Vista 120

Patient Monitoring Solution

Hospitals around the world share a common challenge – to provide the

best possible care in locations with growing populations, stricter financial
regulations and caregivers that are increasingly overloaded. The Vista 120
was engineered to meet your clinical needs and stay within your budget,
allowing you to deliver efficient and high-quality patient care.

380 mm (15") TFT touch screen Device Connectivity

High resolution display (1,024 x 768) is bright Enables true integrated
and easy to read, even from a distance workstation functionality

Conigurable layout
Lets you see the information you
want, the way you want to see it

Core set of essential

parameters
3/5 lead ECG, SpO2,
non-invasive blood pressure,
Enhanced trending respiration and dual
– Stores up to 150 hours of temperature
trend data for all parameters
in tabular and graphic formats
– Stores up to 1,200 NIBP
D-6829-2014

measurements and
200 alarm events Anesthesia support
– 96 hours of full disclosure Displays data from Scio Four
gas measurement modules

Alarms Shortcut keys

Alarm indicator and alarm pause/off Fast access to main functions
02 | Vista 120

Benefits

Fully-integrated workstation solution

The Vista 120 supports adult, pediatric and neonatal patients in a variety of care environments – including
Intensive Care, Operating Rooms, Emergency Departments and Neonatal Intensive Care. Medibus/Medibus-X
connectivity enables the Vista 120 to be used with a complementary Dräger device, such as a ventilator or
anesthesia machine allowing true integrated workstation functionality.

Essential monitoring capabilities, exceptional value

The Vista 120 displays up to 13 waveforms in an easy-to-configure layout and offers a core set of essential
parameters including 3/5 lead ECG, non-invasive blood pressure, respiration and dual temperature. Advanced
parameters including three invasive blood pressures, flexible mainstream and sidestream etCO2 and cardiac
output are also available.

Users can add external parameter modules including SCIO, CO2 and BIS on model C and model C+ after
initial device purchase.

Supports workflow efficiency

The Vista 120 is easy to learn and easy to use. You can configure the display to see the information you want
to see, the way you want to see it. Fast access keys and simplified menus put the data you need right at your
fingertips.

Monitor level of consciousness with flexible Bispectral Index (BIS) measurement

The Vista 120 offers BISx measurement to support clinicians with enhanced information as they monitor the
depth of anesthesia. It allows the ability to better assess patient status and quickly respond to a changing
condition.

Standard built-in gas interface

The Vista 120 provides seamless connectivity to Dräger Scio anesthetic gas measurement modules delivering
precise inspiratory and expiratory values.

Health level-7 (HL7) international interface

The Vista 120 offers direct connection to the hospital information system (HIS) and/or an electronic medical
record in HL7 protocol or a secure connection via the Vista 120 Gateway. The ability for easy access to both of
these important information files help improve workflow efficiency and reduce human error.
 Vista 120 | 03

Benefits

Dräger heritage of quality

Every life is unique. Protecting, supporting and saving lives is the foundation of our company philosophy. Our
goal is to provide product and solutions that support acute care, help improve patient outcomes, reduce costs
and achieve greater overall patient satisfaction.

Related Products

Vista 120 Central Monitoring System

The easy-to-use Vista 120 Central Monitoring System (CMS) lets

you centrally monitor the vital signs of up to 64 patients connected
to Vista 120/Vista 120 S bedside monitors. This central surveillance
streamlines workflow for clinicians, while significantly increasing patient
safety.
D-68804-2012

Vista 120 S

Dräger understands the growing need for a patient monitor with

built-in connectivity that provides essential monitoring at a good value.
The Vista 120 S supports adult, pediatric and neonatal patients and can
be used on its own or with a Dräger therapy device as a fully integrated
workstation.
D-13374-2016
04 | Vista 120

Related Products

Vista 120 SC

Reduce clinicians' workload with an easy-to-use and intuitive user

interface. The Vista 120 SC is designed for spot check and continuous
vital signs monitoring to complete Dräger's hospital-wide solution
offerings.
D-11590-2019
 Vista 120 | 05

