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N19 N22 Physical Specifications

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0% found this document useful (0 votes)
43 views5 pages

N19 N22 Physical Specifications

Uploaded by

ljj19951685419
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
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You are on page 1/ 5

BeneVision N19/N22 PAT I E N T M O N I TO R S

Performance Specifications

Display
Type: Medical-grade color TFT LCD, capacitive touchscreen, support
multi-touch operation
Rotatable screen (landscape and portrait)
Resolution: 1680 x 1050 pixels
Screen:
N22: 22-inch, 178° viewing angle
N19: 19-inch, 170° viewing angle
Waveforms: Up to 16 waveforms (portrait)
Up to 13 waveforms (landscape)
ECG (3, 5, 6, 12-lead)
Leads: I, II, III, aVR, aVL, aVF, V1-V6
Sweep Speed: 6.25 mm/s, 12.5 mm/s, 25 mm/s, 50 mm/s
Gain Selection: x 0.125, x 0.25, x 0.5, x 1, x 2, x 4, auto
Input Signal Range: ±8 mV (p-p) Arrhythmia Analysis
Electrode Offset Patient: Adult/Pediatric
Potential Tolerance: ±500 mV
Monitored Arrhythmias: Asystole, V-Fib/V-Tach, V-Tach, Vent Brady, Extreme Tachy,
Bandwidth
Extreme Brady, Vent Rhythm, PVCs/min, Pauses/min, Couplet,
Diagnostic Mode: 0.05 to 150 Hz Bigeminy, Trigeminy, R on T, Run PVCs, PVC, Tachy, Brady,
Monitor Mode: 0.5 to 40 Hz Missed Beats, Pacer Not Pacing, Pacer Not Capture, Multiform
Surgical Mode: 1 to 20 Hz PVC, Nonsus V-Tach, Pause, Irr Rhythm, A-Fib, SVT, SVCs/min
ST Mode: 0.05 to 40 Hz ST Segment Analysis
High Freq Cut-off (for Patient: Adult/Pediatric
12-lead ECG analysis): 350 Hz, 150 Hz, 35 Hz, 20 Hz selectable
Range: - 2.0 to + 2.0 mV (RTI)
Defibrillator Protection: Withstand 5000 VAC/50 Hz voltage in isolation against
Accuracy: -0.8 to +0.8 mV: ±0.02 mV or ±10%, whichever is greater
electrosurgical interference and defibrillation
Beyond this range: not specified
Recovery Time: ≤5 s
Resolution: 0.01 mV
CMRR ST Adjust Scale: 40 ms after J points, 60 ms after J point (default), 80 ms after
Diagnostic: >90 dB J point and 60/80 ms after J point (80 ms when HR 120 bpm
Monitor, Surgical, or less; 60 ms when HR above 120 bpm)
ST Mode: >105 dB (with notch filter on) ISO Adjust Scale: 4-200 ms before R-Wave (default: 80 ms),
ESU Recovery Time: ≤10 s Step: 4 ms
Heart Rate Meter J Point Adjust Scale: 4-200 ms after R-Wave (default: 48 ms),
Measurement Range Step: 4 ms
Adult: 15 to 300 bpm QT Analysis
Pediatric/Neonate: 15 to 350 bpm Patient: Adult/Pediatric/Neonate
Accuracy: ±1 bpm or ±1 %, whichever is greater. Parameters: QT, QTc, ΔQTc
Resolution: 1 bpm QTc Formula: Bazett, Fridericia, Framingham, or Hodges
Tall T-wave Rejection: When the test is performed based on Clause 201.12.1.101.17 Range:
of ANSI/AAMI/IEC 60601-2-27: 2011, the heart rate calculation QT/QTc: 200 to 800 ms
is not affected for QRS of 1 mV amplitude and 100 ms
duration, T-wave duration of 180 ms and amplitude lower QT-HR: Adult: 15 to 150 bpm
than 1.2 mV, and QT interval of 350 ms. Pediatric/Neonate: 15 to 180 bpm
QT Accuracy: ±30 ms
Pace Pulse
Resolution: QT 4 ms; QTc 1 ms
Pulse Indicator: Pace pulses meeting the following conditions are labelled
with a PACE marker: Respiration
Amplitude: ±2 to ±700 mV Range:
Width: 0.1 to 2 ms Adult: 0 to 120 bpm
Rise Time: 10 to 100 μs (without overshoot) Pediatric/Neonate: 0 to 150 bpm
Pace Pulse Rejection: When tested in accordance with the ANSI/AAMI/ Resolution: 1 rpm
IEC 60601-2-27: 2011: 201.12.1.101.13, the heart rate Apnea Alarm Time: 10, 15, 20, 25, 30, 35, 40 s
meter rejects all pulses meeting the following conditions. Accuracy:
Amplitude: ±2 to ±700 mV 7 - 150 rpm: ±2 rpm or ±2 % (whichever is greater)
Width: 0.1 to 2 ms 0 - 6 rpm: Not specified
Rise Time: 10 to 100 μs (without overshoot) Lead: I, II, or auto (default: lead II)
Sweep Speed: 3 mm/s, 6.25 mm/s, 12.5 mm/s, 25 mm/s, 50 mm/s

