Oxylog 3000 plus Instructions for Use Sw 1.n 6th Edition May 2012.pdf
Page 1
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
Page 2
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 different 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.
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.
Trademarks
–
Oxylog®
–
AutoFlow®
–
DrägerService®
are trademarks owned by Dräger.
–
Sekusept®
is a trademark of ECOLAB.
–
BIPAP*
*
Trademark used under license
2
Instructions for Use Oxylog 3000 plus SW 1.n
Page 3
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
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.
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
Page 4
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
Page 5
Contents
Contents
For Your Safety and that of Your Patients .
7
General Safety Information. . . . . . . . . . . . . . .
Product-specific Safety Information . . . . . . . .
8
11
Application . . . . . . . . . . . . . . . . . . . . . . . . . .
13
Intended use. . . . . . . . . . . . . . . . . . . . . . . . . .
Indications / Contraindications . . . . . . . . . . . .
Environment of use. . . . . . . . . . . . . . . . . . . . .
14
14
15
System Overview . . . . . . . . . . . . . . . . . . . . .
17
Front panel with all options. . . . . . . . . . . . . . .
Range of functions . . . . . . . . . . . . . . . . . . . . .
Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . .
Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
18
22
23
24
Operating Concept . . . . . . . . . . . . . . . . . . . .
27
Switch on or off. . . . . . . . . . . . . . . . . . . . . . . .
Ventilation controls . . . . . . . . . . . . . . . . . . . . .
Display operating controls . . . . . . . . . . . . . . .
Additional function keys . . . . . . . . . . . . . . . . .
Screen window structure . . . . . . . . . . . . . . . .
28
29
30
31
32
Assembly. . . . . . . . . . . . . . . . . . . . . . . . . . . .
35
Internal rechargeable battery . . . . . . . . . . . . .
Connecting the power supply . . . . . . . . . . . . .
External power supply . . . . . . . . . . . . . . . . . .
Connecting the gas supply . . . . . . . . . . . . . . .
Assembling the adult reusable hose system .
Connecting the adult disposable hose system
Connecting the paediatric disposable hose
system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Connecting the bacterial filter or HME . . . . . .
Connecting the CO2 sensor and the cuvette .
Hanging the Oxylog 3000 plus on standard
rail systems. . . . . . . . . . . . . . . . . . . . . . . . . . .
37
38
39
41
43
45
Getting Started . . . . . . . . . . . . . . . . . . . . . . .
51
Charging the battery . . . . . . . . . . . . . . . . . . . .
Determining the approximate pneumatic
operating time. . . . . . . . . . . . . . . . . . . . . . . . .
Checking readiness for operation. . . . . . . . . .
CO2 zero calibration and filter check before
ventilation (optional) . . . . . . . . . . . . . . . . . . . .
52
Instructions for Use Oxylog 3000 plus SW 1.n
46
47
48
49
53
54
Preparation for use after system check, CO2
zero calibration and filter check. . . . . . . . . . .
60
Operation . . . . . . . . . . . . . . . . . . . . . . . . . . .
61
Starting operation . . . . . . . . . . . . . . . . . . . . .
Preparing ventilation mode . . . . . . . . . . . . . .
VC-CMV, VC-AC . . . . . . . . . . . . . . . . . . . . . .
VC-SIMV, VC-SIMV/PS . . . . . . . . . . . . . . . . .
PC-BIPAP, PC-BIPAP/PS . . . . . . . . . . . . . . .
SpnCPAP, SpnCPAP/PS . . . . . . . . . . . . . . . .
NIV – Non-invasive ventilation (Mask
ventilation) . . . . . . . . . . . . . . . . . . . . . . . . . . .
Special functions . . . . . . . . . . . . . . . . . . . . . .
O2 concentration with "O2 blending". . . . . . .
Setting HME correction . . . . . . . . . . . . . . . . .
Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . .
Screen brightness . . . . . . . . . . . . . . . . . . . . .
Alarm volume . . . . . . . . . . . . . . . . . . . . . . . .
Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . .
62
64
65
68
71
73
76
77
79
80
81
81
81
82
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
83
Types of alarms . . . . . . . . . . . . . . . . . . . . . . .
In the event of an alarm. . . . . . . . . . . . . . . . .
Setting alarm limits . . . . . . . . . . . . . . . . . . . .
