Dräger Savina 300 User manual

Instructions for use
Savina 300
Ventilator
Software 5.n
WARNING
To properly use this medical device,
read and comply with these
instructions for use.
DRAFT:19. December 2019 15:22

Information about this document
2 Instructions for use Savina 300 SW 5.n
Information about this document
Typographical conventions
Illustrations
Illustrations of products and screen content in this
document may differ from the actual products
depending on configuration and design.
Use of terms
Dräger uses the term "accessories" not only for
accessories in the sense of IEC 60601-1, but also
for consumables, removable parts, and attached
parts.
1Consecutive numbers indicate steps of action,
with the numbering restarting with "1" for each
new sequence of actions.
Bullet points indicate individual actions or differ-
ent options for action.
– Dashes indicate the listing of data, options, or
objects.
(A) Letters in parentheses refer to elements in the
related illustration.
ALetters in illustrations denote elements referred
to in the text.
> The greater-than symbol indicates the
navigation path in a dialog window.
Bold, italicized text indicates labels on the
device and texts that are displayed on the
screen.

Instructions for use Savina 300 SW 5.n 3
Information about this document
Trademarks
Trademarks owned by Dräger
The following web page provides a list of the
countries in which the trademarks are registered:
www.draeger.com/trademarks
Trademarks owned by third-party
manufacturers
Trademark
Savina®
ATC®
AutoFlow®
LPO®
Spirolog®
MEDIBUS.X®
Trademark Trademark owner
Dismozon®BODE Chemie
Korsolex®
neodisher
MediClean®
Dr. Weigert
acryl-des®Schülke & Mayr
Mikrozid®
Perform®
Actichlor®Ecolab USA
Incidin®
Oxycide®
BruTab 6S®Brulin
Dispatch®Clorox
Klorsept®Medentech
Descogen®Antiseptica
Oxygenon®
SteriMax®Aseptix
Cleanisept®Dr. Schumacher
Trademark used
under license
Trademark owner
BIPAP Respironics

Information about this document
4 Instructions for use Savina 300 SW 5.n
Safety information definitions
WARNING
A WARNING statement provides important
information about a potentially hazardous
situation which, if not avoided, could result in
death or serious injury.
CAUTION
A CAUTION statement provides important
information about a potentially hazardous
situation which, if not avoided, may result in minor
or moderate injury to the user or patient or in
damage to the medical device or other property.
NOTE
A NOTE provides additional information intended
to avoid inconvenience during operation.

Instructions for use Savina 300 SW 5.n 5
Information about this document
User group requirements
The term "user group" describes the personnel
responsible who have been assigned by the
operating organization to perform a particular task
on a product.
Duties of the operating organization
The operating organization must ensure the
following:
– Every user group has the required qualifications
(e.g., has undergone specialist training or
acquired specialist knowledge through
experience).
– Every user group has been trained to perform
the task.
– Every user group has read and understood the
relevant chapters in this document.
User groups
Clinical users
This user group operates the product in
accordance with the intended use.
Users have medical specialist knowledge in the
field of ventilation. Users have knowledge of device
monitoring and ventilation care.
Reprocessing personnel
This user group carries out the necessary activities
to reprocess the product.
Reprocessing personnel has specialist knowledge
in the reprocessing of medical devices.
Service personnel
This user group installs the product and performs
the service activities.
Service personnel has specialist knowledge in
electrical and mechanical engineering and
experience in the servicing of medical devices.
Where product specific knowledge or tools are
required, the service activities must be carried out
by specialized service personnel. The specialized
service personnel was trained by Dräger for these
service activities on this product.

