Dräger Oxylog 3000 plus Instructions For Use Manual
Instructions for Use
Oxylog 3000 plus
WARNING
To properly use this medical device,
read and comply with these
Instructions for Use.
Emergency and Transport Ventilator
Software 1.n
Typographical Conventions
1 Consecutive numbers indicate steps of action,
with the numbering restarting with "1" for each
new sequence of actions.
z Bullet points indicate individual actions or differ-
ent options for action.
– Dashes indicate the listing of data, options, or
objects.
(A) Letters in parentheses refer to elements in the
related illustration.
A Letters in illustrations denote elements referred
to in the text.
Any text shown on the screen and any labeling on
the device are printed in bold and italics, for example, PEEP, Air, or Alarm settings.
Trademarks
– Oxylog
– AutoFlow
– DrägerService
are trademarks owned by Dräger.
– Sekusept
is a trademark of ECOLAB.
– BIPAP*
®
®
®
®
The "greater than" symbol > indicates the navigation path in a dialog window, for example, System
setup > Monitoring > Basic settings. In this
example, System setup represents the dialog window title, Monitoring represents a horizontally
aligned tab, and Basic settings a vertically aligned
tab.
Screen images
Schematic renderings of screen images are used,
which may differ in appearance or in configuration
from the actual screen images.
* Trademark used under license
2 Instructions for Use Oxylog 3000 plus SW 1.n
Safety Information Definitions
WARNING
A WARNING statement provides important
information about a potentially hazardous
situation which, if not avoided, could result in
death or serious injury.
CAUTION
A CAUTION statement provides important
information about a potentially hazardous
situation which, if not avoided, may result in minor
or moderate injury to the user or patient or in
damage to the equipment or other property.
NOTE
A NOTE provides additional information intended
to avoid inconvenience during operation.
Definition of target groups
For this medical device, users, service personnel,
and experts are defined as target groups.
These traget groups must have been instructed in
the use of the medical device and must have the
necessary expertise, training, and knowledge to
use, install, reprocess, maintain or repair the medical device.
Dräger emphasizes that the medical device must
be used, installed, reprocessed, maintained or
repaired exclusively by the defined target groups.
Users
Users are intended operators as defined on
page 14 hereof for the use of the medical device in
accordance with its intended use.
Instructions for Use Oxylog 3000 plus SW 1.n 3
Service Personnel
Service Personnel are persons who are responsible for the maintenance of the medical device
towards the operating organization.
Service Personnel are persons who are authorized
to install, reprocess, or maintain the medical
device.
Experts
Experts are persons who are authorized to carry
out repair or complex maintenance work on the
medical device.
Abbreviations and Symbols
Please refer to "Abbreviations" on page 23 and
"Symbols" on page 24 for explanations.
4 Instructions for Use Oxylog 3000 plus SW 1.n
Contents
Contents
For Your Safety and that of Your Patients .7
General Safety Information. . . . . . . . . . . . . . . 8
Product-specific Safety Information . . . . . . . . 11
Application . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Intended use. . . . . . . . . . . . . . . . . . . . . . . . . . 14
Indications / Contraindications . . . . . . . . . . . . 14
Environment of use. . . . . . . . . . . . . . . . . . . . . 15
System Overview . . . . . . . . . . . . . . . . . . . . . 17
Front panel with all options. . . . . . . . . . . . . . . 18
Range of functions . . . . . . . . . . . . . . . . . . . . . 22
Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . 23
Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Operating Concept . . . . . . . . . . . . . . . . . . . . 27
Switch on or off. . . . . . . . . . . . . . . . . . . . . . . . 28
Ventilation controls . . . . . . . . . . . . . . . . . . . . . 29
Display operating controls . . . . . . . . . . . . . . . 30
Additional function keys . . . . . . . . . . . . . . . . . 31
Screen window structure . . . . . . . . . . . . . . . . 32
Assembly. . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Internal rechargeable battery . . . . . . . . . . . . . 37
Connecting the power supply . . . . . . . . . . . . . 38
External power supply . . . . . . . . . . . . . . . . . . 39
Connecting the gas supply . . . . . . . . . . . . . . . 41
Assembling the adult reusable hose system . 43
Connecting the adult disposable hose system 45
