PNEUMATIC DIAGRAM
Process flows from left to right
12.3 ELECTROMAGNETIC COMPATIBILITY (EMC) INFORMATION
WARNING
• Use of accessories, transducers and cables other than those specified or provided by the
manufacturer of this equipment could result in increased electromagnetic emissions or decreased
electromagnetic immunity of this equipment and result in improper operation.
• Avoid exposure to known sources of EMI (electromagnetic interference) such as diathermy,
lithotripsy, electrocautery, RFID (Radio Frequency Identification), and electromagnetic security
systems such as anti-theft/electronic article surveillance systems, metal detectors. Note that the
presence of RFID devices may not be obvious. If such interference is suspected, reposition the
equipment, if possible, to maximize distances.
• Portable RF communications equipment (including peripherals such as antenna cables and external
antennas) should be used no closer than 30 cm (12 inches) to any part of the device, including
cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment
could result.
• The device should not be used adjacent to or stacked with other equipment. If adjacent or stacked
use is necessary, the device should be observed to verify normal operation. If operation is not
normal, the device or the other equipment should be moved.
Medical electrical equipment needs to be installed and used according to the EMC information in this
manual.
This equipment has been tested and found to comply with EMC limits specified in IEC 60601-1-2. These
limits are designed to provide a reasonable protection against electromagnetic interference in a typical
home environment.
This concentrator contains Transmitter Module IC: 2417C-BX31A. Contains FCC ID: N7NBX31A. This device
complies with Part 15 of the FCC rules. Operation is subject to the following two conditions: (1) this device
may not cause harmful interference, and (2) this device must accept any interference received, including
interference that may cause undesired operation.
12.4 GUIDANCE AND MANUFACTURER'S DECLARATION – ELECTROMAGNETIC IMMUNITY:
The Concentrator is intended for use in the electromagnetic environment of home, institution, vehicle,
and other transport modalities. The user of the concentrator should make sure it is used in such an
environment. During the immunity testing specified below the Rove 6 will continue to deliver oxygen within
specification.
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