Dräger Infinity Delta Series Owner's manual

Supplement
Infinity® Delta Series
Infinity® Patient Monitoring Series
Software VF10.1
WARNING
To properly use this medical device,
read and comply with the instructions
for use and this supplement.

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Supplement for Infinity Delta Series Software
Infinity Delta Series Instructions for use
Software VF10.1
©Drägerwerk AG & Co. KGaA
All rights reserved.
Reproduction in any manner, in whole or in part, in English or in any other languages, except for brief
excerpts in reviews and scientific papers, is prohibited without prior written permission of Dräger.
Before using any Dräger devices, carefully read all the manuals that are provided with your device. Patient
monitoring equipment, however sophisticated, should never be used as a substitute for the human care,
attention, and critical judgment that only trained health care professionals can provide.
ACE®, DrägerService®, MultiMed®, DualHemo®, QuadHemo®, Infinity®, Perseus®, SmartPod®,
Trident®, Pick and Go®, Scio®, and OxiSure® are trademarks of Dräger.
PiCCO®, PULSION®, and PULSIOCATH® are trademarks of PULSION Medical Systems.
CAPNOSTAT® is a trademark of Philips.
A-2000, BIS, BISx, Bispectral Index, Microstream, INVOS, and Nellcor are trademarks and registered
trademarks of a Medtronic company.
CNAP® is a trademark of CNSystems Medizintechnik AG.
Masimo®, Masimo SET®, and Signal Extraction Technology (SET)® are trademarks of Masimo
Corporation.
Dismozon® is a trademark of BODE Chemie.
Oxycide® is a trademark of Ecolab USA.
SILICON SOFTWARE © 1989, 90, 91, 92, 93, 94 Microtec Research Inc.
All rights reserved.
Some graphics courtesy of Covidien.
Unpublished rights reserved under the copyright laws of the United States.
RESTRICTED RIGHTS LEGEND Use, duplication, or disclosure by the Government is subject to
restrictions as set forth in subparagraph (c)(1)(ii) of the Rights in Technical Data & Computer Software
clause at DFARS 252 227:7013.
The capnography component of this product is covered by one of the following US patents: 6,428,483;
6,997,880; 6,437,316; 7,488,229; 7,726,954 and their foreign equivalents. Additional patent applications
pending.
All other brand or product names are trademarks of their respective owners.

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For your safety and that of your patients
Mandatory reporting of adverse events
Serious adverse events with this product must be reported to Dräger and the responsible authorities.
Safety information
Definition of Target Groups
Target groups for this product include users, service personnel, and experts.
These target groups must have received instruction in the use of the product and must have the necessary
training and knowledge to use, reprocess, maintain, or repair the product. Contact Dräger for training
options.
The product must be used, installed, reprocessed, maintained, or repaired exclusively by defined target
groups.
Users
Users are persons who use the product in accordance with its intended use.
Service Personnel
Service personnel are persons who are responsible for the maintenance of the product. Service personnel
must be trained in the maintenance of medical devices and install, reprocess, and maintain the product.
WARNING
A WARNING statement provides important information about a potentially hazardous situation
which, if not avoided, could result in death or serious injury.
CAUTION
A CAUTION statement provides important information about a potentially hazardous situation which, if
not avoided, may result in minor or moderate injury to the user or patient, or in damage to the
equipment or other property.
NOTE
A NOTE provides additional information intended to avoid inconveniences during operation.

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Experts
Experts are persons who perform repair or complex maintenance work on the product. Experts must have
the necessary knowledge and experience with complex maintenance work on the product.
Training
Training for users is available via the responsible Dräger organization (see www.draeger.com).
WARNING
Risk of serious personal injury, death or property damage.
The monitor can detach from the docking station and fall if:
– the mount is faulty
– the monitor is not securely locked in the docking station
If any part of the docking station appears faulty, do not install it or attach a monitor to it. Contact
your hospital’s service personnel.
Follow the installation instructions provided with the mount.
Position the docking station in a safe location away from the patient.
To prevent the monitor from falling, ensure that it is securely locked in the docking station.
When securely locked, the Battery Charge indicator located on the lower-left front panel of the
monitor is lit.
For more information on docking the monitor, see the main IFU.