Connecting the paediatric disposable hose
system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Connecting the bacterial filter or HME . . . . . . 47
Connecting the CO
2 sensor and the cuvette . 48
Hanging the Oxylog 3000 plus on standard
rail systems. . . . . . . . . . . . . . . . . . . . . . . . . . . 49
Getting Started . . . . . . . . . . . . . . . . . . . . . . . 51
Charging the battery. . . . . . . . . . . . . . . . . . . . 52
Determining the approximate pneumatic
operating time. . . . . . . . . . . . . . . . . . . . . . . . . 53
Checking readiness for operation. . . . . . . . . . 54
2 zero calibration and filter check before
CO
ventilation (optional) . . . . . . . . . . . . . . . . . . . . 58
Preparation for use after system check, CO
2
zero calibration and filter check. . . . . . . . . . . 60
Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
Starting operation . . . . . . . . . . . . . . . . . . . . . 62
Preparing ventilation mode . . . . . . . . . . . . . . 64
VC-CMV, VC-AC . . . . . . . . . . . . . . . . . . . . . . 65
VC-SIMV, VC-SIMV/PS. . . . . . . . . . . . . . . . . 68
PC-BIPAP, PC-BIPAP/PS . . . . . . . . . . . . . . . 71
SpnCPAP, SpnCPAP/PS . . . . . . . . . . . . . . . . 73
NIV – Non-invasive ventilation (Mask
ventilation) . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Special functions . . . . . . . . . . . . . . . . . . . . . . 77
O2 concentration with "O2 blending". . . . . . . 79
Setting HME correction . . . . . . . . . . . . . . . . . 80
Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . 81
Screen brightness . . . . . . . . . . . . . . . . . . . . . 81
Alarm volume . . . . . . . . . . . . . . . . . . . . . . . . 81
Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . 82
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83
Types of alarms. . . . . . . . . . . . . . . . . . . . . . . 84
In the event of an alarm. . . . . . . . . . . . . . . . . 85
Setting alarm limits . . . . . . . . . . . . . . . . . . . . 87
Monitoring . . . . . . . . . . . . . . . . . . . . . . . . . . 89
Displaying curves . . . . . . . . . . . . . . . . . . . . . 90
Displaying measured values . . . . . . . . . . . . . 90
2 measurement (optional) . . . . . . . . . . . . 91
CO
Configuration. . . . . . . . . . . . . . . . . . . . . . . . 95
Setting configuration parameters / display
information. . . . . . . . . . . . . . . . . . . . . . . . . . . 96
Displaying configuration and information . . . 97
Customer Service Mode . . . . . . . . . . . . . . . . 98
Customer service manual . . . . . . . . . . . . . . . 110
Problem Solving . . . . . . . . . . . . . . . . . . . . . 111
Alarm - Cause - Remedy. . . . . . . . . . . . . . . . 112
Messages in the alarm window . . . . . . . . . . . 112
Messages in the information window . . . . . . 120
Error messages during the device check . . . 122
Instructions for Use Oxylog 3000 plus SW 1.n 5
Contents
Cleaning, Disinfection and Sterilization . . . 123
Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . 124
Safety Information on reprocessing . . . . . . . . 127
Reprocessing procedure . . . . . . . . . . . . . . . . 127
Reprocessing list . . . . . . . . . . . . . . . . . . . . . . 131
Assembling parts . . . . . . . . . . . . . . . . . . . . . . 131
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . 133
Maintenance intervals of Oxylog 3000 plus . . 134
Safety inspections . . . . . . . . . . . . . . . . . . . . . 135
Exchanging the internal battery . . . . . . . . . . . 136
In case of ventilator failure . . . . . . . . . . . . . . . 136
Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . 137
Disposing of the medical device. . . . . . . . . . . 138
Disposal instructions . . . . . . . . . . . . . . . . . . . 138
Technical Data . . . . . . . . . . . . . . . . . . . . . . . 139
Ambient conditions . . . . . . . . . . . . . . . . . . . . . 140
Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 141
Performance data. . . . . . . . . . . . . . . . . . . . . . 143
Measured values and curves display . . . . . . . 144
Monitoring. . . . . . . . . . . . . . . . . . . . . . . . . . . . 145
Operating data . . . . . . . . . . . . . . . . . . . . . . . . 146
Device specifications . . . . . . . . . . . . . . . . . . . 149
Materials used . . . . . . . . . . . . . . . . . . . . . . . . 150
Technical Documentation for the
Oxylog 3000 plus according to EMC
standard IEC 60601-1-2 . . . . . . . . . . . . . . . . . 152
Principles of Operation . . . . . . . . . . . . . . . . 157
Ventilation modes. . . . . . . . . . . . . . . . . . . . . . 158
AutoFlow . . . . . . . . . . . . . . . . . . . . . . . . . . . . 162
Dead space . . . . . . . . . . . . . . . . . . . . . . . . . . 164
