Instructions for Use

Oxylog 2000 plus

Title

WARNING Emergency and Transport Ventilator

For a full understanding of the perfor-
mance characteristics of this device, Software 1.n
the user should carefully read this man-
ual before use of the device.
Working with these Instructions for Use

Working with these Instructions for Use

The title of the main chapter in the header line Trademarks

helps with orientation and navigation.
The Dräger Oxylog® name is a registered trade-
The Instructions for Use combine text and illustra- mark of Dräger.
tions, providing a comprehensive overview of the
system. The information is presented as sequential
Definitions
steps of action, allowing the user to systematically
learn how to use the device. WARNING
The text provides explanations and instructs the A WARNING statement provides important
user step-by-step in the practical use of the information about a potentially hazardous sit-
product, with short, clear instructions in uation which, if not avoided, could result in
easy-to-follow sequences. death or serious injury.
1 Consecutive numbers indicate the steps of
CAUTION
action, with the numbering restarting with "1" for
each new sequence of actions. A CAUTION statement provides important infor-
mation about a potentially hazardous situation
z Bullet points indicate individual actions or which, if not avoided, may result in minor or mod-
different options for action. erate injury to the user or patient or in damage to
– Dashes indicate the listing of data, options or the equipment or other property.
objects.
NOTE
(A) Letters in parentheses refer to elements in the A NOTE provides additional information intended
relevant illustration. to avoid inconvenience during operation.

The illustrations show the relationship between Abbreviations and Symbols

the text and the device. Elements mentioned in the
Please refer to "Abbreviations" on page 16 and
text are highlighted. Unnecessary details are
"Symbols" on page 17 for additional information.
omitted.
Schematic renderings of screen images guide the
user and allow to reconfirm actions performed. The
actual screen images differ in lock or in configura-
tion.
A Letters denote elements referred to the text.

Typing conventions
Any text shown on the screen and any labeling on
the device are printed in bold and italics, for exam-
ple PEEP, Air or Alarm Settings.

2 Instructions for Use Oxylog 2000 plus SW 1.n

 Contents

Contents

For Your Safety and that of Your Patients . 5 Preparing ventilation mode . . . . . . . . . . . . . . 47
General WARNINGS and CAUTIONS . . . . . . 7 VC-CMV / VC-AC . . . . . . . . . . . . . . . . . . . . . 48
VC-SIMV (optional PS) . . . . . . . . . . . . . . . . . 50
Application . . . . . . . . . . . . . . . . . . . . . . . . . . 9 SpnCPAP (optional PS) . . . . . . . . . . . . . . . . . 52
O2 AirMix or 100% O2 . . . . . . . . . . . . . . . . . 55
Intended use. . . . . . . . . . . . . . . . . . . . . . . . . . 10 Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
Indications/Contraindications . . . . . . . . . . . . . 10 Screen brightness . . . . . . . . . . . . . . . . . . . . . 56
Environment of use. . . . . . . . . . . . . . . . . . . . . 10 Volume loudness . . . . . . . . . . . . . . . . . . . . . . 56
Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
System Overview . . . . . . . . . . . . . . . . . . . . . 11
Front panel with all options. . . . . . . . . . . . . . . 12 Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
Available ventilation modes . . . . . . . . . . . . . . 14 Types of alarms . . . . . . . . . . . . . . . . . . . . . . . 60
Special modes . . . . . . . . . . . . . . . . . . . . . . . . 15 In the event of an alarm. . . . . . . . . . . . . . . . . 61
With monitoring. . . . . . . . . . . . . . . . . . . . . . . . 15 Setting alarm limits . . . . . . . . . . . . . . . . . . . . 63
Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . 16
Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17 Monitoring . . . . . . . . . . . . . . . . . . . . . . . . . . 65
Operating Concept . . . . . . . . . . . . . . . . . . . . 19 Displaying the airway pressure . . . . . . . . . . . 66
Displaying MVe and VTe . . . . . . . . . . . . . . . . 66
Switch ON or OFF . . . . . . . . . . . . . . . . . . . . . 20 Displaying O2 values. . . . . . . . . . . . . . . . . . . 66
Ventilation controls . . . . . . . . . . . . . . . . . . . . . 21 Displaying other measured values . . . . . . . . 67
Display operating controls . . . . . . . . . . . . . . . 22
Screen window structure . . . . . . . . . . . . . . . . 23 Configuration. . . . . . . . . . . . . . . . . . . . . . . . 69
Assembly. . . . . . . . . . . . . . . . . . . . . . . . . . . . 27 Set configuration parameters / display information
70
Dead space . . . . . . . . . . . . . . . . . . . . . . . . . . 28 Displaying configuration and information . . . 71
Assemble the reusable hose system . . . . . . . 29 Customer Service Mode . . . . . . . . . . . . . . . . 72
Connect the disposable hose system. . . . . . . 31
Connecting the power supply . . . . . . . . . . . . . 32 Problem Solving . . . . . . . . . . . . . . . . . . . . . 79
Internal supply with rechargeable battery. . . . 32
Connecting the gas supply . . . . . . . . . . . . . . . 34 Alarm - Cause - Remedy. . . . . . . . . . . . . . . . 80
Hanging the Oxylog 2000 plus on standard rail sys- Messages in the alarm window . . . . . . . . . . . 80
tems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36 Messages in the information window . . . . . . 84
Error messages during the device check . . . 85
Getting Started . . . . . . . . . . . . . . . . . . . . . . . 37
Cleaning, Disinfection and Sterilization . . 87
Charging the battery . . . . . . . . . . . . . . . . . . . . 38
Determining the approximate pneumatic operating Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . 88
time for the Oxylog 2000 plus. . . . . . . . . . . . . 39 Reprocessing procedure . . . . . . . . . . . . . . . . 91
Checking readiness for operation. . . . . . . . . . 40
Maintenance. . . . . . . . . . . . . . . . . . . . . . . . . 95
Perform device check . . . . . . . . . . . . . . . . . . . 41
Preparation for use after system check . . . . . 43 Maintenance intervals . . . . . . . . . . . . . . . . . . 96

Operation. . . . . . . . . . . . . . . . . . . . . . . . . . . . 45 Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99
Starting operation . . . . . . . . . . . . . . . . . . . . . . 46 Safety information . . . . . . . . . . . . . . . . . . . . . 100
Disposal of batteries . . . . . . . . . . . . . . . . . . . 100

Instructions for Use Oxylog 2000 plus SW 1.n 3

Contents

Disposal of the medical device . . . . . . . . . . . . 100

Disposal of the disposable hose system . . . . 101

Technical Data . . . . . . . . . . . . . . . . . . . . . . . 103

Ambient conditions . . . . . . . . . . . . . . . . . . . . . 104
Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 105
Performance data . . . . . . . . . . . . . . . . . . . . . . 106
Measured value display . . . . . . . . . . . . . . . . . 107
Monitoring. . . . . . . . . . . . . . . . . . . . . . . . . . . . 108
Operating data . . . . . . . . . . . . . . . . . . . . . . . . 109
Device specifications . . . . . . . . . . . . . . . . . . . 111
Materials used . . . . . . . . . . . . . . . . . . . . . . . . 112
Technical Documentation for the Oxylog 2000 plus
according to EMC standard IEC/EN 60601-1-2 113

Principles of Operation . . . . . . . . . . . . . . . . 117

Ventilation modes . . . . . . . . . . . . . . . . . . . . . . 118
Functional description . . . . . . . . . . . . . . . . . . 121

List of Accessories . . . . . . . . . . . . . . . . . . . 123

Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 125

4 Instructions for Use Oxylog 2000 plus SW 1.n

 For Your Safety and that of Your Patients

For Your Safety and that of Your Patients

Strictly follow these Instructions for Use Accessories

WARNING WARNING
Any use of the medical device requires full Only the accessories indicated on the list of
understanding and strict observation of all accessories have been tested and approved
portions of these Instructions for Use. The to be used with the medical device. Accord-
medical device is only to be used for the pur- ingly, it is strongly recommended that only
pose specified under "Intended use" these accessories be used in conjunction with
on page 10 and in conjunction with appropri- the specific medical device. Otherwise, the
ate patient monitoring. correct functioning of the medical device may
be compromised.
Strictly observe all WARNING and CAUTION
statements throughout these Instructions for
WARNING
Use and all statements on medical device
labels. Any connected devices, or combination of
devices, not complying with the requirements
mentioned in these Instructions for Use may
Maintenance compromise the correct functioning of the
medical device. Prior to operating the medical
device, consult the respective documentation
WARNING and Instructions for Use of all connected
The medical device must be inspected and devices or combination of devices.
serviced regularly by properly trained service
personnel.
Repair of the device may also only be carried Not for use in explosion hazard areas
out by properly trained service personnel.
Dräger Medical recommends that a service WARNING
contract be obtained with DrägerService and This medical device is neither approved nor
that all repairs also be carried out by them. certified for use in areas where combustible or
Dräger Medical recommends that only authen- explosive gas mixtures are likely to occur.
tic Dräger Medical repair parts be used for
maintenance. Otherwise, the proper function-
ing of the medical device may be
Safe connection with other electrical
compromised.
equipment
Refer to the chapter "Maintenance"
on page 95 for additional information. WARNING
Electrical connections to equipment, which
are not listed in these Instructions for Use,
should only be made following consultation
with the respective manufacturers. Equipment
malfunction may result as well as risk of
patient injury.

Instructions for Use Oxylog 2000 plus SW 1.n 5

For Your Safety and that of Your Patients

Patient safety Functional safety

The design of the medical device, the accompany- The essential performance of the Oxylog 2000 plus
ing literature, and the labeling on the medical is defined as:
device are based on the assumption that the pur- Accuracy of the delivery of ventilation to the patient
chase and use of the equipment are restricted to or generation of a technical alarm condition.
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.
This publication excludes references to various
hazards which are obvious to a medical profes-
sional and operator of this medical device, to the
consequences of medical device misuse, and to
potentially adverse effects in patients with abnor-
mal conditions.
Medical device modification or misuse can be dan-
gerous.

CAUTION
Have a supply of extra batteries available.

Patient monitoring

The operators of the medical device are responsi-

ble for choosing appropriate safety monitoring that
supplies adequate information on medical device
performance and patient condition.
Patient safety may be achieved through a wide
variety of means ranging from electronic surveil-
lance 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.

6 Instructions for Use Oxylog 2000 plus SW 1.n

 For Your Safety and that of Your Patients

General WARNINGS and CAUTIONS

The following WARNINGS and CAUTIONS apply to WARNING

general operation of the device. WARNINGS and
Keep a manual resuscitation bag available!
CAUTIONS specific to subsystems or particular
features appear with those topics in later sections If a failure is detected in the ventilator and its
of the manual. life-support functions can no longer be guar-
anteed (e.g. in case of a power failure or inter-
ruption in the medical gas supply), ventilation
Note on EMC/ESD risk for the device must be started without delay with an inde-
function pendent ventilation device (resuscitation bag)
– using PEEP and/or increased inspired O2
General information on electromagnetic compatibil- concentration as necessary.
ity (EMC) pursuant to international EMC standard
IEC 60601-1-2: WARNING
Always use officially approved gas cylinders
Electromedical devices are subject to special pre-
and pressure regulators that comply with all
cautionary measures concerning electromagnetic
applicable regulations.
compatibility (EMC) and must be installed and put
into operation in accordance with the EMC informa-
tion. Refer to section "Technical Documentation for WARNING
the Oxylog 2000 plus according to EMC standard For proper ventilation, always consider the
IEC/EN 60601-1-2" on page 113. dead space of the total ventilation circuit when
setting ventilation parameters,
Portable and mobile RF communications equip- especially when applying small tidal volumes.
ment can affect medical electrical equipment.
WARNING
WARNING Ventilation with increased oxygen concentra-
Ventilation monitoring is mandatory at all tions may be harmful to the patient. Oxygen
times! Whenever a patient is connected to the must be administered by medical profession-
ventilator, constant attention by qualified als only.
medical staff is required in order to provide
immediate corrective action in case of a
malfunction. Installing accessories
The operator shall not rely on the built-in
CAUTION
monitoring of the ventilator only and must
always assume full responsibility for proper Installations to the basic device must be done in
ventilation and patient safety in all situations. accordance with the Instructions for Use of the
basic device. Make sure that the connection is
securely fitted onto the basic device system.

Strictly follow the Assembly Instructions and

Instructions for Use.

Instructions for Use Oxylog 2000 plus SW 1.n 7

For Your Safety and that of Your Patients

Instructions for Use only available once

CAUTION
Only one copy of the Instructions for Use is
included in the clinical package and should there-
fore be kept in an accessible location for users.

8 Instructions for Use Oxylog 2000 plus SW 1.n

 Application

Application

Intended use . . . . . . . . . . . . . . . . . . . . . . . . . 10

Indications/Contraindications . . . . . . . . . . . 10

Environment of use . . . . . . . . . . . . . . . . . . . 10

Intended use . . . . . . . . . . . . . . . . . . . . . . . . . 10

Indications/Contraindications . . . . . . . . . . . 10

Environment of use . . . . . . . . . . . . . . . . . . . 10

Instructions for Use Oxylog 2000 plus SW 1.n 9

Application

Intended use

The Oxylog® 2000 plus is a time-cycled, volume

controlled emergency and transport ventilator with
pressure support for patients requiring mandatory
or assisted ventilation with a tidal volume of 100 mL
upwards.
For use by and under the supervision of trained
health care professionals.

Indications/Contraindications

For patients requiring a tidal volume of 100 mL

upwards.
WARNING
The Oxylog 2000 plus ventilator may only be
used under the supervision of qualified medi-
cal personnel in order to be able to provide
immediate corrective action in case of a mal-
function.

Environment of use

For use in the following environments:

– Mobile use for emergency patients, for outdoor WARNING
and indoor environments. Do not use the equipment in hyperbaric
chambers!
– During transport in ambulances or aircraft,
including helicopters. The device may malfunction, causing danger
to the patient.
– In accident and emergency departments.
– When moving ventilated patients around the WARNING
hospital. Do not use the equipment in conjunction with
– In the recovery room. magnetic resonance imaging (MRI, NMR, NMI).
The device may malfunction, causing danger
to the patient.

10 Instructions for Use Oxylog 2000 plus SW 1.n

 System Overview

System Overview

Front panel with all options. . . . . . . . . . . . . 12

Side view, right . . . . . . . . . . . . . . . . . . . . . . . . 13
Rear view . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Reusable hose system . . . . . . . . . . . . . . . . . . 14
Disposable hose system. . . . . . . . . . . . . . . . . 14

Available ventilation modes . . . . . . . . . . . . 14

Special modes . . . . . . . . . . . . . . . . . . . . . . . 15

With monitoring . . . . . . . . . . . . . . . . . . . . . . 15

Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . 16

Symbols. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17

Instructions for Use Oxylog 2000 plus SW 1.n 11

System Overview

Front panel with all options

043
A Screen with screen pages for the specific K Display symbols for the power supply
application Charge status of the internal battery
B Key Alarms for setting and displaying
N Mains power supply connected
alarm limits L Central rotary knob for making selections /
settings and for confirming these
C Key Settings for setting other
ventilation parameters on the screen M Control knob for setting O2 AirMix or 100% O2
FiO2
D Key for ventilation modes VC-CMV / VC-AC
N Control knob for setting the maximum
E Key for ventilation modes VC-SIMV (PS)*
inspiratory pressure Pmax
F Key for ventilation modes SpnCPAP (PS)*
O Control knob for setting the ventilation respira-
G Red and yellow lights (LEDs) as alarm tory rate RR
indicators
P Control knob for setting the tidal volume VT
H Key to suppress the audible alarm for
Q Key Values to select the displayed mea-
2 minutes
sured values
I Key Alarm Reset for acknowledging alarm
R Key Values to select the displayed mea-
messages
sured MVe or VTe values
J Start / Standby key O

* VC-SIMV/PS and SpnCPAP/PS are optional features.

12 Instructions for Use Oxylog 2000 plus SW 1.n

 System Overview

Side view, right Rear view

041

042
A Emergency air intake A Filter cartridge for intake of ambient air

WARNING CAUTION
Do not block the emergency air intake. This Do not block the air intake. This may result in
may result in ventilator malfunction. ventilator malfunction.

