The IntelliVue Dock provides an external power supply for the monitor and extension when connected to mains power via AC power connector. IntelliVue Dock has Flexible Sync ... >86 dB (with a 51 kΩ/47 nF imbalance) • Filter Mode: >106 dB (with a 51 kΩ/47 nF imbalance) Electrode Offset Potential Tolerance
Image guided therapy Hemo System Monitor - measure - record Philips Interventional Hemodynamic system with IntelliVue X3 Technical specifications Introduction Improving productivity and patient outcome is vital for healthcare facilities to meet the growing demand for cath lab procedures. To further simplify cath lab workflow, Philips introduces the Interventional Hemodynamic system (Hemo system). Hemo system brings advanced hemodynamic measurements into the interventional lab to support clinical decision making. This system is integrated with the market leading Philips IntelliVue X3 patient monitor mounted at the table side and a hemo workstation in the control room to perform hemodynamic analysis. Furthermore the system can be operated from the table side in the exam room via the Philips Azurion Touch screen module. Key advantages of the Hemo system Integrated IntelliVue X3 patient monitor Control of Philips Hemo on Touch Screen Module Content · Key advantages of the Hemo system · Technical specification of the patient monitor IntelliVue X3, extension and Dock · Patient cables, sensors and accessories · Workstation specification 2 Hemodynamic analyses performed in the control room can be shown in the exam room to help the users to stay focused on the task at hand. Integrated iFR Spot and Scout pullback incoporated Azurion's intuitive workflow approach Confidently used by all staff members with minimal training 3 Technical specifications of the patient monitor IntelliVue X3, measurement extensions and Dock This section describes IntelliVue X3 patient monitor, extension and Dock as a signal acquisition device that provides input to the Hemo system during interventional procedures where all interaction is managed by the Hemo workstation (with Xper Information Management System software and Hemodynamic Application). The IntelliVue X3, extension, Dock with the mounting bracket allow for flexible positioning at the table side. IntelliVue X3, extension and Dock: Weight 2,6 kg Size 120 x 180 x 190 mm The device front panel has patient cable/accessory connectors for invasive blood pressure, ECG, cardiac output, surface temperature, SpO2, etCO2, and noninvasive blood pressure. 1 2 IntelliVue X3 1 Temperature 2 Pressure connector for 2 pressures 3 3 SpO2 (option from Philips FAST , Masimo or Nellcor) 4 ECG 4 5 Noninvasive blood pressure 5 1 Extension 1 EtCO2 (optional Mainstream/Sidestream 2 or Microstream connector) 2 Cardiac Output Thermodilution 3 3 Temperature 4 4 Pressure connector for 2 pressures 5 Connection to IntelliVue X3 5 4 IntelliVue Dock 1. MSL connector for monitor connection 2. Flexible Sync Output connector, to provide signal to other medical devices 3. AC power connector 4. LAN connector for connection to Hemo workstation 1 2 The IntelliVue Dock provides an external power supply for the monitor and extension when connected to mains power via AC power connector. IntelliVue Dock has Flexible Sync Output connector to output and synchronize signals to other 3 4 medical devices. · 1/4 stereo phone jack connector: 2 channels (tip and ring) · 2 programmable analogue outputs: · Analog ECG output (configurable