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B40i Spec Modules ENG

B40I - TECHNICAL SPECIFICATIONS

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

B40i Spec Modules ENG

B40I - TECHNICAL SPECIFICATIONS

Uploaded by

Bui Paul
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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B40i Patient Monitor

Affordable clinical excellence


Patients with acute, life-threatening conditions need the best possible care. The B40i Monitor from GE Healthcare provides
a continuous flow of quality information to enhance clinical decision-making for adult, pediatric and neonatal1 patients in
various care areas.

Advanced clinical parameters Ease of use for fast decision-making


The B40i Monitor is designed with advanced measurement The B40i Monitor makes it easy to acquire accurate patient
technologies for accurate and reliable patient monitoring: data to support timely decision-making:

•• EK-Pro arrhythmia analysis •• 12.1’’ crystal-clear monitor displays up to six


•• DINAMAP* SuperSTAT non-invasive blood pressure waveforms simultaneously

•• TruSignal* enhanced SpO2 saturation monitoring other op- •• Intuitive menus and one-button access to
tions available: Nellcor® OxiMax® SpO2 and Masimo® SET® commonly used functions
SpO2 algorithms •• 72-hour trend display with graphical and numerical data to
•• Datex-Ohmeda* gas technology to support non-invasive review patient progress
monitoring in anesthesia and critical care areas •• HL7 direct output and connectivity with the CARESCAPE*
•• Entropy* monitoring that provides information on the pa- Gateway enables communications to EMR systems
tient’s central nervous system during general anesthesia •• Capability to work in CARESCAPE Network and S/5
•• Comprehensive package of neonatal1 measurements Network environments

Performance and reliability


With its streamlined design, the portable B40i Monitor fits into
crowded spaces and is easily moved to different care areas
as needed. The system’s rugged design stands up to harsh
environments and the everyday wear-and-tear of busy care
areas. It will provide the performance and accuracy that you
expect of GE equipment–so you can provide the care that
your patients expect.

 40i Patient Monitor is not cleared, approved or authorized by the US FDA or other US national regulatory authorities
B
for commercial availability.
1
Impedance respiration is intended for use with only adult and pediatric patients in United States, Guam, Puerto Rico,
Saint Croix, Saint Thomas and Canada. CO2 measurement through E-miniC Module is intended for use with patients
weighing over 5kg (11 lb) only. Entropy is intended for use with adult and pediatric patients older than 2 years.
Technical specifications Arrhythmia analysis  systole, bradycardia, tachy-
A
cardia, ventricular fibrillation,
Display
ventricular tachycardia
Size 12.1 in (diagonal) ST segment analysis Numeric range: -9 to +9 mm
Resolution 800 x 600 pixels (SVGA) (-0.9 to +0.9 mV)
Accuracy: -8 mm to +8 mm;
Number of traces Up to 6
±0.2 mm or ±10%, whichever
Display layout and colors User-configurable is greater
Controls T rim Knob* control and Numeric resolution: 0.1 mm
hard keys (standard) (0.01 mV)
ST Trends: Up to 72 h
Parameters and modules
Impedance respiration
Parameters Modules 2
Range Adult/pediatric: 4 to 120 resp/min
ECG Neonate1: 4 to 180 resp/min
Resp
Accuracy ±5% or ±5 resp/min, whichever
SpO2 Configured is greater
NIBP hemodynamic module Gain range 0.1 to 5 cm/Ohm
Temp SpO2
2 channel InvBP
GE TruSignal SpO2
Entropy E-Entropy2
Measurement range
Sidestream CO2 E-miniC2
Pulse oximetry 1 to 100%
Sidestream CO2, O2 and N2O E-sCO2
Pulse rate 30 to 250 bpm
Sidestream CO2, O2 agents E-sCAiO2
Measurement accuracy
and N20 N-CAiO2
Saturation Without motion-adult/pediatric
NOTE: The monitor also is compatible with the E-sCOV and E-sCAiOV modules with-
out Spirometry function.
Finger sensor: 70 to 100% ±2%
NOTE: When monitoring neonatal1 or other patients that have high respiration rate
Ear sensor: 70 to 100% ±3%
or low tidal volume, the E-sCO or E-sCAiO Modules shall be used within the limits of Without motion-neonate1:
respiration rates and tidal volumes to ensure specified measurement accuracy. 70 to 100% ±3%
ECG With motion-adult/pediatric/
neonate1: 70 to 100% ±3%
Leads available 3-lead configuration: I, II, III
Low perfusion-adult/pediatric:
5-lead configuration: I, II, III, aVR,
70 to 100% ±3%
aVL, aVF and V
(1~69% unspecified)
Sweep speed 12.5, 25 or 50mm/s
Pulse Rate  ithout motion: ±2 bpm
W
Gain range 0.2 to 5.0 cm/mV
(Adult/Pediatric/Neonatal1)
Heart rate accuracy 30 to 300 bpm, ±5% or ±5 bpm, With motion: ±3 bpm
whichever is greater (Adult/Pediatric/Neonatal1)
Bandwidth Low Perfusion: ±5 bpm
50/60 Hz power supply  onitor: 0.5 to 40 Hz
M (Adult/Pediatric)
ST: 0.05 to 40 Hz Nellcor OxiMax
Diagnostic: 0.05 to 150 Hz
Measurement range
Pacemaker detection Range: 2 to 700 mV
Pulse oximetry 1 to 100%
Pulse width: 0.5 to 2 ms
Pulse rate 20 to 250 bpm

