ACCUDIS908 ( Vital Signs Monitor )

748 581 parsian medical

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
Battery7.6 VDC; Li-Ion, RechargeableMaximum ProtectionBattery Operating Time: 4 hoursBattery Charging Time: 4 hours
Fuse500 mA
Resolution
SpO21%
Pulse Rate1 bpm
Temperature0.1°C
Sensor LEDs
Nominal wavelenght and nominal power output values(RED) 660 nm – 1.8 mw and (IRED) 905 nm – 2.0 mw
Battery7.6 VDC; Li-Ion, Rechargeable
Maximum Protection
Battery Operating Time: 4 hours
Battery Charging Time: 4 hours
Alarm Limits
Low SpO20% – 99%
High SpO21% – 100%
Low Pulse Rat30 bpm – 229 bpm
High Pulse Rate31 bpm – 230 bpm
Measurment Range
SpO20% – 100%
Pulse Rate30 – 240 bpm (beat per minute)
Temperature0.0° – 60.0°C (32.0° – 138.9°F )
Perfusion0.02% – 20%
Unit Dimensions & Weight
Dimensions30 x 25 x 10 cm
Weight1.5 kg
Display
TypeHigh Quality TFT Full Colors Liquid Crystal Display (LCD) with LED Backlight
Data DisplayedSpO2, Pulse Rate, Plethysmograph waveform, Temperature, Alarms and Status Message
Note: There is no display delay for the calculated value.
abadis 907 Components
IEC (International Electrotechnical Commission) Classifications
Type of ProtectionCLASS II
Degree of ProtectionType BF
Mode of ProtectionContinuous
Degree of Protection Against Ingress of LiquidsOrdinary (IPX2)
Recommended Methods of Sterilization or DisinfectionUsing 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 AnestheticNot 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 ProtectionCLASS II
Degree of ProtectionType BF
Mode of ProtectionContinuous
Degree of Protection Against Ingress of LiquidsOrdinary (IPX2)
Recommended Methods of Sterilization or DisinfectionUsing 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 AnestheticNot 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
1EN ISO 80601-2-61:2011Medical electrical equipment Part 2-61: Particular requirements for basic safety and essential performance of pulseoximeter equipment
2EN 80601-1-8:2006Medical 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
3EN 60601-1:2006Medical electrical equipment – Part 1: General requirements for basic safety and essential performance
4EN ISO 14971:2007Medical devices – Application of risk management to medical devices (ISO 14971:2007)
5EN 60601-1-2:2001Medical electrical equipment – Part 1-2: General requirements for safety – Collateral standard: Electromagnetic compatibility – Requirements and tests
6ASTM F2761-09Medical 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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