Page 1 of 5
BeneVision N19/N22 PAT I E N T M O N I TO R S

Performance Specifications

Pulse Oximetry Temperature


With Masimo SET® SpO2 Method: Thermal resistance
Range: 1 to 100 % Channels: Up to 8 channels
Resolution: 1% Units of Measure: Selectable °C or °F
Accuracy: ±2 %(70 to 100 %, Adult/Pediatric, non- motion) Range: 0 to 50°C / 32 to 122°F
±3 % (70 to 100 %, motion) Resolution: 0.1°C, 0.1°F
±3 % (70 to 100 %, Neonate, non-motion) Accuracy: ±0.1°C or ±0.2°F (without probe)
0 to 69 % unspecified IBP
Dual-SpO2: Yes, SpO2, SpO2b, ΔSpO2 Number: Up to 8 channels
Pulse Rate Range: 25 to 240 bpm Measurement Range: -50 to 300 mmHg
Pulse Rate Accuracy: ±3 bpm (non- motion) Resolution: 1 mmHg
±5 bpm (motion) Accuracy: ±1 mmHg or ±2 %, whichever is greater (excluding sensor
With Nellcor SpO2 error)
Range: 0 to 100 % Zero Offset Range: ±200 mmHg
Resolution: 1% Excitation: 5V DC, ±2 %
Accuracy: ±2 % (70 to 100 %, Adult/Pediatric) Sensitivity: 5 μV/V/mmHg
±3 % (70 to 100 %, Neonate) Impedance Range: 300 to 3000 Ω
Unspecified (0 to 69 %) PPV Range: 0 to 50 %
Dual-SpO2: Yes, SpO2, SpO2b, ΔSpO2 PAWP: Yes
Pulse Rate Range: 20 to 300 bpm Pulse Rate Range: 25 to 350 bpm
Pulse Rate Accuracy: ±3 bpm (20 - 250 bpm) Pulse Rate Accuracy: ±1 bpm or ±1 %, whichever is greater
Unspecified (251 - 300 bpm)
Sidestream CO2
Refresh Rate: 1s
Measurement Range
Non-Invasive Blood Pressure etCO2: 0 to 150 mmHg
Method: Oscillometry CO2 Accuracy:
Modes: Manual, Auto, STAT, Sequence 0 to 40 mmHg: ±2mmHg
Units of Measure: mmHg, kPa (user-selectable) 41 to 76 mmHg: ±5 % of reading
Resolution: 1 mmHg 77 to 99 mmHg: ±10 % of reading
Systolic Range: 100 to 150 mmHg: ±(3 mmHg+8 % of reading)
Adult: 25 to 290 mmHg Resolution:
Pediatric: 25 to 240 mmHg etCO2: 1 mmHg
Neonate: 25 to 140 mmHg Sample Flow Rate:
Diastolic range: Adult/Pediatric: 120 ml/min
Adult: 10 to 250 mmHg Neonate: 70 ml/min or 90 ml/min
Pediatric: 10 to 200 mmHg Sample Flow Rate Tolerance:
Neonate: 10 to 115 mmHg ±15 ml/min or ±15 %, whichever is greater
Mean range: Warm-up Time: 90 s (maximum), 20 s (typically)
Adult: 15 to 260 mmHg Measured with a Neonatal watertrap and 2.5-meter Neonatal sampling line, or an
Pediatric: 15 to 215 mmHg Adult watertrap and a 2.5-meter Adult sampling line:
Neonate: 15 to 125 mmHg Rise Time
Accuracy: etCO2: ≤250 ms @ 70 ml/min (Neonate watertrap)
Max Mean Error: ±5 mmHg ≤250 ms @ 90 ml/min (Neonate watertrap)
Max Standard ≤300 ms @ 120 ml/min (Adult watertrap)
Deviation: 8 mmHg Sampling Delay Time
Cuff Deflation Technique: Step bleed etCO2: ≤5.0 s @ 70 ml/min (Neonate watertrap)
Initial Cuff Inflation: ≤4.5 s @ 90 ml/min (Neonate watertrap)
Adult: 80 to 280 mmHg (default: 160 mmHg) ≤5.0 s @ 120 ml/min (Adult watertrap)
Pediatric: 80 to 210 mmHg (default: 140 mmHg) awRR Range: 0 to 150 rpm
Neonate: 60 to 140 mmHg (default: 90 mmHg) awRR Accuracy:
Over Pressure Protection: 0 to 60 rpm: ±1 rpm
Adult/Pediatric: 297 ±3 mmHg 61 to 150 rpm: ±2 rpm
Neonate: 147 ±3 mmHg Apnea Alarm Time: 10, 15, 20, 25, 30, 35, 40 s
Max Measurement Time:
Anesthesia Gases
Adult/Pediatric: 180 s
Sampling Rate
Neonate: 90 s
Adult/Pediatric: 200 ml/min
Assisting Venous
Puncture: Yes Neonate: 120 ml/min
Pulse Rate Range: 30 to 300 bpm Sampling Rate Tolerance: ±10 ml/min or ±10 %, whichever is greater.
Pulse Rate Accuracy: ±3 bpm or ±3 %, whichever is greater