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Introduction
Changes in Delta VF10.1
Starting with Delta VF10.1, the following VGA Display requirement has been removed from the Display
Unit (Kappa only) table under the Displays heading.
Output resolution:
High resolution mode: 1024 x 768
Medium resolution mode: 800 x 600
Low resolution mode: 640 x 480
System Components
Applicable Software Options (on a memory option card) include:
Options for Delta only:
– Delta second PodPort option – Pod Comm
Delta, Delta XL and Kappa:
– 4 to 5 channel option – Delta 4-5 Channels
– 6 to 8 channel option – Delta 6-8 Channels
– 3-Lead ST-segment analysis option –
ST Monitoring
– ARIES option – Aries S/W
– Hemodynamic Calculations option – Hemodynamic Calculations
– ACE full arrhythmia option – Arrhythmia II
– Hemo/Oxy/Vent Calculations option package – Hemo/Oxy/Vent Calculations
– OR mode option (loaded in the monitor)
– OR Single Unit
– OR Mode option (loaded in the IDS or Kappa Advanced Communication Option II) – OR Site

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Cybersecurity and Network Stability
Corrected vulnerabilities that may cause device to reboot, lose functionality, and/or lose communication.
Base Unit
Monitor Rear View – Delta XL
Monitor Setup
Main Menu Setup
Date & Time is no longer a selection in the Main Menu > Monitor Setup > Monitor Options submenu.
Date and time changes are only permitted by qualified hospital technical personnel or Dräger Service
personnel in the password-protected Service menu.
Unit Manager
The Unit Manager menu lets supervisory personnel configure monitoring functions for the clinical staff.
Access to this menu is restricted by a password.
1External (lead-acid) battery
compartment (not supported
with software VF9.0 or higher)
2Connector for docking station
interface plate
3Connector for AC adaptor
4Slot for etCO2 modules

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Unit Manager Menu
Menu Item Description Available Settings
The Alarm Control 1 and Alarm Control 2 submenus:
This menu allows the unit manager to configure alarm annunciation. Open the Unit Manager menu,
click on Alarm Control 1 or Alarm Control 2, and then follow the procedures outlined in this table to
execute the indicated functions.
All Alarms OFF
Reminder tone
(Alarm Control 1
submenu)
A reminder tone to indicate all alarms are
OFF permanently.
–Enabled (default)
–Disabled
Enabled when the All Alarms OFF
feature is set to Enabled. A
reminder tone sounds every
30 seconds at 50% volume.
Audio OFF
Reminder (Alarm
Control 1
submenu)
Allows you to set a reminder when the Alarm
Volume is set to OFF.
–Enabled (default) - When the
alarm volume is set to OFF, a
reminder tone sounds every
30 seconds at 50% volume.
For monitors in OR mode: At the
end of an alarm silence or an
alarm off period, if the alarm
condition is still active, the
parameter box flashes and a
reminder tone (high, medium, or
low) sounds every 30 seconds
at 50% volume.
–Disabled -There is no reminder
tone when alarm volume is set
to OFF.
The CODE Setup submenu
This menu allows the unit manager to configure the monitor for quick emergency response. Open the
Unit Manager menu, click on CODE Setup, and then select and execute functions as described in this
table.
Audio OFF Allows you to lower the alarm volume to OFF
when you press the Code fixed key.
NOTE: The central station continues to
sound audio alarms after you press the
Code key.
–Yes - Temporarily sets the alarm
volume and the minimum alarm
volume to OFF when you press
the Code key.
–No (default) - The alarm volume
and the minimum alarm volume
settings do not change when
you press the Code key (i.e.,
retains prior settings).

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Device Markings
The following table contains symbols that have been modified or added to the table in the section on
device markings in the main IFU.
Caution: This product contains
natural rubber latex which may
cause an allergic reaction
Manufacturer’s reorder code
Date of manufacture Device serial number
Acceptable storage temerature ECG waveform out
Acceptable atmospheric pressure
range
ECG Sync out
Acceptable humidity range Arterial waveform out
Contains DEHP Medical Device

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Biomed
Quick Reference - Biomed Menu
Menu Item Description Settings/Procedures
Mainstream CO2
Component Log
This read-only field contains information to
assist with system upgrades and diagnosing
field issues.
The display is read-only.
Press the Menu fixed key.
Select Monitor
Setup>Biomed>Logs>
Component Log