Technical Data

Classification
Protection class Class I equipment and internal powered equipment
Degree of protection against electric shock CF: ECG (RESP), TEMP, IBP, C.O.
BF: SPO2, AG, BIS
Defibrillation protection Yes
Liquid ingress protection IPX 1
Disinfection/sterilization method Refer to chapter "Care and Cleaning" for details.
Mode of operation Continuous
Compliant with standards IEC 60601-1: 2005+A1:2012; IEC 60601-1-2: 2014;
EN 60601-1: 2006+A1:2013; EN60601-1-2: 2015;
IEC 60601-2-49: 2011

Supported Parameters

ECG
Lead mode 3-lead wire: I, II, III
5-lead wire: I, II, III, aVR, aVL, aVF, V
Waveform 3-lead wire: 1-channel waveform
5-lead wire: 2-channel waveform, max. seven waveforms
Lead naming style AHA, IEC
Display sensitivity 1.25 mm/mV (x0.125), 2.5 mm/mV (x0.25), 5 mm/mV (x0.5),
10 mm/mV (x1), 20 mm/mV (x2), 40 mm/mV (x4), AUTO gain
Sweep 6.25, 12.5, 25, 50 mm/s
Bandwidth (-3dB) Diagnosis: 0.05 to 150 Hz
Monitor: 0.5 to 40 Hz
Surgery: 1 to 20 Hz
CMRR Diagnostic: > 95 dB
(Common mode rejection ratio) Monitor: > 105 dB
Surgery: > 105 dB
Notch In diagnosis, monitor and surgery modes: 50 Hz/60 Hz
(Notch filter can be turned on or off manually)
Differential input impendance > 5 MΩ
Input signal range ±10 mVPP
Electrode offset potential tolerance ±800 mV
Auxiliary current Active electrode: < 100 nA
(Leads off detection) Reference electrode: < 900 nA
Recovery time after defibrillation < 5 s (measured without electrodes as IEC60601-2-27:2011,
Sect. 201.8.5.5.1 requires)
Leakage current of patient < 10 μA
Scale signal 1 mVPP, accuracy is ±5
System noise < 30 μVPP
ESU protection Cut mode: 300 W
Coagulation mode: 100 W
Recovery time: ≤ 10 s
Electrosurgical interference suppression Tested according to ANSI/AAMI EC13-2002: Sect. 5.2.9.14,
Complied with ANSI/AAMI EC13:2002, Sect.4.2.9.14
Minimum input slew rate (lead II) > 2.5 V/s
Baseline reset time <3s

Pace Pulse
Pulse indicator Pulse is marked if the requirements of IEC 60601-2-27: 2011,
Sect. 201.12.1.101.12 are met: Amplitude: ±2 mV to ±700 mV
Width: 0.1 ms to 2.0 ms Ascending time: 10 μs to 100 μs
06 | Vista 120

Technical Data

Pulse rejection Pulse is rejected if the requirements of IEC 60601-2-27: 2011,

Sect. 201.12.1.101.13 are met: Amplitude: ±2 mV to ±700 mV
Width: 0.1 ms to 2.0 ms Ascending time: 10 μs to 100 μs

Heart Rate
Range ADU: 15 to 300 bpm
PED/NEO: 15 to 350 bpm
Accuracy ±1% or ±1 bpm, whichever is greater
Resolution 1 bpm
Sensibility ≥ 300 μVPP

PVC
Range ADU: 0 to 300 PVCs/min
PED/NEO: 0 to 350 PVCs/min
Resolution 1 PVCs/min

ST Value
Range -2.0 to +2.0 mV
Accuracy -0.8 mV to +0.8 mV: ±0.02 mV or 10%, whichever is greater
Resolution 0.01 mV

HR Averaging Method
Method 1 Heart rate is computed by excluding the minimum and maximum
values from the 12 most recent RR intervals and averaging the
residual 10 RR intervals
Method 2 If each of three consecutive RR intervals is greater than 1,200 ms,
then the four most recent RR intervals are averaged to compute
the HR