Determining the cycle time, inspiratory time
and expiratory time. . . . . . . . . . . . . . . . . . . . . 164
Functional description . . . . . . . . . . . . . . . . . . 165
List of Accessories . . . . . . . . . . . . . . . . . . . 167
Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 169
6
Instructions for Use Oxylog 3000 plus SW 1.n
For Your Safety and that of Your Patients
For Your Safety and that of Your Patients
General Safety Information . . . . . . . . . . . . . 8
Strictly follow these Instructions for Use. . . . . 8
Maintenance. . . . . . . . . . . . . . . . . . . . . . . . . . 8
Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Connected Devices . . . . . . . . . . . . . . . . . . . . 9
Safe connection with other electrical
equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Modifications. . . . . . . . . . . . . . . . . . . . . . . . . . 9
Patient safety . . . . . . . . . . . . . . . . . . . . . . . . . 9
Patient monitoring. . . . . . . . . . . . . . . . . . . . . . 9
Information on Electromagnetic Compatibility 9
Functional safety . . . . . . . . . . . . . . . . . . . . . . 10
Appropriate monitoring . . . . . . . . . . . . . . . . . . 10
Product-specific Safety Information. . . . . . 11
Installing accessories . . . . . . . . . . . . . . . . . . . 11
Instructions for Use only available once . . . . . 11
Instructions for Use Oxylog 3000 plus SW 1.n 7
For Your Safety and that of Your Patients
General Safety Information
The following WARNINGS and CAUTIONS apply to
general operation of the device. WARNINGS and
CAUTIONS specific to subsystems or particular
features appear with those topics in later sections
of the manual.
Strictly follow these Instructions for Use
WARNING
Risk of incorrect operation and of incorrect
use
Any use of the medical device requires full
understanding and strict observation of all
sections of these Instructions for Use. The
medical device must only be used for the
purpose specified under "Intended use"
on page 14 and in conjunction with
appropriate patient monitoring.
Strictly observe all WARNING and CAUTION
statements throughout these Instructions for
Use and all statements on medical device
labels. Failure to observe these safety
information statements constitutes a use of
the medical device that is inconsistent with its
intended use.
Maintenance
WARNI NG
Risk of medical device failure and of patient
injury
The medical device must be inspected and
serviced regularly by service personnel.
Repair and complex maintenance work carried out on the medical device must be performed by experts.
Dräger recommends that a service contract is
obtained with DrägerService and that all
repairs are performed by DrägerService. For
maintenance Dräger recommends the use of
authentic Dräger repair parts.
If the above are not complied with, medical
device failure and patient injury cannot be
excluded.
Observe chapter "Maintenance".
Accessories
WARNI NG
Risk due to unreleased accessories
If unreleased accessories are used, there is a
risk of patient injury due to medical device
failure.
Only use the medical device together with
released accessories listed in the current list
of accessories.
8
Instructions for Use Oxylog 3000 plus SW 1.n
For Your Safety and that of Your Patients
Connected Devices
WARNING
Risk of electric shock and of device malfunc-
tion
Any connected devices or device combination, not complying with the requirements
mentioned in these Instructions for Use can
compromise the correct functioning of the
medical device and lead to an electric shock.
Before operating the medical device, strictly
comply with the Instructions for Use of all
connected devices or device combinations.
Safe connection with other electrical equipment
CAUTION
Risk of patient injury
Electrical connections to equipment not listed in
these Instructions for Use or these Assembly
Instructions must only be made when approved
by each respective manufacturer.
This publication excludes references to various
hazards which are obvious to a medical
professional and operator of this medical device, to
the consequences of medical device misuse, and
to potentially adverse effects in patients with
abnormal conditions.
Medical device modification or misuse can be
dangerous.
Patient monitoring
The operators of the medical device are
responsible for choosing appropriate safety
monitoring that provides adequate information on
medical device performance and patient condition.
Patient safety may be achieved through a wide
variety of means, ranging from electronic surveillance of medical device performance and patient
condition, to simple, direct observation of clinical
signs.