84
85
87
Monitoring . . . . . . . . . . . . . . . . . . . . . . . . . .
89
Displaying curves . . . . . . . . . . . . . . . . . . . . .
Displaying measured values . . . . . . . . . . . . .
CO2 measurement (optional) . . . . . . . . . . . .
90
90
91
Configuration. . . . . . . . . . . . . . . . . . . . . . . .
95
Setting configuration parameters / display
information. . . . . . . . . . . . . . . . . . . . . . . . . . .
Displaying configuration and information . . .
Customer Service Mode . . . . . . . . . . . . . . . .
Customer service manual . . . . . . . . . . . . . . .
96
97
98
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
58
5
Page 6
Contents
Cleaning, Disinfection and Sterilization . . . 123
Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . .
Safety Information on reprocessing . . . . . . . .
Reprocessing procedure . . . . . . . . . . . . . . . .
Reprocessing list . . . . . . . . . . . . . . . . . . . . . .
Assembling parts . . . . . . . . . . . . . . . . . . . . . .
124
127
127
131
131
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . 133
Maintenance intervals of Oxylog 3000 plus . .
Safety inspections . . . . . . . . . . . . . . . . . . . . .
Exchanging the internal battery . . . . . . . . . . .
In case of ventilator failure . . . . . . . . . . . . . . .
134
135
136
136
Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . 137
Disposing of the medical device. . . . . . . . . . . 138
Disposal instructions . . . . . . . . . . . . . . . . . . . 138
Technical Data . . . . . . . . . . . . . . . . . . . . . . . 139
Ambient conditions . . . . . . . . . . . . . . . . . . . . .
Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Performance data . . . . . . . . . . . . . . . . . . . . . .
Measured values and curves display . . . . . . .
Monitoring. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Operating data . . . . . . . . . . . . . . . . . . . . . . . .
Device specifications . . . . . . . . . . . . . . . . . . .
Materials used . . . . . . . . . . . . . . . . . . . . . . . .
Technical Documentation for the
Oxylog 3000 plus according to EMC
standard IEC 60601-1-2 . . . . . . . . . . . . . . . . .
140
141
143
144
145
146
149
150
152
Principles of Operation . . . . . . . . . . . . . . . . 157
Ventilation modes . . . . . . . . . . . . . . . . . . . . . .
AutoFlow . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Dead space . . . . . . . . . . . . . . . . . . . . . . . . . .
Determining the cycle time, inspiratory time
and expiratory time. . . . . . . . . . . . . . . . . . . . .
Functional description . . . . . . . . . . . . . . . . . .
158
162
164
164
165
List of Accessories . . . . . . . . . . . . . . . . . . . 167
Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 169
6
Instructions for Use Oxylog 3000 plus SW 1.n
Page 7
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 . . . . .
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . .
Accessories . . . . . . . . . . . . . . . . . . . . . . . . . .
Connected Devices . . . . . . . . . . . . . . . . . . . .
Safe connection with other electrical
equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Modifications. . . . . . . . . . . . . . . . . . . . . . . . . .
Patient safety . . . . . . . . . . . . . . . . . . . . . . . . .
Patient monitoring. . . . . . . . . . . . . . . . . . . . . .
Information on Electromagnetic Compatibility
Functional safety . . . . . . . . . . . . . . . . . . . . . .
Appropriate monitoring . . . . . . . . . . . . . . . . . .
8
8
8
9
9
9
9
9
9
10
10
Product-specific Safety Information. . . . . .
11
Installing accessories . . . . . . . . . . . . . . . . . . .
Instructions for Use only available once . . . . .
11
11
Instructions for Use Oxylog 3000 plus SW 1.n
7
Page 8
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
WARNING
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
WARNING
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
Page 9
For Your Safety and that of Your Patients
Connected Devices
WARNING
Risk of electric shock and of device malfunction
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.
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
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
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 communications equipment, e.g., mobile phones, in the
vicinity of the medical device.
9
Page 10
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 O2
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
–
etCO2 (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
10
Instructions for Use Oxylog 3000 plus SW 1.n
Page 11
For Your Safety and that of Your Patients
Product-specific Safety Information
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 O2
concentration as necessary.
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.
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.
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
Page 13
Application
Application
Intended use . . . . . . . . . . . . . . . . . . . . . . . . .
