Invivo Precess - achats

Transcription

Invivo Precess - achats
Invivo Precess
MRI Patient Monitoring Systems
Safer. Smarter. Invivo.
• Designed specifically for high
Don’t Settle For A Copy
Nothing is more important than the quality
of care you provide for your patients.
When you are conducting MRI studies with
critically ill patients, children or patients
who require sedation, errors or delays
are not an option. You need a monitoring
system you can depend on. Invivo has been
designing purpose-built MRI monitors with
industry leading MRI designs for over 20
years., which is why the Invivo Precess MRI
patient monitoring system is your clear
choice.
Specifically designed from the ground up
to withstand demanding environments
with strong magnetic fields, Precess
delivers quality results and increased
patient comfort and safety, and improved
efficiency and reliability.
magnetic field environments,
the Precess MRI patient monitor
operates at the 5,000 Gauss field
line and 4 W/Kg SAR regardless
of option configuration, without
compromising patient safety.
• Wireless ECG and SpO2 feature
shorter cables designed to increase
efficiency. Shorter cables also reduce
the risk of cable heating and are
less prone to damage, reducing
ownership costs.
Wireless technology
Improves Efficiency and
reduces downtime
Invivo’s industry-exclusive direct wireless
technology makes it easy to move the patient
from room to room, expediting patient
management and workflow in the MRI suite.
Sensor setup is fast and simple in the induction
area. Wireless ECG, SpO2 and respiration mean
fewer lines in the MR exam room creating
greater patient access.
• Wireless SpO2 monitoring uses digital
signaling and Invivo exclusive Quick
Connect sensors for precise saturation
values and fast acquisition, even for
difficult pediatric cases.
Remote monitoring allows you to continue
• Six-color waveform capability – two
ECG, SpO2, EtCO2 and two IBP –
provides an easy-to-see overview of
patient status. Anesthetic Agents,
continuous temperature and NIBP
values are easily readable on the large
12” (30.5 cm) displays*.
direct wireless technology increases flexibility
• The smart battery management
system provides a full eight hours of
life on a single charge for each wireless
module. The monitor displays the
remaining battery life for the base unit
and each module. A remote battery
charger charges up to four depleted
batteries at one time.
the risk of cable heating by reducing the
to track vital signs in the MR control room
without the need for extensive – and
expensive – wireless router networks. Invivo’s
allowing you to easily use Precess with
multiple MRI system environments.
Wireless technology helps increase patient
comfort and safety too. Shorter cables reduce
potential for creating loops and are less prone
to damage reducing replacement costs.
inspired by a better way
For more information about Invivo Precess MRI Patient Monitor
or any of the Complete Solution products from Invivo, please contact
your Invivo representative, or visit our web site at www.invivocorp.com.
Invivo Corporation
Orlando, FL, USA
International
T: 877-468-4861
T: +31 (0)499 378299
T: 407-275-3220
[email protected]
E: [email protected]
www.invivocorp.com
Invivo is a Philips company.
Products, services and technical specifications are subject to change without notice.
©2010 Invivo Corporation All Rights Reserved.
* Control Room Display (CRD) is not intended for use in the MR system room
Model Number: 3160
REF: 865323
Descriptif/Présentation détaillé de
l’équipement INVIVO Precess Blue
Le moniteur amagnétique INVIVO Precess est constitué d’un gros socle monté sur 4 roulettes avec un mat supportant
l’écran de visualisation des courbes et données patient avec système de pilotage et contrôle de l’ensemble des
fonctionnalités de l’équipement. Cet ensemble est totalement amagnétique. Il peut être positionné dans la salle d’IRM en
respectant la limite des 5000Gauss soit 0.5Tesla. En vérité, il peut être approché à moins de 50 cm de l’aimant principal.
L’écran de visualisation et contrôle/pilotage n’est pas amovible. Il est solidaire du socle à roulettes. Un deuxième écran
identique avec les mêmes boutons et fonctionnalités, non amagnétique, peut être placé à distance, à l’extérieur de la cage de
Faraday par exemple dans la salle de commande où se trouvent les manipulateurs radio.
La communication entre ces 2 appareils (bidirectionnelle) se fait par communication radio de type WIFI (dans la bande de
fréquence des 2.4 GHz), et ce malgré la cage de Faraday, sans aucun problème.
L’ensemble du système monté sur chariot à roulette est totalement amagnétique. Il a été testé et validé par
l’ensemble des fabriquants d’IRM tant pour des IRM 1.5T que 3T. Il fonctionne sans problème dans la limite de la
courbe des 5000 Gauss ou 0.5 Tesla et il ne perturbe pas le fonctionnement de l’IRM. C’est à dire que l’on peut
approcher l’équipement complet à moins de 50cms de l’aimant.
L’ensemble de l’équipement fonctionne sur batteries ou sur secteur. Le bloc Alim/Chargeur batteries peut être entré dans la
salle d’IRM, mais il doit être maintenu à une distance minimum de 3m de l’aimant. Il est livré avec un câble de
raccordement largement assez long.
