Vista Ifu 2680025 en

Instructions for use
Vista 120 SC
WARNING Vital Signs Monitor

To properly use this medical device, Software 1.n
read and comply with these instructions
for use.
Screen images
Schematic renderings of screen images are used,

which may differ in appearance or in configuration
from the actual screen images.
Definition of Safety Information
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.
Abbreviations and Symbols
For explanations refer to sections “Abbreviations”

and “Symbols” in chapter “Overview”.
Instructions for use Vista 120 SC SW 1.n 1

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2 Instructions for use Vista 120 SC SW 1.n

Contents
Contents
Responsibility of the Manufacturer . . . . . . . 7 Monitoring mode . . . . . . . . . . . . . . . . . . . . . . 49

Responsibility of the Manufacturer . . . . . . . . . . 8 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
Admitting a patient. . . . . . . . . . . . . . . . . . . . . . 50
For your safety and that of your patients. . . 9 Quick admit . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
General safety information . . . . . . . . . . . . . . . . 10 Admit by barcode . . . . . . . . . . . . . . . . . . . . . . 51
Product-specific safety information. . . . . . . . . . 13 Editing patient information . . . . . . . . . . . . . . . . 52
Protecting personal information . . . . . . . . . . . . 19 Monitoring data review . . . . . . . . . . . . . . . . . . 52
Event marking . . . . . . . . . . . . . . . . . . . . . . . . . 53
Application . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Ward round mode . . . . . . . . . . . . . . . . . . . . . 55
Intended use. . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Restrictions for use. . . . . . . . . . . . . . . . . . . . . . 22 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
Intended user . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Create new patient . . . . . . . . . . . . . . . . . . . . . 56
Import Patient . . . . . . . . . . . . . . . . . . . . . . . . . 56
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23 Refresh Patient List . . . . . . . . . . . . . . . . . . . . . 57
Front view . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24 Delete patient . . . . . . . . . . . . . . . . . . . . . . . . . 58
Rear view . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27 Select patient for rounds . . . . . . . . . . . . . . . . . 58
Side view . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28 Ward round record. . . . . . . . . . . . . . . . . . . . . . 59
Bottom view . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Spot-checking mode . . . . . . . . . . . . . . . . . . . 61
Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
Admit patient . . . . . . . . . . . . . . . . . . . . . . . . . . 62
Getting started . . . . . . . . . . . . . . . . . . . . . . . . 35 Modify patient information . . . . . . . . . . . . . . . . 62
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36 Spot-checking data review . . . . . . . . . . . . . . . 62
Initial inspection . . . . . . . . . . . . . . . . . . . . . . . . 36
Networked monitoring . . . . . . . . . . . . . . . . . 65
Mounting the monitor . . . . . . . . . . . . . . . . . . . . 36
Connecting the power cable . . . . . . . . . . . . . . . 36 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66
Checking the monitor . . . . . . . . . . . . . . . . . . . . 37 Cybersecurity . . . . . . . . . . . . . . . . . . . . . . . . . 66
Connecting sensor to patient . . . . . . . . . . . . . . 37 Wi-Fi . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67
Checking the strip recorder . . . . . . . . . . . . . . . 37 e-link function . . . . . . . . . . . . . . . . . . . . . . . . . 69
Setting date and time . . . . . . . . . . . . . . . . . . . . 38 Central Monitoring System . . . . . . . . . . . . . . . 69
Gateway communication . . . . . . . . . . . . . . . . . 70
Operation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39 HL7 communication. . . . . . . . . . . . . . . . . . . . . 71
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40 Inquire for patient information via
Using keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43 network server (ADT) . . . . . . . . . . . . . . . . . . . 71
Work modes . . . . . . . . . . . . . . . . . . . . . . . . . . . 44 Auto uploading data to network server . . . . . . 71
Operating modes . . . . . . . . . . . . . . . . . . . . . . . 45
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
Changing monitor settings . . . . . . . . . . . . . . . . 46
Checking your monitor information. . . . . . . . . . 47 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
Setting languages. . . . . . . . . . . . . . . . . . . . . . . 47 Alarm category . . . . . . . . . . . . . . . . . . . . . . . . 74
Switching on Chinese input . . . . . . . . . . . . . . . 47 Alarm levels. . . . . . . . . . . . . . . . . . . . . . . . . . . 75
Locking touch screen . . . . . . . . . . . . . . . . . . . . 47 Controlling alarm . . . . . . . . . . . . . . . . . . . . . . . 76
Using the barcode scanner. . . . . . . . . . . . . . . . 48 Latching alarms . . . . . . . . . . . . . . . . . . . . . . . . 79
Using mouse. . . . . . . . . . . . . . . . . . . . . . . . . . . 48 Alarm of SpO2 Sensor Off . . . . . . . . . . . . . . . . 79

Contents
Network Disconnected alarms . . . . . . . . . . . . . 79 Procedure of Leakage Test . . . . . . . . . . . . . . . 116

Delete all alarm events . . . . . . . . . . . . . . . . . . . 79 Setting inflation value . . . . . . . . . . . . . . . . . . . 117
Testing alarms . . . . . . . . . . . . . . . . . . . . . . . . . 80 Measuring PR . . . . . . . . . . . . . . . . . . . . . . . . . 117
Alert setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80 NIBP auto recording . . . . . . . . . . . . . . . . . . . . 117
Nurse Call. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82
Monitoring TEMP. . . . . . . . . . . . . . . . . . . . . . 119
Alarm information . . . . . . . . . . . . . . . . . . . . . 83 Infrared TEMP with TAT-5000S-RS232
Physiological alarm information . . . . . . . . . . . . 84 Thermometer. . . . . . . . . . . . . . . . . . . . . . . . . . 120
Technical alarm information . . . . . . . . . . . . . . . 85 Quick TEMP with F3000 module. . . . . . . . . . . 128
Prompts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
Adjustable range of alarm limits . . . . . . . . . . . . 93 Warning-Score system . . . . . . . . . . . . . . . . . 133
Known issues and directions . . . . . . . . . . . . . . 94 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 134
Warning-Score interface . . . . . . . . . . . . . . . . . 134
User Interface . . . . . . . . . . . . . . . . . . . . . . . . . 95 Warning-Score method . . . . . . . . . . . . . . . . . . 135
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 96 Warning-Score criteria. . . . . . . . . . . . . . . . . . . 135
Setting interface style . . . . . . . . . . . . . . . . . . . . 96 Warning-Score result. . . . . . . . . . . . . . . . . . . . 136
Selecting display parameters . . . . . . . . . . . . . . 96 Warning-Score trend table. . . . . . . . . . . . . . . . 137
Changing parameter and waveform colors. . . . 96
Storing data in the storage device. . . . . . . . 139
Monitoring SpO2 . . . . . . . . . . . . . . . . . . . . . . . 97 Setting Storage Mode (For Monitoring
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 98 Mode Only) . . . . . . . . . . . . . . . . . . . . . . . . . . . 140
SpO2 safety information . . . . . . . . . . . . . . . . . . 98 Selecting a storage device . . . . . . . . . . . . . . . 140
Measuring SpO2 . . . . . . . . . . . . . . . . . . . . . . . . 99 Reviewing data stored in the
Measurement limitations . . . . . . . . . . . . . . . . . 101 storage device . . . . . . . . . . . . . . . . . . . . . . . . . 141
Assessing the validity of a SpO2 reading . . . . . 102 Deleting data stored in the storage device . . . 141
SpO2 alarm delay . . . . . . . . . . . . . . . . . . . . . . . 102 Exporting data stored in the internal
Perfusion Index (PI)* . . . . . . . . . . . . . . . . . . . . 103 storage device . . . . . . . . . . . . . . . . . . . . . . . . . 141
Setting pitch tone . . . . . . . . . . . . . . . . . . . . . . . 103 Ejecting a removable device . . . . . . . . . . . . . . 142
Setting sensitivity . . . . . . . . . . . . . . . . . . . . . . . 104 Recording data by recorder. . . . . . . . . . . . . . . 142
Measuring SpO2 and NIBP simultaneously . . . 104 Formatting the internal storage device . . . . . . 142
SatSeconds alarm management*. . . . . . . . . . . 104
Recording. . . . . . . . . . . . . . . . . . . . . . . . . . . . 145
Monitoring PR. . . . . . . . . . . . . . . . . . . . . . . . . 107 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 146
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 108 Performance of the recorder . . . . . . . . . . . . . . 146
PR source. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 108 Starting and stopping recording. . . . . . . . . . . . 146
Setting PR volume . . . . . . . . . . . . . . . . . . . . . . 108 Recorder operations and status messages. . . 148
Monitoring NIBP . . . . . . . . . . . . . . . . . . . . . . . 109 Using battery . . . . . . . . . . . . . . . . . . . . . . . . . 149

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 110 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 150
NIBP safety information . . . . . . . . . . . . . . . . . . 110 Battery safety information . . . . . . . . . . . . . . . . 150
Measurement limitations . . . . . . . . . . . . . . . . . 112 Battery power indicator . . . . . . . . . . . . . . . . . . 151
Measurement methods. . . . . . . . . . . . . . . . . . . 112 Battery status on the main screen. . . . . . . . . . 151
Measurement procedures . . . . . . . . . . . . . . . . 113 Checking battery performance . . . . . . . . . . . . 152
NIBP Multi-Review interface. . . . . . . . . . . . . . . 115 Replacing the battery . . . . . . . . . . . . . . . . . . . 152
Resetting NIBP. . . . . . . . . . . . . . . . . . . . . . . . . 115 Recycling the battery. . . . . . . . . . . . . . . . . . . . 153
Calibrating NIBP. . . . . . . . . . . . . . . . . . . . . . . . 115 Maintaining the battery . . . . . . . . . . . . . . . . . . 153
Leakage test. . . . . . . . . . . . . . . . . . . . . . . . . . . 116

Contents
Reprocessing . . . . . . . . . . . . . . . . . . . . . . . . . 155 Recommended separation distances . . . . . . . 198

Safety instructions . . . . . . . . . . . . . . . . . . . . . . 156
Default settings . . . . . . . . . . . . . . . . . . . . . . . 199
General points . . . . . . . . . . . . . . . . . . . . . . . . . 156
Safety information. . . . . . . . . . . . . . . . . . . . . . . 156 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 200
Information on reprocessing . . . . . . . . . . . . . . . 157 Default configuration . . . . . . . . . . . . . . . . . . . . 200
Classifications for reprocessing . . . . . . . . . . . . 157 User configuration . . . . . . . . . . . . . . . . . . . . . . 200
Patient-specific accessories and Patient information default settings . . . . . . . . . 200
consumables . . . . . . . . . . . . . . . . . . . . . . . . . . 158 Alarm default settings . . . . . . . . . . . . . . . . . . . 201
Before Reprocessing . . . . . . . . . . . . . . . . . . . . 158 SpO2 default settings. . . . . . . . . . . . . . . . . . . . 201
Validated reprocessing procedures . . . . . . . . . 159 PR default settings . . . . . . . . . . . . . . . . . . . . . 202
Storage and transport . . . . . . . . . . . . . . . . . . . . 159 NIBP default settings. . . . . . . . . . . . . . . . . . . . 202
Reprocessing of patient-specific TEMP default settings . . . . . . . . . . . . . . . . . . . 203
accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . 160
After Reprocessing . . . . . . . . . . . . . . . . . . . . . . 161
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . 163
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 164
Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 164
Repair . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 165
Disposal. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 167
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 168
Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . 169
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 170
SpO2 accessories . . . . . . . . . . . . . . . . . . . . . . . 170
NIBP accessories . . . . . . . . . . . . . . . . . . . . . . . 171
TEMP accessories . . . . . . . . . . . . . . . . . . . . . . 172
Other accessories. . . . . . . . . . . . . . . . . . . . . . . 173
Product specification . . . . . . . . . . . . . . . . . . . 175

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 176
Classification . . . . . . . . . . . . . . . . . . . . . . . . . . 176
Physical specifications . . . . . . . . . . . . . . . . . . . 176
Data management . . . . . . . . . . . . . . . . . . . . . . 179
NIBP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 180
SpO2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 183
PR. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 185
TEMP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 185
Wi-Fi . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 187
e-link . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 188
Interfaces . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 188
EMC Information. . . . . . . . . . . . . . . . . . . . . . . 191

Guidance and Manufacture’s Declaration . . . . 192
Electromagnetic immunity . . . . . . . . . . . . . . . . 193
Electromagnetic immunity . . . . . . . . . . . . . . . . 194


Responsibility of the Manufacturer
Responsibility of the Manufacturer . . . . . . . 8

Dräger only considers itself responsible for any

effect on safety, reliability and performance of the
equipment if:
Assembly operations, extensions, re-adjustments,
modifications or repairs are carried out by persons
authorized by Dräger, and
The electrical installation of the relevant room
complies with national standards, and
The instrument is used in accordance with the
instructions for use.

For your safety and that of your patients
General safety information . . . . . . . . . . . . . . 10

Strictly follow these instructions for use . . . . . . 10
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Connected devices . . . . . . . . . . . . . . . . . . . . . . 11
Not for use in areas of explosion hazard . . . . . 11
Safe connection with other electrical
equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Patient safety . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Information on Electromagnetic
Compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Sterile accessories . . . . . . . . . . . . . . . . . . . . . . 12
Installing accessories . . . . . . . . . . . . . . . . . . . . 12
Product-specific safety information . . . . . . . 13
Protecting personal information . . . . . . . . . . 19

General safety information
The following WARNING and CAUTION Maintenance

statements apply to general operation of the
medical device.
WARNING
WARNING and CAUTION statements specific to Risk of medical device failure and of patient
subsystems or particular features of the medical injury
device appear in the respective sections of these
Instructions for Use or in the Instructions for Use of The medical device must be inspected and
another product being used with this device. serviced regularly by service personnel.
Repair and complex maintenance carried out
on the medical device must be performed by
Strictly follow these instructions for use experts.
If the above are not complied with, medical
WARNING device failure and patient injury may occur.
Risk of incorrect operation and of incorrect Read chapter "Maintenance".
use
Dräger recommends that a service contract is
Any use of the medical device requires full obtained with Dräger Service and that all
understanding and strict observation of all repairs are performed by Dräger Service. For
sections of these instructions for use. The maintenance Dräger recommends the use of
medical device must only be used for the authentic Dräger repair parts.
purpose specified under "Intended Use".
Read carefully all WARNING and CAUTION
statements throughout these instructions for Accessories
use and all statements on medical device
labels. Failure to read these safety information WARNING
statements may result in a use of the medical Risk due to incompatible accessories
device contradicting with its intended use.
Dräger has tested only the compatibility of
accessories listed in the chapter
"Accessories".
If other, incompatible accessories are used,
there is a risk of patient injury due to medical
device failure.
Dräger recommends that the medical device is
only used together with accessories listed in
the current list of accessories.

Connected devices Patient safety
WARNING The design of the medical device, the

accompanying documentation, and the labeling on
Risk of electric shock and of device
the medical device are based on the assumption
malfunction
that the purchase and the use of the medical device
Any connected devices or device are restricted to professionals, and that certain
combinations not complying with the inherent characteristics of the medical device are
requirements mentioned in these Instructions known to the user. Instructions and WARNING and
for Use may compromise the correct CAUTION statements are therefore largely limited
functioning of the medical device. Before to the specifics of the Dräger medical device.
operating any combination of devices, refer to
These instructions for use do not contain
and strictly comply with the Instructions for
references to various hazards which are obvious to
Use for all connected devices and device
professionals who operate this medical device as
combinations.
well as references to the consequences of medical
device misuse, and to potentially adverse effects in
WARNING patients with different underlying diseases. Medical
To avoid risk of electric shock, this equipment device modification or misuse can be dangerous.
must be connected to a supply mains with
protective earth. CAUTION
Risk of patient injury
Do not make therapeutic decisions based solely
Not for use in areas of explosion hazard
on individual measured values and monitoring
parameters.
WARNING
Risk of fire
This medical device is not approved for use in Information on Electromagnetic
areas where combustible or explosive gas Compatibility
mixtures are likely to occur.
General information on electromagnetic
compatibility (EMC) according to international EMC
Safe connection with other electrical standard IEC 60601-1-2:
equipment Medical electrical equipment is subject to special
precautionary measures concerning
CAUTION electromagnetic compatibility (EMC) and must be
installed and put into operation in accordance with
Risk of patient injury
the EMC information provided in this Instructions
Electrical connections to equipment not listed in for Use.
these Instructions for Use or these Assembly
Portable and mobile RF communications
Instructions must only be made when approved
equipment can affect medical electrical equipment.
by each respective manufacturer.

WARNING Read carefully Assembly Instructions and

Instructions for Use.
Do not connect connectors with an
ESD warning symbol and do not CAUTION
touch the pins of such connectors
Risk of incorrect use
without implementing ESD
protective measures. Such protective The accessories are not available individually.
measures may include antistatic clothing and Only one copy of the instructions for use is
shoes, touching a ground stud before and included in the bulk package and must therefore
during connection of the pins, or using be kept in a location accessible for users.
electrically insulating and antistatic gloves.
All relevant personnel must be instructed in
these ESD protective measures.
WARNING
Portable RF communications equipment
(including peripherals such as antenna cables
and external antennas) should be used no
closer than 30 cm (12 inches) to any part of
Vista 120 SC, including cables specified by
the manufacturer. Otherwise, degradation of
the performance of this equipment could
occur.
Sterile accessories
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.
Single-use accessories must not be reused,
reprocessed, or resterilized.
Installing accessories
CAUTION
Risk of device failure
Install accessories to the basic device in
accordance with the instructions for use of the
basic device. Make sure that there is a safe
connection to the basic device.

Product-specific safety information
Federal (U.S.) law restricts this device to sale by or WARNING

on the order of a physician.
The simultaneous use of cardiac pacemaker
WARNING and other patient-connected equipment may
cause safety hazard.
To ensure that the monitor works properly,
read the user manual and follow the steps
before using the monitor. WARNING
Extreme care must be exercised when
WARNING applying medical electrical equipment. Many
parts of the human/machine circuit are
Before using the device, the equipment,
conductive, such as the patient, connectors,
patient cable and sensors etc. should be
transducers. It is very important that these
checked. Replacement should be taken if
conductive parts do not come into contact
there is any evident defect or signs of aging
with other grounded, conductive parts when
which may impair the safety or performance.
connected to the isolated patient input of the
device. Such contact would bridge the
WARNING patient’s isolation and cancel the protection
Medical technical equipment such as these provided by the isolated input. In particular,
monitor/monitoring systems must only be there must be no contact of the neutral
used by persons who have received adequate electrode and ground.
training in the use of such equipment and who
are capable of applying it properly. WARNING
Magnetic and electrical fields are capable of
WARNING interfering with the proper performance of the
EXPLOSION HAZARD-Do not use the device device. For this reason make sure that all
in a flammable atmosphere where external devices operated in the vicinity of the
concentrations of flammable anesthetics or monitor comply with the relevant EMC
other materials may occur. requirements. X-ray equipment or MRI devices
are a possible source of interference as they
WARNING may emit higher levels of electromagnetic
SHOCK HAZARD-To avoid the RISK of electric radiation.
shock, this equipment must only be
connected to a SUPPLY MAINS with protective WARNING
earth. Never adapt the three-prong plug from Route all cables carefully to avoid possible
the monitor to fit a two-slot outlet. entanglement, apnea, or electrical
interference. For the device mounted over the
WARNING patient, sufficient precautionary measures
Do not come into contact with the patient, should be taken to prevent it from falling on
table, or the monitor during defibrillation. the patient.
WARNING
Devices connecting with monitor should be
equipotential.

WARNING WARNING
Do not rely exclusively on the auditory alarm If several items of medical equipment are
system for patient monitoring. Adjustment of interconnected, pay attention to the sum of
alarm volume to a low level or off during the leakage currents, otherwise it may cause
patient monitoring may result in a hazard to shock hazard. Consult the service personnel.
the patient. Remember that the most reliable
method of patient monitoring combines close WARNING
personal surveillance with correct operation In monitoring mode, when monitoring is in
of monitoring equipment. process, if the power supply is off and there is
no battery for standby, the monitor will be off.
WARNING The settings configured by the user can be
Accessory equipment connected to the stored, and settings not configured by user
analog and digital interfaces must be certified keep no change. That is, the last settings used
according to the respective IEC/EN standards will be recovered when the power is restored.
(e.g. IEC/EN 60950 for data processing In ward round or spot-checking mode, the
equipment and IEC/EN 60601-1 for medical patient type will be restored to adult by
equipment). Furthermore all configurations default, and the monitor is in status with no
shall comply with the valid version of the patients, and other settings processing after
standard IEC/EN 60601-1. Therefore anybody, power off are the same with that in monitoring
who connects additional equipment to the mode.
signal input or output connector to configure
a medical system, must make sure that it WARNING
complies with the requirements of the valid The device and accessories are to be
version of the system standard IEC/EN 60601- disposed of according to local regulations
1. If in doubt, consult our technical service after their useful lives. Alternatively, they can
department or the local distributor. be to the dealer or the manufacturer for
recycling or proper disposal. Batteries are
WARNING hazardous waste. Do NOT dispose them
Only patient cable and other accessories together with house-hold garbage. At the end
supplied by Dräger can be used. The of their life hand the batteries over to the
performance and electric shock protection applicable collection points for the recycling
cannot be guaranteed, and the patient may be of waste batteries. For more detailed
injured otherwise. Prior to use, check if the information about recycling of this product or
casing of a disposable accessory is intact. Do battery, contact the local Dräger sales
not use it if its casing is damaged. representative.
WARNING WARNING
When interfacing with other equipment, a test If leakage or foul odor is detected, ensure that
for leakage current must be performed by there’s no fire around.
qualified biomedical engineering personnel
before using with patients. WARNING
The packaging is to be disposed of according
to local or hospital’s regulations; otherwise, it
may cause environmental contamination.
Place the packaging at the place which is
inaccessible to children.

WARNING WARNING
This equipment is not intended for home Only items that have been specified as part of
usage. the system or specified as being compatible
with the system can be connected to the
WARNING system.
Do not service or maintain the monitor or any
accessory which is in use with the patient. WARNING
Connecting any accessory (such as external
WARNING printer) or other device (such as the
The appliance coupler or mains plug is used computer) to this monitor makes a medical
as isolation means from supply mains. system. In that case, additional safety
Position the monitor in a location where the measures should be taken during installation
operator can easily access the disconnection of the system, and the system shall provide:
device. a) Within the patient environment, a level of
safety comparable to that provided by
WARNING medical electrical equipment complying
Assembly of the monitor and modifications with IEC/EN 60601-1, and
during actual service life shall be evaluated
b) Outside the patient environment, the
based on the requirements of IEC60601-1.
level of safety appropriate for non-
medical electrical equipment complying
WARNING with other IEC or ISO safety standards.
The monitors are MR Unsafe. The monitors
are not intended for use in an MRI WARNING
environment.
The medical electrical equipment needs to be
installed and put into service according to the
WARNING EMC Information provided in this user
Only recommended batteries can be used for manual.
the monitor.
WARNING
WARNING Portable and mobile RF communications
In monitoring mode, without use of data store equipment can affect medical electrical
function, all data measured (including trend equipment; refer to the recommended
data, review data, alarm events and so on) are separation distances provided in this user
cleared either when the monitor is turned off manual.
or when the monitor is powered down in the
process of monitoring. WARNING
Using accessories other than those specified
WARNING may result in increased electromagnetic
Additional multiple socket-outlets or emission or decreased electromagnetic
extension cords can’t be connected to the immunity of the monitoring equipment.
system.

WARNING WARNING
The monitor should not be used adjacent to or When the monitor is used with HF surgical
stacked with other equipment. If adjacent or equipment, the transducer and the cables
stacked use is necessary, the user must check must be avoided from conductive connection
that normal operation is possible in the to the HF equipment. This is to protect against
necessary configuration before starting burns to the patient.
monitoring patients.
WARNING
WARNING To protect the monitor from damage during
Do not touch accessible parts of medical or defibrillation, for accurate measurement
non-medical electrical equipment in the information and to protect against noise and
patient environment and the patient other interference, use only accessories
simultaneously, such as USB connector, VGA specified by Dräger.
connector or other signal input/output
connectors. WARNING
No modification of this equipment is allowed
WARNING without authorization of the manufacturer. If
SHOCK HAZARD - Don’t connect electrical this equipment is modified, appropriate
equipment, which has not been supplied as a inspection and testing must be conducted to
part of the system, to the multiple portable ensure continued safe operation.
socket-outlet supplying the system.
WARNING
WARNING Clinical decision making based on the output of
SHOCK HAZARD - Don’t connect electrical the device is left to the discretion of the provider.
equipment, which has been supplied as a part
of the system, directly to the wall outlet when WARNING
the non-medical equipment is intended to be The monitor is equipped with wireless AP/Wi-
supplied by a multiple portable socket-outlet Fi to receive RF electromagnetic energy.
with an isolation transformer. Therefore, any other equipment complying
with CISPR radiation requirements may also
WARNING interfere with the wireless communication and
Operation of the equipment exceeding make it interrupted.
specified physiological signal or the
operational specification may cause WARNING
inaccurate results. Wireless LAN equipment contains an
intentional RF radiator that has the potential
WARNING of interfering with other medical equipment,
The equipment can provide protective means including patient implanted devices. Be sure
to prevent the patient from being burned when to perform the electromagnetic compatibility
used with HF SURGICAL EQUIPMENT. The test before installation and any time new
equipment can protect against the effects of medical equipment is added to the Wireless
the discharge of a defibrillator. Use only LAN coverage area.
Dräger-approved accessories.

WARNING CAUTION
If the protective grounding (protective earth) Do not immerse transducers in liquid. When using
system is doubtful, the monitor must be solutions, use sterile wipes to avoid pouring fluids
supplied by internal power only. directly on the transducer.
WARNING CAUTION
Portable RF communications equipment Do not use autoclave or gas to sterilize the
(including peripherals such as antenna cables monitor, recorder or any accessories.
and external antennas) should be used no
closer than 30 cm (12 inches) to any part of the CAUTION
monitor, including cables specified by the
The device and reusable accessories may be
manufacturer. Otherwise, degradation of the
sent back to the manufacturer for recycling or
performance of this equipment could result.
proper disposal after their useful lives.
WARNING
CAUTION
The monitor is suitable for use in the presence
of electrosurgery. When the monitor is used Disposable devices are intended for single use
with HF surgical equipment, user (doctor or only. They should not be reused as performance
nurse) should be cautious about patient could degrade or contamination could occur.
safety.
CAUTION
WARNING Remove a battery whose life cycle has expired
Make sure networking function is used in a from the monitor immediately.
secure network environment.
CAUTION
WARNING To ensure patient safety, use only parts and
To avoid malicious tampering and theft of data accessories manufactured or recommended by
transmitted by the network, it is Dräger.
recommended to switch on the encryption
function. After the encryption function is CAUTION
turned on (it is set to on by default), the Before connecting the monitor to the AC power,
monitor will authenticate the accessed Vista make sure the voltage and the power frequency
120 CMS and GATEWAY devices and encrypt are consistent with the requirements indicated on
the transmitted data to ensure the security. the device label or in this user manual.
CAUTION CAUTION
Electromagnetic Interference - Ensure that the Protect the device against mechanical damage
environment in which the patient monitor is resulting from falls, impacts, and vibration.
installed is not subject to any sources of strong
electromagnetic interference, such as radio CAUTION
transmitters, mobile telephones, microwaves, etc. Do not touch the touch screen with a sharp object.
CAUTION
Keep the environment clean. Avoid vibration.
Keep it far away from corrosive medicine, dust
area, high temperature and humid environment.

CAUTION NOTE
A ventilated environment is required for monitor When there's measurement beyond range, invalid
installation. Do not block up the ventilation grille at measurement or no measurement value, it will
the back of the device. display -?-.
CAUTION NOTE
The device must be connected to the ground to The materials with which the patient or any other
avoid signal interference. person can come into contact conform with the
standard of EN ISO 10993-1: 2009.
CAUTION
NOTE
To protect eyes from damage, don't look directly
at supplementary light for long time. In normal use, the operator shall stand in front of
the monitor.
CAUTION
Poor connection might be caused by frequently
plugging and unplugging the power cord. Check
the power cord regularly and replace it in time.
NOTE
Position the device in a location where the
operator can easily see the screen and access the
operating controls.
NOTE
The monitor can only be used on one patient at a
time.
NOTE
If the monitor gets damp or liquid pours on the
monitor, contact the service personnel of Dräger.
NOTE
This monitor is not a device for treatment
purposes.
NOTE
The pictures and interfaces in this manual are for
reference only.
NOTE
Regular preventive maintenance should be carried
out every two years. The user is responsible for
any requirements specific to his country.