B Screw to secure the battery compartment cover B Rating plate

C Gas outlet for flow measuring hoses
D Gas outlet for ventilation hose
E Connector for medical gas hose
F Socket for DC supply
G Window for Infrared Data Association (IrDA)
interface

Instructions for Use Oxylog 2000 plus SW 1.n 13

System Overview

Reusable hose system Disposable hose system

A
B
A
B
E

C D
D
E C
001

002
A Breathing valve A Breathing valve
B Ventilation hose B Ventilation hose
C Flow and pressure measuring hoses C Flow and pressure measuring hoses
D Angled connector D Flow sensor
E Flow sensor E Angled connector

Available ventilation modes

– VC-CMV / VC-AC – SpnCPAP (PS)

Volume Controlled - Controlled Mechanical Continuous Positive Airway Pressure
Ventilation with PEEP. (Optionally with Pressure Support)
Spontaneous breathing with positive airway
Volume Controlled - Assist Control with PEEP.
pressure.
– VC-SIMV (PS)
Volume Controlled - Synchronized Intermittent
Mandatory Ventilation with PEEP
(Optionally with Pressure Support).
Procedure for weaning patients off the ventilator
after they have started spontaneous breathing.

14 Instructions for Use Oxylog 2000 plus SW 1.n

 System Overview

Special modes

In the ventilation mode SpnCPAP, two special

modes are available.

– Apnea Ventilation
To switch over automatically to volume-con-
trolled mandatory ventilation if spontaneous
breathing stops.
– NIV
For mask ventilation to support non-invasive
ventilation of spontaneously breathing patients
with leakage compensation.

With monitoring

– Airway pressure Paw.

– Expiratory minute volume MVe.
– Apnea.
– Respiratory rate: High respiratory rate alarm.

Instructions for Use Oxylog 2000 plus SW 1.n 15

System Overview

Abbreviations

Abbreviation Explanation
Abbreviation Explanation
PS Pressure Support, pressure assisted
bpm Breaths per minute spontaneous breathing
BTPS Body Temperature, Pressure RF Radio Frequency
Saturated
RR Respiratory Rate (frequency)
Measured values referred to the con-
ditions of the patient's lung, body RRapn Respiratory Rate during apnea
temperature 37 oC, airway pressure, ventilation
water-vapor-saturated gas RRsp Spontaneous Respiratory Rate
C Lung compliance Slope Speed of which inspiratory flow is
EN 794-3 European standard for medical reached
ventilators, Part 3 "Emergency and SpnCPAP Continuous Positive Airway
transport ventilators" Pressure
ESD Electrostatic discharge Spontaneous breathing with
continuous positive pressure
∆Psupp Positive pressure above PEEP
Tapn Time for apnea alarm
FiO2 Fraction of inspiratory oxygen
Te Expiratory time
FRC Functional Residual Capacity
Ti Inspiratory time
HME Heat Moisture Exchange
Tplat % Plateau time in % of inspiratory time
I:E Relation inspiratory time to
expiratory time Taw Airway temperature
IrDA Infrared Data Association VC-AC Volume Controlled
Assist Control with PEEP
MVe Total expiratory minute volume
VC-CMV Volume Controlled
MVi Total inspiratory minute volume
Controlled Mandatory Ventilation
MVspon Spontaneous minute volume
VC-SIMV Volume Controlled
NIV Non-invasive ventilation – mask ven-
tilation Synchronized Intermittent
Mandatory Ventilation
O2 AirMix Inspiratory gas mixture of O2 and
ambient air. VTapn Tidal volume during apnea
ventilation
Paw Airway pressure
VT Tidal volume
PEEP Positive end expiratory pressure
VTe Expiratory tidal volume
PIP Peak inspiratory pressure
VTi Inspiratory tidal volume
Pinsp Inspiratory pressure
Pmax Maximum allowed inspiratory
pressure
Pmean Mean airway pressure
Pplat Plateau pressure

16 Instructions for Use Oxylog 2000 plus SW 1.n

 System Overview

Symbols

Symbol Explanation
Symbol Explanation
E4 10 R-02 XXXX
The device complies with UN
Settings Display screen window "Settings" Regulation no. 10, revision 2 with
respect to EMC for use in motor
vehicles.
Alarms Display screen window "Alarms"
IPX4 Device protected from water
sprayed from all directions, limited
Values Display screen window measured entrance allowed.
"Values" Class II equipment, device pro-
Suppress audible alarm for tected against electric shock with
2 minutes additional safety precautions such
as double or reinforced insulations,
Alarm Acknowledge alarms
Reset without protective earthing.
Do not dispose of the device as
Start / Standby key municipal waste.
Manufacturing date
Upper alarm limit only
Manufacturer
Lower alarm limit only
DC input
! Advisory message
Consult the instructions for use.
!! Caution message
Indoor use only
!!! Warning message
Caution, hot surface!
Strictly follow the Instructions for
! Use! Warning, dangerous voltage!
Type BF applied part (body
floating)
Do not open!
Charge status of the internal
battery
N Mains power supply connected Temperature limitations
Battery charge
(example: three quarters full)

Instructions for Use Oxylog 2000 plus SW 1.n 17

 This page intentionally left blank

18 Instructions for Use Oxylog 2000 plus SW 1.n

 Operating Concept

Operating Concept

Switch ON or OFF. . . . . . . . . . . . . . . . . . . . . 20
Switch ON. . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Switch OFF. . . . . . . . . . . . . . . . . . . . . . . . . . . 20

Ventilation controls . . . . . . . . . . . . . . . . . . . 21

Display operating controls . . . . . . . . . . . . . 22

Changing screen pages in the windows . . . . . 23

Screen window structure. . . . . . . . . . . . . . . 23

Switch ON or OFF. . . . . . . . . . . . . . . . . . . . . 20
Switch ON. . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Switch OFF. . . . . . . . . . . . . . . . . . . . . . . . . . . 20

Ventilation controls . . . . . . . . . . . . . . . . . . . 21

Display operating controls . . . . . . . . . . . . . 22

Changing screen pages in the windows . . . . . 23

Screen window structure. . . . . . . . . . . . . . . 23

Instructions for Use Oxylog 2000 plus SW 1.n 19

Operating Concept

Switch ON or OFF

Oxylog 2000 plus

A
B
003

Switch ON

z To switch ON, briefly press the O key (A).

Switch OFF

1 To switch OFF, hold down the O key (A) for

approximately 3 seconds.
2 Press the rotary knob (B) to confirm the switch
OFF process.

20 Instructions for Use Oxylog 2000 plus SW 1.n

 Operating Concept

Ventilation controls

Selecting the ventilation mode

Oxylog 2000 plus

Oxylog 2000 plus

A
C A

C B
B
004

005
A Keys for selecting the ventilation modes: z Press the appropriate ventilation mode key (A)
– VC-CMV / VC-AC for approximately 3 seconds.
– VC-SIMV (optional PS)
Or
– SpnCPAP (optional PS).
1 Press the appropriate ventilation mode key (A).
B Rotary knob.
2 Press the rotary knob (B) to confirm. The
C Ventilation parameter controls
selected ventilation mode will be activated.
– Inspiratory tidal volume VT [mL],
– Ventilation respiratory rate RR [/min], 3 The active ventilation mode is displayed in the
– Maximum inspiratory pressure Pmax [mbar], upper left corner of the display (C).
– O2 AirMix or 100% O2 FiO2.
Refer to the section "Operation" on page 45 for
NOTE additional information on ventilation mode
Different ventilation modes and their parameters setting.
can be set in the display window via the rotary
knob (e.g. Ti, PEEP, ∆Psupp, 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.

Instructions for Use Oxylog 2000 plus SW 1.n 21

Operating Concept

Routine and additional functions keys A key for suppressing the audible alarm for
2 minutes.
Frequently used keys are positioned on the upper
right corner of the front panel: B Alarm Reset key for acknowledging alarm
messages.

Oxylog 2000 plus

A
B
006

Display operating controls

A Values key; to change screen pages in

the "Measured Values" window, to display MVe
or VTe.
B Values key; to change screen pages in
the "Measured values" window, to display the
Oxylog 2000 plus
measured values.

A C C Settings key; to change screen pages in

the "Setting" window, to set other ventilation
B D parameters.
D Alarms key; to change screen pages in
E the "Alarms" window, to set and display the
alarm limits.
007

E Central rotary knob for selecting and confirming

options on the display.

22 Instructions for Use Oxylog 2000 plus SW 1.n

 Operating Concept

Changing screen pages in the windows

To advance to the next page in a screen window:

Settings and Alarms window:
1 Press the Settings key to display the
settings pages.
2 Press the Alarms key to display the
alarms pages.

Screen window structure

Status and alarm messages window

A Ventilation mode.
A Measured MVe / VTe window. B Trigger indicator.
B Status and alarm message window. C Alarm window.
C Measured values window.
D Airway pressure bar graph.
E Settings and alarms window.
F Information window.

Instructions for Use Oxylog 2000 plus SW 1.n 23

Operating Concept

MVe / VTe window To advance to the next page:

z Press the lower Values key.

Airway pressure bar graph

A B

A Parameter measured.
B Measured value.
C D
C Unit of measure.
A Pmax alarm setting.
D Page number.
B Unit of measure scale.

To advance to the next page: C Pressure measurement of the previous breath.

z Press the upper Values key. D Pressure measurement of the current breath.

Values window Alarms window

A Parameter measured. A Menu for alarm limits and alarm parameters.

For detailed operating instructions, see "Setting
B Measured value. alarm limits" on page 63.
C Page number. B Page number.
D Unit of measure. 1st page of 2 available pages.

24 Instructions for Use Oxylog 2000 plus SW 1.n

 Operating Concept

To advance to the next page: Messages window

z Press the Alarms key.

Settings window

A Numeric values displayed when a control knob

is turned.

A Menu for setting supplementary ventilation

parameters in accordance with the desired ven-
tilation mode:
– I:E
– Ti
– PEEP
– ∆Psupp
– Tapn
– Trigger
– Tplat %
– Slope
– NIV
– Brightness
– RRapn
– VTapn
1st page of 2 available pages.
B Page number.

Instructions for Use Oxylog 2000 plus SW 1.n 25

Operating Concept

Battery capacity indicator

A Battery capacity indicator (example: three quar-

ters full).

O2 consumption

A Actual gas consumption based on current

settings.

26 Instructions for Use Oxylog 2000 plus SW 1.n

 Assembly

Assembly

Dead space . . . . . . . . . . . . . . . . . . . . . . . . . . 28

Assemble the reusable hose system . . . . . 29

Breathing valve assembly. . . . . . . . . . . . . . . . 29
When using a bacterial filter or HME . . . . . . . 30
Hose connections . . . . . . . . . . . . . . . . . . . . . . 30

Connect the disposable hose system . . . . 31

When using a bacterial filter or HME . . . . . . . 31
When changing the ventilation hose system . 31

Connecting the power supply . . . . . . . . . . . 32

Internal supply . . . . . . . . . . . . . . . . . . . . . . . . 32
Additional external power supply . . . . . . . . . . 32

Internal supply with rechargeable battery . 32

Replacing the battery . . . . . . . . . . . . . . . . . . . 32
Checking the charge of the battery. . . . . . . . . 32
Installing the battery . . . . . . . . . . . . . . . . . . . . 33
External power supply with DC/DC converter 33
External power supply from mains power (AC/DC
Power pack) . . . . . . . . . . . . . . . . . . . . . . . . . . 33

Connecting the gas supply . . . . . . . . . . . . . 34

Supply from an O2 cylinder . . . . . . . . . . . . . . 35
Supply from a piped medical gas system . . . . 35

Hanging the Oxylog 2000 plus on standard rail

systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36

Instructions for Use Oxylog 2000 plus SW 1.n 27

Assembly

Reusable or disposable hose systems can be used

with Oxylog 2000 plus. Please refer to the "List of
Accessories" section for ordering information.

NOTE
If the type of the hose system used is changed, the
device must be reconfigured. Refer to the
"Configuration" section for additional information.

Dead space

Dead space is an important aspect of ventilation

management:
Dead space ventilation is the portion of the respira-
tory system, in which no significant gas exchange
occurs. An increase of the proportion of dead space
to alveolar ventilation may lead to an increase of
the retention of carbon dioxide by the patient.
Dead space is present as a component of the
patient’s artificial airway and hose system. If the
volume of the mechanical dead space equals or
exceeds the volume of alveolar ventilation, the
patient may not be able to adequately evacuate
carbon dioxide. Therefore, it is important to prop-
erly manage the ventilation perfusion ratio to
ensure effective elimination of carbon dioxide
gases.

28 Instructions for Use Oxylog 2000 plus SW 1.n

 Assembly

Assemble the reusable hose system

– Parts must always be sterilized before use!

Breathing valve assembly

A

A 008

C
WARNING
The rubber disc (A) in the housing may not be
removed, damaged or bent, otherwise the
valve will not work properly and will endanger D
the patient.
Risk of CO2 rebreathing.

009
1 Place the diaphragm (B) in the breathing valve.
Ensure that it is inserted correctly.
2 Fit the cover (A) and turn it approximately 90o
clockwise to secure into position.
3 Push the flow sensor (C) into breathing valve.
Note the preferred position as indicated by the
groove.
4 Connect the angled adaptor (D) to the flow sen-
sor.
WARNING
Always use an angled adaptor. If the angled
adaptor is not used, the minute volume may
be measured incorrectly.

Instructions for Use Oxylog 2000 plus SW 1.n 29

Assembly

When using a bacterial filter or HME

CAUTION
NOTE Do not use electrically conductive hoses!
When using a bacterial filter or HME, measured
Risk of electric shock.
flows may deviate from the expiratory flows, as
temperature and humidity of the gas are reduced. This can endanger the patient.

B
010

z Connect the bacterial filter or HME to the angled

connector.
WARNING
Bacterial filters increase the exhalation resis-
tance and dead space volume of the ventila-
tion system.

Hose connections
012

A
3 Connect the flow measuring (A) hoses to the
Oxylog 2000 plus.
B 4 Connect the ventilation hose (B) to the gas out-
B put on the Oxylog 2000 plus.
011

1 Connect the ventilation hose (A) to the

breathing valve.
2 Connect the flow measuring hoses (B) to the
nozzles on the flow sensor. Note the different
diameters.

30 Instructions for Use Oxylog 2000 plus SW 1.n

 Assembly

Connect the disposable hose system

When using a bacterial filter or HME

WARNING
Do not use disposable hose systems other NOTE
than those on the "List of Accessories". The When using a bacterial filter or HME, measured
minute volume may be measured incorrectly flows may deviate from the expiratory flows, as
and the device may malfunction. temperature and humidity of the gas are reduced.

A B
C

014
z Connect the bacterial filter or HME.
WARNING
Bacterial filters increase the exhalation resis-
tance and dead space volume of the ventila-
tion equipment.
013

When changing the ventilation hose

WARNING system
Ensure that the flow measuring hoses are cor-
rectly positioned, otherwise the volume will be If the reusable ventilation hose system is to be used
measured incorrectly. instead of a disposable hose system or vice versa:
1 Have the nozzles on the device changed by
1 Connect the blue flow measuring hose (B) to trained service specialists.
the blue gas outlet.
2 Reconfigure the device accordingly. Refer to
2 Connect the transparent flow measuring hose the "Customer Service Mode" on page 72 for
(A) to the other gas outlet. additional information.
3 Connect the ventilation hose (C) to the gas out-
let on the Oxylog 2000 plus.

Instructions for Use Oxylog 2000 plus SW 1.n 31

Assembly

Connecting the power supply

The Oxylog 2000 plus is designed to operate on – with AC/DC power pack
power supplies with different voltages.

WARNING
Internal supply A fully charged battery must always be
installed for safety reasons, even when oper-
– With rechargeable battery (specified Smart ating from an external power supply!
Battery, refer to the "Technical Data"
on page 103 for additional information). To have a fully charged battery on hand, refer to the
"Getting started" section on page 38 for additional
information.
Additional external power supply WARNING
Treatment of batteries:
To recharge the battery and to extend the electrical – Do not throw into fire,
operation time. – Do not force open,
– DC voltage from the on-board power supply via Danger of bodily injury.
DC/DC converter or

Internal supply with rechargeable battery

Replacing the battery 1 Loosen the screw (C) on the battery compart-
ment cover (B) counterclockwise to release the
cover.
2 Remove the battery cover.
3 Remove the battery (A) by pulling the tab.

Checking the charge of the battery

A z Press the button on the rechargeable battery.
The charge status is indicated as a percentage
by LEDs.
B

C
015

32 Instructions for Use Oxylog 2000 plus SW 1.n

 Assembly

Installing the battery

1 Insert a fully charged battery into the battery

compartment.
2 Attach the connector at the bottom. 12 V DC
3 Turn the cover upwards. 24 V DC
Oxylog 2000 plus 28 V DC
4 Tighten the screw.
WARNING A
The Oxylog 2000 plus will interrupt ventilation
when the battery is replaced while the device
is switched on and the external power supply B
is not connected. Ventilation will resume with C
the last values settings approximately 3 sec-
onds after inserting the battery.