Les batteries sont amovibles et interchangeables. Elles offrent une autonomie supérieure à 8H de fonctionnement sans
devoir utiliser le secteur. L’autonomie résiduelle de l’ensemble des batteries du système est affichée en permanence au bas
de l’écran.
Concernant l’acquisition de l’ECG, la respiration et la SPO2, il n’y a aucune liaison filaire entre le patient et l’équipement.
Le patient est connecté au travers des électrodes pour l’ECG, d’un capteur pour la SPO2 et la respiration à des boîtiers de
télémétrie grâce à des câbles d’environ 50cms. Ces boîtiers de télémétrie peuvent être placés sans aucun souci au centre de
l’aimant. La transmission des signaux du patient entre les boîtiers de télémétrie et le socle à roulette qui contient toute
l’électronique de traitement du signal se fait, là aussi, par liaison radio.
Le gros avantage de ce système c’est de ne pas avoir des tas de fils qui traînent autour du patient et peuvent gêner les
manipulateurs ou anesthésistes ou autre intervenants en cas de problème grave du patient nécessitant de l’urgence.
Et n’oublions pas que si le patient est sous anesthésie ou inconscient, il n’est pas rare que les situations deviennent
critiques. Et dans ce cas, la facilité d’accès au patient est très appréciée, d’autant plus que vous continuez à monitorer votre
patient car vous ne risquez pas de vous entraver et débrancher des câbles. Donc très gros avantage d’un point de vue
médico-légal.
Les seuls liens qui subsistent entre le patient et le socle, c’est la tubulure PNI, ainsi que la tubulure de prélèvement des gaz
dans le cas de l’utilisation des options EtCO2 ou Gaz Halogénés. En effet ces paramètres nécessitent une pompe soit pour
gonfler le brassard soit pour prélever des gaz expirés par le patient et qui dit pompe dit moteur électrique donc perturbation
du champ magnétique s’ils étaient intégrés dans des boîtiers de télémétrie.
Comme vous pouvez le constater à la lecture de cette brève présentation, l’équipement a été spécialement étudié pour être
très facile d’utilisation pour le personnel du service et lui permettre de le manipuler en le déplaçant si besoin à l’extérieur
de l’IRM très aisément.
Il reste très convivial et tout à fait comparable à un moniteur classique du marché en ce qui concerne la manipulation
normale.
Durant l’examen, à partir de l’écran déporté qui se trouve à l’extérieur de l’IRM, vous pouvez à tout instant modifier tous
les réglages classiques du moniteur (Limites d’alarmes, amplitude, changement de dérivations, filtres, déclenchement d’un
enregistrement papier, arrêt d’alarme, etc……).Vous êtes en présence d’un moniteur normal vous permettant de surveiller
votre patient durant tout l’examen de l’extérieur de la salle sans jamais avoir à accéder à l’intérieur de l’IRM.
Les gros plus de notre machine, c’est le fait de ne pas avoir de liaison filaire entre la partie à l’intérieur de l’IRM et la partie
commande/visualisation placée à l’extérieur d’où une liberté totale de mouvement ou déplacement par exemple pour un
hôpital qui possède un service avec 2 salles d’IRM ou pour accompagner le patient durant la phase de préexamen ou de
réveil dans une pièce du service attenante.
Invivo
Precess
Technical Data Sheet
(model 3160)
MRI Patient Monitoring System
The Precess MRI Patient Monitoring System is designed to
assist clinicians in monitoring patient vital signs in the
dynamic magnetic resonance environment. The Precess
system combines wireless communication, radio frequency
(RF) shielding, digital signal processing (DSP), to address
the challenges associated with patient monitoring in the
MR environment. The Precess system provides accurate,
continuous, and reliable performance during MRI
applications in a cost efficient package.
