Safety Instructions

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Caution: Basic Safety and Essential Performance
This system should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is
necessary, this system should be observed to verify normal operation in the configuration in which it will be used.
The essential performance of the RecoveryAir PRO system as evaluated in IEC 60601- 1-2 includes treatment com-
pleting cycle, presentation on the display is not interfered, and treatment parameters are not changed unintentionally.
The following, but not limited to, are unacceptable risks that are not allowed: malfunction, non-operation when
operation is required, unwanted operation when no operation is required, deviation from normal operation that poses
unacceptable risk to operator or user, component failure, change in programmable parameter(s), change in operation
mode, reset to factory defaults, and false positive or false negative alarm.
Do not apply the device near any devices with Electromagnetic Interference (EMI), such as cell phones, Magnetic
Resonance Imaging (MRI), computerized axial tomography (CT), diathermy, Radio
Frequency Identification (RFID), etc. or MR environment. EMI, RF devices or MR environments
may affect the normal function of the device or would cause user injury.
Guidance and Manufacturer’s Declaration – Electromagnetic Emission
The RecoveryAir PRO device is intended for use in the electromagnetic environment specified below.
The customer or the user of the device should assure that it is used in such an environment .
Emission Test Compliance Electromagnetic Environment – Guidance
The device uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
IEC 61000-3-3 Class B The device is suitable for use in all establishments, including domestic
establishments and those directly connected to the public low-voltage power
supply network that supplies buildings used for domestic purposes.