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oxygen concentrator (philips)(respironics)

` 45,000.00

  • MRP: `200000.00

PHILIPS OXYGEN CONCENTRATOR RESPIRONICS.

  • Availability: 50 In Stock
  • Min. Qty. Per Consignee: 1
  • Flow Rate (Minimum) at 93% + - 3% oxygen purity - 2 Litres per minute
  • Type - Portable
  • Battery duration (If Battery operated or Electrical cum Battery operated) - 2.5 Hrs
  • Oxygen outlet(s) - Single
  • Operating temperature Range - 40 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 2 Litres per minute
Type Portable
Battery Duration (If Battery Operated Or Electrical Cum Battery Operated) 2.5 Hrs
Battery Charging (If Battery Operated Or Electrical Cum Battery Operated) 1.5 Hrs
Oxygen Outlet(s) Single
Outlet Pressure 226 KPa
Power Consumption 200 Watt
Operating Temperature Range 40 degree C
Operating Humidity Range 85 %
Operating Altitude Range 3500 Meters
Type Of Operation Pulse Dose Type
Adjustable Air Delivery Mechanism Yes
Oxygen Concentration Monitor Yes
Oxygen Tank Capacity 20 Ltrs
Noise Level 48 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 25 Kg
Dimensions (Length) 450 mm
Dimensions (Width) 450 mm
Dimension (height) 650 mm
Flame Retardant YES
Manufacturer Warranty Period 2 Years
Spare Part Availability YES
Comply With International Standards YES
Name Of International Standards FDA
FDA Approved YES
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 CE
Availability Of Test Report From Central Govt./NABL/ILAC Accredited Lab To Prove Conformity To Specification WILL PROVIDE AT THE TIME OF DELIVER
Test Report No. NA
Test Report Date NA
Name Of The Lab NA
Address Of The Lab NA
Power Source Electrical Operated
Power Efficiency 22 W/LPM

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