The Precess MRI Patient Monitoring System consists of the
following primary components:
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The Precess System can be ordered to suit the specific
needs of the MR team
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Cart with Integral LCD Display
Integral DC power supply
Non-invasive blood pressure (NIBP)
Optional Components
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Control Room Display (CRD)
Wireless ECG (WECG) Module
Wireless SpO2 (WSpO2) Module
Wireless Module Battery Charger
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Features and Benefits
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Integral color LCD display
Intuitive graphical user interface
Colored waves and large numeric’s
Portable-8 hour battery
CRD recorder (optional)
Wireless remote recording to CRD (optional)
Simultaneous display of up to eight parameters,
six waveforms, and associated values from each
waveform
Visual displayed and audible alarm signals, pulse
tone, and system status messages
All patient information is displayed on the
integral display
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Main Components
Cart Display (integral display)
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System Parameters Included
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Non-invasive blood pressure (NIBP)
Optional System Parameters
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Dual Channel Electrocardiogram (ECG)
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Pulse Oximetry (SpO2)
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End-tidal CO2 (EtCO2)
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Dual Invasive blood pressure (IBP)
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Pneumatic Respiration
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Axillary Surface Temperature
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Anesthetic Agents
The Precess system includes the ability to display the
following parameters:
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Trends: Heart rate, respiration rate, NIBP
(systolic, mean, diastolic), IBP (systolic
mean, diastolic) temperature, CO2, and
SpO2
Respiration rate (CO2): Respiration rate
derived from EtCO2
CO2: Both EtCO2 and Inspired CO2
O2: Inspired, expired (averaged percent)
Agents: Automatic identification of primary
agent (Desflurane, isoflurane, Enflurane,
Halothane, or Sevoflurane) displaying both
end-tidal and fractionally inspired
concentrations (Et and Fi)
NIBP: (systolic, mean, diastolic), pulse rate
status
Bellows respiration rate: Respiration rate
derived from chest bellows
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800 x 600 pixels color LCD
Screen size: 12 inch (30.5 cm) diagonal
Sweep speed: 25 or 50 mm/second gives 9.2
or 4.6 seconds of display respectively For
respiration waveform sweep speed of, 0.33,
1.56, 3.13, 6.25, 12.5, or 25 mm/second
selectable by user, factory default 12.5
mm/second
Waveform display mode: fixed trace,
moving erase bar
Waveform display height: ≥ 19 mm
Full screen display height: ≥ 75 mm
Front Panel Cart Display (integral display)
The integral cart display provides display and control of
the monitored parameters. The cart display front panel
also provides all of the controls and access for complete
patient monitoring:
Time : Battery-backed quartz clock
Alarms: High and low limits selectable for
each patient parameter
ECG: ECG waveform scale, dual leads
displayed
Heart Rate: factory default derived from
ECG, user selectable to derive from invasive
blood pressure, pulse oximetry, NIBP, or
automatically selected in order of
parameter priority
Pulse Oximeter: Pulse rate, pulse
waveform, and percent saturation
Dual invasive pressures: Systolic, Mean,
diastolic, and waveform
Temperature: axillary surface temperature
(formatted in ° C or ° F)
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Mains power switch (cart and display)
Power indicator
Audio speaker
Rotary navigation knob
Keypad
The cart display (integral display) displays four groups of
user data:
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Informational Display
Vital Signs Trace Display
Vital Signs Numeric Display
System Status Display
Control Room Display (CRD)
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800 x 600 pixels color LCD
Screen size: 12 inch (30.5 cm) diagonal
Sweep speed: 25 or 50 mm/second gives 9.2 or
4.6 seconds of display respectively For
respiration waveform sweep speed of, 0.33,
1.56, 3.13, 6.25, 12.5, or 25 mm/second
selectable by user, factory default 12.5
mm/second
Waveform display mode: fixed trace, moving
erase bar
Waveform display height: ≥ 19 mm
Full screen display height: ≥ 75 mm
Width
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Thermal
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Informational Display
Vital Signs Trace Display
Vital Signs Numeric Display
System Status Display
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Specifications
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Conforms to UL STD 60601-1, Certified to
CAN/CSA STD C22.2 No. 601.1
Complies with: IEC 60601-1, IEC 60601-1-2, IEC
60601-1-4, IEC 60601-1-8, IEC 60601-2-27, IEC
60601-2-30, 60601-2-34, IEC 60601-2-49
Defibrillator protection up to 5 KV
Relative Humidity: 15 80% non-condensing
Electrical Specifications
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Battery: Lithium-ion and lithium polymer
Operating time:
Physical Specifications
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Height
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Operating Temperature: 15 to 35°C (59 to 95°F)
Storage Temperature
o Batteries 0 to 40°C (32 to 104°F)
o Anesthetic Oxygen (O2) Sensor: -40 to
35°C (-40 to 95°F)
o Cart, CRD, wireless modules and
additional accessories: -20 to 60°C (-4
to 140°F)
Transport Temperature: Cart, CRD, wireless
modules, and additional accessories: -20 to 60°C
(-4 to 140°F)
Humidity
Safety Standards