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Temperature Display
All temperature readings appear on the main screen according to their position in Parameter Priority (see
page 2-6). The following display conventions govern temperature labels and values.
The monitor displays temperature values in one parameter box for each pod connector (MultiMed, He-
mo2/Hemo4). The variables “a” and “b” denote the first or second probe connector from the MultiMed with
Y-cable, NeoMed, Hemo2, Hemo4 pod or the MPod – Quad Hemo. When acquired via the MultiMed or
NeoMed pod, temperature signals are displayed as Ta <value> or Tb <value>. (If you are using a MultiMed
without a Y-cable, only Ta displays a value.)
When monitoring temperature using the Hemo2, Hemo4 pod, or the MPod – Quad Hemo, temperature
values are further identified according to where they are connected to the monitor. The temperature value
corresponding to the device hooked up to the Aux/Hemo2 PodCom connector is labeled T2a or T2b, while
the temperature value corresponding to the device hooked up to the Aux/Hemo3 connector is labeled T3a
or T3b.
NOTE
The transient response time for the monitor is less than 2.5 seconds.

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Network Applications
Network Message (Delta/Delta XL/Kappa). . . . 14
Remote View . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Connections to IT networks . . . . . . . . . . . . . 14
Information about connecting to an IT
network. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Disconnecting the monitor from the
network . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Power Sources . . . . . . . . . . . . . . . . . . . . . . . . 17
Battery Power. . . . . . . . . . . . . . . . . . . . . . . . . .17
Admission, Transfer, and Discharge . . . . . . 18
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
General Requirements - Alarm Setup . . . . . . . 19
Alarm History Table . . . . . . . . . . . . . . . . . . . . . 21
Alarm Latching . . . . . . . . . . . . . . . . . . . . . . . . . 21
ECG and Heart Rate . . . . . . . . . . . . . . . . . . . . 22
ECG and Heart Rate . . . . . . . . . . . . . . . . . . . . 22
ECG Leads. . . . . . . . . . . . . . . . . . . . . . . . . . . .22
ECG Setup Menu . . . . . . . . . . . . . . . . . . . . . . . 23
Arrhythmia Monitoring. . . . . . . . . . . . . . . . . . 24
Arrhythmia Ranges and Defaults . . . . . . . . . . . 24
Respiration . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Non-Invasive Blood Pressure . . . . . . . . . . . . 26
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
NBP Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Status Messages . . . . . . . . . . . . . . . . . . . . . . . 29
Continuous Non-invasive Arterial Blood
Pressure (CNAP) Pod. . . . . . . . . . . . . . . . . . . 30
CNAP Calibration . . . . . . . . . . . . . . . . . . . . . . . 31
Status Messages . . . . . . . . . . . . . . . . . . . . . . . 31
Maintenance (CNAP) . . . . . . . . . . . . . . . . . . . 31
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Definition of Maintenance Concepts . . . . . . . . 32
Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Visual Inspection . . . . . . . . . . . . . . . . . . . . . . . 33
Inspection/ Safety Check. . . . . . . . . . . . . . . . . 33
Metrological checks. . . . . . . . . . . . . . . . . . . . . 34
Calculations . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Pulse Oximetry (SpO2) . . . . . . . . . . . . . . . . . 35
Quick Reference Table - SpO2 Setup . . . . . . . 37
New Status Message. . . . . . . . . . . . . . . . . . . . 37
Dräger Mainstream etCO2 Monitoring. . . . . 38
Application. . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
Connecting the Sensor . . . . . . . . . . . . . . . . . . 42
Getting Started . . . . . . . . . . . . . . . . . . . . . . . . 43
Device Conflicts. . . . . . . . . . . . . . . . . . . . . . . . 43
Display Features . . . . . . . . . . . . . . . . . . . . . . . 45
Capnograms . . . . . . . . . . . . . . . . . . . . . . . . . . 49
Troubleshooting. . . . . . . . . . . . . . . . . . . . . . . . 51
Status Messages . . . . . . . . . . . . . . . . . . . . . . . 54
Respiratory Mechanics. . . . . . . . . . . . . . . . . 55
FiO2 (Fractional Inspired O2) monitoring . . 56
Display Features . . . . . . . . . . . . . . . . . . . . . . . 56
MultiGas Monitoring . . . . . . . . . . . . . . . . . . . 56
xMAC (MAC multiple) . . . . . . . . . . . . . . . . . . . 56
Status Messages . . . . . . . . . . . . . . . . . . . . . . . 59
Neuromuscular Transmission (NMT)
Monitoring . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
Patient Preparation . . . . . . . . . . . . . . . . . . . . . 60
Pulse Contour Cardiac Output (PiCCO)
Monitoring . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
Overview of the Infinity PiCCO Pod . . . . . . . . 61
To set up the PiCCO Pod . . . . . . . . . . . . . . . . 63

