A soft nasal mask for patients with sleep apnoea
The AirTouch N20 is a nasal mask that features a memory foam cushion designed to provide a comfortable experience for patients with sleep apnoea. Compatible with AirFit N20 mask1, AirTouch N20 is a good option to offer your patients comfort for daily or occasional use.
Product codes: N20 mask system S, M, L (63909, 63911, 63912) | cushions S, M, L (63950, 63951, 63952)
Designed for great comfort
The AirTouch N20 memory foam cushion can adapt to the unique facial contours of each patient, creating a personalised fit designed to limit red marks2. For a full face mask featuring the AirTouch cushion, visit the AirTouch F20 product page.
Mix and match with the AirFit N20
The AirTouch N20 cushion is compatible with the AirFit N20 nasal mask frame.1 This means that patients can switch between the AirFit N20 and AirTouch N20 cushions as they desire.
Fits a wide range of pressures
The AirTouch N20 memory foam cushion is designed for a good seal across a wide range of therapeutic pressures1: specifically, the mask has been validated for pressures from 4 to 30 cmH201 and can be used with sleep and bilevel ventilation machines.
Buy AirTouch N20 at the ResMed Online Store
ResMed Online Store is the one-stop-shop for sleep professionals, with immediate access to pricing, shipping and invoice details. Contact your ResMed representative to create an account or sign in to start buying and tracking ResMed products.
Warranty & services
Looking for service and warranty information on the AirTouch N20 mask? Find the answers to your questions in our resource centre.
Equip your patient with the AirTouch N20 nasal mask
Assemble/Disassemble the N20 mask
Maintenance and cleaning instructions for the AirTouch N20
Keen to explore other masks?
ResMed’s CPAP mask categories are designed to reflect your patients’ needs and sleep habits. Our Versatile Fit, Freedom and Minimalist mask categories make it easier to find the right mask.
- AirTouch N20 user guide, ResMed Pty Ltd 2019. ID A4670547.
- ResMed external clinical study of 26 patients for 7 nights, conducted between 15/03/2018 and 05/04/2018. Data on file; ID A4575326.