Protecting personal information
Protecting personal health information is a major CAUTION

component of security strategy. To protect the
Ensure that the monitor is connected only to the
personal information and ensure the proper device
device authorized/approved by Dräger. Users
performance, the user should take necessary
should operate all Dräger deployed and
precautions in accordance with local laws and
supported monitors within Dräger authorized
regulations and institution’s policies. Dräger
specifications, including Dräger approved
recommends health care organizations or medical
software, software configuration, security
institutions to implement a comprehensive and
configuration, etc.
multifaceted strategy to protect the information and
systems from internal and external security threats.
CAUTION
To ensure the patients’ safety and protect their Protect all the passwords to prevent unauthorized
personal health information, the user should changes. Only the manufacturer’s service
implement practices or measures that include: personnel are allowed to modify the Factory
1 Physical safeguards - physical safety measures Maintain settings.
to ensure that unauthorized personnel do not
have access to the monitor. CAUTION
Anti-virus measures such as USB device virus
2 Operational safeguards - safety measures
scanning should be carried out prior to using USB
during operation.
flash drive.
3 Administrative safeguards - safety measures in
management. CAUTION
4 Technical safeguards - safety measures in Firewalls and/or other security devices should be
technical field. in place between the medical system and any
externally accessible systems. It’s recommended
CAUTION to use Interfaces defender firewall or any other
The access/operation of the monitor is restricted firewall that can defend against DoS and DDoS
to authorized personnel only. Assign only staff attacks, and keep it up to date.
with a specific role the right to use the monitor.
CAUTION
CAUTION DoS and DDoS protection of the router or switch
Ensure that all device components maintaining must be turned on for defensing against attacks.
personal information (other than removable
media) are physically secure. CAUTION
When building the networking environment: 1) If a
CAUTION wireless router is used, turn on the MAC address
Ensure that the data are deleted after the patient filtering function of the wireless router and add the
is discharged (Refer to Section Deleting data MAC address of the monitor to the rule list. The
stored in the storage device). wireless router only allows devices in the rule list
to access the wireless network. 2) It is suggested
to build a VLAN, assign the LAN ports where the
approved switch port, monitor and Vista 120 CMS
are into the same VLAN, and isolate them from
other VLANs.

CAUTION
When the monitor is returned for maintenance,
disposed of, or removed from the medical
institution for other reasons, it is necessary to
ensure that all patient data are removed from the
monitor (Refer to Section Deleting data stored in
the storage device).
CAUTION
Protect the privacy for the information and the
data displayed on the screen, and for the
information and the data stored in the monitor.
NOTE
Log files generated by the monitor are used for
system troubleshooting and do not contain
protected medical data.

Application
Application
Intended use . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Restrictions for use . . . . . . . . . . . . . . . . . . . . 22
Intended user . . . . . . . . . . . . . . . . . . . . . . . . . 22

Application
Intended use
The monitor is intended to be used by healthcare The monitor is intended for measuring and
professionals whenever there is a need for monitoring physiologic parameters, including
monitoring the physiological parameters of functional arterial oxygen saturation (SpO2), Pulse
patients. The monitor is intended for monitoring, Rate (PR), Non-Invasive Blood Pressure (NIBP)
analyzing, recording, and alarming of multiple and Temperature (TEMP).
physiological parameters in healthcare
The monitor is intended for use only by clinical
environments for adult, pediatric, and neonatal
professionals or under their guidance. It must only
patients.
be used by persons who have received adequate
training.
The monitor is not intended for MRI environments.
F3000 TEMP Module is not for neonates.
Restrictions for use
CAUTION
Device is for use in health care facilities only and
exclusively by persons with specific training and
experience in its use.
Intended user
Users of this device must be trained and

experienced medical professionals.

Overview
Overview
Front view . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Rear view. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Side view . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Bottom view . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . 31
Symbols. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32

Overview
Front view

Overview
A Alarm When an alarm occurs, the alarm indicator will light or flash. The alarm level is
indicator/Stand color coded;
by indicator
Breathing light indicates the standby status.
B AC power When the monitor is connected to AC power, the indicator is in green.
indicator
C Battery Refer to the section Battery power indicator for details.
indicator
D Power On/Off When connected to the AC power supply or battery powered, press the key to turn
switch the monitor on. Press the key again and hold for 3 seconds to turn the monitor off.
An indicator is built in this switch. It turns on when the monitor is on and turns off
when the monitor is off.

Overview
E NIBP Press to inflate the cuff and perform NIBP measurement. Press again to stop the
measurement measurement and deflate the cuff.
F Admit/Create Admit or create new patient;
new patient
Press this button to return to the main interface.
G Switch patient In main interface, press the button to switch the patient type;
type
In other interfaces, press the button to return to the main interface.
H Menu Press the button to open the main menu when there is no menu open. Press it
again to exit.
I Rotary knob The user can turn the rotary knob clockwise or counter-clockwise to highlight the
desired item. Press the rotary knob to select the item.
J TAT-5000S- Provides Temporal Artery (TA) Temperature in about 3 seconds.
RS232
Thermometer
K F3000 TEMP Measures patient’s oral, axillary or rectal temperatures.
module

Overview
Rear view
A Portable handle
B Power supply interface
C Power cord Used to prevent the power cord from detaching. Place the latch on the power cord
safety latch and press it down firmly to ensure that it secures the power cord.
D Equipotential If the monitor is used with other devices, connect this terminal to eliminate
grounding potential ground differences between devices.
terminal
E Network Network interface: standard RJ45 interface that connects the monitor to Vista 120
interface/Nurse CMS 1.62 and above or Vista 120 Gateway.
call port
Nurse call port: it connects the monitor to the hospital’s nurse call system. Alarms
indications are alerted through the nurse call system if configured to do so.
F USB Used to connect the USB devices.
interfaces.

Overview
Side view
Left side

Overview
Right side
A Speaker
B Recorder
C NIBP port
D Dräger SpO2 port
E Nellcor SpO2 port
F TEMP communication interface

Overview
Bottom view
A Heat sink
B Battery compartment door

Overview
Abbreviations
Abbr. Explanation Abbr. Explanation

AC Alternating current MDD Medical Device Directive
ADU Adult MetHb Methemoglobin
ART Arterial MRI Magnetic resonance imaging
BP Blood pressure N/A Not applicable
BTPS Body temperature and pressure, Neo Neonate
saturated NIBP Non-invasive blood pressure
CI Cardiac index O2 Oxygen
CISPR International Special Committee Ped Pediatric
on Radio Interference
Pleth Plethysmogram
CMS Central monitoring system
PR Pulse rate
COHb Carboxyhemoglobin
PVC Premature ventricular complex
DC Direct current
RESP Respiration
DIA Diastolic pressure
RHb Reduced hemoglobin
DoS Denial of Service
RR Respiration Rate
DDoS Distributed Denial of Service
SpO2 Pulse Oxygen Saturation
EEC European Economic Community
SYS Systolic pressure
EMC Electromagnetic compatibility
TB Blood Temperature
EMI Electromagnetic interference
TD Temperature difference
ESU Electrosurgical unit
TEMP Temperature
FCC Federal Communication
Commission USB Universal serial bus
Hb Hemoglobin
Hb-CO Carbon mono-xide hemoglobin
HR Heart rate
ICU Intensive care unit
ID Identification
IEC International Electrotechnical
Commission
IEEE Institute of Electrical and
Electronic Engineers
LCD Liquid crystal display
LED Light emitting diode
MAP Mean arterial pressure

Overview
Symbols
NIBP measurement Equipotential bonding
Admit/Create new patient Caution
Switch patient type Network port
Menu Manufacturer
Type BF applied part Consult Instructions for Use
Warning
Battery indicator (Background: Yellow; Symbol &
outline: black)
Non-ionizing electromagnetic
USB port
radiation
MR Unsafe - Keep away from

magnetic resonance imaging Batch code
(MRI) equipment
CE marking Temperature limitation
Authorised Representative In The

Relative humidity
European Community
Defibrillation-proof type BF
This way up
applied part
Part Number Keep dry
Mains indicator Handle with care
Power supply switch Alternating current

Overview
Ingress Protection: IPX2

(protected against vertically falling
Serial number IPX2 water drops when enclosure tilted
up to 15°)
Disposal instructions Quantity
Recycle Non-sterile
Part number Atmospheric pressure
Date of manufacture Fragile; handle with care
Follow Instructions for Use Stacking limit by number
Caution: Federal (U.S.) Law

restricts this device to sale by or Do not step on
on the order of a physician.


Getting started
Getting started
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Initial inspection . . . . . . . . . . . . . . . . . . . . . . . 36
Mounting the monitor. . . . . . . . . . . . . . . . . . . 36
Connecting the power cable . . . . . . . . . . . . . 36
Checking the monitor. . . . . . . . . . . . . . . . . . . 37
Connecting sensor to patient . . . . . . . . . . . . 37
Checking the strip recorder. . . . . . . . . . . . . . 37
Setting date and time . . . . . . . . . . . . . . . . . . . 38

Getting started
Overview
NOTE
The monitor installations and settings must be
configured by the authorized hospital personnel.
Initial inspection
Before unpacking, check the packaging and ensure Open the package carefully and remove the
that there are no signs of mishandling or damage. monitor and accessories. Check that the contents
If the shipping cartons are damaged, contact the are complete and that the correct options and
local supplier for assistance. accessories have been delivered.
If the user has any question, contact the local
supplier.
Mounting the monitor
If all situations are normal, place the monitor on a

WARNING
flat, level surface, on a trolley or mount on a wall. To
install the trolley or wall mount for the monitor, refer The safe loads of the wall mounting bracket
to Trolley Installation Guide or Wall Mounting and the trolley are 7.5 kg and 11 kg
Bracket Assembly Instruction. respectively. Exceeding the safe load may
cause bracket to fail and the device to fall.
WARNING
The wall mounting bracket can be fixed only
on a concrete wall.
Connecting the power cable
To connect the AC power cable: 2 Connect the power cable provided with the
monitor. Connect the other end of the power
1 Make sure the AC power supply complies with
cable to a grounded power outlet.
the following specifications: 100 V-240 V,
50 Hz/60 Hz. NOTE
Connect the power cable to the socket specialized
for hospital use.

Getting started
NOTE
Only use the power cable supplied by Dräger.
Checking the monitor
Make sure there is no damage on the NOTE

measurement accessories and cables. Then turn
Check that all monitor functions are operating
on the monitor, check whether the monitor can start
correctly.
normally. Make sure all alarm lamps light up and
the alarm sound is heard when turning on the
monitor. Refer to chapter Testing alarms. NOTE
If rechargeable batteries were provided, charge
WARNING them each time before using the device to ensure
Do not use the device if any damage is adequate power.
detected or if the monitor displays error
messages. Contact the hospital technical NOTE
personnel or Dräger Service Representative After long-time continuous running, restart the
immediately. monitor to ensure the monitor’s steady
performance and long lifespan.
Connecting sensor to patient
Connect all the necessary patient sensors.
Checking the strip recorder
If the monitor is equipped with a strip recorder,

verify that paper is properly installed in the strip
recorder by opening the strip recorder’s door. Refer
to the chapter “Recording” for details regarding
installing paper.

Getting started
Setting date and time
To set the date and time:

1 Select Menu > System Setup > Date/Time.
2 Adjust the day/time format based on the user’s
preference.
3 Set the correct time of year, month, day, hour,
min and sec. Display Second can be set to On
or Off as needed.
4 Set Sync Time: default selection is Off.
 CMS is used for time synchronization with
Vista 120 CMS.
 NTP (Network Time Protocol), is used for
time synchronization with the server with
NTP function in hospital. Then, set the Time
Zone of the monitor and NTP Server IP.
WARNING
Changing date and time will affect the storage
of trend data.
NOTE
If the system is not used for a longer period of time,
its system time may be inaccurate. In this case,
readjust the system time after powering on.
NOTE
If the system time cannot be saved and resumes
the default value after restart, contact the service
department of Dräger to replace the button cell on
main board.

Operation
Operation
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
Using keys. . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Permanent keys . . . . . . . . . . . . . . . . . . . . . . . . 43
Shortcut keys . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Hardkeys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Pop-up keys . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Work modes . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Operating modes . . . . . . . . . . . . . . . . . . . . . . 45
Demo Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Standby Mode. . . . . . . . . . . . . . . . . . . . . . . . . . 45
Night Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Changing monitor settings . . . . . . . . . . . . . . 46

Adjusting screen brightness . . . . . . . . . . . . . . . 46
Adjusting volume . . . . . . . . . . . . . . . . . . . . . . . 46
Checking your monitor information . . . . . . . 47
Setting languages. . . . . . . . . . . . . . . . . . . . . . 47
Switching on Chinese input . . . . . . . . . . . . . 47
Locking touch screen . . . . . . . . . . . . . . . . . . 47
Using the barcode scanner . . . . . . . . . . . . . . 48
Using mouse . . . . . . . . . . . . . . . . . . . . . . . . . . 48

Operation
Overview
The user may frequently use the follow functions: Everything the user needs to operate the monitor is
accessible from its user interface. Screen elements
 SpO2 monitoring (Refer to Monitoring SpO2 for
include measurement data, waveforms, screen
more information.)
keys, information fields, alarms fields and menus.
 PR monitoring (Refer to Monitoring PR for more The monitor can be configured in a number of
information.) different ways. For example, the user can access
an item through the on-screen setup menu, via a
 NIBP monitoring (Refer to Monitoring NIBP for
hard key, or via a shortcut key. This Instructions for
more information.)
Use describes how to access items via an on-
 TEMP monitoring (Refer to Monitoring TEMP screen menu.
for more information.)
 Alarm (Refer to Alarms for more information.)
Physiological alarms area

Patient information area
Technical alarms area
Parameters data area
General information area

(Left is function info.; Right is symbol area, from right to left, including data
storage status, USB flash disk, e-link, Wi-Fi network, battery status, wired
network, date & time)
Permanent key & Shortcut key area

Operation
A B C
D
E
H I J K L M N OP QR S
A Bed number K Storage status indicator of the storage device

B Patient name and MRN L Removable storage device symbol of USB flash
disk
C Patient type (click to view/edit patient M e-link connection symbol
information)
D Physiological alarms (click to enter N Wi-Fi status
physiological alarm review interface)
E Technical alarms (click to enter technical alarm O Battery status
review interface)
F Measurement value P Wired network
G Parameter waveform Q Scroll right to display more shortcut keys

Operation
H Alarm reset key R Date and time

I Scroll left to display more shortcut keys S Menu
J Shortcut keys T TEMP measuring position
The icons on the interface and their meanings are

as follows:
In monitoring mode: Medium/Low alarm
In monitoring mode: High alarm icon
In monitoring mode: Audio alarm off
In monitoring mode: Audio alarm paused
In monitoring mode: Parameter alarm off
NIBP SYS alarm off
NIBP MAP alarm off
NIBP DIA alarm off
Patient type: ADU
Patient type: PED
Patient type: NEO
Measuring oral TEMP in ADU mode For device with F3000 TEMP
module only.
Measuring axillary TEMP in ADU mode
Measuring rectal TEMP in ADU mode
Measuring oral TEMP in PED mode
Measuring axillary TEMP in PED mode
Measuring rectal TEMP in PED mode

Operation
Taking Temporal Artery (TA) Temperature via TAT- For device with TAT-5000S-
5000S-RS232 Thermometer RS232 Thermometer only.
Using keys
The monitor has four different types of keys. If the In monitoring mode, the displayed keys are: Alarm
key sound is enabled, the monitor gives a normal Mute, Admission, Review, NIBP measurement,
key sound when the operation is valid. General, Standby mode, Record, Barcode
scanning, Night Mode and Score.
In ward round mode, the displayed keys are:
Permanent keys Review, NIBP AVG, NIBP measurement, General,
Standby mode, Barcode scanning and Score.
A permanent key is a graphical key that is In spot-checking mode, the displayed keys are:
permanently located at the bottom of the main Record, Review, NIBP AVG, NIBP measurement,
screen allowing fast, direct access to functions. General, Standby mode, Barcode scanning and
Score.
Menu, to display the main setup menu
Audio alarm paused/off
Alarm Reset, to reset the alarm for

monitoring mode only Enter score interface
New Patient, to create new patient for

General setup
spot-checking mode only
Select Patient, to select patient for ward Record output

round mode only
Review (in monitoring or spot-

checking mode)
Shortcut keys
Barcode scanning
A shortcut key is a configurable graphical key
located at the bottom of the main screen. It gives
the user direct access to functions. The selection Select this item by the rotary knob
of shortcut keys available on the monitor depends to enable the touch screen
on the monitor configuration and options operation
purchased. Enter into Menu > User Maintain >
Shortcut to choose and configure. Quickly admit a patient
NIBP measurement

Operation
Hardkeys
Standby mode
A hardkey is a physical key on a monitoring device,
such as the main menu key on the front panel.
NIBP average measurement Refer to the illustration in Front view for more
information.
Night mode
Pop-up keys
Review (in ward round mode)
Pop-up keys are task-related graphical keys that
appear automatically on the screen when required.
For example, the confirmation pop-up key appears
only when the user needs to confirm a change.
Work modes
The monitor offers multiple work modes, including NOTE

Monitoring, Ward Round, and Spot-checking. Each
In these 3 modes, each setting item is respectively
work mode gives the user access to a different set
independent, except language and network
of features. Choose the work mode that best suits
setups. For instance, in monitoring mode, NIBP
the needs.
parameter is selected in parameters setup, but this
Select Menu > System Setup > Mode to choose setting is not affected and still keeps unchanged
Monitoring, Spot-checking or Ward Round. The when the monitor enters spot-checking mode or
selected working mode will be displayed in left part ward round mode.
of general information area.
Monitoring mode is designed for continuous
bedside single patient monitoring and
management. Ward Round mode is optimized for
rapid multi-patient vitals capture and multiple
patient review. Spot-checking mode is optimized for
unattended episodic interval monitoring of a single
patient with multiple patient review. Refer to specific
chapter for details of these 3 modes.
NOTE
The history data in each mode can be viewed only
in corresponding mode.

Operation
Operating modes
Demo Mode 2 The monitor stops monitoring and measuring.

The monitoring data before entering standby
will be stored.
WARNING
The Demo Mode is for demonstration 3 The monitor won’t respond to all alarms and
purposes only. The user must not change to prompts, except Battery Low alarm.
Demo Mode during patient monitoring. In 4 Audio alarm paused status discontinues. Audio
Demo Mode, all stored trend information is alarm off, alarm off, alarm reset and alarm latch
deleted from the monitor’s memory. status are not influenced.
To change from operating mode to demo mode: 5 Continuous real-time recording will stop
immediately, and other recording task will stop
1 Select Menu > Common Function > Demo
after current recording finishes.
Mode from the pop-up dialog box.
6 Vista 120 CMS won’t update monitoring data,
2 Type the password into the displayed dialog
and will display monitor's standby mode. If
box.
network is disconnected, monitor will make
To exit the Demo Mode, select Menu > Common request for connection.
Function > Demo Mode.
The monitor exits standby mode in any of the
conditions:
Standby Mode 1 The user clicks anywhere on the screen or

presses any key.
To enter into standby mode: 2 Battery Low alarm occurs.
1 Manual standby: press the shortcut key 3 Vista 120 CMS sends exit order to monitor.
on screen directly or select Menu > Common
Function > Standby. After exiting standby mode, the monitor resumes
monitoring, including parameter monitoring,
2 Automatic standby: In spot-checking or ward storage and alarm; users need to press Record key
round mode, if there is no measurement, alarm to restart recording.
and operation in process, the monitor can enter
standby mode automatically without any NOTE
operations in specified time. Enter Menu > The monitor is unable to enter into standby mode
System Setup > General > Auto Standby to when exporting data.
choose time from 1 min, 2 min, 5 min, 10 min,
30 min, 1 hour or Off. 30 min is default setting.
In monitoring mode, permanent setting is Off.
Night Mode
In standby mode:
To switch to night mode,
1 The light indicator will be lighted or not based on
selection (Setting path: Menu > System Setup  Select the shortcut key on the main
> General > Standby Indicator). screen, or
 Select Menu > Common Function > Night
Mode.

Operation
NOTE
In night mode, the sound of key and pulse is
muted; the alarm volume and screen brightness
are down to their minimum; the settings including
key volume, PR volume, alarm volume and screen
brightness are unavailable.
Changing monitor settings
Adjusting screen brightness
To change the screen brightness, select Menu >

System Setup > General, and select the
appropriate setting for the screen brightness. 10 is
the brightest, 1 is the least bright.
Adjusting volume
Adjusting key volume Adjusting alert volume

The key volume is audible when the user selects In ward round or spot-checking mode, to change
any field on the monitor screen or when the user the alert volume, select Menu > System Setup >
turns the knob. To adjust the key volume, select General and select the desired setting for the Alert
Menu > System Setup > General, then select the Volume item: five bars represent the maximum
appropriate setting: five bars represent the volume and one bar represents the minimum
maximum volume and one bar represents the volume. If none of bars are selected, the alert
minimum volume. If none of bars are selected, the volume will be off.
key volume will be off.
Adjusting alarm volume

The monitor provides five levels of alarm volume:
five bars represent the maximum volume and one
bar represents the minimum volume.
To change the alarm volume, select Menu >
System Setup > General and select the desired
setting.

Operation
Checking your monitor information
To check the monitor information, select Menu > About includes: software version, serial number,
Common Function > Device Information. device name and so on.
Monitor information includes Config, About,
Network includes: Network type, Local Net No.,
Network.
Server IP (such as Vista 120 CMS), Local Mask
Config includes: the configuration monitor No., Local Gateway No., Mac address,
supported (such as Wi-Fi, Wired, USB, Barcode, Communication protocol and so on.
etc.), the currently used configurations are marked
with √. NOTE
The contents related with network can be set in
User Maintain > Network.
Setting languages
To change the language: 2 Select Common > Language option on the

pop-up dialog box to display the language list.
1 Select Menu > User Maintain, then type the
maintenance password into the displayed 3 Select the desired language from the list. To get
dialog box. the change effective, restart the monitor.
Switching on Chinese input
To set Chinese input method: 2 Select Common > Chinese Input option on the
pop-up dialog box to toggle between On and
1 Select Menu > User Maintain, then type the
Off.
maintenance password into the displayed
dialog box.
Locking touch screen
The user can disable touch screen operation by of screen. To enable the touch screen operation,
selecting and holding the permanent key select and hold the menu key for three
for three seconds. A message of Screen Locked seconds again.
and the symbol will be displayed at the bottom

Operation
Using the barcode scanner
To enter the barcode setup menu, select Menu > If the scanner is connected for the first time, the
User Maintain. After entering the required monitor will pop up a confirmation message to ask
password, select Common > Barcode Setup. user whether the new USB device is added as
Then the user can set MRN, last name, first name scanner. Choose Yes to add as scanner, choose
and so on. No to add as USB device.
User can also check relevant scanner device NOTE
information in Scanner Management.
The start and end code should be set before using
scanner to update patient, otherwise the barcode
can’t be recognized correctly. After setting start
and end code, user should also set male code and
female code to distinguish the gender.
Using mouse
The monitor supports mouse operation via USB

port. Mouse is used for controlling cursor.

Monitoring mode
Monitoring mode
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
Admitting a patient . . . . . . . . . . . . . . . . . . . . . 50
Patient category . . . . . . . . . . . . . . . . . . . . . . . . 50
Quick admit . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
Admit by barcode . . . . . . . . . . . . . . . . . . . . . . 51
Editing patient information . . . . . . . . . . . . . . 52
Monitoring data review . . . . . . . . . . . . . . . . . 52

Trend graph review. . . . . . . . . . . . . . . . . . . . . . 52
Trend table review . . . . . . . . . . . . . . . . . . . . . . 52
NIBP review . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
Alarm review. . . . . . . . . . . . . . . . . . . . . . . . . . . 53
Technical alarm checking . . . . . . . . . . . . . . . . . 53
Event marking. . . . . . . . . . . . . . . . . . . . . . . . . 53

Monitoring mode
Overview
Monitoring mode is used for single patient’s

monitoring and management.
Admitting a patient
The monitor displays physiological data and  Doctor: Enter the attending doctor for the
records the information in trends. This allows the patient.
user to monitor unadmitted patients. It is however
 Gender: Male, Female and N/A.
important to admit patients properly so that the user
can identify the patient on recordings, reports, and  Type: Choose the patient type, either Adult,
networked devices. Pediat, or Neonat.
During admission, the patient category setting  BloodType: N/A, A, B, AB and O.
determines the algorithm that the monitor uses to
 Date of Birth: Enter the patient’s date of
process and calculate measurements. These
birth.
include safety limits that are applied for specific
measurements and alarm limit ranges.  Date of Admission: Enter the patient’s date
of admission.
To admit a patient:
 Height: Enter the patient’s height.
1 Select Menu > Patient Management > New
Patient, or press the Admit/Create new patient  Weight: Enter the patient’s weight.
 Height unit: cm or inch.
hardkey on the front panel, then a  Weight unit: kg or lb.
message is displayed to ask the user to confirm
to update patient. NOTE
2 Click No to cancel this operation; click Yes, the Admitting new patient will clear the history data in
Patient Info interface is displayed. the monitor associated with the patient.
3 Enter the patient information:

 MRN: Enter the patient’s medical record Patient category
number.
The patient category setting determines the
 Last Name: Enter the patient’s last name algorithm which the monitor uses to process and
(family name). calculate some measurements, the safety limits
 First Name: Enter the patient’s first name. that are applied for some measurements, and the
alarm limit ranges.
 Bed No.: supports up to 8 characters.
Chinese, English, number and special
characters can be input.

Monitoring mode
WARNING
Changing the patient category may change
the relevant configuration (such as alarm
limits). Always check alarm limits to make
sure that they are appropriate for the patient.
Quick admit
If the user does not have the time or information to 3 Click No to cancel this operation; click Yes to
fully admit a patient, the user can use Quick Admit continue and the Quick Admit interface is
to quickly admit a patient and fill in the rest of the displayed.
patient information later. To quickly admit a patient:
4 Configure Type to the correct setting.
1 Select the shortcut key on the screen

directly, or
2 Select Menu > Patient Management > Quick
Admit, a message is displayed requesting that
the user confirm the patient update.
Admit by barcode
To admit a patient by barcode,

 In the interface of creating new patient, the
patient information from barcode is directly
updated to the interface. User can input
relevant information and click Confirm to finish.
 In other interfaces, if the monitor is connected
with network server and ADT Query (in User
Maintain > Network) is also set to on, the
monitor will automatically inquire for patient
information from the server via MRN. The
corresponding patient information in the monitor
will be updated after user’s confirmation.
NOTE
Patient information obtained from network server
cannot be edited.

Monitoring mode
Editing patient information
To edit the patient information after a patient has

been admitted, select Menu > Patient
Management > Patient Info., and make the
required changes through the pop-up dialog box.
Monitoring data review
In monitoring mode, the monitor provides 120-hour NOTE

trend data of all parameters, storage of 1200 NIBP
Select 1 sec interval if completed NIBP data is
measurement results, 200 alarm events and so on.
expected to display on the screen.
Trend graph review

Trend table review
To review Trend Graph, press the Review shortcut
To review the trend table, press the Review
key on the screen or select Menu >

shortcut key on the screen or select
Review > Trend Graph.
Menu > Review > Trend Table.
In the trend graph, the y-axis stands for the
In the trend table review interface:
measurement value and x-axis stands for the time.
With the exception of NIBP and TEMP, other trends  Select Interval to change the interval of the
are displayed as continuous curves. trend data. 1 s, 5 s, 30 s, 1 min, 3 min, 5 min,
10 min, 15 min, 30 min, 60 min and NIBP are
In the trend graph review interface:
optional. Select NIBP to view the trend data
 Select beside the parameter name and according to the NIBP measurement time.
choose the desired parameter.
 Select and to scroll the screen manually
 Select Zoom to adjust the trend scale. to browse the trend table.
 Select Interval to change the length of trend  Select Record to print out the currently
data displayed on the current screen. 1 s, 5 s, displayed trends by the recorder.
1 min, 5 min and 10 min are optional.
 Select Record All to print out all the trends by
the recorder.
 Select beside Cursor to move the cursor

left or right.
 Select and to scroll the screen left and
right manually to browse the trend graph.
 Select Record to print out the currently
displayed trends by the recorder.