Range of Sinus and SV Rhythm

Tachycardia Adult: RR interval for 5 consecutive QRS complex ≤ 0.5 s.
Pediatric/neonatal: RR interval for 5 consecutive QRS complex
≤ 0.375 s
Normal Adult: 0.5 s < RR interval for 5 consecutive QRS complex < 1.5 s.
Pediatric/neonatal: 0.375 s < RR interval for 5 consecutive QRS
complex < 1 s
Bradycardia Adult: RR interval for 5 consecutive QRS complex ≥ 1.5 s.
Pediatric/neonatal: RR interval for 5 consecutive QRS complex
≥1s

Range of Ventricular Rhythm

Ventricular tachycardia The interval of 5 consecutive ventricular complexes is less than
600 ms
Ventricular rhythm The interval of 5 consecutive ventricular complexes ranges from
600 ms to 1,000 ms
Ventricular bradycardia The interval of 5 consecutive ventricular complexes is higher than
1,000 ms

Startup Time for Tachycardia

Ventricular tachycardia Gain 0.5: 10 s
1 mV 206 bpm Gain 1.0: 10 s
Gain 2.0: 10 s
Ventricular tachycardia Gain 0.5: 10 s
2 mV 195 bpm Gain 1.0: 10 s
Gain 2.0: 10 s
 Vista 120 | 07

Technical Data

Response time of heart rate HR range: 80 to 120 bpm

meter to change in HR Range: within 11 s
HR range: 80 to 40 bpm
Range: within 11 s
Tall T-wave rejection Complied with IEC 60601-2-27: 2011, Sect. 201.12.1.101.17 minimum recommended 1.2 mV T-wave
amplitude
Accuracy of heart rate meter Complied with IEC 60601-2-27: 2011,
and response to irregular Sect. 201.7.9.2.9.101 b) 4).
rhythm The HR value after 20 s:
Ventricular bigeminy: 80 ±1 bpm
Slow alternating ventricular bigeminy: 60 ±1 bpm
Rapid alternating ventricular bigeminy: 120 ±1 bpm
Bidirectional systoles: 91 ±1 bpm
Time to alarm for heart rate Asystole alarm: ≤ 10 s
alarm conditions HR low alarm: ≤ 10 s
HR high alarm: ≤ 10 s
Arrhythmia analyses Asystole V-fib/V-tach Couplet
Run PVCs PVC bigeminy PVC trigeminy
Vent rhythm R on T PVCs high
Tachy Brady Missed beat
Irr rhythm Vent brady Pacer not capture
Pacer not pacing

Respiration
Method Impedance between RA-LL, RA-LA
Baseline impedance range 200 Ω to 2,500 Ω (with ECG cables of 1 KΩ resistance)
Measuring sensitivity Within the baseline impedance range: 0.3 Ω
Waveform bandwidth 0.2 to 2.5 Hz (-3 dB)
RR measuring and alarm range: Adult: 0 to 120 rpm
Neo/Ped: 0 to 150 rpm
Resolution 1 rpm
Accuracy Adult: 6 rpm to 120 rpm: ±2 rpm
0 rpm to 5 rpm: not specified
Neo/Ped: 6 rpm to 150 rpm: ±2 rpm
0 rpm to 5 rpm: not specified
Gain selection x0.25, x0.5, x1, x2, x3, x4, x5
Sweep 6.25 mm/s, 12.5 mm/s, 25 mm/s, 50 mm/s
Apnea alarm time setup 10 s, 15 s, 20 s, 25 s, 30 s, 35 s, 40 s; default value is 20 s

NIBP
Method Oscillometric
Mode Manual, auto, continuous
Measuring interval in auto mode (unit: minutes) 1/2/2.5/3/4/5/10/15/30/60/90/120/180/240/360/480
Continuous 5 min, interval is 5 s
Measuring type Systolic pressure, diastolic pressure, mean pressure
Alarm type SYS, DIA, MAP

Measuring and Alarm Range

Adult mode SYS: 40 to 270 mmHg
DIA: 10 to 215 mmHg
MAP: 20 to 235 mmHg
Pediatric mode SYS: 40 to 230 mmHg
DIA: 10 to 180 mmHg
08 | Vista 120

