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clinician; SmartStart automatically disabled. Use of a ResMed Full Face mask. SmartStart does not work with a full-face mask as the anti-asphyxia valve will not allow sufficiently high pressure on exhalation. Breath not deep enough to trigger Take a deep breath in and out through the mask. SmartStart. Problem/Possible Cause Solution Excessive leak. Adjust position of mask and headgear. Replace caps if missing from ports on mask. Air tubing may not be connected properly. Connect firmly at both ends. Air tubing may be kinked or punctured. Straighten or replace. Displays error message: SYSTEM ERRxxxx Call Service!or Exxxx (where xxxx defines an error) Component failure. Record error number and call service. Displays error message: Check tube!! Key if done Air tubing is loose or blocked. Check that the air tubing is connected securely to your mask and the air outlet to the front of the S8 Series II. When you have checked the air tubing, press the Start/ Stop key to restart the device. If this does not clear the message, disconnect the power cord and then reconnect it to restart the device. The following message is displayed on the LCD after you try to update settings or copy data to the Data Card: Card Error Remove Card Data Card is not inserted correctly. Check that the Data Card is inserted into the Data Card module with the arrow facing up, while the S8 Series II is switched on and not delivering therapy (standby mode). The Data Card is only partly Ensure that the Data Card is inserted into the Data Card inserted. slot as far as it will go. You may have removed the Data Reinsert the Data Card and wait for the Settings Card before settings were copied to Success Remove Card message to appear on the the S8 II. LCD. The card is not a ResScan Data Only use a ResScan Data Card. Card. The following message is displayed on the LCD after you try to update settings or copy data to the Data Card: Settings Error Remove Card There is a data error on the Data Contact your clinician immediately. Card. The following message is NOT displayed on the LCD after you try to update the settings using the Data Card: Settings Success Remove Card The settings were not updated. Contact your clinician immediately. Troubleshooting Problem/Possible Cause Solution The following message is displayed on the LCD after you try to update settings or copy data to the Data Card: Settings Invalid Remove Card The identification details on the Contact your clinician immediately. Data Card do not match the identification details on your device. Technical Specifications . Operating pressure range 4 to 20 cm H2O Dimensions (H x W x D) 112 mm x 164 mm x 145 mm Weight 1.4 kg Operating Temperature +5°C to +36°C Power Supply • Input range for S8 Series II with H4i:100–240V, 50/60Hz; 110V, 400Hz; 2.5A < 140VA (110W) (maximum power consumption). Instantaneous peak power consumption <340VA. • Refer to the DC-12 converter instructions for DC ratings. Only use the ResMed DC-12 converter for DC input. • Typical power consumption at 20 cm H20 is 39VA or 20.7W. Operating Humidity 10%–95% non-condensing Storage and Transport -20.C to +60.C Temperature Storage and Transport 10%–95% non-condensing Humidity Operating Altitude Sea level to 2,591 m Electromagnetic Product complies with all applicable electromagnetic compatibility Compatibility requirements (EMC) according to IEC60601-1-2, for residential, commercial, and light industry environments. The electromagnetic compatibility tables for these ResMed devices can be found on on the Products page under Service & Support. Click on the PDF file for your device. Air Filter Two-layered, powder-bonded, polyester non-woven fiber Air Tubing Flexible plastic, 2 m Air Outlet The 22 mm conical outlet complies with EN 1281-1 IEC 60601-1 Classifications Class II (double insulation), Type CF Housing Construction Flame retardant engineering thermoplastic DECLARED DUAL-NUMBER NOISE EMISSION VALUES in accordance with ISO 4871: Sound Pressure Level 24 dBA with uncertainty of 2 dBA as measured according to ISO 17510-1: 2002 26 dBA with uncertainty of 2 dBA as measured according to ISO 17510-1: 2007 Sound Power Level 34 dBA with uncertainty of 2 dBA as measured according to ISO 17510-1: 2007 Supplemental Oxygen Recommended maximum supplemental oxygen flow: 4 L/min The manufacturer reserves the right to change these specifications without notice. Symbols which appear on the device Attention, consult accompanying documents; Follow instructions for use; Drip proof; Type CF equipment; Dangerous voltage; Class II equipment; Start/Stop; Manufacturer; Environmental information WEEE 2002/96/EC is a European Directive that requires the proper disposal of electrical and electronic equipment. This device should be disposed of separately, not as unsorted municipal waste. To dispose of your device, you should use appropriate collection, reuse and recycling systems available in your region. The use of these collection, reuse and r...

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