Datascope Product Detail
Model: Trio
The Trio is a portable, configured monitor designed for use in many hospital departments and outpatient areas – from traditional bedside monitoring to intra-hospital transport. Its high-resolution color display far exceeds the standard in compact patient monitors.
The Trio, with a rechargeable battery, allows you to continuously monitor vital signs while transporting the patient.
Features:
- 8.4'' color TFT display with a resolution of 800 x 600 provides optimal visualization of patient data
- Standard features include up to 4 waveforms, 3 or 5 lead ECG, Respiration, NIBP, SpO2 and Temperature
- Many options available including Masimo SET motion tolerant SpO2, Nellcor OxiMax SpO2, invasive blood pressure, Lithium Ion battery and a dual trace recorder
- 24 hour graphic and list trends with event markers provide extended review of all patient data
- Default menu stores user configured settings for each patient size
- Waveform and numeric data are configurable to five colors
- Ergonomically designed fold-away handle with built-in bed rail hook provides maximum flexibility and easy handling
- Built-in Power Supply for direct AC connection allows for convenient transport from one location to the next
- Navigator Control Knob and quick action keys make for easy-to-use functions
Specifications:
- ECG
- Input: 5-lead or 3-lead selectable
- Leads: I, II, III, aVR, aVL, aVF, V
- Gain: x0.25; x0.5; x1; x2
- Sweep Speed: 12.5 mm/s, 25 mm/s, 50 mm/s
- Frequency Response to Screen
- Extended Mode: 0.05–100 Hz, -3 dB max
- Monitor Mode: 0.5–40 Hz, -3 dB max
- Surgical Mode: 1–20 Hz, -3 dB max
- CMRR
- Extended Mode: >90 dB min
- Monitor Mode: >105 dB min
- Surgical Mode: >105 dB min
- Analog Output (ECG):
- Delay: 25 ms
- Sensitivity: 1 V/mV of input, ± 10%
- Heart Rate Meter
- Range: 15-300 BPM Adult, 15-350 BPM Pediatric
- Accuracy: ±1 BPM or ±1% whichever is greater
- Pacer Rejection: Rejects all pulses of amplitude ±2.0 mV to ±700 mV and duration. 0.1 ms to 2 ms with no tail per ANSI/AAMI EC13-2002 4.1.4.1. Rejects all pulses of amplitude ±2.0 mV to ±700 mV and duration. 0.1 ms to 2 ms with 100 ms time constant tail of less than 2.0 mV, or 4 ms time constant tail of less than 2.0 mV per ANSI/AAMI EC13-2002 4.1.4.2
- Tall T-Wave Rejection: Rejects all T-Waves less than 120% of a 1 mV, 100 ms QRS, and a T-Wave duration of 180 ms and a Q-T interval of 350 ms per ANSI/AAMI EC13-2002 4.1.2.1c.
- Display
- Size: 8.4 inch (21.3 cm) Color TFT
- Resolution: VGA 800 x 600
- Waveforms: 4
- Sweep Speed: 6.25 mm/s, 12.5 mm/s, 25 mm/s, 50 mm/s
- IBP Information
- Range: Sys/Dia/Mean -50 to +300 mmHg
- Accuracy: ± 1 mmHg or ± 2% whichever is greater
- Default Scale: ART: 0-150 mmHg, PA: 0-100 mmHg, CVP: 0-40 mmHg, RAP:0-40 mmHg, LAP: 0-40 mmHg, ICP: 0-40 mmHg
- Zero Range: ± 200 mmHg
- Excitation: 5 Volts DC, ± 2%
- Frequency Response: DC to 16 Hz ± 1 Hz, -3 db
- Pressure Labels: ART, PA, CVP, RAP, LAP, ICP
- Analog Output (IBP):
- Delay: 25 ms, without sensor, measured using a simulator as the input
- Sensitivity: 1 V/100 mmHg, ± 10%
- Non-Invasive BP
- Technique: Oscillometric
- Measurement Intervals: 1 min, 2 min, 3 min, 4 min, 5 min, 10 min, 15 min, 30 min, 1 hr, 2 hrs, 4 hrs, CONT, OFF
- Systolic Range: Adult: 40-255 mmHg Pediatric: 40-200 mmHg
- Diastolic Range: Adult: 10-210 mmHg Pediatric: 10-150 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
- Connector Type: Rectus
- Temperature
- Scale: Selectable °C or °F
- Range: 0–50 °C / 32–122 °F
- Accuracy: ± 0.1 °C (0–50 °C) exclusive of probe errors. ± 0.2 °F (32–122 °F) exclusive of probe errors
- Respiration (ECG)
- Method: RA-LL impedance
- Range: Adult: 6–120 BPM, Pediatric: 6–150 BPM
- Accuracy: ± 2% or ± 2 breaths per minute, whichever is greater
- Lead: II
- Recorder
- Pulse Oximetry
- Masimo SET SpO2 Saturation Accuracy with no motion conditions
- Adult/Pediatric: 70% to 100% ±2 digits SpO2
- Masimo SET SpO2 Saturation Accuracy during motion conditions
- Adult/Pediatric: 70% to 100% ±3 digits SpO2
- Response Time: 20 seconds to 95% of final step of % SpO2 value from 60–95% at 75 BPM. Averaging set at 8 seconds.
