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oxygen concentrator Nuvo (nidek)(nidek 5)

` 63,400.00

  • MRP: `85200.00

Oxygen Concentrator.

  • Availability: 2 In Stock
  • Min. Qty. Per Consignee: 1
  • Flow Rate (Minimum) at 93% + - 3% oxygen purity - 5 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 - 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 5 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 7 KPa
Power Consumption 290 Watt
Operating Temperature Range 40 degree C
Operating Humidity Range 30 %
Operating Altitude Range 2287-4000 Meters
Type Of Operation Continuous Flow Type
Adjustable Air Delivery Mechanism Yes
Oxygen Concentration Monitor Yes
Oxygen Tank Capacity 5 Ltrs
Noise Level 40 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 13.6 Kg
Dimensions (Length) 36 mm
Dimensions (Width) 22 mm
Dimension (height) 58 mm
Flame Retardant YES
Manufacturer Warranty Period 1 Years
Spare Part Availability YES
Comply With International Standards YES
Name Of International Standards US 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 3443-4-2016
Test Report No. 3443-4-2016
Test Report Date 15/4/2016
Name Of The Lab DEPARTMENT OF HEALTH AND HUMAN SERVICES
Address Of The Lab FOOD AND DRUG ADMINISTRATION 10903 NEW HAMPSHIRE AVENUE SILVER SPRING MD 20993
Power Source Electrical Operated
Power Efficiency na W/LPM

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