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Cart: 75 ± 0.5 lbs (34 ± 0.2 Kg)
CRD: 17 lbs (7.7 Kg)
Wireless ECG module: 5.4 oz (153 gm)
Wireless SpO2 module: 5.2 oz (147 gm)
Environmental Specifications
Power Switch
Power indicator
Audio Speaker
Rotary navigation knob
Keypad
The CRD displays four groups of user data:
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Cart: 17.5 ± 0.5 inches (44.5 ± 1.3 cm)
CRD: 4.6 inches (11.7 cm)
Wireless ECG module: 0.91 inches (2.3 cm)
Wireless SpO2 module: 0.91 inches (2.3 cm)
Weight
The Control room display (CRD) provides, display, control
and documentation of the monitored parameters. The
CRD display also includes an antenna for wireless
communication. The CRD front panel also provides all of
the controls and access for complete patient monitoring:
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Cart: 17.5 ± 0.5 inches (44.5 ± 1.3 cm)
CRD: 15.3 inches (38.9 cm)
Wireless ECG module: 2.5 inches 96.4 cm)
Wireless SpO2 module: 2.5 inches 96.4 cm)
Depth
Front Panel Control Room Display (CRD)
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Wireless ECG module: 4.7 inches (11.9 cm)
Wireless SpO2 module: 5.5 Inches (13,9 cm)
Cart: 48.5 ± 0.5 Inches (123.2 ± 1.3 cm)
CRD: 10.4 inches (26.4 cm)
Cart: 8 hours
Modules: 8 hours
Application Features
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Trends
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Automatically stores the parameter trend
information for heart rate, NIBP, SpO2, CO2, and
respiration
Trend feature is user configurable graphical
trends to graph multiple or individual trends
Multi Trends opens a graphical representation of
the selected parameters from the following
available parameters
Parameters:
o HR
o NIBP
o P1 (invasive pressure)
o P2 (invasive pressure)
o Sp02
o EtCO2
o Respiration (from EtCO2)
o Temperature
Lead Fail: Passive, sensing signal imbalance
ECG Input Impedance: >2.5MΩ (according to IEC
60601-2-27, 50.102.3)
Heart Rate
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Range: 30 to 240 bpm (Adult)
30 to 300 bpm (Neonate, Pediatric)
Accuracy: ±1% or ±1bpm, whichever is greater,
in the absence of a MRI gradient artifact
Resolution: 1BPM
Cardiotach
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Sensitivity (Monitor filter):
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Adult ECG mode: > 200 µV
o Neonale/Pediatric ECG mode: > 100 µV
Bandwidth: Monitor Mode: 0.5 to 40 Hz
Tall T-Wave Rejection capability for Heart Rate
Indication:
o 2 mV with a 1 mV QRS Amplitude
Alarms
Alarms
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One alarm severity (high)
o Visual alarm indicators,
flashing numeric panes,
alarm message, alarm icons
o Audible alarms, user
configurable for volume,
tone, and silence
Configurable alarm limits
Auto-set alarm limits allow alarm limits to be
quickly set
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Test/Calibration
Square Wave Test Signal: 60 bpm ± 1 bpm, 1 mV ± 10%
Non-Invasive Blood Pressure (NIBP)
Printer
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Oscillometric method (with inflatable cuff). Determines
systolic, diastolic, and ,mean arterial pressures, and pulse
rate.
Chart speed: 25 or 50 mm/second
Number of channels: 2
Paper type and size: Non-grid thermal paper, 50
mm wide
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Cart: ECG and peripheral gating output port
CRD: Serial data port for connections to facility
information system
Measurement Specifications
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Electrocardiogram (ECG)
ECG Amplifier
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Patient Types: Adults, Pediatric, Neonate
Pneumatic System
Device Connections
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Lower Alarm Limits: 30 to 249 bpm (or off)
Upper Alarm Limits: 60 to 249 bpm (or off)
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Protected against defibrillator and
electrosurgery potentials
Standard Lead Configurations:
I, II, III, AVR, AVL, AVF
Initial Cuff inflation Pressure:
o Adult: 170 mmHg
o Pediatric: 130 mmHg
o Neonate: 120 mmHg
o Subsequent inflation pressures
determined by last NIBP measurement
Overpressure Protection:
o Adult and Pediatric: Automatically
releases cuff pressure if inflation
pressure exceeds 285 mmHg
o Neonate: 150 mmHg absolute, > 142
mmHg and < 150 mmHg for 15 seconds
Unit of Measure: mmHg or KPa user selectable
Measurement Range
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Systolic:
o Adult, Pediatric: 45 to 260 mmHg
o Neonate: 45 to 125 mmHg
Diastolic:
o Adult, Pediatric: 15 to 235 mmHg
o Neonate: 15 to 85 mmHg
Mean Arterial:
o Adult, Pediatric: 25 to 255 mmHg
o Neonate: 25 to 95 mmHg
Pulse Rate Rage:
o Adult, Pediatric: 40 to 200 bpm
o Neonate: 40 to 230 bpm
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Alarm Limits
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Accuracy
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Pulse Rate:
o Within 2% of the pulse rate range
Pressure Transducer Accuracy:
o ± 3 mmHg or 2% of the reading at or
above 200 mmHg
Pressure Transducer Range
o 0 mmHg to 307 mmHg
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Number of Pressure Channels: 2 (P1 and P2)
Pressure Amplifier
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Systolic:
o Adult, Pediatric: 46 to 254 mmHg
o Neonate: 46 to 124 mmHg
Mean:
o Adult, Pediatric: 26 to 239mmHg
o Neonate: 26 to 94 mmHg
Diastolic:
o Adult, Pediatric: 16 to 224 mmHg
o Neonate: 16 to 84 mmHg
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Manual:
o Immediate upon operator command
Automatic:
o Determinations automatically made
with user selectable intervals of 1, 2,
2.5, 3, 5, 10, 15, 20, 30, and 45
minutes; and 1, 2, 3, and 4 hours
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ART, PAP, CVP, LAP, and ICP
Pressure Wave Display
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Pitch of pulse tone is modulated by saturation value.
