Page 1
VPAP™ III ST-A with QuickNav User Guide English • • 简体中文 繁體中文...
Page 3
153516, ES 156136, FR 021395, GB 3001819, GB 3001820, JP 1164265, JP 1164266, NZ 527088, SE 75598, SE 75600, US D467335, US D476077, US D477868, US D487311. SmartStart, TiCONTROL, VPAP, and Vsync are trademarks of ResMed Ltd and SmartStart and VPAP are registered in U.S. Patent and Trademark Office.
Page 4
248210/4 08 10 VPAP™ III ST-A with QuickNav USer APAC Global leaders in sleep and respiratory medicine www.resmed.com...
..........1 User/Owner Responsibility Medical Information Intended Use Contraindications Adverse Effects The VPAP III ST-A with QuickNav Masks Humidifiers Setting up the device Attaching a Humidifier Using the LCD QuickNav Screen and Keypad...
• Medical Information Intended Use The VPAP III ST-A system is intended to provide non-invasive ventilation for patients with respiratory insufficiency or obstructive sleep apnoea (OSA), in the hospital or home. Contraindications This device should not be used if you have an insufficient respiratory drive to endure brief interruptions in non-invasive ventilation therapy.
IEC 60950 or equivalent. Masks You will also need a ResMed mask (supplied separately). For information on using your mask, see your mask manual. For the latest available masks, or to select the appropriate setting for your mask, see www.resmed.com on the Products page under Service &...
Power switch Connect the power cord. Note: ResMed recommends using the AC power cord supplied with the unit. If a replacement power cord is required, contact your ResMed service centre. Plug the free end of the power cord into a power outlet.
The HumidAire 2i or 2iC attaches to the front of the device to provide heated or passover humidification, respsectively. No other accessories are required for its use. The VPAP III ST-A with QuickNav automatically detects the presence of the HumidAire 2i. HumidAire or Passover Humidifier Medium size (52 cm) air tubing is a necessary accessory for connecting the device to the HumidAire or Passover humidifier.
To assist you in adjusting the device, the keypad and LCD are equipped with a backlight. The LCD backlight comes on when the device is turned on or when you press a key, and turns off after two minutes. The LCD backlight may be set to be on continually. The keypad backlight is on at all times when the device is powered.
Using the HumidAire 2i Warm-up Feature If using a HumidAire 2i with the device, you can use the Warm- up feature to pre-heat the water in the humidifier prior to starting treatment. The humidifer will be automatically detected when the device is turned on and the standby screen will give you the option to start warming up the humidifier.
Using the Mask-Fit Feature This device includes a mask-fit feature to help you fit your mask properly. If a Ramp time is selected, the mask can be adjusted at a pressure closer to the prescribed pressure. To use the mask-fit feature: Fit your mask as described in the user instructions.
“Patient Home Screen/Treatment Screen” on page 6. Patient Summary Menu The patient summary menu allows you to view details about the time used, a summary of your device settings, and the current software version of your VPAP III ST-A with QuickNav. Soft key display 6mths...
(eg, a day, a week, a month, etc.). Patient Settings Menu The Patient Settings menu allows you to view and change settings such as mask type, tube length and the humidifier used. You can also access the Mask-Fit feature. 21:53 SETTINGS...
Function Default SmartStart™ (SmrtStrtStp) If you select “Mir Full” as the mask option, SmartStop is automatically disabled. SmartStart may not work with a full face mask due to safety features of the mask. † When the Leak or Low MV Alarms are set to ON, SmartStop is automatically disabled. SmartStop cannot be used with the Leak or Low MV Alarms because, if either of these conditions occur, SmartStop will stop treatment before the alarm signal is activated.
The most common reason for an alarm to sound is because the system has not been properly assembled. Check that the air tubing has been properly attached to the flow generator and mask (and humidifier if used). When an alarm has been activated, the LCD screen will display either alarm information or recommended instructions for you or your clinician.
Page 18
1. Check the air circuit for a blockage. 2. Remove blockage. 3. Re-start therapy. If the alarm persists, return the unit to ResMed for servicing. Continue using and contact your clinician about this alarm. Device settings may require adjustment.
Do not store the air tubing in direct sunlight as the tubing may harden over time and eventually crack. Humidifier If you are using a humidifier, clean it according to the instructions supplied with the humidifier. Weekly Cleaning Remove the air tubing from the device and the mask.
(VPAP III ST-A with QuickNav) be inspected by an authorised ResMed Service Centre five years from the date of purchase. Applicable ResMed warranty details are provided with the device at the time of original supply.
HumidAire 2i is attached. The case temperature should be less than 50°C at an ambient temperature of 35°C. (For VPAP III ST-A with QuickNav temperature specifications, see “System Specifications” on page 16.) Troubleshooting If there is a problem, try the following suggestions. If the problem cannot be solved, contact your equipment supplier or ResMed.
Press the Start/Stop key. Enable SmartStart/Stop. SmartStop does not work with a full face mask. Use only equipment as recommended and supplied by ResMed. Consult your clinician. SYSTEM ERROR Call service! Return your device for servicing. Return your device for servicing.
Page 23
• The manufacturer reserves the right to change these specifications without notice. • Further clinical information is available through your authorised ResMed service centre. 270 mm x 230 mm x 141 mm 2.3 kg 22 mm taper, compatible with ISO 5356-1:2004 Anaesthetic &...
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 25
RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the VPAP III ST-A with QuickNav is used exceeds the applicable RF compliance level above, the VPAP III ST-A with QuickNav should be observed to verify normal operation.
Page 26
Warnings: The VPAP III ST-A with QuickNav should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the VPAP III ST-A with QuickNav should be observed to verify normal operation in the configuration in which it will be used.
ResMed shall not be responsible for any incidental or consequential damages claimed to have occurred as a result of 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. This warranty gives you specific legal rights, and you may also have other rights which vary from region to region.