Monitoring mode
NIBP review  Select Time Index to set end time of alarm

review.
To review the NIBP measurement data, press the – Current Time: the alarm events occurring
before the current time are displayed on the
alarm event review interface.
Review shortcut key on the screen,
select Menu > Review > NIBP, or click NIBP Multi- – User Define: the user can define the review
Review area at the bottom of main interface. time by setting time box displayed on the
interface. The alarm events occurring
In the NIBP review interface: before the User Define option are displayed
 Select Unit to change the pressure unit. on the alarm event review interface.
 Select and to browse more NIBP  Select and to browse more alarm events.
measurement data.  Click certain alarm event and select Record to
 Select Record to print out the NIBP print out the alarm data by the recorder. Click
measurement data by the recorder. Alarm List to return to the alarm event list.
NOTE
Alarm review The monitor can store a maximum of 200 alarm
events. As soon as the alarm event storage is full,
To review the alarm event, press the Review the earliest alarm event will be replaced by the
latest one.
shortcut key on the screen or select

Menu > Review > Alarm. Technical alarm checking
In the alarm review interface:
Click technical alarm area to check the current
 Select Event Type to choose the required technical alarms.
parameter from the popup list and the user can
review alarm event of the specific parameters.
Event marking
Event mark is used to note the classified events

which are related with patient or may have
influence on parameters monitoring, such as take
or inject medicine, or kinds of treatments. There are
four kinds of event marking at most: event A, event
B, event C and event D.
Access Menu > Common Function > Event
Marker to check event mark. Besides, the event
mark will also be displayed in trend graph, trend
table and alarm review.


Ward round mode
Ward round mode
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
Create new patient . . . . . . . . . . . . . . . . . . . . . 56
Import Patient . . . . . . . . . . . . . . . . . . . . . . . . . 56
Refresh Patient List . . . . . . . . . . . . . . . . . . . . 57
Delete patient . . . . . . . . . . . . . . . . . . . . . . . . . 58
Select patient for rounds . . . . . . . . . . . . . . . . 58
Ward round record . . . . . . . . . . . . . . . . . . . . . 59

Data Update . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
Ward round record confirmation . . . . . . . . . . . . 59
Ward round record review . . . . . . . . . . . . . . . . 59

Ward round mode
Overview
Ward round mode is used for parameter Select Menu > Patient Management to check the
measurement and for multiple patients’ round data patient list. If the monitor is powered off, the patient
management (maximum 1000 patients). list will be stored. The user can also create, edit,
import and delete patients in this interface.
Create new patient
2) In other interfaces, scan the barcode:

To create new patient,
a If the patient information via MRN has
1 Select Menu > Patient Management > New been stored in the monitor before, this
Patient, or patient information will be inquired from
2 Press Admit/Create new patient hardkey the monitor and be updated as current
patient to be measured. Measurement
will start without Select Patient
on the front panel, or operation.
3 Use Select Patient permanent key, and then b If the patient information via MRN hasn’t
click icon + in popup window, or been stored in the monitor before:
4 Scan patient barcode by using barcode When monitor is connected with network
server and ADT Query (in User
Maintain) is also set to on, the monitor
scanning shortcut key . The barcode is will automatically inquire for patient
based on patient MRN. information from the server via MRN.
The corresponding patient information in
1) In the interface of creating new patient, scan
the monitor will be updated after user’s
the barcode:
confirmation.
The monitor will update the patient
information from the identified MRN. In this NOTE
interface, user can complete relevant Either Bed No. or MRN should be input.
information inputting.
Import Patient
To import patient to the patient list, select Patient  If USB flash disk is selected, prior to importing,
Management > Import and choose Source (USB set the import data file as following steps:
flash disk or Network).

Ward round mode
Step 1: Use Excel to input the patient information

with the format below. Patient type can only be
numbers, 1 for Adult, 2 for Pediatric and 3 for
Neonate. Patient information should include: bed
No., first name, last name, patient type, and MRN.
bed No. first name last name patient type MRN
23 Xiaoming Wang 1 12345
… … … … …
Step 2: Save the file as CSV with comma delimiter  If Network is selected, input the query
format. The file name should be fixed as conditions (Department, Admission Date),
‘ImportPatientList.csv’, and the encoding format of
the file should be UTF-8. and then click query button . A list
including all the patients that meet the query
NOTE
conditions is displayed. Select patients from the
In the patient list of CSV data file, first name, last list, and click Import.
name and MRN cannot be more than 63 bits for
each.
User can also directly click shortcut key
NOTE
In importing process, the monitor will import the > icon to import patient from Network.
patient information that meets the requirements,
and the wrong patient information will be During importing, if the total patients in the monitor
prompted. The wrong patient information needs to exceed upper limit (1000 patients), a confirmation
be revised and re-imported. box will be popped up. Choose OK to enter Patient
Management interface, and user should manually
Step 3: Choose patients and click Import. delete the patients till the monitor can import
patients again. Choose No to return to Import
Patient interface, and user should delete patients
to be imported, then import again.
Refresh Patient List
If monitor is connected with network server and patients > click Refresh List, and then all eligible
ADT Query (in User Maintain) is also set to on, patients will be refreshed to the window of Select
Patient.
click shortcut key > icon to set query NOTE

condition (such as Admission Date, The operation of Import Patient will keep the
patients those exist in the monitor but not found on
Department) > click query icon to show the EMR. However, the operation of Refresh Patient
List will delete those patients.

Ward round mode
NOTE
During importing or refreshing, if MRN or bed No.
has conflicts, the monitor will replace all conflicting
patient information. The measurement status will
keep unchanged if there is a MRN conflict, and
restore to the initial unmeasured status if there is a
bed No. conflict.
Delete patient
To delete patients, This operation only deletes the patient information

in Patient Management interface but will not
1 Select Patient Management > Delete Patient;
delete patient history data.
2 Choose specific patients, or directly select
If the selected patients are in measurement, there
PAGE or ALL;
will be a confirmation ‘Delete the currently
3 Select Delete. measured patient, confirm?’. Choose Yes to
delete and the monitor will return to no patient
status.
Select patient for rounds
Choose a specific patient for measurement and the  Select New Round to clear all patients’
patient information will be displayed on the main measurement status and measurement time.
interface. Measurement status will all return to ‘not
measured’ status. When the user sets Scale to
Current in Review interface, Current
Click Select Patient permanent key : measurement data will be cleared.
 All patients’ bed No., name, measurement time
and measurement status will be displayed. The
circle next to bed No. shows measurement
status by colour. Green means the patient has
normal measurement value; no colour means
the patient has invalid measurement value or no
measurement value.
 Click one patient to choose patient for current
measurement, and the patient information will
be displayed on the main interface.
 Click icon + to create new patient.

Ward round mode
Ward round record
Data Update  Click All to display all ward round records in

specified period. Abnormal value is displayed in
In main interface, for quick TEMP module, only red. Choose Alert to display abnormal value in
measurement data in predict/quick predict will be specified period. All is the default setting which
updated. will be recovered if user exit and enter this
interface again.
SpO2 data will be updated by following ways:
 The ward round record can be sequenced by
 By time interval: Click SpO2 parameter area to Bed No. or Time. Time sequence is the default
enter SpO2 parameter setup menu > SpO2 setting if user exits and enters this interface
Storage Inteval, choose from 30 S, 1 min, again.
2 mins and 5 mins. 30 S is default setting.
Then the monitor will store SpO2 original data or  Upload, Record, Export or Delete is used for
SpO2 spot-checking data according to the uploading, record outputting, exporting or
selected interval. deleting the selected ward round records
(excluding original data). Refer to chapter
 By spot-checking data: when TEMP value or Uploading data to network server and Exporting
NIBP value is obtained. data stored in the internal storage device for
details about uploading and exporting.
Ward round record confirmation  Click the icon on the right of one ward round
record to enter Patient Measurement Data
In main interface: window. In this window, user can view the
corresponding original data (20 groups at
Generate manually: by clicking Save, the most), including patient information, parameters
measurement data in main interface will be stored value and this ward round record. User can also
as a round record in Review menu. User can Save click Record to output the original data in this
multiple ward round records for a patient. interface, or modify the ward round record and
The measurement time of ward round record is click Save to complete.
subject to the time of clicking Save. If monitor is powered off, ward round record will be
stored. 1 MB space can store 100 groups of ward
round records at least, including patient information
Ward round record review and 20 original records.
Select Menu > Review, or click Review shortcut

key directly to enter ward round record review
interface.
 Set Scale to display ward round record in
specified period. The Current ward round
record will be displayed by default.


Spot-checking mode
Spot-checking mode
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
Admit patient. . . . . . . . . . . . . . . . . . . . . . . . . . 62
Modify patient information . . . . . . . . . . . . . . 62
Spot-checking data review . . . . . . . . . . . . . . 62

Spot-checking mode
Overview
Spot-checking mode is used for spot-checking

measurement and for management of multiple
patients’ spot-checking data.
Admit patient
If monitor is connected to network server, the 3 Scan patient barcode by using barcode
patient information can be synchronized to the scanning shortcut key.
network server after admission. To admit patient,
 In creating new patient interface, user can scan
1 Select Menu > Patient Management, click the barcode through scanner. The patient
New Patient to enter new patient interface. information is directly updated to this interface
according to barcode information, and user
2 Select New Patient permanent key, or press
should Confirm it.
 In other interfaces, serial No. will be
Admit/create new patient hardkey automatically added by one, and the patient
(without key sound), the monitor will information is directly updated to main interface
automatically admit new patient (that is, series according to barcode information.
No. will be automatically added by one and
other setting items are empty by default).
Modify patient information
Select Patient Management > Patient Info, or If the monitor is powered off and restarted, the bed
directly click patient information area in main No.1 patient will be automatically selected as
interface to view or modify patient information current measured patient, the patient type is adult
(serial No. is not editable). and the other information is blank.
Spot-checking data review
Select Menu > Review, or directly select Review  Set Scale to display spot-checking data in
shortcut key to enter review interface. specified period. The valid spot-checking data
in 12 hours before the latest valid spot-checking
 Click and to turn page.
data will be displayed by default.

Spot-checking mode
 Click All to display all spot-checking data in

specified period. Abnormal value is displayed in
red. Choose Alert to display abnormal value in
specified period. All is the default setting which
will be recovered if user exit and enter this
interface again.
 Upload, Record, Export or Delete is used for
uploading, record outputting, exporting or
deleting all spot-checking data in specified
period. User can choose patient data manually
and upload as needed, including the data which
have been uploaded. Refer to chapter
Uploading data to network server and Exporting
data stored in the internal storage device for
details about uploading and exporting.
 Click the icon on the right of one spot-checking
record to view the details, including patient
information, parameters value. User can also
click Record to output the data in this window.


Networked monitoring
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66
Cybersecurity . . . . . . . . . . . . . . . . . . . . . . . . . 66
Wi-Fi. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67
e-link function . . . . . . . . . . . . . . . . . . . . . . . . . 69
Central Monitoring System . . . . . . . . . . . . . . 69
Gateway communication . . . . . . . . . . . . . . . . 70
HL7 communication . . . . . . . . . . . . . . . . . . . . 71
Inquire for patient information via network

server (ADT) . . . . . . . . . . . . . . . . . . . . . . . . . . 71
Auto uploading data to network server . . . . 71

Overview
The monitor can be connected to the wired network NOTE

and the wireless network. If the monitor is
Be aware that some network-based functions may
networked, a network symbol is displayed on the
be limited for monitors on wireless networks in
screen.
comparison to those on wired networks.
NOTE
When selecting dynamic IP mode, check the IP
address from Vista 120 CMS.
Cybersecurity
For more security operations, select Menu > User  Step 1, in CA Certificate column, select
Maintain and input user maintain password > corresponding CA certificate whose suffix
Security. In this menu: should be ‘.cer’.
 Select User Password > Modify to enter  Step 2, in Client Certificate column, select
Modify User Password submenu, the user can corresponding client certificate whose suffix
change the password according to the prompts. should be ‘.cer’.
For safety considerations, change the
 Step 3, in Private Key Certificate column,
password periodically, and a combination of
select corresponding private key whose
words and numbers is recommended. If Old
suffix should be ‘.pem’.
Password is forgotten, contact Dräger Service.
 Step 4, in Password column, input
NOTE corresponding password.
When the monitor is turned on for the first time,
 Step 5, click Confirm.
modify the User Maintain password according to
the prompts. The default initial User Maintain Steps of importing certificate for HL7:
password can be found in Section Passwords.
 Step 1, in CA Certificate column, select
corresponding CA certificate whose suffix
 Set CMS/Gateway Encryption to Off, AES
should be ‘.cer’.
(default) or TLS when user connects the
monitor with network server (Vista 120 CMS or  Step 2, in Server Certificate column, select
gateway). corresponding server certificate whose
suffix should be ‘.cer’.
 Click Load Certificate to install/upgrade the
Certificate via USB flash drive. The certificate  Step 3, in Private Key Certificate column,
issued by Certificate Authority (CA) is select corresponding private key whose
recommended and self-signed certificate suffix should be ‘.pem’.
should be avoided.
 Step 4, in Password column, input
Steps of importing certificate for Vista 120 CMS corresponding password.
and Gateway:
 Step 5, click Confirm.

NOTE NOTE
CA certificate is the root certificate of CA The storage path for certificate related to TLS
institution. enterprise-level encryption method:
For Vista 120 CMS\gateway: root directory of USB
NOTE flash drive\certs\cms\
Client certificate/Server certificate are the SSL For HL7: root directory of USB flash drive
certificate obtained from CA institution and it is \certs\hl7\
recommended to use OV-SSL certificate type.
 Set Firewall to On to protect against hacker
attacking.
NOTE
The private key shall be generated by the RSA-  Click Firewall Rules to check rule details.
2048 algorithm and be encrypted by using the  Set Packets Limit value for traffic monitoring. If
AES-256 algorithm. The password for encryption the data traffic per minute exceeds the
shall be at least 8 characters (a combination of threshold, the monitor will trigger the alarm to
letters and numbers). remind the user.
 Set Auto Login to On/Off. When it is set to On,
NOTE
the user can directly enter the main interface;
The certificate format is as follows: For CA and otherwise, the user needs to enter a password
Client certificate/Server certificate, ‘.cer’ is for identity authentication.
supported; for private key, ‘.pem’ is supported. All
the certificates should comply with X.509 format.  Setting User Login Timeout allows the user to
lock the screen when the monitor has been idle
for a certain amount of time, so that others
cannot access the monitor without entering the
password. If Never is chosen, the user has no
need to login again once the authorization is
successful.
Wi-Fi
Wi-Fi modules are optional to be configured in the 4 Choose a network from the interface, in which
monitors. And the user should configure the the user can check the network’s encryption
settings on the monitor following the steps below information (Security). The user will be
before connecting the monitor to a wireless prompted to enter the password of that network
network: if a password is required. After entering the
password and setting the IPv4 address, the
1 Select Menu > User Maintain, and input the
user can click to connect the network.
password.
5 Or select to connect the hidden networks.
2 In the User Maintain menu, select Network.
After entering Network Name, Security,
3 In the Network menu, select Wi-Fi from the password and setting the IPv4 address, the
Network Type list. And click Config to open the user can click to connect the hidden
Wi-Fi Setup interface. The available networks network.
will be listed in this interface.

If the monitor is successfully connected to the Show password

selected network, it will be indicated by the
message Connected, and the local IP address of Connect the network
the monitor will be displayed in the Wi-Fi Setup
interface. Also, a symbol indicating the networking Disconnect the network
state will be displayed on the lower portion of the
main screen. The meanings of the networking state
symbols are explained below: NOTE
Be aware that some network-based functions may
Wi-Fi signal intensity: Level 4 be limited for monitors on wireless networks in
comparison with those on wired networks.
Wi-Fi signal intensity: Level 3
NOTE
The obstacle may interfere with data transmission
Wi-Fi signal intensity: Level 2
and even cause data loss.
Wi-Fi signal intensity: Level 1 NOTE

Click to review the historically connected Use the wireless device recommended by Dräger,
networks. After choosing certain network, the user otherwise some exceptional situations such as
can select Forget This Network or Join This frequent network disconnection may occur on the
Network. monitor.
If the encryption information of the currently

NOTE
connected network is modified, the network will
automatically disconnect and attempt to reconnect. When signal intensity is level 2 or less, signal may
At this time, click first to ignore this network and be unstable and quality of the signal transmission
then connect manually. may be degraded.
The following symbols may appear when

NOTE
configuring Wi-Fi:
When the monitor is connected to Vista 120
CMS/GATEWAY via the wireless network, the user
Symbol Description should set the router to a secure
encryption/authentication mode and use the non-
Connect to hidden networks
dictionary password.
View historically connected networks  Recommended options: WPA2-PSK (supports
AES / TKIP);
Refresh network list
 Other options: WPA-PSK, WPA2-Enterprise
Turn the page left and right to view (includes EAP-TLS / EAP-TTLS / EAP-PEAP).
more networks
NOTE
Secure network
The storage path for certificate related to EAP-TLS
enterprise-level encryption method: root directory
Insecure network (not
of USB flash drive\certs\wlan\
recommended). Icon color is red.
Hide password

WARNING WARNING
Before monitoring patient, the Network Type If Wi-Fi is unavailable, restart the monitor
(wired or Wi-Fi) should be selected, it is not (refer to Section Front view) to restore Wi-Fi
allowed to be switched during monitoring. function under the precondition of ensuring
Otherwise, the Wi-Fi may be unavailable. patient’s safety.
e-link function
A monitor with e-link module can transmit data

through e-link and also displays the status between Symbol Description
the monitor and the communication device in the
general information area. e-link successfully connected
To enable e-link function,

e-link disconnected
1 Select Menu > User Maintain, and input the
password.
Data transmission
2 In the User Maintain menu, select Network.
The supported data includes: patient information
3 Set e-link to On.
(doctor, blood type and department information are
4 Set the e-link Name. E-link name setup for excluded), parameter measurement data.
monitors of same model has fixed rules.
The monitor responds to the communication
20 characters are supported at most.
device’s request to transmit data. The data to be
5 In order to transmit data, the user shall pair first transmitted include:
and then connect the monitor and the
The data displayed in current interface: NIBP,
communication device. Configure e-link Key to
SpO2, PR, TEMP, transmission time.
set the pairing code which supports 6 numbers
at most. Default pairing code is 1234. NOTE
The supported e-link version is BLE4.0, which is
applicable in 3 system environments: iOS, Android
and Windows.
Central Monitoring System
The monitor can be connected to the central

monitoring system only in monitoring mode.
Through the network:
1 The monitor sends patient information, real-
time monitoring or measurement data to the
central monitoring system.

2 The real-time monitoring information is NOTE

displayed on the central monitoring system as
The time synchronization function might not be
the same to the monitor, and the central
available to all software versions of Vista 120
monitoring system can perform some bilateral
CMS. Consult our technical service department or
control. For example: changing patient
the local distributor for more information.
information, receiving patient, discharging
patient and so forth.
NOTE
For detailed information, refer to Vista 120 CMS
The monitor and Vista 120 CMS/Gateway will pack
Central Monitoring System User Manual.
and transmit the data via their own protocol. When
And the monitor supports HL7 protocol. receiving the data, they will confirm the
correctness of the data package. Only the data
NOTE that meets the protocol’s requirements will be
Use wired instead of wireless networking when received.
connecting the monitor to central monitoring
system in the operating room because the ESU NOTE
will interfere with a wireless network, which may
When deploying the network of the monitor and
cause networking failure.
Vista 120 CMS/Gateway, it is recommended to
isolate the network and the Intranet system of the
NOTE hospital by using VLAN so as to ensure the
Make sure the network connection between the network security. Only trusted devices are allowed
monitor and Vista 120 CMS is in good condition to join the VLAN network.
when the time synchronization function (refer to
section Setting date and time) on the monitor is NOTE
active. If the setting is on, the monitor will accept
For more instructions on how to connect or install
time synchronization from Vista 120 CMS.
and disconnect or uninstall the Vista 120
CMS/Gateway, refer to Vista 120 CMS Central
Monitoring System Installation Guide/Vista 120
Gateway User Manual.
Gateway communication
The monitor can be connected to the Gateway, For more information about Gateway
which provides clinicians with the capability of communication, refer to Vista 120 Gateway User
viewing and collecting patient data remotely and Manual.
the data exchange of selected clinical and
administrative information between Vista 120
Network and the hospital network.
To set the monitor server IP address, select User
Maintain > Network > Server IP. Make sure the
monitor share the same server IP with the
computer in which the Vista 120 CMS software is
installed.

HL7 communication
The monitor supports HL7 protocol to upload data.  Set HL7 Encryption method to Off or TLS
Select Menu > User Maintain and input user (default).
maintain password > Security. In this menu:
To set HL7 IP address of the client-side, select
 Set HL7 to On/Off. When it is set to On, set User Maintain > Network > HL7 IP.
Firewall to On to protect against hacker
For more information about HL7 communication,
attacking.
refer to HL7 Communication Protocol Service
Manual.
Inquire for patient information via network server (ADT)
The user can obtain patient information from the NOTE

network server to the monitor by inputting MRN or
The user can load patient information from the
scanning barcode.
network server only when ADT Query is enabled.
To obtain patient information from the network Default setting is off. Setting path: Menu > User
server, Maintain > Network > ADT Query.
1 In monitoring or ward round mode, press
NOTE
If patient information is modified on the network
Admit/Create new patient hardkey on server, the monitor can update the modified
the front panel to enter New Patient interface; contents correspondingly only when the monitor is
in monitoring mode and relevant settings on the
In spot-checking mode, select Menu > Patient network server have also been set to on. If patient
Management > New Patient to enter New information is modified on the monitor in
Patient interface; monitoring mode, the modified contents will also
2 Input MRN or scan barcode, and then click be updated to network server.
to get patient information. The patient

information can be updated to the monitor.
Auto uploading data to network server
Ward round records and spot-checking data can be

uploaded to network server.

In User Maintain > Network > Real-time Upload,

if it is set to On, when monitor is in networking and
is also connected with network server, the monitor
will upload the stored ward round record or the real-
time spot-checking measurement data to network
server in real time. The upload result will be
prompted in the general information area of main
interface, and in review interface, the icon
indicates the data have been successfully sent to
the network server.

Alarms
Alarms
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
Alarm category . . . . . . . . . . . . . . . . . . . . . . . . 74
Physiological alarms. . . . . . . . . . . . . . . . . . . . . 74
Technical alarms. . . . . . . . . . . . . . . . . . . . . . . . 74
Prompts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
Alarm levels . . . . . . . . . . . . . . . . . . . . . . . . . . 75
Controlling alarm . . . . . . . . . . . . . . . . . . . . . . 76
Setting parameter alarm . . . . . . . . . . . . . . . . . . 76
Audio alarm paused . . . . . . . . . . . . . . . . . . . . . 77
Audio alarm off . . . . . . . . . . . . . . . . . . . . . . . . . 78
Alarm reset . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
Latching alarms . . . . . . . . . . . . . . . . . . . . . . . 79
Alarm of SpO2 Sensor Off . . . . . . . . . . . . . . . 79
Network Disconnected alarms . . . . . . . . . . . 79
Delete all alarm events. . . . . . . . . . . . . . . . . . 79
Testing alarms . . . . . . . . . . . . . . . . . . . . . . . . 80
Alert setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . 80
Adjustable range of alert limits . . . . . . . . . . . . . 81
Nurse Call . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82

Alarms
Overview
WARNING
A potential hazard can exist if different alarm
presets are used for the same or similar
equipment in different areas, e.g., an intensive
care unit or a cardiac operating room.
Alarm category
 In monitoring mode: Technical alarms

The monitor provides two types of alarm,
physiological alarms and technical alarms. Also, If one or several technical status of the device is in
the monitor provides prompts. abnormal status, the monitor will give an alarm. And
this type of alarm is called technical alarms.
 In ward round or spot-checking mode: Technical alarms can’t be disabled. About the
The monitor provides vital signs alarms (such as detailed alarm information, refer to Section
SpO2 No Pulse, SpO2 Desat), and also provides Technical alarm information.
alert information (refer to chapter Alert setup for
details) instead of physiological alarms. Parameter
area displays alarm off symbol. In addition Battery Prompts
Low alarm, some technical alarms are acted as
prompts. Battery Low is acted as low-level The monitor can give the character indication of
technical alarm. monitoring process or other functions. And this
character is called prompts. About the detailed
alarm information, refer to Section Prompts.
Physiological alarms
If one or several physiological parameters of the

currently monitored patient exceed the predefined
alarm limit, the monitor will give an alarm, and this
type of alarm is called physiological alarms. About
the detailed alarm information, refer to the Section
Physiological alarm information.

Alarms
Alarm levels
In terms of severity, the device’s alarm levels can A medium level alarm warns the operator of a
be classified into three categories: high level medium priority alarm condition which requires
alarms, medium level alarms and low level alarms. prompt operator response. Failure to respond to
the cause of the alarm condition is likely to
1 High level alarms
result in reversible injury of the patient.
A high level alarm intensively warns the
3 Low level alarms
operator of a high priority alarm condition which
requires immediate operator response. Failure A low level alarm reminds the operator of a low
to respond to the cause of the alarm condition is priority alarm condition which requires
likely to result in death or irreversible injury of response. And the response time for a low
the patient. priority alarm condition can be greater than that
for a medium priority alarm condition. Failure to
2 Medium level alarms
respond to the cause of the alarm condition is
likely to result in discomfort or reversible minor
injury of the patient.
The high/medium/low-level alarms are indicated by
the system in following different ways:
Standard
Alarm level Prompt

High Mode is “DO-DO-DO------DO-DO, DO-DO-DO------DO-DO”, which is triggered
once every 8-10 seconds. The alarm indicator flashes in red, with frequency of 1.4
Hz~2.8 Hz. The alarm message flashes with red background, and the symbol *** is
displayed at the alarm area.
Medium Mode is “DO-DO-DO”, which is triggered once every 23-25 seconds. The alarm
indicator flashes in yellow, with frequency of 0.4 Hz~0.8 Hz. The alarm message
flashes with yellow background, and the symbol ** is displayed at the alarm area.
Low Mode is “DO-”, which is triggered once every 28-30 seconds. When physiological
alarm is triggered, the alarm indicator is constantly yellow. While for technical
alarm, the alarm indicator is constantly blue. The alarm message flashes with
yellow background, and the symbol * is displayed at the alarm area.
The sound pressure range for standard audible The parameter area has two flash methods to
alarm signals is from 45 dB to 85 dB. prompt alarms: background flash and text flash.
User can click respective parameter area to enter
When different level alarms occur at the same time,
parameter setup menu > Alarm > Visual Effect:
alarm sound and alarm indicator prompt the highest
level alarm, alarm messages display in turn. 1 Text Flash: text flashes with frequency of 1 Hz.
2 Background Flash: background flashes with
frequency of 1 Hz.

Alarms
WARNING WARNING
Do not rely exclusively on the audible alarm Ensure the volume is properly set up. When
system for patient monitoring. Adjustment of the sound pressure of audible alarm is below
alarm volume to a low level or off during or equivalent to the ambient noise, it may be
patient monitoring may result in patient difficult for the operator to distinguish the
danger. Remember that the most reliable audio alarm.
method of patient monitoring combines close
personal surveillance with correct operation
of monitoring equipment.
Controlling alarm
Setting parameter alarm
In monitoring mode, parameter alarm settings

including alarm switch, alarm record, alarm level
and alarm limit are available on the respective
alarm setup menu for each parameter. Click
respective parameter area to enter parameter
setup menu > Alarm to open the menu shown
below for alarm settings of each parameter. Also,
click Alarm Rec. Time to set the waveform length
of alarm record. 8 s, 16 s and 32 s are optional.
When alarm switch is off, the parameter alarm off
icon will be displayed in the corresponding

parameter displaying area.

Alarms
Upper arrow or
lower arrow to
increase or
decrease the
alarm limit
Setting value of
low alarm limit
Setting value of
high alarm limit
WARNING Audio alarm paused

When the alarm is set to Off, the monitor won’t
In monitoring mode, the user can temporarily
give an alarm prompt even if an alarm occurs.
prevent alarms from sounding by pressing shortcut
In order to avoid endangering the patient’s
life, the user should use this function
cautiously. key .
The user can set the alarm pause time as desired.
WARNING The default alarm pause time is 120 s.
Prior to monitoring, make sure that the alarm
limit settings are appropriate for the patient. 1 Select Menu > User Maintain, and enter the
required password.
WARNING 2 Select Alarm, and set Pause Time to 60 s,

Setting alarm limits to extreme values may 120 s, or 180 s.
cause the alarm system to become ineffective. When alarms are paused,
It is recommended to use the default settings.
 The audio alarm is turned off, and no alarms are
sounding.
 The visual alarm indications are still displayed.