Page 2 of 5
BeneVision N19/N22 PAT I E N T M O N I TO R S

Performance Specifications

Anesthesia Gases (continued) N2O: ≤4.2 s


Sampling Delay Time: <4 s O2: ≤4 s
Refresh Rate: 1s Enf /Iso/Hal/Sev/Des: ≤4.4 s
Warm-up Time: 45 s to warm-up status Sampling flow 200ml/min, using Adult/Pediatric DRYLINE II™ watertrap and an Adult
10 min to ready-to-measure status 2.5m sampling line:
Measurement Range CO2: ≤4.2 s
CO2: 0 to 30 % N2O: ≤4.3 s
N2O: 0 to 100 % O2: ≤4 s
Des/Sev/Enf/Iso/Hal: 0 to 30 % Enf/Iso/Hal/Sev/Des: ≤4.5 s
O2: 0 to 100 % Apnea Alarm time: 10, 15, 20, 25, 30, 35, 40 s
awRR: 2 to 100 rpm Oridion Microstream CO2
Resolution Measurement Range: 0 to 99 mmHg
CO2: 0.1 % Resolution: 1 mmHg
N2O: 1% Accuracy:
Des/Sev/Enf/Iso/Hal: 0.1 % 0 to 38 mmHg: ±2 mmHg
O2: 1% 39 to 99 mmHg: ±5 % +0.08 % of the reading –38 mmHg
awRR: 1 rpm Sample Flow Rate: 50 (-7.5 +15) ml/min
Full Accuracy Start-up Time: = 180 s max
Gases Range (%REL) Accuracy (%ABS) Auto-Zeroing Interval: At start-up, and every 12 hrs thereafter
Cc: 0 to 1 % ±0.1 % awRR Range: 0 to 150 rpm
1 to 5 % ±0.2 % awRR Accuracy:
5 to 7 % ±0.3 % 0 to 70 rpm: ±1 rpm
7 to 10 % ±0.5 % 71 to 120 rpm: ±2 rpm
>10 % Not specified 121 to 150 rpm: ±3 rpm
N2O: 0 to 20 % ±2 % Apnea Alarm Time: 10, 15, 20, 25, 30, 35, 40 s
20 to 100 % ±3 % Cardiac Output
Des: 0 to 1 % ±0.15 % Method: Thermodilution
1 to 5 % ±0.2 % Measurement Range: 0.1 - 20 L/min
5 to 10 % ±0.4 % Resolution: 0.1 L/min
10 to 15 % ±0.6 % Accuracy: ±0.1 L/min or ±5 %, whichever is greater
15 to 18 % ±1 % Blood Temp Range: 23 to 43°C (73.4 to 109.4°F)
>18 % Not specified Blood Temp Accuracy: ±0.1°C (±0.2°F) (without sensor)
Sev: 0 to 1 % ±0.15 % Blood Temp Resolution: 0.1°C (0.2°F)
1 to 5 % ±0.2 %
5 to 8 % ±0.4 % Continuous Cardiac Output Interface
>8 % Not specified Measured Parameter: Consistent with CCO-related parameters outputted by
Edwards Lifescience Vigilance II®, Vigileo™, EV1000 or
Enf/Iso/Hal: 0 to 1 % ±0.15 % HemoSphere monitor
1 to 5 % ±0.2 %
>5 % Not specified FloTrac™ Specifications
O2: 0 to 25 % ±1 % Standard: Meets the requirements of IEC 60601-2-34: 2011
25 to 80 % ±2 % Measured Parameter Display Range Remark
80 to 100 % ±3 % CCO: 1.0 to 20.0 L/min
awRR: 2 to 60 rpm ±1 rpm Reproductibility1: ±6% or 0.1 L/min, whichever is greater
>60 rpm Not specified CCI: 0.0 to 20.0 L/min/m2 /
Rise Time SV: 0 to 300 mL/b /
Sampling flow 120 ml/min, using the Neonatal DRYLINE II™ watertrap and a Neonatal SVI: 0 to 200 mL/b/m2 /
2.5m sampling line: SVR: 0 to 5000 dyne-s/cm5 /
CO2/N2O: ≤250 ms SVRI: 0 to 9950 dyne-s-m2/cm5 /
Iso/Hal/Sev/Des: ≤300 ms SVV: 0 to 99% /
Enf: ≤350 ms PPV: 0 to 99% /
O2: ≤600 ms Blood pressure 2 live
Sampling flow 200ml/min, using Adult/Pediatric DRYLINE II™ watertrap and an Adult pressure: -34 to 312 mmHg
2.5m sampling line: MAP/DIA/SYS: 0-300 mmHg
CO2/N2O: ≤250 ms Accuracy: ±4% or ±4 mm Hg, whichever is greater, from -30 mmHg to
Iso/Hal/Sev/Des: ≤300 ms 300 mmHg
Enf: ≤350 ms PR: 0 to 220 bpm Accuracy 3: Arms ≤3 bpm
O2: ≤500 ms 1Coefficient of variation: measured using electronically generated data.
2 Parameter specifications compliant with IEC 60601-2-34. Testing performed under
Sampling Delay Time
laboratory conditions.
Sampling flow 120 ml/min, using the Neonatal DRYLINE II™ watertrap and a Neonatal
3 Accuracy tested under laboratory conditions.
2.5m sampling line:
CO2: ≤4 s

