Description
Lumis 100 VPAP S is a non invasive ventilator designed for spontaneously breathing non dependent patients with respiratory insufficiency. It is easy to set up and use
Key Features –
Key Features –
- Vsync
- TiControl
- 5 Trigger and Cycle Senstivities
- QuickNav for low touch therapy adjustments
- Climate Control Auto for automatic humidification
- Ramp and Ramp Down for extra comfort
SPECIFICATIONS
- Height – 150 mm
- Weight – 1106 gm
- Breadth – 205 mm
- Length – 116 mm
- Modes – CPAP, S
- Operating pressure range – 2–25 cm H2O (2–25 hPa) in S mode 4–20 cm H2O (4–20 hPa) in CPAP mode
- Sound pressure level – 26.6 dBA with uncertainty of 2 dBA as measured according to ISO 17510-1:2009 (CPAP mode)
- Dimensions (H x W x D) – 116 mm x 255 mm x 150 mm (Device with HumidAir humidifier)
- Weight (Device with HumidAir humidifier) – 1268 gm
- Power Supply – 90W power supply unit Input range: 100–240V, 50–60Hz, 57VA (typical power consumption) 108VA (peak power consumption)
- Operating temperature/ humidity/altitude – +5°C to +35°C/ 10–95% relative humidity, non-condensing/ Sea level to 2,591 m; air pressure range 1013 hPa to 738 hPa
- Storage and transport temperature/humidity – -20°C to +60°C/ 5–95% relative humidity, non-condensing
- Housing construction – Flame retardant engineering thermoplastic
- Supplemental oxygen – Recommended maximum flow: 15 L/min (CPAP, S)
- Standard air filter – Polyester non-woven fibre
- Tubing – SlimLine™ and ClimateLineAir (15 mm); Standard (19 mm)
- Air outlet – 22 mm air outlet complies with ISO 5356-1:2004
- Electromagnetic compatibility – Requirements (EMC) according to IEC60601-1-2:2007 for residential, commercial, and light industry environments
- Aircraft use – ResMed confirms that device meets the Federal Aviation Administration (FAA) requirements (RTCA/DO-160, section 21, category M) for all phases of air travel
- IEC 60601-1: 2006 classification – Class II (double insulation), Type BF Ingress protection IP22
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