Technical Specifications - ResMed Lumis 100 VPAP ST User Manual

• Keep the area around the device dry, clean and clear of anything (eg, clothes or bedding)
that could block the air inlet or cover the power supply unit.
• Do not place the device on its side as water might get into the device.
• Incorrect system setup may result in incorrect mask pressure reading. Ensure the system is
correctly set up.
• Do not use bleach, chlorine, alcohol, or aromatic-based solutions, moisturising or
antibacterial soaps or scented oils to clean the device, the humidifier or air tubing. These
solutions may cause damage or affect the humidifier performance and reduce the life of
the products.
• If you use the humidifier, always place the device on a level surface lower than your head
to prevent the mask and air tubing from filling with water.
• Leave the humidifier to cool for ten minutes before handling to allow the water to cool and
to make sure that the humidifier is not too hot to touch.
• Make sure that the humidifier is empty before transporting the device.
Notes:
• The device is not intended to be operated by persons (including children) with reduced physical,
sensory or mental capabilities without adequate supervision by a person responsible for the
patient's safety.
• For any serious incidents that occur in relation to this device, these should be reported to
ResMed and the competent authority in your country.

Technical specifications

Units are expressed in cm H
90W power supply unit
AC input range:
DC output:
Typical power consumption:
Peak power consumption:
Environmental conditions
Operating temperature:
Operating humidity:
Operating altitude:
Storage and transport temperature:
Storage and transport humidity:
Electromagnetic compatibility
The Lumis complies with all applicable electromagnetic compatibility requirements (EMC) according to IEC 60601-1-2:2014,
for residential, commercial and light industry environments. It is recommended that mobile communication devices are kept
at least 1 m away from the device.
Information regarding the electromagnetic emissions and immunity of this ResMed device can be found on
www.resmed.com/downloads/devices
Classification: EN60601-1:2006/A1:2013
Class II (double insulation), Type BF, Ingress protection IP22.
18
O and hPa. 1 cm H
2
O is equal to 0.98 hPa.
2
100–240V, 50–60Hz 1.0–1.5A, Class II
115V, 400Hz 1.5A, Class II (nominal for aircraft use)
24V 3.75A
53W (57VA)
104W (108VA)
+5°C to +35°C
Note: The air flow for breathing produced by this therapy
device can be higher than the temperature of the room.
Under extreme ambient temperature conditions (40°C) the
device remains safe.
10 to 95% relative humidity, non-condensing
Sea level to 2,591 m; air pressure range 1013 hPa to
738 hPa
-20°C to +60°C
5 to 95% relative humidity, non-condensing