016
1 Plug the large connector (A) of the DC/DC con-
NOTE
verter into the on-board supply.
It is recommended to use fully charged internal
batteries. 2 Plug the small connector (B) into the DC nozzle
of the Oxylog 2000 plus.
3 When the Oxylog 2000 plus is connected to an
External power supply with external supply, the indicator N (C) lights up
DC/DC converter and displays the internal battery status.

WARNING
Use only a specified DC/DC converter. External power supply from mains
power (AC/DC Power pack)
Otherwise the device can malfunction.
Refer to the "List of Accessories" on page 108 WARNING
for additional information. Use only a specified AC/DC power pack
equipped with a correct mains plug.
The DC/DC converter must be used to connect the
Oxylog 2000 plus to on-board supplies of different Otherwise the device can malfunction.
voltages (12 V, 24 V, 28 V DC). Refer to the "List of Accessories" on page 108
The voltage of the on-board supply may fluctuate, for additional information.
depending on the amount of power required. The
supply voltage may fall below or exceed the range WARNING
permitted by the Oxylog 2000 plus. The on-board The AC/DC power pack may not be used
voltage is converted into a constant DC voltage of outdoors.
approximately 19 V DC by the DC/DC converter:
Risk of electric shock or equipment damage.
– When connected to an external power supply
(e.g. the on-board power supply of the vehicle),
the ventilator must always be connected via the
DC/DC converter, refer to the "List of Accesso-
ries" on page 123 for additional information.

Instructions for Use Oxylog 2000 plus SW 1.n 33

Assembly

1 Connect the mains plug (A) to the mains outlet.

2 Connect the DC plug (B) to the DC outlet on the
Oxylog 2000 plus.
A
O xylog 2000 plus 3 When the Oxylog 2000 plus is connected to an
external supply, the indicator N (C) lights up
and displays the internal battery status.

C
B
017

Connecting the gas supply

Take care when handling O2: WARNING

WARNING Only use medical grade oxygen that is dry and
Secure O2 cylinders so they cannot fall over free from dust and oil.
and keep away from excessive heat.
Contaminated gas can cause device
Risk of explosion! malfunction.

WARNING WARNING
Do not grease or lubricate O2 fittings, such as Always provide adequate ventilation in order
cylinder valves and pressure reducers and do to maintain ambient O2 concentration < 24%,
not handle with greasy hands. to prevent risk of fire.

Risk of fire! WARNING

Always use extreme caution when using oxy-
WARNING gen, to prevent risk of fire.
Operate cylinder valves by hand and rotate
smoothly to prevent the risk of fire or
explosion.
Do not use tools.

WARNING
No smoking or open flames.
O2 is combustible and can intensity fires.

34 Instructions for Use Oxylog 2000 plus SW 1.n

 Assembly

Supply from an O2 cylinder 5 Rotate the cylinder valve (C) slowly and open
fully.
WARNING
Only use compressed gas cylinders and pres- CAUTION
sure reducers, which comply with all applicable
Do not connect flow control valves or flowmeters
regulations and have been approved.
in the gas supply to Oxylog 2000 plus.
1 Use a full O2 cylinder. The ventilator could malfunction!
2Connect the pressure reducer (270 to 600 kPa
WARNING
delivery pressure, 500 kPa nominal pressure)
to the O2 cylinder. Always check the O2 pressure of cylinder
before use, to prevent insufficient oxylog sup-
WARNING
ply during use.
Only use a pressure reducer with a relief valve at
the outlet to limit the delivery pressure to a max-
imum of 1000 kPa in case of a malfunction, to
prevent damage to the ventilator! Supply from a piped medical gas system

A A

C
B
B
O2
019

1 Connect the O2 medical gas hose (A) to the

Oxylog 2000 plus.
018

3 Connect the O2 medical gas hose (A) to the 2 Connect the gas hose (B) to the O2 terminal unit
Oxylog 2000 plus. until the supply of O2 is confirmed.

4 Connect the O2 medical gas hose to the pres-

sure reducer (B).

Instructions for Use Oxylog 2000 plus SW 1.n 35

Assembly

Hanging the Oxylog 2000 plus on standard rail systems

The Oxylog 2000 plus can be hung on various rail

systems measuring up to 35 mm diameter by
means of the claw.
– Ensure that the rail is completely inserted in the
claw.
– To ensure optimal functioning of the claw, a dis-
tance of at least 25 mm between rail and wall is
required.
CAUTION
The Oxylog 2000 plus is only held by its own
weight when hung on a bar or rail. The Oxylog
2000 plus must be secured additionally when
being transported, otherwise vibrations may
cause accidental dislodgement.

36 Instructions for Use Oxylog 2000 plus SW 1.n

 Getting Started

Getting Started

Charging the battery . . . . . . . . . . . . . . . . . . 38

Indication of battery capacity / battery operation 38

Determining the approximate pneumatic oper-

ating time for the Oxylog 2000 plus . . . . . . 39

Checking readiness for operation . . . . . . . 40

Perform device check . . . . . . . . . . . . . . . . . 41

Connect the test lung . . . . . . . . . . . . . . . . . . . 41
Switch ON. . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
Check connections . . . . . . . . . . . . . . . . . . . . . 42
System check . . . . . . . . . . . . . . . . . . . . . . . . . 42
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . 43

Preparation for use after system check . . . 43

Instructions for Use Oxylog 2000 plus SW 1.n 37

Getting Started

Charging the battery

The actual screen display may differ in appearance Indication of battery capacity / battery
or configuration. operation

CAUTION
The ambient temperature must be between
0 and 35 oC when charging the batteries.

When an external supply is available:

Oxylog 2000 plus

The remaining capacity of the battery is indicated
by Oxylog 2000 plus in 25% increments in the lower
right section of the information window when power
is ON:

A – when charging from an external power supply,

– as the battery is discharged during operation.
B
Example: 75% charge
020

1 The green lamp N (B) lights up when the bat- – The accuracy of the battery capacity indicator
tery is actively charging. can vary, depending on the age and condition of
the battery. Refer to "Technical Data"
2 A three colored indicator (A) lights up to on page 103 for additional information.
show the current charge status of the internal
battery: – The capacity indication is overwritten if higher
priority messages are activated.
– Green: when the battery has been fully
charged. – Additional alarms can draw attention to the
remaining operating time of the battery.
– Yellow: while the battery is being charged.
– When operated via the rechargeable battery,
– Red: if a battery has not been inserted or a the brightness of the ventilator screen is
technical failure occurred. reduced in order to save power.
– Indicators (A) and (B) remain off while the – The screen brightness is automatically
ventilator is being operated from the internal increased to maximum for one minute while
battery. settings are being made.

An external battery charging station connected to

the mains supply can be used to charge an extra
battery. Refer to the "List of Accessories"
on page 123 for additional information.

38 Instructions for Use Oxylog 2000 plus SW 1.n

 Getting Started

Determining the approximate pneumatic operating time for the

Oxylog 2000 plus

Example for supply of medical gas: Example:

– Cylinder pressure measured on the pressure
gauge of the pressure reducer: 2000 kPa
– Liquid capacity of the O2 cylinder: 2.1 L
Supply of medical gas:
2.1 L x 2000 kPa = approximately 420 L

Example for pneumatic operation time:

– VC-CMV mode, respiratory rate
10 breaths /min, VT = 1 L, O2 = 100% O2 consumption = 2.1 L/min
– Minute volume = 10 breaths /min x 1 L =
10 L/min

Operation time = Medical gas supply [L]

(MV +0.5*) [L/min]

* Calculated with average gas consumption of

ventilator: 0.5 L/min

Operation time = 420 = approx. 40 minutes

10.5

The pneumatic operation time increases when

Oxylog 2000 plus operates with O2 AirMix, as
ambient air is drawn into the device.
The amount of gas from the high-pressure supply,
which is currently being consumed, is indicated by
the Oxylog 2000 plus in the lower left section of the
information window in L/min. This display is over-
written when a higher priority message is activated.

Instructions for Use Oxylog 2000 plus SW 1.n 39

Getting Started

Checking readiness for operation

– Whenever the ventilator has been serviced or

the ventilation hoses changed.
– At the latest every six months.
The following functions are checked with the menu-
based test:
– Gas supply present.
– Hose system / breathing valve connected and
OK.
– Alarm functions OK.
– Ventilation functions OK.
– Monitor functions OK.
Oxylog 2000 plus interrupts the test if a fault is
detected.
The relevant fault is indicated on the screen.

WARNING
The patient may be endangered if the above
device check is not completed.

40 Instructions for Use Oxylog 2000 plus SW 1.n

 Getting Started

Perform device check

The device check consists of the following steps. Switch ON

– Duration is approximately 3 minutes.

Connect the test lung

Oxylog 2000 plus

A
B

A
B
C

022
1 To switch ON briefly press the O key (B).
The device performs a self-test and the
operator is prompted, on the display, to activate the
021

configuration menu or device check:

1 Connect the angled adapter (A) to the Press rotary knob for device check and
breathing valve. configuration

2 Connect the catheter connector (B), diameter

7 mm, to the angled adapter.
The catheter connector simulates the
resistance of the airways.
3 Connect the test lung (C).

CAUTION
BTPS values of a test lung are not the same as the
screen 6

BTPS values of a patient. The Oxylog 2000 plus

measures and adapts according to BTPS values of
a patient. Therefore, when a test lung is con-
2 Press the rotary knob (A) to confirm, before the
nected, the MVe and VTe indicated on display may
bar is full.
differ from the MVe and VTe that is set by the
operator. 3 Select Device check in the main menu and
confirm.
NOTE:
The device check can be discontinued at any time
by pressing the Alarm Reset key.

Instructions for Use Oxylog 2000 plus SW 1.n 41

Getting Started

Check connections System check

1 Ensure that the gas supply has been

connected.
2 Ensure that the test lung has been connected.

The Oxylog 2000 plus automatically checks if a test

lung has been connected. The device check is Oxylog 2000 plus

aborted if a test lung is not detected within one

minute.
The check is continued when the test lung is
detected.

3 Ensure that the configured hose system has A

been connected, either

023
– the disposable hose system
or 1 Set the controls (A) below the display to the
required values.
– the reusable hose system. The Oxylog 2000 plus successively activates the
4 Confirm the appropriate hose system. The sec- audible and visual alarm signals and prompts the
ond page of the device check appears. operator to acknowledge each signal.
2 Confirm the audible and visual alarm signals.
If the wrong hose system has been configured: The device check continues automatically.
1 Press the Alarm Reset key to cancel the device During the automatic test sequence, the Oxylog
check. 2000 plus checks the flow, pressure levels and
alarm signals. Corresponding sounds are heard.
2 Select the correct hose system. Refer to "Select The bar graph shows the progress made by the
hose type" on page 74. check.
3 Restart the device check. The result is displayed on the Oxylog 2000 plus.
3 Confirm. The system returns to the menu
screen.
A monthly check of the power failure alarm is
recommended.
1 Disconnect the external power supply.
2 Remove the battery to activate the audible
alarm signal.
3 Listen for the audible alarm.
NOTE:
Contact DrägerService if no alarm is heard.
4 When the power failure alarm test is completed,
reinstall the battery into the battery compart-
ment of the Oxylog 2000 plus.

42 Instructions for Use Oxylog 2000 plus SW 1.n

 Getting Started

Troubleshooting 3 Contact your local DrägerService for support.

WARNING
The ventilator is ready for operation only after
all functional tests have been successfully per-
formed.

If the device check is not completed successfully:

1 Refer to "Error messages during the device
check" on page 85 of the section "Problem
Solving".
2 Check the configuration, please refer to the
"Operation" section.

Preparation for use after system check

1 Assemble the Oxylog 2000 plus for

operation. Refer to the "Assembly" section.
2 Connect to the power supply and gas supply.
Refer to the "Connecting the power supply"
section.
3 Start the ventilator:
z Select Ventilation from the device check
and confirm.
Or
z Press the Alarm Reset key.

Instructions for Use Oxylog 2000 plus SW 1.n 43

 This page intentionally left blank

44 Instructions for Use Oxylog 2000 plus SW 1.n

 Operation

Operation

Starting operation. . . . . . . . . . . . . . . . . . . . . 46
Switch ON. . . . . . . . . . . . . . . . . . . . . . . . . . . . 46

Preparing ventilation mode . . . . . . . . . . . . . 47

To activate the ventilation mode . . . . . . . . . . . 47
Set ventilation parameters . . . . . . . . . . . . . . . 47

VC-CMV / VC-AC . . . . . . . . . . . . . . . . . . . . . . 48
Trigger (VC-AC) . . . . . . . . . . . . . . . . . . . . . . . 49
For heart-lung resuscitation . . . . . . . . . . . . . . 49

VC-SIMV (optional PS) . . . . . . . . . . . . . . . . . 50

Pressure support (optional) . . . . . . . . . . . . . . 51

SpnCPAP (optional PS) . . . . . . . . . . . . . . . . 52

Apnea ventilation . . . . . . . . . . . . . . . . . . . . . . 52
Pressure support (optional) . . . . . . . . . . . . . . 53
NIV – Non-invasive ventilation Mask ventilation
(optional). . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54

O2 AirMix or 100% O2 . . . . . . . . . . . . . . . . . 55

Calibration. . . . . . . . . . . . . . . . . . . . . . . . . . . 56

Screen brightness . . . . . . . . . . . . . . . . . . . . 56

Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . 57

Instructions for Use Oxylog 2000 plus SW 1.n 45

Operation

Starting operation

The actual screen display may differ in appearance

or configuration.

WARNING
Only use a ventilator that has been cleaned
and successfully tested for operation, to pre-
vent a health risk for the patient and user.

Switch ON

screen 6
Upon completion of the self-test, the ventilator
automatically begins ventilation with the default
settings.
The opening display with configured settings is
displayed if the central rotary knob is not pressed.
Oxylog 2000 plus

A
024

z Briefly press the O key (A).

The Oxylog 2000 plus performs a self-test.
The manufacturer's default settings are:
– The sef-test will be completed in approxi-
mately six seconds. – Ventilation mode VC-CMV.

During the self-test, the system briefly displays the – Ventilation time ratio I:E = 1:1.5.
starting page with the software version and a – Positive end expiratory pressure
prompt for the operator to select the configuration PEEP = 5 mbar.
menu, or to activate the device check by pressing
the rotary knob. – Plateau time Tplat % = 0%.

The bar graph indicates the progress of the self- – Trigger = OFF.
test. The manufacturer's default settings can be
adjusted in Customer Service Mode. Refer to the
"Set startup settings" section.

46 Instructions for Use Oxylog 2000 plus SW 1.n

 Operation

Preparing ventilation mode

To activate the ventilation mode

1 Press and hold the ventilation mode key for

approximately 3 seconds.
Or
2 Press the ventilation mode key and confirm by
pressing the rotary knob.
The new ventilation mode selected is now effective.

Set ventilation parameters

1 Set the required control below the display.

Or
2 Select, set and confirm a parameter on the
display with the rotary knob.
The former settings are retained if confirmation is
not received within 15 seconds. Attention is drawn
to this fact by the advisory message ! Settings not
confirmed.
screen 7

When the PEEP-setting is increased above 10

mbar, a message Confirm PEEP above 10 mbar?
will appear to request confirmation of the change.
The PEEP setting can be increased to the desired
testting after the message is acknowledged with
the rotary knob.

Instructions for Use Oxylog 2000 plus SW 1.n 47

Operation

VC-CMV / VC-AC

The following can be set on the display:

Paw
Plateau time
Tplat

Pmax
P plat

PEEP

t
Tinsp Te

screen 3
1
RR
Flow – Positive end expiratory pressure PEEP.
Insp. Flow
– Ventilation time ratio I:E.

t – Plateau time Tplat %, in % of the inspiration

time.
When setting the ventilation respiratory rate RR,
tidal volume VT or ventilation time ratio I:E, the
025

VC-CMV – Volume Controlled - Controlled Mecha- associated values for inspiration time Ti and
nical Ventilation. inspiration flow are automatically displayed in the
information window.
Volume-controlled ventilation with fixed mandatory
minute volume MV, set with tidal volume VT and
respiratory rate RR.
WARNING
Only use VC-CMV for patients who are not
spontaneously breathing.
Otherwise, the patient may be put at risk by not
receiving sufficient ventilation.
Use VC-AC for patients with partial
spontaneous breathing.

Set the ventilation pattern with the controls below

the display:
– Tidal volume VT.
– Ventilation respiratory rate RR.
(minimum possible respiratory rate: 5 per min).
– Maximum airway pressure Pmax.
– O2 setting, O2 AirMix or 100% O2 FiO2.