Alarms
 The monitor displays the audio alarm paused Alarm reset

icon . In monitoring mode, select the shortcut key
 The monitor displays the remaining pause time
in seconds with red background. on the screen directly. When the alarm is
When the alarm pause time expires, the audio reset,
alarm paused status is automatically terminated  No alarms are sounding until a new alarm
and alarm is sounding. The user can also terminate occurs.
the alarm paused status by pressing shortcut key
 As for the active alarms, the visual alarm
indications are still displayed.
.
 All latching alarms are cleared. If the alarm
NOTE condition is no longer present, all alarm
If a new alarm occurs during the audio alarm indications stop and the alarm is reset.
paused period, the new alarm will not be sounding.  It will not influence the configuration of
physiological alarm off, audio paused, and
audio off status.
Audio alarm off
NOTE
In monitoring mode, set Pause Time to If a new alarm occurs after the alarm is reset, the
new alarm will be sounding.
Permanent, press shortcut key , the
monitor displays information: please confirm
whether to activate audio alarm off function?
Click Yes, the monitor will enter into audio alarm off
status. Click No, the monitor will keep current
status.
 The audio alarm is turned off, and no alarms are
sounding.
 The visual alarm indications are still displayed.
Remind signal: Audio alarm off symbol and

Audio Alarm off on a red colored background are
displayed with an interval of 2 s during the audio
alarm off status.
Pressing shortcut key again can

resume the audio alarm.
NOTE
If a new alarm occurs during the audio alarm off
period, the new alarm will not be sounding.

Alarms
Latching alarms
In monitoring mode, to configure the alarm latching

setting, select Menu > User Maintain > Alarm and
choose Alarm Latch which can be set to On or Off. The user can use the permanent key on
When it is set to Off, alarm indications end when the screen to acknowledge the latched alarm.
the alarm condition ends. When it is set to On, the
visual and audible alarm indications are still
displayed after the alarm condition ends;
meanwhile, the alarm time is also displayed for the
latched alarm for reference. The indication lasts
until the alarm is acknowledged.
Alarm of SpO2 Sensor Off
In monitoring mode, user can enter Menu > User In ward round or spot-checking mode, it is acted as
Maintain > Alarm to set the alarm level of SpO2 prompt and the level is not user-selectable.
Sensor Off to High, Med. or Low. It is set to Low
by default.
Network Disconnected alarms
To configure the network disconnected alarms, NOTE

select Menu > User Maintain > Network and
If Disconnect Alarm occurs during audio alarm
choose Disconnect Alarm which can be set to On
paused or audio alarm off status, the monitor will
or Off. The alarm is off by default.
prompt a sounding alarm with information of
NOTE NetWork Disconnect. During the network
disconnected status, activating audio alarm
When the monitor is connected with the central
paused or audio alarm off function can disable the
monitoring system, the user must set Disconnect
audio alarm signal of Disconnect Alarm.
Alarm to On.
Delete all alarm events
Select Menu > User Maintain > Alarm > Clear

Alarm Log to delete.

Alarms
WARNING
The deleted alarm events are beyond retrieve.
Use this function cautiously.
Testing alarms
When the user switches the monitor on, the monitor NOTE
will prompt two “Di” tone that means the audio in
The monitor will reboot in 3 seconds due to self-
selftest is normal. The user must check that the
test failure.
alarm indicator light is normal (it lights in red, yellow
and blue in turn during starting up). This indicates
that the visible and auditory alarm indicators are
functioning correctly. For further testing of
individual measurement alarms, perform the
measurement on a subject or use a simulator.
Adjust alarm limits and check that appropriate
alarm behavior is observed.
Alert setup
In ward round mode or spot-checking mode, the  Alert information area displays prompts with
monitor provides vital signs alarms (SpO2 No blue background. (Alert information area is the
Pulse, SpO2 Desat), and if physiological physiological alarm area in monitoring mode.)
parameters of the currently monitored patient
NOTE
exceed the predefined limit, the monitor will give
alert information instead of physiological alarms. For TEMP module, TEMP alert can only be used in
predictive mode of quick TEMP and in infrared
Enter the respective parameter setup menu to set TEMP.
alert limit and alert switch.
Alert can be indicated by the system in following NOTE
different ways: Generally, monitor displays SYS alert value. When
 User can select Background Flash or Text multiple values are abnormal, alert value will be
Flash in the parameter area. displayed in order of SYS, DIA and MAP.
 A sound of DU is used to indicate alert.

NOTE
 Parameters storage table (including the table in When alert is set to Off, the monitor won’t give a
main interface and the table in data prompt even if an alert occurs. In order to avoid
management interface) and has red mark to endangering the patient’s life, the user should use
indicate the alert value. this function cautiously.

Alarms
NOTE NOTE
Prior to monitoring, make sure that the limit Setting limits to extreme values may cause the
settings are appropriate for the patient. alert system to become ineffective. It is
recommended to use the default settings.
Adjustable range of alert limits
SpO2 20% ~ 100%

PR 30 bpm ~ 300 bpm
NIBP mmHg
Dräger NIBP
Patient Type High Limit Low Limit
ADU SYS 270 40
DIA 215 10
MAP 235 20
PED SYS 230 40
DIA 180 10
MAP 195 20
NEO SYS 135 40
DIA 100 10
MAP 110 20
SunTech NIBP
ADU SYS 260 40
DIA 200 20
MAP 220 26
PED SYS 230 40
DIA 160 20
MAP 183 26
NEO SYS 130 40
DIA 100 20
MAP 110 26

Alarms
TEMP
ADU/PED/NEO +42 ºC (+107.6 ºF) +35.5 ºC (+95.9 ºF)
Nurse Call
The monitor provides dedicated nurse call port

which is connected to nurse call system through the
nurse call cable to perform the nurse call function.
Enter Menu > User Maintain > Common > Nurse
Call to choose On or Off (default).
NOTE
Before using the function of nurse call, check if it is
functioning normally.

Alarm information
Alarm information
Physiological alarm information . . . . . . . . . . 84
Technical alarm information . . . . . . . . . . . . . 85
Prompts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
Adjustable range of alarm limits . . . . . . . . . . 93
Known issues and directions . . . . . . . . . . . . 94

Alarm information
Physiological alarm information
WARNING
During monitoring, the physiological alarms
SpO2 No Pulse and SpO2 Desat are preset to
be on and cannot be turned off.
Message Cause Alarm level

SpO2
SpO2 High SpO2 measuring value is above upper alarm limit. User-selectable
SpO2 Low SpO2 measuring value is below lower alarm limit. User-selectable
SpO2 No Pulse The signal of the measurement site is too weak due to High
insufficient blood supply and environmental factors, so the
monitor can’t detect the pulse signal.
SpO2 Desat SpO2 measuring value is below the SpO2 Desat Limit. High
PR
PR High PR measuring value is above upper alarm limit. User-selectable
PR Low PR measuring value is below lower alarm limit. User-selectable
NIBP
SYS High SYS measuring value is above upper alarm limit. User-selectable
SYS Low SYS measuring value is below lower alarm limit. User-selectable
DIA High DIA measuring value is above upper alarm limit. User-selectable
DIA Low DIA measuring value is below lower alarm limit. User-selectable
MAP High MAP measuring value is above upper alarm limit. User-selectable
MAP Low MAP measuring value is below lower alarm limit. User-selectable
TEMP
TEMP High Measuring value of TEMP is above upper alarm limit. User-selectable
TEMP Low Measuring value of TEMP is below lower alarm limit. User-selectable

Alarm information
Technical alarm information
Message Cause Alarm Level Action Taken
SpO2
Make sure the sensor is

well connected to the
SpO2 sensor may be
patient’s finger or other
disconnected from the
parts. Make sure the
SpO2 Sensor Off patient measuring site. User-selectable monitor and cables are
Or SpO2 sensor may have well connected.
malfunction.
Or replace the SpO2
sensor.
Malfunction in the SpO2 Replace the SpO2

SpO2 Sensor Err sensor or in the extension Low sensor or the extension
cable. cable.
Make sure the monitor

No SpO2 sensor was and sensor are well
SpO2 No Sensor Low
connected to the monitor. connected, reconnect
the sensor.
High
Stop using measuring
(monitoring
function of SpO2
mode)
SpO2 module failure or module, and notify
SpO2 Comm Fail Low
communication failure biomedical engineer or
(spot-checking
manufacturer’s service
or ward round
staff.
mode)
Reconnect the SpO2

sensor and change the
SpO2 Low The pulse signal is too
measurement site. If
Perfusion weak or the perfusion of
Low problem exists, notify
the measurement site is too
(Dräger SpO2) biomedical engineer or
low.
staff.

Alarm information
There is interference with

Check the condition of
SpO2 measurement
SpO2 Noisy Signal signals due to patient patient and avoid patient
movement, ambient light, Low movement; make sure
(Dräger SpO2) the cable is well
electrical interference or
else. connected.
SpO2 Light Reduce interference of

Ambient light around the the ambient light and
Interference Low
sensor is too strong. avoid sensor’s exposure
(Dräger SpO2) to strong light.
NIBP
High
(monitoring
function of NIBP module,
mode)
NIBP module failure or and notify biomedical
NIBP Comm Fail Low
communication failure. engineer or
(spot-checking or
ward round
staff.
mode)
Check the connections
and the wrapped cuff to
see whether they are all
NIBP Leak NIBP pump, valve, cuff or prepared well.
Low
(Dräger NIBP) tube has a leakage. If failure persists, notify
biomedical engineer or
staff.
NIBP Excessive Pressure has exceeded the Measure again, if failure
Low
Pressure specified upper safety limit. persists, stop measuring
function of NIBP module
and notify biomedical
NIBP Init Pressure The initial pressure is too engineer or
Low
High high during measuring manufacturer’s service
staff.
Notify biomedical
NIBP Aux Pressure has exceeded the
engineer or
Excessive second safety limit as High
Pressure specified.
staff.

Alarm information
Measuring time has Measure again or use

NIBP Time Out exceeded the specified Low other measuring
time. method.
Measure again, if failure
persists, stop using
measuring function of
NIBP Self Test Error Sensor or other hardware NIBP module and notify
High
errors. biomedical engineer or
staff.
NIBP Cuff Type The cuff type used isn’t Confirm the patient type
Error consistent with the patient Low and change the cuff.
type.
Check whether the
Atmospheric pressure or airway is occluded or
NIBP System system pressure is pressure sensor works
Pressure abnormal. The valve is Low properly. If the problem
Abnormality occluded so that deflation is still exists, contact the
failed. service personnel.
NIBP System Contact the service
Failure NIBP is not calibrated. High
personnel.
Use other methods to
Cuff is too loose or patient
NIBP Weak Signal Low measure blood
pulse is too weak.
pressure.
NIBP Range Maybe the patient blood

Use other methods to
Exceeded pressure value is beyond High
measure blood pressure.
the measurement range.
Cuff is not properly
NIBP Loose Cuff wrapped or no cuff is Low Properly wrap the cuff.
connected.
Signal noise is too large or
Make sure that the
pulse rate is not regular
NIBP Interference Low patient under monitoring
due to the patient
is motionless.
movement.

Alarm information
TAT-5000S-RS232 Thermometer
High
(monitoring
function of TEMP
mode)
Temp Comm Fail TEMP module failure or module; notify biomedical
Low
communication failure. engineer or
(spot-checking or
Manufacturer’s service
ward round
staff.
mode)
1. Check the patient and

provide any necessary
clinical care.
2. Take measurement as
Temp exceed limit The TEMP value is out of
Medium described in the user
the measurement range.
manual.
3. If message persists,
contact Manufacturer’s
service staff.
The remaining battery

power of TAT-5000S-RS232 Change the battery or
Battery Low Medium
Thermometer is 10% ~ charging.
20%.
The battery power of TAT-
Battery Depleted 5000S-RS232 Change the battery or
Medium
charging.
Thermometer is depleted.
Temperature not Contact Manufacturer’s
functional Temp problem detected Medium
service staff.
Ambient TEMP Too 1. Make sure the room
High Temp probe too warm. Low
temperature is within the
operating temp of the
temp scanner.
2. Allow the temp
Ambient TEMP Too scanner to come to room
Low Temp probe too cold. Low temperature (~30 min)
3. If message persists,
contact Manufacturer’s
service staff.

Alarm information
F3000 TEMP
System error during

TEMP Error E1 Medium
synchronization.
System error during patient

thermistor calibration.
System error during heater

thermistor calibration.
TEMP Error E4 System timing error. Medium
Probe Heater error Heater error. Medium Stop using measuring

function of TEMP
Monitoring mode patient module; notify
TEMP Error P2 thermistor unstable or out of Low biomedical engineer or
range. Manufacturer’s service
staff.
Monitoring mode heater
TEMP Error P3 thermistor unstable or out of Low
range.
Predict Mode patient

range.
Predict Mode heater

range.

function of TEMP
module; notify
biomedical engineer or
Unable to pre-heat probe staff.
TEMP Error P6 Low
tip. NOTE: Measure
readings displayed on
the screen are unreliable
when the monitor
indicates Temp Error
P06.

Alarm information
High
(monitoring
function of TEMP
mode)
TEMP module failure or module; notify
Temp COMM Fail Low
communication failure. biomedical engineer or
(spot-checking or
ward round
staff.
mode)
The TEMP value is out of Put the probe into the

Temp exceed limit the range of +30 °C ~ Medium probe well; take it out
+43 °C. and measure again.
Well connect the probe

Probe configuration (or no
No TEMP Sensor Low and the monitor, and
probe connected) error.
measure again.
The probe in use is not Correctly set the

Measure Site Error consistent with the measure Medium measure position on the
position set on the monitor. monitor.
The original temperature of

Probe TEMP Too Wait for probe temp drop
sensor >+33 °C and Low
High and start measuring.
≤+40 °C.
Others
High
(monitoring
mode)
Change the battery or
Battery Low Battery Low Low
charging.
(spot-checking or
ward round
mode)
Replace the battery and

restart the monitor. If the
Battery Error Malfunction in Battery 1 Low problem persists, notify
the manufacturer’s
service staff.
Recorder Out Of
Recorder Out Of Paper Low Install the paper.
Paper
The user presses the Notify the manufacturer’s

Recorder Setup
RECORD button when Low service staff to install and
Needed
Recorder is not configured. set the recorder.

Alarm information
Delete some data in the

Insufficient storage Less than 10M space is left
Low device or use another
space in the device.
device.
Repair the device or

Read-only storage
The device is read-only. Low replace it with a new
device
one.
1) Check if the network

cable is well connected.
2) Check if the Vista 120
CMS is turned on.
3) Check if the IP of
bedside monitor and
In distributed alarm system,
Network Vista 120 CMS are on
the monitor’s network is Low
Disconnect the same network
disconnected.
segment.
4) Contact the
professionals authorized
by manufacturer to
check the network
problem.
Disconnect the network

to make the monitor work
Abnormal network traffic
properly, and then
Network traffic has been detected. The
High contact the professionals
anomaly data traffic exceeds the
authorized by
limit.
manufacturer to check
the network problem.
Prompts
Message Cause
SpO2 Search Pulse SpO2 module is analyzing the patient signal and searching for the
pulse to compute the saturation, when sensor is connected with
patient.

Alarm information
Message Cause
SpO2 Noisy Signal There is interference with SpO2 measurement signals due to patient
movement, ambient light, electrical interference or else. (Nellcor
SpO2)
Manual Measuring In manual measuring mode.
Continual Measuring In continuous measuring mode.
Auto Measuring In automatic measuring mode.
AVG Measuring In average measuring mode.
Measurem. Canceled Press the “Start/stop NIBP measurement” button to stop the
measurement.
Calibrating During calibrating.
Calibrat. Canceled Calibration is over.
Leak. Test Running The leakage test is in process.
Leak.Test Canceled Pneumatic test over.
Resetting NIBP module in resetting.
Please Start NIBP module is in idle status.
Done NIBP measurement is completed.
Measure time out No measuring result after the module entering Predict state for 30 s.
TEMP Is Warming Up User takes the sensor out of the bracket and TEMP is warming up
Warm-up Over The monitor displays this message after taking the sensor out of the
bracket and warm-up is over.
Predict Over After the Predict measuring is over, the data and message display
on the interface.
Incomplete parameter input, In Warning-Score System interface, parameters are not completely
unable to score input.
No WIFI module detected No Wi-Fi module is detected.
Quick Predict Over Quick prediction measurement is completed.
PlaceProbeOnMeasurePlace Probe isn’t placed on the measurement site.

Alarm information
Adjustable range of alarm limits
SpO2 alarm limits are listed as follows (unit %): TEMP alarm limits are listed as follows:
Adjustable Range Patient Type Adjustable Range
SpO2 20 to 100 +35.5 °C (+95.9 ºF) ~ +42 °C
ADU/PED/NEO
(+107.6 ºF)
SpO2 Desat Limits are listed as follows (unit %):
Adjustable Range
SpO2 Desat Limit 20 to 99
NOTE
User can set the range through User Maintain >
Alarm > SpO2 Desat Limit. SpO2 Desat Limit
should be less than or equal to SpO2 alarm low
limit.
PR alarm limits are listed as follows: unit (bpm)

Adjustable Range
Dräger 30 to 300
PR (SpO2)
Nellcor 30 to 300
PR (NIBP) Dräger 40 to 240
PR (IBP) Dräger 30 to 300
NIBP alarm limits are listed as follows: unit

(mmHg):
Patient Adjustable Range

Type Dräger SunTech
SYS 40~270 40~260
ADU DIA 10~215 20~200
MAP 20~235 26~220
SYS 40~230 40~230

PED DIA 10~180 20~160
MAP 20~195 26~183
SYS 40~135 40~130

NEO DIA 10~100 20~100
MAP 20~110 26~110

Alarm information
Known issues and directions
No. Known issues Directions

1 When the trend graph is recorded in the Re-print trend graph, and do not press
monitoring mode and if the Record shortcut Record shortcut key in printing process.
key is pressed manually to stop the recording
in the process of recording the second
parameter trend graph, the record paper will
not be left blank after the second parameter
trend graph.
2 In spot-checking mode, press Admit/Create N/A
new patient hardkey, there is no key sound.
3 Switching Network Type may lead to Wi-Fi If Wi-Fi is unavailable, restart the monitor
unavailable. (refer to Section Front view) under the
precondition of ensuring patient’s safety.
4 In ward round or spot-checking mode, N/A
Removable Device can be selected, while
storage device is fixed as Internal Storage
Device.

User Interface
User Interface
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 96
Setting interface style . . . . . . . . . . . . . . . . . . 96
Selecting display parameters . . . . . . . . . . . . 96
Changing parameter and

waveform colors . . . . . . . . . . . . . . . . . . . . . . . 96

User Interface
Overview
Changing some settings may have the risk, so only

the authorized person can change them. After
changing the settings, notify the operator.
Setting interface style
The user can set the interface based on the

requirement, such as: Parameters needing to be
monitored.
Selecting display parameters
The user can select the display parameters based Exit the menu and the screen will adjust the
on the monitoring and measurement requirements. parameters automatically.
Click Menu > Parameters Setup to select the
required parameters from the popup interface >
Confirm.
Changing parameter and waveform colors
The user can set the display colors of parameter

and waveform as desire. Click respective
parameter area to enter parameter setup menu >
Color Setup to make color changes on parameter
and waveform.
NOTE
The colors won’t be affected by the default factory
Settings.

Monitoring SpO2
Monitoring SpO2
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 98
SpO2 safety information . . . . . . . . . . . . . . . . 98
Measuring SpO2 . . . . . . . . . . . . . . . . . . . . . . . 99
Measurement Procedure . . . . . . . . . . . . . . 99
Measurement limitations . . . . . . . . . . . . . . . . 101
Assessing the validity of a SpO2 reading . . 102
SpO2 alarm delay . . . . . . . . . . . . . . . . . . . . . . 102
Perfusion Index (PI)* . . . . . . . . . . . . . . . . . . . 103
Setting pitch tone . . . . . . . . . . . . . . . . . . . . . . 103
Setting sensitivity. . . . . . . . . . . . . . . . . . . . . . 104
Measuring SpO2 and NIBP simultaneously . 104
SatSeconds alarm management* . . . . . . . . . 104

Describing SatSeconds . . . . . . . . . . . . . . . 104
SatSeconds “Safety Net” . . . . . . . . . . . . . . 105
Setting SatSeconds duration . . . . . . . . . . . 105

Monitoring SpO2
Overview
SpO2 is used to measure arterial blood oxygen

saturation, which is the percentage of
oxyhemoglobin in the arterial blood. SpO2
parameter can also provide pulse rate (PR) and a
plethysmogram wave (Pleth).
SpO2 safety information
WARNING WARNING
Do not use the SpO2 sensors if the packaging Neonate SpO2 sensor can only be used when
or the sensor is damaged and return them to required, no more than 20 min at a time.
the vendor.
WARNING
WARNING Use only Dräger permitted sensors and
If the SpO2 sensor does not work properly, extension cables with the oximeter. Other
reconnect the sensor or use a new one. sensors or extension cables may cause
improper monitor performance and/or minor
WARNING personal injury.
Correct and proper sensor application: if the
sensor is too loose, it might compromise the WARNING
optical alignment, and even cause the sensor High oxygen levels may predispose a
to fall off. If the sensor is too tight, (such as premature infant to retrolental fibroplasia. If
the application site is too large or becomes this is a consideration do NOT set the high
too large due to edema), excessive pressure alarm limit to 100%, which is equivalent to
and local tissue ischemia, hypoxia and lack of switching the high limit alarm off.
nutrition may occur on the application site.
Prolonged and continuous monitoring may WARNING
increase the risk of skin irritations or When serious arrhythmia is present, the SpO2
lacerations. To avoid these damages, users pulse rate may differ from ECG heart rate but
should periodically check surrounding skin of this does not indicate an inaccurate PR (SpO2)
application site according to the patient's value.
condition and pressure sensor, inspect the if
there is sign of stress-related damage in WARNING
surrounding tissue, and regularly change the
Misapplied sensor or sensor that becomes
application site. For the patients whose fluid is
partially dislodged may cause either over or
easy to transfer and/or the patients with
under reading of actual arterial oxygen
systemic or localized edema, users should
saturation.
inspect the skin and change application site
more frequently.

Monitoring SpO2
NOTE NOTE
Avoid placing the sensor on extremities with an Functional tester or simulator can not be used to
arterial catheter, intravascular venous infusion assess the SpO2 accuracy. However, it can be
line, or inflated NIBP cuff. When measuring SpO2 used to demonstrate that a particular monitor
on the limb with inflated NIBP cuff, turn on the reproduces a calibration curve that has been
NIBP Simul function. independently demonstrated to meet a particular
accuracy.
NOTE
When a trend toward patient deoxygenation is NOTE
indicated, analyze the blood samples with a If the surrounding temperature increases, the
laboratory co-oximeter to completely understand operator should pay attention to the site of poor
the patient’s condition. perfusion, and increase the frequency of checking
the skin and changing the measurement site to
NOTE prevent burns. If the initial skin temperature is less
than 35 °C, the temperature of all the listed
SpO2 waveform is not directly proportional to the
sensors on the skin will not exceed 41 °C during
pulse volume.
working.
NOTE
NOTE
The device is calibrated to display functional
The cumulative use time for SpO2 sensor in a
oxygen saturation.
single patient should be less than 30 days.
Measuring SpO2
1 Select the correct patient category setting Before Applying the Sensor
(adult/pediatric and neonatal), as this is used to
Be sure to understand all warnings listed in the
optimize the calculation of the SpO2 and pulse
previous section before applying any sensor to a
numerics.
patient. Also,check the sensor as follows:
2 During measurement, ensure that the
 Check the sensor outside and inside. To inspect
application site:
the inside, gently open the sensor cavity and
 has a pulsatile flow, ideally with a good check splits on or next to the transparent
circulation perfusion. silicone that covers the optical elements.
 has not changed in its thickness, causing an  Any sensor showing signs of damage or
improper fit of the sensor. alteration must not be used for further patient
monitoring; instead, dispose of it using proper
disposal procedures.
Measurement Procedure
1 Switch on the monitor.

2 Attach the sensor to the appropriate site of the
patient.

Monitoring SpO2
Applying Finger/Soft-tip Sensors: NOTE

 Nip the clamp, and choose a site that is well Injected dyes such as methylene blue or
perfused and minimally restricts a conscious intravascular dyshemoglobins such as
patient’s movements. The ring finger of the non- methemoglobin and carboxyhemoglobin may lead
dominant hand is preferred. Alternatively, the to inaccurate measurements.
other fingers on the non-dominant hand may be
used. NOTE
 The big toe or long toe (next to the big toe) may Inspect the sensor to ensure that the light emitter
be used on restrained patients or patients and receiver are aligned with each other and there
whose hands are unavailable. is no gap between the sensor and the finger. All the
light emitted by the light emitter must pass through
 Place the finger into the sensor according to the the patient's tissue. The sensor cable should be
direction of the symbol on the sensor. Adjust the placed on the back of the hand.
finger to ensure that the pad of the finger
completely covers the sensor detection window. NOTE
 Orient the sensor so that the cable will be Clean and remove any substances such as nail
running towards the top of the patient’s hand. polish from the application site. Periodically check
to ensure that the sensor remains properly
 Connect the sensor with the monitor (or with the positioned on the patient.
extension cable if needed).
Applying Neonatal Finger (or Toe) Wrap
Sensors:
 When the user performs the measurement,
position the sensor over the hand or foot with
optical components opposite each other.
 Hold the sensor, and insert stretched strap into
slot, hold it there while threading end through
latch. If strap is too long, thread it through
second latch.
 Connect the sensor with the monitor (or with the
extension cable if needed).
3 Plug the connector of the sensor extension
cable into the SpO2 socket.
WARNING
Inspect the application site every two to three
hours to ensure skin quality and correct
optical alignment. If the skin quality changes,
move the sensor to another site. Change the
application site at least every four hours. For
neonate, change the measuring site every
20 minutes.

Monitoring SpO2
Measurement limitations
Certain patient conditions can affect the NOTE

measurements or cause the loss of the pulse
To prevent interference from ambient light, ensure
signal.
that the sensor is properly applied, and cover the
Inaccurate measurements can be caused but not sensor site with opaque material.
limited by:
 incorrect sensor application NOTE
Adjacent SpO2 sensors may interfere with each
 high levels of ambient light sources, such as other (eg, multiple SpO2 measurements in the
surgical lights (especially those with a xenon same patient). Be sure to cover the sensor with
light source), bilirubin lamps, fluorescent lights, opaque material to reduce cross-interference.
infrared heating lamps, and direct sunlight
 failure to cover the sensor with opaque material NOTE
in high levels of ambient light conditions Move the sensor to a less active site, and keep the
 dysfunctional hemoglobins patient still, if possible.
 low peripheral perfusion NOTE

 excessive or violent patient movement For Nellcor SpO2 module, the algorithm
automatically extends the amount of data required
 venous pulsations
for measuring SpO2 and PR depending on the
 intravascular dyes, such as indocyanine green measurement conditions. During normal
or methylene blue measurement conditions the averaging time is 6 to
7 seconds. During conditions such as those
 externally applied coloring agents (nail polish,
caused by low perfusion, interference (e.g.,
dye, pigmented cream)
external interference such as ambient light or
 defibrillation patient movement), or a combination of these, the
algorithm automatically extends the amount of
 placement of the sensor on an extremity with a
data required beyond 7 seconds. If the resulting
blood pressure cuff, arterial catheter, or
dynamic averaging time exceeds 20 seconds, the
intravascular line
screen will display prompt message “SpO2 Search
 electromagnetic interference Pulse” and SpO2 and PR will continue to be
updated every second. As these conditions
Loss of pulse signal can occur for the following
extend, the amount of data required continues to
reasons:
increase. If the dynamic averaging time reaches
 the sensor is applied too tightly 40 seconds, the screen will display high-level
alarm message “SpO2 No Pulse” indicating a loss-
 a blood pressure cuff is inflated on the same
of-pulse condition.
extremity as the one with the sensor attached
 there is arterial occlusion proximal to the sensor
 low peripheral perfusion

Monitoring SpO2
Assessing the validity of a SpO2 reading
The user can check the quality of the pleth wave NOTE
and the stability of the SpO2 values to assess
The SpO2 accuracy has been validated in
whether the sensor functions properly and whether
controlled human studies against arterial blood
the SpO2 readings are valid. Always use these two
sample reference measured with a CO-oximeter.
indications simultaneously to assess the validity of
SpO2 measurements are statistically distributed,
a SpO2 reading.
only about two-thirds of the measurements can be
Generally, the quality of the SpO2 pleth wave expected to fall within the specified accuracy
reflects the quality of the light signals obtained by compared to CO-oximeter measurements. The
the sensor. A wave of poor quality manifests a volunteer population in the studies are composed
decline of the signal validity. On the other hand, the of healthy men and women from age 19 to 37 (for
stability of the SpO2 values also reflects the signal Dräger SpO2 module), from 18 to 50 (for Nellcor
quality. Different from varying SpO2 readings SpO2 module), with various skin pigmentations.
caused by physiological factors, unstable SpO2 Note that the study population was healthy adults
readings are resulted from the sensor’s receiving and not in the actual intended use population.
signals with interference. The problems mentioned
above may be caused by patient movement, wrong NOTE
sensor placement or sensor malfunction. To obtain The pulse rate accuracy is obtained by comparison
valid SpO2 readings, try to limit patient movement, to the pulse rate generated with an arterial oxygen
check the placement of the sensor, measure simulator (also an electronic pulse simulator).
another site or replace the sensor.
NOTE
During monitoring, if the monitor's reading differs
significantly from the patient's physiological
condition, it indicates that the signal may be
disturbed, resulting in an inaccurate reading. In
this case, the artifact can disguise as a similar
reading, causing the monitor to fail to send an
alarm. In order to ensure reliable monitoring, it is
necessary to regularly check whether the sensor is
wearing properly and the signal quality is good.
SpO2 alarm delay
There is a delay between a physiological event at

the measurement site and the corresponding alarm
at the monitor. This delay has two components:

Monitoring SpO2
1 The time between the occurrence of the

physiological event and when this event is
represented by the displayed numerical values.
This delay depends on the algorithmic
processing time and the sensitivity setting. The
lower the sensitivity configured, the longer the
time needed until the numerical values reflect
the physiological event.
2 The time between the displayed numerical
values exceeding an alarm limit and the alarm
indication on the monitor. This delay is the
combination of the configured alarm delay time
plus the general system delay time.
Perfusion Index (PI)*
* Only applicable to the Dräger SpO2 module. PI is indicated by a value ranging from 0 to 10. The
bigger the value is, the better the perfusion and the
PI is a numeric value indicating perfusion level. It
signal quality will be. The perfusion level and the
reflects the perfusion level at the monitoring site.
signal quality are at their maximum when the value
As the measurement of SpO2 is based on the reaches 10. When PI is below 2, it indicates the low
pulsation caused by the blood flow through the perfusion and the poor signal quality at the monitoring
vessel, PI is in relation to the strength of the pulse. site; the user needs to reposition the sensor or find a
Also, the user can use PI as a signal quality indicator better site.
for the measurement of SpO2.
The PI value will be displayed in the SpO2 parameter
area.
Setting pitch tone
If tone modulation is on, the PR sound lowers when

the SpO2 level drops. In the SpO2 Setup menu,
select pitch tone to toggle between On and Off. The
lower SpO2 value is, the lower the frequency of Pitch
tone is.

