ResMed’s softest mask ever
Superior comfort and uncompromising seal
Unique to ResMed’s AirTouch F20, our new UltraSoft memory foam cushion adapts to your facial profile, seals naturally and prevents leaks for a light and gentle experience of sleep therapy. Foam has unique properties that provide less friction and contact pressure than a standard silicone cushion, even when it’s sealed firmly against your face. This reduces the likelihood of red facial marks. And because foam is permeable, it allows a very small amount of air to pass through your cushion – providing a more natural sleeping experience without compromising your therapy.
Easy to care for
Thanks to a regularly replaceable cushion, the AirTouch 20 series helps you refresh your experience of sleep therapy and allows for a simpler, smoother cleaning process. No more mask cleaning when you wake up each morning – a simple wipe down with a CPAP wipe is all that’s needed!
Freedom of choice
AirTouch F20 is made with interchangeable components that allow you to easily mix and match them with AirFit F20 mask. AirTouch F20 cushions are also compatible with AirFit F20 for Her masks, so female patients can enjoy the comfort of Ultra-Soft foam alongside the outstanding fit of a female-specific mask.
A wider set of options makes it easier to find a solution that maximises comfort, therapy compliance and success.
Relax in quiet comfort
Featuring the revolutionary QuietAir diffuser vent, ResMed AirTouch F20 is our quietest mask ever. With QuietAir, noise is minimised and airflow is so soft you might not feel it at all. You can simply enjoy a more peaceful night’s sleep and the freedom to sleep closer and more naturally with your partner.
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Please refer to the user guides for relevant information related to any warnings and precautions to be considered before and during use of the products.
Use of masks with magnetic components is contraindicated in patients with the following pre-existing conditions: a metallic haemostatic clip implanted in the head to repair an aneurysm and/or metallic splinters in one or both eyes.
1. ResMed external clinical study of 10 experienced patients for 7 nights, conducted between 29/08/2016 and 19/09/2016. Data on file; ID A3907045.