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Range: +300 mmHg
Zero Accuracy: ±1.0 mmHg
Response Time: 1 Second, with notification upon
completion
User Configurable Labels
Pulse Oximeter
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Range: -10 to 248 mmHg
Sensitivity: 5µV/V/mmHg
Gain Accuracy: ± 0.5% or ±1mmHg which ever is
greater
Bandwidth: 0Hz to 10 Hz (-3dB)
Auto Zero
Modes
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SpO2 Alarm limits:
o Low: 50 to99, or off
o High: 70 to 99 or off
Pulse Alarm Limits (when “HR” derived from
SpO2):
o Low: 30 to 249
o High: 60 to 249
Invasive Blood Pressure
Alarm Limits
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Wavelength Range: 500 to 1000 nm: Information
about wavelength range can be especially useful
to clinicians (for instance, when photodynamic
therapy is performed)
Emitted Light Energy: <15 mW
Pulse Oximeter Calibration Range: 70 to 100%
Number of Waveform Channels: 0, 1, or 2
ART, PAP, and LAP: Numeric display of systolic,
mean, and diastolic pressures
CVP and ICP: Numeric display of the mean
pressure only
Pressure Scale (user selectable)
Saturation Range: 0 to 100%
Saturation Accuracy: ± 3% at 70% to 100% (the
specified accuracy is the root –mean square
(RMS) difference between the measured values
and the reference values)
Pulse Range: 30 to 250 bpm
Pulse Accuracy: ± 2% OR 1 bpm, whichever is
greater
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0 to 250 mmHg
0 to 200 mmHg
0 to 150 mmHg
0 to 100 mmHg
0 to 75 mmHg
0 to 45 mmHg
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Pulse Rate Derived from P1 or P2
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Range: 30 to 249 bpm
Accuracy: 2% full scale
Resolution: 1 bpm
Alarms
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Transducer Disconnect: Alarm delay 6 seconds
Pressure Disconnect: Alarm delay 6 seconds
High and Low Pressure: Alarm delay 10 seconds
Anesthetic Agents
Technique: Side Stream, non-dispersive infrared (NDIR)
absorption technique, including water trap filtration
system and microprocessor logic control of sample
handling and calibration
Alarm Limits
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Pulse Rate Limit:
o Low: 30 to 249 bpm
o High: 60 to 249 bpm
Systolic, Mean, Diastolic:
o Low: - 10 to 249 mmHg (-1.3 to 33.2
KPa)
o High: -10 to 249 mmHg (-1.3 to 33.2
KPa)
Measurement Range (after maximum warm-up period)
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Carbon Dioxide: 0 to 10.0 Vol%
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Sesflurane: 0 to 18.0 Vol%
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Enflurane: 0 to 5,0 Vol%
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Halothane: 0 to 5.0 Vol%
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Isoflurane: 0 to 5.0 Vol%
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Sevoflurane: 0 to 8.0 Vol%
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Nitrus Oxide: 0 to 100 Vol%
Connector Pin Configuration
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Pin A: - Signal
Pin B: +Excitation
Pin C: +Signal
Pin D: -Excitation
Pin E: Shield
Accuracy (includes stability and drift):
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Carbon Dioxide:
o ±0.10 Vol% at 0 -1.00 Vol%
o ±0.20 Vol% at 1.00 – 5.00 Vol%
o ±0.30 Vol% at 5.00 – 7.00 Vol%
o ±0.50 Vol% at 7.00 – 10.00 Vol%
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Desflurane:
o ±0.15 Vol% at 0 – 1.00 Vol%
o ±0.20 Vol% at 1.00 - 5.00 Vol%
o ±0.40 Vol% at 5.00 - 10.00 Vol %
o ±0.60 Vol% at 10.00 – 15.00 Vol%
o 1.0 Vol% at 15.00 – 18.00 Vol%
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Enflorane:
o ±0.15 Vol% at 0-1.00 Vol%
o ±0.20 Vol% at 1.00 – 5.00 Vol%
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Halothane:
o ±0.15 Vol% at 0 – 1.00 Vol%
o ±0.20 Vol% at 1.00 – 5.00 Vol%
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Isoflurane:
o ±0.15 Vol% at 0 – 1.00 Vol%
o ±0.20 Vol% at 1.00 – 5.00 Vol%
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Sevoflurane:
o ±0.15 Vol% at 0 – 1.00 Vol%
o ±0.20 Vol% at 1.00 – 5.00 Vol%
o ±0.40 Vol% at 5.00 – 8.00 Vol%
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Nitrous Oxide:
o ±2.0 Vol% at 0 – 20 Vol%
o ±3.0 Vol% at 20.0 to100 Vol%
Low-flow End-tidal CO2
Side stream: non-dispersive infrared absorption technique.
