Atlan A300 series Instructions for Use sw 1.0n Edition 2 April 2019 .pdf
Page 1
Instructions for use
Atlan
A300, A300 XL, A350, A350 XL
WARNING
To properly use this medical
device, read and comply with
these instructions for use.
Anesthesia workstation
Software 1.0n
Page 2
This page has been left blank intentionally.
2
Instructions for use
| Atlan A300, A300 XL, A350, A350 XL SW 1.0n
Page 3
Contents
Contents
1
2
Information about this document ...........................................................
7
1.1
1.2
1.3
1.4
Typographical conventions .............................................................
Use of terms ...................................................................................
Illustrations......................................................................................
Trademarks.....................................................................................
7
7
7
7
Safety-related information.......................................................................
9
2.1
2.2
2.3
2.4
2.5
2.6
2.7
2.8
2.9
3
4
5
6
Instructions for use
Intended use ...................................................................................
Indications.......................................................................................
Contraindications ............................................................................
Environments of use .......................................................................
Essential performance features ......................................................
User group requirements ................................................................
Information on safety instructions and precautionary statements...
Safety instructions ..........................................................................
Additional information .....................................................................
9
9
9
10
10
11
11
12
14
Overview ...................................................................................................
15
3.1
3.2
3.3
Hardware ........................................................................................
Functional scope.............................................................................
Gas flow diagram............................................................................
15
31
42
Assembly and preparation ......................................................................
4.1
Safety instructions ..........................................................................
4.2
Mounting of accessories .................................................................
4.3
Before first operation ......................................................................
4.4
Intrahospital transport .....................................................................
4.5
Gas supply......................................................................................
4.6
Connecting to the gas scavenging system .....................................
4.7
Preparation for an operation day / after cleaning and sterilization..
4.8
Selecting and connecting patient-specific accessories...................
4.9
Connecting and replacing consumables.........................................
45
Operating concept....................................................................................
79
5.1
5.2
5.3
Screen ............................................................................................
Color concept..................................................................................
Selecting and setting ......................................................................
79
83
84
Getting started..........................................................................................
86
6.1
6.2
6.3
6.4
6.5
86
86
86
87
88
Safety instructions ..........................................................................
Turning on the device .....................................................................
Checking the device configuration..................................................
Checking the operational readiness ...............................................
Emergency start-up ........................................................................
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52
55
59
59
65
67
67
75
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Contents
7
Operation ..................................................................................................
7.1
7.2
7.3
7.4
7.5
7.6
7.7
7.8
7.9
7.10
7.11
7.12
7.13
7.14
8
9
Safety instructions ..........................................................................
Starting the therapy ........................................................................
Adjusting the therapy ......................................................................
Special forms of therapy .................................................................
Using fields with special functions ..................................................
Customizing the screen display ......................................................
Displaying additional data...............................................................
Setting the volume ..........................................................................
Adjusting the alarms .......................................................................
Changing the patient data...............................................................
Exporting data.................................................................................
Other settings .................................................................................
Ending the therapy..........................................................................
Change of patient ...........................................................................
89
93
96
100
103
107
113
115
116
119
119
120
122
124
Tests ..........................................................................................................
126
8.1
8.2
8.3
8.4
Status of the device functions.........................................................
Available test types.........................................................................
Performing the tests........................................................................
Checklist in the walk-through mode................................................
126
127
127
136
Ending operation......................................................................................
151
At the end of the OR day ................................................................
Storing the device ...........................................................................
Disconnecting the mains power supply ..........................................
151
151
151
9.1
9.2
9.3
10 Alarms .......................................................................................................
10.1
10.2
10.3
10.4
10.5
10.6
10.7
152
Safety instructions ..........................................................................
Displaying alarms ...........................................................................
Response to alarms........................................................................
Adopting alarm settings when changing the ventilation mode........
Alarm delay and alarm escalation...................................................
Activation of alarms after breath detection .....................................
Intelligent alarm behavior................................................................
152
152
154
159
160
163
164
11 Configuration............................................................................................
165
11.1
11.2
11.3
11.4
11.5
11.6
Device settings ...............................................................................
Setting the date and time................................................................
Specifying the start settings............................................................
Transferring device configurations..................................................
Activating software options .............................................................
Overview of configurable screen contents......................................