Monitoring SpO2
Setting sensitivity
The different sensitivity indicates different refresh 1 Select the SpO2 Setup menu;
frequency. High indicates the refresh frequency of
2 Select Sensitivity on the interface and select
SpO2 value is the most frequent. To change the
the desired sensitivity from the popup list.
sensitivity, follow the steps:
Measuring SpO2 and NIBP simultaneously
While measuring SpO2 and NIBP on the same limb

simultaneously, the user can set NIBP Simul to On
in SpO2 Setup menu to lock the SpO2 alarm status
until the NIBP measurement ends. If NIBP Simul is
set to Off, low perfusion caused by NIBP
measurement may lead to inaccurate SpO2 readings
and therefore cause false physiological alarms.
SatSeconds alarm management*
* Only applicable to the Nellcor SpO2 module. With the SatSeconds technique, upper and lower
* Not applicable to Vista 120 CMS. SpO2 alarm limits are set in the same way as
traditional alarm management. However, the user can
also set a SatSeconds limit that allows monitoring of
Describing SatSeconds SpO2 below the selected lower alarm limit and above
the selected upper alarm limit for a period of time
With traditional alarm management, upper and lower before an alarm is triggered.
alarm limits are set for monitoring oxygen saturation. The method of calculation is as follows:
During monitoring, as soon as an alarm limit is
violated by as little as one percentage point, an alarm The number of percentage points that the SpO2 falls
is immediately triggered. When the SpO2 level outside the alarm limit is multiplied by the number of
fluctuates near an alarm limit, the alarm is triggered seconds that the SpO2 level remains outside that
each time the limit is violated. Such frequent alarms limit. This can be stated as an equation:
can be distracting. Points × Seconds = SatSeconds
Where:
Points = SpO2 percentage points outside of the limit
Seconds = number of seconds that SpO2 remains at
that point outside of the limit

Monitoring SpO2
The alarm response time, assuming a SatSeconds SatSeconds “Safety Net”

limit set at 50 and a lower alarm limit set at 90, is
described and illustrated below. The SatSeconds “Safety Net” is for patients whose
In this example, the SpO2 level drops to 88 (2 points saturation makes frequent excursions below or
below the limit) and remains there for a period of above the SpO2 limit but does not remain in
2 seconds (2 points × 2 seconds = 4 SatSeconds). violation long enough for the SatSeconds limit to be
The SpO2 then drops to 86 for 3 seconds and then to reached. If three or more SpO2 alarm limit
84 for 6 seconds. The resulting SatSeconds values violations occur within a 60-second period, an
are shown below: alarm will be triggered even if the SatSeconds limit
has not been reached.
SpO2 Seconds SatSeconds
2 x 2 = 4
Setting SatSeconds duration
4 x 3 = 12
The user can set SatSeconds to Off or to the
6 x 6 = 36
duration among 10, 25, 50 and 100. To configure
Total SatSeconds = 52 the SatSeconds settings, enter the SpO2 Setup
menu and select the desired SatSeconds setting
After approximately 10.7 seconds, a SatSeconds from the SatSeconds list.
alarm will be triggered, because the limit of 50
SatSeconds has been exceeded. See arrow (↑) in
the following figure.
50 SatSeconds
Alarm Point
SECONDS
Alarm Response with SatSeconds
Saturation levels may fluctuate rather than

remaining steady for a period of several seconds.
Often, the patient SpO2 may fluctuate above and
below the alarm limit, re-entering the non-alarm
range several times. During such fluctuation, the
monitor integrates the number of SpO2 points, both
positive and negative, until either the SatSeconds
limit is reached, or the patient SpO2 returns within a
normal range and remains there.


Monitoring PR
Monitoring PR
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 108
PR source . . . . . . . . . . . . . . . . . . . . . . . . . . . . 108
Setting PR volume . . . . . . . . . . . . . . . . . . . . . 108

Monitoring PR
Overview
The pulse numeric counts the arterial pulsations

that result from the mechanical activity of the heart
in beats per minute (bpm). The user can obtain a
pulse from any measured SpO2 signal or NIBP
measurement.
PR source
PR source can be from SpO2 or NIBP, and is not

selectable. SpO2 is preferred source if PR from
SpO2 is valid. If PR is on, and SpO2 & NIBP both
are off, PR parameter area will display No source.
Setting PR volume
Select PR Setup > Function > PR Volume. Five

bars represent the maximum volume and one bar
represents the minimum volume. If none of bars are
selected, the PR volume will be off. Beat frequency
has positive correlation with measurement value.

Monitoring NIBP
Monitoring NIBP
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 110
NIBP safety information. . . . . . . . . . . . . . . . . 110
Measurement limitations . . . . . . . . . . . . . . . . 112
Measurement methods . . . . . . . . . . . . . . . . . 112
Measurement procedures . . . . . . . . . . . . . . . 113

Operation prompts . . . . . . . . . . . . . . . . . . . . . . 114
Correcting the measurement if limb
is not at heart level . . . . . . . . . . . . . . . . . . . . . . 115
NIBP Multi-Review interface . . . . . . . . . . . . . 115
Resetting NIBP . . . . . . . . . . . . . . . . . . . . . . . . 115
Calibrating NIBP . . . . . . . . . . . . . . . . . . . . . . . 115
Leakage test . . . . . . . . . . . . . . . . . . . . . . . . . . 116
Procedure of Leakage Test . . . . . . . . . . . . . . 116
Setting inflation value . . . . . . . . . . . . . . . . . . 117
Measuring PR . . . . . . . . . . . . . . . . . . . . . . . . . 117
NIBP auto recording. . . . . . . . . . . . . . . . . . . . 117

Monitoring NIBP
Overview
This monitor uses the oscillometric method for The blood pressure measurements determined
measuring NIBP. It can be used for adult, pediatric with this device comply with the American National
and neonatal patients. It is also intended for use Standard for Electronic or Automated
with pregnant, including pre-eclamptic patients. Sphygmomanometers (ISO 81060-2:2013) in
relation to mean error and standard deviation. In
Oscillometric devices measure the amplitude of
clinical investigation method with a reference
pressure changes in the occluding cuff as the cuff
sphygmomanometer, the fifth Korotkoff sound was
deflates from above systolic pressure. The
used to determine adult diastolic pressure, and the
amplitude suddenly increases as the pulse breaks
fourth Korotkoff sound was used to determine
through the occlusion in the artery. As the cuff
pediatric diastolic pressure.
pressure decreases further, the pulsations increase
in amplitude, reach a maximum (which The invasive blood pressure is used to determine
approximates to the mean pressure), and then the neonate pressure in clinical investigation, and
diminish. the arterial reference sites include umbilical artery,
arteria cruralis, axillary artery, brachial artery,
dorsalis pedis, and radial artery.
NIBP safety information
WARNING WARNING
Do not measure NIBP on patients with sickle- Do not apply the cuff to a limb that has an
cell disease or any condition where skin intravenous infusion or catheter in place. This
damage has occurred or is expected. could cause tissue damage around the
catheter when infusion is slowed or blocked
WARNING during cuff inflation.
Do not measure NIBP on the arm of the same
side with a mastectomy. WARNING
Do not attach the cuff to a limb being used for
WARNING IV infusions as the cuff inflation can block the
Use clinical judgment to decide whether to infusion, potentially causing harm to patient.
perform frequent blood pressure
measurements on patients with severe blood WARNING
clotting disorders because of the risk of Do not apply the cuff to a limb where
hematoma in the limb fitted with the cuff. intravascular access or therapy, or an arterio-
venous (A-V) shunt is present, otherwise, it
may result in injury to the patient.

Monitoring NIBP
WARNING NOTE
Ensure that the correct patient type is selected If the user spills liquid onto the equipment or
before performing measurements. Do not accessories, particularly if there is a chance that it
apply the higher adult inflation, overpressure can get inside the tubing or the measurement
limits and measurement duration for neonatal device, contact the service personnel.
patients. Not using the neonate mode on a
neonatal patient can block the blood flow, NOTE
potentially causing harm to the patient. Continuous use of the automatic measuring mode
for short intervals may lead to the discomfort of
WARNING patient. Continuous measuring and automatic
Make sure that the air tubing connecting the measuring in neonatal or pediatric mode may
blood pressure cuff and the monitor is neither result in tissue damage or ischemia to the patient.
blocked nor tangled.
NOTE
WARNING NIBP measurement can be affected by extremes
Measuring of blood pressure can temporarily of temperature, humidity and altitude.
cause malfunctioning of other medical
monitoring devices on the same limb. NOTE
NIBP measurement value should be explained by
WARNING qualified professionals.
NIBP readings can be affected by the
measurement site, the position of the patient, NOTE
exercise, or the patient's physiologic The pulse rate based on the NIBP measurement
conditions. may differ from the heart rate based on the ECG
waveform. NIBP measures the number of
WARNING peripheral pulse pulsations, and the heart rate is
Continuous cuff pressure due to connection measured by the electrical signal of the heart.
tubing kinking can block the blood flow, and When the electrical signals of the heart
may result in injury to the patient. occasionally fail to cause the peripheral blood
vessels to pulse or the patient's peripheral
WARNING perfusion is poor, the difference happens.
Verifying the calibration is only applicable for
adults, and it cannot be operated in automatic NOTE
measuring interval. Continuous measuring The cumulative use time for NIBP cuff in a single
cannot be operated in automatic measuring patient should be less than 30 days.
interval either.
NOTE
It is suggested that the user should not start NIBP
measuring when the low battery displays, or the
monitor may be turned off automatically.

Monitoring NIBP
Measurement limitations
Measurements are impossible with pulse rate  Patients with excessive and continuous
extremes of less than 40 bpm or greater than movement such as shivering or convulsions.
240 bpm, or if the patient is on a heart-lung
 Patients with rapid blood pressure changes.
machine.
 Patients with severe shock or hypothermia that
The measurement may be inaccurate or impossible
reduces blood flow to the peripheries.
in the following situations:
 Patients with obesity, where a thick layer of fat
 A regular arterial pressure pulse is hard to
surrounding a limb dampens the oscillations
detect.
coming from the artery.
 Patients with cardiac arrhythmias.
 Patients on an edematous extremity.
Measurement methods
There are four methods of measuring NIBP: WARNING

 Manual - measurement on demand. Manual is Prolonged non-invasive blood pressure
the default setting in ward round and spot- measurements in AUTO mode may be
checking mode. associated with purpura, ischemia and
neuropathy in the limb wearing the cuff. When
 Auto - continually repeated measurements
monitoring a patient, examine the extremities
(between 1 and 480 minute adjustable interval).
of the limb frequently for normal color, warmth
After the first measurement starts manually, the
and sensitivity. If any abnormality is observed,
monitor will automatically measure NIBP as
stop the blood pressure measurements.
preset interval. Auto is used in monitoring mode
only.
 Continual - the measurement will run
consecutively in five minutes with intervals of
5 seconds, then the monitor enters manual
mode or auto mode.
 Average - between 1 and 5 minute adjustable
AVG interval, measurement will run as specified
AVG times (3 or 5 times are optional), then gets
average value. Average is used in ward round
or spot-checking mode only. After finishing
average measurement, the monitor enters
manual mode.
To change Measure Mode, Interval, AVG
Measurement Interval and AVG Measurement
Times, select NIBP Setup > Function.

Monitoring NIBP
Measurement procedures
To obtain accurate measurements, the following 4 Select a measurement mode and unit (mmHg,
operating steps need to be observed: cmH2O or kPa, 1 mmHg = 0.133 kPa,
1 mmHg=1.36 cmH2O) in the NIBP Setup
1 Ensure the patient position in normal use,
menu. Refer to section Operation Prompts for
including
details.
 Comfortably seated or lie flat, legs
uncrossed;
5 Press the button on the front panel to
 Feet flat on the floor start a measurement.
 Back and arm supported 6 Wait until the first reading is taken.
 Relax as much as possible, neither talking
nor applying external pressure against the NOTE
cuff. Rest for five minutes in a quiet The width of the cuff is either approximately 40%
environment. of the limb circumference or 2/3 of the upper arm
length. The inflatable part of the cuff should be
2 Connect the air hose and switch on the monitor. long enough to encircle 80-100% of the limb. The
Apply the blood pressure cuff to the patient's wrong size of cuff can cause erroneous readings.
arm and follow the instructions below. Ensure If the cuff size is in question, use another cuff with
that the cuff is completely deflated. suitable size to avoid errors.
Apply the appropriate size cuff to the patient
(About the cuff size selection, refer to Section NOTE
NIBP accessories), and make sure that the If an NIBP measurement is suspect, repeat the
symbol "Φ" is over the artery. Ensure that measurement. If the user is still uncertain about
middle of the cuff is at the level of the right the reading, use another method to measure the
atrium of the heart and the cuff is not wrapped blood pressure.
too tightly around the limb. Excessive tightness
may cause discoloration and eventual ischemia NOTE
of the extremity.
Make sure the cuff is well connected. A leak of air
may cause measurement error.
NOTE
Select the cuff with the suitable size. An unsuitable
cuff may cause incorrect measurements.
NOTE
Avoid incursion of liquid into the cuff. If this
happens, desiccate the cuff completely.
Cuff Usage
NOTE
3 Check whether the patient type is appropriately NIBP parameter area can display real-time cuff
selected. Clicking patient information area or pressure value till displaying SYS value.
pressing Switch Patient Type hardkey can
change patient Type.

Monitoring NIBP
NOTE Access the NIBP Setup menu; click Continuous to

start a continuous measurement. The continuous
NIBP parameter area keeps measured value for
measurement will last 5 minutes.
30 mins. If there is no measurement to continue,
the area will display invalid value after 30 mins. 4 AVG Measurement
Access NIBP Setup > Function menu, set AVG
Measurement interval and AVG Measurement
Operation prompts times, and click NIBP AVG; or click AVG shortcut
1 Manual Measurement
Access the NIBP Setup > Function menu and
key directly to start measurement. During
set the Measure Mode item to Manual. Then measurement:
 Invalid value will not be used for counting
press the button on the front panel to
average. Invalid value every measurement will
start a manual measurement. During
result in invalid average;
measurement, pressing this button at any time
can stop measurement.  There will have sounding of DU… after entire
measurement is finished. At that time, a final
2 Automatic Measurement
average value can be displayed. Meanwhile,
Access the NIBP Setup > Function menu and alert information of the last measurement and
set the Measure Mode item to AUTO, select technical alarms of the last measurement will be
cleared, and alert information can work
time interval as need, then press the normally. The value for each measurement and
button on the front panel. During measurement: final average value will be stored in ward round
records/spot-checking trend table which uses
 If measurement is failed or monitor receives the icon * to mark the average value;
command for suspending, measurement will be
stopped. The next measurement will be  In specified interval, if interval and times have
continued after interval. If alarms of NIBP been changed again, the whole average
Excessive Pressure or NIBP Aux Excessive measurement will be ended and measurement
Pressure are present, the whole measurement times will be zero;
will be stopped. Manually operation is  Other operations, such as changing patient
necessary for a new auto measurement. type, entering DEMO or standby mode and so
 During interval, if interval is changed, after on, can stop the measurement. Meanwhile,
ending of new interval countdown, monitor will parameter interface will be updated;
start measurement automatically.  At the end of the last measurement, if user
 During interval, if user manually starts the presses NIBP measurement key before monitor
measurement, the next auto measurement will gets average value with DU… sounding, a new
start after the ending of countdown which starts round of average measurement will be started
from the latest manual measurement; During with prompt NIBP AVG-1 (n) and NIBP average
interval, if user makes a continuous value of the last round will not be displayed. '-1
measurement, the whole measurement will be (n)' means the first measurement of N times.
over on the basis of continuous measurement. 5 Stopping Measurement
3 Continuous Measurement
During measurement, press the button on
the front panel at any time to stop measurement.

Monitoring NIBP
NOTE Correcting the measurement if limb is

In auto or average mode, when measurement is in not at heart level
To correct the measurement if the limb is not at

process, pressing the button can only
heart level to the displayed value:
stop the current measurement, and cannot end the
entire measurement mode. At the end of
countdown, monitor continues to finish the NIBP Add 0.75 mmHg Deduct 0.75 mmHg
measurement; when measurement is in interval, (0.10 kPa) for each (0.10 kPa) for each
centimeter higher or centimeter lower or
pressing the button can start Add 1.9 mmHg Deduct 1.9 mmHg
measurement in advance. (0.25 kPa) for each (0.25 kPa) for each inch
inch higher lower
NOTE
To end the whole AVG measurement, click AVG
measurement shortcut key, or click Stop in NIBP
setup menu.
NIBP Multi-Review interface
In monitoring mode, clicking the triangle icon at the

bottom of main interface can display/hide NIBP
multi-review interface.
Resetting NIBP
Available for Dräger module only. When the pressure does not work properly and the
system fails to give a message for the problem, pick
Reset in the User Maintain > NIBP menu to
activate self-test procedure, and thus restore the
system from abnormal performance.
Calibrating NIBP
NIBP is not user-calibrated. Cuff-pressure qualified service professional. See the Service
transducers must be verified and calibrated, if Manual for details.
necessary, at least once every two years by a

Monitoring NIBP
Leakage test
Leakage test is used to detect the air tightness of WARNING

the NIBP pump, valve, and trachea. If not, the
This leakage test other than being specified in
system will display NIBP leakage. NIBP leak
the ISO 81060-1 standard is to be used by the
detection should be performed at least once every
user to simply determine whether there are air
two years or when the user thinks the
leaks in the NIBP airway. If at the end of the
measurement is inaccurate.
test the system gives the prompt that the NIBP
airway has air leaks, contact the manufacturer
for repair.
Procedure of Leakage Test
1 Connect the cuff securely with the socket for NOTE

NIBP air hole.
When applying high pressures; take special care
2 Wrap the cuff around the cylinder of an to increase the pressure at a rate that will not
appropriate size; don’t wrap the cuff around cause unwanted overpressure errors (300 mmHg).
limbs.
Manually inflate the pneumatic system to
3 Make sure the patient type has been set to approximately 250 mmHg. Start the timer and wait
Adult. 60 seconds for the pneumatic system to reach its
4 Access Menu > User Maintain. pressure equilibrium point. After the waiting period,
record the pneumatic pressure level (P1) and wait
5 Select Leakage Test in NIBP. Then the prompt another 60 seconds and record the pneumatic
Leak. Test Running will appear indicating that pressure level again (P2). Safety circuitry on the
the system has started the leakage test. module only allows the pressure in the pneumatic
For Dräger module: system to remain above 10mmHg for 180 seconds.
When this safety time limit is exceeded, the valves
The system will automatically inflate the pneumatic will open releasing the pressure. Subtract P2 from
system to about 180 mmHg. After 20 seconds to P1 and this is the leak rate per minute.
40 seconds, if system leakage has detected, the
system will automatically open the deflating valve 6 If the alarm information NIBP Leak appears, it
to stop the leak test and indicates NIBP Leak. If no indicates that the airway may have air leaks. In
system leakage is detected when the pneumatic this case, the user should check for loose
system is inflated to 180 mmHg, the system will connection. After confirming secure
perform a deflation to an approximate value of connections, the user should re-perform the
40 mmHg and subsequently perform the second leakage test. If the failure prompt still appears,
phase leak test. After 20 seconds to 40 seconds, contact the manufacturer for repair.
the system will automatically open the deflating
valve and provide corresponding indication based
on the test result.
For SunTech module:

Monitoring NIBP
Monitor Cylinder
NIBP Hose Cuff
Diagram of NIBP Air Leakage Test
Setting inflation value
To change the inflation value:  If other inflation values are chosen, the
preset value by users will be adopted as the
1 Select NIBP Setup > Function > Inflation
inflation value when measuring blood
value;
pressure.
2 Choose AUTO or other inflation values from the
 If AUTO is chosen, the default value will be
pull-down list.
adopted as the inflation value when
measuring blood pressure.
Measuring PR
Access NIBP Setup > Function, and set PR to On  Monitor will not record PR from NIBP;
or Off.
 PR from NIBP will be displayed in NIBP review
 The NIBP parameter area displays PR from table but not in other review tables.
NIBP;
NIBP auto recording
In monitoring mode, the monitor supports NIBP

recording for each valid measurement. Access
Menu > System Setup > Recorder > NIBP
Trigger Recording to choose On. Default setting
is Off.


Monitoring TEMP
Monitoring TEMP
Infrared TEMP with TAT-5000S-RS232 Ther-

mometer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 120
Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . 120
Preparation before Use . . . . . . . . . . . . . . . . . . 121
Measuring Procedure . . . . . . . . . . . . . . . . . . . . 122
Setting Exergen Temp scanner unit . . . . . . . . . 126
Replacing Exergen Temp scanner’s battery. . . 127
Quick TEMP with F3000 module . . . . . . . . . . 128

Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . 128
Probe covers —applying & removing . . . . . . . . 129
Changing isolation chambers and probes . . . . 130
Measuring mode. . . . . . . . . . . . . . . . . . . . . . . . 130
Measuring procedure . . . . . . . . . . . . . . . . . . . . 131
TEMP setup for F3000 module. . . . . . . . . . . . . 132

Monitoring TEMP
Infrared TEMP with TAT-5000S-RS232 Thermometer
Introduction CAUTION
Always store this thermometer in a clean, dry
The Exergen Temporal Scanner, Model TAT-
place where it will not become excessively cold
5000S-RS232 Thermometer has the capability of (-4 °F/-20 °C), or hot (122 °F/50 °C) or humid
taking Temporal Artery (TA) Temperature in about (max RH 93% non-condensing, at 50 to 106 kPa).
3 seconds. The Exergen Temp scanner has the
ability to measure the patient’s Arterial temperature
in °F or °C. CAUTION
The thermometer is not shockproof. Do not drop it
Vista 120 SC monitor with Exergen Temp scanner or expose it to electrical shocks.
is indicated for use in adult, pediatric and neonatal
patient populations.
CAUTION
WARNING Do not Autoclave. Note cleaning and sterilizing
No modification of this equipment is allowed. procedures in this manual.
WARNING CAUTION
Do not use this thermometer if it is not In addition to the battery, there are no other parts
working properly, if it has been exposed to available to the user for maintenance. When the
temperature extremes, damaged, been battery power is low, the user shall replace the
subject to electrical shocks or immersed in battery according to the instructions in this
water. manual. For service, repair or adjustments, return
the thermometer to the manufacturer.
WARNING
CAUTION
Not suitable for use in the presence of
flammable anesthetic mixtures. Never drop or insert any object into any opening,
unless stated in this manual.
WARNING
CAUTION
Do not take temperature over scar tissue,
open sores or abrasions. If the thermometer is not used regularly, remove
the battery to prevent possible damage due to
chemical leakage.
CAUTION
Use this product only for its intended use as
CAUTION
described in this manual.
Disposal of used Exergen scanner must be
performed in accordance with current medical
CAUTION
practices or local regulations regarding disposal
The operating environmental temperature range of infectious, biological medical waste.
for this product is 60 to 104 °F (15.5 to 40 °C).

Monitoring TEMP
CAUTION
Follow the battery manufacturer’s
recommendations or the hospital policy for the
disposal of used batteries.
Preparation before Use
Sensor Lens
Metal Probe Cone
ON Button
Pinhole (on side)
LED Display
Battery
Compartment
Access Door
Front Rear
Using the Exergen Temp Scanner  Clicking: Each fast click indicates a rise to a
higher temperature, similar to a radar detector.
 To Scan: Depress the ON button. The
Slow clicking indicates that the thermometer is
thermometer will continually scan for the
still scanning, but not finding any higher
highest temperature (peak) as long as the ON
temperature.
button is depressed.

Monitoring TEMP
 To Retain or Lock Reading: The reading will Factors That May Affect Measurement
remain on the LED display for 30 seconds after Accuracy
button is released. If measuring room
 Sweating
temperature, the temperature will remain on the
LED display for only 5 seconds. When a fever resolves, the body may bring its
temperature down by sweating. The temp scanner
 To Restart: Depress the ON button to restart. It
detects this reduction in temperature immediately.
is not necessary to wait until the LED display is
However, sweating also causes extra cooling of the
clear, the thermometer will immediately begin a
skin. As a result the reading given by the temp
new scan each time the ON button is
scanner may be low. The user should therefore
depressed.
either wait until the sweating has stopped (wiping of
Alternate sites when temporal artery or behind the forehead is not recommended, since the
ear are unavailable sweating immediately begins again), or use the
following method:
 Femoral artery: slowly slide the scanner
across groin. 1 Scan the temperature as normal, keeping the
button depressed;
 Lateral thoracic artery: slowly scan side-to-
side in the area - midway between the axilla and 2 Gently nestle the temp scanner on the neck
the nipple. directly behind the ear lobe;
3 Release the button and read the temperature.
Measuring Procedure The artery behind the ear lobe does not provide a
sufficiently accurate reading. However, this area is
Measure only the side of the head exposed to the less affected by sweating than the forehead. In
environment. Anything covering the area to be addition, during sweating, increased blood flow
measured (hair, hat, wig, bandages, etc.) would produces higher skin temperatures, equivalent to
insulate the area, resulting in falsely high readings. TA temperature, resulting in a good reflection of
body temperature.
Slide the thermometer straight across the forehead,
not down the side of the face. Midline on the  Environmental Effects
forehead, the TA is about a millimeter below the The temp scanner measures the temperature of the
skin, whereas at the side of the face, the TA is much surrounding environment. For this measurement to
deeper, and measuring there would result in falsely be accurate, it needs to have become acclimated to
low readings. the temperature of the room in which it is to be
Wait about 30 seconds before measuring the same used.
person again to avoid excessive cooling of the skin.
CAUTION
An infant is frequently swaddled in blankets and
Allow the temp scanner to acclimate for at least
clothing covering the neck area. Unless visible
30 minutes before use if it is taken from a cold
sweating, one measurement at the TA area is
room into a hot room, or vice versa. Avoid holding
typically all that is required. Should the user feel the
the temp scanner by the probe as it will mistake
temperature is low, then push aside any clothing or
the temperature of hand for that of the room.
blankets covering the neck area for about 30
seconds or so, and repeat the measurement on the  Movement
neck behind the ear.
If the patient is agitated, or squirms away before
completing the measurement, just keep the button
depressed and continue the measurement without
having to wait.

Monitoring TEMP
Temperature Measurement 2 Slide across forehead

Follow this procedure to take a temperature:  Place probe on center of forehead and
depress ON button.
1 Remove temp scanner from cradle
 Keeping ON button depressed, slowly slide
 Gently tilt the temp scanner up from the
probe mid-line across forehead to the hair
bottom of the cradle.
line.
 Lift the temp scanner’s probe over the
cradle’s fingers (probe).
3 Slide behind ear (Only applicable to adult)  Remove from head.

