AirFit™ F30
Small, quiet and designed for freedom
Ultra-compact mask delivering full face functionality in a small, quiet1, comfortable format2. The snug cushion of the AirFit F30 nestles under the nose, offering more visual and physical freedom and eliminating discomfort and red marks on the nasal bridge.
Visual freedom
The under-the-nose design means the AirFit F30 is noticeably smaller, more discreet and more attractive than a traditional full-face mask. With nothing on your nasal bridge, you can easily rediscover simple pleasures like wearing glasses and reading in comfort.
Peace and quiet
AirFit F30 with the QuietAir™ elbow is quieter than the leading ultra-compact full face mask competitor1. The QuietAir elbow gently and quietly diffuses exhaled air from your mask to create a quieter, more restful atmosphere with almost no noticeable drafts².
Nothing over your nose
The F30’s ultra-compact frame sits comfortably under your nose, not over it. Less facial contact looks good, feels good and means you can say goodbye to red marks and pressure on the bridge of your nose.
Shop online
Need new equipment, accessories or spare parts? It’s quick and convenient to shop on the ResMed online store from anywhere, at any time. Register for our membership programme and you’ll also receive information on our latest products and promotions.
How do I fit my AirFit F30 mask?
How do I assemble/disassemble my AirFit F30 mask?
How do I maintain/clean my AirFit F30 mask?
Interested in exploring other mask options?
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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.
References:
- Sound power level with QuietAir of 21 dBA – AirFit F30 user guide, ResMed Pty Ltd 2019. ID A4500405.
- ResMed external 7-day clinical study of 21 ResMed and non-ResMed patients, conducted between 16/04/2018 – 05/05/2018. Data on file; ID A4356449.
