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: • • • The Precess System can be ordered to suit the specific needs of the MR team 1 Cart with Integral LCD Display Integral DC power supply Non-invasive blood pressure (NIBP) Optional Components • • • • • Control Room Display (CRD) Wireless ECG (WECG) Module Wireless SpO2 (WSpO2) Module Wireless Module Battery Charger • • • • Features and Benefits • • • • • • • • • 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 • • Main Components Cart Display (integral display) • • • System Parameters Included • Non-invasive blood pressure (NIBP) Optional System Parameters • Dual Channel Electrocardiogram (ECG) • Pulse Oximetry (SpO2) • End-tidal CO2 (EtCO2) • Dual Invasive blood pressure (IBP) • Pneumatic Respiration • Axillary Surface Temperature • Anesthetic Agents The Precess system includes the ability to display the following parameters: • • • • • • • 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 • • • 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) • • • • • 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: • • • • 2 Informational Display Vital Signs Trace Display Vital Signs Numeric Display System Status Display Control Room Display (CRD) • • • • • • • • 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 • • • • • • • • • • • • Thermal • • Informational Display Vital Signs Trace Display Vital Signs Numeric Display System Status Display • Specifications • • 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 • Battery: Lithium-ion and lithium polymer Operating time: Physical Specifications • • Height • • 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 • 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: • 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: • • • • 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) • • • • • 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 3 • • Trends • • • 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 • • • 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 • • • Sensitivity (Monitor filter): o 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 • • • 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 • • Test/Calibration Square Wave Test Signal: 60 bpm ± 1 bpm, 1 mV ± 10% Non-Invasive Blood Pressure (NIBP) Printer • • • 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 • • Cart: ECG and peripheral gating output port CRD: Serial data port for connections to facility information system Measurement Specifications • Electrocardiogram (ECG) ECG Amplifier • • Patient Types: Adults, Pediatric, Neonate Pneumatic System Device Connections • • Lower Alarm Limits: 30 to 249 bpm (or off) Upper Alarm Limits: 60 to 249 bpm (or off) • 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 4 • • • • • 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 • • Alarm Limits • • Accuracy • • • 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 • • Number of Pressure Channels: 2 (P1 and P2) Pressure Amplifier • • • 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 • • • • • 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 • ART, PAP, CVP, LAP, and ICP Pressure Wave Display • • • Pitch of pulse tone is modulated by saturation value. • • Range: +300 mmHg Zero Accuracy: ±1.0 mmHg Response Time: 1 Second, with notification upon completion User Configurable Labels Pulse Oximeter • • 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 • 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 • 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 • • • • • • 5 0 to 250 mmHg 0 to 200 mmHg 0 to 150 mmHg 0 to 100 mmHg 0 to 75 mmHg 0 to 45 mmHg • • Pulse Rate Derived from P1 or P2 • • • Range: 30 to 249 bpm Accuracy: 2% full scale Resolution: 1 bpm Alarms • • • • 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 • • 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) • Carbon Dioxide: 0 to 10.0 Vol% • Sesflurane: 0 to 18.0 Vol% • Enflurane: 0 to 5,0 Vol% • Halothane: 0 to 5.0 Vol% • Isoflurane: 0 to 5.0 Vol% • Sevoflurane: 0 to 8.0 Vol% • Nitrus Oxide: 0 to 100 Vol% Connector Pin Configuration • • • • • Pin A: - Signal Pin B: +Excitation Pin C: +Signal Pin D: -Excitation Pin E: Shield Accuracy (includes stability and drift): • 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% • 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% • Enflorane: o ±0.15 Vol% at 0-1.00 Vol% o ±0.20 Vol% at 1.00 – 5.00 Vol% • Halothane: o ±0.15 Vol% at 0 – 1.00 Vol% o ±0.20 Vol% at 1.00 – 5.00 Vol% • Isoflurane: o ±0.15 Vol% at 0 – 1.00 Vol% o ±0.20 Vol% at 1.00 – 5.00 Vol% • 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% • 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 • • • • • • • • • 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: • CO2: N2O, O2, Any Agent = 0.1 allowance for each 6 inaccuracy • • Inspired CO2: • 25 mmHg (fixed) N2O: CO2, O2, Any Agent = 0.1 inaccuracy allowance for each inaccuracy allowance Agents: CO2, = 0 N2O: • Display Resolution: • 0.1% Volume 80% (fixed) Et Halothane: • Low: Off, 0.1 to 5.0 Vol% • High: Off, 0.1 to 5.0 Vol% Flow Rate: • Adult, Pediatric: 200 ml/min ±20ml/min • Neonate: 150 ml/min ±15ml/min Fi Halothane: • Low: Off, 0.1 to 5.0 Vol% • High: Off, 0.1 to 5.0 Vol% Response Time: • Agents: not specified • 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] 14 15