ResMed III ST-A user manual Portable and mobile RF communications

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

The VPAP III ST-A is intended for use in the electromagnetic environment specified below. The customer or the user of the VPAP III ST-A 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 III ST-A, 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 III ST-A is used exceeds the applicable RF compliance level above, the VPAP III ST-A should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the VPAP III ST-A.

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 Vpap III ST-A ROW ENG System Components Illustrations52 cm 3 m 248139/3 05 Manufactured by Contents System Specifications Limited Warranty Index What the Vpap III ST-A is Intended for IntroductionMedical Information User/Owner ResponsibilityPage Adverse Effects Page Masks Vpap III ST-A SystemHumidifiers AccessoriesSetting up the Vpap III ST-A Setting up the Vpap III ST-A SystemAttaching a HumidAire Humidifier Attaching a HumidifierAttaching a HumidAire 2i Humidifier Attaching a HumidAire 2iC HumidifierAttaching a Passover Humidifier Using the LCD Screen and Keypad LCD ScreenLEDs Vpap III ST-A keypad has the following keys Keypad KeysPage Ramp Time Starting TreatmentUsing the HumidAire 2i Warm-up Feature Using the Mask-Fitting FeatureStopping Treatment High Leak Page Periodic Cleaning Cleaning and MaintenanceDaily Cleaning Weekly CleaningTesting the Alarm Replacing the Air FilterServicing How to Use the Vpap III ST-A Menus How to Use the Standard MenuRamp Screen Settings Summary Screens How to Use the Detailed Menu if enabled by your clinicianMIRAGE, MIR Full STANDARD, Ultra Menu Functions Detailed Menu only Settings MenuSmartStart Options Menu Results MenuServicing Menu Treatment ScreensOxygen saturation This screen only Level SpO2 98% Non-vented Mask Alarm Screen Page Testing the Alarm AlarmsAlarms Troubleshooting Alarm Mute KeyLCD Ipap Lower LCD System Error LCD LOW MV Alarm Nasal Irritation Using a Battery to Power the Vpap III ST-AHelpful Hints Starting outResMed DC-24/30 Converter No display TroubleshootingSystem Error Dynamic pressure characteristics System SpecificationsIEC 60601-1 Classifications Pressure Variation Pressure Volume CurveEnvironmental information Symbols which may Appear on the ProductEmissions test Compliance Next Portable and mobile RF communications Separation distance according to frequency of transmitter Limited Warranty Page Index Index

III ST-A specifications

The ResMed III ST-A is a state-of-the-art ventilator specifically designed for patients with respiratory challenges, particularly those suffering from obstructive sleep apnea, neuromuscular conditions, or chronic obstructive pulmonary disease (COPD). It stands out due to its user-friendly features, advanced technologies, and robust performance, making it a preferred choice for both clinicians and patients.

One of the main features of the ResMed III ST-A is its intelligent algorithm designed to optimize minute ventilation. This provides variable support that adapts to the patient's breathing patterns, enhancing comfort and ensuring effective ventilation. By offering a range of modes, including spontaneous timed (ST) and volume-assured pressure support (VAPS), this device caters to various clinical needs, facilitating customized therapy based on individual patient requirements.

The built-in leak compensation feature of the ResMed III ST-A allows it to maintain accurate pressure delivery even in the presence of large leaks, which is crucial for ensuring effective therapy. This is particularly beneficial for patients who may have difficulty achieving a proper seal with their masks.

Incorporating advanced technologies, the ResMed III ST-A features AutoSet technology, which automatically adjusts pressure levels in response to detected changes in airflow. This promotes optimal treatment at all times, reducing the burden on patients and allowing for a more seamless sleep experience. The device also supports a range of connectivity options, enabling healthcare providers to monitor patient compliance and therapy effectiveness remotely through ResMed's cloud-based platform.

The ResMed III ST-A is designed with a user-friendly interface, including a bright, easy-to-read display and simplified controls, promoting ease of operation for both healthcare professionals and patients. Its compact size and lightweight design enhance portability, making it suitable for home and travel use.

Furthermore, the device's comprehensive data logging capabilities allow clinicians to access a wealth of information regarding patient adherence and sleep patterns, thus supporting informed decision-making. The ResMed III ST-A also prioritizes patient safety, featuring alarms and alerts for high- and low-pressure conditions.

In conclusion, the ResMed III ST-A embodies cutting-edge technology and thoughtful design, providing versatile and effective respiratory support. With its combination of intelligent algorithms, user-friendly features, and robust patient monitoring capabilities, it is well-positioned to enhance the quality of life for individuals with respiratory challenges.