 Keeping ON button depressed, lift probe  Read value on probe and monitor.
from forehead, touch behind ear halfway
down the mastoid process and slide down to
the soft depression behind the earlobe.
5 Return scanner back to cradle (or when not in

use)
 Lay the temp scanner probe into the cradle’s
4 Read Temp
fingers (probe).
 Release ON button.

Monitoring TEMP
 Gently lay the temp scanner down into the

bottom of the cradle.
 The temp scanner may be gently pushed
into the cradle until the retaining clips are
engaged around the body of the temp
scanner.
How to Improve Accuracy of Infant
Measurements
Preferred site:
 The preferred site is the temporal artery area.
 Unless visibly diaphoretic, one measurement
here is typically all that is required.
 Measure straight across the forehead and not
down the side of the face.
 At the mid-line, the temporal artery is about
2 mm below the surface, but can go deeply
below the surface on the side of the face.
Alternate site:
 If the temporal artery is covered, then the area
behind the ear, if exposed, can be an alternate
site.
 Brush the hair aside if covering the area to be

measured.
 The Measurement site must be exposed.

Monitoring TEMP
How to Improve Accuracy of Adult Measure exposed skin:

Measurements
 Brush the hair and bangs aside if covering the
Non-insulated forehead: area to be measured.
 Measure only the up-side on a patient in a
lateral position.
 The down-side will be insulated preventing the
heat from dissipating, resulting in falsely high
readings.
If an abnormally high or low reading is

obtained:
 Repeat the reading with the same Temp
scanner; a correct reading will be reproducible.
 Repeat the reading with another Temp scanner.
Think of a sweatband: Two Temp scanners with the same reading will
confirm the reading.
 Measure straight across the forehead and not
down the side of the face.  Sequential readings on the same patient in
rapid succession will cool the skin; it is best to
 At the mid-line, the temporal artery is about
wait about 30 seconds for the skin to recover
2 mm below the surface, but can go deeply
from the cold probe.
below the surface on the side of the face.
 Refer to the table below for Possible Causes of
Abnormal Exergen Temp Readings.

Monitoring TEMP
Type of Abnormal
Possible Cause Action Taken
Temperature
Dirty Lens. Clean lens of scanner every two weeks.
Releasing the button before finished Release the button after finished
measuring. measuring.
Measuring when an ice pack or wet Remove ice pack or wet compress, wait
compress is on the forehead. 2 minutes, and re-take temperature.
Complete diaphoresis includes
diaphoresis of area behind the ear and
Abnormally low
suggests that the temperature is rapidly
temperature
Measuring a completely diaphoretic dropping. Use an alternative method of
patient. temperature measurement in these
cases until the patient is dry and the
temporal artery measurement can be
repeated.
Scan straight across forehead. The
Improperly scanning down the side
temporal artery is closest to skin in that
of the face.
area.
Confirm measurement site has not
recently been in contact with heat
Anything covering the area to be
insulators such as hats, blankets, and
Abnormally high measured would insulate and
hair. Scan the area not covered or wait
temperature prevent heat from dissipating,
about 30 seconds for the previously
resulting in false high readings.
covered area to equilibrate to the
environment.
Setting Exergen Temp scanner unit 1 Insert a pointed object (e.g., the end of
straightened paperclip) into the hole on the right
NOTE rear of the temp scanner (looking at the back of
the temp scanner).
If the monitor and Exergen Temp scanner units are
each set to a different unit (e.g., one °F and the 2 Pushing in and release the battery
other °C), the monitor will automatically switch to compartment access door.
the Temp units set in the Exergen Temp scanner, 3 Remove the battery compartment access door
once a valid temperature measurement has been from the temp scanner.
completed.
4 Remove the 9 V battery from the temp scanner
Follow this procedure to change the temp scanner battery compartment - There is no need to
Temp LED display units: disconnect the battery from the temp scanner.
5 Locate the F/C switch, and slide to desired
display temp units: °C or °F (marked on the
switch).

Monitoring TEMP
6 Reinstall the 9 V battery back into the temp 7 Reinstall the battery compartment access door.
scanner battery compartment.
Pinhole (on side)

Battery & Harness
F/C Switch
F/C Switch
Replacing Exergen Temp scanner’s 4 Remove the 9 V battery from the battery
battery compartment of the temp scanner.
5 Disconnect the battery from the battery
When the Exergen temp scanner battery fails to harness.
hold a charge it will need to be replaced or if the
Exergen temp scanner will not be used regularly, CAUTION
remove the battery to prevent possible damage due If the battery leaks, remove it carefully. Do not
to chemical leakage. allow bare skin to touch leaking fluids.
Follow this procedure to remove/replace the
battery: CAUTION
1 Insert a pointed object (e.g., the end of Properly dispose of used batteries. Do not wrap
straightened paperclip) into the hole on the right them in metal or aluminum foil. Wrap them in
rear of the temp scanner (looking at the back of paper before disposing of them, batteries may
the temp scanner). explode if overheated.
2 Pushing in and release the plastic battery 6 Connect a new 9 V battery to the battery
compartment door. harness, noting the proper polarity of the 9 V
3 Remove the plastic battery compartment door battery pins.
from the temp scanner. 7 Install a new 9 V battery into the temp scanner
battery compartment.

Monitoring TEMP
8 Position the battery compartment door over the 9 Gently push down on the compartment door
battery compartment by aligning the tabs with until the door is fully seated into the temp
the slots at the bottom of the battery scanner’s recess. A click should be heard when
compartment. the latch is engaged.
NOTE
Use only high quality alkaline batteries in the
Exergen temp scanner.
Quick TEMP with F3000 module
Introduction WARNING
Use probe covers supplied by the
The monitor with the F3000 module measures
manufacturer with this thermometer only. Use
patient temperatures by oral, axillary or rectal
of any other probe cover will result in
means.
erroneous temperature readings.
The monitor can only measure temperature of adult
and pediatric patients. If the user measure WARNING
temperature of neonate patient, the monitor will not The thermometer and probe covers are Non-
display data. sterile. Do not use on abraded tissue.
The electromagnetic compatibility of this device
has been verified by test according to the WARNING
EN60601-1-2: 2015 requirements. To limit cross contamination, use Blue
devices for Oral and Axillary temperature
WARNING
taking only.
Do not use this device near flammable
anesthetics. Not suitable for use in the
WARNING
presence of flammable anesthetic mixture
with air, oxygen or nitrous oxide. Use RED devices only for RECTAL
temperatures.
WARNING
WARNING
Do not use this thermometer without first
installing a new probe cover. Thoroughly dry all electrical contacts on both
probe and thermometer after washing, or
device may fail to function properly.
WARNING
Do not reuse the disposable probe covers.
WARNING
For re-calibration, service or integrity checks,
refer to a qualified Biomedical Technician or
return to the manufacturer.

Monitoring TEMP
WARNING NOTE
Do not open the F3000 module. No user- Even though this device has been designed to
serviceable parts inside. Opening of the minimize the effects of electromagnetic
module may affect calibration and voids interference, it does generate radio frequency
warranty. energy. If not used in accordance with the
instructions, the device could cause interference in
WARNING other equipment operating within its vicinity. If the
device is causing interference, the following
Disposal of used probe covers must be
actions may be taken in an attempt to correct the
performed in accordance with current medical
interference:
practices or local regulations regarding
disposal of infectious, biological medical  Re-orient or re-locate the receiving device.
waste.
 Increase the separation between the devices.
WARNING  Consult a customer service representative.

Cleaning frequency and practices must be
consistent with institutional policy for NOTE
cleaning of non-sterile devices. Verification of the temperature module is
necessary as frequently as dictated by the Hospital
Procedures Policy. When the user needs to
WARNING
calibrate the temperature measurement, contact
The F3000 module is not intended for neonatal
the manufacturer.
patients.
NOTE
WARNING
The reference body site temperature is the same
In monitoring mode of TEMP module, no as the temperature of the measuring site.
physiological alarms are available.
NOTE
WARNING The cumulative use time for the oral or rectal
Verification of the temperature module is temperature probe in a single patient should be
necessary as frequently as dictated by the less than 24 hours.
Hospital Procedures Policy. When the user
needs to calibrate the temperature
measurement, contact the manufacturer. Probe covers —applying & removing
1 Open probe cover box by lifting tab at top corner

and pulling to remove top panel.
2 Insert box of probe covers into top of isolation
chamber.
NOTE
To aid infection control, never switch boxes
between blue and red isolation chambers. Also,
never switch probes between blue and red
isolation chambers. Keep similar colors together.

Monitoring TEMP
3 Remove probe from the probe well. This 6 To change probes, remove the isolation
automatically turns on the thermometer. chamber as described previously.
4 To help remind the user to apply or remove a 7 Grasp the sides of the L-shaped connector
probe cover, a probe icon with flashing probe piece with one hand and then using other hand
cover will be displayed when the probe is pull backward on the latch holding the end of
withdrawn from the probe well and following a the L-shaped connector.
completed temperature measurement.
8 Once free of the latch, slide the L-shaped
5 Insert the probe end into a cover in the box. connector out of isolation chamber.
Push the handle firmly until the cover snaps into
9 To replace, properly align the top of the L-
place.
shaped connector to the slot on the back of the
6 Take appropriate temperature measurement isolation chamber.
(oral, axillary or rectal).
10 Then slide the connector up into the slot
7 Eject the used cover into bio-waste container by pressing firmly on the bottom of the connector
pressing top button. until it “clicks” into place.
8 Remove, discard and replace box when empty.
Measuring mode
Changing isolation chambers and
probes Predictive Mode
When MEASURE MODE is set to PREDICT, the
NOTE monitor operates in Predictive Mode to provide fast
For aiding in infection control, use only the Blue and accurate temperature measurements.
probe and Blue isolation chamber for Oral and
Axillary temperature taking. The Red probe and Quick Predictive Mode
Red isolation chamber must only be used for rectal
temperature taking. When MEASURE MODE is set to QUICK
PREDICT, the monitor operates in Quick Predictive
NOTE Mode which is an oral predictive measurement
mode intended for situations where fast
Do not attach a Red probe to a Blue isolation
temperature measurements are desired.
chamber or vice-versa.
Quick Predictive Mode allows clinicians to rapidly
1 To remove or replace any isolation identify patients with “normal” body temperatures. If
chamber/probe assembly, grasp the isolation the patient temperature is outside of the “normal”
chamber from each side as shown. range, the monitor will automatically switch into its
2 Squeeze inward releasing the snaps and slide standard predictive mode to provide a more
the isolation chamber up to pull off. accurate reading.
3 To replace, align probe well finger with opening Quick Predictive Mode is not available when in Low
in the top of the unit. Temp. Mode.
4 Slide the isolation chamber down until the side

snaps “click” into place.
5 The probe is connected to the thermometer
automatically.

Monitoring TEMP
Monitoring Mode NOTE

When MEASURE MODE is set to MONITOR, the Accurate body temperature readings can only be
monitor will perform continual temperature obtained in one of these two “heat pocket”
measurement for a maximum of 10 minutes. Only locations as shown. Temperatures taken in other
measure mode ‘MONITOR’ can be displayed in mouth locations will result in inaccurate body
TEMP parameter area. temperature readings.
Besides, in the following instances, the monitor will
automatically switch to Monitoring Mode and
perform temperature measurement for a maximum
of 5 minutes until the temperature stabilizes:
1 When the monitor operates in Predictive Mode,
no measurement site is detected or the
temperature does not stabilize.
2 When the monitor operates in Predictive Mode
or Quick Predictive Mode, the ambient
temperature shall be greater than 35 °C (95 °F).
Low Temp. Mode

4 Patient’s mouth must be CLOSED.
Low Temp. Mode is provided for use in applications
where body temperatures may be lower than 5 Securely hold the probe in place until the
“normal”, such as for patients recently out of temperature is displayed.
surgery.
6 For Axillary temperatures, have the patient
The accuracy and measurement time of Low Temp. raise the arm, then place the probe tip in the
Mode measurements are equivalent to standard axilla. Press gently to assure good contact. For
prediction measurements at the respective body the most accurate temperature the probe tip
sites. should be placed directly against the patient’s
skin.
7 Have the patient then lower the arm and remain
Measuring procedure as still as possible. Hold the probe parallel to the
arm as shown.
Oral and Axillary Temperature Taking
1 Make certain that the Blue isolation
chamber/probe unit is attached.
2 Withdraw probe and apply a probe cover. The
thermometer turns on automatically and a beep
will be heard when the probe completes warm-
up.
3 For Oral temperatures, insert the probe tip deep
into the sublingual pocket next to the frenulum
linguae, (vertical fold of tissue in middle of
tongue), on one side or the other, toward the
back of the mouth.

Monitoring TEMP
8 If three short beeps are heard, it means the unit TEMP setup for F3000 module
switched to Monitoring Mode for this
temperature only. In TEMP SETUP interface, the following settings
9 Two beeps are sounded when measurement is are available:
complete and the final temperature is displayed. MEASURE MODE: Set the measuring mode to
10 Eject the used cover into a bio-waste container PREDICT, QUICK PREDICT or MONITOR.
by pushing top button. MEASURE POS: Set the measuring position to
ORAL, AXILLARY or RECTAL.
Rectal Temperature Taking Low Temp. Mode: Activate /deactivate the Low
1 Make certain that the Red isolation Temp. Mode by setting it to On/Off.
chamber/probe unit is attached.
NOTE
2 Withdraw the probe and apply a probe cover. The QUICK PREDICT mode is for oral
Thermometer turns on automatically a beep will measurement only.
be heard when the probe completes warm-up.
3 Apply lubrication if desired. NOTE
Low Temp. Mode can be set to On only when
4 Insert the probe into the patient’s rectum. To
measure mode is PREDICT.
ensure proper tissue contact, angle the probe
slightly after insertion.
NOTE
5 Depth of insertion is recommended at 1/2” to Make sure all settings of TEMP Setup are properly
3/4” (12 mm ~ 19 mm) for adults and 1/4” to 1/2” set up every time before the user withdraws the
(6 mm ~ 13 mm) for children. probe from the probe well. If the user modifies the
6 If three short beeps are heard, it means the unit settings immediately a measurement is
switched to Monitoring Mode for this completed, the new settings will be effective for the
temperature only. next measurement.
7 Two beeps are sounded when measurement is
complete and the final temperature is displayed.
8 Eject the used cover into a bio-waste container
by pushing top button.
NOTE
Probe movement during a measurement can
affect the thermometer’s ability to measure the site
temperature and may lengthen the time required to
obtain a reading.
NOTE
If a beep is not heard 10 seconds after withdrawing
the probe from the probe well and starting
temperature measurement in Predictive Mode or
Quick Predictive Mode, check the physical
connection of the F3000 module.

Warning-Score system
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 134
Warning-Score interface . . . . . . . . . . . . . . . . 134
Warning-Score method . . . . . . . . . . . . . . . . . 135
Warning-Score criteria . . . . . . . . . . . . . . . . . . 135
Warning-Score result . . . . . . . . . . . . . . . . . . . 136
Warning-Score trend table. . . . . . . . . . . . . . . 137

Overview
Click User Maintain > EWSTYPE to turn on one of NOTE

the warning-score function.
MEWS, EWS and NEWS are not available in USA.
User can use warning-score system to get score
and sum up based on measurement value or input NOTE
value of each vital sign. Depending on the score The score results are for reference only and the
calculated, an action list with appropriate score significance must be determined by the
recommendations is displayed. Warning-score physician.
system includes EWS (Early Warning Score),
NEWS (National Early Warning Score System) and
MEWS (Modified Early Warning Score) system,
which are mutual excluded. That is, only one
system can be used at the same time. Contact the
Dräger service personnel for activation.
Warning-Score interface
The interface includes EWS, NEWS and MEWS NOTE

sub-interface.
Operations, including power-off, updating patient
To enter the interface: 1. By shortcut key. Click and entering standby or Demo mode, will stop
User Maintain > Shortcut to select Score. Then current warning-score, and also monitor will exit
click Score shortcut key to enter; 2. By menu. Click this function.
Menu > Score to enter.
To exit the interface: 1. By shortcut key. Click Score
shortcut key to exit; 2. By menu. Click X button on
the top right of the interface.
Before exiting interface, if selected Method is score
calculator, the monitor can exit not only this
interface, but also this function; if selected Method
is auto score, the monitor can only exit this interface
instead of this function.
The above rule is also applicable to the switchover
between sub-interface. (e.g., if selected Method is
auto score, sub-interface is switched over from
EWS to NEWS, however, EWS function is still
working.)

Warning-Score method
Warning-Score method includes score calculator NOTE

(default) and auto score. If score calculator is
If any of above information is not completely input,
selected, user needs to input HR/PR, TEMP, RR,
the monitor will prompt information: Incomplete
SYS, SpO2, Oxygen, Age and Consciousness
parameter input, unable to score.
manually, if auto score is selected, user needs to
input TEMP, RR, Oxygen, Consciousness and
Age manually (HR/PR, SYS, SpO2 value will be
obtained automatically), and then click Start. The
monitor will calculate and display score result.
Warning-Score criteria
In EWS interface, select Criteria to check score

criteria as following:
Value
3 2 1 0 1 2 3
HR (bpm) ≤40 41~50 51~100 101~110 111~129 ≥130
SYS (mmhg) ≤70 71~80 81~100 101~199 ≥200
RESP (rpm) ≤8 9~20 21~24 25~29 ≥30
TEMP (°C) ≤35 35.1~36.0 36.1~37.9 38~38.9 ≥39
SpO2 (%) <86 86~91 92~93 ≥94
Consciousness NC A V P U
In NEWS interface, select Criteria to check score

Value
3 2 1 0 1 2 3
RESP (rpm) ≤8 9~11 12~20 21~24 ≥25
SpO2 (%) ≤91 92~93 94~95 ≥96
TEMP (°C) ≤35.0 35.1~36.0 36.1~38.0 38.1~39.0 ≥39.1
SYS (mmHg) ≤90 91~100 101~110 111~219 ≥220
HR (bpm) ≤40 41~50 51~90 91~110 111~130 ≥131

Consciousness A V/P/U
Oxygen Yes No
In MEWS interface, select Criteria to check score

Value
3 2 1 0 1 2 3
HR (bpm) ≤40 41~50 51~100 101~110 111~129 ≥130
SYS (mmhg) ≤70 71~80 81~100 101~199 ≥200
RESP (rpm) <9 9~14 15~20 21~29 ≥30
TEMP (°C) <35.0 35.0~38.4 ≥38.5
Consciousness A V P U
Age <50 50~70 >70
The relationship between consciousness level and

its display result is as below:
Consciousness Displayed Result

Sober A
Responsive to Voice V
Responsive to Pain P
Unresponsive U
Warning-Score result
Warning-Score results include parameter value,

score value, time and severity level. The relation for
value and severity level is as following:
EWS Severity Level Color Warning-score Remindings

Keep close to the condition of patient’s life
EWS=0~2 / Off-white
signs.
Inform medical personnel that observing and
EWS=3 Low Green checking should be taken every 1 hr. Or call the
doctor to give appropriate actions if necessary.

EWS Severity Level Color Warning-score Remindings

Inform medical personnel that observing and
checking should be taken every 20 mins~1 hr.
EWS=4~5 Medium Amber
Or call the doctor to give appropriate actions if
necessary.
Inform medical personnel and emergency team
that consultation should be taken every
EWS≥6 High Red
10 mins, keep close to blood gas condition, and
start emergency plan.
NEWS Severity Level Color Warning-score Remindings

Observing and checking should be taken every
NEWS=0 / Off-white 12 hrs at least, and keep close to the condition
of patient’s life signs.
Observing and checking should be taken every
NEWS=1~4 Low Green 4 hrs~6 hrs at least. Or increase monitoring
frequency or nurse-care level, if necessary.
NEWS=5~6
One single Observing and checking should be taken every
parameter’s Medium Amber 1 hr at least. Or call the doctor to give
score appropriate actions if necessary.
value=3
points
NEWS Severity Level Color Warning-score Remindings

For stable life signs and no life danger, normal
MEWS<5 Non-urgent Off-white
handling is recommended.
Keep close to the condition of patient’s life
MEWS=5 Observing Green
signs, and appropriate treatment can be taken.
The condition is urgent and may be worse.
5<MEWS≤9 Warning Amber
Keep close observing and give treatment timely.
The condition is bad. Urgent rescue and
MEWS>9 Critical Red
treatment are recommended.
Warning-Score trend table
Trend table provides the monitored patient’s scores in Warning-Score interface. EWS, NEWS and
during a period of time; it includes score time, score MEWS can respectively support 1200 groups of
parameters and value, EWS/NEWS/MEWS score. trend review at least.
To check the trend table, click Trend Table button


Storing data in the storage device
Setting Storage Mode (For Monitoring

Mode Only) . . . . . . . . . . . . . . . . . . . . . . . . . . . 140
Selecting a storage device . . . . . . . . . . . . . . 140
Reviewing data stored in the

storage device . . . . . . . . . . . . . . . . . . . . . . . . 141
Deleting data stored in the storage

device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 141
Exporting data stored in the internal

storage device . . . . . . . . . . . . . . . . . . . . . . . . 141
Ejecting a removable device . . . . . . . . . . . . . 142
Recording data by recorder. . . . . . . . . . . . . . 142
Formatting the internal storage

device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 142

Setting Storage Mode (For Monitoring Mode Only)
NOTE When data reach the maximum, the user can

choose to Keep Storing (default) or Stop Storing
The storage time varies according to the patient's
by selecting Menu > System Setup > Storage > if
parameter data volume. When store time for single
storage space is full.
patient data reaches 240 hours, the monitor will
create a new folder for continuous data store. If Keep Storing is selected, as soon as the data is
full, the earliest data will be replaced by the latest
Refer to Section Data management for more one.
information about data volume in each work mode.
If Stop Storing is selected, the monitor will stop
data storing and the latest data cannot be stored
when the data reach the maximum.
Selecting a storage device
To configure the storage device, select Menu > After configuring the appropriate storage device,
System Setup > Storage > Storage Device, and click exit. If the storage device is successfully
choose the storage medium from the pop-up list as starting data storing, the monitor will be indicated
desired.
by the symbol . If there is no enough space in
In ward round or spot-checking mode, Storage storage device, or the storage device is read-
Device is fixed as Internal Storage Device.
only/damaged, the symbol will be displayed.
NOTE
In ward round or spot-checking mode, if storage The monitor will stop storing data in the storage
space of the system is <200 M, a prompt will be device under the following circumstances:
given out. In order to store data normally, please  There is no enough space in the storage device
clean the space in time. for storing data.
In monitoring mode, Internal Storage Device  The removable device is read-only.

(default) and Removable Device can be selected.  The monitor is switched off.
If Removable Device is selected, the user can
perform data storage after inputting User Maintain  The power supply is off.
password.
CAUTION
When Internal Storage Device is selected as the
Not all the removable devices are compatible with
storage medium, if configured, the storage device
the monitor, Use the removable devices
name will automatically become Internal Storage
recommended by Dräger.
Device. The user can select a removable device as
a working one among the plugging devices by
selecting Menu > System Setup > Storage > CAUTION
Storage Device and choosing the device name Do not set the read-only switch on the removable
from the list. device to on when the removable device is
inserted in the monitor.

CAUTION
It is recommended to format the USB flash drive
to the FAT file type via PC prior to use.
Reviewing data stored in the storage device
In monitoring mode: If Internal Storage Device is selected, clicking

Export all data can export all patients’ data.
To review data stored in the storage device, select
Choosing one patient’s data in history patient list,
Menu > Review > History Patient. The user can
and clicking Export Current Data can export this
choose to review the storage device as desired
patient’s data.
from the pop-up list. Choose a patient from the list
to review the data including patient information, In ward round or spot-checking mode:
trend graph, trend table, NIBP measurements,
Refer to chapter Ward round record review or Spot-
alarm event and waveform.
checking data review for data review.
Deleting data stored in the storage device
CAUTION To delete data of all patients, select Menu >

Review > History Patient and click Delete all data
When the lifecycle of the device ends, delete all
on the History Patient Review menu. Further
patient information before disposal of the device.
confirmation is required.
In monitoring mode: In ward round or spot-checking mode:
To delete data of one patient, choose the patient Refer to chapter Ward round record review or Spot-
from the list after selecting Menu > Review > checking data review for data review.
History Patient, and then click Delete data on the
Review menu. Further confirmation of deletion is
required.
Exporting data stored in the internal storage device
 In monitoring mode, to export data of one Choose the patient from the list after selecting
patient from the internal storage device to the Menu > Review > History Patient, click Export
removable device: Data on the Review menu, and then input User
Maintain password.

To export data of all patients, select Menu >  In ward round or spot-checking mode, User
Review > History Patient, click Export all data, Maintain password is necessary for exporting
and then input User Maintain password. ward round records/spot-checking data in the
specified time to the removable device , and
NOTE also to the internal storage device. If no
In monitoring mode, the data in internal storage removable device is used, the data will be
device is not encrypted. Protect privacy exported to internal storage device directly.
information.
Choose Menu > Review > Export, and confirm the
operation as needed.
In ward round and spot-checking mode, the formats
of exported CSV data file names are ‘XXX- Round-
Records’ and ‘XXX-Spot-Review.csv’ respectively,
in which the XXX means export time.
Ejecting a removable device
Before unplugging a removable device from the CAUTION

monitor, the user needs to select Menu > System
Do not remove the removable device without
Setup > Storage > Removable Device and click
ejecting it during data storing, or the removable
Eject to uninstall the removable device. In this
device might be damaged.
menu, the user can also check the remaining
capacity of the storage device.
Recording data by recorder
In monitoring mode: The data to be recorded include: trend graph, trend

table, NIBP review and alarm review.
To recording the review data, enter Menu >
Review > History Patient > choose one patient In ward round or spot-checking mode:
data in history patient interface > Review > choose
Refer to chapter Ward round record review or Spot-
the desired data to review > Record.
checking data review for data review.
Formatting the internal storage device
To format the internal storage device, select Menu NOTE

> User Maintain > Common > Format internal
As soon as the internal storage device is
storage device. Further confirmation is required.
formatted, all the data will be cleared.

NOTE
No need to restart the monitor after formatting is
successful. The internal storage device can be
identified and loaded automatically.
NOTE
If formatting is failed, try again. Restart the monitor
and retry the formatting, or contact the service
personnel of the manufacturer if formatting is failed
repeatedly.


Recording
Recording
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 146
Performance of the recorder . . . . . . . . . . . . . 146
Starting and stopping recording . . . . . . . . . . 146
Recorder operations and status messages . 148

Record paper requirement . . . . . . . . . . . . . . . . 148
Proper operation. . . . . . . . . . . . . . . . . . . . . . . . 148
Paper out . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 148
Replacing paper . . . . . . . . . . . . . . . . . . . . . . . . 148
Removing paper jam . . . . . . . . . . . . . . . . . . . . 148

Recording
Overview
A thermal dot matrix recorder is used for the

monitor and can support a number of recording
types and output patient information, measurement
data, review data waveform and so forth.
Performance of the recorder
 Waveform record is printed at the rate of  Auto recording interval is set by the user and
12.5 mm/s, 25 mm/s or 50 mm/s; default setting the waveform displays in real time.
is 25 mm/s.
NOTE
 49 mm ~ 50 mm wide printout paper.
Do not use the strip recorder with a low battery as
 Record one SpO2 waveform; default setting is recorder usage will more quickly deplete the
off. battery.
 User-selectable real-time recording time and
waveform.
Starting and stopping recording
The monitor provides several types of stripe

recording. The strip recording can be started and
stopped in the following ways:
Recording Type Description/ Procedure

Continual real-time In monitoring mode, enter Menu > System Setup > Recorder, select
recording Continual in R-T Rec Time, and press Record shortcut key to start or stop
recording.
8-second real-time In monitoring mode, select 8 s in R-T Rec Time, set Record Interval as
recording needed, and press Record shortcut key to start recording. Press the key
again to stop recording or when R-T Rec time ends, the monitor stops
recording automatically. The runtime for each wave is 8 seconds. The record
Interval can be set as: Off, 10 min, 20 min, 30 min, 40 min, 50 min, 1 h, 2 h,
3 h, 4 h.

Recording
Recording Type Description/ Procedure

Trend graph recording In monitoring mode, select Menu > Review > Trend Graph, click Record in
trend graph interface to start recording. Press Record shortcut key to stop the
recording.
NOTE:
When the trend graph is recorded in the monitoring mode and if the Record
shortcut key is pressed manually to stop the recording in the process of
recording the second parameter trend graph, the record paper will not be left
blank after the second parameter trend graph.
Trend table recording In monitoring mode, select Menu > Review > Trend Table, click Record in
trend table interface to start recording. Press Record shortcut key to stop the
recording.
NIBP review recording In monitoring mode, select Menu > Review > NIBP, click Record in NIBP
review interface to start recording. Press Record shortcut key to stop the
recording.
Alarm review In monitoring mode, select Menu > Review > Alarm, select one alarm and
recording click Record in alarm review interface to start recording. Press Record
shortcut key to stop the recording.
Recording manually In spot-checking mode, press Record shortcut key in main interface to output
current measurement value and patient information;
In spot-checking or ward round mode, click Record or press Record shortcut
key in Review interface to output corresponding spot-checking data or ward
round record.
Pressing Record shortcut key again can stop recording.
NIBP auto triggered In monitoring mode, support NIBP auto triggered recording. Refer to NIBP
recording Auto recording for details.
To manually stop recording, click Record again in

the related interfaces.
The recorder will stop recording in the following
situations:
 The recording task is finished.
 No paper in the recorder.
 Malfunction stops the recorder from running
properly.
NOTE
The Record shortcut key enables users to
manually start or stop recording.