Page 3 of 5
BeneVision N19/N22 PAT I E N T M O N I TO R S

Performance Specifications

ScvO2 Delta, Theta, Alpha, Beta: 0 to 100% / 1%


Range: 0 to 99 % Alpha/Delta (for EEG-1/
Accuracy: ±3 % (50 to 80 %) aEEG module): 0 to 99 (invalid if Delta is 0%) / 0.1

rSO2 iView
Patient: Weight greated than 2.5 kg CPU: Intel Pentium N4200 2.5 GHz
Method: INVOS, NIRS (Near Infrared Spectroscopy) Memory: 8 GB
Number: Up to 4 channels Hard-disk: mSATA SSD 128 GB
Measurement Range: 15 to 95 % OS: Windows 10

BIS Recorder
Standard: Meets the standard of IEC 60601-2-26: 2012 Type: Thermal array
Technique: Bispectral index Speed: 25 mm/s, 50 mm/s
Measured Parameters: EEG Trace: Up to 3
BIS, BIS L, BIS R: 0 to 100 Data Storage
Calculated Parameters: SQI, SQI L, SQI R: 0 to 100% Trends Data: >120 hrs @ 1min, 4 hrs @ 5 s
EMG, EMG L, EMG R: 0 to 100 dB Events: 1000 events, including parameter alarms, arrhythmia events,
SR, SR L, SR R: 0 to 100% technical alarms, and so on
SEF, SEF L, SEF R: 0.5 to 30.0 Hz NIBP: 1000 sets
TP, TP L, TP R: 40 to 100 dB Interpretation of Resting
BC, BC L, BC R: 0 to 30 12-lead ECG Results: 20 sets
sBIS L, sBIS R: 0 to 10.0 Full Disclosure: Up to 48 hrs
sEMG L, sEMG R: 0 to 10.0 OxyCRG: 48 hrs
ASYM: 0 to 100% ST Review: 120 hrs @1 min
Impedance Range: 0 to 999 kΩ Wi-Fi Communications
Sweep Speed: 6.25 mm/s, 12.5 mm/s, 25 mm/s or 50 mm/s, ±10% error Protocol: IEEE 802.11a/b/g/n
Input Impedance: >5 MΩ Modulation Mode: DSSS and OFDM
Noise (RTI): <0.3 μV (0.25 to 50 Hz) Operating Frequency
Input Signal Range: ±1 mV IEEE 802.11b/g/n (2.4G):
EEG Bandwidth: <0.25 to 100 Hz FCC: 2.4 to 2.483 GHz
Patient Leakage Current: <10 μA MIC: 2.4 to 2.495 GHz
Alarm Limit IEEE 802.11a/n (5G):
BIS High Range: (low limit + 5) to 100 Step: 5 FCC: 5.15 to 5.35 GHz, 5.725 to 5.82 GHz
BIS Low Range: 0 to (high limit - 5) Step: 5 MIC: 5.15 to 5.35 GHz
Channel Spacing: 5 MHz @ 2.4 GHz, 20 MHz @ 5 GHz
NMT
Wireless Baud Rate: IEEE 802.11a: 6 to 54 Mbps
Sensor Type: Acceleromyography sensor
IEEE 802.11b: 1 to 11 Mbps
Stimulation Modes: ST, TOF, PTC, DBS3.2, DBS3.3
IEEE 802.11g: 6 to 54 Mbps
Stimulation Current
Range: 0 to 60 mA IEEE 802.11n: 6.5 to 72.2 Mbps
Stimulation Current Output Power: <30 dBm (FCC requirement, detection mode - peak power)
Accuracy: ±5 % or ±2 mA, whichever is greater. Operating Mode: Infrastructure
Stimulation Pulse Width: 100, 200 or 300 μs, monophasic rectangle pulse Data Security: WPA-PSK, WPA2-PSK, WPA-Enterprise, WPA2-Enterprise
Stimulation Pulse Width (EAP-FAST, EAP-TLS, EAP-TTLS, PEAP-GTC, PEAP-MSCHAPv2,
Accuracy: ±10 % PEAP-TLS, LEAP)
Max. Output Voltage: 300 V Encryption: AES

