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portable oxygen concentrator (sanrai)(inogenone G3 System)

` 294,000.00

  • MRP: `350000.00

Oxygen Concentrator.

  • Availability: 1 In Stock
  • Min. Qty. Per Consignee: 1
  • Flow Rate (Minimum) at 93% + - 3% oxygen purity - 93 Litres per minute
  • Type - Portable
  • Battery duration (If Battery operated or Electrical cum Battery operated) - 4 Hrs
  • Oxygen outlet(s) - Single
  • Operating temperature Range - 0 degree C
Other Specifications Download Specification
Conformity To ISO 80601-2-69:2014 Of The Medical Electrical Equipment – Part 2-69: Particular Requirements For Basic Safety And Essential Performance Of Oxygen Concentrator Equipment Yes
Flow Rate (Minimum) At 93% + - 3% Oxygen Purity 93 Litres per minute
Type Portable
Battery Duration (If Battery Operated Or Electrical Cum Battery Operated) 4 Hrs
Battery Charging (If Battery Operated Or Electrical Cum Battery Operated) 3 Hrs
Oxygen Outlet(s) Single
Outlet Pressure 1050 KPa
Power Consumption 240 Watt
Operating Temperature Range 0 degree C
Operating Humidity Range 0 %
Operating Altitude Range 0 Meters
Type Of Operation Pulse Dose Type
Adjustable Air Delivery Mechanism Yes
Oxygen Concentration Monitor Yes
Oxygen Tank Capacity 0 Ltrs
Noise Level 39 dB
Continuous Flow 5 LPM
Digital Display LCD
Audio Alarm YES
Visual Alarm YES
Alert Of Technical Fault YES
Alert Of Wrong Battery YES
Alert Of Depleted Battery YES
Alert Of High Breath Rate YES
Alert Of Low Oxygen Purity YES
Alert Of No Breath YES
Alert For No Flow YES
Alert For Low Flow YES
Alert For High Flow YES
Alert Of Low Pressure YES
Alert Of High Pressure YES
Alert Of High Temperature YES
Alert For Power Failure YES
Alert For Service Requirement YES
Weight 2.20 Kg
Dimensions (Length) 8.75 mm
Dimensions (Width) 3.0 mm
Dimension (height) 8.25 mm
Flame Retardant YES
Manufacturer Warranty Period 1 Years
Spare Part Availability YES
Comply With International Standards YES
Name Of International Standards 0
FDA Approved No
Availability Of Test Report CE Or EC Certification In Accordance With Appendix II(excluding Section 4) Of Medical Device Directive 93/42/EC & Its Amendment Or Equivalent Yes
Availability Of Test Report From Central Govt./NABL/ILAC Accredited Lab To Prove Conformity To Specification Yes
Test Report No. 0
Test Report Date 0
Name Of The Lab 0
Address Of The Lab 0
Power Source Electrical cum Battery Operated
Power Efficiency 0 W/LPM

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