6 Instructions for use Savina 300 SW 5.n
This page has been left blank intentionally.

Instructions for use Savina 300 SW 5.n 7
Contents
Contents
Information about this document . . . . . . . . . 2
For your safety and that of your patients. . . 9
General safety information . . . . . . . . . . . . . . . . 10
Product-specific safety information. . . . . . . . . . 13
Additional information. . . . . . . . . . . . . . . . . . . . 16
Application . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Intended use. . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Contraindications . . . . . . . . . . . . . . . . . . . . . . . 18
Environments of use. . . . . . . . . . . . . . . . . . . . . 18
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Savina 300 . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Trolley. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Range of functions . . . . . . . . . . . . . . . . . . . . . . 25
Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Product labels. . . . . . . . . . . . . . . . . . . . . . . . . . 33
Operating concept . . . . . . . . . . . . . . . . . . . . . 35
Control and display unit . . . . . . . . . . . . . . . . . . 36
Fixed function keys. . . . . . . . . . . . . . . . . . . . . . 36
Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Assembly and preparation . . . . . . . . . . . . . . 41
Safety information. . . . . . . . . . . . . . . . . . . . . . . 42
Preparing the trolley . . . . . . . . . . . . . . . . . . . . . 42
Fitting an additional monitor . . . . . . . . . . . . . . . 50
Preparing the ventilator . . . . . . . . . . . . . . . . . . 52
Connecting the power supply . . . . . . . . . . . . . . 60
Connecting the gas supply . . . . . . . . . . . . . . . . 62
Connecting the nurse call. . . . . . . . . . . . . . . . . 63
Using the MEDIBUS or MEDIBUS.X
protocol. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65
Removing and fitting the filter cover . . . . . . . . . 67
Connecting the potential equalization cable . . . 67
Intrahospital transport of the device . . . . . . . . . 68
Getting started. . . . . . . . . . . . . . . . . . . . . . . . 69
Safety information . . . . . . . . . . . . . . . . . . . . . . 70
Switching on the ventilator . . . . . . . . . . . . . . . 70
Selecting the breathing circuit and the
humidification type. . . . . . . . . . . . . . . . . . . . . . 72
Checking the operational readiness . . . . . . . . 73
Selecting the therapy type and the
application mode . . . . . . . . . . . . . . . . . . . . . . . 79
Selecting the start settings for ventilation . . . . 80
Starting the therapy. . . . . . . . . . . . . . . . . . . . . 82
Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83
Ventilation settings . . . . . . . . . . . . . . . . . . . . . 84
Adjusting the ventilation settings . . . . . . . . . . . 86
Non-invasive ventilation (NIV) . . . . . . . . . . . . . 89
Suction maneuver with oxygenation . . . . . . . . 90
Medication nebulization. . . . . . . . . . . . . . . . . . 92
Manual inspiration – Inspiration hold. . . . . . . . 95
Special maneuvers . . . . . . . . . . . . . . . . . . . . . 96
O2 therapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . 97
Day/Night screen switch-over . . . . . . . . . . . . . 99
Key lock. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99
Low Pressure Oxygen (LPO) . . . . . . . . . . . . . 100
Transporting patients. . . . . . . . . . . . . . . . . . . . 103
Interrupting the therapy – standby mode. . . . . 104
Ending operation . . . . . . . . . . . . . . . . . . . . . . . 105
Storing the device . . . . . . . . . . . . . . . . . . . . . . 106
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 107
Display of alarms. . . . . . . . . . . . . . . . . . . . . . . 108
Alarm silence. . . . . . . . . . . . . . . . . . . . . . . . . . 110
Dismissing alarm messages . . . . . . . . . . . . . . 110
Setting the alarm limits . . . . . . . . . . . . . . . . . . 111
Trends and data. . . . . . . . . . . . . . . . . . . . . . . 113
Opening the dialog window . . . . . . . . . . . . . . . 114
Displaying measured values and set values . . 114
Displaying trends. . . . . . . . . . . . . . . . . . . . . . . 115
Displaying the logbook . . . . . . . . . . . . . . . . . . 117
Displaying waveforms and measured values
on the main screen . . . . . . . . . . . . . . . . . . . . . 118