165
165
166
181
182
184
12 Troubleshooting .......................................................................................
190
12.1
12.2
12.3
12.4
12.5
4
89
Leakage ..........................................................................................
Power supply failure .......................................................................
Failure of the gas supply.................................................................
Failure of fresh-gas delivery (electronically controlled gas mixture)
Failure of the piston ventilator.........................................................
Instructions for use
190
191
192
194
195
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Contents
12.6
12.7
12.8
12.9
12.10
12.11
12.12
12.13
Failure of the O2 sensor..................................................................
Flow measurement failure ..............................................................
Screen fault or failure of the graphical user interface .....................
Complete failure..............................................................................
Problems with the active anesthetic gas receiving system (AGS) ..
Cylinder pressure reducer ..............................................................
Support request ..............................................................................
Alarm – Cause – Remedy...............................................................
195
198
198
198
199
201
201
201
13 Reprocessing............................................................................................
222
13.1
13.2
13.3
13.4
13.5
13.6
13.7
13.8
13.9
13.10
13.11
13.12
13.13
Safety instructions ..........................................................................
Information on reprocessing ...........................................................
Classifications for reprocessing ......................................................
Reprocessing list ............................................................................
Reprocessing procedures...............................................................
Preparation .....................................................................................
Surface disinfection with cleaning...................................................
Disassembly ...................................................................................
Disassembling the breathing system ..............................................
Machine reprocessing.....................................................................
Fitting and assembly.......................................................................
Preparation before the next use .....................................................
Brief instructions for reprocessing ..................................................
222
223
224
225
225
227
229
230
238
242
249
258
260
14 Service ......................................................................................................
262
14.1
14.2
14.3
14.4
14.5
Safety instructions ..........................................................................
Definition of service terminology.....................................................
Inspection .......................................................................................
Maintenance ...................................................................................
Repair .............................................................................................
262
262
262
265
265
15 Disposal ....................................................................................................
266
15.1
15.2
15.3
Safety instructions ..........................................................................
Disposing of the device...................................................................
Disposing of accessories ................................................................
266
266
266
16 Technical data ..........................................................................................
267
16.1
16.2
16.3
16.4
16.5
16.6
16.7
16.8
16.9
16.10
16.11
16.12
16.13
16.14
Instructions for use
Safety instructions ..........................................................................
General information ........................................................................
Ambient conditions .........................................................................
Fresh-gas delivery ..........................................................................
Fresh-gas delivery with electronically controlled gas mixer ............
Fresh-gas delivery with mechanically controlled gas mixer ............
Ventilator.........................................................................................
Breathing system ............................................................................
External fresh-gas outlet.................................................................
Anesthetic gas receiving system (AGS) .........................................
Active AGS .....................................................................................
Passive AGS...................................................................................
Measuring systems and displays....................................................
Gas measurement ..........................................................................
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268
268
269
269
270
270
272
274
274
274
275
275
279
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Contents
16.15
16.16
16.17
16.18
16.19
16.20
16.21
16.22
16.23
16.24
16.25
16.26
Gas measurement with PGM..........................................................
Gas measurement with O2 sensor..................................................
Display of calculated values ...........................................................
Operating characteristics ................................................................
Interfaces and ports ........................................................................
Relevant standards.........................................................................
Diagrams ........................................................................................
EMC declaration .............................................................................
Device combinations.......................................................................
Emission of high-frequency energy ................................................
Connections to IT networks ............................................................
Open-source software ....................................................................
279
281
282
283
287
289
290
291
293
293
294
297
17 Principles of operation ............................................................................
297
17.1
17.2
17.3
17.4
17.5
17.6
17.7
17.8
Safety instructions ..........................................................................
Description of the ventilation modes...............................................
Description of the ventilation drive..................................................
Improving the CO2 measurement by means of an HME filter.........
Minimum O2 delivery ......................................................................
Influence of patient category, weight, and age on device behavior
Support of Infinity ID accessories ...................................................
Schematic illustration of the acoustic signals .................................
297
298
307
308
310
311
312
313
18 Annex ........................................................................................................
314
18.1
18.2
18.3
18.4
Abbreviations ..................................................................................
Symbols ..........................................................................................
Product labels .................................................................................
Overview of the menu structure......................................................
