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Pressure Swing Absorption Technology, Adjustable Flowrate, Large LCD Display, Digital Pressure, Temperature, Maintenance reminding and Nebulizer.
| 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 | 0.07 KPa |
| Power Consumption | 530 Watt |
| Operating Temperature Range | 70 degree C |
| Operating Humidity Range | 93 % |
| Operating Altitude Range | 230 Meters |
| Type Of Operation | Continuous Flow Type |
| Adjustable Air Delivery Mechanism | Yes |
| Oxygen Concentration Monitor | Yes |
| Oxygen Tank Capacity | 5 Ltrs |
| Noise Level | 50 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) | 365 mm |
| Dimensions (Width) | 373 mm |
| Dimension (height) | 600 mm |
| Flame Retardant | YES |
| Manufacturer Warranty Period | 1 Years |
| Spare Part Availability | YES |
| Comply With International Standards | YES |
| Name Of International Standards | Longfian |
| 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 | YES |
| Test Report No. | YES |
| Test Report Date | YES |
| Name Of The Lab | YES |
| Address Of The Lab | YES |
| Power Source | Electrical Operated |
| Power Efficiency | 106 W/LPM |
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