ACCUCAP901 ( Capnography )

581 452 parsian medical

Mainstream / Microstream Capnography Monitoring

  • Continues Monitoring of EtCO2, Respiration Rate and FiCO2
  • Real Time CO2 Waveform
  • High Accuracy and Stability
  • The Most Efficient Capnography System for Neonates
  • In Comply with New International Standard, ISO 80601-2-55: 2011

Technical Specification

  • Internal Rechargeable Battery with 5 Hours Working Capacity
  • ETHERNET Connection Complying HL7 Protocols
  • USB Connector
  • Unlimited Trend for Several Patients
  • 7 inch TFT LCD with CAPACITIVE TOUCH panel
  • Capability to Install other Vital Sign Modules
  • Auto-Rotate Sensor for Detecting Horizontal or Vertical Positions
accucap901 digital capnography Technical Specification
Electrical Characteristics
Input Voltag 100-140 VAC, 50-60 Hz
Power Consumption 17VA
Battery Type Li-Ion
Battery Capacity 2400 mAH
Battery Charge Time 5 Hours
Fuses 250V, 500mA, 5x20mm
General Specification
Output Interfaces USB and Etherne
Trending Time  Every Second
Display  7” TFT LCD Touch Panel
Network Protocol  ER7
Dimensions (WxHxD)  30x25x10 cm3
Weight  1.5 Kg
Alarms
Audible and Visual Alarms
According to IEC 60601-1-8 :2006
High and Low EtCo2
High and Low Respiration Rate
High FiCo2
Low Battery
Related Accessories
Microstream or Mainstream Sensor
Power Cable
User Manual
Trolley
Wall stand
Extra Fuse
LOFLO® CO2 SENSOR – SPECIFICATIONS
Transducer Type Sidestream CO2Sensor
Principle of Operation Non-dispersive infrared (NDIR) single beam optics, dual wavelength, no moving parts
Initialization Time Capnogram displayed in less than 20 seconds, at an ambient temperature of 25°C
CO2 Measurement Range 0 to 150 mm Hg, 0 to 19.7%, 0 to 20 kPa (at 760 mm Hg) Barometric Pressure supplied by host
Rise Time Less than 60 ms – Adult Reusable or Single-Patient-Use Airway Adapter Less
than 60 ms – Infant Reusable or Single-Patient-Use Airway Adapter
CO2 Resolution 0.1 mm Hg    0 to 69 mm Hg
0.25 mm Hg  70 to 150 mm Hg
CO2 Accuracy 0 – 40 mm Hg ±2 mm Hg
41 – 70 mm Hg ±5% of reading
71–100 mm Hg ±8% of reading
101 – 150 mm Hg ±10% of reading
CO2 Stability Short Term Drift: Drift over four hours shall not exceed 0.8 mm Hg max.
Long Term Drift: Accuracy specification will be maintained over a 120-hour period
CO2 Noise RMS noise of the sensor shall be less than or equal to 0.25 mm Hg at 5% CO2
Respiration Rate Range 2 to 150 Breaths Per Minute (BPM)
Respiration Rate Accuracy ±1 Breath
Compensations (Host Supplied) Barometric Pressure 400 mm Hg to 850 mm Hg
Operator selectable O2, N2O, HE and Agent compensation.
Calibration No routine user calibration required.
Sample Cell/Filter Proprietary single patient use sample cell and inline filter are integrated with the sample line which eliminates contamination of the internal system
Nasal Sampling Kits for Non-intubated Patients Adult, pediatric and infant nasal CO2 sampling, nasal CO2 sampling and O2 delivery
Adult and pediatric nasal/oral CO2 sampling, nasal/oral CO2 sampling and O2 delivery
On-Airway Adapter KITS for Intubated Patients Adult/Pediatric with and without dehumidification tubing Pediatric/Infant, low dead space, with and without dehumidification tubing Taper meets ISO 5356-1
Sample Kit Hours of Use Nasal Cannula (all styles) – up to 12 hours
On-Airway Adapter Kits without dehumidification tubing–up to 12 hours
On-Airway Adapter Kits with dehumidification tubing–up to 120 hours
Sample Cell Detection Insertion automatically turns sampling pump on. Removal automatically turns sampling pump off.
Flow Control Via DP measurement across a capillary tube
Scavenging Port Yes