Recording
Recorder operations and status messages
Record paper requirement Removing paper jam
CAUTION When the strip recorder malfunctions, open the

strip recorder door to check for a paper jam.
Only use standard thermo-sensitive record paper.
Remove the paper jam in the following way:
If non-standard record paper is used, the recorder
might not function, the recording quality may be  Cut the record paper from the feeding edge.
poor, and the thermo-sensitive printhead could be
 Open the strip recorder door.
damaged.
 Re-install the paper.
NOTE
Proper operation
If the monitor is not configured with the recorder
 When the strip recorder is operating, do not pull function, it will indicate Recorder Setup Needed
the paper. after the Record button is pressed.
 Do not operate the strip recorder without record NOTE

paper.
Do not touch the thermo-sensitive print head when
performing continuous recording.
Paper out
When the Recorder Out Of Paper alarm is

displayed, the strip recorder will not start.
Replacing paper
1 Pull outwards the upper arc part of the strip

recorder casing to release the casing.
2 Insert a new roll of paper into the paper
cassette, printing side facing upwards.
3 Position the paper correctly.
4 Pull 2 cm of paper out and close the strip
recorder casing.
NOTE
Be careful when inserting papers. Avoid damaging
the thermo-sensitive print head. Do not leave the
strip recorder door open except to insert paper or
troubleshoot printing problems.

Using battery
Using battery
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 150
Battery safety information . . . . . . . . . . . . . . . 150
Battery power indicator . . . . . . . . . . . . . . . . . 151
Battery status on the main screen . . . . . . . . 151
Checking battery performance . . . . . . . . . . . 152
Replacing the battery . . . . . . . . . . . . . . . . . . . 152
Recycling the battery . . . . . . . . . . . . . . . . . . . 153
Maintaining the battery . . . . . . . . . . . . . . . . . 153

Using battery
Overview
This monitor can run on battery power, which

ensures its uninterrupted operation even when AC
power supply is interrupted. The battery recharges
whenever the monitor is connected to the AC
power source. During monitoring, if the AC power is
interrupted, the monitor will take power from the
internal battery. If the monitor is powered by battery,
the monitor will switch off automatically before the
battery is completely depleted.
Battery safety information
WARNING WARNING
Before using the rechargeable lithium-ion Do not unplug the battery when working is in
battery (hereinafter called battery), be sure to process.
read the user manual and safety precautions
thoroughly. WARNING
Do not heat or throw the battery into a fire.
WARNING
The service life of the battery depends on the WARNING
service frequency and time. The service life of
Do not use, leave the battery close to fire or
the battery is about three years if the battery is
other places where temperature may be above
well maintained and stored. The service life of
60 °C.
the battery may shorten if it is used
inappropriately. If the battery life is exhausted
and not replaced in time, it may cause damage WARNING
or heat to the device. Do not immerse, throw, or wet the battery in
water/seawater.
WARNING
Periodic checks on the battery performance WARNING
are required. Change the battery if necessary. Do not destroy the battery: do not pierce the
battery with a sharp object such as a needle;
WARNING do not hit with a hammer, step on or throw or
drop to cause strong shock; do not
Do not connect the positive (+) and negative (-)
disassemble or modify the battery.
terminals with metal objects, and do not put the
battery together with metal objects, which can
result in short circuits. WARNING
The recommended battery can only be used
for this monitor. Do not solder the leading wire
and the battery terminal directly.

Using battery
WARNING WARNING
If liquid leaking from the battery gets into the Do not use a battery with serious scratch or
eyes, do not rub the eyes. Wash them well with deformation.
clean water and go to see a doctor
immediately. If liquid leaks of the battery WARNING
splash onto the skin or clothes, wash well with
When the monitor is running on battery power,
fresh water immediately.
do not replace the battery during monitoring
patients; or the monitor will be powered off,
WARNING which may result in patient injury.
Keep away from fire immediately when
leakage or foul odor is detected. WARNING
Do not place battery in the monitor with the (+)
WARNING and (-) in the wrong way.
Stop using the battery if abnormal heat, odor,
discoloration, deformation or abnormal WARNING
condition is detected during use, charge, or
Due to high ambient temperature, the monitor
storage. Keep it away from the monitor.
gives out Battery Error alarm. To protect the
battery from damage, take battery out for
cooling and then charge.
Battery power indicator
The indicator labeled Battery on the front panel of

the monitor illuminates in green when the monitor is
battery powered and illuminates in yellow when
battery is being charged. The indicator is not
illuminated when the monitor is not powered or
when AC power is applied.
Battery status on the main screen
Battery status symbols show the status of each

Remaining battery power: 75%.
battery detected and the combined battery power
remaining.

Remaining battery power: 25%

Using battery
Batteries are almost depleted and

need to recharge immediately.
No battery is installed.
Battery Error
Checking battery performance
The performance of rechargeable batteries may 3 Disconnect monitor from mains power and let
deteriorate over time. Battery maintenance as the monitor run until there is no battery power
recommended here can help to slow down this left and the monitor shuts off.
process.
4 The running time of the battery reflects the
1 Disconnect the patient from the monitor and battery performance.
stop all monitoring and measurement.
If the running time is obviously less than the
2 Switch the monitor power on and charge the specified time in the specification, change the
battery for more than 6 hours continuously. battery or contact the service personnel.
Replacing the battery
To install or replace the battery, follow the 3 Insert the new battery into the battery
procedure: compartment.
4 Close battery latch.
1 Pull the battery latch according to the arrow

direction in the figure.
2 Take battery out.

Using battery
Recycling the battery
When the battery no longer holds a charge, it WARNING

should be replaced. Remove the old battery from
Do not disassemble batteries, put them into
the monitor and recycle it properly.
fire or cause them to short circuit. They may
ignite, explode or leak, causing personal
injury.
Maintaining the battery
Batteries should be conditioned regularly to

maintain their useful life.
Remove the batteries from the monitor if they are
not used for a longer period of time. And recharge
the batteries at a minimum of every 6 months when
they are stored.
Discharge the battery completely once every
month.


Reprocessing
Reprocessing
Safety instructions . . . . . . . . . . . . . . . . . . . . . 156
General points . . . . . . . . . . . . . . . . . . . . . . . . 156
Safety information . . . . . . . . . . . . . . . . . . . . . 156
Information on reprocessing. . . . . . . . . . . . . 157
Classifications for reprocessing. . . . . . . . . . 157

Classification of medical devices . . . . . . . . . . . 157
Classification Explanation. . . . . . . . . . . . . . . . . 157
Classification of device-specific components . . 157
Patient-specific accessories and

consumables. . . . . . . . . . . . . . . . . . . . . . . . . . 158
Reusable products:. . . . . . . . . . . . . . . . . . . . . . 158
Disposable products: . . . . . . . . . . . . . . . . . . . . 158
Classification of device-specific
components . . . . . . . . . . . . . . . . . . . . . . . . . . . 158
Before Reprocessing . . . . . . . . . . . . . . . . . . . 158
Validated reprocessing procedures . . . . . . . 159

Surface disinfection with cleaning . . . . . . . . . . 159
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 159
Surface Disinfection . . . . . . . . . . . . . . . . . . . . . 159
Additional Information. . . . . . . . . . . . . . . . . . . . 159
Storage and transport . . . . . . . . . . . . . . . . . . 159
Reprocessing of patient-specific
accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . 160
Categorization of accessories . . . . . . . . . . . . . 160
Reprocessing of the category "[1] SpO2
Sensors", "[2] NIBP Cuffs" . . . . . . . . . . . . . . . . 160
Storage and transport . . . . . . . . . . . . . . . . . . . . 161
Other agents and reprocessing procedures . . . 161
After Reprocessing . . . . . . . . . . . . . . . . . . . . 161

Reprocessing
Safety instructions
Reusable products  Check the products for signs of wear and

replace them if necessary.
Reusable products must be reprocessed,
otherwise there is an increased risk of infection. Disposable products
 Follow the infection prevention policies and Disposable products have been designed, tested,
reprocessing regulations of the health-care and manufactured exclusively for single use.
facility. Reuse, reprocessing, or sterilization can result in
failure of the accessory, incorrect measurements,
 Follow the national infection prevention policies
and injury to the patient.
and reprocessing regulations.
 Do not reuse disposable products.
 Use validated procedures for reprocessing.
 Do not reprocess disposable products.
 Reprocess reusable products after every use.
 Do not use any disinfectants.
 Follow the manufacturer's instructions for
cleaning agents, disinfectants, and
reprocessing devices. Signs of wear, e.g.,
cracks, deformation, discoloration, or peeling,
may occur with reprocessed products.
General points
Keep the monitor, cables and accessories free of  Unless otherwise specified, do not immerse any
dust and dirt. To prevent the device from damage, part of the equipment or any accessories in
follow the procedure: liquid.
 Use only recommended cleaning substances  Do not pour liquid onto the system.
and disinfectants listed in this manual. Others
 Do not allow liquid to enter the case.
may cause damage (not covered by warranty),
reduce product lifetime or cause safety  Never use abrasive material (such as steel wool
hazards. or silver polish).
 Always dilute according to the manufacturer’s  Inspect the monitor and reusable accessories
instructions. after they are cleaned and disinfected.
Safety information
CAUTION Signs of wear, e.g., cracks, deformation,

discoloration, or peeling, may occur with
Risk due to faulty products
reprocessed products.

Reprocessing
 Check the products for signs of wear and  If the user spills liquid on the equipment,
replace them if necessary. battery, or accessories, or they are accidentally
immersed in liquid, contact the service
personnel or Dräger service engineer.
Information on reprocessing
Follow the national infection prevention policies Follow the infection prevention policies and
and reprocessing regulations. reprocessing regulations of the healthcare facility
(e.g., concerning the reprocessing cycles).
Classifications for reprocessing
Classification of medical devices
The classification depends on the intended use of

the medical device. The risk of infection
transmission through the application of the product
to the patient without proper reprocessing is the
basis of the Spaulding classification.
Classification Explanation
Classification Explanation
Non-critical Components that come into contact only with skin that is intact
Semi-critical Components that carry breathing gas or come into contact with mucous
membranes or pathologically altered skin
Critical Components that penetrate skin or mucous membranes or come into contact with
blood
Classification of device-specific Non-critical

components – Device surface
The following classification is a recommendation – Screen

from Dräger.

Reprocessing
Patient-specific accessories and consumables
The patient-specific accessories and consumables Disposable products:

must be removed from the monitor and, if
necessary, disassembled.  Dispose of the disposable products.
Reusable products: Classification of device-specific

components
 If the reusable product has its own instructions
for use, perform reprocessing in accordance The following classification is a recommendation
with the separate instructions for use. Further from Dräger.
information can be found in the list of
accessories. Non-critical
 If no separate instructions for use are available – NIBP Cuff

for the reusable product, perform reprocessing – SpO2 Sensors
in accordance with the instructions in these
instructions for use (see "Reprocessing of – TEMP Sensors
patient-specific accessories").
Before Reprocessing
For device specific components, observe before

disassembly
1 Switch off the monitor.
2 Disconnect it from the power line.
For patient specific accessories and consumables
NIBP Cuffs
1 Remove NIBP Cuffs from the monitor.
2 Take out the air bladder.
SpO2 Sensors
1 Remove SpO2 sensors from the monitor.
Quick Temps
1 Remove quick temp module from the monitor.

Reprocessing
Validated reprocessing procedures
Surface disinfection with cleaning
Surface Disinfectant Manufacturer Concentration Contact Times

Ethanol* N/A 75% 3 minutes
Dismozon Plus BODE Chemie GmbH 1.6% 15 minutes
*Ethanol is not for Germany, Switzerland and Surface Disinfection

Austria.
Prerequisites: 1 Wipe cleaned surfaces again to visibly wet all
surfaces to be disinfected with surface
– The surface disinfectant has been prepared in disinfectant.
accordance with the manufacturer's instructions.
2 Wait for the surface disinfectant contact time.
– The manufacturer's instructions, e.g., regarding
shelf life or application conditions, are observed. 3 At the end of the contact time, moisten a new,
uncontaminated and lint-free cloth with water
– An uncontaminated, lint-free cloth soaked in (at least drinking water quality).
surface disinfectant is used for the cleaning surface
disinfection. 4 Wipe all surfaces until no remains of the surface
disinfectant, such as foam residues or streaks,
are visible.
Cleaning 5 Dry the monitor for at least 30 minutes in a
ventilated and cool place.
1 Wipe the entire exterior surface, including the
6 Check the surfaces for visible damage and, if
screen, of the equipment using a soft cloth
necessary, replace the product.
dampened with the cleaning solution.
2 Wipe thoroughly until no visible contaminants
remain. Additional Information
Regarding the reprocessing of Quick Temp Module

please refer to the respective IFU by Exergen.
Storage and transport
After reprocessing, there are no special – Avoid recontamination and damage during
requirements for storage and transport of the transport
product. However, the following must be observed:
All further information on storage and transport
– Store dry and free of dust included in the accompanying documents must be
observed.

Reprocessing
Reprocessing of patient-specific accessories
Categorization of accessories
Category Classification Part Number Description of Procedure

1 SpO2 Sensors Non-Critical 2606151, 2606152, see "Surface disinfection with
2606153, 2606154 cleaning"
2606155, 2606156
2 NIBP Cuffs Non-Critical 2606483, 2606484 see "Surface disinfection with
2606485, 2606486 cleaning"
2606487, 2607047
7262764
Reprocessing of the category "[1] SpO2

Sensors", "[2] NIBP Cuffs"
Surface disinfection with cleaning
Surface Disinfectant Manufacturer Concentration Contact Times

Ethanol TBD 75% 3 minutes
Dismozon Plus BODE Chemie GmbH 1.6% 15 minutes
Prerequisites: Surface Disinfection

– The surface disinfectant has been prepared in 1 Wipe cleaned SpO2 sensors, NIBP Cuff and air
accordance with the manufacturer's instructions. bladder again to visibly wet all surfaces to be
disinfected with surface disinfectant.
– The manufacturer's instructions, e.g., regarding
shelf life or application conditions, are observed. 2 Wait for the surface disinfectant contact time.
– An uncontaminated, lint-free cloth soaked in 3 At the end of the contact time, moisten a new,
surface disinfectant is used for the cleaning surface uncontaminated and lint-free cloth with water
disinfection. (at least drinking water quality).
Cleaning 4 Wipe all accessories until no remains of the
surface disinfectant, such as foam residues or
1 Wipe the SpO2 sensors, NIBP cuff and the air
streaks, are visible.
bladder with a soft cloth dampened with the
disinfectant solution. 5 Dry the accessories for at least 30 minutes in a
ventilated and cool place.
2 Wipe thoroughly until no visible contaminants
remain.

Reprocessing
Storage and transport Other agents and reprocessing

procedures
After reprocessing, there are no special
requirements for storage and transport of the Disinfections
product. However, the following must be observed:
Use nationally approved disinfectants suitable for
– Store dry and free of dust the respective reprocessing process and the
– Avoid recontamination and damage during intended application.
transport Surface disinfectants
All further information on storage and transport The manufacturers of the surface disinfectants
included in the accompanying documents must be have verified at least the following spectra of
observed. activity:
– Bactericidal
– Yeasticidal
– Virucidal or virucidal against enveloped viruses
Follow the manufacturer's instructions for surface
disinfectants
The following surface disinfectants were
compatible with the material at the time of testing:
Class of Active Surface Disinfectant Manufacturer Listing

Ingredient
Quaternary Cleanisept Wipes Maxi Dr. Schumacher GmbH CE
Ammonium Compounds
Dräger states that oxygen-releasing agents and Other surface disinfectants are used at one's own
chlorine-releasing agents may cause color change risk.
in some materials. Color change does not indicate
that the product is not functioning correctly.
After Reprocessing
Assembling and attaching device-specific Preparation before next use of device

components
Assembling and fitting patient-specific accessories
Prerequisite: and consumables, i.e. SpO2 sensors and NIBP
Cuffs.
– All components have been reprocessed and are
dry.


Maintenance
Maintenance
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 164
Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . 164
Repair . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 165

Maintenance
Overview
WARNING WARNING
Failure on the part of the responsible The maintenance operations such as software
institution to implement a satisfactory upgrade of the device shall only be conducted
maintenance schedule may cause undue by Dräger-qualified service professionals. The
equipment failure and possible health history data in monitor may be deleted due to
hazards. software upgrade. Before software upgrade,
backup the data in the monitor to avoid data
WARNING loss. For data backup methods, refer to the
section Exporting data stored in the internal
If the monitor is mechanically damaged, or if it
storage device to export the data, or refer to
is not working properly, do not use it. Contact
the section Uploading data to network server
technical personnel.
to load the data to HIS system.
WARNING WARNING
If the user finds any problems with the Any serious incident that has occurred in
equipment, contact service personnel or relation to the device should be reported to
authorized supplier. the manufacturer and the competent authority
of the Member State in which the user and/or
patient is established.
Inspection
The overall check of the monitor, including the  If all functions are in good conditions.
safety check, should be performed only by qualified
 If the grounding resistance and leakage current
personnel every 24 months, and each time after fix
meet requirement.
up.
If any damage or abnormality is found, don’t use the
The following items should be checked:
monitor and contact local Customer Service
 If the environment condition and power supply Center.
meet requirement.
Maintenance shall be carried out at least once
 If the power supply cord has damage and every two years, or as specified by local
insulativity meets requirement. regulations. The following tasks are for Dräger-
qualified service professionals only. Contact an
 If the device and accessories have damage.
Dräger-qualified service provider if the monitor
 Specified accessories. needs a safety or performance test. Clean and
disinfect equipment to decontaminate it before
 If the alarm system can work properly.
testing or maintaining it.
 If the recorder can work properly and the paper
meets the requirement.
 Battery performance

Maintenance
Maintenance and Test Schedule Frequency

Safety checks. Selected tests on At least once every two years, or as needed, after any repairs where
the basis of IEC60601-1 the power supply is removed or replaced, or if the monitor has been
dropped.
Check all monitoring functions and At least once every two years, or as needed.
measuring functions
Repair
Dräger recommends that all repairs are carried out

by Dräger Service and that only authentic Dräger
spare parts are used.


Disposal
Disposal
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 168

Disposal
Overview
CAUTION
The device and its components must be
disinfected and cleaned before disposal!
For countries subject to EU Directive

2002/96/EC:
This device is subject to EU directive 2002/96/EC
(WEEE). In order to comply with its registration
according to this directive, it may not be disposed
of at municipal collection points for waste electrical
and electronic equipment. Dräger has authorized a
company to collect and dispose of this device. To
initiate take-back or for further information, visit us
on the Internet at www.draeger.com and navigate
to the Dräger Service area where the user will find
a link to “WEEE”. If the user has no access to our
website, contact the local Dräger organization.

Accessories
Accessories
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 170
SpO2 accessories . . . . . . . . . . . . . . . . . . . . . . 170
NIBP accessories . . . . . . . . . . . . . . . . . . . . . . 171
TEMP accessories . . . . . . . . . . . . . . . . . . . . . 172
Other accessories . . . . . . . . . . . . . . . . . . . . . 173

Accessories
Overview
Accessories can be ordered from the local Dräger WARNING

representative.
Only use accessories that are approved by
WARNING Dräger. Using accessories that are not
approved by Dräger may compromise device
Never reuse disposable transducers, sensors
functionality and system performance and
or other accessories that are intended for
cause a potential hazard. It is not
single-use or single patient use only. Reuse
recommended to use accessories supplied by
may compromise device functionality and
Dräger with patient monitors by other
system performance and cause a potential
manufacturers.
hazard.
NOTE
Transducers and sensors have a limited shelf life.
Refer to the package labeling.
The following cables may not all be available in all

countries. Check availability with the local Dräger
supplier.
SpO2 accessories
Part Number Accessories

For Dräger Module
2606484 SpO2 Finger Sensor, adult, 1 m, reusable
2606485 SpO2 Silicone Soft-tip Sensor, adult, 1 m, reusable
2606486 SpO2 Silicone Soft-tip Sensor, pediatric, 1 m, reusable
2606487 SpO2 Extension cable, 2 m
2606483 SpO2 Finger Sensor, adult, 2.5 m, reusable
2607047 SpO2 Sensor, Ear Clip, Adult/Pediatric, 1 m, reusable
2606208 SHD-A SpO2 Sensor, adult, disposable
2606209 SHD-P SpO2 Sensor, pediatric, disposable
2606210 SHD-I SpO2 Sensor, Infant, disposable
2606211 SHD-N SpO2 Sensor, Neonate, disposable
For Dräger Module

Accessories

7262764 Nellcor Reusable Adult SpO2 Sensor (DS-100A OxiMax)
8201013 Nellcor Reusable Adult/Neonate SpO2 Sensor (OXI-A/N OxiMax)
MP00748 or Nellcor SpO2 Extension cable (Compatible with Nellcor OXI-Max SpO2 module
MS20979 and Nellcor sensor)
MX50070 Nellcor forehead sensor, Adult/Pediatric, >10 kg, MAX-FAST
2170221 OXIBAND-ADH.WRAP P/I (100 PCS)
MX01004 Nellcor multisite sensor, >1 kg, hand, D-YS
MX50065 or Nellcor sticking sensor, Adult, >30 kg, hand, MAX-A/MAX-AL
MX50071
MX50068 Nellcor sticking sensor, Neonatal/Adult < 3kg or >40 kg, foot, MAX-N
MX50067 Nellcor sticking sensor, Infant, 3 kg-20 kg, foot, MAX-I
MX50066 Nellcor sticking sensor, Pediatric, 10 kg-50 kg, hand, MAX-P
NIBP accessories

For Dräger Module
2606155 NIBP Cuff, Adult, 27 cm-35 cm, reusable
2606156 NIBP Cuff, Larger Adult, 34 cm-43 cm, reusable
2606153 NIBP Cuff, Child, 16 cm-21.5 cm, reusable
2606151 NIBP Cuff Infant, 10 cm-15 cm, reusable
2606152 NIBP Cuff, Small Child, 13 cm-17 cm, reusable
2606154 NIBP Cuff, Small Adult, 20.5 cm-28 cm, reusable
2601195 NIBP Tube 3 m
For SunTech Module
2607034 NIBP Cuff, neonatal #1, 3 cm-6 cm, disposable

Accessories

2600930 APC Cuff, Child (Green), range: 12 cm-19 cm
2600932 APC Cuff, Small Adult (Royal Blue), range: 17 cm-25 cm
2600933 APC Cuff, Adult (Navy Blue), range: 23 cm-33 cm
2600934 APC Cuff, Large Adult (Burgundy), range: 31 cm-40 cm
2600935 OPC Cuff, Child, range: 12 cm-19 cm
2600936 OPC Cuff, Small Adult, range: 17 cm-25 cm
2600937 OPC Cuff, Adult, range: 23 cm-33 cm
2600938 OPC Cuff, Large Adult, range: 31 cm-40 cm
TEMP accessories

TEMP (For TAT-5000S-RS232 Thermometer)
2600946 TAT-5000S-RS232-QR, Arterial, Deg C

2600947 TAT-5000S-RS232-QR to 740 SELECT monitor Interface cable
TAT-5000S-RS232-QR Resposable Probe Caps, latex free Box of 1000 -
2600948
20 sleeves of 50 each
TAT-5000S-RS232-QR Sheaths, Latex free, Complete covering for cross
2600949
contamination protection Box of 250
TEMP (For F3000 Module)
2600939 Filac 3000 Oral Probe 4ft

2600940 Filac 3000 Oral Probe 9ft
2600942 Filac 3000 Rectal Probe 4ft
2600943 Filac 3000 Rectal Probe 9ft
2600945 Filac 3000 Probe Covers
2600146 Covidien Quick Temp Pod Oral/Axi
2600147 Covidien Quick Temp Pod Rectal

Accessories
Other accessories

2606229 Rechargeable Lithium-Ion Battery/TWSLB-003
2607073 Unicode EPRT-48mm printer
2606231 Printing Paper 4 pcs
2606232 Ground Cable
2606234 Power Cord Europe
2606235 Power Cord North America
2606237 Power Cord Australia
2606238 Power Cord UK
2606239 Power Cord Argentina
2606240 Power cord Korea
2606241 Power cord Israel
2606242 Power Cord South Africa
2606243 Power Cord India
2606244 Power Cord Brazil
2600168 Vista 120 SC Roll Stand
2601380 Mounting Adaptor for GCX
MS27314 Ethernet patch cable 15 m
MS26956 Ethernet patch cable 5 m
MS26955 Ethernet patch cable 2.4 m
MS26957 Ethernet patch cable 1.5 m
NOTE
The part description may vary depending on
context, but the part number is constant.