Technical Data

MAP: 20 to 195 mmHg

Neonatal mode SYS: 40 to 135 mmHg
DIA: 10 to 100 mmHg
MAP: 20 to 110 mmHg
Cuff pressure measuring range 0 to 300 mmHg
Pressure resolution 1 mmHg
Maximum mean error ±5 mmHg
Maximum standard deviation 8 mmHg

Maximum Measuring Period

Adult/pediatric 120 s
Neonate 90 s
Typical measuring period 20 to 35 s (depend on HR/motion disturbance)

Overpressure Protection
Adult 297 ±3 mmHg
Pediatric 245 ±3 mmHg
Neonatal 147 ±3 mmHg

Pulse Rate
Measuring range 40 to 240 bpm
Accuracy ±3 bpm or 3.5%, whichever is larger

SpO2
Measuring range 0 to 100%
Resolution 1%

Accuracy
Adult (including pediatric) ±2% (70 to 100% SpO2)
Undefined (0 to 69% SpO2)
Neonate ±3% (70 to 100% SpO2)
Undefined (0 to 69% SpO2)

Perfusion Index
Measuring range 0 – 10, invalid PI value is 0
Resolution 1

Pulse Rate
Measuring range 25 to 300 bpm
Resolution 1 bpm
Adjustable range of alarm limits 30 to 300 bpm
Accuracy ±2 bpm

Nellcor Module
Measuring range 1% to 100%
Alarm range 20% to 100%
Resolution 1%
Data update period 1s
Accuracy (70% to 100% SpO2):
DS-100A, OXI-A/N (adult) ±3%
OXI-A/N (neonate) ±4%
D-YS (infant to adult) ±3%
D-YS (neonate) ±4%
D-YS with D-YSE ear clip ±3.5%
MAX-FAST ±2%
 Vista 120 | 09

Technical Data

Pulse Rate
Measuring range 20 to 300 bpm
Resolution 1 bpm
Accuracy ±3 bpm (20 to 250 bpm)
Sensor wavelength Approximately 660 and 900nm
Emitted light energy <15 mW

NOTE
Information about the wavelength range can be especially useful to clinicians (for instance, when photodynamic therapy is performed).

Temperature
Channels 2
Measuring and alarm range 0 to 50°C (32 to 122°F)
Sensor type YSI 2.252K/YSI 10K
Resolution 0.1°C (0.1°F)
Accuracy (without sensor) ±0.1°C
Refresh time Every 1 to 2 s

IBP
Accuracy (not including sensor) ±2% or ±1 mmHg, whichever is greater
Resolution 1 mmHg

Pressure Sensor
Sensitivity 5 (μV/V/mmHg)
Impedance range 300 Ω to 3,000 Ω
Filter DC~ 12.5 Hz; DC~ 40 Hz
Zero Range: ±200 mmHg

Measuring and Alarm Range

Art 0 to 300 mmHg
PA -6 to 120 mmHg
CVP/RAP/LAP/ICP -10 to 40 mmHg
P1/P2 -50 to 300 mmHg

CO2
Complies with ISO 80601-2-55: 2011.
Intended patient Adult, pediatric, neonatal
Measure parameters etCO2, FiCO2, AwRR
Unit mmHg, %, kPa
Measuring range CO2 0 mmHg to 150 mmHg (0% to 20%)
AwRR 2 rpm to 150 rpm
Resolution etCO2 1 mmHg
FiCO2 1 mmHg
AwRR 1 rpm
Accuracy etCO2 ±2 mmHg, Respiratory rate Typical conditions:
0 mmHg to 40 mmHg ≤ 60 rpm Ambient temperature:
±5% of reading, (25±3)°C
41 mmHg to 70 mmHg Barometric pressure:
±8% of reading, (760±10) mmHg
71 mmHg to 100 mmHg Balance gas: N2
±10% of reading, Sample gas flow rate:
101 mmHg to 150 mmHg 100 ml/min
±12% of reading or Respiratory rate All conditions
10 | Vista 120