Including multiple water trap filtration system and
microprocessor logic control of sample handling and
calibration
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Total Respiration Range: 4 to 100 rpm
Total System Response Time: Response time
measured from step change of 10% to 90% of
CO2 level through complete pneumatic system
including patient sample line
o Adult, pediatric: ≤ 800 ms
o Neonate: ≤ 320 ms
Operating Temperature: 15 to 35°C (59 to 95°F)
Output: CO2 waveform, EtCO2, FiCO2,
Respiration Rate
CO2 units of measurement: mmHg and KPa
CO2 measurement range: 0 to 76 mmHg ( 0 to
10.1 KPa)
CO2 measurement resolution: 1 mmHg or 0.1
KPa
Accuracy:
o CO2: ± 4 mmHg or 12% whichever is
greater
o Respiration: ± 1 rpm or ± 3% whichever
is greater
Warm-up time: ≤ 2 minutes
Zero Calibration interval: Automatic or user
request
Flow Rate: 80 mL/minute ±16 mL/minute
Full Accuracy Respiration Range (rate permitting
specified CO2 accuracy)
o Accuracy: 4 to 60 rpm
Interference Gas:
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CO2: N2O, O2, Any Agent = 0.1
allowance for each
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inaccuracy
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Inspired CO2:
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25 mmHg (fixed)
N2O: CO2, O2, Any Agent = 0.1
inaccuracy
allowance for each
inaccuracy allowance
Agents: CO2, = 0
N2O:
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Display Resolution:
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0.1% Volume
80% (fixed)
Et Halothane:
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Low: Off, 0.1 to 5.0 Vol%
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High: Off, 0.1 to 5.0 Vol%
Flow Rate:
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Adult, Pediatric: 200 ml/min ±20ml/min
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Neonate: 150 ml/min ±15ml/min
Fi Halothane:
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Low: Off, 0.1 to 5.0 Vol%
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High: Off, 0.1 to 5.0 Vol%
Response Time:
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Agents: not specified
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CO2:
o Adult, Pediatric: <330 ms
o Neonatal: <290 ms
Note: based on 10% to 90% step change of
measured CO2 level through pneumatic system
including patient sample line
Et Isoflurane:
•
Low: Off, 0.1 to 5.0 Vol%
•
High: Off, 0.1 to 5.0 Vol%
Fi Isoflurane:
•
Low: Off, 0.1 to 5.0 Vol%
•
High: Off, 0.1 to 5.0 Vol%
Full Accuracy Respiration Rate (range permitting specified
gas accuracy:
•
2 to 60 rpm
Et Enflurane:
•
Low: Off, 0.1 to 5.0 Vol%
•
High: Off, 0.1 to 5.0 Vol%
Total Respiration Range:
•
2 to 100 rpm, accuracy unspecified from 60 to
100 rpm
Relevant interference:
•
0.5 mmHg equivalent with 37.5°C saturated with
H2O (0.1% relative max)
Display resolution:
•
0.1 percent Volume
Fi Enflurane:
•
Low: Off, 0.1 to 0.5 Vol%
•
High: Off, 0.1 to 5.0 Vol%
Et Sevoflurane:
•
Low: Off, 0.1 to 8.0 Vol%
•
High: Off, 0.1 to 8.0 Vol%
Fi Sevoflurane:
•
Low: Off, 0.1 to 8.0 Vol%
•
High: Off, 0.1 to 8.0 Vol%
Maximum Warm-up Time:
•
10 minutes: ISO accuracy is achieved in <45
seconds
Auto ID Threshold: (full accuracy mode)
•
0.15 percent
Et Desflurane:
•
Low: Off, 0.1 to 18.0 Vol%
•
High: Off, 0.1 to 18.0 Vol%
Fi Desflurane:
•
Low: Off, 0.1 to 18.0 Vol%
•
High: Off, 0.1 to 18.0 Vol%
Multiple Agents Alarm Threshold:
•
0.3% (0.5% during ISO accuracy mode) or 5
(10% isoflurane) of primary agent >10% (for
halothane add 0.1
to threshold values)
Oxygen:
•
Low: 15 to 99%
•
High: 16 to 99%, Off
CO2 Ambient Pressure Compensation Range:
•
500 to 900 mmHg
Calibration Interval: Calibration verification (as described
in the maintenance instructions) must be performed at a 1
year interval
Oxygen
Range:
•
Alarm Limits
0 to 100%
Signal Output (at constant temperature and pressure):
•
10mV ±1.5mV at 20°C/20.95% O2
CO2 Alarms Limits:
•
Low: Off, 5 to 60 mmHg
•
High: Off, 5 to 80 mmHg
7
Maximum Response Time (21% to 100% step change
through patient sample line as seen by the cart gas
monitor window)
•
Adult, Pediatric: <7.3 seconds
•
Neonate: <8.2 seconds
Range:
•
Accuracy (includes stability and drift), full scale:
•
±1% at 0 to 40%
•
±2% at 40 to 60%
•
±3% at 60 to 80%
•
±4% at 80 to 100%
Note: Gas measurement performance requirements are
met after the maximum warm-up period
Accuracy:
•
± 0.5°C (0.9°F)
Offset:
•
Resolution:
•
0.1°C (0.1°F)
Response Time:
•
1 second
Numeric Display Update Time:
•
2 seconds
Sensor Type:
•
Fiber Optic
±1%
O2 Interfering Gas Effects:
•
N2O: <0.3 Vol% at 80 Vol% N2O