Contents
8 Instructions for use Savina 300 SW 5.n
Monitoring. . . . . . . . . . . . . . . . . . . . . . . . . . . . 121
Information on monitoring. . . . . . . . . . . . . . . . . 122
Flow monitoring . . . . . . . . . . . . . . . . . . . . . . . . 122
FiO2 monitoring . . . . . . . . . . . . . . . . . . . . . . . . 124
CO2 monitoring. . . . . . . . . . . . . . . . . . . . . . . . . 126
Configuration . . . . . . . . . . . . . . . . . . . . . . . . . 133
Information on configuration. . . . . . . . . . . . . . . 134
Configuring the ventilation functions . . . . . . . . 134
Configuring the start settings . . . . . . . . . . . . . . 135
Configuring the device settings . . . . . . . . . . . . 141
Configuring country-specific settings . . . . . . . . 142
Configuring the data interface . . . . . . . . . . . . . 143
Enabling software options . . . . . . . . . . . . . . . . 143
Scanning the QR code . . . . . . . . . . . . . . . . . . . 144
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . 145
Failure of the power supply . . . . . . . . . . . . . . . 146
Failure of the gas supply . . . . . . . . . . . . . . . . . 146
High ambient temperature . . . . . . . . . . . . . . . . 146
Alarm – Cause – Remedy . . . . . . . . . . . . . . . . 147
Reprocessing . . . . . . . . . . . . . . . . . . . . . . . . . 171
Safety information . . . . . . . . . . . . . . . . . . . . . . 172
Information on reprocessing . . . . . . . . . . . . . . . 173
Classifications for reprocessing . . . . . . . . . . . . 174
Before reprocessing . . . . . . . . . . . . . . . . . . . . . 174
Validated reprocessing procedures . . . . . . . . . 178
Other agents and reprocessing procedures . . . 181
After reprocessing . . . . . . . . . . . . . . . . . . . . . . 184
Service. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 185
Safety information . . . . . . . . . . . . . . . . . . . . . . 186
Definition of service terminology . . . . . . . . . . . 187
Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 187
Maintenance. . . . . . . . . . . . . . . . . . . . . . . . . . .189
Repair. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 190
Replacing the microfilter. . . . . . . . . . . . . . . . . . 190
Replacing the dust filter set . . . . . . . . . . . . . . . 191
Replacing the O2 sensors . . . . . . . . . . . . . . . . 192
Replacing the diaphragm of the reusable
expiratory valve . . . . . . . . . . . . . . . . . . . . . . . .192
Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 193
Safety information . . . . . . . . . . . . . . . . . . . . . . 194
Disposing of the packaging material . . . . . . . . 194
Disposing of the batteries. . . . . . . . . . . . . . . . . 194
Disposing of the O2 sensors . . . . . . . . . . . . . . 195
Disposing of the device . . . . . . . . . . . . . . . . . . 195
Technical data . . . . . . . . . . . . . . . . . . . . . . . . 197
Ambient conditions . . . . . . . . . . . . . . . . . . . . . 198
Set values . . . . . . . . . . . . . . . . . . . . . . . . . . . . 198
Performance characteristics . . . . . . . . . . . . . . 201
Displayed measured values . . . . . . . . . . . . . . 203
Monitoring . . . . . . . . . . . . . . . . . . . . . . . . . . . . 208
Operating data. . . . . . . . . . . . . . . . . . . . . . . . . 210
Alarm system of Savina 300 . . . . . . . . . . . . . . 216
Automatic alarm limits . . . . . . . . . . . . . . . . . . . 217
Device combinations . . . . . . . . . . . . . . . . . . . . 218
EMC declaration . . . . . . . . . . . . . . . . . . . . . . . 219
Connections to IT networks. . . . . . . . . . . . . . . 221
Open-source software. . . . . . . . . . . . . . . . . . . 222
Principles of operation . . . . . . . . . . . . . . . . . 223
Ventilation modes . . . . . . . . . . . . . . . . . . . . . . 224
Additional settings . . . . . . . . . . . . . . . . . . . . . . 236
Therapy types and application modes. . . . . . . 244
Special maneuvers . . . . . . . . . . . . . . . . . . . . . 245
Low Pressure Oxygen (LPO) . . . . . . . . . . . . . 246
Automatic leakage compensation . . . . . . . . . 248
Measurements. . . . . . . . . . . . . . . . . . . . . . . . . 250
Pneumatic functional description . . . . . . . . . . 251
Overview of the menu structure . . . . . . . . . . . 254
References . . . . . . . . . . . . . . . . . . . . . . . . . . . 258
Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 259
Labels for options . . . . . . . . . . . . . . . . . . . . . 263
User password for Savina 300 SW 5.n . . . . 271
Information on the user password . . . . . . . 271