at tip or ring) 2V/mV (default, 4V/mV; 1V/mV; 0.5V/mV; 0.25 V/mV selectable)) · Analog pressure output (configurable at tip or ring): 1V/100 mmHG; voltage swing ±4V · Digital ECG pulse output (configurable at ring) Possibility to split the signal if you want to use ECG lead I/ II for different devices as the input. On X3 you can choose between QRS, primary lead or one of the pressure channels. Signals can be split if necessary. Care and Cleaning The X3 measurement extensions and Dock deploy chemicallyresistant surface materials, designed to resist deterioration from cleaning and disinfection agents. Even against very aggressive disinfectants, the X3's the housing materials have been tested, and found to resist deterioration about 60 times longer than the housing material used for preceeding products. See the list of tested agents in the monitor's Instructions for Use. Mounting bracket General IntelliVue X3, extension and Dock Power Consumption: < 20W when on IntelliVue Dock Operating Voltage 36 to 60 V dc floating Operating Temperature Range: 0 to 35°C (32 to 95°F) when charging the battery Operating Relative Humidity Range: 15% to 95% humidity, non-condensing Ingress Protection IntelliVue X3, extension and Dock IP32 when mounted horizontally Definition of IP 32: Protected against ingress of water when the water is dripping vertically and monitor is tilted up to 15°, and ingress of solid foreign objects 2,5 mm in diameter or larger Internal Battery (453564526811) The battery is required for the operation of the monitor. The battery lifetime is 3 years from manufacturing date or 500 charge/ discharge cycles. 5 Fits your clinical workflow Choose the set-up that works best with your lab Basic Basic monitoring and hemodynamic analysis capabilities for main stream Interventional Cardiac procedures Performance Comprehensive monitoring and hemodynamic analysis capabilities for wide range of Interventional Cardiac procedures Clinical and workflow functionality: · Non-invasive blood pressure · Body surface temperature · 12 lead ECG · 2 invasive blood pressures · Calculated Cardiac Output Fick · Respiration rate · SpO2 Philips FAST, Nellcor (Covidien) or Masimo · Capture and store hemodynamic waveforms and ECG's · Full disclosure (record and store all waveforms data for post case review and analysis) · End case report (hemodynamic measurements and calculations) · Print waveforms and hemodynamic analysis · Store patient data · Visualization of ST values · Aortic Regurgitation (AR) Index Clinical Options: · Integrated Philips iFR/FFR · Integrated FFR (compatible with Abbott) Work Flow Options: · Ability to operate in patient area · Trolley Integrated with Philips image guided therapy system · Hemo control from Touch Screen Module · Patient demographics · Connected to FlexVision or Monitor Ceiling Suspension 6 Clinical and workflow functionality: · Non-invasive blood pressure · Body surface temperature · 12 lead ECG · 4 invasive blood pressures · Thermodilusion Cardiac Output (and calculated Fick) · Respiration rate · SpO2 Philips FAST, Nellcor (Covidien) or Masimo · Capture and store hemodynamic waveforms and ECG's · Full disclosure (record and store all waveforms data for post case review and analysis) · End case report (hemodynamic measurements and calculations) · Print waveforms and hemodynamic analysis · Store patient data · Visualization of ST values · Aortic Regurgitation (AR) Index Clinical Options: · EtCO2: · Respironics LowFlo CO 2 · Covidien Microstream® CO 2 · Integrated Philips iFR/FFR · Integrated FFR (compatible with Abbott) Work Flow Options: · Ability to operate in patient area · Trolley Integrated with Philips image guided therapy system · Hemo control from Touch Screen Module · Patient demographics · Connected to FlexVision or Monitor Ceiling Suspension 7 Measurement Specifications - ECG IEC 60601227:2011 ECG Specifications HR Range 15300 bpm maximum delay: 10 seconds according to IEC 60601227 ST Numeric Range -2020 mm Accuracy ±0.5 mm or 15% whichever is greater Resolution 0.1 mm QT-HR Numeric Range - Adult 15150 bpm Range - Pedi/neo 15180 bpm Resolution 1 bpm Sinus and SV Rhythm Ranges Brady · Adult: · Pedi: · Neo: 1559 bpm 1579 bpm 1589 bpm Normal · Adult: · Pedi: · Neo: 60100 bpm 80160 bpm 90180 bpm Tachy · Adult: · Pedi: · Neo: >100 bpm >160 bpm >180 bpm Bandwidth Diagnostic mode Adult/neo/pedi: 0.05150 Hz Monitoring mode · Adult: · Neo/pedi: 0.540 Hz 0.555 Hz Notch filter 50/60 Hz Differential Input Impedance · >2 M RA-LL leads (Resp) · >5 M at all other leads (at 10 Hz including patient cable) Common Mode Rejection Ratio · Diagnostic Mode: >86 dB (with a 51 k/47 nF imbalance) · Filter Mode: >106 dB (with a 51 k/47 nF imbalance) Electrode Offset Potential Tolerance ±500 mV Auxiliary Current (Leads off Detection) · Active Electrode: <100 nA · Reference Electrode: <900 nA Input Signal Range ±5 mV 8 Respiration Respiration Performance Specifications Respiration Rate Range · Adult/pedi: · Neo: 0120 rpm 0170 rpm Accuracy · At 0120 rpm ±1 rpm · At 120170 rpm ±2 rpm Resolution 1 rpm Bandwidth 0.32.5 Hz (-6 dB) Noise <25 m (rms) referred to the input Respiration Alarm Specifications High Range · Adult/pedi: · Neo: 10100 rpm 30150 rpm Adjustment · <20 rpm: 1 rpm steps · 20 rpm: 5 rpm steps Delay Maximum 14 seconds Low Range Adjustment Delay Apnea Alarm Range Adjustment · Adult/pedi: · Neo: 095 rpm 0145 rpm · <20 rpm: 1 rpm steps · 20 rpm: 5 rpm steps · For limits from 0 to 20 rpm: maximum 4 seconds · For limits above 20 rpm: maximum 14 seconds 1040 seconds 5 second steps 9 Noninvasive Blood Pressure (NBP) Complies with: · IEC 80601230:2010 + A1:2013 · EN 80601230:2010 + A1:2015 NBP Performance Specifications Systolic Range · Adult: 30270 mmHg (436 kPa) · Pedi: 30180 mmHg (424 kPa) · Neo: 30130 mmHg (417 kPa) Diastolic Range · Adult: 10245 mmHg (1.532 kPa) · Pedi: 10150 mmHg (1.520 kPa) · Neo: 10100 mmHg (1.513 kPa) Mean Range · Adult: 20255 mmHg (2.534 kPa) · Pedi: 20160 mmHg (2.521 kPa) · Neo: 20120 mmHg (2.516 kPa) Accuracy Max. Std. Deviation 8 mmHg (1.1 kPa) Max. Mean Error ±5 mmHg (±0.7 kPa) Measurement Time Typical at HR >60 bpm Auto/Manual · Adult: · Neo: · Stat: 30 seconds 25 seconds 20 seconds Maximum time · Adult/pedi: 180 seconds · Neo: 90 seconds Cuff Inflation Time Typical for normal adult cuff <10 seconds Typical for neonatal cuff <2 seconds Initial Cuff Inflation Pressure · Adult: · Pedi: · Neo: 165 ±15 mmHg 130 ±15 mmHg 100 ±15 mmHg Maximum Cuff · Adult/pedi: 300 mmHg Pressure · Neo: 150 mmHg NBP Alarm Specifications Systolic Range · Adult: 30270 mmHg (436 kPa) · Pedi: 30180 mmHg (424 kPa) · Neo: 30130 mmHg (417 kPa) Adjustment · 1030 mmHg (1.54 kPa): 2 mmHg (0.5 kPa) · >30 mmHg (>4 kPa): 5 mmHg (1 kPa) Diastolic Range · Adult: 10245 mmHg (1.532 kPa) · Pedi: 10150 mmHg (1.520 kPa) · Neo: 10100 mmHg (1.513 kPa) Adjustment · 1030 mmHg (1.54 kPa): 2 mmHg (0.5 kPa) · >30 mmHg (>4 kPa): 5 mmHg (1 