Impedance respiration is intended for use with only adult and pediatric patients in United States, Guam, Puerto Rico, Saint Croix, Saint Thomas and Canada. CO2 measurement through
1

E-miniC Module is intended for use with patients weighing over 5kg (11 lb) only. Entropy is intended for use with adult and pediatric patients older than 2 years.

Refer to B40i User’s Guide for more information.


2
Measurement accuracy Invasive blood pressure
Saturation  dult: 70 to 100% ±2%
A Measurement range -40 to 320 mmHg (-5.3 to 42.7 kPa)
Neo: 70 to 100% ±3% Measurement accuracy ±5% or ±2 mmHg, whichever
Low perfusion: 70 to 100% ±2% is greater
Pulse Rate ±3 bpm Frequency response 4 to 22 Hz
Masimo SET Transducer sensitivity 5 μV/V/mmHg
Measurement range Temperature
Pulse oximetry 1 to 100% Numerical display T1, T2, T2-T1
Pulse rate 25 to 240 bpm Measurement range 10 to 45°C (50 to 113°F)
Measurement accuracy Measurement accuracy ±0.1°C without probe
Saturation  ithout motion-adult/pediatric:
W Display resolution ±0.1°C at 25 to 45°C with
70 to 100% ±2% reusable probes
Without motion-neonate1:
70 to 100% ±3% Probe  SI probes recommended by
Y
With motion-adult/pediatric/ GE Healthcare
neonate1: 70 to 100% ±3%
Networking
Low perfusion: 70 to 100% ±2%
(0~69% unspecified) Compatibility  ARESCAPE Network and
C
S/5 Network
Pulse rate  ithout motion: ±3 bpm
W
With motion: ±5 bpm Software version
NIBP VSP-B_1.20

Measurement technique Oscillometric with step deflation I/O connectors


Modes Manual, automatic and stat RS-232 computer serial output, Defibrillation synch, Nurse call

NIBP Measurement ranges Mounting


Systolic  dult/Pediatric: 30 to 290 mmHg
A GCX compatible
Neonate1: 30 to 140 mmHg Integrated carrying handle
MAP 
Adult/Pediatric: 20 to 260 mmHg Paper Recorder
Neonate : 20 to 125 mmHg
1
Method Thermal dot array
Diastolic  dult/Pediatric: 10 to 220 mmHg
A
Horizontal resolutions 24 dots/mm (600 dpi)
Neonate1: 10 to 110 mmHg
Vertical resolution 8 dots/mm (200 dpi)
Accuracy Meets AAMI SP10
Waveforms Selectable 1, 2, or 3 waveforms
Default initial  dult/Pediatric: 135 ±15 mmHg
A
inflation pressure Neonate1: 100 ±15 mmHg Numerics  R, SpO2, NIBP, IBP1, IBP2, ETCO2,
H
T1, T2, Resp, O2, AA
Maximum  dult/Pediatric: 2 min
A
determination time Neonate1: 85 s Tabular trend printout  R, NIBP, IBP1, IBP2, T1, T2, Et/
H
FiCO2, RR, Et/Fi O2, Et/Fi AA
Over pressure monitor  dult/Pediatric: 300 ±6 to
A
330 mmHg Graphical trend printout  R, ST, IBP1, IBP2, NIBP, SpO2, Pleth,
H
Neonate1: 150 ±3 to 165 mmHg CO2, N2O, O2, AA, Resp, T1+T2,
Entropy
Paper width 50 mm, printing width 48 mm
Paper speed 1, 6.25, 12.5, 25 mm/s
Printing
Network laser printer supported in S/5 network.