48 Instructions for Use Oxylog 2000 plus SW 1.n

 Operation

Trigger (VC-AC) Activating/setting the trigger

NOTE
If in VC-CMV the trigger is set »on«, the ventilation
mode changes into VC-AC.
Refer to the previous section.

VC-AC – Volume Controlled - Assist Control Oxylog 2000 plus

For synchronisation with the patient's spontaneous

breathing efforts. A
The mandatory ventilation strokes are synchro-
nized with the patient's spontaneous breathing
efforts when the trigger is activated and the trigger
sensitivity is set.

026
The actual respiratory rate may be higher than the
set ventilation respiratory rate RR in this case. 1 Press the key Settings (A) until the trig-
The trigger can be deactivated if synchronisation ger parameter is displayed.
with the patient's spontaneous breathing efforts is 2 Select the line Trigger on the display and then
not desired. set and confirm the value with the rotary knob.
Successful patient triggering is briefly indicated by Small value = high sensitivity.
an asterisk (*) in the middle of the status and alarm The ventilation mode VC-AC is shown on the dis-
message window. play.

Deactivate trigger
1 Set a value less than 3 L/min or greater than
15 L/min (off is displayed instead of a value).
2 Press the rotary knob to confirm.
The last effective trigger value is adopted by the
ventilator when changing from VC-AC to
SpnCPAP.

For heart-lung resuscitation

During heart-lung resuscitation, the airway pres-

sure Paw is limited to the set Pmax value by the
Oxylog 2000 plus, without ending inspiration
prematurely (pressure-limited, nonconstant-vol-
ume ventilation when Pmax is reached).
If Pmax is set to a higher value, a higher minute
volume is possible.

Instructions for Use Oxylog 2000 plus SW 1.n 49

Operation

VC-SIMV (optional PS)

The following are set on the display:

Paw Pressure
support PS

P max rapid slow

rise time rise time
PEEP

t
Trigger window
Ti

screen 9
1
Flow RR
– Inspiration time Ti.
Insp. Flow
– Plateau time Tplat %, in % of the inspiration
t time.
– Positive end expiratory pressure PEEP.
027

Volume Controlled - Synchronized Intermittent

Mandatory Ventilation
For patients with inadequate spontaneous breath-
ing, or for patients who are to be weaned gradually.
Fixed mandatory minute volume MV is set with tidal
volume VT and ventilation respiratory rate RR. The
patient can breathe spontaneously between the
mandatory ventilation strokes and thus contribute
screen 10

to the total minute volume. Spontaneous breathing

can be assisted with PS.
– Sensitivity Trigger.
Set the ventilation pattern with the controls below
the display: Successful patient triggering is indicated by an
asterisk (*) in the center of the status and alarm
– Tidal volume VT.
message window.
– Respiratory Rate RR.
When setting the ventilation respiratory rate RR,
(minimum possible respiratory rate: 2 per min).
tidal volume VT or inspiration time Ti, the associ-
– Maximum airway pressure Pmax. ated values for inspiration flow time ratio I:E are
automatically displayed in the information window.
– O2 setting FiO2.

50 Instructions for Use Oxylog 2000 plus SW 1.n

 Operation

Pressure support (optional)

The following can also be set on the display for

VC-SIMV / PS:

screen 26

– Setting on page 1: Pressure support ∆Psupp

above PEEP.
– Setting on page 2: Pressure rise time Slope
steep slope = short pressure rise time
flat slope = long pressure rise time.

Instructions for Use Oxylog 2000 plus SW 1.n 51

Operation

SpnCPAP (optional PS)

Apnea back-up ventilation is only applicable when

using the SpnCPAP mode. In the event of an
Continuous Positive Airway Pressure
apnea, the ventilator will automatically activate
WARNING volume-controlled mandatory ventilation
Only use SpnCPAP for patients with sufficient (VC-CMV).
spontaneous breathing.
When an apnea occurs, the device simultaneously
Otherwise there is a risk of the patient issues an alarm signal and switches to volume con-
receiving insufficient ventilation. trolled ventilation with the parameters respiratory
rate RRapn, tidal volume VTapn, and the maxi-
Spontaneous breathing can optionally be assisted mum airway pressure Pmax when the apnea time
with PS and NIV. Tapn has been reached. The ventilation time ratio
I:E is set to 1:1.5. The plateau time Tplat % is 0.
The patient can breathe spontaneously during
Set the ventilation pattern with the controls below apnea ventilation. The mandatory frequency
the display: RRapn remains constant.
– Maximum airway pressure Pmax.
– O2 setting FiO2. Setting apnea ventilation

Apnea ventilation

Paw Oxylog 2000 plus

Pmax
A

t
Apnea alarm time 1 C B
Tapn RR
Start
030

Flow apnea ventilation

with apnea alarm On the display:
1 Press the Settings key (A) until
t page 2/3 appears.
2 Set Tapn with the rotary knob (B) to a value
between 15 and 60 seconds.
029US

52 Instructions for Use Oxylog 2000 plus SW 1.n

 Operation

The parameters RRapn and VTapn, which are Pressure support (optional)
required for setting apnea ventilation, are now
displayed: The following can additionally be set on the display
for SpnCPAP / PS:

screen 13

screen 12
3 Set RRapn and VTapn.
– Sensitivity Trigger (for synchronization with the
4 Set Pmax. This determines the maximum air- patient's spontaneous breathing efforts).
way pressure allowed during apnea ventilation. Successful patient triggering is briefly indicated
The ventilation time ratio I:E = 1:1.5 and the plateau by an asterisk (*) in the middle of the status
time Tplat % = 0 are preset during apnea alarm messages window.
ventilation. – Pressure support ∆Psupp above PEEP.
– Pressure rise time Slope (for pressure
To switch apnea ventilation OFF support ∆Psupp).
z Set Tapn to OFF.

To end apnea ventilation

z Press the Alarm Reset key.
The ventilator resumes ventilating with the original
mode and parameter settings.

The manufacturer default settings are:

– RRapn = 12 /min
– VTapn = 500 mL
These default settings can be configured.
Refer to the "Customer Service Mode" section for
additional information.
NOTE
Apnea ventilation can only be activated in
the ventilation mode SpnCPAP without NIV.
The minimum ventilation required by the patient
must be monitored via the lower alarm limit
MV .

Instructions for Use Oxylog 2000 plus SW 1.n 53

Operation

NIV – Non-invasive ventilation – The supplement NIV appears in the upper

Mask ventilation (optional) section of the display.

NIV can only be activated as a supplementary

function in the pressure-controlled ventilation
modes SpnCPAP and SpnCPAP / PS. Mask leak-
ages are detected by the device, compensated and
included in the measured values for VTe and MVe.
WARNING
If NIV is not activated, measured values for VTe
and MVe will be inconsistent if there are

screen 14
leakages during ventilation.

Oxylog 2000 plus automatically adjusts to the

Use of NIV requirements of mask ventilation. Leakage flows
are compensated automatically and the leakage
WARNING alarm is inactive.
Dead space increases when using masks. WARNING
Note the mask manufacturer's instructions!
Set the lower alarm limit MV according to
the minimum ventilation required for the
WARNING
patient.
Application mode NIV may not be activated
with intubated patients! Otherwise, there is a risk of the patient
receiving insufficient ventilation.
Risk of undetected leaks and inadequate ven-
tilation! Apnea ventilation is not permitted by the ventilator
when NIV is active.
WARNING
Check MV alarm limits after deactivating NIV
mode!

WARNING
Avoid high airway pressure.
Risk of aspiration!

To switch on NIV
1 Press the Settings key until display page
2/3 appears.
2 Activate the line NIV off.
3 Select NIV on and confirm.

54 Instructions for Use Oxylog 2000 plus SW 1.n

 Operation

O2 AirMix or 100% O2

The FiO2 concentration can be set to O2 AirMix or

100% O2, regardless of the ventilation mode.
O2 (%)
When set to O2 AirMix the injector principle of the
Oxylog 2000 plus will draw in ambient air, to realize
85 (%)
an FiO2 concentration of approximately 40%.
However, the O2 concentration, which can be
40
realized depends on the mean airway pressure and
the inspiratory flow. The O2 concentration can 20
Flow
(L/min.)
never be lower than 40%. This is shown in the fol- 0 15 30 100
O 2 = f(Flow, Paw)
lowing graphics:

033
O2 (%) O2 concentration which can be realized at a Pmean
of 30 mbar.
80 (%)

O2 (%)
40

20
Flow
93 (%)
0 3 40 100 (L/min.)
O2 = f(Flow, Paw)
031

O2 concentration which can be realized at a Pmean 40

of 5 mbar. 20
Flow
0 20 100 (L/min.)
O2 = f(Flow, Paw)

031
O2 (%)
O2 concentration which can be realized at a Pmean
of 60 mbar.
82 (%)
The O2 concentration is a calculated value. It is not
measured by an internal O2 sensor.
40
When the O2 concentration has been set, the value
Flow
20 will be displayed after approximately 30 seconds.
0 10 35 100 (L/min.)
O2 = f(Flow, Paw)
WARNING
032

In toxic surroundings:
O2 concentration which can be realized at a Pmean – The patient must be ventilated with 100%
of 15 mbar. O2 so that toxic constituents do not enter
into the breathing gas.
– The patient must be immediately trans-
ferred to a breathable atmosphere in order
to prevent inhalation of toxic air when
spontaneous breathing resumes.

Instructions for Use Oxylog 2000 plus SW 1.n 55

Operation

Calibration

The pressure and flow sensors are automatically The saved calibration values are retained even
calibrated by the device at regular intervals without when the device is switched OFF.
interrupting ventilation.

Screen brightness

The screen brightness levels can be set on the last – The setting Brightness is active during
page of the Settings menu, from level 1/4 to 4/4: battery operation, when no controls have been
set for a period longer than one minute.
– The setting Brightness is active in both
mains and battery operation when adjusting the
settings on the ventilator.

Volume loudness

The volume loudness level can be set on the last

page of the Alarms menu, from level 1/4 to 4/4.

56 Instructions for Use Oxylog 2000 plus SW 1.n

 Operation

Shutdown

– After disconnecting the patient

Switch the ventilator OFF:

Oxylog 2000 plus

B A
035

1 Press the key O (A) for approximately

3 seconds. The yellow lamp flashes and
ventilation is terminated by the device.
2 Press the rotary knob (B) to acknowledge the
alarm !!! Confirm device OFF with rotary
knob.

When O2 is supplied from a cylinder:

3 Close the cylinder valve.
WARNING
The cylinder valve must be closed completely
to avoid gas flow leakage by the device.

When medical gas is supplied from the pipeline

system:
4 Disconnect the high pressure connection from
the source.

Instructions for Use Oxylog 2000 plus SW 1.n 57

 This page intentionally left blank

58 Instructions for Use Oxylog 2000 plus SW 1.n

 Alarms

Alarms

Types of alarms . . . . . . . . . . . . . . . . . . . . . . 60

In the event of an alarm . . . . . . . . . . . . . . . . 61

Setting alarm limits . . . . . . . . . . . . . . . . . . . 63

Instructions for Use Oxylog 2000 plus SW 1.n 59

Alarms

Types of alarms

The actual screen display may differ in appearance Caution

or configuration.
An alarm of medium priority.
z The alarm LED (A) flashes yellow.
Oxylog 2000 plus assigns a priority to the alarm Caution messages are highlighted by two exclama-
message. This message highlights the text with the tion marks.
appropriate number of exclamation marks and
generates different tone sequences for the respec- Example: !! No int. battery ?
tive alarms. Oxylog 2000 plus generates a three-tone
!!! = Warning sequence, which is repeated approximately every
!! = Caution 20 seconds.
! = Advisory
Refer to the list "Alarm – Cause – Remedy" on
page 79 for information on how to remedy the Advisory
faults. An alarm of low priority.
z The yellow alarm LED (A) lights up.
Advisory messages are identified by one exclama-
tion mark.

Example:
A
Oxylog 2000 plus
! Settings not confirmed
Low-priority alarm.
B The Oxylog 2000 plus generates a two-tone alarm
sequence, which sounds only once.
036

Warning
An alarm with high priority
z The alarm LED (A) flashes in red.
Warnings are highlighted by three exclamation
marks and displayed in inverted form (B).

Example: !!! Apnea

The Oxylog 2000 plus generates a sequence of five
tones, which sound twice and are repeated appro-
ximately every 7 seconds.

60 Instructions for Use Oxylog 2000 plus SW 1.n

 Alarms

In the event of an alarm

Oxylog 2000 plus

Oxylog 2000 plus
A A
C B

038
037

z The LED (A) flashes red or yellow. 1 Press the key (A).
Or The yellow LED lights up and all alarm tones are
z The alarm message appears on the right of the suppressed for approximately 2 minutes.
status and alarm message window (C). Alarm tones are resumed by the device after
these 2 minutes.
CAUTION
When the fault has been remedied the alarm tone
To be notified of new audible alarms, the
is cancelled.
2 minutes alarm silence must be reset.
Alarms which have been remedied remain on the
display and can be acknowledged (reset):
NOTE
1 Press the Alarm Reset key (B).
The alarm message is removed from the The loudness of alarm tones can be adjusted.
display. Refer to section "Volume loudness" on page 56.
Every alarm which has been remedied, but not
If alarm tones are to be heard again before the
acknowledged, will be overwritten by a new alarm
2 minutes have expired:
or advisory message.
2 Press the key (A) again and its LED goes
out.
Suppress alarm tones
WARNING
Check the display regularly for alarm mes-
sages when the alarm tones are silenced.
Otherwise, alarms can be missed.

NOTE
Alarm tones are suppressed for a maximum of
2 minutes.

Instructions for Use Oxylog 2000 plus SW 1.n 61

Alarms

In the event of a gas failure

CAUTION
In the event of a gas failure, the Oxylog 2000 plus
cannot continue ventilation and issues the alarm
!! Supply pressure low.

Immediately start ventilating the patient with an

independent manual ventilation device (resuscita-
tion bag) using PEEP and/or increased inspiratory
oxygen concentration where appropriate.

In the event of an internal power failure

WARNING
In the event of an internal power failure, auto-
matic ventilation, volume measurement and
alarms do not operate!

An audible alarm goes off to indicate the inter-

nal power failure.

Spontaneous breathing can continue through

the emergency air intake.

Immediately start ventilating the patient with

an independent manual ventilation device
(resuscitation bag) using PEEP and/or
increased inspiratory oxygen concentration
where appropriate.

62 Instructions for Use Oxylog 2000 plus SW 1.n

 Alarms

Setting alarm limits

CAUTION To set alarm limits for MV and RRsp

Set alarm values carefully. 2 Press the key Alarms (A).
Extreme alarm values can render the alarm Display example Alarms screen with variable
system useless. alarm limits.
= lower alarm limit.
= upper alarm limit.
Upper alarm limit for Paw
Pressure limitation with Pmax
Alarm Range
Regardless of the set ventilation mode, the airway
MV 2 to 41 L/min
pressure is controlled by the ventilator and limited
to the set maximum inspiratory pressure Pmax. MV 0.5 to 40 L/min
Pmax appears in the pressure bar graph as a RRsp 10 to 100 /min
dashed line.
When this dashed line is reached, Oxylog 2000
Example: Setting the upper alarm limit for MV.
plus issues a !!! Paw high alarm. The volume-con-
trolled stroke is terminated (ventilation with noncon- 1 Select and activate the line MV on the dis-
stant volume). play.
2 Set and confirm the value.
WARNING
Set the lower alarm limit MV according to
the minimum ventilation required for the
patient.
Oxylog 2000 plus

Otherwise, there is a risk of the patient

receiving insufficient ventilation.
A

B
039

1 Set the maximum airway pressure Pmax via the

Pmax control (B).
The airway pressure is limited when Pmax is rea-
ched; inspiration will not be terminated prematurely.

Lower alarm limit for Paw

A lower alarm limit need not be set for the airway
pressure Paw. Oxylog 2000 plus automatically
generates an alarm when it no longer detects a
pressure difference of more than 5 mbar between
inspiratory and expiratory pressure.

Instructions for Use Oxylog 2000 plus SW 1.n 63

Alarms

Setting alarm limits automatically

WARNING
After using the function Auto alarm limits:
check if the new alarm limits are appropriate
for the patient.
Risk of hypoventilation.

The function Auto alarm limits sets the alarm

limits on the basis of the following actual measured
values at the time of activation:
MV : Measured value MV +2 L/min
MV : Measured value MV –2 L/min
RRsp : Measured value RRsp +5/min, with a
minimum of 10/min.
This automatic selection of alarm limits is perfor-
med only once, when confirmed, via the rotary
knob. The alarm limits refer to the current measu-
red values for MV and RRsp.