kPa) Mean Range · Adult: 20255 mmHg (2.534 kPa) · Pedi: 20160 mmHg (2.521 kPa) · Neo: 20120 mmHg (2.516 kPa) Adjustment · 1030 mmHg (1.54 kPa): 2 mmHg (0.5 kPa) · >30 mmHg (>4 kPa): 5 mmHg (1 kPa) NBP Overpressure Settings (Not User Adjustable) Adult >300 mmHg (40 kPa) >2 seconds Pedi >300 mmHg (40 kPa) >2 seconds Neo >150 mmHg (20 kPa) >2 seconds 10 Invasive Blood Pressure Supports up to two pressure transducers via one connector and one Y-cable. Complies with: · IEC 60601234:2011 · EN 60601234:2014 Temperature Complies with: · ISO 80601256:2009 · EN ISO 80601256:2012 Invasive Pressure Performance Specifications Measurement Range -40360 mmHg Input Sensitivity Sensitivity 5 V/V/mmHg (37.5 V/V/kPa) Adjustment range ±10% Transducers (Compliant with ANSI/AAMI BP22) Load impedance 2002000 (resistive) Output impedance 3000 (resistive) Frequency Response DC to 12 Hz or 40 Hz Zero Adjustment Range ±200 mmHg (±26 kPa) Accuracy ±1 mmHg (±0.1 kPa) Drift <0.1 mmHg/°C (0.013 kPa/°C) Gain Accuracy Accuracy ±1% Drift <0.05%/°C Non-linearity and Error of 0.4% FS (@CAL 200 mmHg) Hysteresis Overall Accuracy (Including Transducer) ±4% of reading or ±4 mmHg (±0.5 kPa), whichever is greater Invasive Pressure Alarm Specifications Pressure Range -40360 mmHg (-5.048 kPa) Adjustment · -4050 mmHg (-54 kPa): 2 mmHg (0.5 kPa) · >50 mmHg (>4 kPa): 5 mmHg (1 kPa) Delay Maximum 12 seconds Transducer and pressure cable should be ordered via established supplier chain in the hospital. We suggest to order: Edwards TrueWare PX series Single adult transducer and the pressure cable from the front end to the transducer. Temperature Performance Specifications Temperature Range (absolute) -145°C (30113°F) Range (differential) ±46°C (±115°F) Resolution 0.1°C (0.1°F) Accuracy ±0.1°C (±0.2°F) Average Time Constant <10 seconds Temperature Alarm Specifications Temperature High/Low Alarms Range -145°C (30113°F) Adjustment · -130°C (3086°F), 0.5°C (1.0°F) steps · 3045°C (86113°F), 0.1°C (0.2°F) steps 11 Cardiac Output Thermodilution Specifications End tidal CO (867040) 2 Complies with: · ISO 80601255:2011 · EN ISO 80601255:2011 Cardiac Output Blood Temperature Range 1743°C (62.6109.5°F) Blood Temperature Accuracy 0.1°C (0.2°F) (Excluding Probe) Injectate Temperature Range -130°C (30.286.0°F) Injectate Temperature Accuracy (Excluding Probe) 0.1°C (0.2°F) Cardiac Output (Right Heart) C.O. Range 0.120 l/min Instrument Specification (Measured Electronically) C.O. Instrument Accuracy ±3% or 0.1 l/min C.O. Repeatability ±2% or 0.1 l/min 12 Mainstream CO2 Performance Specifications CO2 Range 0150 mmHg (020 kPa) Accuracy After two minutes warm-up: · For values between 0 and 40 mmHg (0 and 5,3 kPa): ±2.0 mmHg (±0.29 kPa). · For values from 4170 mmHg (5.49.3 kPa): ±5% of reading. · For values from 71100 mmHg (9.413.3 kPa) ±8% of reading. · For values from 101150 mmHg (13.420 kPa): ±10 % of reading the specifications are valid for standard gas mixtures, balance air, fully hydrated at 35°C, Pabs = 760 mmHg (101.3 kPa), flow rate = 2 l/min Resolution · Numeric: 1.0 mmHg (0.1 kPa) · Wave: 0.1 mmHg (0.01 kPa) Stability: Short-term Drift Long-term Drift ±0.8 mmHg (0.11 kPa) over four hours Accuracy specification is maintained over a 120hour period Warm-up Time Two minutes with CO transducer 2 attached for full accuracy specification Response Time <60 ms (with adult or infant reusable or disposable adapter) Sidestream CO2 Performance Specifications CO2 Range 0150 mmHg (020 