EEG Auxiliary Output


EEG Channels: Up to 4 channels Standard: Meets the requirements of ANSI/AAMI/IEC 60601-1 for
short-circuit protection and leakage current
Bandwidth: 0.5 to 50 Hz (-3 dB)
ECG Analog Output
Input Signal Range: - 2 mVp-p to + 2mVp-p
Bandwidth (- 3 dB; reference frequency: 10 Hz)
Max. Input DC Offset: ±500 mV
Diagnostic Mode: 0.05 to 150 Hz
CMRR: ≥100 dB @51 kΩ imbalance and 60 Hz
Monitor Mode: 0.5 to 40 Hz
Noise Level: ≤0.5 μV rms (1 Hz to 30 Hz)
Surgical Mode: 1 to 20 Hz
Differential Input
Impedance: >15 MΩ @10 Hz ST Mode: 0.05 to 40 Hz
Electrode Impedance: QRS Delay: ≤25 ms (in diagnostic mode, and non-paced)
Range: 0 to 90 kΩ Sensitivity: 1 V/mV, ±5 %
Accurancy: ±1 kΩ or ±10 %, whichever is greater Pace Enhancement:
Measured Parameters: Measurement Range / Resolution Signal Amplitude: Voh ≥2.5 V
SEF, MF, PPF: 0.5 to 30 Hz / 0.5 Hz Pulse Width: 10 ms ±5 %
TP: 40 to 100 dB / 1 dB Signal Rising and
Falling Time: ≤100 μs
SR: 0 to 100% / 1%

Page 4 of 5
BeneVision N19/N22 PAT I E N T M O N I TO R S

Physical Specifications

Auxiliary Output (continued) Display, 22"


