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Successful therapy starts with the right device

Successful therapy starts with the right device

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Philips, following consultation with the Therapeutic Goods Administration (TGA), announced it is conducting an Urgent Product Defect Correction for specific devices in the sleep and respiratory care portfolio. For more information please 

click here or call 1800 009 579.

References

  1. 2015 User Preference Questionnaire, data on file.
  2. Mask does not directly contact the bridge of the nose or nostrils.
  3. In a retrospective review conducted by Philips Respironics of approximately 15,000 System One patients, patients who used SleepMapper, which has been rebranded DreamMapper, demonstrated 22% greater adherence to the therapy than patients who did not use SleepMapper. To see which therapy devices are compatible with DreamMapper, visit www.dreammapper.com/compatible .

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By clicking on the link, you will be leaving the official Royal Philips ("Philips") website. Any links to third-party websites that may appear on this site are provided only for your convenience and in no way represent any affiliation or endorsement of the information provided on those linked websites. Philips makes no representations or warranties of any kind with regard to any third-party websites or the information contained therein.

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