The responsibility for the selection of the best level
of patient monitoring lies solely with the medical
device operator.
Information on Electromagnetic
Modifications
WARNING
Modification of the device is not allowed.
Patient safety
The design of the medical device, the accompanying literature, and the labeling on the medical
device are based on the assumption that the use of
the equipment is restricted to trained professionals,
and that certain inherent characteristics of the medical device are known to the trained operator.
Instructions, warnings, and caution statements are
limited, therefore, largely to the specifics of the
Dräger design.
Instructions for Use Oxylog 3000 plus SW 1.n 9
Compatibility
General information on electromagnetic
compatibility (EMC) pursuant to international EMC
standard IEC 60601-1-2:
Electromedical devices are subject to special
precautionary measures concerning
electromagnetic compatibility (EMC) and must be
installed and put into operation in accordance with
the EMC information. Refer to section "Technical
Documentation for the Oxylog 3000 plus according
to EMC standard IEC 60601-1-2" on page 152.
WARNING
Do not use portable and mobile HF communi-
cations equipment, e.g., mobile phones, in the
vicinity of the medical device.
For Your Safety and that of Your Patients
Functional safety
The essential performance of the Oxylog 3000 plus
is defined as:
Appropriate delivery of ventilation to the patientconnection port or generation of an alarm condition.
Appropriate monitoring
CAUTION
Always use a separate SpO2 monitor for
patients who are dependent on an exact O
concentration.
The monitoring functionality of the
Oxylog 3000 plus ensures appropriate monitoring
of ventilation therapy. To ensure appropriate
monitoring during ventilation, always set the
following alarm limits:
– Airway pressure, Paw
– Expiratory minute volume, MVe
– Respiratory rate (if applicable), RR
–etCO
2 (if applicable)
Not setting appropriate alarm limits could suppress
alarms related to:
– Acute changes in the patient’s condition
– Incorrect settings and faulty handling
– Hose system leakage
2
10
Instructions for Use Oxylog 3000 plus SW 1.n
Product-specific Safety Information
For Your Safety and that of Your Patients
WARNING
Ventilation monitoring is mandatory at all
times! Whenever a patient is connected to the
ventilator, constant attention by qualified
medical staff is required in order to provide
immediate corrective action in case of a
malfunction.
The operator shall not solely rely on the builtin monitoring of the ventilator and must
always assume full responsibility for proper
ventilation and patient safety in all situations.
WARNING
Keep a manual breathing bag available.
If a failure is detected in the ventilator and its
life-support functions can no longer be
guaranteed (e.g. in case of a power supply
failure or interruption in the O2 supply),
ventilation must be started without delay with
an independent ventilator (breathing bag) –
using PEEP and/or increased inspired O
concentration as necessary.
WARNING
To ensure proper ventilation, consider the
total dead space of the breathing circuit, especially when using small tidal volumes.
Observe for signs of rebreathing.
Risk of CO2 rebreathing.
2
Installing accessories
CAUTION
Installations on the Oxylog 3000 plus must be
done in accordance with these Instructions for
Use. Make sure that the connections are securely
fitted onto the basic system.
Strictly follow the Assembly Instructions and
Instructions for Use.
Instructions for Use only available once
NOTE
Only one copy of the Instructions for Use is
included in the clinical package and should therefore be kept in an accessible location for users.
NOTE
An etCO2 value by itself is insufficient as a basis
for medical decisions.
Instructions for Use Oxylog 3000 plus SW 1.n 11
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12 Instructions for Use Oxylog 3000 plus SW 1.n
Application
Intended use . . . . . . . . . . . . . . . . . . . . . . . . . 14
Indications / Contraindications. . . . . . . . . . 14
Environment of use . . . . . . . . . . . . . . . . . . . 15
Application
Instructions for Use Oxylog 3000 plus SW 1.n 13
Application
Intended use
The Oxylog 3000 plus is a time-cycled, volumecontrolled and pressure-controlled emergency and
transport ventilator for patients requiring mandatory
or assisted ventilation with a tidal volume from
50 mL upwards.
Intended operator: the device is intended for use by
and under the supervision of trained healthcare
professionals, e.g. doctors, nurses, emergency
medical technicians, respiratory therapists, and
paramedics.
Indications / Contraindications
The device is intended for use with patients with a
tidal volume of 50 mL upwards.
