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S9
Auto 25
™
POSITIVE AIRWAY PRESSURE DEVICE
Information Guide
English
English
Please read the entire Information and Welcome Guides before using your device.
Indications for use
The S9 Auto 25 is indicated for the treatment of obstructive sleep apnoea (OSA) in patients weighing
more than 30 kg. The S9 Auto 25 is intended for home and hospital use.
Contraindications
Positive airway pressure therapy may be contraindicated in some patients with the following pre-
existing conditions:
•
severe bullous lung disease
•
pneumothorax or pneumomediastinum
•
pathologically low blood pressure, particularly if associated with intravascular volume depletion
•
dehydration
•
cerebrospinal fluid leak, recent cranial surgery, or trauma.
Adverse effects
Patients should report unusual chest pain, severe headache, or increased breathlessness to their
prescribing physician. An acute upper respiratory tract infection may require temporary
discontinuation of treatment.
The following side effects may arise during the course of therapy with the device:
•
drying of the nose, mouth, or throat
•
nosebleed
•
bloating
•
ear or sinus discomfort
•
eye irritation
•
skin rashes.
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Summary of Contents for ResMed S9 Auto 25
- Page 1 Please read the entire Information and Welcome Guides before using your device. Indications for use The S9 Auto 25 is indicated for the treatment of obstructive sleep apnoea (OSA) in patients weighing more than 30 kg. The S9 Auto 25 is intended for home and hospital use.
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Page 2: Troubleshooting
Troubleshooting If there is a problem, try the following suggestions. If the problem cannot be solved, contact your equipment supplier or ResMed. Do not attempt to open the device enclosure. Problem/Possible cause Solution No display Power is not connected. Ensure the power cable is connected and the power outlet (if available) is on. - Page 3 Leak Alert is enabled. SmartStart/Stop is enabled but the device does not stop automatically when you remove your mask Incompatible mask system Only use equipment recommended by ResMed. being used. The patient is using a nasal Disable SmartStart/Stop...
- Page 4 The DC plug is partially inserted into the back of the device or inserted too slowly. A non-ResMed power supply Remove the power supply unit and replace with a ResMed power unit is connected to the device. supply unit. The power supply unit is being Make sure that the power supply unit is free from bedding, clothes covered by bedding.
- Page 5 Operating altitude: Sea level to 2,591m Storage and transport temperature: -20°C to +60°C Storage and transport humidity: 10 to 95% non-condensing ResMed confirms that the device/s meets the Federal Aviation Administration Aircraft use (FAA) requirements (RTCA/DO-160, section 21, category M) for all phases of air travel.
- Page 6 It is recommended that mobile communication devices are kept at least 1 m away from the device. Information regarding the electromagnetic emissions and immunity of this ResMed device can be found on www.resmed.com, on the Products page under Service and Support. Click on the PDF file for your language. IEC 60601-1...
- Page 7 Sound Pressure level (CPAP mode) DECLARED With SlimLine air 26 dBA with uncertainty of 2 dBA as measured according DUAL-NUMBER tubing: to EN ISO 17510-1:2009 NOISE EMISSION With Standard air 27 dBA with uncertainty of 2 dBA as measured according VALUES in tubing: to EN ISO 17510-1:2009...
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Page 8: Humidifier Performance
• The electrical connector end of the heated air tubing is only compatible with the H5i air outlet and should not be fitted to the device or mask. Humidifier performance The following settings have been tested at 22°C ambient temperature: Mask pressure RH output % Nominal system output AH... -
Page 9: Displayed Values
Displayed values Value Range Accuracy Display resolution Pressure sensor at air outlet Pressure 4 to 25 cm H ±0.5 cm H O (±4% of 0.1 cm H measured value) Flow derived values Leak 0–200 L/min 1 L/min Tidal volume 0–4000 mL ±10% 1 mL Respiratory rate... -
Page 10: Environmental Information
If you need information on these disposal systems, please contact your local waste administration. The crossed-bin symbol invites you to use these disposal systems. If you require information on collection and disposal of your ResMed device please contact your ResMed office, local distributor or go to www.resmed.com/environment. -
Page 11: Limited Warranty
Portable diagnostic/screening devices This warranty is only available to the initial consumer. It is not transferable. If the product fails under conditions of normal use, ResMed will repair or replace, at its option, the defective product or any of its components. - Page 12 ResMed shall not be responsible for any incidental or consequential damages claimed to have resulted from the sale, installation or use of any ResMed product. Some regions or states do not allow the exclusion or limitation of incidental or consequential damages, so the above limitation may not apply to you.
- Page 13 • Only use the ResMed 90W or 30W power supply unit. Use the 90W power supply unit to power the system comprising the device, H5i, air tubing, DC/DC converter and battery pack. The 30W power supply unit is designed to power the device only and recommended for traveling.
- Page 14 • Do not open the device enclosure. There are no user serviceable parts inside. Repairs and servicing should only be performed by an authorised ResMed service agent. • Do not use bleach, chlorine, alcohol, or aromatic-based solutions, moisturising or antibacterial soaps or scented oils to clean the device, humidifier or air tubing.
- Page 15 Manufacturer: ResMed Ltd 1 Elizabeth Macarthur Drive Bella Vista NSW 2153 Australia. Distributed by: ResMed Corp 9001 Spectrum Center Boulevard San Diego CA 92123 USA. ResMed (UK) Ltd 96 Milton Park Abingdon Oxfordshire OX14 4RY UK. See www.resmed.com for other ResMed locations worldwide.
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