64 Instructions for Use Oxylog 2000 plus SW 1.n

 Monitoring

Monitoring

Displaying the airway pressure. . . . . . . . . . 66

Displaying MVe and VTe . . . . . . . . . . . . . . . 66

Displaying O2 values . . . . . . . . . . . . . . . . . . 66

Displaying other measured values . . . . . . . 67

Instructions for Use Oxylog 2000 plus SW 1.n 65

Monitoring

Displaying the airway pressure

The actual screen display may differ in appearance

or configuration.
The airway pressure is displayed in a bar graph
indicator on the display.
Refer to the "Operating concept" section on
page 24 for additional information.

Displaying MVe and VTe

MVe and VTe are displayed in the measured MVe / To switch between the values:
VTe window.
z Press the upper Values key: the next
Refer to the "Operating concept" section on value is displayed on the screen.
page 24 for additional information.

Displaying O2 values

The O2 concentration can be displayed in the mea-

sured values window.
NOTE
This value is a calculated value, based on the
measured air intake and total flow. It is not based
on a measurement by an O2 sensor!

When the O2 AirMix – 100% O2 switch has been

changed, the calculated value will be updated after
approximately 30 seconds.
Refer to "Values window" on page 24 for additional
information.

66 Instructions for Use Oxylog 2000 plus SW 1.n

 Monitoring

Displaying other measured values

Additional measured values are displayed in the

measured values window.
Refer to the "Operating concept" section on
page 24 for additional information.

To switch between the values:

z Press the lower Values key: the next
value is displayed on the screen.
In the values window five different values can be
displayed.
These five values can be selected out of eight
measured values options, in any desired order.
Refer to "Abbreviations" on page 16. These options
are:
– O2
– RR
– RRsp
– PEEP
– Pmean
– PIP
– Pplat
– MVespon

The five values displayed in the measured values

window can be configured in the customer service
mode. Refer to the "Set the measured values dis-
play window" on page 75 for additional information.

Instructions for Use Oxylog 2000 plus SW 1.n 67

 This page intentionally left blank

68 Instructions for Use Oxylog 2000 plus SW 1.n

 Configuration

Configuration

Set configuration parameters / display informa-

tion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70

Displaying configuration and information . 71

Set language . . . . . . . . . . . . . . . . . . . . . . . . . 71
Display the battery type . . . . . . . . . . . . . . . . . 71

Customer Service Mode. . . . . . . . . . . . . . . . 72

To enter customer service mode . . . . . . . . . . 73
Set startup settings. . . . . . . . . . . . . . . . . . . . . 74
Exit customer service mode . . . . . . . . . . . . . . 78

Instructions for Use Oxylog 2000 plus SW 1.n 69

Configuration

Set configuration parameters / display information

The actual screen display may differ in appearance

or configuration.

1 Switch the Oxylog 2000 plus ON. Press the O

key.
The device performs a self-test and the
operator is prompted to enter the configuration
menu or device check:
Press rotary knob for device check and con-
figuration.
2 Press the rotary knob and confirm.
The main menu is then displayed:
screen 15

Select and confirm Configuration and informa-

tion.

70 Instructions for Use Oxylog 2000 plus SW 1.n

 Configuration

Displaying configuration and information

– The settings made via the "Configuration" are 3 Select the language and confirm.
retained after the ventilator is switched OFF. The new language selected is effective
immediately.
– Configuration can be cancelled by pressing the
Alarm reset key or by startup of ventilation.
The following settings can be made for the applica-
tion concerned via Configuration and informa-
tion:
– Language

screen 16
The following ventilator data can be displayed via
Configuration and information:
– Identification No. (Device-ID)
– Total hours of operation (Working hours)
Display the battery type

– Hours of operation since the last inspection and z Press the key Settings to select the
maintenance (Hours since service time) menu Configuration and information 2/2 .
– Battery type and battery capacity. The performance data of the inserted battery
are displayed on the device.
screen 16

screen 17

3 Select and confirm Configuration and infor-

mation.

Set language

1 Press the key Settings to select the

menu Configuration and information 1/2 .
2 Select and activate the line Language.

Instructions for Use Oxylog 2000 plus SW 1.n 71

Configuration

Customer Service Mode

WARNING
Ventilation is not possible in customer service
mode.

In customer service mode, the ventilator performs

function tests, outputs status information and
permits configuration of parameter settings.
Displays in customer service mode appear in Eng-
lish and cannot be changed to any other language.
001 Set startup settings. Configure start-up settings, restore manufacturer's
default settings.
002 Select hose type. Determine which ventilation hose system is used
(reusable or disposable hose system).
003 Set date and time Set date and time.
(Greenwich Mean Time GMT).
004 Set measured values display window. Configure the layout of measured values in the measured
values window or restore manufacturer's default settings.
005 Enter activation code. Enter the activation code for options.
006 Test buttons and potentiometer. Check for correct functioning of keys and controls.
007 Test loudspeaker, buzzer, LEDs and Check for correct functioning of loudspeaker, buzzer,
display. LEDs and display.
008 Display accu and supply data. Display battery data and condition of the supply voltage.
009 Display actual technical errors. Display any active technical errors.
010 Display error and info logbook. Calibration logbook and technical errors in chronological
order.
011 Display settings logbook. Logbook of operating phases and ventilator settings.
012 Display language text. Display screen texts in two selectable languages.

72 Instructions for Use Oxylog 2000 plus SW 1.n

 Configuration

To enter customer service mode Settings in customer service mode

1 Select the required function with the cursor

(asterisk).
– To select the parameter: turn the rotary
knob.
Oxylog 2000 plus
– To activate the parameter: press the rotary
knob.
A – To set the value: turn the rotary knob.
B
– To confirm the value: press the rotary knob.

C D
E 040
To exit the parameter settings menu

1 Turn controls (C) and (D) VT and RR all the way

to the right.
2 Switch ON (E) the device (briefly press O key)
and simultaneously press and hold the Values
key (A) and the Values key (B) until
the main Customer Service Mode menu
appears.
3 Set the number of the required test in the main

screen 19
menu with the central rotary knob.

1 Select the line EXIT.

2 Press the rotary knob and confirm.
The set values are saved and remain effective
whenever ventilation is started after switching
ON.
11737170.tiff

4 Activate test = press rotary knob.

Instructions for Use Oxylog 2000 plus SW 1.n 73

Configuration

Set startup settings

Advance to the second page:
Range of the settings: 1 Select the line Page, confirm and turn rotary
Parameter Range knob.
Trigger 0 (OFF) 3 to 15 L/min
PEEP 0 to 20 mbar
I:E 3:1 to 1:4
Ti 0.2 to 10.0 s
Tplat % 0 to 50%
∆Psupp 0 to 35 mbar
Slope SLOW, STANDARD, FAST
NIV ON, OFF
Tapn 0 (OFF), 15 to 60 s

screen 21
VTapn 50 to 2000 mL
RRapn 12 to 60 bpm
MV-high 2.0 to 41 L/min To restore the manufacturer's defaults:
MV-low 0.5 to 40 L/min
2 Select and confirm line Set factory default.
RR 10 to 100 bpm
Loudness 1/4 to 4/4
Brightness 1/4 to 4/4 Select hose type

The default settings for the parameters are dis-

played on the screen when the ventilator is
switched ON. The settings can be adjusted.

screen 24

The type of ventilation hose (reusable or

disposable hose system) can be configured.
The gas output sockets for the flow measuring
screen 20

hoses must correspond to the hose type system

selected.

74 Instructions for Use Oxylog 2000 plus SW 1.n

 Configuration

Set date and time

The date and time can be set. NOTE
It is recommended that you have the O2 value as
a displayed value.

To define the five values to be displayed:

z Start configuration on page 1/5 and continue
through to 5/5.

Enter activation code

10237170
1 Set the current date and time with the positions
Year, Month, Day, Hour and Minute and confirm.
2 The date and time can be confirmed with »Set«.

Set the measured values display window

In the measured values window five different
values can be displayed.

The activation codes for options can be entered.

The activated options are then displayed.

Test buttons and potentiometer

screen 32

These five values can be selected out of a total of

eight measured values, in any desired order.
These are:
– O2
screen 25

– RR
– RRsp The operating elements on the front panel are dis-
played schematically on the screen.
– PEEP
– Display = screen
– Pmean
– B = buttons
– PIP
– Pplat
– MVespon

Instructions for Use Oxylog 2000 plus SW 1.n 75

Configuration

The selected test remains active until the rotary

Set the controls accordingly for the test: knob is pressed again.
– VT to 500 mL
Display accu (battery) and supply data
– RR to 20 /min
The parameters of the replaceable battery and the
– Pmax to 40 mbar
status of the external power supply are displayed.
– FiO2 to O2 AirMix
Display (example):

These settings are displayed on the screen.

To test the buttons:
1 Briefly press the corresponding button.
The associated letter on the screen changes
from "B" to "X". If the button has an LED, it will
be illuminated by the device. If there are buttons
without LED, the yellow warning LED will light
up on the device. fd

2 Briefly press the O key. 1 Advance to the second page:

The ventilator switches OFF if it is pressed for
longer than 3 seconds. 2 Select the line Page, confirm and turn rotary
knob.
The function of the rotary knob is not included in the
test. Display (example):

Test loudspeaker, buzzer, LEDs and display

To test the loudspeaker, buzzer, all LEDs and the
display:
1 Select the required test

2 Start the test. Each function is tested by the

device.
To test the screen display (Test display):
3 Turn the rotary knob; various test cards are dis-
played.

76 Instructions for Use Oxylog 2000 plus SW 1.n

 Configuration

Display actual technical error Display settings logbook

Momentarily active technical errors are displayed
with the error number and a brief description.
Display (example):

screen 24
The operating phases with ventilator settings and
time are listed in chronological order.

Advance to the next page:

Display error and info logbook
z Select line Page, confirm and turn the rotary
Any technical errors and/or special occurrences, knob.
such as activation of a software option, completion
of the device check and device calibration, are
listed in chronological order. Display language text
Display (example):

10137170
Alarm messages and advisory messages are
Advance to the next page: displayed by the ventilator in the selected display
languages – one text per page.
z Select line Page, confirm and turn the rotary
knob. Advance to the next page:
1 Select line Page, confirm and turn the rotary
knob.

Choose another language:

2 Select line Language 1 or Language 2, confirm
and turn the rotary knob.

Instructions for Use Oxylog 2000 plus SW 1.n 77

Configuration

Exit customer service mode

1 Press the key O for approximately

3 seconds; the LED flashes yellow.

To switch ventilation ON:

2 Briefly press the key O.

To switch OFF:
3 Press the rotary knob.

78 Instructions for Use Oxylog 2000 plus SW 1.n

 Problem Solving

Problem Solving

Alarm - Cause - Remedy . . . . . . . . . . . . . . . 80

Messages in the information window. . . . . 84

Error messages during the device check . 85

Instructions for Use Oxylog 2000 plus SW 1.n 79

Problem Solving

Alarm - Cause - Remedy

Oxylog 2000 plus classifies alarm messages In the following table, the alarm messages are
according to three priority levels and identifies listed in alphabetical order. If an alarm occurs, the
these accordingly with the aid of exclamation table helps to identify causes and remedies. The
marks: different causes and remedies should be worked
through in the order listed until the cause of the
alarm has been resolved.
Warning !!! High priority alarm message
When multiple alarms occur, they are displayed
Caution !! Medium priority alarm according to their Alarm Rank, as illustrated in the
message table below. A lower number has a higher rank.
Advisory ! Low priority alarm message

Messages in the alarm window

Alarm Cause Remedy Alarm

Rank
!!! Apnea Spontaneous breathing by Ventilate in VC-CMV mode. 6
the patient has failed, or dis-
Ensure that hose connections are
connection.
tight.
Faulty flow sensor. Replace flow sensor.
!!! Apnea ventila- The ventilator has automati- Check ventilation mode. Return to 5
tion (only for cally switched over to man- original ventilation mode: Press
SpnCPAP) datory ventilation after the Alarm Reset key.
detecting an apnea (only in
SpnCPAP mode).
!! Charge int. bat- Oxylog 2000 plus draws its The ventilator must immediately 16
tery power from the internal bat- be reconnected to the mains sup-
tery due to the absence of ply, an onboard DC supply or a
an external DC supply. Only fully charged battery.
a few minutes of operating
time remain (approximately
10 minutes).
!! Check settings The flow resulting from the Change tidal volume VT or inspira- 14
flow settings for "Tidal volume tory time Ti or ventilation time ratio
VT per unit time" is not pos- I:E.
sible.

80 Instructions for Use Oxylog 2000 plus SW 1.n

 Problem Solving

Alarm Cause Remedy Alarm

Rank
!! Check settings The expiration time result- Change RR or I:E or Ti. 13
time ing from the settings for RR
and I:E or Ti is not possible.
!!! Confirm device Key O has been pressed To switch OFF: confirm. ---
OFF with rotary for 3 seconds.
To continue ventilation, press key
knob
O again.
!!! Device failure Technical defect. Contact your local DrägerService 1
for additional support.
!! Flow measure- Measurement hoses for Ensure flow measurement hoses 23
ment inop flow measurement hoses are connected correctly.
kinked, disconnected or
leaking.
Flow sensor defective. Replace flow sensor.
Technical defect. Contact your local DrägerService
for additional support – restricted
operation is now possible.
!! Gas delivery fail- Technical defect. Contact your local DrägerService 20
ure for additional support – restricted
operation is now possible.
!! High respiratory Patient breathes at a high Check patient's condition, check 15
rate spontaneous rate. ventilation pattern, correct alarm
limit RRsp if necessary.
!! Int. battery Technical defect. Contact your local DrägerService 17
charging inop for additional support – restricted
operation is now possible.
!!! Int. battery dis- The operating time for oper- The ventilator must immediately 2
charged ation with the internal bat- be reconnected to a mains supply,
tery has expired and an an on-board DC supply or a fully
external DC supply has not charged battery.
been connected.
!! Int. battery in use Oxylog 2000 plus draws its Press the Alarm Reset key to 12
power from the internal bat- confirm the alarm.
tery due to the absence of
an external DC supply.
!! Key failed Technical defect. Contact your local DrägerService 19
for additional support – restricted
operation is now possible.

Instructions for Use Oxylog 2000 plus SW 1.n 81

Problem Solving

Alarm Cause Remedy Alarm

Rank
!!! Leakage The measured expiratory Repair leaks in hose system and 9
tidal volume VTe is approxi- possibly in the tube. Check place-
(not in NIV)
mately 40% lower than the ment of lower sentence.
inspiratory value.
Use new flow measuring hoses.
Faulty flow sensor. Replace flow sensor.
The ventilator may not func- Contact your local DrägerService
tion properly. for additional support.
!! Loss of data Technical defect. Contact your local DrägerService 21
for additional support – restricted
operation is now possible.
!! Loudspeaker Technical defect. Contact your local DrägerService 22
inop for additional support – restricted
operation is now possible.
!!! MV high The upper alarm limit for the Check patient's condition, check 8
minute volume MV has ventilation pattern, adjust alarm
been exceeded. limits if necessary.
Faulty flow sensor. Replace flow sensor.
The ventilator may not func- Contact your local DrägerService
tion properly. for additional support.
!!! MV low The minute volume MV has Check patient's condition, check 7
dropped below its lower ventilation pattern, adjust alarm
alarm limit. limits if necessary.
Leak in exhalation system. Ensure connections in exhalation
system are tight.
Faulty flow sensor. Replace flow sensor.
The ventilator may not func- Contact your local DrägerService
tion properly. for additional support.
!! No int. battery ? Internal battery not Fit battery or confirm alarm or 24
installed, faulty or wrong change internal battery.
battery installed.
! No int. battery ? Internal battery not Advisory message, is displayed 25
installed, faulty or wrong continuously when confirmed.
battery installed. Change internal battery.
! No int. battery Internal battery cannot be Press the Alarm Reset key to 26
charging charged. confirm the alarm. Change inter-
nal battery.

82 Instructions for Use Oxylog 2000 plus SW 1.n

 Problem Solving

Alarm Cause Remedy Alarm

Rank
!!! Paw high The alarm limit Pmax for the Check patient's condition, check 3
airway pressure has been ventilation pattern, adjust alarm
reached. Patient "fights" the limits if necessary.
ventilator, coughing.
Ventilation hose kinked, or Check hose system, breathing
obstructed. valve and tube.
!!! Paw low No pressure difference >5 Inflate cuff and check for leaks. 4
mbar between inspiration
and expiration or set pres-
sure level is not achieved.
Leak in cuff.
Leakage or disconnection. Check hose system for leaking
connections. Ensure that the
breathing valve has been installed
correctly.
!! Paw measure- Fault in flow measurement Ensure hose system for loose con- 18
ment inop hoses. nections. Ensure flow measure-
ment hoses are connected
correctly.
Technical defect. Contact your local DrägerService
for additional support – restricted
operation is now possible.
! Self test OK The device has been The message can be confirmed or 28
switched on and the self- it will be cancelled automatically
test completed successfully. with the next message.
!! Set correct FiO2 The control knob for setting Set the Control knob in the right or 10
O2 AirMix or 100% O2 is set left position.
in a middle position.
! Settings not con- Parameters have been Press the rotary knob to confirm 27
firmed changed on the screen but the parameter changes.
not confirmed.
!! Supply pressure Supply pressure <270 kPa. Ensure that supply pressure 11
low exceeds 270 kPa.

