ResMed S9 V-Auto Information Manual
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ResMed S9 V-Auto Information Manual

Positive airway pressure device
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S9
V-Auto
™
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 V-Auto is indicated for the treatment of obstructive sleep apnoea (OSA) in patients weighing
more than 30 kg. The S9 V-Auto 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
1
English

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Summary of Contents for ResMed S9 V-Auto

  • Page 1 Please read the entire Information and Welcome Guides before using your device. Indications for use The S9 V-Auto is indicated for the treatment of obstructive sleep apnoea (OSA) in patients weighing more than 30 kg. The S9 V-Auto is intended for home and hospital use.

  • Page 2: Troubleshooting

    • skin rashes. 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(s). Problem/possible cause Solution No display Power is not connected.
  • 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 being Only use equipment recommended by ResMed. used. The patient is using a nasal pillows Disable SmartStart/Stop.
  • Page 4 Turn the humidifier setting down and empty the water from resulting in accumulation of water in the air tubing. the air tubing. Check ResMed 30/90W Power Supply Unit and fully insert the Displays error message: connector The DC plug is partially inserted into Fully insert the DC plug.
  • 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 tube: 26 dBA with uncertainty of 2 dBA as measured DUAL-NUMBER according to EN ISO 17510-1:2009 NOISE With Standard tube: 27 dBA with uncertainty of 2 dBA as measured EMISSION according to EN ISO 17510-1:2009 VALUES in With either SlimLine or 28 dBA with uncertainty of 2 dBA as measured...

  • Page 8: Humidifier Performance

    3. Tube 4. Mask Flow (maximum) at set pressures The following are measured at the end of the specified tubing: Pressure, cm H S9 V-Auto and S9 V-Auto, H5i S9 V-Auto and S9 V-Auto, H5i Standard air and Standard air...
  • Page 9 Maximum dynamic pressure variation according to EN ISO 17510-1:2009 Pressure (cm H 10 BPM 15 BPM 20 BPM S9 V-Auto and Standard tube without H5i / S9 V-Auto and Standard tube with H5i 0.18 / 0.18 0.30 / 0.30 0.51 / 0.51 0.21 / 0.20...

  • 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 See www.resmed.com for other ResMed locations worldwide. For patent information, see www.resmed.com/ip. S9, H5i, ClimateLine, SlimLine and SmartStart are trademarks of ResMed Pty Ltd and S9, ClimateLine, SlimLine and SmartStart are registered in U.S. Patent and Trademark Office. © 2012 ResMed. 368776/2 2012-05 www.resmed.com...

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