314
317
322
323
19 Password ..................................................................................................
325
19.1
6
Configuration password for Atlan A300, A300 XL, A350, A350
XL Software 1.0n ............................................................................
325
Index ..........................................................................................................
327
Instructions for use
| Atlan A300, A300 XL, A350, A350 XL SW 1.0n
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Information about this document
1
Information about this document
1.1
Typographical conventions
Text
Bold, italicized text indicates labels on the device and screen text.
1.
Numbers with a period indicate the individual steps within a process
sequence. The numbering for each new process sequence starts once
more at number 1.
a.
Lower-case letters with a period indicate secondary process steps. The lettering for each new higher-level process step starts once more with the
letter a.
►
This triangle indicates individual steps without any specific order.
(1)
Numbers in parentheses refer to elements in illustrations.
1
Numbers in illustrations denote elements referred to in the text.
–
Dashes indicate listings.
>
The greater-than symbol indicates the navigation path in a dialog.
This symbol indicates information that will facilitate the use of the product.
1.2
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.
The product "Atlan A300, A300 XL, A350, A350 XL" is also referred to as "Atlan".
1.3
Illustrations
Illustrations of products and screen content in this document may differ from the
actual products depending on configuration and design.
1.4
Trademarks
1.4.1
Trademarks owned by Dräger
Trademark
Atlan®
AutoFlow®
Infinity®
D-Vapor®
Drägersorb®
MEDIBUS®
ServiceConnect®
WaterLock®
Instructions for use
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Information about this document
Trademark
E-Vent®
The following web page provides a list of the countries in which the trademarks are
registered: www.draeger.com/trademarks
1.4.2
Trademarks owned by third-party manufacturers
Trademark
®
Selectatec
Trademark owner
Datex-Ohmeda
Dismozon®
Mikrobac®
BODE Chemie
Korsolex®
Neodisher
Mediclean®
Dr. Weigert
acryl-des®
Mikrozid®
Schülke & Mayr
Perform®
Actichlor®
OxyCide®
Ecolab USA
BruTab 6S®
Brulin
Dispatch®
Clorox
Klorsept®
Medentech
Descogen®
Oxygenon®
Antiseptica
Virkon®
DuPont
SteriMax®
Aseptix
Cleanisept®
Dr. Schumacher
Trademark used Trademark owner
under license
BIPAP
8
Respironics
Instructions for use
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Safety-related information
2
Safety-related information
2.1
Intended use
This device is intended for use in anesthetizing adults, pediatric patients, and
neonates. The device can be used for mechanical ventilation, manual ventilation,
pressure-supported spontaneous breathing, and spontaneous breathing.
The device is equipped with the following basic functions:
– Ventilation monitoring
– Inspiratory O2 measurement
– Device monitoring
– Anesthetic gas receiving system
The following options are additionally available:
– Patient-gas measurement module for O2, CO2, N2O, and anesthetic gases
– O2 insufflation
Anesthesia is achieved through a mixture of pure oxygen and Air (medical
compressed air) or pure oxygen and nitrous oxide, with the addition of volatile
anesthetic agents.
Ventilation is accomplished on the patient through a laryngeal mask, a breathing
mask, or an endotracheal tube.
The integrated breathing system can be used with partial rebreathing (low-flow or
minimum-flow).
A non-rebreathing system, such as the Bain, Mapleson, Kuhn, or Waters system,
may be used at the external fresh-gas outlet.
2.2
Indications
The device is specified for inhalational anesthesia and/or patient ventilation in
accordance with the intended use during surgical or diagnostic interventions.
2.3
Contraindications
The device has no product-specific contraindications.
It is the responsibility of the user to select the appropriate treatment for the patient’s
underlying disease. The patient's condition must be continually monitored for any
potential changes.
The safety information must be followed for patients suspected of malignant
hyperthermia, patients with ketoacidosis, and patients who are under the influence
of alcohol. Observe the following information: "Therapy and applications", page 89.
The device administers medical gases such as O2, N2O, Air (medical
compressed air), and volatile anesthetic agents (halothane, enflurane, isoflurane,
sevoflurane, desflurane). For contraindications to the applied medical gases, strictly
follow the instructions for use of the medical gases.
