Datascope Product Detail
Model: Passport 2
The Passport 2 is a portable bedside monitor that can be configured to meet the demands of many hospital departments. The Passport 2, with rechargeable batteries, allows continuous vital signs monitoring during patient transport.
Features:
- 10.4 inch color TFT display with auto-adjustable large numerics optimizes visibility
- Navigator knob and dedicated function keys provide instant access to critical monitoring functions
- Standard features include 6 waveforms, 3 or 5-lead ECG, lead-selectable respiration, NIBP, Masimo SET motion tolerant SpO2 and temperature
- Many options available including ventricular arrhythmia analysis, Microstream ETCO2, Nellcor SpO2, dual invasive pressures, 3-lead ST analysis with trends and alarms and dual trace recorder
- Optional View 12 ECG Analysis Module includes 12-leads of continuous ST, arrhythmia and diagnostic interpretations printable to a laser printer
- List and graph trends store up to 120 patient time measurements - expandable to 500 entries with extended memory
- Software enhancements, memory expansion, and data transfers are quick and easy with the use of dual PCMCIA ports
- Complete 5-agent auto ID, CO2, O2 and N2O analysis available with optional Gas Module SE
- Network to Panorama Central Station for continuous data storage
Specifications:
- Display
- Size: 10.4 inch (26.4 cm) Color TFT
- Resolution: VGA 640-480
- Waveforms: 3 to 6
- ECG (3-Lead and 5-Lead)
- Leads: I, II, III, aVR, aVL, aVF, V
- Cable Detection: Autodetecting Datascope 3 or 5 wire
- Display Sensitivity: 0.25, 0.5, 1.0, 2.0, 3.0, 4.0, cm/mV ± 10%
- Frequency Response To Screen
- Extended Mode: 0.05 100 Hz, -3db max @ 1mVpp input
- Monitor Mode: 0.5 40 Hz, -3db max @ 1mVpp input (ESU filter disabled)
- ST Mode: 0.05 40 Hz, -3db max @ 1mVpp input
- CMRR: 90 db min, Maximum output of 1mVp-p (RTI) over 60 seconds at 50/60 Hz, with parallel combination 51K Ω and 0.047 uF imbalance and ± 300 mV. DC offset per AAMI EC13-1992 3.2.9.10
- ECG Sync Pulse for Cardioversion:
- Delay: ≤35 ms max between QRS Peak and rising edge of Sync Pulse
- Amplitude: 2Vp minimum into a 5k ohm load
- Width: 2-7 msec
- Analog Output (ECG): Supports slaving of an IABP with ECG
- Delay: 25 ms max
- Sensitivity: 1 V/mV of input, ± 10%
- Defibrillator Overload Protection: Withstand 360 Joule discharge as per IEC 60601-2-27, 51.101.1
- Recovery Time: Time for recovery to within 1mV in < 8 seconds automatically. 3 seconds from 1Vpp at 60Hz
- ECG (12-Lead)
- Leads: I, II, III, aVR, aVL, aVF, V1, V2, V3, V4, V5, V6
- Connection Type: Type II PCMCIA card to be installed in PCM 1 slot
- Cable Detection: Automatically enabled when 12-lead Card is inserted into PCM 1 slot
- Frequency Response
- Extended Mode: 0.05 100 Hz, -3db max @ 1mVpp input
- Monitor Mode: 0.5 40 Hz, -3db max @ 1mVpp input (ESU filter disabled)
- ST Mode: 0.05 40 Hz, -3db max @ 1mVpp input
- CMRR: 90 db min, Maximum output of 1mVp-p (RTI) over 60 second period at 50/60 Hz, with a parallel combination 51K Ω and 0.047 uF imbalance and ± 300 mV DC offset per ANSI/AAMI EC11-1991, 3.2.11
- Analog Output (ECG): Disabled when 12-lead ECG analysis is enabled
- Defibrillator Overload Protection: Withstand 360 joule discharge as per IEC 60601-2-27, 51.101.1
- Heart Rate Meter
- Range: 30 300 BPM Adult/Pediatric, 30 350 BPM Neonate 3-lead and 5-lead / 30 300 BPM 12-lead
- Accuracy: ± 3 BPM or ± 3% at 30 250 BPM whichever is greater, ± 5% at 251 350 BPM
