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: 2018
Technical Specification
- Internal Rechargeable Battery with 5 Hours Working Capacity
- ETHERNET Connection Complying HL7 Protocols
- USB Connector
- Unlimited Trend for Several Patients
- 7.8 inch TFT LCD with CAPACITIVE TOUCH panel
- Capability to Install other Vital Sign Modules
- Auto-Rotate Sensor for Detecting Horizontal or Vertical Positions of Display
| Electrical Characteristics | |
|---|---|
| Input Voltag | 80-264VAC, 47-63Hz |
| Power Consumption | 45W |
| Battery Type | Li-Ion |
| Battery Capacity | 2400 mAH |
| Battery Charge Time | 3 Hours |
| Fuses | 250V, 500mA, 5x20mm |
| General Specification | |
|---|---|
| Output Interfaces | USB and Etherne |
| Trending Time | Every Second |
| Display | 7” TFT LCD Wide +Touch Panel |
| Network Protocol | HL7 |
| Dimensions (WxHxD) | 25x 8 x 22 cm3 |
| Weight | 1 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 |
| 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 IEC80601-2-55:2018. 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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