Introduction
This manual is intended for clinicians using the ResMed CPAP S6 device.
Important Safety Information
The device is contraindicated in patients with severe bullous lung disease, pneumothorax or pneumomediastinum, pathologically low blood pressure, dehydration, cerebrospinal fluid leak, recent cranial surgery, or trauma.
Adverse effects may include unusual chest pain, severe headache, or increased breathlessness.
Device Information
The ResMed CPAP S6 is manufactured by ResMed Ltd in Australia.
The device is protected by various patents, and trademarks include AutoScan, Bubble Cushion, HumidAire, Mirage, SmartStart, and Ultra Mirage.
Manual:
Download: ResMed CPAP S6 Clinician’s Manual
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