- Pacer Rejection: Rejects all pulses of amplitude ± 2.0 mV to 700 mV and duration 0.1 to 2 ms with no tail. AAMI EC-13-1992 3.1.4.1 (3-Lead and 5-Lead) Rejects all pulses of amplitude ± 2.0 mV to 700 mV and duration 0.1 to 2 ms with 100 ms time constant tail of less than 2.0 mV, or 4 ms time constant tail of < 2.0 mV per AAMI EC-13-1992 3.1.4.2
- Tall T-Wave Rejection: Rejects all T-Waves less than 120% of 1 mV QRS and Q-T interval of 350 ms per AAMI EC-13-1992 3.1.2.1 (c)
- ST Analysis
- 3-lead or 5-lead Range: -9.9 mm to +9.9 mm
- 12-lead Absolute Range: -10 mm to +10 mm
- 12-lead Delta Range: -20 mm to +20 mm
- Resolution: 0.1 mm
- Default ST Measuring Point: 80 ms after J point for HR ≤ 120 BPM, 60 ms after J point for HR >120 BPM
- Arrhythmia Analysis
- 3-lead or 5-lead cables: Adult / Pediatric Only: Asystole, Irregular Heart Rate, Couplets, Bigeminy, Trigeminy, Ventricular Tachycardia, Ventricular Fibrillation, PVCs per minute, Runs, Ventricular Rhythm and Bradycardia
- 12-lead: Adult / Pediatric Only: Asystole, Couplets, Runs, Bigeminy, Trigeminy, Ventricular Tachycardia, Ventricular Fibrillation, PVCs per minute, Ventricular Rhythm, and Pause
- Respiration (ECG)
- Range: 4 to 199 BPM
- Accuracy: ± 2% or 2 breaths per minute whichever is greater from 4 to 150 BPM, ± 4% from 151 to 199 BPM
- Lead: I or II
- Temperature
- Scale: Selectable C or F
- Range: 15 to 45 C / 59 to 113 F
- Accuracy: ± 0.1 C (15 C to 45 C) exclusive of probe errors. ± 0.2 F (59 F to 113 F) exclusive of probe errors.
- Non-Invasive BP
- Technique: Oscillometric
- Systolic Range: Adult 55-235 mmHg Pediatric 55-160 mmHg Neonate 45-120 mmHg
- Diastolic Range: Adult 30-200 mmHg Pediatric 30-150 mmHg Neonate 20-100 mmHg
- Systolic Accuracy: Mean Error less than ± 5 mmHg, Standard Deviation less than ± 8 mmHg
- Diastolic Accuracy: Mean Error less than ± 5 mmHg, Standard Deviation less than ± 8 mmHg
- Pulse Rate Range: Adult/Pediatric: 35 to 245 BPM Neonate: 70 to 245 BPM
- Pulse Rate Accuracy: ± 3 BPM or 3% whichever is greater
- Connector Type: Rectus
- Cuff Inflation: Volume of 500cc to 300 mmHg in ≤35 sec
- Pulse Oximetry
- Classification per ISO 9919: Functional Saturation Oximeter
- Masimo SET SpO2 Accuracy Saturation with no motion conditions
- Adult/Pediatric: 70% to 100% ± 2 digits SpO2, 0-69% unspecified
- Neonate: 70% to 100% ± 3 digits SpO2, 0-69% unspecified
- Ear Sensor (Adult/Pediatric): 70% to 100% ± 4 digits SpO2, 0-69% unspecified
- Masimo SET SpO2 Accuracy Saturation during motion conditions
- Adult/Pediatric/Neonate: 70% to 100% ± 3 digits SpO2
- Response Time: 18 seconds to 95% of final step of % SpO2 value from 60-95% at 75 BPM. Averaging set at 8 seconds.
- Pulse Rate Range Masimo with no motion conditions
- Adult/Pediatric/Neonate: 30-235 ± 3 BPM, Ear Sensor (Adult/Pediatric) 30-235 ± 3 BPM
- Pulse Rate Range Masimo during motion conditions
- Adult/Pediatric/Neonate: 30-235 ± 5 BPM
- Low Perfusion Performance
- Masimo: > 0.02% Pulse Amplitude and % Transmission > 5% / Saturation (% SpO2) ± 2 digits; Pulse ± 3 digits
- Nellcor OxiMax SpO2 Saturation Accuracy
- Adult/Pediatric/Neonate: 70% to 100% ± 3 digits
- Pulse Rate Range Nellcor: 20-249 ± 3 BPM
- IBP
- Range: Sys/Dia/Mean -30 +300 mmHg
- Accuracy: ± 2 mmHg or 2% whichever is greater
- Scale: -10 to 10, 0-20, 0-40, 0-160, 0-225, 0-320, 60-140 mmHg
- Zero Range: ± 120 mmHg
- Excitation: 5V DC ± 2%
- Frequency Response: DC to 16 Hz ± 1Hz, -3db
- Analog Output (IBP): Supports slaving of an IABP with IBP
- Delay: 25 ms max
- Sensitivity: 1 V/100 mmHg ± 10%
- Recorder
- Speed: 3.125, 6.25, 12.5, 25mm, and 50mm/sec Note: 3.125 speed is for CO2/Resp only.