IBP Analog Output Dimension: 15.1" (H) x 22.3" (W) x 1.9" (D)
Bandwidth (-3 dB; reference frequency: 10 Hz) 0 to 40 Hz 38.3 cm (H) x 56.6 cm (W) x 4.8 cm (D)
Max. Transmission Delay: 30 ms Weight: 16.3 lb (7.4 kg) excluding handle
Sensitivity: 1 V/100 mmHg, ±5 % Main Unit
Dimension: 10.5" (H) x 10.5" (W) x 2.7" (D)
Interfacing 26.8 cm (H) x 26.8 cm (W) x 6.8 cm (D)
Main Unit: 1 AC Power Connector
2 RJ45 Network Connector, 100 Base-TX, IEEE 802.3 Weight: 7.5 lb (3.4 kg) including battery
6 USB 2.0 Connector Environmental
3 Nonstandard USB SMR Connector Operating Temperature:
1 VP Connector, VP1 for the secondary display 0°C to 40°C Main unit, MPM module, individual module of SpO2, TEMP, IBP,
1 BNC Connector CO, CCO/SvO2, NMT, EEG, and BeneLink, recorder
1 Equipotential Grounding Terminal 0°C to 40°C Microstream CO2 module
Modular iView: 1 VP Connector, VP2 5°C to 40°C Sidestream CO2 module
4 USB 2.0 Connector 10°C to 40°C AG module, ScvO2 module
1 RJ45 Network Connector, 100 Base-TX, IEEE 802.3 16°C to 32°C rSO2 module
Multifunction Connector for Defib Sync and Analog Output 10°C to 32.5°C FloTrac module
1 on multi-parameter module Storage Temperature:
Barcode Scanner: Support 1D and 2D barcode -20°C to 60°C Main unit, MPM module, individual module of SpO2, TEMP, IBP,
Keyboard and Mouse: Support wire and wireless type CO, CCO/SvO2, ScvO2, NMT, AG, Microstream/Sidestream CO2,
EEG, and BeneLink, recorder
Remote Control: Support
-20°C to 70°C rSO2 module
Network Printer: Support
-18°C to 45°C FloTrac module
Battery Operating Humidity:
Type: Rechargeable lithium-ion 15 to 95 %
Number of Battery: 1 (non condensing): Main unit, MPM module, individual module of SpO2, TEMP, IBP,
Capacity: 5600 mAh, 11.3 VDC CO, CCO/SvO2, NMT, AG, Microstream/Sidestream CO2, EEG,
Run Time: >1 hrs and BeneLink, recorder
When powered by a new fully-charged battery at 25 ºC±5 ºC 15 to 75 %
with 12-lead ECG , Resp, SpO2, 4-ch IBP, 2-ch Temp, CO2, C.O. (non condensing): ScvO2 module
and NIBP measurements every 15 min, WiFi enabled, and 20 to 80 %
screen brightness set to default 5 (non condensing): rSO2 module
Recharge Time: 5 hrs to 90 % when the monitor is off 20 to 90 %
(non condensing): FloTrac module
Physical BeneVision N19
Storage Humidity:
Main Unit and Primary Display Installed Together with Handle 10 to 95 %