Instructions for Use Oxylog 2000 plus SW 1.n 83

Problem Solving

Messages in the information window

(Numerical examples)

Message Cause Explanation/Remedy

RR = 12 per min or Change in Ti, RR or VT in ventila-
VT = 800 mL tion mode VC-SIMV.
I : E = 1 : 1.5
Flow = 15 L/min
RR = 12 per min or Change in I/E, RR or VT in ventila-
VT = 800 mL tion mode VC-CMV, VC-AC.
Ti = 0.7 s
Flow = 35 L/min
I : E = 1 : 1.5 Change in Ti.
Ti = 2 s

Confirm PEEP above 10 mbar ? PEEP >10 mbar has been set but The required setting of
not confirmed. PEEP >10 mbar is only possible
when confirmed via the rotary
knob.
Gas consumption = 10 L/min Standard display in information
window for the current gas
consumption.
Standard display in information
window for the current battery
(Battery capacity)
capacity.
Psupp = 22 mbar Change in ∆Psupp or PEEP. Psupp is the absolute pressure
resulting from PEEP + ∆Psupp.

84 Instructions for Use Oxylog 2000 plus SW 1.n

 Problem Solving

Error messages during the device check

Message Cause Explanation/Remedy

No communication control- / Device defective Contact your local DrägerService
charge-board for additional support.
System leakage Leak in ventilation hose system Check hoses, breathing valve,
and/or test lung. flow sensor and test lung for leaks
and replace if necessary.
No test lung Test lung not connected or mayor Connect test lung.
leakage
Check hoses, breathing valve,
flow sensor and test lung for leaks
and replace if necessary.
Breathing valve inop PEEP >10 mbar has been set but The required setting of
not confirmed. PEEP >10 mbar is only possible
when confirmed via the rotary
knob.
Pressure measurement inop The ventilation hose system has Connect ventilation system cor-
not been connected correctly. rectly.
Pressure measurement is not pos- Contact your local DrägerService
sible. for additional support.
PEEP-valve inop Internal leak in system Check hoses, breathing valve,
flow sensor and test lung for leaks
and replace if necessary.
Device defective Contact your local DrägerService
for additional support.
Patient flow measurement Flow measurement implausible Replace flow sensor.
inop Contact your local DrägerService
for additional support.

Instructions for Use Oxylog 2000 plus SW 1.n 85

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86 Instructions for Use Oxylog 2000 plus SW 1.n

 Cleaning, Disinfection and Sterilization

Cleaning, Disinfection and Sterilization

Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . 88
Disassemble the reusable hose system . . . . . 88
Remove the disposable hose system. . . . . . . 90

Reprocessing procedure . . . . . . . . . . . . . . . 91
Cleaning and disinfecting . . . . . . . . . . . . . . . . 91
Sterilizing the reusable hose system . . . . . . . 92
After care . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
Note service life of the hose system. . . . . . . . 93

Instructions for Use Oxylog 2000 plus SW 1.n 87

Cleaning, Disinfection and Sterilization

Disassembly

Disassemble the reusable hose system

B
B
A
C

011
WARNING
When disconnecting the ventilation hose,
always grip the sleeve (A) and not the corruga-
tions (B)!
If this is not done, the corrugations or hose
may be torn from the sleeve.
011

1 Disconnect the ventilation hose (A) from the gas

output.
2 Disconnect the flow measuring hoses (B) from
the nozzles.
3 Disconnect the medical gas hose (C) from the
Oxylog 2000 plus.

88 Instructions for Use Oxylog 2000 plus SW 1.n

 Cleaning, Disinfection and Sterilization

Breathing valve, disassembly

D A

A B
B

C
011

011
4 Disconnect the flow sensor (A) from the breath- 8 Turn the cover (A) about 90o
ing valve. counterclockwise to unlock the cover.
WARNING 9 Remove the silicone diaphragm (B).
Do not twist or use force when disconnecting WARNING
the flow measuring hoses from the flow sen-
Do not disassemble breathing valve any fur-
sor nozzles. This can damage the flow sensor.
ther.
5 Carefully detach the flow measuring hoses (B) Do not allow any objects to enter the housing
from the flow sensor. of the breathing valve to prevent risk of mal-
Pull in the axial direction of the hose nozzles. functions!
6 Detach the angled connector (C) from the flow Do not damage the silicone diaphragm and
sensor. other parts.
WARNING
Do not allow any objects to enter the flow sen-
sor to prevent risk of malfunctions.
Do not purge with compressed air. The wind
vane inside may be damaged and cause mea-
suring errors!

7 Detach the ventilation hose (D) from the brea-

A
thing valve.
011

Instructions for Use Oxylog 2000 plus SW 1.n 89

Cleaning, Disinfection and Sterilization

WARNING
The rubber disc (A) in the housing must not be
removed, damaged or bent, otherwise the
valve will not work properly and endangers
the patient.
Risk of CO2 rebreathing.

Remove the disposable hose system

A B
C
047

1 Disconnect flow measuring hoses (A and B).

2 Disconnect the ventilation hose (C).
3 Correctly dispose of the complete disposable
hose system. Refer to the chapter "Disposal"
on page 99.

CAUTION
The disposable hose system must not be
sterilized: it cannot withstand high temperatures
and may be damaged!

90 Instructions for Use Oxylog 2000 plus SW 1.n

 Cleaning, Disinfection and Sterilization

Reprocessing procedure

– Clean breathing valve, flow sensor, angled

adapter and ventilation hoses of the reusable CAUTION
hose system after use.
Disinfectants based on:
– Always exchange the disposable hose system – compounds containing alkylamine
after use on a patient. – compounds containing phenol
– The disposable hose system must always be – compounds releasing halogen
disposed of correctly. Refer to the chapter "Dis- – strong organic acids
posal" on page 99. – compounds releasing oxygen

– Clean the ventilator and medical gas hoses with may cause damage, which is not always immedi-
a disposable cloth if heavily soiled. ately apparent, to materials, particularly those
used for the breathing valve, flow sensor and
– Replace the disposable hose system in case of angled connector.
contamination by e.g. vomitus or coughing.
CAUTION
– Clean the reusable hose system in case of con-
tamination by e.g. vomitus or coughing. Sterilization of the ventilator itself with ethylene
WARNING oxide (EtO) is not recommended.
Always follow hospital/EMS procedures for
WARNING
handling equipment contaminated with body
fluids. Always follow accepted hospital/EMS proce-
dures for disinfecting equipment contami-
WARNING nated with body fluids (protective clothing,
Always follow local regulations governing the eyewear, etc.).
disposal of infectious waste and materials
contaminated with body fluids to prevent the
risk of infection. Users in the Federal Republic of Germany are
recommended to use only disinfectants on the cur-
rent DGHM list (DGHM: German Society for Hygi-
ene and Microbiology).
Cleaning and disinfecting
The following disinfectants on the DGHM list are
recommended:
To ensure material compatibility, use disinfectants
– Dismozon pur
based on:
– Incidur
– aldehydes
– Sekusept Powder
– alcohols
– Trichlorol
– quaternary ammonia compounds.
The DGHM list (published by: mhp-Verlag, Wiesba-
den) also specifies the active ingredient in each dis-
infectant. Disinfectants based on the active
ingredients aldehydes, alcohols or quaternary
ammonia compounds are recommended for users
in those countries in which the DGHM list is not
available.

Instructions for Use Oxylog 2000 plus SW 1.n 91

Cleaning, Disinfection and Sterilization

Disinfecting by wiping Bath disinfection for reusable hose system

Ventilator and medical gas hose: Disassembled parts of the breathing valve, flow
sensor, ventilation hose and flow measuring hoses:
– Follow the manufacturer's instructions. Remove
heavy soiling with a disposable cloth first.
WARNING WARNING
Do not allow any liquid to enter the ventilator Follow the manufacturer's instructions.
or medical gas hose! Agitate parts thoroughly in the solution.
Do not clean with a hard brush!
Risk of malfunction.
WARNING
Do not allow any objects to enter the breathing
valve or flow sensor!
Risk of malfunction.

WARNING
Rinse parts thoroughly with distilled water.
Disinfectant residues can cause the rubber
disc to become jammed in the breathing
valve!

WARNING
Allow to dry completely. The breathing valve
and flow measuring hoses may not function
correctly if water remains in these parts!

Sterilizing the reusable hose system

– Disassemble the breathing valve, flow sensor

and angled connector. When disassembling the
breathing valve from the flow sensor, pull in a
straight line.
Do not rotate the parts, as this may damage the
flow sensor. Dismantle the breathing valve.
– The disassembled parts of the breathing valve,
the flow sensor, the angled connector, the flow
measuring hoses and the ventilation hose can
be sterilized in hot steam at 134 oC in accor-
dance with EN 285 (Sterilization – Steam
sterilization – Large-scale sterilization) for at
least 3 minutes, up to 10 minutes.
– The hose system can be sterilized up to a
100 times.

92 Instructions for Use Oxylog 2000 plus SW 1.n

 Cleaning, Disinfection and Sterilization

– Sterilization for longer than 10 minutes is

permissible, but will decrease the service life of
the hose system.

After care

– Reassemble, refer to the "Assembly" section for

information.
– Connect to the power supply and gas supply,
refer to the "Assembly" section for information.
– Check readiness for operation, refer to the
"Assembly" section for information.

Note service life of the hose system

The parts of the breathing valve, the flow sensor,

the angled connector, the flow measuring hoses
and the ventilation hose are resistant to the recom-
mended disinfectants and to the temperatures
occurring during sterilization.
However, every disinfection and sterilization cycle
also means wear on the parts concerned.
For this reason, the parts must be examined for
cracks and permanent deformation after the
cleaning procedure.
NOTE
Damaged or deformed parts must be replaced.

Instructions for Use Oxylog 2000 plus SW 1.n 93

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94 Instructions for Use Oxylog 2000 plus SW 1.n

 Maintenance

Maintenance

Maintenance intervals . . . . . . . . . . . . . . . . . 96
In case of ventilator failure . . . . . . . . . . . . . . . 97

Instructions for Use Oxylog 2000 plus SW 1.n 95

Maintenance

Maintenance intervals

Inspection examination of actual condition.

Service measures to maintain specified
condition.
Repair measures to restore specified
condition.
Maintenance inspection, service, and repair,
where necessary.
Preventive maintenance measures at regular
Maintenance intervals.

CAUTION
In order to avoid malfunctioning of the device,
maintenance must be carried out by properly
trained service personnel.

CAUTION
Have the ventilator inspected and serviced at
regular two-year intervals.
Keep a record on all preventive maintenance.

WARNING
Clean and disinfect the device or device parts
before each maintenance step – and also
when returning for repair to prevent risk of
infection.
Task Frequency Performed by
1)
Replace dust filter. Every two years. Trained service personnel.
Replace internal battery. – Every two years Trained service personnel.
– When the battery no longer
remains charged for the speci-
fied operating time2).
Device inspection and maintenance. Every two years. Trained service personnel.
1) The dust filter can be treated as household waste.
2) Refer to "Technical Data" section for the battery operating time.

96 Instructions for Use Oxylog 2000 plus SW 1.n

 Maintenance

In case of ventilator failure

CAUTION
Never operate a ventilator if it has suffered physi-
cal damage or does not seem to operate properly.
In this case, always refer servicing to factory
trained and authorized personnel.

Instructions for Use Oxylog 2000 plus SW 1.n 97

 This page intentionally left blank

98 Instructions for Use Oxylog 2000 plus SW 1.n

 Disposal

Disposal

Safety information . . . . . . . . . . . . . . . . . . . . 100

Disposal of batteries . . . . . . . . . . . . . . . . . . 100

Disposal of the medical device . . . . . . . . . . 100

Disposal of the disposable hose system . . 101

Instructions for Use Oxylog 2000 plus SW 1.n 99

Disposal

Safety information

For countries subject to the EU directive

2002/96/EC
This device is subject to EU Directive 2002/96/EC
(WEEE). In order to comply with its registration,
according to this directive, it may not be disposed
of at municipal collection points for electrical and
electronic equipment waste. Dräger Medical has
authorized a company to collect and dispose of this
device. To initiate take-back or for further informa-
tion, visit us on the Internet at www.draeger-medi-
cal.com and navigate to the DrägerService area,
where you will find a link to "WEEE". If you do not
have access to our website, contact your local
Dräger Medical Organization.

Disposal of batteries

WARNING
Risk of explosion! Do not throw in fire.
Risk of corrosion! Do not open using force.

The medical device battery contains pollutant sub-

stances.
The applicable local regulations for battery disposal
must be observed in all countries.

Disposal of the medical device

When disposing of the medical device:

– Consult the relevant waste disposal company
for appropriate disposal.
– Observe the applicable local regulations.

100 Instructions for Use Oxylog 2000 plus SW 1.n

 Disposal

Disposal of the disposable hose system

Always follow local regulations governing the

disposal of disposable hose systems according to
established hospital/EMS procedures.

Instructions for Use Oxylog 2000 plus SW 1.n 101

 This page intentionally left blank

102 Instructions for Use Oxylog 2000 plus SW 1.n

 Technical Data

Technical Data

Ambient conditions . . . . . . . . . . . . . . . . . . . 104

During operation . . . . . . . . . . . . . . . . . . . . . . . 104
During storage and transportation . . . . . . . . . 104

Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 105

Performance data . . . . . . . . . . . . . . . . . . . . . 106

Measured value display . . . . . . . . . . . . . . . . 107

Airway pressure measurement. . . . . . . . . . . . 107
Flow measurement . . . . . . . . . . . . . . . . . . . . . 107
Frequency measurement . . . . . . . . . . . . . . . . 107
Pressure Bar graph . . . . . . . . . . . . . . . . . . . . 107

Monitoring . . . . . . . . . . . . . . . . . . . . . . . . . . . 108
Expiratory minute volume MVe. . . . . . . . . . . . 108
Airway pressure Paw . . . . . . . . . . . . . . . . . . . 108
Apnea alarm time Tapn. . . . . . . . . . . . . . . . . . 108

Operating data . . . . . . . . . . . . . . . . . . . . . . . 109

Power supply . . . . . . . . . . . . . . . . . . . . . . . . . 109
Gas supply . . . . . . . . . . . . . . . . . . . . . . . . . . . 110

Device specifications . . . . . . . . . . . . . . . . . . 111

Materials used. . . . . . . . . . . . . . . . . . . . . . . . 112

Technical Documentation for the Oxylog 2000

plus according to EMC standard IEC/EN 60601-
1-2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 113
General Information . . . . . . . . . . . . . . . . . . . . 113
Electromagnetic Emissions . . . . . . . . . . . . . . 114
Electromagnetic Immunity . . . . . . . . . . . . . . . 114

Instructions for Use Oxylog 2000 plus SW 1.n 103

Technical Data

WARNING
Do not use the device outside the specified
environmental and supply conditions, as the
device may not operate according to its spec-
ifications and may become inoperative.

Ambient conditions

During operation
Temperature –20 to 50 oC
Atmospheric pressure 570 to 1200 hPa
Relative humidity 5 to 95%

During storage and transportation

Ventilator without replaceable battery,
with reusable hose system
Temperature –40 to 75 oC
Atmospheric pressure 570 to 1200 hPa
Relative humidity 5 to 95%
Disposable hose system
Temperature –20 to 70 oC
Atmospheric pressure 570 to 1200 hPa
Relative humidity 30 to 50%
Replaceable battery
Temperature –20 to 35 oC
Atmospheric pressure 570 to 1200 hPa
Relative humidity 5 to 95%

104 Instructions for Use Oxylog 2000 plus SW 1.n

 Technical Data

Settings

Ventilation modes VC-CMV, VC-AC, VC-SIMV, SpnCPAP,

Optional: Pressure support for VC-SIMV
and SpnCPAP.

Ventilation frequency RR 2 to 50 /min ±1 /min (VC-SIMV)

5 to 50 /min ±1 /min (VC-CMV, VC-AC)
12 to 50 /min ±1 /min for apnea ventilation.