- Nellcor OxiMax SpO2 Saturation Accuracy
- Adult/Pediatric: 70% to 100% ±2 digits SpO2
- Sensors: MAX-A, MAX-AL, MAX-N, MAX-P, MAX-I, MAX-FAST
- Adult/Pediatric: 70% to 100% ±3 digits SpO2
- Sensors: DS-100A, OXI-A/N, OXI-P/I, D-YS
- Pulse Rate Range Masimo with no motion conditions - Adult/Pediatric: 30-235 BPM ±3 BPM
- Pulse Rate Range Masimo during motion conditions - Adult/Pediatric: 30-235 BPM ±5 BPM
- Pulse Rate Range Nellcor Adult/Pediatric: 20–250 BPM ±3 BPM
- Electrical Ratings
- AC Voltage: AC100240 V, 50/60 Hz
- Battery Type: Sealed Lead Acid or Lithium Ion
- Number of Batteries: 1
- Battery Voltage:
- Sealed Lead Acid: 12 Vdc
- Lithium Ion: 10.8 Vdc
- Battery Capacity:
- Sealed Lead Acid: 2.3 A-Hr
- Lithium Ion: 3.6 A-Hr
- Battery Run Time:
- Sealed Lead Acid: 75 minutes from one fully charged new battery at 25 °C with ECG, SpO2, and NIBP every 15 minutes.
- Lithium Ion: 3 hours from one fully charged new battery at 25 °C with ECG, SpO2, and NIBP every 15 minutes.
- Battery Recharge Time:
- Sealed Lead Acid: 8 hours max
- Lithium Ion: 6.5 hours max
- Environmental Conditions
- Storage Altitude: -1,000 to 20,000 ft ASL, 1050 hPa to 466 hPa, 788 mmHg to 349 mmHg
- Storage Temperature: -20 to 60 °C/ -4 to 140 °F
- Storage Humidity: 10–95% non-condensing
- Operating Altitude: -1,000 to 9,889 ft ASL, 1050 hPa to 700 hPa, 788 mmHg to 525 mmHg
- Operating Temperature: 5 °C to 40 °C/ 41 °F to 104 °F
- Operating Humidity: 15–95% non-condensing
- Physical
- Monitor Size: 241 mm W x 228 mm H x 174 mm D (9.49" W x 8.98" H x 6.85" D)
- Monitor Weight: 4 kg (8.8 lbs) excluding battery & optional accessories. 4.66 kg (10.25 lbs) including 1 sealed lead acid battery excluding optional accessories. 4.33 kg (9.52 lbs) including 1 lithium ion battery excluding optional accessories.
- Agency Compliances
- Safety: IEC 60601-1:1988 +A1:1991, A2:1995/EN 60601-1:1990 +A1:1993, A2:1995, A13:1995, UL 2601-1:1997, CSA Standard C22.2 No.601.1M90, IEC 60601-1-4:1996 / EN 60601-1-4:1996 + A1:1999, IEC 60601-2-30:1999/EN 60601-2-30:2000, IEC 60601-2-34:2000/EN 60601-2-34:2000, IEC 60601-2-27:1994 / EN 60601-2-27:1994, EN 12470-4:2000
- Hazard: EN 1441:1997, EN ISO 14971:2000
- Performance: EN 865:1997, EN 1060-1:1995, EN 1060-3:1997, ANSI/AAMI EC13:2002, ISO 3744:1994, ANSI/AAMI/ISO 10993-1:1997, AAMI SP10:1992, EN 475:1995, EN 1041:1998, EN 980:1996 + A1:1999 + A2:2001, IEC 878:1998, ISO 1000:1992 + A1:1998
- Environmental: IEC 60601-1-2:2001/EN 60601-1-2:2001, IEC 68-2-6:1982 +A1:1983 +A2:1985, IEC 68-2-27:1987, IEC 68-2-37:1973 +A1:1983, IEC 529: 1989, ISTA: 1998 Procedure 1A, ECRI PB-296892:1979 (Drop and impact)
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