kPa) Accuracy After two minutes warm-up: · For values between 0 and 40 mmHg (0 and 5,3 kPa): ±2.0 mmHg (±0.29 kPa). · For values from 4170 mmHg (5.49.3 kPa): ±5% of reading. · For values from 71100 mmHg (9.413.3 kPa) ±8% of reading. · For values from 101150 mmHg (13.420 kPa): ±10% of reading. At respiration rates above 80 rpm, all ranges are ±12% of reading. The specifications are valid for gas mixtures of CO2, balance N2, dry gas at 760 mmHg (101.3 kPa) within specified operating temperature range. Microstream CO 2 (867041) Resolution · Numeric: 1.0 mmHg (0.1 kPa) · Wave: 0.1 mmHg (0.01 kPa) Stability: Short-term Drift Long-term Drift ±0.8 mmHg (0.11 kPa) over four hours Accuracy specification is maintained over a 120hour period Warm-up Time Two minutes with CO sensor 2 attached for full accuracy specification Sample Flow Rate 50 ±10 ml/minute Total System Response Time 3 seconds CO2 Alarm Specifications EtCO High 2 Range 2095 mmHg (213 kPa) Adjustment 1 mmHg (0.1 kPa) steps Delay <14 seconds EtCO2 Low Range 1090 mmHg (112 kPa) Adjustment 1 mmHg (0.1 kPa) steps Delay <14 seconds Performance Specifications Measurement Range Accuracy (After 5 minutes warmup) 0150 mmHg (020.0 kPa) or 20% CO , whichever is lower 2 These specifi cations are valid for: · 21% O2 and balance N2 · Up to 35° C ambient temperature · Up to 60 rpm for adults and 100 rpm for neonates · Values between 0 and 40 mmHg (0 and 5,3 kPa): ±2.2 mmHg ±0.30 kPa) · Values above 40 mmHg (5.3 kPa): ± (5% + 0.08% per mmHg above 40 mmHg) of reading Resolution · Numeric: 1 mmHg (0.1 kPa) · Wave: 0.1 mmHg (0.02 kPa) Warm-up Time Up to 5 minutes, with an accuracy of ±4 mmHg or ± 12% of reading, whichever is greater Sample Flow Rate 50 + 15 ml/min - 7.5 ml/min Rise Time Step Response 1090% · 190 ms for neonatal patients (measured with M1923A FilterLine H Set Infant/Neonatal) · 240 ms for adult patients (measured with M1921A FilterLine H Set Adult/ Pediatric) Gas Sampling Delay Time Sampling delay time from an input step change at the airway adapter until the measured signal changes by 10% of the input step. 2 m Sample Lines Maximum 3 seconds 4 m Sample Lines Maximum 6 seconds Total System Response Time Sum of Gas Sampling Delay Time and Rise Time Endtidal CO2 (et CO2) Alarm Limits Range · EtCO low: 1090 mmHg (112 kPa) 2 · EtCO2 high: 2095 mmHg (213 kPa) Adjustments 1 mmHg (0.1 kPa) steps CO2 Alarm Delay <14 seconds (excluding Total System Response Time) 13 Philips FAST SpO 2 (867030 SP1) Complies with: · ISO 80601261:2011 · EN ISO 80601261:2011 Nellcor OxiMax SpO 2 (867030 SP6) Complies with: · ISO 80601261:2011 · EN ISO 80601261:2011 Philips FAST SpO2 Performance Specifications Range and Resolution Range 0100% Resolution 1% Perf Range 0.0230.0 Resolution 0.1, 0.01 for small values Pulse Range 30300 bpm Accuracy ±2% or 1 bpm, whichever is greater Resolution 1 bpm Pulse Oximetry Performance Specifications SpO2 Measurement range 1100% Resolution 1% Accuracy For information about accuracy see Philips 867030 Technical Data Sheet Low perfusion accuracya 2% (70100%) Pulse Range 25300 bpm Resolution 1 bpm Accuracy ±3 bpm (20250 bpm) a Specification applies to the performance of the device. Reading accuracy in the presence of low perfusion (detected IR pulse modulation amplitude 0.031.5%) was validated using signals supplied by a patient simulator. SpO2 and pulse rate values were varied across the monitoring range over a range of weak signal conditions and compared to