . . . . . . . . . . . . . . . . 10-2

Electromagnetic compatibility (EMC) . . . . . . . . . . . . . . . . 10-26

In this section Intended use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2

Symbols used in the manual or on the equipment

On (power) Off (power)

Type BF equipment Type B equipment

Dangerous voltage Frame or chassis ground

Direct current Alternating current

Caution Attention, refer to product instructions

Refer to product instructions Exhaust

Electrical input Electrical output

Electrical input/output Sample gas inlet to scavenging

Pneumatic inlet Pneumatic outlet

Equipotential Lamp, lighting, illumination

Protective earth ground Earth ground

Variability Variability in steps

Suction bottle outlet Vacuum inlet

+ Plus, positive polarity

Bag position/manual ventilation Mechanical ventilation

Inspiratory flow Expiratory flow

Movement in one direction Movement in two directions

Isolation transformer Low pressure leak test

134°C Autoclavable Not autoclavable

Bellows volumes are approximate

APL settings are approximate Anesthetic Gas Scavenging System

Pinch hazard Read to top of float

EZchange Canister (CO2 bypass) Caution: federal law prohibits dispensing

Open drain (remove liquid) Close drain

Alarm silence touch key Menu touch key

End case touch key Cylinder

Manufacturer Date of manufacture

Indicates that the waste of electrical and GOST R Russian certification

This way up USB port

Ethernet connection This product consists of devices that

Typeface conventions used

ABS Advanced breathing system

ACGO Auxiliary common gas outlet

AGSS Anesthetic gas scavenging system

APL Adjustable pressure-limiting valve