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Quick Reference - PiCCO Setup . . . . . . . . . . . 66
Optimizing Results for PiCCO
Measurements . . . . . . . . . . . . . . . . . . . . . . . . . 66
Peripheral Devices and Associated
Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67
Analysis Tool. . . . . . . . . . . . . . . . . . . . . . . . . . . 67
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67
Compatible devices . . . . . . . . . . . . . . . . . . . . . 68
Precautions. . . . . . . . . . . . . . . . . . . . . . . . . . . . 71
Ventilation and Anesthesia Devices . . . . . . . . . 71
Atlan, Primus, Zeus, Apollo, and Perseus
Anesthesia Devices . . . . . . . . . . . . . . . . . . . . . 75
Covidien/Medtronic INVOS
Cerebral/Somatic Oximeter 5100C. . . . . . . . . . 79
Information on reprocessing. . . . . . . . . . . . . 79
Safety information. . . . . . . . . . . . . . . . . . . . . . . 79
Classifications for reprocessing. . . . . . . . . . 80
Classification of medical devices . . . . . . . . . . . 80
Classification of device-specific components . . 80
Reprocessing list . . . . . . . . . . . . . . . . . . . . . . 81
Reprocessing procedures . . . . . . . . . . . . . . . 81
Validated reprocessing procedures . . . . . . . . . 81
Disinfectants . . . . . . . . . . . . . . . . . . . . . . . . . . . 81
Surface disinfection with cleaning . . . . . . . . . . 83
Cleaning and Disinfecting . . . . . . . . . . . . . . . 83
IBP - Infinity PiCCO Pod. . . . . . . . . . . . . . . . . . 83
etCO2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
To dry the sidestream pump subsystem . . . . . . 85
Technical Data . . . . . . . . . . . . . . . . . . . . . . . . 85
Electromagnetic Compatibility (EMC). . . . . . . . 85
Electromagnetic Emissions . . . . . . . . . . . . . . . 88
Electromagnetic Immunity . . . . . . . . . . . . . . . . 89
Recommended separation distances . . . . . . . . 90
EMC declaration . . . . . . . . . . . . . . . . . . . . . . . 91
General information . . . . . . . . . . . . . . . . . . . . . 91
Electromagnetic environment. . . . . . . . . . . . . . 91
Recommended separation distances from
wireless communication devices . . . . . . . . . . . 92
System Components . . . . . . . . . . . . . . . . . . . . 93
Monitoring Accessories . . . . . . . . . . . . . . . . . . 94
Monitoring Specifications. . . . . . . . . . . . . . . . . 96
Approved Options and Accessories . . . . . . 108
Temperature probe covers . . . . . . . . . . . . . . . 108
Invasive Blood Pressure (IBP) . . . . . . . . . . . . 109
Pulse Oximeter (SpO2) . . . . . . . . . . . . . . . . . . 109
Nellcor FLEXMAX reusable sensors . . . . . . . . 112
Mainstream etCO2 . . . . . . . . . . . . . . . . . . . . . 113
Infinity PiCCO Pod . . . . . . . . . . . . . . . . . . . . . 113
Infinity PiCCO Pod Connecting Cables . . . . . . 113
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . 114
Admission, Transfer, and Discharge . . . . . . . . 114
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 114
Trends . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115
ECG and Heart Rate . . . . . . . . . . . . . . . . . . . . 115
Respiration . . . . . . . . . . . . . . . . . . . . . . . . . . . 115
Pulse Oximetry (SpO2) . . . . . . . . . . . . . . . . . . 116
Dräger Mainstream etCO2 Monitoring . . . . . . 116
Pulse Contour Cardiac Output (PiCCO)
Monitoring . . . . . . . . . . . . . . . . . . . . . . . . . . . . 117
Peripheral Devices and Associated
Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 117

