Technical Specifications - ResMed AirCurve 10 VAUTO Clinical Manual

• Do not use bleach, chlorine, alcohol, or aromatic-based solutions, moisturizing or
antibacterial soaps or scented oils to clean the device, the water tub 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 the
patient's head to prevent the mask and air tubing from filling with water.
• Do not overfill the water tub as water may enter the device and air tubing.
• Leave the water tub to cool for ten minutes before handling to allow the water to cool and
to make sure that the water tub is not too hot to touch.
• Make sure that the water tub is empty before transporting the device.

Technical specifications

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 AirCurve 10 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: IEC 60601-1:2005+A1:2012
Class II (double insulation), Type BF, Ingress protection IP22.
Sensors
Pressure sensor:
Flow sensor:
Maximum single fault steady pressure
Device will shut down in the presence of a single fault if the steady state pressure exceeds:
30 cm H O (30 hPa) for more than 6 sec or 40 cm H
2
36
100–240V, 50–60Hz 1.0–1.5A, Class II
115V, 400Hz 1.5A, Class II (nominal for aircraft use)
24V
53W (57VA)
104W (108VA)
+41°F to +95°F (+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
(104°F/40°C) the device remains safe.
10 to 95% relative humidity, non-condensing
Sea level to 8,500' (2,591 m); air pressure range 1013 hPa to
738 hPa
-4°F to +140°F (-20°C to +60°C)
5 to 95% relative humidity, non-condensing
Internally located at device outlet, analog gauge pressure
type, -5 to +45 cm H
Internally located at device inlet, digital mass flow type, -70
to +180 L/min
O (40 hPa) for more than 1 sec.
2
3.75A
O (-5 to +45 hPa)
2