•
CO2: <0.3 Vol% at 5 Vol% CO2
•
Halothane: <0.3 Vol% at 5 Vol% HAL
•
Enflurane: <0.3 Vol% at 5 VOl% ENF
•
Isoflurane: <0.3 Vol% at 5 Vol% ISO
•
Desflurane: <0.3 Vol% at 18 Vol% DES
•
Sevoflurane: <0.3 Vol% at 8 Vol% SEV
•
Acetone: <0.3 Vol% at 1 Vol% Acetone
•
Ethanol: < 0.3 Vol%
Alarm Limits
•
•
Ambient Humidity (non-condensing):
•
10% to 99% RH (non-condensing)
•
•
Oxygen Sensor, Storage Temperature:
•
-40 to 35°C (-40 to 95°F)
Oxygen Sensor Expected operating Life:
•
9 months (2500 hours at 100% O2)
•
Exchange recommended every 9 months
Oxygen Sensor Shelf Life:
•
3 months in sealed container
Temperature
For use with Invivo Fiber optic Sensor (utilizes Fabry-Perot
interferometer technology)
Number of Temperature Channels:
•
One
Units:
•
Degrees Celsius:
o Low: Off, 20.0 to 44.0°C
o High: Off, 20 to 44.0°C
Degrees Fahrenheit
o Low: Off, 68.0 to 111.2°F
o High: Off, 68.0 to 111.2°F
Respiration
Operating Temperature:
•
15 to 35°C (59 to 95°F)
•
20 to 44°C (68.0°F to 111.2°F)
Celsius (°C) or Fahrenheit (°F) User configurable
8
Respiration is displayed numerically by detecting
the patient’s abdominal or chest wall motion
through a pneumatic bellows placed at the
patient’s chest
There are no user adjust options for this
parameter, including alarms because this
parameter is not intended for vital sign
monitoring.
Ordering information
9016C
Precess MRI Patient monitoring System
Divided Pediatric Cannula
9016B
Standard Features
Divided Small Infant Cannula
Precess Cart: 865323
9025
Includes:
• Precess with integral Display
• Integral charger
• NIBP
Endotracheal Airway Adapter 50-Pk
9027
Female Luer Lock Adapters (Qty 10)
Options:
EtCO2: G01
Agents: G02
IBP:
P01
TEMP: T01
9014
Infant Disposable Cannula
9010F
Maintenance CO2 Calibration Gas, Aerosol
Precess Control CRD: 865485
9013
With/Out Recorder: D01
With Recorder: D02
• Includes roll of recorder paper (MP05)
Pediatric Disposable Cannula
Wireless SpO2 Module: 989803163111
Scavenger Hose
Wireless ECG Module: 989803163121
9015
Module 3.7 volt battery: 9065
Small Infant Disposable Cannula
9471
CO2 (Low Flow)
Module Battery charger: 989803152891 (9023)
94020
CO2/Anesthetic Agents
Low Flow Disposable Water Trap (Blue)
Accessories
94022
9012
Low Flow CO2 Kit (Blue)
Adult Disposable Cannula
Contains:
•
Low-Flow Blue Water Trap (94020)
•
Low-Flow EtCO2 Blue Sample Line (94021)
•
Pediatric Cannulas (9013)
•
Adult Cannulas (9012)
9016
Divided Adult Cannula Disposable
9016A
94021
Divided Infant Cannula
Low Flow CO2 Sample Line (Blue)
9
94013
CO2 (Standard Flow)/Anesthetic
Neonatal Starter Kit
Agents
Contains:
•
Neonatal ECG Lead Cable (9222)
•
(Box of 10) Neonatal Quadtrodes (9372A)
•
Prep Gel (453564120521)
989803162051
Anesthetic Oxygen (O2) Sensor, Artema
•
•
•
•
•
•
989803162961
Anesthetic Oxygen (O2) Sensor Installation Tool
94012
Neonatal NIBP Hose (989803169421)
Neonatal #3 BP Cuff (989803170401)
Neonatal #5 BP Cuff (989803170421)
(Pack of 3) Neonatal Grip Sensors (9399AN)
(Pack of 3) Infant Grip Sensors (9399AI)
(2 Each) Infant Cannulas (9014 and 9015)
Standard Flow Disposable Water Trap (Clear)
94019
9222
Standard Flow CO2/Agent Kit (Clear)
Neonatal ECG Cable
Contains :
•
Standard-Flow Clear Water Trap (94012)
•
Standard-Flow Clear Sample Lines (94018)
9372A
94018
9009
Standard Flow CO2/Agent Sample Line (Clear)
Prep Gel, Box of 3 Tubes
ECG
452213305301
Neonatal Quadtrodes (Qty 10)
Special Apps ECG Lead Cable
989803163121
94016
Wireless ECG Module
Standard ECG Kit
989803170121
Contains:
Advanced Filter ECG Cable
•
•
•
94015
CV ECG Starter Kit
Contains:
•
•
•
ECG Lead Cable (9224)
(Box of 10) Standard Quadtrodes (9303A)
Prep Gel (453564120521)
9224
Prep Gel (453564120521)
ECG Leadwires (9223)
(Box of 10) CV Quadtrodes (9371A)
Standard ECG Lead Cable
9303A
9223
Standard Quadtrodes (Qty 10)
CV ECG Lead Cable
9303N
9371A
Standard Quadtrodes (Qty 50)
CV Quadtrode (Qty 10)
10
Gating Options
989803170421
9292
Disposable Neonatal NIBP Cuff, Colder Connector
GE Excite Gating Interface
(8-15 cm)
9293
94013
Hitachi/Toshiba Gating Interface
Neonatal Starter Kit
9291
Contains:
•
Neonatal ECG Lead Cable (9222)
•
(Box of 10) Neonatal Quadtrodes (9372A)
•
Prep Gel (453564120521)
Siemens Gating Interface
9294
•
•
•
•
•
•
Vector Gating Interface
Invasive Blood Pressure
Invivo recommends using the following transducer and
adapter cables with the Expression MRI Patient Monitoring
System: Edwards Lifesciences Transducer, Model PX260 Please contact Edwards Lifesciences for an adapter cable
that is compatible with Invivo devices. For additional
questions, please contact your Invivo sales representative.