Voltage Requirements 5.0 VDC ±5%
Power Rating Rated input: Less than 1.3 Watts typical. Steady State Less than 2.0 Watts maximum on power up (warm up)
Temperature and Humidity Operating: 0 to 45ºC, 10 to 90% RH, non-condensing
Storage: -40 to 70ºC, <90% RH, non-condensing
Water Resistance IPX4 – Splash-proof (When sample cell is inserted in sample cell receptacle
Shock Impact IEC TR 60721-4-7 Class 7M3 (designed to withstand environments subject to significant vibrations or high shock levels)
EN60068-2-27 Shock
EN60068-2-64 Random vibration
Regulatory Designed to meet IEC 60601-1-2, EN55011 – CISPIR 11 Class B (Radiated and Conductive Emissions), IEC 61000-4-2 Electrostatic Discharge Immunity, IEC 61000-4-3 Radiated Immunity,Designed to comply with 93/42/EEC (MDD CE Marking), FDA Standards, ASTM F1456-01 Minimum Performance and Safety Requirements for Capnometers and IEC80601-2-55:2011. Medical Electrical Equipment performance requirements for the basic safety and essential performance of respiratory gas monitors.
CAPNOSTAT© 5 MAINSTREAM CO2 SENSOR – SPECIFICATION
Transducer Type Mainstream CO2Sensor
Principle of Operation Non-dispersive infrared (NDIR) single beam optics, dual wavelength, no moving parts
Initialization Time  Capnogram, displayed in less than 15 seconds at an ambient temperature of25ºC, full specifications within 2 minutes
CO2 Measurement Range 0 to 150 mm Hg, 0 to 19.7%, 0 to 20 kPa (at 760 mm Hg) Barometric Pressure supplied by host
Rise Time Less than 60 ms – Adult Reusable or Single-Patient-Use Airway Adapter Less than 60 ms – Infant Reusable or Single-Patient-Use Airway Adapter
CO2 Resolution 0.1 mm Hg    0 to 69 mm Hg
0.25 mm Hg  70 to 150 mm Hg
CO2 Accuracy 0 – 40 mm Hg ±2 mm Hg
41 – 70 mm Hg ±5% of reading
71–100 mm Hg ±8% of reading
101 – 150 mm Hg ±10% of reading
CO2 Stability Short Term Drift: Drift over four hours shall not exceed 0.8 mm Hg max.
Long Term Drift: Accuracy specification will be maintained over a 120-hour period
CO2 Noise  RMS noise of the sensor shall be less than or equal to 0.25 mm Hg at 7.5% CO2
Respiration Rate Range 2 to 150 Breaths Per Minute (BPM)
Respiration Rate Accuracy ±1 Breath
Compensations (Host Supplied) Barometric Pressure 400 mm Hg to 850 mm Hg
Operator selectable O2, N2O, HE and Agent compensation.
Calibration  No routine user calibration required. An airway adapter zero is required when changing to a different style of airway adapter.
Airway Adapters  Single-patient-use or reusable, < 5 cc dead space (adult), <1 cc dead space infant Adapter taper meets ISO 5356-1
Voltage Requirements  +5.0 VDC, 1.125 W Typical, 1.5 W Maximum.
Power Rating  Rated input: 1.1 Watts typical. Steady State Up to 1.5 Watts maximum on power up (warm up)
Temperature and Humidity  Operating: 0 to 45ºC, 10 to 90% RH, non-condensing
Storage: -40 to 70ºC, <90% RH, non-condensing
Water Resistance  IPX4 – Splash-proof (sensor head only)
Shock Impact EN60068-2-6 Sinusoidal Vibration
EN60068-2-27 Shock
EN60068-2-64 Random Vibration
Able to withstand repeated 6-foot drops onto tiled floor while operating
Regulatory Designed to meet IEC 60601-1-2, EN55011 – CISPIR 11 Class B (Radiated and Conductive Emissions), IEC 61000-4-2 Electrostatic Discharge Immunity, IEC 61000-4-3 Radiated Immunity, Designed to comply with 93/42/EEC (MDD CE Marking), FDA Standards, ASTM F1456-01 Minimum Performance and Safety Requirements for Capnometers and IEC 80601-2-55:2011. Medical Electrical Equipment performance requirements for the basic safety and essential performance of respiratory gas monitors.

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