Axia TRIA Touch Screen Patient Monitor

  • Axia TRIA Touch Screen Patient Monitor Multiparameter and ECG Monitors

The Axia TRIA is a new and intuitive approach to patient vital signs measurements. The TRIA can be configured to measure any combination of non-invasive blood pressure, SpO2, rapid temperature and capnography (EtCO2).

The TRIA is well suited for any patient care area by offering a multitude of vital sign combinations. The TRIA can be used as a basic pulse oximeter or configured to an NIBP / SpO2 / Temp spot-check monitor. The TRIA can also be configured to be a stand-alone capnograph or a combination of capnograph SpO2 / NIBP monitor. The TRIA is well suited for bedside and mobile spot check use.

Description

Axia TRIA Touch Screen Patient Monitor Features

  • Touch screen
  • Simple interface
  • Intuitive
  • Long life Lithium Battery
  • Mobile (Backup battery powered)
  • Portable (weight 1.71 lbs)
  • Color waveforms
  • Neonatal, pediatric and adult patient applications

Axia TRIA Touch Screen Patient Monitor Specifications

Axia TRIA Touch Screen Patient Monitor Dimensions & Weight:

  • 8 x 4.5 x 4 (HxWxD inches)
  • 2.5 LBS

DISPLAY

  • Display: 5.0 inch (Diagonal) color TFT
  • Resolution: 800 × 3(RGB) × 480
  • Trace: 2 waveforms
  • Waveforms: PLETH, ETCO2
  • Indicator: Alarm Indicator, Power Indicator, Pulse Beep and Alarm Sound
  • Trend time: From 1 to 72 hours

LCD

  • Display Type: TFT color LCD
  • Size (diagonal): 5.0 inch
  • Active Area: 152.4 (W) × 91.44 (H) mm
  • Color arrangement: RGB-stripe
  • Dot pitch: 0.0635(W) × 0.1905(H) mm
  • Display Mode: Normally white, Transmissive
  • Interface: Digital (TTL)
  • Surface: Treatment: Anti-Glare

TOUCHSCREEN

  • Type: Four-Wire Analog Resistive Touch Panel
  • Input Mode: Stylus Pen or Finger
  • Connector: FPC
  • Insulation resistance: 25MΩ
  • Voltage: 7VDC
  • Chattering: 10ms
  • Transparency: 80%
  • Surface hardness: 3H
  • Durability-surface scratching: Write 100,000
  • Active force: 80gf
  • Knock Test: 1,000,000 times

PERFORMANCE

SPO2

  • ASpO2: Anti-motion SpO2
  • SpO2% Range: 0 ~ 100%
  • SpO2 Accuracy: ±2% (70 ~ 100%,non-motion) ±3% (70 ~ 100%, motion)
  • Pulse Rate Range: 30-250 bpm
  • Pulse Rate Accuracy: ±2 bpm(non-motion), ±3 bpm (motion)
  • Alarm Upper-lower Limit: Upper limit 70 ~ 100%, Lower limit 70 ~ 100%
  • SpO2 Probe:
    • Red light LED wavelength: 660nm±5nm
    • Infrared light LED wavelength: 940nm±10nm
  • Standards: Meets performance of EN ISO 9919:2015

NIBP

  • Measuring Technology: Automatic oscillating measurement
  • Cuff Inflating: <30s (0 ~ 300 mmH, standard adult cuff)
  • Measuring Period: AVE<40s
  • Mode: Manual, Auto, STAT in AUTO Mode: 2 min ~ 4 hrs
  • Pulse Rate Range: 30 bpm ~ 250 bpm
  • Measuring Range:
    • Adult/Pediatric Mode
      • SYS: 40 ~ 250 (mmHg)
      • DIA: 15 ~ 200 (mmHg)
    • Neonatal Mode
      • SYS: 40 ~ 135 (mmHg)
      • DIA: 15 ~ 100 (mmHg)
  • Resolution: 1mmHg
  • Pressure Accuracy: Maximum Mean error: ±5mmHg
  • Deviation: 8mmHg
  • Overpressure Protection:
    • Adult Mode: 280(mmHg)
    • Neonatal Mode: 150 (mmHg)
  • Alarm Limit:
    • SYS: 50 ~ 240 mmHg
    • DIA: 15 ~ 180 mmHg
  • Standards: Meets performance standards ANSI/AAMI SP10:2002