14
Indications / Contraindications . . . . . . . . . .
14
Environment of use . . . . . . . . . . . . . . . . . . .
15
Instructions for Use Oxylog 3000 plus SW 1.n
13
Page 14
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
Page 15
Application
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.
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
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16
Instructions for Use Oxylog 3000 plus SW 1.n
Page 17
System Overview
System Overview
Front panel with all options. . . . . . . . . . . . .
18
Side view, right . . . . . . . . . . . . . . . . . . . . . . . .
Rear view . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Adult hose system, reusable . . . . . . . . . . . . .
Adult hose system, disposable . . . . . . . . . . . .
Paediatric hose system, disposable . . . . . . . .
19
19
20
20
21
Range of functions . . . . . . . . . . . . . . . . . . . .
22
Ventilation functions of the Oxylog 3000 plus.
22
Abbreviations . . . . . . . . . . . . . . . . . . . . . . . .
23
Symbols. . . . . . . . . . . . . . . . . . . . . . . . . . . . .
24
Instructions for Use Oxylog 3000 plus SW 1.n
17
Page 18
System Overview
Front panel with all options
A
BC D E FG
H
I
J
K
L
M
V
U
T
R
Q
P
O
N
Front
S
A Screen with screen pages for the specific
application
L Key Insp. Hold for initiating a manual inspiration or for extending the current inspiratory time.
B Key Alarms
to display the alarm settings
in the "Settings and Alarms" window and to
change screen pages
M Key
C Key Settings
to display ventilation
parameters (ventilation screen) in the "Settings
and Alarms" window and to change screen
pages
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
D Key for setting the ventilation mode SpnCPAP
P Control knob for setting the O2 concentration
FiO2
E Key for setting the ventilation modes VC-CMV /
VC-AC
Q Control knob for setting the maximum
inspiratory pressure Pmax
F Key for setting the ventilation mode VC-SIMV
R Control knob for setting the respiratory rate RR
G Key for setting the ventilation mode PC-BIPAP
S Control knob for setting the tidal volume VT
H Red and yellow alarm indicators
T Explanation of color codes for quick pre-setting
of RR and VT
I
J
Key
for suppressing the acoustic alarm signal for 2 minutes
Key Alarm Reset for acknowledging alarm
messages
K Key O2 inhalation for O2 inhalation or key
100 % O2 for 100 % O2 application, depending
on the option installed at manufacture
18
Curves
U Key Curves
to change between the
pressure, flow or CO2 (optional) curve in small
and large presentation
V Key Values
to change screen pages in
the "Measured Values" window
Instructions for Use Oxylog 3000 plus SW 1.n
Page 19
System Overview
Side view, right
Rear view
A
H
G
B
C
C
A
B
D
Side
Rear
E
F
A Emergency air intake
CAUTION
Do not block the emergency air intake. This may
result in ventilator malfunction.
A Emergency air intake
CAUTION
Do not block the air intake. This may result in
ventilator malfunction.
B Knob to secure the battery compartment cover
B Fresh-gas intake with a filter cartridge
C Connectors for flow measuring lines
C Protection bracket
D Gas outlet for breathing hose
E Connector for O2 supply
F Connector for power supply
CAUTION
Do not use the protection bracket as a handle.
Tilting the device to a vertical position may lead to
airway pressure oscillation.
G Connector for CO2 sensor
H Connector for data communication cable
Instructions for Use Oxylog 3000 plus SW 1.n
19
Page 20
System Overview
Adult hose system, reusable
C
Adult hose system, disposable
C
D
D
E
B
B
E
002
A
001
A
A Angled connector
A Angled connector
B Flow sensor
B Flow sensor
C Breathing valve
C Breathing valve
D Breathing hose
D Breathing hose
E Flow and pressure measuring hoses
E Flow and pressure measuring hoses
20
Instructions for Use Oxylog 3000 plus SW 1.n
Page 21
System Overview
Paediatric hose system, disposable
C
A B
D
08137170
E
A Angled connector
B Flow sensor
C Breathing valve
D Breathing hose
E Flow and pressure measuring hoses
Instructions for Use Oxylog 3000 plus SW 1.n
21
Page 22
System Overview
Range of functions
Ventilation functions of the
Oxylog 3000 plus
Ventilation modes:
–
–
–
Volume-controlled ventilation:
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.
