ResMed 248127 user manual Portable and mobile RF communications

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Guidance and manufacturer’s declaration – electromagnetic immunity (Continued)

The VPAP is intended for use in the electromagnetic environment specified below. The customer or the user of the VPAP should assure that it is used in such an environment.

Immunity

IEC60601-1-2

Compliance

Electromagnetic environment –

test

test level

level

guidance

 

 

 

 

 

 

 

Portable and mobile RF communications

 

 

 

equipment should be used no closer to any

 

 

 

part of the VPAP, including cables, than the

 

 

 

recommended separation distance

 

 

 

calculated from the equation applicable to

 

 

 

the frequency of the transmitter.

 

 

 

Recommended separation distance

Conducted RF

3 Vrms

3 Vrms

d = 1.17 P

IEC 61000-4-6

150 kHz to 80 MHz

 

 

Radiated RF

10 V/m

10 V/m

d = 0.35 P 80 MHz to 800 MHz

IEC 61000-4-3

80 MHz to 2.5 GHz

 

 

 

 

 

d = 0.70 P 800 MHz to 2.5 GHz

 

 

 

where P is the maximum output power

 

 

 

rating of the transmitter in watts (W)

 

 

 

according to the transmitter manufacturer

 

 

 

and d is the recommended separation

 

 

 

distance in meters (m).

 

 

 

Field strengths from fixed RF transmitters, as

 

 

 

determined by an electromagnetic site

 

 

 

survey,a should be less than the compliance

 

 

 

level in each frequency range.b

 

 

 

Interference may occur in the vicinity of

 

 

 

equipment marked with the following

 

 

 

symbol:

 

 

 

 

NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.

NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

aField strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the VPAP is used exceeds the applicable RF compliance level above, the VPAP should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the VPAP.

bOver the frequency range 150 kHz to 80 MHz, field strengths should be less than 10 V/m.

System Specifications

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Contents 248127/1 05 Illustrations 52 cm 3 m English Manufactured by Contents Limited Warranty Index Introduction Medical InformationUser/Owner Responsibility What the Vpap III and Vpap III ST are Intended forPage Adverse Effects Medical InformationPage Vpap System MasksAccessories HumidifiersSetting up the Vpap System Setting Up The VpapAttaching a Humidifier Attaching a HumidAire 2i Humidifier Attaching a HumidAire 2iC HumidifierAttaching a HumidAire Humidifier Attaching a Passover Humidifier Using the LCD Screen and Keypad LCD ScreenKeypad Keys KeyFunction FrontKey Function Left green Right redPage Starting Treatment Ramp timeStarting Treatment Using the HumidAire 2i Warm-Up Feature Using the Mask-Fitting FeatureStopping Treatment High Leak Page Cleaning and Maintenance Daily CleaningWeekly Cleaning Periodic CleaningReplacing the Air Filter ServicingHow to Use the Vpap Menus How to Use the Standard MenuRamp Screen How to Use the Detailed Menu if enabled by your clinician To exit out of the menu Press the Right key exitVpap Detailed Menu Series if enabled by your clinician Settings Menu Menu Functions Detailed menu onlyTo enter a submenu Press the Left key enter Function Default Function Description Setting Options Settings for mask types MaskSettings Mask Results Menu Function Function Description Setting OptionsResults Menu Options Menu Servicing MenuTreatment Screens Treatment screenHow to Use the Vpap Menus Page Using a Battery and an Inverter Helpful HintsStarting out Nasal IrritationPage Troubleshooting TroubleshootingProblem Possible Cause Solution Check tube Key if doneLast session Page System Specifications Dynamic pressure characteristicsIEC 60601-1 Classifications Flow sensor in flow generatorPressure Volume curve Pressure VariationPressure cm H2O BreathsSymbols which appear on the product Environmental informationEmissions test Compliance Next Portable and mobile RF communications Separation distance according to frequency of transmitter Limited Warranty Product Warranty PeriodLimited Warranty Page Index

248127 specifications

ResMed 248127 is a state-of-the-art device designed to enhance patients' experience in managing sleep apnea and other respiratory conditions. As a leader in innovative technologies, ResMed continues to focus on developing equipment that promotes better sleep and overall health.

One of the key features of the ResMed 248127 is its advanced integrated monitoring capabilities. This device provides real-time data on various parameters that are crucial for effective therapy management. Patients and healthcare providers can easily access important information, such as adherence rates and overall treatment effectiveness. This transparency helps to ensure that users remain compliant with their prescribed therapies, which is essential for achieving desired outcomes.

The ResMed 248127 also features a user-friendly interface with an intuitive design. The device is equipped with a high-resolution display that presents information clearly, making it easier for users to navigate through different settings and options. This simplicity is particularly beneficial for older adults or those who may not be technologically savvy, allowing for an efficient user experience without overwhelming the patient.

Another standout characteristic is its whisper-quiet operation. Sleep therapy devices often come under scrutiny for their noise levels, which can disrupt sleep patterns. The ResMed 248127 addresses this concern by utilizing advanced sound dampening technologies that ensure a peaceful night's sleep, creating a harmonious environment for both the patient and their sleep partner.

The device also incorporates SmartStart technology, which automatically starts or stops therapy as soon as the mask is put on or removed. This functionality not only enhances the convenience of use but also ensures that therapy is delivered effectively and promptly as needed.

Furthermore, the ResMed 248127 is designed with portability in mind. Its lightweight and compact design make it easy for users to transport the device, facilitating therapy adherence even while traveling. This flexibility allows patients to maintain their treatment regimen when they are away from home, ensuring that sleep quality is preserved regardless of location.

In conclusion, the ResMed 248127 combines innovative technology, user-friendly features, and unmatched portability to provide users with an effective solution for managing sleep apnea and other respiratory conditions. Its advanced monitoring capabilities, quiet operation, and convenience-oriented design make it a valuable tool in the quest for better sleep health. This device demonstrates ResMed's commitment to improving patient outcomes through technological advancements in the realm of sleep therapy.