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oxygen concentrator dual flow (silverline meditech pvt ltd)(silverdxx)

` 84,500.00

  • MRP: `110000.00

OXYGEN CONCENTRATOR FOR AIR.

  • Availability: 15 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) - 0 Hrs
  • Oxygen outlet(s) - Single or Dual
  • Operating temperature Range - 60 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) 0 Hrs
Battery Charging (If Battery Operated Or Electrical Cum Battery Operated) 0 Hrs
Oxygen Outlet(s) Single or Dual
Outlet Pressure 48 KPa
Power Consumption 400 Watt
Operating Temperature Range 60 degree C
Operating Humidity Range 95 %
Operating Altitude Range 3500 Meters
Type Of Operation Pulse Dose Type
Adjustable Air Delivery Mechanism Yes
Oxygen Concentration Monitor Yes
Oxygen Tank Capacity 5 Ltrs
Noise Level 45 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) 440 mm
Dimensions (Width) 440 mm
Dimension (height) 640 mm
Flame Retardant YES
Manufacturer Warranty Period 1 Years
Spare Part Availability YES
Comply With International Standards YES
Name Of International Standards USFDA
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 YES
Availability Of Test Report From Central Govt./NABL/ILAC Accredited Lab To Prove Conformity To Specification EUROPEAN CONFIRMITY By TUV
Test Report No. 16802952001
Test Report Date 25/04/2014
Name Of The Lab TUV Rheinland Of North America, Inc
Address Of The Lab NORTH AMERICA
Power Source Electrical Operated
Power Efficiency 53 W/LPM

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