WARNING
The Oxylog 3000 plus ventilator may only be
used under the supervision of trained
healthcare professionals in case immediate
corrective action is required in the event of a
device failure.
14
Instructions for Use Oxylog 3000 plus SW 1.n
Environment of use
Intended environment of use:
– Mobile use for emergency patients, in both
outdoor and indoor environments.
– During transport in ambulances or aircraft,
including helicopters.
– In accident and emergency departments.
– When moving ventilated patients around the
hospital.
– In the recovery room.
WARNING
Do not use the medical device in hyperbaric
chambers.
The medical device may malfunction, causing
danger to the patient.
WARNING
Do not use the medical device in conjunction
with magnetic resonance imaging (MRI, NMR,
NMI).
The medical device may malfunction, causing
danger to the patient.
Application
WARNING
This medical device is neither approved nor
certified for use in areas where combustible or
explosive gas mixtures are likely to occur.
Instructions for Use Oxylog 3000 plus SW 1.n 15
This page intentionally left blank
16 Instructions for Use Oxylog 3000 plus SW 1.n
System Overview
Front panel with all options. . . . . . . . . . . . . 18
Side view, right . . . . . . . . . . . . . . . . . . . . . . . . 19
Rear view . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Adult hose system, reusable . . . . . . . . . . . . . 20
Adult hose system, disposable. . . . . . . . . . . . 20
Paediatric hose system, disposable . . . . . . . . 21
Range of functions . . . . . . . . . . . . . . . . . . . . 22
Ventilation functions of the Oxylog 3000 plus. 22
Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . 23
Symbols. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
System Overview
Instructions for Use Oxylog 3000 plus SW 1.n 17
System Overview
ABCDEFG
H
I
J
K
L
M
NOPQRS
T
U
V
Front panel with all options
A Screen with screen pages for the specific
application
B Key Alarms to display the alarm settings
in the "Settings and Alarms" window and to
change screen pages
C Key Settings to display ventilation
parameters (ventilation screen) in the "Settings
and Alarms" window and to change screen
pages
D Key for setting the ventilation mode SpnCPAP
E Key for setting the ventilation modes VC-CMV /
VC-AC
F Key for setting the ventilation mode VC-SIMV
G Key for setting the ventilation mode PC-BIPAP
H Red and yellow alarm indicators
I Key for suppressing the acoustic alarm sig-
nal for 2 minutes
J Key Alarm Reset for acknowledging alarm
messages
K Key O
100 % O2 for 100 % O2 application, depending
on the option installed at manufacture
2 inhalation for O2 inhalation or key
L Key Insp. Hold for initiating a manual inspira-
tion or for extending the current inspiratory time.
M Key Start/Standby
N Display symbols for the power supply
Charge status of the internal battery
Mains power supply connected
O Rotary knob for making selections, changing
and confirming settings
P Control knob for setting the O
2 concentration
FiO2
Q Control knob for setting the maximum
inspiratory pressure Pmax
R Control knob for setting the respiratory rate RR
S Control knob for setting the tidal volume VT
T Explanation of color codes for quick pre-setting
of RR and VT
U Key Curves to change between the
pressure, flow or CO
and large presentation
V Key Values to change screen pages in
the "Measured Values" window
Curves
2 (optional) curve in small
Front
18
Instructions for Use Oxylog 3000 plus SW 1.n
System Overview
B
C
D
E
F
A
G
H
A
B
C
Side view, right
A Emergency air intake
CAUTION
Do not block the emergency air intake. This may
result in ventilator malfunction.
B Knob to secure the battery compartment cover
C Connectors for flow measuring lines
D Gas outlet for breathing hose
E Connector for O
F Connector for power supply
G Connector for CO
H Connector for data communication cable
2 supply
2 sensor
Rear view
Side
A Emergency air intake
CAUTION
Do not block the air intake. This may result in
ventilator malfunction.
B Fresh-gas intake with a filter cartridge
C Protection bracket
CAUTION
Do not use the protection bracket as a handle.
Tilting the device to a vertical position may lead to
airway pressure oscillation.