Technical Data

±4 mmHg, > 60 rpm

whichever is greater
AwRR ±1 rpm
Drift of measure Meets the requirements of the measure accuracy
accuracy
Sample gas flow rate 70 ml/min or 100 ml/min(default), accuracy: ±15 ml/min
Warm-up time Display reading within 20 s; reach to the designed accuracy within 2 minutes.
Rise time < 400 ms (water trap with 2 m gas sampling tube, sample gas flow rate: 100 ml/min)
Response time < 4 s (water trap with 2 m gas sampling tube, sample gas flow rate: 100 ml/min)
Work mode Standby, measure
O2 compensation Range: 0% to 100%
Resolution: 1%
Default: 16%
N2O compensation Range: 0% to 100%
Resolution: 1%
Default: 0%
AG compensation Range: 0% to 20%
Resolution: 0.1%
Default: 0%
Humidity compensation ATPD(default), BTPS
method
Barometric pressure Automatic (The change of barometric pressure will not add additional errors to the measurement values.)
compensation
Zero calibration Support
Calibration Support
Alarm etCO2, FiCO2, AwRR
Apnea alarm delay 10 s, 15 s, 20 s, 25 s, 30 s, 35 s, 40 s, 60 s; default value is 20 s.
Data sample rate 100 Hz
etCO2 change1 AwRR >80 rpm, etCO2 descending 8%
AwRR >120 rpm, etCO2 descending 10%

NOTE
Use a test device equivalent to EN ISO 80601-2-55 fig 201.101 to measure at 1:2 I/E ratio. Respiration rate accuracy is determined
by frequency of device, and ET READING change refers to the nominal value.

Interfering Gas Effects:

Gas Gas Level (%) Quantitative Effect/Comments
Nitrous oxide 60 The interfering gas will have no effect on
Halothane 4 the measurement value if compensation
Enflurane 5 of O2, N2O, anesthetic agents has been
Isoflurane 5 correctly set.
Sevoflurane 5
Desflurane 15

Respironics Module
Applicable patient type Adult, pediatric and neonatal patients
Technique Infra-red absorption technique
Measure parameters etCO2, FiCO2, AwRR
Unit mmHg, %, Kpa

Measuring Range
etCO2 0 mmHg to 150 mmHg
FiCO2 3 mmHg to 50 mmHg
 Vista 120 | 11

Technical Data

AwRR 0 rpm to 150 rpm (mainstream)

2 rpm to 150 rpm (sidestream)
Resolution etCO2 1 mmHg
FiCO2 1 mmHg
AwRR 1 rpm
etCO2 accuracy ± 2 mmHg, 0 mmHg to 40 mmHg
± 5% of reading, 41 mmHg to 70 mmHg
± 8% of reading, 71 mmHg to 100 mmHg
± 10% of reading, 101 mmHg to 150 mmHg
± 12% of reading, RR is over 80 rpm (sidestream)
There will be no degradation in performance due to respiration rate (mainstream)
AwRR accuracy ± 1 rpm
Operation mode Measure, standby
Sample gas flow rate (sidestream) (50 ±10) ml/min

O2 Compensation
Range 0% to 100%
Resolution 1%
Default 16%
Barometric pressure compensation User setup

Anesthetic Gas Compensation

Range 0% to 20%
Resolution 0.1%
Default 0.0%
Balance gas compensation Room air, N2O, helium

Stability
Short-term drift Drift over 4 hours < 0.8 mmHg
Long-term drift 120 hours
Zero calibration Support
Alarm type etCO2, FiCO2, AwRR
Apnea alarm delay 10 s, 15 s, 20 s, 25 s, 30 s, 35 s, 40 s; default value is 20 s
Data sample rate 100 Hz
CO2 rise time/response time (mainstream) Less than 60 ms
Sensor response time (sidestream) < 3 seconds, including transport time and rise time

Interfering Gas and Vapor Effects on etCO2 Measurement Values:

Nitrous oxide 60 Dry and saturated gas
Halothane 4 (0 ~ 40) mmHg: ±1 mmHg additional error
Enflurane 5 (41 ~ 70) mmHg: ±2.5% additional error
Isoflurane 5 (71 ~ 100) mmHg: ±4% additional error
Sevoflurane 5 (101 ~ 150) mmHg: ±5% additional error
Xenon 80 Note: Additional worst case error when
Helium 50 compensation for PB, O2, N2O, anesthetic
Desflurane 15 agents, or helium is correctly selected
for the actual fractional gas constituents
present.
Desflurane:
The presence of desflurane in the exhaled
breath at concentrations greater than 5%
will positively bias carbon dioxide values by
up to an additional 3 mmHg at
12 | Vista 120

Technical Data

38 mmHg.
Xenon:
The presence of xenon in the exhaled
breath will negatively bias carbon dioxide
values by up to an additional 5 mmHg at
38 mmHg.

Barometric Pressure on etCO2 Measurement Values:

Quantitative Effect
Ambient barometric, operational
(0 ~ 40) mmHg: ± 1 mmHg additional error
(41 ~ 70) mmHg: ± 2.5% additional error
(71 ~ 100) mmHg: ± 4% additional error
(101 ~ 150) mmHg: ± 5% additional error
Note: Additional worst case error when compensation for PB, O2, N2O, anesthetic agents, or helium is correctly selected for the actual
fractional gas constituents present.

NOTE
Respiration rate accuracy was verified by using a solenoid test setup to deliver a square wave of known CO2 concentration to the
device. 5% and 10% CO2 concentrations were used. Respiration rate was varied over the range of the device. Pass/fail criteria was
comparison of the respiratory rate output from the sensor to the frequency of the square wave.

Dräger MCable Mainstream CO2 Module

Measure parameters etCO2, FiCO2, AwRR
Unit mmHg, %, Kpa

Measuring Range
etCO2 0 mmHg to 100 mmHg
FiCO2 0 mmHg to 100 mmHg
AwRR 3 rpm to 150 rpm (PGM algorithm)
Resolution etCO2 1 mmHg
FiCO2 1 mmHg
AwRR 1 rpm
etCO2 accuracy < 0.5 mmHg rms, 0 mmHg to 40 mmHg
< 1 mmHg rms, 40.1 mmHg to 100 mmHg
Operation mode Measure, standby
Local barometric pressure 57 kPa to 110 kPa

O2 Compensation
Range 0% to 100%
Resolution 1%
Default 16%

N2O Compensation
Range 0% to 100%
Resolution 1%
Default 0%

He Compensation
Range 0% to 100%
Resolution 1%
 Vista 120 | 13

Technical Data

Default 0%

Xe Compensation
Range 0% to 100%
Resolution 1%
Default 0%
Zero calibration Support
Alarm type etCO2, FiCO2, AwRR
Apnea alarm delay 10 s, 15 s, 20 s, 25 s, 30 s, 35 s, 40 s; default value is 20 s
Data reporting rate Every 10 msec or 20 msec
Response time Rise time: t10–90 = 24 msec
Delay time: 150 msec
Warm up The sensor meets the specified operating performance within
2 minutes typical from power on or reset at ambient temperatures
from 20°C to 40°C (68°F to 104°F). At 10°C (50°F) ambient
temperature, time from power on to reach the specified operating
performance is 10 min approximately.

Interfering Gases and Vapours

N2O 100 vol.% 0.00 vol.%
Halothane 5 vol.% 0.02 vol.%
Enflurane 5 vol.% 0.03 vol.%
Isoflurane 5 vol.% 0.02 vol.%
Sevoflurane 5 vol.% 0.02 vol.%
Desflurane 20 vol.% 0.00 vol.%
Ethanol 4‰ * 0.00 vol.%
Acetone 1‰ * 0.00 vol.%
Isopropanol 1% 0.00 vol.%
Methane 3 vol.% <0.02 vol.%
NO 100 ppm 0.01 vol.%
NO2 50 ppm 0.00 vol.%
CO 4 vol.% 0.00 vol.%
Freon R21 100 vol.% 0.07 vol.%
Freon R134a 100 vol.% 0.19 vol.%
Heptafluorpropane 0.7 vol.% 0.00 vol.%
Water vapour 37°C saturated 0.01 vol.%
*blood concentration equivalent

NOTE
The numbers given at the end of each line are typical CO2 readings of the sensor for the pure interfering gas or vapour, balance
N2 (if applicable), without CO2 content. CO2 reading of common mixtures like CO2, O2, N2O, anaesthetic agent (in physiological
concentration) or CO2, O2, N2, water vapour is within specified bias, provided that the major foreign gases (see above: O2, N2O, He,
Xe) are entered to the sensor.