Instructions for use
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Safety-related information
2.4
Environments of use
The device is designed for use in rooms in which therapeutic or diagnostic
interventions can be performed under constant supervision of users. According to
IEC 60601-1-2, the use of the device is only permissible in hospitals and
comparable facilities with a Class A electromagnetic environment.
Do not use the device in the following environments:
– Outside buildings
– On intensive care units
– During patient transport
– In vehicles, airplanes, helicopters, and on ships
– In areas where oxygen concentrations above 25 Vol% or combustible or
explosive gas mixtures can occur.
– In rooms with magnetic field applications (e.g., magnetic resonance imaging)
2.5
Essential performance features
Correct functioning of the essential performance features ensures that the product
can be used in accordance with its intended use. The product has the following
essential performance features:
General
– Supply of the anesthesia workstation with O2:
If the O2 supply (central gas supply or gas cylinder) fails, an alarm is issued.
– Supply of the patient with adequately oxygenated breathing gas:
If the breathing gas contains insufficient levels of O2, an alarm is issued.
– Supply of an adequate anesthetic gas concentration to the patient:
When the anesthetic gas is measured by means of an integrated patient-gas
measurement module, an alarm will be generated if the anesthetic gas
concentrations are too high.
– Monitoring of the airway pressure:
Alarms are issued depending on the set alarm limits.
Gas measurement
– Breathing gas monitoring:
– Set values for FiO2
– Inspiratory and expiratory measured values for O2, CO2, N2O, and
anesthetic gas; automatic anesthetic agent identification (patient-gas
measurement module)
The gas composition is measured with ISO accuracy.
– Monitoring of breathing gas concentrations:
Alarms will be issued depending on the set alarm limits or if the gas
measurement fails.
10
Instructions for use
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Safety-related information
2.6
User group requirements
The term "user group" describes the responsible personnel who have been
assigned by the operating organization to perform specific tasks on the product.
2.6.1
Duties of the operating organization
The operating organization must ensure the following:
– Each user group has the required qualification (e.g., has undergone specialist
training or acquired specialist knowledge through experience).
– Each user group has been trained to perform the task.
– Each user group has read and understood the relevant chapters in this
document.
2.6.2
User groups
Clinical users
This user group uses the product in accordance with the intended use.
Reprocessing personnel
This user group performs reprocessing activities.
Service personnel
This user group installs the product and performs service activities.
If product-specific skills or tools are required, then the service activities must be
performed by specialized service personnel. The specialized service personnel
have been trained by Dräger to perform these specific service activities on this
specific product.
2.7
Information on safety instructions and precautionary
statements
Safety instructions and precautionary statements warn of risks and give instructions
for the safe use of the product. Failure to observe them may lead to personal injury
or property damage.
2.7.1
Safety instructions
This document contains sections with safety instructions which warn of risks. The
type of risk and the consequences of non-compliance are described in each safety
instruction.
2.7.2
Precautionary statements
Precautionary statements relate to action steps and warn of risks that may arise
when performing the action steps. Precautionary statements precede the action
steps.
Instructions for use
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Safety-related information
The following warning signs and signal words indicate precautionary statements
and differentiate the possible consequences of non-compliance.
Warning sign Signal word
WARNING
Consequences of non-compliance
May result in death or serious injury.
CAUTION
May result in moderate or minor injury.
NOTICE
May result in property damage.
2.8
Safety instructions
2.8.1
Instructions for use
Personal injury and property damage may arise if this product is used contrary to
the information in these instructions for use.
► Follow these instructions for use.
► Only use this product in accordance with its intended use.
► Keep these instructions for use in an accessible location. Make sure that the
instructions for use are compatible with the device software.
► Follow the instructions for use of all the products that are used with this product.
These instructions for use do not provide any information on the following:
– Risks that are obvious to the user
– Consequences of foreseeable misuse of the product
– Possible negative effects on patients with one or more diseases
2.8.2
Symbols and product labels
Failure to observe symbols and product labels may result in personal injury and
property damage.
► Observe the symbols and product labels.
2.8.3
Monitoring the patient's condition
The monitoring of the patient's condition can range from direct observation to
electronic monitoring by means of medical devices. If the patient's condition is not
adequately monitored, the patient may be put at risk.
► Monitor the patient's condition in an appropriate manner and at appropriate
intervals.