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Network Message (Delta/Delta XL/Kappa)
The Condition for the Duplicate Address message should read as follows:
More than one monitor configured for the same IP address.
Remote View
Remote view of an IACS or M540 monitor from a Delta Series Monitor may not display all of the
information properly. Refer to the primary source device for all diagnostic and therapeutic decisions.
Remote view of a Delta Series Monitor from an IACS or M540 monitor may not display all of the
information properly. Refer to the primary source device for all diagnostic and therapeutic decisions.
Connections to IT networks
In an IT network, data can be exchanged by means of wired or wireless technologies. An IT network can
be any data interface (e.g., RS232, LAN, USB, printer interface) that is described in standards and
conventions.
During operation, this device can exchange information with other devices by means of IT networks and
supports the following functions:
– Display of waveforms and parameter data
– Signaling of alarms
– Recording, storing, and printing
– Remote control (e.g., alarm management)
– Bed view by remote access
– Access to saved patient data
– Transfer of device settings and patient data
Connecting this device to a network that incorporates other devices or making subsequent changes to that
network can lead to new risks for patients, users, and third parties. Before the device is connected to the
network or the network is changed, these risks must be identified, analyzed, and evaluated, and
appropriate measures taken.
Examples of subsequent changes to the network:
– Changing the network configuration
– Removing devices from the network
CAUTION
If the Duplicate Address network message is displayed, contact your Biomed or local DrägerService.

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– Adding new devices to the network
– Performing upgrades or updates on devices that are connected to the network
Information about connecting to an IT network
Prerequisites
This device must only be connected to the network by service personnel. The IT representative of the
hospital must be consulted in advance.
The following documents must be observed:
– Accompanying documents of this device
– Descriptions of the network
– Description of the network-based alarm systems
Dräger recommends complying with IEC 80001-1 (risk management for IT networks with medical
devices).
LAN networks
– LAN networks are usually configured in a star topology. Individual devices can be combined into groups
by means of layer-n-switches. Other data traffic is decoupled by means of separate VLAN networks.
Configure the network settings of the device in accordance with these instructions for use and the network
specifications.
– Specifications for LAN connections are described in the following standards:
– Wired networks: IEEE˽802.3
– Wireless networks: IEEE˽802.11 (b, g)
– If the device is used with a layer-2-switch or a layer-3-switch, the port settings must be configured on
the network switch. Before the device is shipped, Dräger can configure the network settings of the
device so that they are compatible with the specifications of the operating organization.
– This device exchanges data with other medical devices over the LAN network. The network must
support the following transmissions and protocols:
– TCP/IP
– Unicast (static or dynamic addressing with the ARP or RARP network protocols)
– Multicast
– Broadcast
– IGMP (version 2)
This device can join or leave an IP multicast group by using the IGMP network protocol.

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VLAN networks
If data is being exchanged within a single physical network and a clinical information system is used, an
independent VLAN network must be set up for the clinical information system. Additionally, at least one of
the following independent VLAN networks must be set up:
– Network for medical devices for intrahospital use
– Network for portable patient monitors
WLAN networks
– On Dräger devices, the Advanced Encryption Standard (AES) WPA2 with pre-shared key
administration is used during installation.
– With some Dräger clinical devices, the installation is carried out using SSL and additional functions
that are defined in the form "Manufacturer Disclosure Statement for Medical Device Security" (MDS2).
Serial interfaces
The following interfaces are supported:
– RS232 interfaces conforming to EIA RS232 (CCITT V.24/V.28) for the following applications:
– MEDIBUS, MEDIBUS.X
– Paging systems
– Connections to medical devices from other manufacturers
– Interfaces conforming to IEEE˽1073 (Medical Information Bus) for connection to medical devices from
other manufacturers
The requirements of IEEE 1073.3.2 or the combined requirements of IEEE 1073.3.1 and IEEE
1073.4.1 must be complied with.
Consequences of using an unsuitable network
If the network does not meet the requirements, hazardous situations can result. The following situations
can occur with this device:
– Due to unsafe distributed alarm system:
– Alarms are not transmitted.
– Alarms or data are delayed.
– False alarms are indicated.
– During an interruption of the network connection:
– Alarms are not transmitted.
– Suppressed alarms or alarm tones are not reactivated, but remain suppressed.
– Without firewall and antivirus software:
– Data are not protected.
– Device settings are changed.
– The device generates false alarms or no alarms.
– Data are sent incomplete, sent to the wrong device, or not sent at all.
– Patient data are intercepted, falsified, or damaged.