Neonatal NIBP Hose (989803169421)
Neonatal #3 BP Cuff (989803170401)
Neonatal #5 BP Cuff (989803170421)
(Pack of 3) Neonatal Grip Sensors (9399AN)
(Pack of 3) Infant Grip Sensors (9399AI)
(2 Each) Infant Cannulas (9014 and 9015)
989803169461
Large Adult NIBP Cuff, Colder Connector (39-62 cm)
989803169421
Miscellaneous
Neonatal NIBP Hose, Colder Connector
453564125581
989803169411
2.4GHz Antenna
Adult NIBP Hose, Colder Connector
9059
94014
2.4GHz Passive Antenna Kit
NIBP Starter Kit
9180T
HP107
Contains 1 Each:
•
MRI NIBP Hose (989803169411)
•
Adult Cuff (989803169451)
•
Pediatric Cuff (989803169441)
Zero Port Filter
989803169441
NIBP
Pediatric NIBP Cuff, Colder Connector (9-25 cm)
989803169451
989803169431
Adult NIBP Cuff, Colder Connector (17-45 cm)
Infant NIBP Cuff, Colder Connector (5-15 cm)
989803170401
989803170431
Disposable Neonatal NIBP Cuff, Colder Connector (6-11
cm)
Disposable Infant NIBP Cuff (10-15cm)
Printer Paper (Qty 10)
11
989803170441
9023
Disposable Pediatric NIBP Cuff (14-21 cm)
Wireless Module Battery Charger 3.7V
989803170451
453564123631
Disposable Small Adult NIBP Cuff (20-28 cm)
CRD Power Converter Kit
989803170461
SpO2
Disposable Adult NIBP Cuff (27-36 cm)
989803163121
989803170471
Wireless ECG Module
Disposable Extra Long Adult NIBP Cuff (27-36 cm)
989803162491
989803170481
Grip Sensor Starter Kit
Disposable Large Adult NIBP Cuff (35-45 cm)
Disposable Large Extra Long Adult NIBP Cuff (35- 45 cm)
Contains 1 Each:
•
AN-Type (989803161961) grip
•
P-Type (989803161971) grip
Note: Compatible with the 989803161981 Senso
989803166531
989803170501
Quick Connect SpO2 Clip, Adult
Disposable NIBP Cuff Sample Kit
989803166541
Pneumatic Respiration
Quick Connect SpO2 Clip, Pediatric
94023
989803166551
Chest Bellows
Quick Connect SpO2 Grip, Adult, 20/box
Replacement Power
989803166571
989803169491
Quick Connect SpO2 Grip, Infant, 20/box
14.8V Battery (each)
989803166581
AS18
Quick Connect SpO2 Grip, Neonatal, 20/box
Power Cord, US 110V
989803166561
AS18G
Quick Connect SpO2 Grip, Pediatric, 20/box
Power Cord, European 220-230V
989803167111
AS18A
Quick Connect SpO2 Grip, Starter Pack for use with
989803161991 Quick Connect SpO2 probe
989803170491
Power Cord, Universal 220V
Contains 5 Each:
9065
•
Wireless Module Battery 3.7V (each)
12
Quick Connect Disposable Sensor (Adult,
Pediatric, Infant and Neonatal)
989803161991
Quick Connect SpO2 Sensor, MRI
452213305371
SpO2 Fiber Optic Sensor
989803162501
SpO2 Sensor Grip Adult/Neonatal (Qty 2)
989803162511
SpO2 Sensor Grip Infant/Pediatric (Qty 2)
Temperature
9320
Fiber Optic Temperature Sensor
9321
FiberTEMP Surface Applicators (Qty 30)
13
Invivo is part of Royal Philips
Electronics
For more information about Invivo Expression MRI
Patient Monitoring Systems or any of the Complete
Solution products from Invivo, please do not hesitate
to contact us. We would be glad to hear from you.
Invivo
Orlando, FL, USA
www.invivocorp.com
North America
T: 800-331-3220
T: 407-275-3220
E: [email protected]
Europe
T: +31 (0)499 378624
E: [email protected]
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