N2O, O2, CO2 and, where necessary, anesthetic gases must be monitored when
patients are ventilated. If no monitoring is available or the sensors are not ready for
operation, the patient will not be adequately monitored and may be put at risk.
► Provide for suitable monitoring of O2, CO2, N2O, and anesthetic gases in
accordance with ISO 80601-2-55.
► Provide for suitable substitute monitoring in the event of a fault.
12
Instructions for use
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Safety-related information
2.8.4
Accessories and components
Compatible accessories
The use of faulty or incompatible accessories may compromise the functional
integrity of the product. Personal injury and property damage may occur as a
consequence.
► Use only compatible accessories. The accessories that are compatible with this
product are listed in the list of accessories supplied with the product.
► Use only accessories that are in good working order.
Instructions for use for accessories
If accessories or connected devices are used contrary to the information in the
associated instructions for use, this may lead to user errors, incorrect use, or
incorrect reprocessing. Personal injury and property damage may occur as a
consequence.
► Follow the instructions for use for all accessories, e.g.:
– Water traps
– Flow sensors
– CLIC adapter
– CLIC absorber
– Soda lime
– Breathing hoses
– Masks
– Filter
– Bronchial suction
– Vaporizer
– Manual resuscitator
– AGSS terminal unit
2.8.5
Color codes and labels
In some countries, the arrangement and display of the gases on the status display
and the virtual flow tubes on the screen may deviate from the illustrations shown in
this document.
► Always pay attention to the respective color codes and labels.
2.8.6
Device
Penetrating liquid
Penetrating liquid may cause the following:
– Damage to the device
– Electric shock
– Device malfunctions
Personal injury and property damage may occur as a consequence.
► Ensure that no liquid penetrates the device.
► Do not place any containers containing liquids above or on the device.
Instructions for use
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Safety-related information
Housing
Under the housing, there are live electrical components, which may cause an
electric shock.
► The housing may only be opened by those user groups that are assigned to that
particular measure.
2.8.7
Service
If service activities are not performed regularly or properly, malfunctions may occur
that can result in personal injury and property damage.
► Perform the service in accordance with the chapter "Service".
2.8.8
Reprocessing
Reusable products must be reprocessed, otherwise there is an increased risk of
infection.
► Perform the reprocessing in accordance with the chapter "Reprocessing".
2.8.9
Modifications to the product
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.
2.8.10
Network security
The impermissible use of data interfaces may result in property damage and
personal injury.
► Only make connections to data interfaces with permission from the responsible
organization (IT representative and the hospital equipment officer).
► Observe the following information: "Connections to IT networks", page 294.
2.9
Additional information
2.9.1
Use of Infinity ID components
Ownership or purchase of this medical device with RFID technology only includes
the right to use the medical device and RFID technology in conjunction with
products approved by Dräger and in strict compliance with these instructions for
use. No intellectual property rights or any rights to the use of the medical device or
RFID technology are hereby granted, either explicitly or implicitly, which are
contrary to the above-mentioned conditions.
2.9.2
Training
Training for users is available via the Dräger organization responsible (see
www.draeger.com).
14
Instructions for use
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Overview
Overview
3.1
Hardware
3.1.1
Front
3.1.1.1
Large version
36437
3
No.
1
2
3
4
5
6
7
8
9
10
Instructions for use
Designation
Screen
Description
Enables user inputs by touchscreen and
rotary knob.
Plug-in connectors for vaporiz- Enable the connection of up to 3 vaporizers.
ers
Backup manual switch (behind Used to switch to backup manual mode in
the flap)
the event of malfunctions of the device.
Gas mixing unit
Produces a gas mixture from the selected
gases (e.g., O2 and Air).
Work surface
Used for storing, e.g., documents.
Pull-out writing tray (option)
Provides additional work surface.
Viewing window for piston ven- Allows visual checking of the movement of
tilator
the piston ventilator.
Lockable drawer
Provides additional storage space.
Trolley with footrest and cen- Used for moving the device. The central
tral brake
brake locks the two front castors.
CO2 absorber
Absorbs CO2 from the patient’s breathing
gas.
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Page 16
Overview
No.
11
12
13
14
Description
Used for suctioning and scavenging excess
anesthetic gas and breathing gas. Used to
reduce the anesthetic gas concentration
released into the environment by the anesthesia machine, and to scavenge the sample gases from an anesthetic gas monitor.