Ventilation time ratio I:E (VC-CMV, VC-AC) 1:4 to 3:1

Inspiration time Ti (VC-SIMV, VC-SIMV / PS) 0.2 to 10 s

Inspiration tidal volume VT 0.1 to 2.0 L, BTPS1)

Accuracy of Setting ±15% of set value or ±25 mL, whichever is greater.

O2 concentration 100 vol.% (No-AirMix) or

approximately 40 vol.% (O2 AirMix).

Positive end expiratory pressure PEEP 0 to 20 mbar ±2 mbar, no negative pressure.

Trigger sensitivity (flow trigger) 3 to 15 L/min

Pressure support ∆Psupp 0 to 35 mbar (relative to PEEP) ±2 mbar

Rise time for pressure slow (1 s), standard (0.4 s), fast (0 s).
support

1) BTPS
Body Temperature, Pressure, Saturated.
Measured values referred to the conditions of the patient's lungs,
body temperature 37 oC, airway pressure, water-vapor-saturated gas.

Instructions for Use Oxylog 2000 plus SW 1.n 105

Technical Data

Performance data

Control principle Time-cycled, volume-constant, pressure supported.

Maximum inspiratory flow 100 L/min1)

Device compliance
with 1.5 m ventilation hose< 1 mL/mbar
with 3 m ventilation hose < 2 mL/mbar

Inspiration resistance < 6 mbar at 60 L/min

< 4 mbar at 30 L/min
< 2 mbar at 5 L/min
Expiration resistance < 6 mbar at 60 L/min
< 4 mbar at 30 L/min
< 2 mbar at 5 L/min

Dead space including flow sensor approximately 35 mL (reusable hose system).

approximately 33 mL (disposable hose system).

Supplementary functions
Demand valve Opens the breathing system upon failure of the gas
supply, permits spontaneous breathing with ambient
air.
Relief valve Opens the breathing system at
approximately 80 mbar.

Patient connection 22 mm ISO conical connector.

1) At service pressures >350 kPa.

The maximum inspiratory flow is reduced to 80 L/min at service pressures <350 kPa and to 39 L/min at service
pressures <280 kPa.

106 Instructions for Use Oxylog 2000 plus SW 1.n

 Technical Data

Measured value display

Airway pressure measurement

Range 0 to 99 mbar
Resolution 1 mbar
Accuracy ±2 mbar
Maximum airway pressure PIP
Positive end expiratory pressure PEEP
Mean airway pressure Pmean
Plateau pressure Pplat

Flow measurement
Minute volume MVe
Range 0 to 99 L/min, BTPS
Resolution 0.1 L/min
Accuracy ±15% of measured value, or ±1 L/min, whichever is
greater.

Tidal volume VTe

Range 0 to 5000 mL, BTPS
Resolution 1 mL
Accuracy ±15% of measured value, or ±25 mL, whichever is
greater.

Frequency measurement
Range 0 to 99 /min
Resolution 1 /min
Accuracy ±1 /min

Pressure Bar graph

Airway pressure Paw –7 to 60 mbar

Instructions for Use Oxylog 2000 plus SW 1.n 107

Technical Data

Monitoring

Expiratory minute volume MVe

Alarm, upper alarm limit When the upper alarm limit has been exceeded.
Range of settings 2 to 41 L/min
Alarm, lower alarm limit When the level drops below the lower alarm limit.
Range of settings 0.5 to 40 L/min

Airway pressure Paw

Alarm, upper alarm limit When value "Pmax" is exceeded.
Range of settings 20 to 60 mbar
Alarm, lower alarm limit When the pressure difference between inspiratory
and expiratory phases is less than 5 mbar.
Or
If the set pressure level is not attained.

Apnea alarm time Tapn

Alarm When respiratory activity is no longer detected.
Range of settings 15 to 60 s, can be set in 1 s increments.

108 Instructions for Use Oxylog 2000 plus SW 1.n

 Technical Data

Operating data

Power supply
Power supply
Input voltage 19 V ±0.5 V DC
Oxylog 2000 plus
With DC/DC converter 12 / 24 / 28 V DC

Current consumption
With battery charge 2.1 A
Operating time with fully
charged internal battery approximately 4 hours
without mains supply for
"typical" ventilation
Battery type Lithium ion battery
Charging times approximately 5 hours
The specified charging time applies when recharging
the battery completely after it has been depleted.

Permissible ambient temperature during charging 0 oC to 35 oC

Indication of battery capacity in 25% increments.

Accuracy of the capacity indication The indicated capacity is determined by the battery
itself. The accuracy depends on the type and manu-
facturer and may deteriorate with frequent partial
discharge and during operation in extreme tempera-
tures. The internal battery is only reconditioned after
being discharged completely and recharged at room
temperature 25 oC.
The criteria for the warnings !!! Int. battery dis-
charged and !! Charge int. battery are therefore
based on measurement of the battery voltage. The
capacity indicated at this moment may differ from the
actual capacity of the internal battery.
Battery storage time The internal battery must always be removed from
the ventilator for storage and recharged completely
after 12 months at the latest (e.g. in the external
battery charging station).

Instructions for Use Oxylog 2000 plus SW 1.n 109

Technical Data

AC/DC power pack

Temperature range –20 oC to 50 oC
Protection class to Class II, the earthing is used for EMC purposes.
EN 60601
Input 100 to 240 V~/ 50 to 60 Hz / 0.6 - 0.3 A
Output 19 V ±0.5 V / 2.1 A

DC/DC converter
Temperature range –20 oC to 50 oC
Input 12 / 24 / 28 V DC / 9 A
Output 19 V ±0.5 V / 2.1 A

Gas supply From a pipeline system or from a medical gas

cylinder.
O2 service pressure 270 kPa to 600 kPa maximum 100 L/min
Supply gas Medical oxygen.
O2 inlet connection either:
NIST1) to EN 739, or
DISS2) to CGA V5-1989, or
N-F3) S90-116
WARNING
Only use medical grade oxygen that is dry and
free from dust and oil.
Contaminated gas can cause device malfunction.

Gas cylinders and WARNING

pressure reducers
Only use compressed gas cylinders and pres-
sure reducers, which comply with all applicable
regulations and have been approved.
Pressure reducer Must have a vent valve on the output side to limit the
delivery pressure to approximately 1000 kPa in the
event of a fault.
Gas consumption for Average 0.5 L/min
internal control
Accuracy of gas 15% or ±1 L/min, whichever is greater.
consumption indication

1) NIST = Non Interchangeable Screw Thread Connection

2) DISS = Diameter Index Safety Systems
3) N-F = French standard

110 Instructions for Use Oxylog 2000 plus SW 1.n

 Technical Data

Device specifications

Noise pressure <45 dB (A) for typical ventilation at a distance of

1 m.

Dimensions (W x H x D)
Basic unit 285 x 184 x 175 mm (without handle)
AC/DC power supply 161 x 63 x 118 mm
DC/DC converter 162 x 42 x 69 mm

Weight
Basic unit without internal approximately 4.9 kg
battery
Basic unit with internal approximately 5.4 kg
battery
AC/DC power pack approximately 0.8 kg
DC/DC converter approximately 0.4 kg

Electromagnetic compatibility (EMC). EN 60601-1-2, EN 794-3 (36.101)

10 V/m, ISO 10651-3 (36.202.2.1) 30 V/m and
UN Regulation nr. 10, revision 2, with respect to EMC
for use in motor vehicles.
E4 10 R-02 XXXX

Classification Class IIb

according to Directive 93/42/EEC.

UMDNS-Code 18 – 098
Universal Medical Device Nomenclature System.

Protection class, ventilation hose systems Type BF (body floating).

(disposable or reusable).

Type of protection against ingress of liquids. IPX4

Instructions for Use Oxylog 2000 plus SW 1.n 111

Technical Data

Materials used

Housing, Oxylog 2000 plus. Acrylonitrile styrene acrylate/polycarbonate

(ASA/PC).
Housing, AC/DC power pack. Acrylonitrile butadiene styrene/polycarbonate
(ABS/PC).
Housing, DC/DC converter. Polycarbonate (PC).
Touch sensitive keypad on ventilator. Polyester film.

NOTE
All Dräger ventilation hoses are latex-free.

Reusable hose system.

Ventilation hose, flow Silicone rubber.
measuring hoses.
Flow sensor housing, Polysulphone (PSU).
breathing valve.
Vane in flow sensor. Stainless steel.
Diaphragms in breathing Silicone rubber.
valve.

Disposable hose system.

Ventilation hose. Polyethylene (PE).
Non-return valve. Synthetic resin.
Breathing valve. Polyethylene (PE).
Flow sensor housing. Polymethyl methacrylate (PMMA).
Film in flow sensor. Polyester.
Adapter. Silicone rubber.
Patient connection. Polypropylene (PP).

Display
Technology. Electro-luminescence (EL).
Pixels. 240 x 128
Visible area. 108 x 56 mm

112 Instructions for Use Oxylog 2000 plus SW 1.n

 Technical Data

Technical Documentation for the Oxylog 2000 plus according to EMC

standard IEC/EN 60601-1-2

General Information

The EMC conformity of the Oxylog 2000 plus includes the use of following external cables, transducers
and accessories:

AC/DC power pack 100 - 240 V / 50 - 60 Hz

DC/DC Converter
All-round Wall holder
Carrying System

Refer to the "List of Accessories" on page 123 for additional information.

Additionally, accessories may be used, which do not affect EMC compliance, if no other reasons contradict
the use of them. The non-observance may result in increased emissions or decreased immunity of the
Oxylog 2000 plus.

The Oxylog 2000 plus should not be used adjacent to or stacked with other equipment; if adjacent or
stacked use is inevitable, the Oxylog 2000 plus should be observed to verify normal operation in the
configuration in which it will be used.

Instructions for Use Oxylog 2000 plus SW 1.n 113

Technical Data

Electromagnetic Emissions
Electromagnetic Emissions
The Oxylog 2000 plus is intended for use in the electromagnetic environment specified below.
The user of the Oxylog 2000 plus should make sure that it is used in such an environment.
Emissions Compliance Electromagnetic environment
according to
RF emissions (CISPR 11) Group 1 The Oxylog 2000 plus uses RF energy only for its internal
function.
Therefore, its RF emissions are very low and are not likely
to cause any interference in nearby electronic equipment.
Class B The Oxylog 2000 plus is suitable for use in all establish-
ments including domestic establishments and those
directly connected to the public low-voltage power supply
network that supplies buildings used for domestic
purposes.
Harmonic emissions Class A
(IEC 61000-3-2)
Voltage fluctuations / flicker Complies
(IEC 61000-3-3)

Electromagnetic Immunity
Electromagnetic Immunity
This Oxylog 2000 plus is intended for use in the electromagnetic environment specified below.
The user of the Oxylog 2000 plus should make sure that it is used in such an environment.
Immunity against IEC 60601-1-2 test level Compliance Electromagnetic environment
level (of the
Oxylog 2000
plus)
electrostatic contact discharge: 6 kV 8 kV Floors should be wood, concrete
discharge, ESD air discharge: 8 kV 15 kV or ceramic tile. If floors are cove-
(IEC 61000-4-2) red with synthetic material, the
relative humidity should be at
least 30%.
electrical fast – power supply lines: 2 kV – 2 kV – Mains power quality should
transients / bursts be that of a typical commer-
(IEC 61000-4-4) cial or hospital environment.
– longer input / output – N/A – No input/output lines.
lines: 1 kV

114 Instructions for Use Oxylog 2000 plus SW 1.n

 Technical Data

Immunity against IEC 60601-1-2 test level Compliance Electromagnetic environment

level (of the
Oxylog 2000
plus)
surges on AC mains common mode: 2 kV 2 kV Mains power quality should be
lines differential mode: 1 kV 1 kV that of a typical commercial or
(IEC 61000-4-5) hospital environment.
power frequency 3 A/m N/A Test is not necessary because
magnetic field the Oxylog 2000 plus is not likely
50/60 Hz to be sensitive to magnetic field
(IEC 61000-4-8) disturbances, such as CRT
monitors or hall elements.
voltage dips and dip >95%, 0.5 periods N/A No voltage dips or short interrup-
short dip 60%, 5 periods tions, since a fully charged bat-
interruptions on AC dip 30%, 25 periods tery must be installed for safety
mains input lines dip >95%, 5 seconds reasons, even when operating
(IEC 61000-4-11) from an external supply.
radiated RF 80 MHz - 2,5 GHz: 10 V/m 30 V/m Recommended separation dis-
(IEC 61000-4-3) tance from portable and mobile
RF transmitters with transmis-
sion power PEIRP to the
Oxylog 2000 plus including its
lines:
1.84 m * PEIRP (X1)
RF coupled into lines 150 kHz - 80 MHz: 10 V 10 V Recommended separation dis-
(IEC 61000-4-6) within ISM bands, tance from portable and mobile
3 V outside ISM bands (X2) 10 V RF transmitters with transmis-
sion power PEIRP to the
Oxylog 2000 plus including its
lines:
(X1)
1.84 m * PEIRP
I

Information regarding separation distances (IEC 60601-1-2, tables 205 and 206).
X1) For PEIRP the highest possible "equivalent isotropic radiated power" of the adjacent RF transmitter has to be inserted
(value in Watt). Also in the vicinity of equipment marked with the symbol interference may occur. Field strengths from
fixed, portable or mobile RF transmitters at the location of the Oxylog 2000 plus should be less than 3 V/m in the frequency
range from 150 kHz to 2.5 GHz and less than 1 V/m above 2.5 GHz.
X2) ISM bands in this frequency range are: 6.765 MHz - 6.795 MHz, 13.553 MHz - 13.567 MHz,
26.957 MHz - 27.283 MHz, 40.66 MHz - 40.70 MHz.

Instructions for Use Oxylog 2000 plus SW 1.n 115

Technical Data

Recommended separation distances

Recommendated separation distances between
portable and mobile RF-Telecommunication
devices and the Oxylog 2000 plus.
The table below gives examples of the most com-
mon devices. If a device is not listed, do as follows:
1 Check the product manual of the device for the
energy (W) and the frequency (GHz) values that
the device transmits.
2 In the table below, search for the energy (W)
value of the device in the PEIRP (W) column.
3 On the correct table row, search for the distance
that corresponds to the frequency of the device.
– If the frequency is between 150 kHz to 2.5 GHz,
use the 3 V/m distance column.
– Otherwise, use the 1 V/m distance column.

Recommended separation distances between portable and mobile RF-Telecommunication

devices and the Oxylog 2000 plus
maximum 3 V/m 1 V/m Examples
PEIRP (W) distance (m) distance (m)
0.001 0.06 0.17
0.003 0.10 0.30
0.010 0.18 0.55 e.g. Garage door openers
0.030 0.32 0.95 e.g. WLAN 5250 / 5775 (Europe)*
0.100 0.58 1.73 e.g. WLAN 2440 (Europe), Bluetooth*
0.200 0.82 2.46 e.g. WLAN 5250 (not in Europe)*
0.250 0.91 2.75 e.g. DECT devices*
1.000 1.83 5.48 e.g. GSM 1800- / GSM 1900- / UMTS- mobiles,
WLAN 5600 (not in Europe)*
2.000 2.60 7.78 e.g. GSM 900 mobiles*
3.000 3.16 9.49

Information regarding separation distances (IEC 60601-1-2, tables 205 and 206).

* Telecommunication devices. For the correct type, check the product manual of the device.

116 Instructions for Use Oxylog 2000 plus SW 1.n

 Principles of Operation

Principles of Operation

Ventilation modes. . . . . . . . . . . . . . . . . . . . . 118

VC-CMV . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 118
VC-AC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 118
PS (optional). . . . . . . . . . . . . . . . . . . . . . . . . . 119

Functional description . . . . . . . . . . . . . . . . . 121

Gas supply . . . . . . . . . . . . . . . . . . . . . . . . . . . 121
Inspiration . . . . . . . . . . . . . . . . . . . . . . . . . . . . 121
Expiration . . . . . . . . . . . . . . . . . . . . . . . . . . . . 121
Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 122
Monitoring. . . . . . . . . . . . . . . . . . . . . . . . . . . . 122

Instructions for Use Oxylog 2000 plus SW 1.n 117

Principles of Operation

Ventilation modes

VC-CMV VC-SIMV

Volume-Constant Mandatory Ventilation stroke Synchronized Intermittent Mandatory Ventilation

Paw Paw Unsynchronized

mandatory
Synchronized
mandatory
with plateau without plateau ventilation stroke ventilation stroke
Tplat%

Pplat
PEEP
PEEP

t t
Trigger
window T i Spontaneous Spontaneous
Ti Te breathing time breathing time + T
Set mandatory
T= 1
RR 1 Set mandatory
cycle time
Flow RR
cycle time
1
RR

042
t Combination of mandatory ventilation and sponta-
neous breathing
041

VC-SIMV enables the patient to breathe

The ventilation pattern is specified by the settings spontaneously in regular prescribed cycles, with
for tidal volume VT, respiratory rate RR, ventilation the mechanical mandatory ventilation strokes
time ratio I:E and PEEP. providing a minimum ventilation during the
remaining cycles.
At the end of the flow phase, the expiration valve
remains closed until the end of the inspiration time The minimum ventilation is controlled by the two set
Ti. This phase, the inspiratory pause, can be identi- values of the tidal volume VT and respiratory rate
fied as the plateau Pplat. RR and is determined from the product of VT x RR.
The ventilation pattern results from the ventilation
parameters of the tidal volume VT, respiratory rate
VC-AC RR and inspiration time Ti.

