ResMed Travel Letter


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RE: Traveling with a ResMed device To whom it may concern, With regard to the patient in possession of this letter and the accompanying ResMed medical device, please read the following: The ResMed CPAP is a medical device cleared for sale by the Food and Drug Administration, a branch of the United States government, for the treatment of sleep-disordered breathing (SDB) such as sleep apnea, and has been prescribed for use on or by the order of a physician. ResMed medical devices include the following products: AutoSet family ApneaLink H4i H5i HumidAire family ResControl (I and II)

ResLink ResTraxx S6 Series S7 Series S8 Series S8 Series II

S9 Series Sullivan V family VPAP Adapt SV VPAP II family VPAP III family VPAP Tx

If you have any questions regarding this device, please contact ResMed Customer Service in the United States at (800) 424-0737. Our European offices, located in France, Germany, Sweden and the United Kingdom, can be contacted through: ResMed (UK) Limited 67b Milton Park Abingdon Oxfordshire OX14 4RX UK Tel: +44 (1235) 862 997 Fax: +44 (1235) 831 336 Email: [email protected] Best regards,

Jim Cassi Vice President, Quality ResMed Corp

ResMed Ltd 1 Elizabeth Macarthur Drive, Bella Vista NSW 2153 Australia Tel: +61 2 8884 1000 Fax: +61 2 8883 3114 ABN 30 003 765 142

Global leaders in sleep and respiratory medicine

www.resmed.com