External fresh-gas outlet
Gas outlet for a mixture of fresh gas and
anesthetic gas which is fed to a nonrebreathing system.
External O2 flowmeter (option) Supplies pure oxygen for O2 insufflation.
Rail
Used for fastening additional components.
Compact version
36438
3.1.1.2
Designation
Anesthetic gas receiving system
No.
1
2
3
4
5
6
7
8
9
16
Designation
Screen
Description
Enables user inputs by touchscreen and
rotary knob.
Plug-in connectors for vaporiz- Enable the connection of up to 2 vaporizers.
ers
Backup manual switch (behind Used to switch to backup manual mode in
the flap)
the event of malfunctions of the device.
Swiveling shelf (option)
Used for storage.
Work surface
Used for storing, e.g., documents.
Viewing window for piston ven- Allows visual checking of the movement of
tilator
the piston ventilator.
Lockable drawer
Provides additional storage space.
Trolley with footrest and cen- Used for moving the device. The central
tral brake
brake locks the two front castors.
CO2 absorber
Absorbs CO2 from the patient’s breathing
gas.
Instructions for use
| Atlan A300, A300 XL, A350, A350 XL SW 1.0n
Page 17
Overview
Designation
Anesthetic gas receiving system
11
Gas mixing unit
12
External fresh-gas outlet
13
Rail
Description
Used for suctioning and scavenging excess
anesthetic gas and breathing gas. Used to
reduce the anesthetic gas concentration
released into the environment by the anesthesia machine, and to scavenge the sample gases from an anesthetic gas monitor.
Produces a gas mixture from the selected
gases (e.g., O2 and Air).
Gas outlet for a mixture of fresh gas and
anesthetic gas which is fed to a nonrebreathing system.
Used for fastening additional components.
Screen
36441
3.1.2
No.
10
No.
1
2
Designation
Touchscreen
Alarm silence key
3
Rotary knob
4
5
Working light
6
Instructions for use
key
key
Description
Calls up functions or dialogs when touched.
Suppresses the alarm tones of all active
alarms for 2 minutes.
Used for selecting, adjusting, and confirming settings. Lights up in color in certain situations.
Illuminates the work surface.
Turns the working light on or off. Dims the
illuminance in 3 steps (dark, medium, and
bright).
Turns the device on or off.
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Overview
3.1.3
Breathing system and other components
3.1.3.1
Overview
36446
The following illustration shows the device and the breathing system.
18
No.
1
Designation
Pressure gauge (option)
2
Inspiratory port
3
Bag elbow with circuit plug
4
APL valve
5
Breathing system cover
6
Expiratory port
7
8
Holder
Handles
9
CO2 absorber
10
Anesthetic gas receiving system
Instructions for use
Description
Indicates the airway pressure in the internal
breathing system.
Used to connect the inspiratory hose to the
device.
Used to connect the breathing bag hose.
The circuit plug is used to seal the Y-piece
during an automatic test.
Limits the maximum airway pressure in the
Manual / Spontaneous mode.
Protects the breathing system underneath
and provides climate control for the breathing system.
Used to connect the expiratory hose to the
device.
Used for parking the breathing bag hose.
Used for aligning the device and for stowing
used breathing hoses.
Absorbs CO2 from the patient’s breathing
gas.
Used for suctioning and scavenging excess
anesthetic gas and breathing gas, to reduce
the anesthetic gas concentration released
into the environment by the anesthesia
machine, and to scavenge the sample
gases from an anesthetic gas monitor.
| Atlan A300, A300 XL, A350, A350 XL SW 1.0n
Page 19
Overview
No.
11
12
13
3.1.3.2
Designation
Water trap with connection for
sample line
Patient-gas measurement
module
Guide clip
Description
Collects condensed water which forms in
the sample line.
Measures and monitors various gas concentrations in the breathing gas (O2, CO2,
N2O, and anesthetic gases).
Used to securely lay the O2 insufflation
hose.
Version with O2 sensor
36447
The following illustration shows the device without its breathing system cover and
illustrates the position of the O2 sensor.
Instructions for use
No.
1
Designation
O2 sensor
2
Sealing cap
Description
Measures the inspiratory O2 concentration
in the breathing gas.