Assisted ventilation with continuous positive airway To prevent the mandatory ventilation stroke from
pressure. being applied during spontaneous expiration, the
flow trigger of the ventilator ensures that the venti-
The mandatory ventilation stroke begins when the lation stroke is triggered in synchrony with the
patient reaches an inspiratory flow corresponding patient's spontaneous inspiratory effort within a
at least to the set flow trigger. "trigger window".
The current ventilation respiratory rate may be The trigger window is 5 seconds long. If the
greater than the set respiratory rate for the same expiration times are less than 5 seconds, the
trigger. trigger window covers the entire expiration time
minus a minimum expiration time of 500 ms.

118 Instructions for Use Oxylog 2000 plus SW 1.n

 Principles of Operation

Since the synchronization of the mandatory ventila- PS (optional)

tion stroke reduces the effective VC-SIMV time,
which would result in an undesirable increase in Pressure Support
effective respiratory rate, Oxylog 2000 plus pro-
longs the subsequent spontaneous breathing time Paw
by the missing time difference ∆T – thus preventing
an increase in SIMV respiratory rate. The respira- Phase
tory rate parameter RR remains constant. This I II
parameter, in combination with the tidal volume VT, PPS
sets the minimum ventilation. over PEEP
During the spontaneous breathing phases, the DPS
patient can be assisted with pressure by PS
CPAP
pressure support.
In the course of progressively weaning the patient t
from artificial ventilation, the ventilation respiratory Start of inspiration End of inspiration
rate RR is further reduced while the spontaneous
breathing time is increased, so that the required Insp.
total minute volume is increasingly supplied by Flow
spontaneous breathing. max. 4 s

25 % Insp. Flow

043
Pressure support for insufficient spontaneous
breathing.
The device takes over part of the inhalation func-
tion, with the patient maintaining control of sponta-
neous breathing.
The SpnCPAP system supplies the spontaneously
breathing patient with breathing gas, even if the
inspiration effort is weak.
The pressure support of the PS system is started:
when the spontaneous inspiration flow reaches the
set value of the flow trigger, or at the latest
when the spontaneous inspired volume exceeds
25 mL.

Instructions for Use Oxylog 2000 plus SW 1.n 119

Principles of Operation

The device then produces an increase in pressure

up to the preselected PS pressure ∆Psupp above
PEEP, which is adjustable to the breathing require-
ment of the patient.
The time for this pressure increase (Slope) is
adjustable:
– In case of rapid increase in pressure, the
Oxylog 2000 plus supports the insufficient
spontaneous breathing of the patient with a high
peak flow.
– In case of slow increase in pressure, the
Oxylog 2000 plus begins gently with regular
inspiratory flow. The patient has to take over
more breathing effort.
With the patient adjusted pressure increase and the
pressure ∆Psupp above PEEP, the patient's own
breathing activity defines the required inspiration
flow.

PS is terminated:
– when the inspiration flow returns to zero during
phase I, i.e. when the patient exhales or fights
the ventilator.

Or
– when the inspiration flow in phase II falls below
25% of the inspiration flow previously supplied
(and thus ∆Psupp above PEEP is reached).

Or
– after 4 seconds if the two other criteria have not
come into operation.

120 Instructions for Use Oxylog 2000 plus SW 1.n

 Principles of Operation

Functional description

Microprocessor system

Gas blender E
Pressure control V6
S4 P

O2 F1 DR V1 - 3 V10

SV NV
S3 P
E
S8

F2
V7 V8

P P P P
E E E E

S9 S7 S5 S6

044
The variable pneumatic actuators in the applied tidal volume corresponds with that set for
Oxylog 2000 plus are controlled by the micropro- BTPS, taking into account the ambient pressure. In
cessor system via digitized electrical signals. this way, Oxylog 2000 plus meters and measures
roughly 10% less volume in operation with a test
lung (dry gas at room temperature).
Gas supply

The supply gas O2 is purified by filter F1 and Expiration

adjusted to a constant pressure by pressure
regulator DR. Ambient air is taken in via filter F2 as During volume-controlled inspiration, pressure con-
required. The supply pressure is monitored by trol V6 closes the inspiratory canal and controls the
pressure sensor S3. PEEP pressure during expiration or reduces the
pressure in the inspiration hose to control the PS,
Pinsp or Pmax pressure when the target values are
Inspiration reached. Breathing valve V10 on the patient side,
which is indirectly controlled by V6, seals off
Gas blender V1-3 delivers the variable inspiration against atmospheric air during inspiration and
flow as a mixture of supply gas O2 and ambient air adjusts the required patient pressure during expira-
in accordance with the ventilation mode and tion by controlling the pressure in the inspiration
required O2 concentration. The tidal volume is hose. The measured value of the airway pressure
applied regardless of ambient pressure (absolute sensor S5 on the patient side serves as a set point
pressure sensors S7 and S9) under patient condi- for pressure regulation.
tions BTPS for volume-controlled breathing; the

Instructions for Use Oxylog 2000 plus SW 1.n 121

Principles of Operation

Safety

In the event of a fault, gas blender V1-3 closes and

pressure control V6 opens to the atmosphere. The
pneumatic demand valve NV (spontaneous breath-
ing) opens in the presence of negative pressure.
The pneumatic relief valve SV (set to approximately
80 mbar) opens in the presence of excess
pressure.

Monitoring

The flow measured on the patient side by S8 is

transmitted to the internal electronic pressure
difference sensor S6 as a differential pressure
signal. The measured monitoring values of the tidal
volume, minute volume and respiratory rate are
derived from the measured expiratory flow. The
inspiratory flow signal is used for detection of the
flow trigger. System leakages can be identified from
the balance of inspiratory and expiratory tidal
volumes (e.g. leakage alarm, NIV).
Airway pressure measurement on the patient side
supplies the Paw values for the airway pressure on
the display via S5, as well as for the derived
measured values PEEP, PIP, Pplat, Pmean. The
plausibility of this airway pressure measurement on
the patient side is monitored by a redundant inter-
nal airway pressure measurement in the ventilator
via S4 in the inspiratory duct.

122 Instructions for Use Oxylog 2000 plus SW 1.n

 List of Accessories

List of Accessories

Part name Part No.

Part name Part No.
Reusable hose system,
Workstation comprising:
Oxylog 2000 plus 57 05 080 – Reusable hose system, 1.5 m 84 12 068
– Reusable hose system, 3 m 84 12 913
Basic unit – Breathing valve 84 12 001
Oxylog 2000 plus 57 05 081 – Flow sensor 84 12 034
– Angled connector 84 12 235
Accessories required for
operation
Power supply:
Disposable ventilation hose, 1.5 m 57 02 871
AC/DC power pack 2M 86 730
Disposable ventilation hose, 1.5 m 57 03 041
100-240 V/50-60 Hz
(set of 5)
Available power cables:
– Germany and Europe 18 24 481
Conversion kit Reusable ME 05 133
– Denmark 18 68 950 (nozzle kit)
– United Kingdom 18 44 369 Conversion kit Disposable ME 05 134
– Australia 18 51 705 (nozzle kit)
– Switzerland 18 44 377
– USA 18 41 793 Connecting hoses
– China 18 59 706 Gas Supply System 57 04 500
– Brazil 18 68 160
Special accessories
DC/DC converter 2M 86 731 Equipment Holder 2M 86 900
Battery Charger 2M 86 729
Lithium ion battery 2M 86 733 All-round Wall holder 57 04 216
Carrying System 2M 86 975
Test lung 84 03 201

Options
Pressure support (PS) 57 05 161
Non-invasive ventilation (NIV) 57 05 083

Instructions for Use Oxylog 2000 plus SW 1.n 123

 This page intentionally left blank

124 Instructions for Use Oxylog 2000 plus SW 1.n

 Index

Index

Numerics D
100% O2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55 DC/DC converter . . . . . . . . . . . . . . . . . . . . . . . 33
Dead space . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
A Device check . . . . . . . . . . . . . . . . . . . . . . . 41, 85
Device specifications . . . . . . . . . . . . . . . . . . . 111
Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . 16 Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87
AC, VC- . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48 Display operating controls . . . . . . . . . . . . . . . . 22
AC/DC power pack . . . . . . . . . . . . . . . . . . . . . . 33 Disposable hose system . . . . . . . . . . . . . . 14, 31
Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . 123 Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99
Advisory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
Airway pressure bar . . . . . . . . . . . . . . . . . . . . . . 24 E
Airway pressure Paw . . . . . . . . . . . . . . . . . . . . 108
Alarm - Cause - Remedy . . . . . . . . . . . . . . . . . . 80 Electromagnetic Emissions . . . . . . . . . . . . . . 114
Alarm limits, setting . . . . . . . . . . . . . . . . . . . . . . 63 Electromagnetic Immunity . . . . . . . . . . . . . . . 114
Alarm reset . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 EMC . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7, 8, 113
Alarm tones, suppress . . . . . . . . . . . . . . . . . . . . 61 EMC/ESD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Alarm, in the event of . . . . . . . . . . . . . . . . . . . . . 61 Environment of use . . . . . . . . . . . . . . . . . . . . . 10
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60, 80 Error messages during device check . . . . . . . . 43
Alarms window . . . . . . . . . . . . . . . . . . . . . . . . . 24
Alarms window, messages . . . . . . . . . . . . . . . . 80 F
Ambient conditions . . . . . . . . . . . . . . . . . . . . . 104
Apnea alarm, time for . . . . . . . . . . . . . . . . . . . . 52 FiO2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Apnea ventilation . . . . . . . . . . . . . . . . . . . . . . . . 52 Front panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Functional description . . . . . . . . . . . . . . . . . . 121
B
G
Bacterial filter . . . . . . . . . . . . . . . . . . . . . . . . 30, 31
Battery capacity indicator . . . . . . . . . . . . . . 26, 32 Gas failure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
Battery, charging . . . . . . . . . . . . . . . . . . . . . . . . 38 Gas supply . . . . . . . . . . . . . . . . . . . . . . . . 34, 110
Battery, installing . . . . . . . . . . . . . . . . . . . . . . . . 33
Battery, internal . . . . . . . . . . . . . . . . . . . . . . . . . 32
Breathing valve, assembly . . . . . . . . . . . . . . . . . 29
H
Breathing valve, disassembly . . . . . . . . . . . . . . 89 HME . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30, 31
BTPS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16, 41
I
C
Indications/Contraindications . . . . . . . . . . . . . . 10
Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56 Information window, messages . . . . . . . . . . . . 84
Caution . . . . . . . . . . . . . . . . . . . . . . . . . 2, 7, 8, 60 Intended use . . . . . . . . . . . . . . . . . . . . . . . . . 9, 10
Changing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Checking readiness for operation . . . . . . . . . . . 40
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87 L
CMV, VC- . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48 Language . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71
Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . 69 Language, set . . . . . . . . . . . . . . . . . . . . . . . . . . 71
CPAP, Spn- . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52
Customer Service Mode . . . . . . . . . . . . . . . . . . 72

Instructions for Use Oxylog 2000 plus SW 1.n 125

Index

M Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Screen brightness . . . . . . . . . . . . . . . . . . . . . . 56
Maintenance intervals . . . . . . . . . . . . . . . . . . . . 96 Screen window structure . . . . . . . . . . . . . . . . . 23
Manufacturer’s default settings . . . . . . . . . . . . . 46 Separation distances . . . . . . . . . . . . . . . . . . . 116
Materials used . . . . . . . . . . . . . . . . . . . . . . . . . 112 Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 105
Measured value display . . . . . . . . . . . . . . . . . . 107 Settings window . . . . . . . . . . . . . . . . . . . . . . . . 25
Measured values display window . . . . . . . . . . . 75 Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
Messages window . . . . . . . . . . . . . . . . . . . . . . . 25 Side view, right . . . . . . . . . . . . . . . . . . . . . . . . . 13
Monitoring . . . . . . . . . . . . . . . . . . . . . . . . . . 15, 65 SIMV, VC- . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
MVespon . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67 Single use hose system . . . . . . . . . . . . . . . 14, 31
Special modes . . . . . . . . . . . . . . . . . . . . . . 10, 15
N SpnCPAP . . . . . . . . . . . . . . . . . . . . . . . . . . 21, 52
Standard rail systems . . . . . . . . . . . . . . . . . . . . 36
NIV . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54 Startup settings . . . . . . . . . . . . . . . . . . . . . . . . 74
Status window . . . . . . . . . . . . . . . . . . . . . . . . . 23
O Sterilization . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87
Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
O2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67 System check . . . . . . . . . . . . . . . . . . . . . . . . . . 42
O2 AirMix . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55 System overview . . . . . . . . . . . . . . . . . . . . . . . 11
O2 concentration with O2 blending . . . . . . . . . . 55
O2 cylinder . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35 T
Operating concept . . . . . . . . . . . . . . . . . . . . . . . 20
Operating data . . . . . . . . . . . . . . . . . . . . . . . . . 109 Technical Data . . . . . . . . . . . . . . . . . . . . . . . . 103
Operating time . . . . . . . . . . . . . . . . . . . . . . . . . . 39 Trigger . . . . . . . . . . . . . . . . . . . . . . . . . 49, 50, 53
Operating time, pneumatic . . . . . . . . . . . . . . . . 39
V
P
Values window . . . . . . . . . . . . . . . . . . . . . . . . . 24
PEEP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67 VC-AC . . . . . . . . . . . . . . . . . . . . . . . . 21, 48, 118
Performance data . . . . . . . . . . . . . . . . . . . . . . 106 VC-CMV . . . . . . . . . . . . . . . . . . . . . . . 21, 48, 118
PIP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67 VC-SIMV . . . . . . . . . . . . . . . . . . . . . . . . . 21, 118
Pmax . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 Ve / VTe window . . . . . . . . . . . . . . . . . . . . . . . 24
Pmean . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67 Ventilation controls . . . . . . . . . . . . . . . . . . . . . . 21
Power failure . . . . . . . . . . . . . . . . . . . . . . . . . . . 62 Ventilation mode, select . . . . . . . . . . . . . . . . . . 21
Power supply . . . . . . . . . . . . . . . . . . . . . . . 32, 109 Ventilation modes . . . . . . . . . . . . . . . . . . . . . . . 14
Pplat . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67 Ventilation modes, description . . . . . . . . . . . . 118
Pressure limitation . . . . . . . . . . . . . . . . . . . . . . . 63 Volume loudness . . . . . . . . . . . . . . . . . . . . . . . 56
Pressure support . . . . . . . . . . . . . . . . . 51, 53, 119 VT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21

R W
Rear view . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13 Warning . . . . . . . . . . . . . . . . . . . . 2, 7, 60, 61, 64
Recommended separation distances . . . . . . . 116 Warnings, general . . . . . . . . . . . . . . . . . . . . . . . 7
Restrictions of use . . . . . . . . . . . . . . . . . . . . . . . 10 Windows . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Resuscitation . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
Resuscitation, heart-lung . . . . . . . . . . . . . . . . . . 49
Reusable hose system . . . . . . . . . . . . . . . . 14, 29
RR . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21, 67
RRsp . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67

S
Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

126 Instructions for Use Oxylog 2000 plus SW 1.n

 This page intentionally left blank

Instructions for Use Oxylog 2000 plus SW 1.n 127

These Instructions for Use only apply to Oxylog
2000 plus SW 1.n with the Serial No.:
If no Serial No. has been filled in by Dräger,
these Instructions for Use are provided for gen-
eral information only and are not intended for
use with any specific machine or device.
This document is provided for customer informa-
tion only, and will not be updated or exchanged
without customer request.
0344

Directive 93/42/EEC
concerning Medical Device

Manufacturer

Dräger Medical b.v.

Kanaaldijk 29
5683 CR BEST
The Netherlands.
+31 499 331 331
FAX +31 499 331 335
http://www.draeger-medical.com

57 05 035 - 03 – GA 5664.650 En
© Dräger Medical b.v.
1st Edition – January 2008
Dräger Medical reserves the right to make
modifications to the equipment without prior
notice.