Pressure-controlled ventilation:
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 [cmH2O].
–
One [mbar] equals approximately one [cmH2O].
–
VC-CMV / VC-AC,
–
VC-SIMV.
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.
Special procedures:
–
Inspiration hold,
–
O2 inhalation (optional), with an inhalation
mask.
22
Instructions for Use Oxylog 3000 plus SW 1.n
Page 23
System Overview
Abbreviations
Abbreviation Explanation
Abbreviation Explanation
100 % O2
100 % O2 flow
PIF
Peak Inspiratory Flow
AF
AutoFlow
Pinsp
Inspiratory pressure
BF
Body Floating
PIP
Peak Inspiratory Pressure
bpm
Breaths per minute
Pmax
BTPS
Body Temperature, Pressure
Saturated
Maximum allowed inspiratory
pressure
Pmean
Mean airway pressure
C
Lung compliance
Pplat
Plateau pressure
CO2
Carbon dioxide
PS
Pressure Support
CSM
Customer Service Mode
R
Resistance
ΔPsupp
Positive pressure above PEEP
RF
Radio Frequency
EMC
Electromagnetic Compatibility
RR
Respiratory Rate (frequency)
ESD
Electrostatic Discharge
RRapn
etCO2
Endtidal CO2 concentration
Respiratory Rate during apnoea
ventilation
FiO2
Fractional inspired oxygen
concentration
RRsp
Spontaneous Respiratory Rate
SpnCPAP
Spontaneous Continuous Positive
Airway Pressure
FRC
Functional Residual Capacity
HME
Heat and Moisture Exchange
SpO2
Saturation of peripheral oxygen
I:E
Ratio inspiratory time to expiratory
time
Tapn
Time before apnoea is recognized
Te
Expiratory time
IPX2
Ingress Protection level 2
Ti
Inspiratory time
IPX4
Ingress Protection level 4
Tplat %
Plateau time in % of inspiratory time
MVe
Expiratory minute volume
UN
United Nations
MVi
Inspiratory minute volume
VC-AC
Volume Controlled - Assist Control
MVespon
Spontaneous expiratory minute
volume
VC-CMV
Volume Controlled - Controlled
Mandatory Ventilation
NIV
Non-invasive ventilation –
mask ventilation
VC-SIMV
Volume Controlled - Synchronized
Intermittent Mandatory Ventilation
O2
Oxygen
VT
Tidal volume
O2-Inhalat.
O2 inhalation
VTapn
Paw
Airway pressure
Tidal volume during apnoea
ventilation
PC-BIPAP
Pressure Controlled - Biphasic
Positive Airway Pressure
VTe
Expiratory tidal volume
VTi
Inspiratory tidal volume
PEEP
Positive End Expiratory Pressure
Instructions for Use Oxylog 3000 plus SW 1.n
23
Page 24
System Overview
Symbols
Symbol
Insp.
hold
Explanation
Key for initiating a manual
inspiration or for extending the
current inspiratory time.
Symbol
*
Explanation
Trigger indicator
Warning
Settings
Key to display ventilation
parameters (ventilation screen) in
the "Settings and Alarms" window
and to change screen pages.
Alarms
Key to display the alarm settings in
the "Settings and Alarms" window
and to change screen pages.
Charge status of the internal battery
Values
Key to change screen pages in the
"Measured Values" window.
External power supply connected
Key to change between the
pressure, flow or CO2 (optional)
curve in small and large
presentation.
Battery charge
(example: three quarters full)
Curves
Key for suppressing the acoustic
alarm signal for 2 minutes.
Alarm
Reset
Key for acknowledging alarm
messages.
Defibrillation-proof type BF applied
part
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.
Rotary knob
Manufacturing date
Start / Standby key
Manufacturer
Upper alarm limit
DC input
Lower alarm limit
Operating instructions
!
Advisory message
!!
Caution message
!!!
Warning message
24
Follow Instructions for Use
Instructions for Use Oxylog 3000 plus SW 1.n
Page 25
System Overview
Symbol
Explanation
Symbol
Explanation
For dry locations only
Slope (steep, medium, flat)
Caution, hot surface!
Quantity
Warning, dangerous voltage!
Temperature limitations
Latex free
Do not reuse
Do not use oil and grease
Non-sterile
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