RAPID TEMPERATURE (OPTION)

  • Measurement Range: 30°C to 43°C (86°F to 109°F)
  • Typical Measurement Times (after insertion into measurement site):
    • Oral (Quick Mode): 3-5 seconds (non-fever temps), 8-10 seconds (fever temps)
    • Oral (Standard Mode): 6-10 seconds
    • Axillary Mode: 8-12 seconds
    • Rectal Mode: 10-14 seconds
    • Direct Mode (All Sites): 60-120 seconds
  • Pulse Timer: 60 Second count with a “beep” at 15 seconds, 2 “beeps” at 30 seconds, 1 “beep” at 45 seconds, and 2 “beeps”at 60 seconds
  • Patient Accuracy: A Standard Prediction Mode reading and a Direct Mode reading will differ by less than ±0.2°C (±0.4°F) on 98% of tested patients
  • Batteries: Four “AA” Required, Standard IEC package size. Alkaline –1.5 Volt, Approx. 6000 temperature readings
  • Standards: Meets performance standards of EN 12470-3:2000 and ASTM E1112:2006

ETCO2 (OPTION)

  • Mode of Sampling: Sidestream or Mainstream
  • Principle of Operation: Non-dispersive infrared (NDIR) single beam optics, dual wavelength, no moving parts.
  • CO2 measurement Range: 0 to 150 mmHg (0 to 19.7%, 0 to 20 kPa)
  • CO2 Calculation Method: BTPS (Body Temperature Pressure Saturated)
  • CO2 Resolution: 0.1mmHg (0-69mmHg), 0.25mmHg (70-150mmHg)
  • CO2 Accuracy:
    • 0 ~ 40 mmHg ± 2 mmHg
    • 41 ~ 70 mmHg ± 5% of reading
    • 71 ~ 100 mmHg ± 8% of reading
    • 101 ~ 150 mmHg ± 10% of reading
    • Above 80 breath per minute ± 12%of reading
  • Sampling rate: 100Hz
  • Respiration Rate: 2 ~ 150 bpm
  • Respiration Rate accuracy: ±1 breath
  • Response Time: <3 seconds -includes transport time and rise time
  • Measurement Range: 3 ~ 50 mmHg
  • Standards: Meets performance standards of ISO/ FDIS 21647:2004 (E)

NETWORKING

  • Wired Networking:
    • Industry standard: 802.11b/g wired network
    • Frequency Range: 2.412 ~ 2.484 GHz
    • Connected bedside number: Up to 16 bedside monitors
  • Wireless Networking: Up to 100m indoors Industry standard 802.11b/g wireless Supports TCP/IP and UDP/IP Protocols

POWER

  • Source: External AC power or internal battery
  • AC Power: 100 ~ 240VAC, 50/60Hz, 150VA
  • Battery: Built-in and lithium-Ion rechargeable, 12.6V/5Ah
  • Charge Time: 8 hours
  • Operating Time: 3 hours
  • FUSE: 3.15A/250V

SAFETY

  • Meet the requirement of EN60601 series, CE marking according to MDD93/42/EEC
  • Type of Protection: Class I (on AC power) , internally powered equipment (on battery power): Per I.E.C. 60601-1, clause 2.2.4
  • Degree of Protection: Type BF, defibrillator-proof CF – Applied part
  • Sterilization or Disinfection methods: 70% isopropyl alcohol solution or a non staining disinfectant. Equipment not suitable for use in the with air or with oxygen or nitrous oxide
  • Operation Mode: Continuous
  • Protection Against Ingress of Liquids: IPXO

Additional information

Brand

Axia