- CO2 (MICROSTREAM MINIMEDI)
- Range: 0 99 mmHg
- Accuracy:
- 0 38 mmHg: ± 2 mmHg
- 39 99 mmHg: ± 5% of reading + 0.8% for every 1 mmHg above 38 mmHg
- Respiration Rate: 0 150 breaths per minute
- Respiration Accuracy:
- 0 70 BPM: ± 1 BPM
- 71 120 BPM: ± 2 BPM
- 121 150 BPM: ± 3 BPM
- Sampling Rate: 50 ml/min ± 7.5 ml/min
- Electrical Rating:
- AC Voltage: 100 240 VAC ± 10%, 50/60 Hz ± 3 Hz
- Battery Type: Lithium-ion
- Number of Batteries: 2
- Battery Voltage: 11.1 Vdc
- Battery Capacity: 4.4 AH each
- Battery Run Time: 5 hrs from two fully charged batteries at 25 C with ECG, SpO2 and 1 NIBP every 15 minutes, no recording, no CO2
- Recharge Time: 5 hrs max
- Environmental
- Storage Temperature: -20C - + 60C/-4F - +140F
- Storage Humidity: 10 to 95% non-condensing
- Operating Altitude: -1250 to 9,889 feet ASL, 1060hPa to 700hPa, 795 mmHg to 525 mmHg
- Operating Temperature: 5C to 40C/41F - 104F
- Operating Humidity: 15% to 95%, non-condensing
- Physical
- Monitor Size: 24.1cm H X 30.2cm W X 18.8cm D, 9.5" H x 11.9" W x 7.4" D
- Weight: 5.9 kg (13 lbs.) including (2) lithium-ion batteries, 5.2 kg (11.4 lbs.) excluding batteries
- Agency compliances
- Safety: IEC 60601-1:1988 + A1:1991 + A2:1995, UL 60601-1:2003, CSA Standard C22.2 No. 601.1M90, EN 60601-1-1:2001/IEC 601-1-1:2000, IEC 60601-1-2:Ed 2.1, EN 60601-1-4:1996 + A1:1999/IEC 601-1-4:1996 + A1:1999, EN 60601-2-30:2000/IEC 601-2-30:1999, EN 60601-2-34:2000/IEC 601-2-34:2000, EN 60601-2-49:2001/IEC 60601-2-49:2001
- 3/5 Lead ECG: EN 60601-2-25:1993/IEC 60601-2-25:1993 + A1:1999, section 36.202.101, EN 60601-2-27:1994/IEC 601-2-27:1994. 12 Lead ECG: EN 60601-2-25:1993/IEC 601-2-25:1993 + A1:1999
- Hazard Analysis (Risk Management): EN ISO 14971:2000 + A1:2003.
- Performance / Accuracy: EN 475:1995, EN 864:1996, EN 865:1997, EN 1060-1:1995 + A1:2002, EN 1060-3:1997. + A1:2005, ANSI/AAMI/ISO 10993-10:1995, ANSI/AAMI/ISO 10993-1:1995, AAMI SP10:1996, AAMI EC13:1992, AAMI EC11:1991, ISO 3744:1994
- Environmental / EMC: IEC 60068-2-6:1995 + Corrigendum 1, IEC 60068-2-27:1987, IEC 60068-2-64:1994 +. Corrigendum 1, EN60529:1991 + A1:2001 + Corrigendum 1, EN 55011:1998 + A1:1999 + A2:2002 (CISPR 11), EN 61000-3-2:2000 + A1:2001 + A2:2005, EN 61000-3-3:1995. + A1:2001 + A2:2005, EN 61000-4-6: 2003 + A1:2004 + A2:2006, EN 61000-4-3:2006, EN 61000-4-8:1993 + A1:2001, EN 61000-4-2:1995 + A1:1998 + A2:2001, EN 61000-4-4:2004, EN 61000-4-5:2005, EN 61000-4-11:2004, ECRI PB-296892:1979 (for Drop and Impact requirements), ISTA: 1994 procedure 1A, 2002/96/EC: 2003
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