Instructions for use Savina 300 SW 5.n 9
For your safety and that of your patients
For your safety and that of your patients
General safety information . . . . . . . . . . . . . . 10
Strictly follow these instructions for use . . . . . . 10
Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Not for use in areas of explosion hazard . . . . . 10
Connected devices. . . . . . . . . . . . . . . . . . . . . . 10
Patient safety . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Patient monitoring. . . . . . . . . . . . . . . . . . . . . . . 11
Electromagnetic compatibility (EMC) . . . . . . . . 11
Disposable products. . . . . . . . . . . . . . . . . . . . . 12
Sterile-packaged accessories. . . . . . . . . . . . . . 12
Installing accessories . . . . . . . . . . . . . . . . . . . . 12
Storing the instructions for use . . . . . . . . . . . . . 12
Product-specific safety information . . . . . . . 13
Functional safety . . . . . . . . . . . . . . . . . . . . . . . 15
Monitoring ventilation . . . . . . . . . . . . . . . . . . . . 15
Backup ventilation with an independent
manual ventilation device . . . . . . . . . . . . . . . . . 15
Additional information . . . . . . . . . . . . . . . . . . 16
Training. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Mandatory reporting of adverse events . . . . . . 16

For your safety and that of your patients
10 Instructions for use Savina 300 SW 5.n
General safety information
The following WARNING and CAUTION
statements apply to general operation of the
medical device.
WARNING and CAUTION statements specific to
subsystems or particular features of the medical
device appear in the respective sections of these
instructions for use or in the instructions for use of
another product being used with this medical
device.
Strictly follow these instructions for use
Service
Accessories
Not for use in areas of explosion hazard
Connected devices
WARNING
Risk of incorrect operation and of incorrect
use
Any use of the medical device requires full un-
derstanding and strict observation of all sec-
tions of these instructions for use. The medi-
cal device must only be used for the purpose
specified under "Intended use" on page 18
and in conjunction with appropriate patient
monitoring (see page 11).
Strictly observe all WARNING and CAUTION
statements throughout these instructions for
use and all statements on medical device la-
bels. Failure to observe these safety informa-
tion statements constitutes a use of the medi-
cal device that is inconsistent with its intend-
ed use.
WARNING
Risk if service is not performed regularly
If service is not performed regularly, malfunc-
tions may occur, which can result in personal
injury and property damage.
Perform the service in accordance with the
chapter "Service".
WARNING
Risk due to incompatible accessories
The use of incompatible accessories may ad-
versely affect the functional integrity of the
product. Personal injury and property damage
may occur as a consequence.
Use only compatible accessories. The acces-
sories that are compatible with this product
are listed in the list of accessories supplied
with the product.
WARNING
Risk of fire
The medical device is not approved for use in
areas where combustible or explosive gas
mixtures are likely to occur.
WARNING
Risk of electric shock and of device malfunc-
tion
Electrical connections to equipment not listed
in these instructions for use or these assem-
bly instructions must only be made when ap-
proved by each respective manufacturer.
Before operating the medical device, strictly
comply with the instructions for use of all con-
nected devices or device combinations.