Effects of Humidity or Condensate

The airway adapter windows are indirectly heated via the sensor to prevent moisture condensation. While by sensor design the effect
of water droplets spilled onto the airway adapter windows and of contamination, as long as still some measurement light passes
the airway adapter windows, is largely compensated for, water droplets and other window contamination may slightly influence
measurement bias, up to 0.3 Vol.% approximately at 5 Vol.% CO2 (normally much less). Precision, of course, worsens if less light
passes (i.e., noise of reading gets higher). After some time, water droplets are heated away.
If measurement light is blocked such that noise of reading gets unacceptably high, an error message is sent from the CO2 sensor
indicating that the airway adapter has to be checked (cleaned or replaced).
14 | Vista 120

Technical Data

BIS

Technique Bispectral Index, Power Spectrum Analysis

Measure parameters Primary parameter BIS 0 to 100
Secondary parameters SQI 0% to 100%
SR 0% to 100%
EMG 30 dB to 80 dB
SEF 0.5 Hz to 30.0 Hz
TP 40 dB to 100 dB
BC (only applicable to BIS™ 0 to 30
extend sensor)
Sweep speed 6.25 mm/s, 12.5 mm/s, 25 mm/s, 50 mm/s
Wave scale 50 μv, 100 μv, 200 μv, 500 μv
BIS trend Length of BIS trend: 6 min, 12 min, 30 min, 60 min
Smoothing rate 10 s, 15 s, 30 s
Noise (EEG waveform) < 0.3 μV (0.25 Hz ~ 50 Hz)
EEG bandwidth 0.25 Hz ~ 50 Hz
BIS alarm range 0 ~ 100

C.O.
Measure parameters C.O., TB, TI
Measurement method Thermodilution technique

Measuring Range
C.O. 0.1 l/min ~ 20 l/min
TB 23°C ~ 43°C
TI -1°C ~ 27°C

Resolution
C.O. 0.1 l/min
TB, TI 0.1°C (+0.1°F)

Accuracy
C.O. ±5% or 0.2 l/min, whichever is greater
TB ±0.1°C (without sensor)
TI ±0.1°C (without sensor)

Trend review
Short 1 hr, 1 s. resolution
Long 150 hrs, 1 min. resolution
NIBP measurement data review 1200 sets
Alarm review 200 sets
Arrhythmia review 200 sets

NOTE
Regarding the AG specifications, refer to the Supplement Scio Four modules.

Wireless
IEEE 802.11 b/g/n
Frequency band 2.4 GHz ISM band
Modulation OFDM with BPSK, QPSK, 16-QAM, and 64-QAM 802.11 b with
CCK and DSSS
Typical transmit power (±2 dBm) 17 dBm for 802.11 b DSSS, 17 dBm for 802.11 b CCK, 15 dBm for
802.11 g/n OFDM
 Vista 120 | 15

Technical Data

Device Connectivity
Protocol Medibus/Medibus.X
Supported device Atlan, Fabius Plus/XL, Fabius GS Premium, Fabius Tiro,
Fabius MRI, Primus/IE, A500, Zeus IE, Evita V500, Evita VN500,
V300, Savina/300/Classic/Select, Babylog 8000 Plus,
Babylog VN500, Oxylog 3000 Plus

