This monitor is consisting of pulse oximetry and capnography parameters. It can use in the field of anesthesia monitor. Big screen with high acuity on parameters can provide better solution for physicians and hospital responsible personals to monitor patient safely.
Digital pulse oximeter with high accuracy capnography together make system more useful to achieve better options for patient monitoring. Alarms are providing according to related standards and system designed to connect to all ICE servers base on HL& protocols for transferring patient data.
Light weight and high battery capacity can help to use this system as portable system with patient.
Vital Signs Monitor Including:
- Oxygen Saturation (SpO2)
- Pulse Rate (PR)
- Plethysmograph Waveform
- Perfusion Index (PI)
- Continues Monitoring of EtCO2
- Respiration Rate (RR)
- FiCO2
- Real Time CO2 Waveform
Setting for all Patient Type:
- Adult
- Pediatric
- Neonate
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
| Electrical Characteristics | |
|---|---|
| Power Requirements (AC Line) | 100-240VAC; 50-60 Hz; 23-30VA |
| Battery | 7.6 VDC; Li-Ion, RechargeableMaximum ProtectionBattery Operating Time: 4 hoursBattery Charging Time: 4 hours |
| Fuse | 500 mA |
| Resolution | |
|---|---|
| SpO2 | 1% |
| Pulse Rate | 1 bpm |
| Temperature | 0.1°C |
| Sensor LEDs | |
|---|---|
| Nominal wavelenght and nominal power output values | (RED) 660 nm – 1.8 mw and (IRED) 905 nm – 2.0 mw |
| Battery | 7.6 VDC; Li-Ion, Rechargeable Maximum Protection Battery Operating Time: 4 hours Battery Charging Time: 4 hours |
| Alarm Limits | |
|---|---|
| Low SpO2 | 0% – 99% |
| High SpO2 | 1% – 100% |
| Low Pulse Rat | 30 bpm – 229 bpm |
| High Pulse Rate | 31 bpm – 230 bpm |
| Measurment Range | |
|---|---|
| SpO2 | 0% – 100% |
| Pulse Rate | 30 – 240 bpm (beat per minute) |
| Temperature | 0.0° – 60.0°C (32.0° – 138.9°F ) |
| Perfusion | 0.02% – 20% |
| Unit Dimensions & Weight | |
|---|---|
| Dimensions | 30 x 25 x 10 cm |
| Weight | 1.5 kg |
| Display | |
|---|---|
| Type | High Quality TFT Full Colors Liquid Crystal Display (LCD) with LED Backlight |
| Data Displayed | SpO2, Pulse Rate, Plethysmograph waveform, Temperature, Alarms and Status Message |
| Note: There is no display delay for the calculated value. | |
| IEC (International Electrotechnical Commission) Classifications | |
|---|---|
| Type of Protection | CLASS II |
| Degree of Protection | Type BF |
| Mode of Protection | Continuous |
| Degree of Protection Against Ingress of Liquids | Ordinary (IPX2) |
| Recommended Methods of Sterilization or Disinfection | Using a soaked swab with alcohol for the external parts of system, SpO2 sensor and extension cable for appropriate cleaning instructions. |
| Degree of Safety of Application in the Presence of a Flammable Anesthetic | Not suitable for use in the presence of a flammable anesthetic mixture with air, oxygen or nitrous oxide. |
| Do not use functional tester to assess the accuracy of pulseoximeter probes and monitor. | |
| IEC (International Electrotechnical Commission) Classifications | |
|---|---|
| Type of Protection | CLASS II |
| Degree of Protection | Type BF |
| Mode of Protection | Continuous |
| Degree of Protection Against Ingress of Liquids | Ordinary (IPX2) |
| Recommended Methods of Sterilization or Disinfection | Using a soaked swab with alcohol for the external parts of system, SpO2 sensor and extension cable for appropriate cleaning instructions. |
| Degree of Safety of Application in the Presence of a Flammable Anesthetic | Not suitable for use in the presence of a flammable anesthetic mixture with air, oxygen or nitrous oxide. |
| Do not use functional tester to assess the accuracy of pulseoximeter probes and monitor. | |
| List of Relevant Standard | ||
|---|---|---|
| 1 | EN ISO 80601-2-61:2011 | Medical electrical equipment Part 2-61: Particular requirements for basic safety and essential performance of pulseoximeter equipment |
| 2 | EN 80601-1-8:2006 | Medical electrical equipment – Part 1-8: General requirements for safety – Collateral standard: 2. General requirements, tests and guidance for alarm systems in medical electrical equipment and medical |
| 3 | EN 60601-1:2006 | Medical electrical equipment – Part 1: General requirements for basic safety and essential performance |
| 4 | EN ISO 14971:2007 | Medical devices – Application of risk management to medical devices (ISO 14971:2007) |
| 5 | EN 60601-1-2:2001 | Medical electrical equipment – Part 1-2: General requirements for safety – Collateral standard: Electromagnetic compatibility – Requirements and tests |
| 6 | ASTM F2761-09 | Medical Devices and Medical Systems — Essential safety requirements for equipment comprising the patient-centric integrated clinical environment (ICE) — Part 1: General requirements and conceptual model |
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