Impedance respiration is intended for use with only adult and pediatric patients in United States, Guam, Puerto Rico, Saint Croix, Saint Thomas and Canada. CO2 measurement through
1

E-miniC Module is intended for use with patients weighing over 5kg (11 lb) only. Entropy is intended for use with adult and pediatric patients older than 2 years.
Performance specifications Environmental specifications
Alarms Operating conditions
Priority High, Medium, Low and Message Temperature 5 to 40°C (41 to 104°F)
Notification Audible and visual Relative humidity 20 to 90% noncondensing
Setting Default and individual Atmospheric pressure  00 to 1060 hPa
7
(525 to 795 mmHg)
Visual alarm notification  ed, yellow, cyan
R
Audio silence message Storage and transport conditions
General alarm message -20 to 60°C (-4 to 140°F)
Temperature
Audio pause 2 min Relative humidity 10 to 90% noncondensing
Adjustment  entral alarm display and
C Atmospheric pressure  00 to 1060 hPa
7
adjustment page (525 to 795 mmHg)
Trending  0 min graphical trends referenced
1
to set alarm limits
Power specifications
Trends AC input 100 to 240V ±10%, 50/60 Hz, 150VA
Graphical  ll parameters, selectable time
A
scales from 20 min to 72 h Protection Class I
Numerical  ll parameters, every 5 min sam-
A Battery  xchangeable lithium-ion,
E
pling or after NIBP determination 2 pcs max
Snapshot  p to 10 snapshots Manual or
U Charging time 2 h per battery pack
alarm triggered Run time Up to 4.5 h
OCRG trend  eal time or snapshot Neonate
R
mode only
Physical specifications
Trend cursor In both graphical and Dimensions (H x W x D)  ithout extension rack:
W
numerical trends 31 x 31 x 16 cm (12.2 x 12.2 x 6.3 in)
Minitrends  or 30 min minitrends can be
5  ith extension rack:
W
displayed for a continuous 31 x 35 x 18 cm (12.2 x 13.8 x 7 in)
historical view <=7kg (15 lb)
Weight
Ingress protection IP21

Warranty
One year.

Certifications
IEC 60601-1 passed
CE marking according to Directive 93/42/ EEC

Impedance respiration is intended for use with only adult and pediatric patients in United States, Guam, Puerto Rico, Saint Croix, Saint Thomas and Canada. CO2 measurement through
1

E-miniC Module is intended for use with patients weighing over 5kg (11 lb) only. Entropy is intended for use with adult and pediatric patients older than 2 years.
About GE Healthcare © 2014 General Electric Company – All rights reserved.

GE Healthcare provides transformational medical  eneral Electric Company reserves the right to make
G
changes in specifications and features shown herein, or
technologies and services that are shaping a new age of discontinue the product described at any time without
notice or obligation. Contact your GE representative for
patient care. Our broad expertise in medical imaging and the most current information.
information technologies, medical diagnostics, patient T rademark of General Electric Company is the preferred
monitoring systems, drug discovery, biopharmaceutical form of trademark notice. This form of notice can be used
with registered and unregistered marks, and marks that
manufacturing technologies, performance improvement are the subject of a pending application.

and performance solutions services help our customers  E and the GE Monogram are trademarks of
G
the General Electric Company.
to deliver better care to more people around the world * Trademarks of General Electric Company.
at a lower cost. In addition, we partner with healthcare  asimo and SET are trademarks of Masimo Corporation.
M
leaders, striving to leverage the global policy change Nellcor and OxiMax are trademarks of Nellcor Puritan
Bennett, Inc.
necessary to implement a successful shift to sustainable
 eneral Electric Company, by and through its
G
healthcare systems. GE Healthcare division.

Our “healthymagination” vision for the future invites


the world to join us on our journey as we continuously
develop innovations focused on reducing costs,
increasing access and improving quality around the
world. Headquartered in the United Kingdom,
GE Healthcare is a unit of General Electric Company
(NYSE: GE). Worldwide, GE Healthcare employees are
committed to serving healthcare professionals and
their patients in more than 100 countries. For more
information about GE Healthcare, visit our website at
www.gehealthcare.com.

GE Healthcare Finland Oy
Kuortaneenkatu 2
00510 Helsinki, Finland
Europe

DOC1481839 rev2 2/14

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