Instructions for use Savina 300 SW 5.n 11
For your safety and that of your patients
Patient safety
The design of the medical device, the
accompanying documentation, and the labeling on
the medical device are based on the assumption
that the purchase and the use of the medical device
are restricted to persons familiar with the most
important inherent characteristics of the medical
device.
Instructions and WARNING and CAUTION
statements are therefore largely limited to the
specifics of the Dräger medical device.
The instructions for use do not contain any
information on the following points:
– Risks that are obvious to users
– Consequences of obvious improper use of the
medical device
– Potentially negative effects on patients with
different underlying diseases
Medical device modification or misuse can be
dangerous.
Patient monitoring
The user of the medical device is responsible for
choosing a suitable patient monitoring system that
provides appropriate information on medical device
performance and patient condition.
Patient safety can be achieved by a wide variety of
means ranging from electronic surveillance of
medical device performance and patient condition
to direct observation of clinical signs.
The responsibility for selecting the best level of
patient monitoring lies solely with the user of the
medical device.
Electromagnetic compatibility (EMC)
Medical electrical equipment is subject to special
precautionary measures concerning
electromagnetic compatibility. During installation
and before initial operation, follow the information in
section: "EMC declaration" (page 219).
This device can be affected by other electrical
devices.
CAUTION
Risk of patient injury
Do not make therapeutic decisions based solely
on individual measured values and monitoring pa-
rameters.
WARNING
Risk due to electrostatic discharge
Malfunctions that endanger the patient may
occur if no protective measures against elec-
trostatic discharge are employed in the follow-
ing situations:
– When touching the pins of connectors that
carry the ESD warning symbol.
– When establishing connections with these
connectors.
To prevent malfunctions, observe the follow-
ing measures and train the relevant person-
nel:
– Observe the ESD protective measures.
Such measures may include wearing anti-
static clothing and shoes, touching a po-
tential equalization pin before and while
making the connection, or using electrical-
ly insulating and antistatic gloves.
– Observe the requirements for the electro-
magnetic environment. Observe the fol-
lowing section: "Electromagnetic environ-
ment" (page 219).

For your safety and that of your patients
12 Instructions for use Savina 300 SW 5.n
Disposable products
Sterile-packaged accessories
Installing accessories
Strictly observe instructions for use and assembly
instructions.
Storing the instructions for use
WARNING
Risk due to electromagnetic disturbance
Wireless communication devices (e.g., cellu-
lar phones) and medical electrical equipment
(e.g., defibrillators, electrosurgical devices)
emit electromagnetic radiation. When such
devices are operated too close to this device
or its cables, the functional integrity of this de-
vice may be compromised by electromagnetic
disturbances. As a result, the patient could be
put at risk.
Maintain a distance of at least 0.3 m (1.0 ft) be-
tween this device and wireless communica-
tion devices, to ensure that the essential per-
formance of this device is fulfilled.
Maintain an adequate distance between this
device and other medical electrical equip-
ment.
WARNING
Risk of patient injury due to failure of accesso-
ries
Disposable products are developed, tested
and manufactured for disposable use only.
Reuse, reprocessing, or sterilization can lead
to a failure of accessories and cause injury to
the patient.
Do not reuse, reprocess, or sterilize dispos-
able products.
CAUTION
Risk of medical device failure and of patient injury
Do not use sterile-packaged accessories if the
packaging has been opened, is damaged, or if
there are other signs of non-sterility.
CAUTION
Risk of device failure
Install accessories to the basic device in accor-
dance with the instructions for use of the basic de-
vice. Make sure that there is a safe connection to
the basic device.
CAUTION
Risk of incorrect use
Instructions for use must be kept accessible to the
user.