Seals the O2 sensor port during calibration
of the O2 sensor.
| Atlan A300, A300 XL, A350, A350 XL SW 1.0n
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Page 20
Overview
Side view from left
36462
3.1.4
No.
1
2
3
4
20
Designation
Castor brake
Gas cylinder holder (option)
Rail
Hanger yoke system (option)
Instructions for use
Description
Prevents movement of the rear castor.
Secures the gas cylinders.
Used for fastening additional components.
Enables the connection of gas cylinders
with a pin-index connector.
| Atlan A300, A300 XL, A350, A350 XL SW 1.0n
Page 21
Overview
Side view from right
36468
3.1.5
No.
1
Instructions for use
Designation
Standard rail with handle
Description
Allows the device to be maneuvered during
intrahospital transport and also the attachment of accessories.
| Atlan A300, A300 XL, A350, A350 XL SW 1.0n
21
Page 22
Overview
3.1.6
Device column
36469
The illustration shows the left side of the device.
22
No.
1
Designation
Column cover
2
Holder for hoses and cables
3
Cable holder with cable
channels
Instructions for use
Description
Depending on the version, allows a patient
monitor or other workplace components to
be mounted.
Used for storing and winding up central supply hoses and cables.
For passing hoses and cables through.
| Atlan A300, A300 XL, A350, A350 XL SW 1.0n
Page 23
Overview
Rear
3.1.7.1
Version with screw connections for standing gas cylinders
36470
3.1.7
No.
1
2
Designation
Storage compartment
Holder for hoses and cables
3
Gas supply block
4
5
7
Gas cylinder holder (option)
Strain relief for compressed
gas hoses
Auxiliary power sockets
(option)
Vent
8
Ventilation slot
9
Connectors
6
Instructions for use
Description
Can be used as storage space.
Used for storing and winding up central supply hoses and cables.
Provides connectors for gases from the
central gas supply system and for gas cylinders.
Secures the gas cylinders.
Protects the compressed gas hoses from
loosening inadvertently.
Allow other devices to be connected.
Discharges warmed air from the device into
the environment.
Feeds ambient air to the device for ventilation.
Provides connectors for power cable,
potential equalization, and interfaces. Used
for data exchange between external
devices, additional components, and networks.
| Atlan A300, A300 XL, A350, A350 XL SW 1.0n
23
Page 24
Overview
Version with pin-index connector for suspended gas cylinders (option)
36471
3.1.7.2
No.
1
2
Designation
Storage compartment
Holder for hoses and cables
3
Gas supply block
4
Hanger yoke system (option)
5
Strain relief for compressed
gas hoses
Vent
6
7
8
24
9
Gas cylinder holder (option)
Auxiliary power sockets
(option)
Ventilation slot
10
Connectors
Instructions for use
Description
Can be used as storage space.
Used for storing and winding up central supply hoses and cables.
Provides connectors for gases from the
central gas supply system and for gas cylinders.
Enables the connection of gas cylinders
with a pin-index connector.
Protects the compressed gas hoses from
loosening inadvertently.
Discharges warmed air from the device into
the environment.
Secures the gas cylinders.
Allow other devices to be connected.
Feeds ambient air to the device for ventilation.
Provides connectors for power cable,
potential equalization, and interfaces. Used
for data exchange between external
devices, additional components, and networks.
| Atlan A300, A300 XL, A350, A350 XL SW 1.0n
Page 25
Overview
Connectors
36474
3.1.8
No.
1
Designation
Serial port (COM 1 and
COM 2)
2
Main switch
3
5
Connector for workplace light
(option)
Power inlet (connector for
power cable)
Potential equalization pin
6
7
Network port
USB port
4
Instructions for use
Description
This serial port (RS232) supports the MEDIBUS.X protocol for data exchange between
the anesthesia machine and external
devices.
Turns the device off and minimizes the current consumption when the power plug is
pulled out. To be used when the device is to
be disconnected from the power supply for
longer than 2 weeks and during service
activities.
Used for connecting an external workplace
light.
Used to connect the device to the mains
power supply.
Used for connecting a potential equalization
cable. This will minimize differences in electrical potential.
Enables data transfer within an IT network.
Used to transfer data to a USB mass storage device.
| Atlan A300, A300 XL, A350, A350 XL SW 1.0n
25