ResMed Lumis HFT User Manual page 22

Physical - device and humidifier
Dimensions (H x W x D):
Air outlet (complies with ISO 5356-1:2015):
Weight (device and cleanable humidifier):
Housing construction:
Water capacity:
Cleanable humidifier - material:
Temperature
Maximum heater plate:
Cut-out:
Maximum gas temperature:
Air filter
Standard:
Hypoallergenic:
Wireless module
Technology used:
It is recommended that the device is a minimum distance of 2 cm from the body during operation. Not applicable to masks,
tubes or accessories. Technology may not be available in all regions.
Declaration of Conformity (DoC to the Radio Equipment Directive)
ResMed declares that the Lumis HFT device (models 285xx) is in compliance with the essential requirements and other
relevant provisions of Directive 2014/53/EU (RED). A copy of the Declaration of Conformity (DoC) can be found on
Resmed.com/productsupport
This device can be used in all European countries without any restrictions.
All ResMed devices are classified as medical devices under the Medical Device Directive. Any labelling of the product and
printed material, showing
amendment (2007/47/EC).
Supplemental oxygen
Maximum flow:
Device air leak at 25 cmH2O:
Pneumatic flow path
Design life
Device, power supply unit:
Cleanable humidifier tub:
0123, relates to the Council Directive 93/42/EEC including the Medical Device Directive
116 mm x 265 mm x 150 mm
22 mm
1290 g
Flame retardant engineering thermoplastic
To maximum fill line 380 mL
Injection moulded plastic, stainless steel and silicone seal
76°C
78°C
≤ 43°C
Material: Polyester non-woven fibre
Average arrestance: >75% for ~7 micron dust
Material: Acrylic and polypropylene fibres in a polypropylene
carrier
Efficiency: >98% for ~7-8 micron dust; >80% for ~0.5 micron
dust
4G (LTE)
10 L/min
≤ 2L/min
1. Flow sensor
2. Blower
3. Pressure sensor
4. Nasal cannula
5. Air tubing
6. Humidifier
7. Device
8. Inlet filter
9. Low flow oxygen input (up to 10 L/min)
3 years
3 months
English 21