Rear
Instructions for Use Oxylog 3000 plus SW 1.n 19
System Overview
A
E
B
C
D
E
D
C
A
B
Adult hose system, reusable
A Angled connector
B Flow sensor
C Breathing valve
D Breathing hose
E Flow and pressure measuring hoses
Adult hose system, disposable
001
A Angled connector
B Flow sensor
C Breathing valve
D Breathing hose
E Flow and pressure measuring hoses
002
20
Instructions for Use Oxylog 3000 plus SW 1.n
Paediatric hose system, disposable
D
A
E
C
B
A Angled connector
B Flow sensor
C Breathing valve
D Breathing hose
E Flow and pressure measuring hoses
System Overview
08137170
Instructions for Use Oxylog 3000 plus SW 1.n 21
System Overview
Range of functions
Ventilation functions of the Oxylog 3000 plus
Ventilation modes:
– Volume-controlled ventilation:
– VC-CMV / VC-AC,
–VC-SIMV.
– Pressure-controlled ventilation:
–PC-BIPAP.
– Support of spontaneous breathing:
– SpnCPAP.
Additional settings for ventilation:
– Pressure Support: in the ventilation modes
VC-SIMV, PC-BIPAP, SpnCPAP,
– Apnoea ventilation: in the ventilation mode
SpnCPAP,
– AutoFlow (optional): in the ventilation modes
VC-CMV, VC-AC and VC-SIMV.
– NIV: in the ventilation modes: SpnCPAP (/PS),
PC-BIPAP (/PS), VC-CMV / AF, VC-AC / AF
and VC-SIMV / AF.
For a detailed description of the ventilation modes
and the additional settings, refer to "Principles of
Operation" on page 157. For abbreviations, see
"Abbreviations" on page 23.
NOTE
In these Instructions for Use the unit of measurement for airway pressure is expressed in [mbar].
However, in some languages the display of the
Oxylog 3000 plus shows [cmH
One [mbar] equals approximately one [cmH
2O].
2O].
Special procedures:
– Inspiration hold,
–O
2 inhalation (optional), with an inhalation
mask.
22
Instructions for Use Oxylog 3000 plus SW 1.n
Abbreviations
System Overview
Abbreviation Explanation
100 % O
2 100 % O2 flow
AF AutoFlow
BF Body Floating
bpm Breaths per minute
BTPS Body Temperature, Pressure
Saturated
C Lung compliance
2 Carbon dioxide
CO
CSM Customer Service Mode
ΔPsupp Positive pressure above PEEP
EMC Electromagnetic Compatibility
ESD Electrostatic Discharge
2 Endtidal CO2 concentration
etCO
2 Fractional inspired oxygen
FiO
concentration
FRC Functional Residual Capacity
HME Heat and Moisture Exchange
I:E Ratio inspiratory time to expiratory
time
IPX2 Ingress Protection level 2
IPX4 Ingress Protection level 4
MVe Expiratory minute volume
MVi Inspiratory minute volume
MVespon Spontaneous expiratory minute
volume
NIV Non-invasive ventilation –
mask ventilation
2 Oxygen
O
2-Inhalat. O2 inhalation
O
Paw Airway pressure
PC-BIPAP Pressure Controlled - Biphasic
Positive Airway Pressure
PEEP Positive End Expiratory Pressure
Abbreviation Explanation
PIF Peak Inspiratory Flow
Pinsp Inspiratory pressure
PIP Peak Inspiratory Pressure
Pmax Maximum allowed inspiratory
pressure
Pmean Mean airway pressure
Pplat Plateau pressure
PS Pressure Support
R Resistance
RF Radio Frequency
RR Respiratory Rate (frequency)
RRapn Respiratory Rate during apnoea
ventilation
RRsp Spontaneous Respiratory Rate
SpnCPAP Spontaneous Continuous Positive
Airway Pressure
2 Saturation of peripheral oxygen
SpO
Tapn Time before apnoea is recognized
Te Expiratory time
Ti Inspiratory time
Tplat % Plateau time in % of inspiratory time
UN United Nations
VC-AC Volume Controlled - Assist Control
VC-CMV Volume Controlled - Controlled
Mandatory Ventilation
VC-SIMV Volume Controlled - Synchronized
Intermittent Mandatory Ventilation
VT Tidal volume
VTapn Tidal volume during apnoea
ventilation
VTe Expiratory tidal volume
VTi Inspiratory tidal volume
Instructions for Use Oxylog 3000 plus SW 1.n 23
System Overview
Insp.
hold
Alarms
Symbols
Symbol Explanation
Key for initiating a manual
inspiration or for extending the
current inspiratory time.