Dimension (horizontal): 16.6" (H) x 20.0" (W) x 4.5" (D) (non condensing): Main unit, MPM module, individual module of SpO2, TEMP, IBP,
42.3 cm (H) x 50.9 cm (W) x 11.5 cm (D) CO, CCO/SvO2, ScvO2, NMT, AG, Microstream/Sidestream CO2,
Dimension (vertical): 23.0" (H) x 13.7" (W) x 4.5" (D) EEG, and BeneLink, recorder
58.4 cm (H) x 34.8 cm (W) x 11.5 cm (D) 10 to 90 %
Weight: 22.7 lb (10.3 kg) including battery, iView module, WiFi module, (non condensing): ScvO2 module
display with handle and navigation knob 20 to 90 %
Display, 19" (non condensing): FloTrac module
Dimension: 13.7" (H) x 20.0" (W) x 1.9" (D) Operating Atmospheric Pressure:
34.8 cm (H) x 50.9 cm (W) x 4.8 cm (D) 427.5 to 805.5 mmHg Main unit, MPM module, individual module of SpO2, TEMP, IBP,
Weight: 13.7 lb (6.2 kg) excluding handle CO, CCO/SvO2, ScvO2, NMT, EEG, and BeneLink, recorder
Main Unit 430 to 790 mmHg Microstream/Sidestream CO2 module
Dimension: 10.5" (H) x 10.5" (W) x 2.7" (D) 525 to 805.5 mmHg AG module, and rSO2 module
26.8 cm (H) x 26.8 cm (W) x 6.8 cm (D) 522.8 to 759.8 mmHg FloTrac module
Weight: 7.5 lb (3.4 kg) including battery
Safety
Physical BeneVision N22 Type of Protection: Class I
Main Unit and Primary Display Installed Together Degree of Protection: MPM/IBP/C.O./NMT/EEG module: CF
Dimension (horizontal): 18.0" (H) x 22.3" (W) x 4.5" (D) ScvO2/CO2/AG/rSO2 module: BF
45.8 cm (H) x 56.6 cm (W) x 11.5 cm (D) Protection Against
Dimension (vertical): 25.2" (H) x 15.0" (W) x 4.5" (D) Ingress of Fluids: IPX1
64.1 cm (H) x 38.3 cm (W) x 11.5 cm (D)
Power Requirements
Weight: 25.3 lb (11.5 kg) including battery, iView module, WiFi module,
AC Voltage: 100 to 240 VAC (±10 %)
display with handle and navigation knob
Current: 2.8 to1.6 A
Frequency: 50 Hz/60 Hz (±3 Hz)
Fuse: Time-lag 250 V T4A
Page 5 of 5

Mindray DS USA, Inc.


800 MacArthur Blvd., Mahwah, NJ 07430
Tel: 800.288.2121 Tel: 201.995.8000 Fax: 800.926.4275 www.mindray.com
©2023 Mindray DS USA, Inc.
Mindray® is a registered trademark of Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights reserved.
All brands and product names are trademarks of their respective owners. Specifications subject to change without notice.
Contact your Mindray Representative for the most current information. 08/23 P/N: 0002-08-8102 Rev 1.0

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