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– Data have incorrect time stamps.
Requirements for the electrical characteristics of connected devices and networks
The LAN interfaces and the serial interfaces are only suitable for the connection of devices or networks
that have a rated voltage of at most 24 V DC on the network side and that meet the requirements of one
of the following standards:
– IEC 60950-1: Ungrounded SELV circuits
– IEC 60601-1 (as of 2nd edition): Touchable secondary circuits
Disconnecting the monitor from the network
1Hold the monitor firmly by its handle. Slide the lever to the left to disengage the power supply. The mon-
itor automatically switches to battery power.
2Continue to move the lever to the left until it clicks. Use both hands to tilt the monitor forward and lift it
off the IDS or Docking Station.
3When docking and undocking the monitor to and from an IDS, a minimum 15 second delay between
undocking and redocking the monitor is required, for loading the default IDS profile to the monitor.
Power Sources
Battery Power
The following information refers to the table on battery charge display as described in the main IFU.
NOTE
When the internal battery has approximately 20 minutes remaining, a low priority alarm sounds and
the message Monitor Internal Battery Low appears. The alarm can be silenced; however, the
banner message remains visible.

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Admission, Transfer, and Discharge
Admitting a patient at the Central Station
1Select the viewport that corresponds to the room/patient monitor.
2Click on Admit/Standby.
3Click on the Demographics tab if it is not already selected.
4Enter the patient information in the appropriate fields.
5Click on Apply to confirm your entry.
If you pre-admit a patient to a discharged Delta patient monitor, the monitor exits discharge.
NOTE
To change the patient’s category (adult, pediatric, or neonatal), you must access the Patient
Setup menu at the bedside monitor.
If you change a patient’s category, the weight selection is cleared and must be entered again.
In neonatal mode, additional settings (gestational age and birth weight) are available at the
bedside monitor only. Day of Life and corrected GA values also appear in a read only field.
Entries and changes regarding a patient’s height and weight affect all other monitor menus and
displays that use this information.
For more information on admission at the Delta, see the Instructions For Use for the Delta
monitor.
Dräger recommends that patients be admitted at the Infinity CentralStation.

Supplement – Infinity® Delta Series Software VF10.1 19
Supplement for Infinity Delta Series Software
Alarms
General Requirements - Alarm Setup
Upper and Lower Alarm Limits
In addition to those listed in the main IFU, alarm limits should be set according to your patient’s prevailing
condition within the predefined ranges of the monitor as listed in the following table:
Parameter Predefined Alarm Range and
Resolution
Default State Default Alarm Setting
inCO2/inCO2* 2 to 10 mmHg (0.3 to 1.3 kPa) (upper
limit only) increments of 1 mmHg or
0.1 kPa
ON High: 4 mmHg (0.5 kPa)
PLS 30 to 240 in increments of 5 bpm ON Adult:
Low 45 bpm
High 120 bpm
Pediatric:
Low 50 bpm
High 150 bpm
Neonatal:
Low 80 bpm
High 180 bpm

Supplement for Infinity Delta Series Software
20 Supplement – Infinity® Delta Series Software VF10.1
Auto Set Alarm Limits
Alarm Limits Table
Function Description Available Settings
Auto Set Sets alarm limits based on current values: Not applicable
NOTE:
• The monitor recalculates the upper
and lower alarm limits based on the
parameter values in the Current
column.
•Auto Set applies to all displayed
parameters and ST parameters
only.
• If a calculated limit value falls
outside the range for that
parameter, the parameter’s alarm
limits remain unchanged.
Parameters Upper Limit Lower Limit
Ta, T1a, T1b,
T2a, T2b, T3a,
T3b
< 107% of
current value
< 93% of
current value
ΔT1, ΔT2, ΔT3,
PVC/min,
inCO2/inCO2*
No change No change
SpO2/SpO2* Adults 100
Neonates 98
Current value
–(value x 5%)
ΔSpO2% Current value
+20%
None
ST Current value
+2.0 mm
Current value
–2.0 mm
MultiGas Agent < 105% of
current value
< 95% of
current value
BIS No change No change
TOF-Cnt No change No change
PCCO Current value
+30%
Current value
–30%
PCCI Current value
+30%
Current value
–30%
MultiGas O2 100% 21%
tp < 125% of
current value
< 80% of
current value
All others Current value
+25%
Current value
–20%