Product specification
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 176
Classification . . . . . . . . . . . . . . . . . . . . . . . . . 176
Physical specifications . . . . . . . . . . . . . . . . . 176

Size and weight . . . . . . . . . . . . . . . . . . . . . . . . 176
Function configuration . . . . . . . . . . . . . . . . . . . 177
Environment specification. . . . . . . . . . . . . . . . . 177
Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 178
Battery specification . . . . . . . . . . . . . . . . . . . . . 178
Recorder. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 178
Data management. . . . . . . . . . . . . . . . . . . . . . 179

Data review. . . . . . . . . . . . . . . . . . . . . . . . . . . . 179
Data storage . . . . . . . . . . . . . . . . . . . . . . . . . . . 179
NIBP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 180
SpO2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 183
PR. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 185
TEMP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 185
Wi-Fi. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 187
e-link . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 188
Interfaces. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 188
Nurse Call. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 188
USB Interfaces . . . . . . . . . . . . . . . . . . . . . . . . . 188
Wired Network Interface . . . . . . . . . . . . . . . . . . 189

Overview
NOTE
The performance of the equipment with ☆ mark is
determined to be essential performance.
Classification
Anti-electroshock type Class I equipment and internal powered equipment
Anti-electroshock degree SpO2, NIBP, TEMP: BF
Ingress Protection IPX2

With TAT-5000S-RS232 Thermometer or F3000 TEMP module:
Ordinary equipment (Sealed equipment without liquid proof)
Disinfection/sterilization method Refer to Chapter Care and cleaning for details.
Working system Continuous operation equipment
Compliant with Standards IEC 60601-1: 2005+A1 :2012; IEC 60601-1-2: 2014;
EN 60601-1: 2006+A1 :2013; EN 60601-1-2: 2015;
IEC 60601-2-49: 2011
Physical specifications
Size and weight
Size 155 mm (W) × 250 mm (H) × 165 mm (D)
Weight < 3 kg (standard configuration, without accessories and battery)

Function configuration
Product Model Standard Configuration

 Dräger SpO2, Dräger NIBP
A
 Recorder, Wi-Fi, touch screen
 Dräger SpO2, Dräger NIBP, External temperature module
Vista 120 SC B
 Recorder, Wi-Fi, Bluetooth, touch screen
 Nellcor SpO2, SunTech NIBP, External temperature module
C
 Wi-Fi, Bluetooth, touch screen
Environment specification When the monitor and related products have

differing environmental specifications, the effective
The monitor may not meet the performance range for the combined products is that range
specifications given here if stored or used outside which is common to the specifications for all
the specified temperature and humidity ranges. products.
Temperature
Working +0 °C to +40 °C (32 °F~104 °F)

For F3000 TEMP Module, +10 °C to +40 °C (50 °F~104 °F)
For Exergen TEMP Module, +16 °C to +40 °C (60 °F~104 °F)
Transport and Storage -20 °C to +55 °C (-4 °F~131 °F)
Humidity
Working 15%RH ~ 95%RH (non-condensing)
Transport and Storage 15%RH ~ 95%RH (non-condensing)
Altitude
Working 86 kPa ~ 106 kPa
Transport and Storage 70 kPa ~ 106 kPa
Power Supply 100 V-240 V~, 50 Hz/60 Hz
Current: 1.4 A-0.7 A

Display
Display Messages
Display screen: 8-inch color One power on/off LED, green

TFT, supporting touch screen
One battery charge LED, yellow/green
Resolution: 800×600
One AC power LED, green
One alarm LED, red/yellow/blue
Battery specification
Number 1
Battery Type Lithium battery
Capacity ≥5000 mAh
Condition Standard configuration, at 20 °C ~ 30 °C, with (a) new fully charged

battery/batteries, continuous SpO2 measurement and NIBP automatic
measurement mode at interval of 15 minutes, recording at interval of
15 minutes, screen brightness set to “1”.
Operating Time ≥8 hrs
Charging Time ≤390 min, at 20 °C ~ 30 °C; the monitor is off.
Recorder
Record Width 49 mm~50 mm
Paper Speed 12.5 mm/s, 25 mm/s, 50 mm/s
Trace 1

Recording types Continual real-time recording

8 seconds real-time recording
Recording manually
Physiological Alarm recording
Trend graph recording
Trend table recording
NIBP review recording
Alarm review recording
NIBP auto triggered recording
Data management
Data review
Trend graph/trend table 3 hrs, at 1 Second Resolution

review
120 hrs, at 1 min. Resolution
Alarm/Monitoring Event data Up to 200 sets
NIBP Measurement Review 1200 sets
Refer to Chapter Monitoring data review for more

information about data review.
Data storage
In monitoring mode, a single piece of patient data maximally contains the following information:
Patient information MRN, name, date of birth, date of admission, gender, type, height,
weight, blood type, doctor, bed No., department
Trend graph and trend table 240 hours
NIBP measurement review 1200 sets
Alarm review 200 sets

1 GB extension space for data storage: ≥400 hrs

With all parameters on, storage interval of 1 s, one SpO2 wave, and one alarm event occurring for each
10 s.
In ward round mode, storage data maximally contains the following information:
Ward round MRN, name, type, bed No., ward round record Up to 800 thousand sets
record and original record
SpO2 Storage starting time, SpO2 value, PR value Up to 20 sets for a single patient
NIBP SYS, DIA, MAP, PR, measurement time Up to 20 sets for a single patient
TEMP TEMP value, measurement time Up to 20 sets for a single patient
1 GB space for data storage: ≥100 thousand sets of ward round records. Up to 800 thousand sets of
ward round records are supported (one ward round record has 20 original records).
In spot-checking mode, storage data maximally contains the following information:
16 million sets of spot-checking data for multiple patients.
Refer to Section Storing data in the storage device

for more information about storing data in the
storage medium.
NIBP
Complies with IEC 80601-2-30: 2009+A1: 2013;

EN80601-2-30:2010+A1:2015.
Dräger Module
Technique Oscillometry
Mode Manual, Auto, Continuous, Average
Measuring Interval in AUTO 1/2/3/4/5/10/15/30/60/90/120/180/240/360/480

Mode (unit: minutes)
Continuous 5 min, interval is 5 s
Measuring Type SYS, DIA, MAP, PR
Average measurement Interval (unit: minutes) 1/2/3/4/5
times 3/5

☆ Measuring Range
☆ Adult Mode SYS: 40 mmHg to 270 mmHg

DIA: 10 mmHg to 215 mmHg
MAP: 20 mmHg to 235 mmHg
☆ Pediatric Mode SYS: 40 mmHg to 230 mmHg

☆ Neonatal Mode SYS: 40 mmHg to 135 mmHg

☆ Alarm Type SYS, DIA, MAP
☆ Cuff Pressure Measuring 0 mmHg to 300 mmHg

Range
Pressure Resolution 1 mmHg
☆ Maximum Mean Error ±5 mmHg
☆ Maximum Standard 8 mmHg

Deviation
Maximum Measuring Period
Adult/Pediatric 120 s
Neonate 90 s
Typical Measuring Period 20 s to 35 s (depend on HR/motion disturbance)
Dual Independent Channel Overpressure Protection
Adult (297±3) mmHg
Pediatric (245±3) mmHg
Neonatal (147±3) mmHg
Pre-inflation Pressure
Adult Mode Default: 160 mmHg

Range: 80/100/120/140/150/160/180/200/220/240 mmHg

Pediatric Mode Default: 140 mmHg

Range: 80/100/120/140/150/160/180/200 mmHg
Neonatal Mode Default: 100 mmHg

Range: 60/70/80/100/120 mmHg
SunTech Module
Method Oscillometric
Mode Manual, Auto, Continuous, Average
Measuring Interval in AUTO 1/2/3/4/5/10/15/30/60/90/120/180/240/360/480

Mode (unit: minute)
Continuous 5 min, interval is 5 s
Average measurement Interval (unit: minutes) 1/2/3/4/5
times 3/5
☆ Measuring Type SYS, DIA, MAP, PR
☆ Measuring Range
☆ Adult Mode SYS: 40 mmHg ~ 260 mmHg

DIA: 20 mmHg ~ 200 mmHg
MAP: 26 mmHg ~ 220 mmHg
☆ Pediatric Mode SYS: 40 mmHg ~ 230 mmHg

☆ Neonatal Mode SYS: 40 mmHg ~ 130 mmHg

☆ Alarm Type SYS, DIA, MAP
Pressure Resolution 1 mmHg
☆ Maximum mean error ±5 mmHg
☆ Maximum standard 8 mmHg

deviation
Maximum measuring period

Adult 130 s
Pediatric 90 s
Neonate 75 s
Overpressure protection
Adult/Pediatric <300 mmHg
Neonate <150 mmHg
Pre-inflation Pressure
Adult Mode 120 mmHg, 140 mmHg, 150 mmHg, 160 mmHg, 180 mmHg,
200 mmHg, 220 mmHg, 240 mmHg, 260 mmHg, 280 mmHg
Default: 160 mmHg
Pediatric Mode 80 mmHg, 100 mmHg, 120 mmHg, 140 mmHg, 150 mmHg,
160 mmHg, 180 mmHg, 200 mmHg, 220 mmHg, 250 mmHg
Default: 120 mmHg
Neonatal Mode 60 mmHg, 70 mmHg, 80 mmHg, 90 mmHg, 100 mmHg, 120 mmHg,
140 mmHg
Default: 90 mmHg
SpO2
Complies with EN/ISO 80601-2-61: 2017.

Dräger Module
Measuring Range 0% to 100%
Resolution 1%
☆ Data Update Period 1s
☆ Accuracy
☆ Adult/Pediatric ±2% (70% to 100% SpO2)
Undefined (0% to 69% SpO2)
☆ Neonate ±3% (70% to 100% SpO2)
Undefined (0% to 69% SpO2)

SpO2 Storage Inteval In ward round mode

30 S (default), 1 min, 2 mins, 5 mins
Sensor
Red Light (660±3) nm
Infrared Light (905±10) nm
Emitted Light Energy < 15 mW
PI
Measuring Range 0-10, invalid PI value is 0.
Resolution 1
Nellcor Module
Measuring Range 0% to 100%
Resolution 1%
☆ Data Update Period 1s
DS-100A, OXI-A/N (Adult)

D-YS (Adult and Pediatric) ±3% (70% to 100% SpO2)
OXI-P/I (Pediatric)
MAX-A, MAX-AL, MAX-N, MAX-P, MAX-I, MAX-

☆ Accuracy ±2% (70% to 100% SpO2)
FAST (Adult and Pediatric)
MAX-A, MAX-AL, MAX-N, MAX-P, MAX-I, MAX-

±3% (60% to 80% SpO2)
FAST (Adult and Pediatric)
If sensor is used for neonate as recommended, the accuracy will be larger than adult
by ±1.
SpO2 Storage In ward round mode

Inteval
30 S (default), 1 min, 2 mins, 5 mins
Sensor Wave length: approximately 660 nm and 900 nm
Emitted light energy: <15 mW
NOTE
The information about wavelength range can be
especially useful to clinicians (for instance, when
photodynamic therapy is performed).

PR
Measuring range Accuracy Resolution

PR Dräger 25 bpm to 300 bpm ±2 bpm 1 bpm
(SpO2) Nellcor 20 bpm to 300 bpm ±3 bpm (20 bpm to 250 bpm) 1 bpm
PR Dräger 40 bpm to 240 bpm ±3 bpm or 3.5%, whichever is greater 1 bpm
(NIBP) SunTech 30 bpm to 220 bpm ±3 bpm or ±2%, whichever is greater 1 bpm
TEMP
Complies with EN/ISO 80601-2-56: 2018.

TAT-5000S-RS232 Thermometer:
☆ Measuring Range 16 °C ~ 43 °C (61 °F ~ 110 °F)
Arterial Heat Balance Range for Body 34.5°C ~ 43 °C (94 °F ~ 110 °F)
Temperature 1
Clinical Accuracy ±0.1 °C or 0.2 °F

per ASTM E1112
Clinical Performance (versus Oral Clinical Bias: 0.52 °C

Thermometry), per ISO 80601-2-56
Limits of Agreement: 1.24
Clinical Repeatability: 0.13
Clinical Performance (versus Rectal Clinical Bias: 0.02 - 0.07 °C

Thermometry), per ISO 80601-2-56
Limits of Agreement: 0.87 - 1.15
Clinical Repeatability: 0.13
Operating Environment 16°C ~ 40°C (60 °F ~ 104 °F)
Storage Environment -20°C ~ 50°C (-4 °F ~ 122 °F)
Resolution 0.1 °C or °F
Response Time ~ 0.04 seconds
Time displayed on scanner 30 seconds
Battery type and life 9-volt alkaline battery, providing 15,000 readings 2

NOTE WARNING
1 Automatically applied when temperature is within The monitor may not meet performance
normal body temperature range, otherwise reads specifications if stored or used outside
surface temperature. temperature and humidity ranges. When
2 Approximate number of readings when scanning moving the monitor from a storage location,
for 5 seconds and reading the temperature display wait at least one-hour or more prior to use to
for 3 seconds before turning off the thermometer. allow the monitor to adjust to room
temperature.
☆ Measuring range 30 °C~43 °C
Prediction measurement range 35 °C~43 °C
Low Temp. Mode prediction measurement 33 °C~43 °C

range
Working temperature 10 °C ~ 40 °C
Transport and Storage -20 °C ~ 55 °C
Sensor type Oral /axillary /rectal
☆ Adjustable range of alarm limits 35.5 °C ~42 °C
Resolution 0.1 °C
☆ Accuracy Monitoring Mode and Preditive Mode: ±0.1 °C

Quick Predictive Mode: ±0.3 °C
Typical measurement time (after insertion Oral (Quick Predictive Mode): (3~5) s (non-fever
into measurement site) temps); (8~10) s (fever temps)
Oral (Predictive Mode): (6~10) s
Axillary: (8~12) s
Rectal: (10~14) s
Monitoring Mode (all sites): (60~120) s
Measuring Mode Direct Mode /Adjusted Mode
Transient Response Time ≤30 s monitoring mode
Clinical Bias (-0.2 to -0.4 )°C
Limits of Agreement 0.49
Stability 0.14 °C

NOTE
The direct mode refers to monitoring mode, while
adjusted mode refers to predictive mode and quick
predictive mode.
Wi-Fi
IEEE 802.11 a/b/g/n
Frequency Band 2.4 GHz & 5 G ISM band
Modulation OFDM with BPSK, QPSK, 16-QAM, and 64-QAM

802.11b with CCK and DSSS
Typical Transmit Power 2.4 G

(±2 dBm) 17 dBm for 802.11b DSSS
17 dBm for 802.11b CCK
17 dBm for 802.11g OFDM
16 dBm for 802.11n OFDM
5 G (not available in USA and in Canada)
10 dBm for 802.11a OFDM
9 dBm for 802.11n OFDM
I/U Ratio (co-channel) ≤20 dB
I/U Ratio (adjacent channel) ≤1 dB
Throughput ≥0.01 Mbps
Latency ≤1 s
Jitter ≤1 s
PER ≤10%

e-link
Transmit Frequency 2402 MHz ~ 2480 MHz
Frequency Band 2402 MHz ~ 2480 MHz
Modulation FHSS, GFSK, DPSK, DQPSK
Transmit Power ≥ 0 dBm
I/U Ratio ≤1 dB
Throughput ≥0.01 Mbs
Latency (one way delay) ≤1 s
Jitter (latency variation) ≤1 s
PER ≤10%
Interfaces
Nurse Call
Drive Mode Voltage output
Power Supply 11.4 V ~ 12.6 V
Interface Signal 12 V power supply and PWM waveform
Interface Type Standard RJ-45 network interface
USB Interfaces
Number of USB Interfaces Standard: 2
Drive Mode HOST interface, USB1.0/2.0 protocol
Power Supply 5 VDC±5%, 500 mA Max.

Interface Type USB A-type port
Wired Network Interface
Specification 100-Base TX (IEEE802.3)
Interface Type Standard RJ-45 network interface


EMC Information
EMC Information
Guidance and Manufacture’s Declaration . . 192

Electromagnetic emissions. . . . . . . . . . . . . . . . 192
Electromagnetic immunity. . . . . . . . . . . . . . . 193
Electromagnetic immunity. . . . . . . . . . . . . . . 194
Recommended separation distances . . . . . . 198

EMC Information
Guidance and Manufacture’s Declaration
Electromagnetic emissions
Guidance and manufacture’s declaration – electromagnetic emission

Vista 120 SC is intended for use in the electromagnetic environment specified below. The customer or
the user of Vista 120 SC should assure that they are used in such an environment.
Emission test Compliance Electromagnetic environment – guidance
RF emissions Group 1 Vista 120 SC uses RF energy only for their
internal function. Therefore, their RF emissions
CISPR 11
are very low and are not likely to cause any
interference in nearby electronic equipment.
RF emission Class A Vista 120 SC is suitable for use in all
establishments, other than domestic
CISPR 11
establishments and those directly connected to
Harmonic emissions N/A the public low-voltage power supply network that
supplies buildings used for domestic purposes.
IEC/EN 61000-3-2
Voltage fluctuations/ N/A
flicker emissions
IEC/EN 61000-3-3
NOTE
The EMISSIONS characteristics of Vista 120 SC
make it suitable for use in industrial areas and
hospitals (CISPR 11 class A). If it is used in a
residential environment (for which CISPR 11 class
B is normally required) Vista 120 SC might not
offer adequate protection to radio-frequency
communication services. The user might need to
take mitigation measures, such as relocating or re-
orienting the equipment.

EMC Information
Electromagnetic immunity
Guidance and manufacture’s declaration – electromagnetic immunity

Immunity test IEC/EN 60601 test Compliance level Electromagnetic environment -
level guidance
Electrostatic ± 8 kV contact ± 8 kV contact Vista 120 SC uses RF energy only
discharge (ESD) for their internal function. Therefore,
± 15 kV air ± 15 kV air
their RF emissions are very low and
IEC/EN 61000-4-2
are not likely to cause any
interference in nearby electronic
equipment.
Electrical fast ±2 kV for power ±2kV for power Mains power quality should be that of
transient/burst supply lines supply lines a typical commercial or hospital
environment.
IEC/EN 61000-4-4
Surge ±1 kV for line to line ±1 kV for line to line Mains power quality should be that of
a typical commercial or hospital
IEC/EN 61000-4-5 ±2 kV for line to ±2 kV for line to
environment.
ground ground
Power frequency 30 A/m 30 A/m Power frequency magnetic fields
should be at levels characteristic of a
(50/60Hz)
typical location in a typical
magnetic field commercial or hospital environment.
IEC/EN 61000-4-8
Voltage dips, short 0 % UT; 0.5 cycle 0 % UT; 0.5 cycle Mains power quality should be that of
interruptions and At 0°, 45°, 90°, 135°, At 0°, 45°, 90°, 135°, a typical commercial or hospital
voltage variations on 180°, 225°, 270° 180°, 225°, 270° and environment. If the user of Vista 120
power supply input and 315° 315° SC requires continued operation
lines during power mains interruptions, it
is recommended that Vista 120 SC
IEC/EN 61000-4-11
0 % UT; 1 cycle 0 % UT; 1 cycle be powered from an uninterruptible
and and power supply or a battery.
70 % UT; 25/30 70 % UT; 25/30
cycles ) cycles )
Single phase: at 0° Single phase: at 0°
0 % UT; 250/300 0 % UT; 250/300

cycle cycle
NOTE UT is the a.c. mains voltage prior to application of the test level.

EMC Information
Electromagnetic immunity
Guidance and manufacture’s declaration – electromagnetic immunity

Immunity test IEC/EN 60601 test Compliance level Electromagnetic environment -
level guidance
Portable and mobile RF
communications equipment should
be used no closer to any part of Vista
120 SC, including cables, than the
recommended separation distance
calculated from the equation
applicable to the frequency of the
transmitter.
Conducted RF 3 Vrms 3 Vrms
Recommended separation
IEC/EN 61000-4-6 150 kHz to 80 MHz 150 kHz to 80 MHz
distance
Radiated RF 6Vrmsc in ISM bands 6Vrmsc in ISM bands
between 0.15 MHz between 0.15 MHz
d = 1.2 P 150KHz to 80MHz
IEC/EN 61000-4-3
and 80 MHz and 80 MHz
3 V/m 3 V/m d = 1.2 P 80 MHz to 800 MHz

80 MHz to 2.7 GHz 80 MHz to 2.7 GHz d = 2.3 P 800 MHz to 2.7 GHz
See table 1 Comply with table 1 d=6 P /E at RF wireless

communications equipment bands
(Portable RF communications
equipment (including peripherals
such as antenna cables and external
antennas) should be used no closer
than 30 cm (12 inches) to any part of
the Vista 120 SC, including cables
specified by the manufacturer).
Where P is the maximum output

power rating of the transmitter in
watts (W) according to the
transmitter manufacturer and d is the
recommended separation distance
in meters (m).

EMC Information
Field strengths from fixed RF

transmitters, as determined by an
electromagnetic site survey,a should
be less than the compliance level in
each frequency range.b
Interference may occur in the vicinity
of equipment marked with the
following symbol:
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones
and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be
predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF
transmitters, an electromagnetic site survey should be considered. If the measured field strength in the
location in which Vista 120 SC is used exceeds the applicable RF compliance level above, Vista 120
SC should be observed to verify normal operation. If abnormal performance is observed, additional
measures may be necessary, such as reorienting or relocating Vista 120 SC.
b Over the frequency range 150kHz to 80MHz, field strengths should be less than 3V/m.
c The ISM (industrial, scientific and medical) bands between 0.15 MHz and 80 MHz are 6.765 MHz to
6.795 MHz; 13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz.
The amateur radio bands between 0.15 MHz and 80 MHz are 1.8 MHz to 2.0 MHz, 3.5 MHz to 4.0 MHz,
5.3 MHz to 5.4 MHz, 7 MHz to 7.3 MHz, 10.1 MHz to 10.15 MHz, 14 MHz to 14.2 MHz, 18.07 MHz to
18.17 MHz, 21.0 MHz to 21.4 MHz, 24.89 MHz to 24.99 MHz, 28.0 MHz to 29.7 MHz and 50.0 MHz to
54.0 MHz.

EMC Information
Table 1 Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless

communications equipment
Test Immunity
Band a) Maximum Distance
frequency Service a) Modulation b) test level
(MHz) power (W) (m)
(MHz) (V/m)
Pulse
385 380-390 TETRA 400 modulation b) 1.8 0.3 27
18 Hz
FM c)
GMRS 460, ± 5 kHz
450 430-470 deviation 2 0.3 28
FRS 460
1 kHz sine
710
Pulse
LTE Band 13,
745 704-787 modulation b) 0.2 0.3 9
17
217 Hz
780
810 GSM
800/900,
870 Pulse
TETRA 800,
800-960 modulation b) 2 0.3 28
iDEN 820,
18 Hz
930 CDMA 850,
LTE Band 5
1720 GSM 1800;

CDMA 1900;
1845 Pulse
GSM 1900;
1700-1990 modulation b) 2 0.3 28
DECT; LTE
217 Hz
1970 Band 1, 3, 4,
25; UMTS
Bluetooth,
WLAN, Pulse
2450 2400-2570 802.11 b/g/n, modulation b) 2 0.3 28
RFID 2450, 217 Hz
LTE Band 7
5240
Pulse
WLAN
5500 5100-5800 modulation b) 0.2 0.3 9
802.11 a/n
217 Hz
5785

EMC Information
Test Immunity
Band a) Maximum Distance
frequency Service a) Modulation b) test level
(MHz) power (W) (m)
(MHz) (V/m)
NOTE If necessary to achieve the IMMUNITY TEST LEVEL, the distance between the transmitting
antenna and the ME EQUIPMENT or ME SYSTEM may be reduced to 1 m. The 1 m test distance is
permitted by IEC 61000-4-3.
a) For some services, only the uplink frequencies are included.

b) The carrier shall be modulated using a 50 % duty cycle square wave signal.
c) As an alternative to FM modulation, 50 % pulse modulation at 18 Hz may be used because while it
does not represent actual modulation, it would be worst case.

EMC Information
Recommended separation distances
Recommended separation distances between portable and mobile RF communications

equipment and Vista 120 SC
Vista 120 SC is intended for use in an electromagnetic environment in which radiated RF disturbances
are controlled. The customer or the user of Vista 120 SC can help prevent electromagnetic interference
by maintaining a minimum distance between portable and mobile RF communications equipment
(transmitters) and Vista 120 SC as recommended below, according to the maximum output power of
the communications equipment.
Rated maximum Separation distance according to frequency of transmitter(m)

output power of
transmitter 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.7 GHz
(W) d = 1.2 P d = 1.2 P d = 2.3 P

0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation
distance d in meters (m) can be estimated using the equation applicable to the frequency of the
transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the
transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.

Default settings
Default settings
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 200
Default configuration . . . . . . . . . . . . . . . . . . . 200
User configuration . . . . . . . . . . . . . . . . . . . . . 200
Patient information default settings . . . . . . . 200
Alarm default settings . . . . . . . . . . . . . . . . . . 201
SpO2 default settings . . . . . . . . . . . . . . . . . . . 201
PR default settings . . . . . . . . . . . . . . . . . . . . . 202
NIBP default settings . . . . . . . . . . . . . . . . . . . 202
TEMP default settings . . . . . . . . . . . . . . . . . . 203

Default settings
Overview
This appendix documents the most important

default settings of the monitor as it is delivered from
the factory.
NOTE
If the monitor has been preconfigured according to
the requirements, the settings at delivery will be
different from the default settings listed below.
Default configuration
To set default configuration, select Menu > Default To check the configuration currently used, select
Setup. On the Profile menu, users can choose a Menu > Default Setup. The one labeled with ● is
factory configuration (adult, pediatric or neonate) current configuration. If there's no labeled
based on the patient category. Also, users can configuration, it means the currently used
choose a user configuration saved in the monitor if configuration is not one of them.
it is available. For more information about user
configuration, refer to User configuration.
User configuration
Select Menu > Default Setup > User Configure,

enter the required password, users can save the
current monitor’s configuration, delete the saved
user configuration and rename it. Three pieces of
user configuration can be saved in the monitor.
User can select as desire. The one labeled with ● is
current configuration.
Patient information default settings
Patient Information Settings

Patient Type Adult

Default settings
Alarm default settings
Alarm Settings
Pause Time 120 s
Alarm Latch Off
SpO2 default settings
SpO2 Settings ADU PED NEO

Alarm Switch On
Alarm Record Off
Alarm Level Medium
Alarm High Limit 100 100 95
Alarm Low Limit 90 90 88
NIBP/SpO2 Simul Off
Measurement
Pitch Tone On
Sensitivity Medium
SatSeconds (Nellcor Off
Module)
Sweep 12.5 mm/s
Alert Switch On
Alert High Limit 100 100 95
Alert Low Limit 90 90 88
SpO2 Desat Limit 80%

Default settings
PR default settings
PR Settings ADU PED NEO

PR Source SpO2
Alarm Switch On
Alarm Record Off
Alarm Level Medium
Alarm High Limit 120 160 200
Alarm Low Limit 50 75 100
Pulse Volume 3
Alarm Source SpO2 or NIBP
NIBP default settings
NIBP Settings ADU PED NEO

Alarm Switch On
Alarm Record Off
Alarm Level Medium
Alarm High Limit (SYS) 160 120 90
Alarm Low Limit (SYS) 90 75 40
Alarm High Limit (MAP) 110 90 70
Alarm Low Limit (MAP) 60 50 30
Alarm High Limit (DIA) 90 70 60
Alarm Low Limit (DIA) 50 40 20
Dräger Module
Inflation value 160 140 100
SunTech Module
Inflation value 160 140 90
Unit mmHg

Default settings
Interval 1 minute
Interval (Average) 1 minute
Measurement times 3
(Average)
PR Switch On
Auto Recording Off
Alert Switch On
Alert High Limit (SYS) 160 120 90
Alert Low Limit (SYS) 90 70 40
Alert High Limit (MAP) 110 90 70
Alert Low Limit (MAP) 60 50 30
Alert High Limit (DIA) 90 70 60
Alert Low Limit (DIA) 50 40 20
TEMP default settings
TEMP Settings ADU PED

Alarm Switch On
Alarm Record Off
Alarm Level Medium
Measurement Mode Predictive
Measurement Position Oral or rectal
Low Temp. Mode Off
Alarm High Limit 39.0 39.0
Alarm Low Limit 36.0 36.0
Alert Switch On
Alert High Limit 39.0 39.0
Alert Low Limit 36.0 36.0
Unit °C



These instructions for use apply only to
Vista 120 SC 1.n
with the Serial No.:
If no Serial No. has been filled in by Dräger,
these Instructions for Use are provided for
general information only and are not intended for
use with any specific machine or unit.
This document is provided for customer
information only, and will not be updated or
exchanged without customer request.
Directive 93/42/EEC
concerning Medical Devices
Manufacturer:
Shanghai Dräger Medical Instrument Drägerwerk AG & Co. KGaA

Co., Ltd. Moislinger Allee 53-55
23542 Lübeck
3#, No.229, Hupo Road,
Germany
Shanghai International Medical Zone,
Pudong New Area, 201321 Shanghai,
PEOPLE’S REPUBLIC OF CHINA +49 451 8 82-0
+86 21 3108 6000 FAX +49 451 8 82-20 80
FAX +86 21 3108 6011 http://www.draeger.com
http://www.draeger.com
26 80 025 – GA 6498.020 en
© Shanghai Dräger Medical Instrument Co., Ltd.
Edition: 2 – 2020-02
Dräger reserves the right to make modifications
to the equipment without prior notice.

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Instructions for use

WARNING Vital Signs Monitor

Schematic renderings of screen images are used,

Definition of Safety Information

Abbreviations and Symbols

For explanations refer to sections “Abbreviations”

Instructions for use Vista 120 SC SW 1.n 1

2 Instructions for use Vista 120 SC SW 1.n

Responsibility of the Manufacturer . . . . . . . 7 Monitoring mode . . . . . . . . . . . . . . . . . . . . . . 49

Instructions for use Vista 120 SC SW 1.n 3

Network Disconnected alarms . . . . . . . . . . . . . 79 Procedure of Leakage Test . . . . . . . . . . . . . . . 116

Monitoring NIBP . . . . . . . . . . . . . . . . . . . . . . . 109 Using battery . . . . . . . . . . . . . . . . . . . . . . . . . 149

4 Instructions for use Vista 120 SC SW 1.n

Reprocessing . . . . . . . . . . . . . . . . . . . . . . . . . 155 Recommended separation distances . . . . . . . 198

Product specification . . . . . . . . . . . . . . . . . . . 175

EMC Information. . . . . . . . . . . . . . . . . . . . . . . 191

Instructions for use Vista 120 SC SW 1.n 5

6 Instructions for use Vista 120 SC SW 1.n

Responsibility of the Manufacturer

Responsibility of the Manufacturer . . . . . . . 8

Instructions for use Vista 120 SC SW 1.n 7

Responsibility of the Manufacturer

Dräger only considers itself responsible for any

8 Instructions for use Vista 120 SC SW 1.n

For your safety and that of your patients

General safety information . . . . . . . . . . . . . . 10

Product-specific safety information . . . . . . . 13

Protecting personal information . . . . . . . . . . 19

Instructions for use Vista 120 SC SW 1.n 9

General safety information

The following WARNING and CAUTION Maintenance

10 Instructions for use Vista 120 SC SW 1.n

Connected devices Patient safety

WARNING The design of the medical device, the

Instructions for use Vista 120 SC SW 1.n 11

WARNING Read carefully Assembly Instructions and

12 Instructions for use Vista 120 SC SW 1.n

Product-specific safety information

Federal (U.S.) law restricts this device to sale by or WARNING

Instructions for use Vista 120 SC SW 1.n 13

14 Instructions for use Vista 120 SC SW 1.n

Instructions for use Vista 120 SC SW 1.n 15

16 Instructions for use Vista 120 SC SW 1.n

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Protecting personal information

Protecting personal health information is a major CAUTION

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Restrictions for use . . . . . . . . . . . . . . . . . . . . 22

Instructions for use Vista 120 SC SW 1.n 21

Restrictions for use

Users of this device must be trained and

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Instructions for use Vista 120 SC SW 1.n 25

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