the known true saturation and pulse rate of the input signals. Masimo rainbow SET SpO (867030 SP5) 2 Complies with: · ISO 80601261:2011 · EN ISO 80601261:2011 Measurement Accuracy SpO2, no motion · 6080 ±3%, Adult/pedi/infant · 70100 ±2%, Adult/pedi/infant, ±3% Neo Measurement Range and Resolution SpO2 Range 0100% Resolution 1% Pulse Range 25-240 bpm Resolution 1 bpm For more information on Philips IntelliVue X3 (867030), measurement extensions (867039, 867040, 867041), and Dock (867043), refer to the separate technical data sheets. 14 15 Patient cables, sensors and Accessories for Philips Hemo system Category ECG SpO 2 NIBP (NBP) CO Temp Name CBL 5+5: 10 lead ECG trunk cable, AAMI/IEC, 2.7m CBL 5 lead ECG trunk, AAMI/IEC, 2.7m CBL 5 leadset, grabber, chest, AAMI/ICU CBL 5 leadset, grabber, limb, AAMI/ICU CBL 5 leadset, grabber, chest, IEC/ICU CBL 5 leadset, grabber, limb IEC/ICU Disposable radiolucent leads IEC Disposable radiolucent leads AAMI CBL SpO 9-pin D-sub adapter 1.1 m (8-pin) 2 Reusable clip adult SpO sensor 2 Disposable adult/pedi SpO2 sensor Infant disposable SpO sensor 2 Neo / infant / adult disposable SpO sensor 2 Wristband Reusable NIBP Comfort Cuff assortment NIBP Hose Reusable NIBP Comfort Cuff Adult Long Kit - 3 sizes Reusable NIBP Comfort Cuff, infant Reusable NIBP Comfort Cuff, pediatric Reusable NIBP Comfort Cuff, small adult Reusable NIBP Comfort Cuff, small adult XL Reusable NIBP Comfort Cuff, adult Reusable NIBP Comfort Cuff, adult XL Reusable NIBP Comfort Cuff, large adult Reusable NIBP Comfort Cuff, large adult XL Reusable NIBP Comfort Cuff, thigh Reusable NIBP Comfort Cuff assortment, smaller sizes (infant, pediatric, small adult, adult) Reusable NIBP Comfort Cuff assortment, larger sizes (small adult, adult, large adult, thigh) Ice bath temperature probe Cardiac output cable, 4.8 m CO-Set injectate temp probe, 0.5 m Skin surface temperature probe Gobi reusable skin probe 16 Philips ID old P/N M1949A M1668A M1976A M1968A M1978A M1971A 989803156271 989803156261 M1943A M1196A M1131A M1132A M1133A M1627A M1579A M1599B M1579XL M1571A M1572A M1573A M1573XL M1574A M1574XL M1575A M1575XL M1576A M1577A M1578A 23002A M1643A 23001A 21078A 989803203581 Respironics etCO2 Capnostat 5 Mainstream intubated Mainstream CO2 sensor Airway Adapter Adult/Pediatric Reusable Use with ET tube > 4mm Airway Adapter Infant Reusable Use with ET tube < 4mm Deadspace < 1cc Single patient use adult airway adapter Single patient use infant airway adapter Gas cylinder regulator GAS Verification gas Respironics Lo-Flo etCO2 Sidestream non-intubated Sidestream CO2 sensor CO nasal cannula - adult 2 CO2 nasal cannula - pediatric CO2 nasal cannula - infant CO /O nasal cannula - adult 2 2 CO2 /O2 nasal cannula - pediatric CO2 oral-nasal cannula - adult CO oral-nasal cannula - pediatric 2 CO /O oral-nasal cannula - adult 2 2 CO2/O2 nasal cannula - pediatric Airway Adapter Set - ET > 4.0 mm Airway Adapter Set H - ET > 4.0 mm Airway Adapter Set H - ET > 4.0 mm Airway Adapter Set ET > 4.0 mm EtCO /O Nasal Cannula - Infant/ Neonate 2 2 Straight Sample Line, non-humidified Straight Sample Line H, humidified Straight airway adapter. Single patient use Reusable Nafion sample tube Elbow airway adapter. Single patient use Bacteria filter (0.45 micron). Single patient use Hybrid Nafion polyethylene sample tube. Single patient use Nafion length: 6 ft (1.8m) Polyethylene length: 9 ft (2.7m) CO2 Microstream intubated and non-intubated