Instructions for use Savina 300 SW 5.n 13
For your safety and that of your patients
Product-specific safety information
WARNING
Risk of incorrect use
This medical device is only intended to be
used by the user group "users".
WARNING
Risk of not hearing alarm signals
If the alarm volume is too low, alarm signals
may not be heard.
– Set the alarm volume loud enough so that
the alarm signals can be heard in the envi-
ronment where the device is located.
– The user must remain within hearing dis-
tance of the alarm signals.
WARNING
Risk due to modifications
Modifications to the product may lead to
malfunctions and unforeseen risks. This may
result in injury to the patient or the user or in
property damage.
Do not modify this product.
WARNING
Risk of electric shock
If the connectors of the interfaces and the pa-
tient are touched simultaneously, there is a
risk of electric shock.
Do not simultaneously touch the connectors
of the interfaces and the patient.
WARNING
Risk of patient injury
Penetrating liquid may cause malfunction of
the device, which may endanger the patient.
Do not place any containers with liquid on or
above the device.
During surface disinfection, make sure no
liquids penetrate into the device.
WARNING
Risk of fire
The flow sensor can ignite medications or oth-
er substances based on highly flammable
substances.
– Do not nebulize medications or other sub-
stances that are easily flammable or spray
them into the device.
– Do not use substances containing alcohol.
– Do not allow flammable or explosive sub-
stances to enter the breathing system or
the breathing circuit.
WARNING
Risk of failure of flow measurement
Deposits that were not removed during repro-
cessing can damage the measuring wires in
the flow sensor or cause a fire.
– Before inserting the flow sensor check for
visible damage, soiling, and particles.
Repeat this check regularly.
– Replace flow sensors when damaged,
soiled, or not particle-free.

For your safety and that of your patients
14 Instructions for use Savina 300 SW 5.n
WARNING
Risk of fire
When using O2 pressure reducers that are not
approved, excess pressure can cause a fire.
When supplying the ventilator with oxygen
from a compressed gas cylinder, only use
pressure reducers that comply with
ISO 10524.
Open pressure reducers slowly by hand.
Do not use tools.
WARNING
Risk of fire
Do not use the medical device in conjunction
with flammable gases or flammable solutions
that can mix with air, oxygen, nitrous oxide, or
other sources of ignition since the medical de-
vice could ignite.
Do not allow the medical device to come into
contact with sources of ignition.
WARNING
Risk of patient injury
Magnetic resonance imaging (MRI, NMR, NMI)
may impair correct functioning of the medical
device.
Do not use the medical device during magnet-
ic resonance imaging.
WARNING
Risk of patient injury
Hyperbaric chambers may impair correct
functioning of the medical device.
Do not use the medical device in hyperbaric
chambers.
WARNING
Risk of electric shock
There are live components under the housing
cover.
Do not remove the cover.
WARNING
Risk of fire
Due to oxygen enrichment in the ambient air
and overheating, the medical device can ig-
nite.
A distance of at least 10 cm (3.9 in) must be
maintained between the rear of the medical
device and walls or large-scale obstacles.
Do not cover the rear during operation or
standby mode so that air circulation is en-
sured.
Only use the medical device in adequately
ventilated rooms.
CAUTION
Risk of unnoticed change in the inspiratory
O2concentration
If an additional flow (e.g., NO, nitrous oxide) is de-
livered from an external flow source, the actual
O2concentration may deviate from the displayed
values.
If required, use additional monitoring, e.g., exter-
nal SpO2 monitoring.
CAUTION
Risk of overheating of the medical device
Sources of heat such as direct sunlight, heat radi-
ators or spotlights may cause the medical device
to overheat.
Keep sources of heat away from the medical de-
vice. Only use the medical device in adequately
ventilated rooms.
CAUTION
Risk of patient injury
Positive-pressure ventilation can lead to negative
effects, such as barotrauma or strain on the circu-
latory system.
Monitor the patient's condition.