Recorder
Record width 48 mm (1.9 inch)
Paper width 50 mm
Paper speed 12.5, 25, 50 mm/s
Trace Up to 3 waveforms
Recording types ‒ Continuous real-time recording
‒ 8/20 seconds real-time recording
‒ Oxygenation calculation result recording
‒ Ventilation calculation result recording
‒ Renal function calculation result recording
‒ Trend graph recording
‒ Trend table recording
‒ NIBP review recording
‒ Arrhythmia review recording
‒ Alarm review recording
‒ C.O. measurement recording
‒ Frozen waveform recording
‒ Drug calculation titration recording
‒ Hemodynamic calculation result recording

Display Specifications
Display screen 380 mm (15 inch) color TFT
Resolution 1024 x 768
Maximum number of waveforms 13
Indicator LEDs 1 power, 2 alarm, 1 charge

Physical Specification
Size (H x W x D) (408±2) mm x (316±2) mm x (157±2) mm (12.4 x 16.1 x 6.2 inch)
Weight <7.0 kg (15.4 lbs)

Electrical Specification
Power supply 100 V – 240 V~, 50 Hz/60 Hz
Current 1.4 A-0.7 A
FUSE T 3.15 AH, 250 VP

Classification
Protection class Class I equipment and internal powered equipment
EMC type Class A
Degree of protection against electric shock CF: ECG (RESP), TEMP, IBP, C.O.
BF: SpO2, NIBP, CO2, AG, BIS
Liquid ingress protection IPX1
Mode of operation Continuous

Lithium-ion Battery (optional)

Quantity 1
Capacity 5,000 mAh
16 | Vista 120

Technical Data

Battery life ≥ 300 min (At 25±2°C, with (a) new fully charged battery/
batteries, continuous SpO2 measurement and NIBP automatic
measurement mode at interval of 15 minutes, Dräger ECG/TEMP
module connected, recording at interval of 10 minutes, brightness
set to “1”)
Battery charge time ≤ 390 min, 100% charge (monitor is on or in standby mode)
≤ 351 min, 90% charge (monitor is on or in standby mode)

Enviromental Requirements
The monitor may not meet the performance specifications given here if stored or used outside the specified temperature and humidity
ranges. When the monitor and related products have differing environmental specifications, the effective range for the combined
products is that range which is common to the specifications for all products.

Temperature Range
Operating 0 to 40°C (32 to 104°F)
Transport and storage -20 to 55°C (-4 to 131°F)

Relative Humidity
Operating 15% RH ~ 95% RH (non-condensing)
Transport and storage 15% RH ~ 95% RH (non-condensing)

Atmospheric Pressure
Operating 86 kPa ~ 106 kPa
Transport and storage 70 kPa ~ 106 kPa

Standards
IEC 60601-1: 2005+A1 :2012; IEC 60601-1-2: 2007; EN 60601-1: 2006+A1 :2013; EN 60601-1-2: 2007; IEC 60601-2-49: 2011
The Vista 120 monitors comply with the Medical Device Directive (MDD) 93/42/EEC.

Vista 120 MS34008 MS34010 MS34009 MS34011

3/5 lead ECG X X X X
Proprietary SpO2 X X
Nellcor SpO2 X X
NBP X X X X
Dual temps X X X X
3IBP X X
CO X X
etCO2 X X
BISx X X
Built-in recorder X X X
Gas bench X X X X
LAN X X X X
Wireless X X X X
Vista 120 monitors are available in select markets only.
For availability in your area, please contact the appropriate Dräger office from those listed below.
 Vista 120 | 17

Notes
18 | Vista 120

Notes

91 05 981 | 20.06-3 | HQ | PP | Subject to modifications | © 2020 Drägerwerk AG & Co. KGaA

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in which this material is released. Go to www.draeger.com/trademarks to find the current status.

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Drägerwerk AG & Co. KGaA Drägerwerk AG & Co. KGaA Draeger Singapore Pte. Ltd.
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Fax +49 451 882 2080 Tel: +65 6872 9288
[email protected] Fax: +65 6259 0398
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Manufacturer: REGION MIDDLE EAST, AFRICA .
Drägerwerk AG & Co. KGaA Drägerwerk AG & Co. KGaA REGION CENTRAL AND
Moislinger Allee 53-55 Branch Office SOUTH AMERICA
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