ResMed 248551/1, 2011-09 manual General warnings and cautions

Page 36

•The device must only be used with masks (and connectors1) recommended by ResMed, or by a clinician or respiratory therapist. A mask should not be used unless the device is turned on and operating properly. The vent hole or holes associated with

the mask should never be blocked.

Explanation: The Stellar is intended to be used with special masks (or connectors1) which have vent holes to allow continuous flow of air out of the mask. When the device is turned on and functioning properly, new air from the device flushes the exhaled air out through the mask vent holes. However, when the device is not operating, insufficient fresh air will be provided through the mask, and the exhaled air may be rebreathed. Rebreathing of exhaled air for longer than several minutes can, in some circumstances, lead to suffocation. This applies to most Positive Airway Pressure devices.

•In the event of power failure2 or machine malfunction, remove the mask or the catheter mount from the tracheostomy tube.

•Explosion hazard – do not use in the vicinity of flammable anesthetics.

•Do not use the device if there are obvious external defects, unexplained changes in performance.

•Only use orignal and approved ResMed accessories and parts.

•Use only accessories from the original package. If the packaging is damaged, the respective product must not be used, and should be disposed along with the packaging.

•Before using the device and the accessories for the first time, ensure that all components are in a proper condition and that their operational safety is guaranteed. If there are any defects, the system should not be used.

•Additional equipment connected to medical electrical equipment must comply with the respective IEC or ISO standards (eg, IEC 60950 for data processing equipment). Furthermore all configurations shall comply with the requirements for medical electrical systems (see IEC 60601-1-1 or clause 16 of the 3Ed. of IEC 60601-1, respectively). Anybody connecting additional equipment to medical electrical equipment configures a medical system and is therefore responsible that the system complies with the requirements for medical electrical systems. Attention is drawn to the fact that local laws take priority over the above mentioned requirements. If in doubt, consult your local representative or the technical service department.

CAUTIONS

A caution explains special measures for the safe and effective use of the device.

•When using accessories, read the manufacturer’s User Manual. For consumables important information can be provided on the packaging, see also symbols on page 30.

•At low pressures, the flow through the mask vent holes may be inadequate to clear all exhaled gas, and some rebreathing may occur.

•The device may not be exposed to excessive force.

•If the device should fall accidentally on the ground, please contact your authorised service agent.

•Pay attention to leaks and other unusual sounds. If there is a problem, contact an authorised service agent.

Notes:

A note advises to special product features.

•The above are general warnings and cautions. Further specific warnings, cautions and notes appear next to the relevant instructions in the user guide.

•Only trained and authorised personnel are allowed to make clinical setting changes.

English

1 Ports may be incorporated into the mask or in connectors that are near the mask.

2 During partial (below rated minimum voltage) or total power failure, therapy pressures will not be delivered. When power is restored, operation can be proceeded with no change to settings.

General warnings and cautions

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Contents Stellar User GuideRespiratory Care Solutions Making quality of care easy Stellar 100 Stellar Contents Cleaning and maintenance Introduction Indications for useContraindications Adverse effectsStellar at a glance Internal battery Patient interfaceHumidification ResMed USB stickSetting up for noninvasive use Mobile useSetting up for invasive use Attaching the H4i heated humidifier for noninvasive useHmef Working with other optional accessories Attaching the pulse oximeterAdding supplemental oxygen Starting therapy using oxygen Stopping therapy using oxygenUsing the FiO2 monitoring sensor Connecting a sensor Attaching an antibacterial filterStellar basics About the control panelStarting therapy LCD screenPerforming a functional test Starting therapy Stopping therapyCheck the FiO2 monitoring sensor if in use Check pulse oximeter if in useTurning off the power Working with alarmsTailoring treatment setup options Using mask-fitUsing the menus Enu Alarm Settings Alarm Volume Enu OptionsSetup menu Configuration Menu Parameter DescriptionOptions On, Auto Info menu Event SummaryUsed Hours Device InformationCleaning and maintenance Data managementDaily Weekly MonthlyReplacing the air filter DisinfectionTroubleshooting Alarm troubleshootingMultipatient use ServicingProblem / possible cause Action LCD Internal Battery Empty LCD High Temperature 10, 11, 12LCD System Failure LCD Over PressureProblem / possible cause Action LCD Circuit disconnected LCD Internal Battery LowLCD Low Minute Ventilation LCD Low Respiratory Rate!, High Respiratory RateOther troubleshooting Problem / possible cause Solution Device does not start when you breathe into the maskDevice does not stop when you remove your mask Treatment pressure seems highTechnical specifications Alarm Volume Range Dimensions L x W x HWeight Air outlet Power supplyIEC ClassificationsAir travel requirements Vrms Symbols General warnings and cautionsGeneral warnings and cautions Limited warranty Product Warranty periodApac
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