Instructions for use Savina 300 SW 5.n 15
For your safety and that of your patients
Functional safety
The essential performance consists in a controlled
and monitored patient ventilation with user-defined
settings for the monitoring functions
– minimum ventilation flow,
– maximum airway pressure,
– minimum and maximum O2 concentration in the
breathing gas,
or, if a set limit is exceeded, an appropriate alarm.
The integrated monitoring also generates an alarm
in the following situations:
– Failure of the external power supply
– Discharge of the internal battery
– Failure of the O2 supply (HPO mode)
The medical device is equipped with basic safety
features to reduce the possibility of patient injury
while the cause of an alarm is remedied.
Monitoring ventilation
The following parameters are monitored by the
integrated monitoring:
– Airway pressure
– Expiratory minute volume
– Respiratory rate
– Apnea
– Inspiratory O2 concentration
– Inspiratory breathing gas temperature
– Inspiratory tidal volume
– End-expiratory CO2 concentration
Changes in these parameters may be caused by:
– Acute changes in the patient's condition
– Incorrect settings and faulty handling
– Device malfunctions
– Failure of power and gas supplies
If the built-in monitoring fails, use substitute
monitoring.
During O2 therapy, the monitoring functions of the
medical device are limited.
Backup ventilation with an independent
manual ventilation device
CAUTION
Risk of malfunction
The touch screen has a sensitive surface. Dam-
age to the surface results in malfunctions of the
touch-sensitive controls.
Never use sharp objects to operate the screen.
Do not damage the surface of the screen during
cleaning or transport.
CAUTION
Risk of electric shock
If a faulty device without safety extra-low voltage
(SELV) is connected to the medical device, there
is a risk of electric shock when the housing is
touched.
Only connect devices with safety extra-low volt-
age (SELV) to the connections for the serial port
and the nurse call.
WARNING
Risk of patient injury
If a fault is evident at the medical device, its
life-support functions may be affected.
Ventilation of the patient using an indepen-
dent ventilation device must be started with-
out delay, if necessary with PEEP and/or an in-
creased inspiratory O2 concentration
(e.g., with the manual resuscitator MR-100).

For your safety and that of your patients
16 Instructions for use Savina 300 SW 5.n
Additional information
Training
Training for users is available from the Dräger
organization responsible, see www.draeger.com.
Mandatory reporting of adverse events
Serious adverse events with this product must be
reported to Dräger and the responsible authorities.

Instructions for use Savina 300 SW 5.n 17
Application
Application
Intended use . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Contraindications . . . . . . . . . . . . . . . . . . . . . . 18
Environments of use . . . . . . . . . . . . . . . . . . . 18

Application
18 Instructions for use Savina 300 SW 5.n
Intended use
Savina 300 is a ventilator intended for the
ventilation of adults and pediatric patients.
Savina 300 offers mandatory ventilation modes,
ventilation modes supporting spontaneous
breathing, and airway monitoring.
Contraindications
When using small minute volumes, it takes longer
for a modified oxygen concentration to reach the
patient.
For the ventilation of neonates, the use of special
neonatal ventilators is therefore recommended.
Environments of use
Savina 300 is intended for the following
environments of use:
– In intensive care wards, in recovery rooms and
generally for hospital use
– During the transfer of patients within the
hospital

Instructions for use Savina 300 SW 5.n 19
Overview
Overview
Savina 300 . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Ventilator with trolley. . . . . . . . . . . . . . . . . . . . .20
Control and display unit . . . . . . . . . . . . . . . . . . 20
Patient connection panel . . . . . . . . . . . . . . . . . 22
Rear . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Trolley . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Range of functions. . . . . . . . . . . . . . . . . . . . . 25
Therapy types. . . . . . . . . . . . . . . . . . . . . . . . . .25
Ventilation functions . . . . . . . . . . . . . . . . . . . . . 25
Monitoring functions . . . . . . . . . . . . . . . . . . . . . 25
Displays on the screen . . . . . . . . . . . . . . . . . . . 26
Additional functions . . . . . . . . . . . . . . . . . . . . . 26
Power supply . . . . . . . . . . . . . . . . . . . . . . . . . .26
Gas supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Data transfer. . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Medication nebulization . . . . . . . . . . . . . . . . . . 26
Transport of patients. . . . . . . . . . . . . . . . . . . . . 26
Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . 27
Symbols. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Product labels. . . . . . . . . . . . . . . . . . . . . . . . . 33

Overview
20 Instructions for use Savina 300 SW 5.n
Savina 300
Ventilator with trolley
AControl and display unit
BPatient connection panel
CDräger Savina 300 trolley
DDräger Savina 300 compact trolley
Control and display unit
ATouch screen
BFixed function keys
CRotary knob
DPower supply display
001
A
B
CD
003
AB
C
D