Key to display ventilation
Settings
parameters (ventilation screen) in
the "Settings and Alarms" window
and to change screen pages.
Key to display the alarm settings in
the "Settings and Alarms" window
and to change screen pages.
Key to change screen pages in the
Values
"Measured Values" window.
Key to change between the
Curves
pressure, flow or CO
2 (optional)
curve in small and large
presentation.
Key for suppressing the acoustic
alarm signal for 2 minutes.
Key for acknowledging alarm
Alarm
Reset
messages.
Rotary knob
Start / Standby key
Upper alarm limit
Lower alarm limit
! Advisory message
!! Caution message
Symbol Explanation
* Trigger indicator
Warning
Defibrillation-proof type BF applied
part
Charge status of the internal battery
External power supply connected
Battery charge
(example: three quarters full)
Class II equipment, device protected against electric shock with
additional safety precautions such
as double or reinforced insulations,
without protective earthing.
Do not dispose of the device as
municipal waste.
Manufacturing date
Manufacturer
DC input
Operating instructions
Follow Instructions for Use
!!! Warning message
24
Instructions for Use Oxylog 3000 plus SW 1.n
System Overview
Symbol Explanation
For dry locations only
Caution, hot surface!
Warning, dangerous voltage!
Temperature limitations
Latex free
Do not reuse
Do not use oil and grease
Non-sterile
Symbol Explanation
Slope (steep, medium, flat)
Quantity
Keep away from sunlight
For indoor use only
Do not open
Prohibition: Do not obstruct emergency air intake or fresh gas intake
Pediatric
Adult
Paediatric
Adult
Instructions for Use Oxylog 3000 plus SW 1.n 25
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26 Instructions for Use Oxylog 3000 plus SW 1.n
Operating Concept
Switch on or off . . . . . . . . . . . . . . . . . . . . . . 28
Switch on . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Switch off . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Ventilation controls . . . . . . . . . . . . . . . . . . . 29
Display operating controls . . . . . . . . . . . . . 30
Additional function keys . . . . . . . . . . . . . . . 31
Screen window structure. . . . . . . . . . . . . . . 32
Operating Concept
Instructions for Use Oxylog 3000 plus SW 1.n 27
Operating Concept
Oxylog 3000 plus
AB
Switch on or off
Switch on
z To switch the device ON, briefly press the
key (A).
00337170
Switch off
Refer to "Shutdown" on page 82.
28
Instructions for Use Oxylog 3000 plus SW 1.n
Ventilation controls
BC
A
Oxylog 3000 plus
Operating Concept
General ventilation controls
A Keys for selecting the ventilation modes:
– VC-CMV / VC-AC
–VC-SIMV
– SpnCPAP
– PC-BIPAP.
B Rotary knob.
C Ventilation parameter controls:
– Inspiratory tidal volume VT [mL],
– Ventilation respiratory rate RR [/min],
– Maximum inspiratory pressure Pmax
[mbar],
–O
2 concentration FiO2 [%].
Selecting the ventilation mode
Oxylog 3000 plus
00137170
BC
z Press the appropriate ventilation mode key (A)
for approximately 3 seconds.
Or
1 Press the appropriate ventilation mode key (A).
2 Press the rotary knob (B) to confirm.
The selected ventilation mode will be activated.
The active ventilation mode is displayed in the
upper left corner of the display (C).
A
08537170
Instructions for Use Oxylog 3000 plus SW 1.n 29
Operating Concept
Oxylog 3000 plus
B C
D
E
A
Curves
Display operating controls
A Rotary knob for making selections, changing
and confirming settings.
NOTE
Different parameters can be set in the display
window via the rotary knob (e.g. Ti, PEEP, ΔPsupp,
Pinsp).
– To select the parameter: turn rotary knob.
– To activate the parameter: press rotary knob.
– To set the value: turn rotary knob.
– To confirm the value: press rotary knob.
00237170
B Key Values to change screen pages in
the "Measured Values" window.
C Key Curves to change between the
pressure, flow or CO2 (optional) curve in small
and large presentation.
D Key Settings to display ventilation
parameters (ventilation screen) in the "Settings
and Alarms" window and to change screen
pages.
E Key Alarms to display the alarm settings
in the "Settings and Alarms" window and to
change screen pages.
30
Instructions for Use Oxylog 3000 plus SW 1.n
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