FilterLine Set, Adult/Pedi, Intubated FilterLine H Set, Adult/Pedi, Intubated FilterLine H Set, Infant/Neonatal, Intubated FilterLine® Set Long, Adult/Pediatric FilterLine H Set Long, Adult/Pediatric FilterLine H Set Long, Infant/Neonatal VitaLineTM H Set, Adult/Pediatric VitaLineTM H Set, Infant/Neonatal Smart CapnoLine® O Pediatric 2 Smart CapnoLine® O2 Adult/Intermediate Smart CapnoLine® Pediatric M2501A M2513A M2516A M2533A M2536A M2505A M2506A M2741A M2744A M2745A M2746A M2750A M2751A M2756A M2757A M2760A M2761A M2768A M2772A M2773A 989803144531 989803144471 M2776A M2777A M1612A 13901A 13902A 13904A 13905A M1920A M1921A M1923A 989803160241 989803160251 989803160261 989803159571 989803159581 M2520A M2522A M2524A 17 Workstation specification CO2 Microstream intubated and non-intubated Other Smart CapnoLine® Adult/Intermediate Smart CapnoLine® O2 Pediatric Long Smart CapnoLine® O Plus Adult Long 2 Smart CapnoLine® Plus Adult Long CapnoLine® H O2 Adult CapnoLine® H O Pediatric 2 NIV Adult NIV Pediatric CapnoLine® H Adult CapnoLine® H Infant/Neonatal Smart CapnoLine® H O2 Adult Smart CapnoLine® H O Adult Long 2 Smart CapnoLine® H O2 Pediatric Smart CapnoLine® H O2 Pediatric Long CapnoLine® H O Infant/Neonatal 2 CapnoLine® H Infant/Neonatal Long Nasal FilterLine® Infant/Neonatal Smart CapnoLine® Guard Smart CapnoLine® Guard O 2 Smart CapnoLine® Guard O2 Long Hook and Loop Strap Nasal FilterLine® O Adult 2 Nasal FilterLine® O2 Adult Long Nasal FilterLine® O2 Pediatric Calibration Regulator TRADE COMPLIANT: FILTERLINE, ADULT/PED TRADE COMPLIANT:FILTERLINE H, ADULT/PED TRADE COMPLIANT:FILTERLINE H, INFANT/NEO TRADE COMPLIANT:VITALINEH SET, ADULT/PED TRADE COMPLIANT:SMART CAPNOLINE O2 PED TRADE COMPLIANT:SMART CAPNOLINE O ADULT 2 TRADE COMPLIANT:SMARTCAPNOLINEH O2 ADULT TRADE COMPLIANT:SMARTCAPNOLINEO2,ADULT4M TRADE COMPLIANT:SMART CAPNOLINE GUARD O 2 TRADE COMPLIANT:SMARTCAPNOLINEGUARDO2 4M TRADE COMPLIANT:CAPNOLINE H O2 ADULT Patient cable organizer For more information about s complete set of the supplies and accessories, refer to the separate "Philips IntelliVue Accessories" Technical Data Sheet M2526A 989803160271 989803160281 989803160301 M4680A M4681A M4686A M4687A M4689A M4691A 989803177951 989803177961 989803177971 989803177981 989803178001 989803178011 989803178021 989803178031 989803178041 989803178051 989803178071 989803179101 989803179111 989803179121 M2267A 989803182911 989803182921 989803182931 989803182941 989803182951 989803182961 989803182971 989803182981 989803182991 989803183001 989803183071 M2281A Control room workstatioin: 8 GB RAM Intel Core i5 8500 6C CPU HDD 500GB HDD 1TB (Standalone only) NVIDIA Quadro P400 2GB Exam room workstation: 4 GB RAM Intel Core i5-6300U HDD 500GB Displays: Control room display: 1920x1200 24" or 1920x1080 24" Exam Room displays 1280x1024 19" or 1920x1080 27" Size of displayed ECG waves: To ensure that the size of ECG waves on the attached displays are within 10% of the size indicated by the Philips Hemodynamic Application, the pixel density of the display should be 89 +/- 10% dpi (i.e. the dot size should be 0.285 +/- 10% mm). 18 19 © 2020 Koninklijke Philips N.V. All rights reserved. Specifications are subject to change without notice. Trademarks are the property of Koninklijke Philips N.V. or their respective owners. 4522 991 57361 * Mar 2020 How to reach us Please visit www.philips.com healthcare@philips.comAdobe PDF Library 15.0 Adobe InDesign 15.0 (Macintosh)