Intel Corporation A2RX ユーザーズマニュアル
IMPORTANT SAFETY & REGULATORY INFORMATION
DO NOT DISCARD – DOCUMENT MUST REMAIN WITH PRODUCT
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Monday, April 04, 2016
Model: A2RX (Sea Dunes) PRU Module – Regulatory Information
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.
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.
Modifications made to this device, unless expressly approved by the manufacturer, may void the user’s
rights to operate this equipment.
rights to operate this equipment.
Note: This equipment generates, uses and can radiate radio frequency energy and, if not installed and
used in accordance with the instructions, may cause harmful interference to radio communications.
However, there is no guarantee that interference will not occur in a particular installation. If this
equipment does cause harmful interference to radio or television reception, which can be determined by
turning the equipment off and on, the user is encouraged to try to correct the interference by one or
more of the following measures:
—Reorient or relocate the receiving antenna.
—Increase the separation between the equipment and receiver.
—Connect the equipment into an outlet on a circuit different from that to which the receiver is
connected.
—Consult the dealer or an experienced radio/TV technician for help.
used in accordance with the instructions, may cause harmful interference to radio communications.
However, there is no guarantee that interference will not occur in a particular installation. If this
equipment does cause harmful interference to radio or television reception, which can be determined by
turning the equipment off and on, the user is encouraged to try to correct the interference by one or
more of the following measures:
—Reorient or relocate the receiving antenna.
—Increase the separation between the equipment and receiver.
—Connect the equipment into an outlet on a circuit different from that to which the receiver is
connected.
—Consult the dealer or an experienced radio/TV technician for help.
Radio Frequency Exposure and Compatibility with Implantable Cardiac Medical Devices.
Wireless Power devices are designed to meet all applicable RF health and safety regulations prescribed
by individual countries around the world. Through complex testing procedures we have demonstrated to
appropriate country regulators that the RF emissions from our wireless power devices meet the basic
exposure restrictions set forth in ICNIRP or IEEE or similar international RF safety standards. Based on
readily available information, Intel’s wireless power device should not cause interference with any
implantable cardiac device. However because each cardiac device can be different and some may be
affected by low powered RF fields, individuals wearing implantable cardiac devices should not be in
very close proximity ( or direct contact) with the wireless power device. Individuals should discuss any
concerns about the compatibility of their medical device with their physician or medical device
manufacturer.
by individual countries around the world. Through complex testing procedures we have demonstrated to
appropriate country regulators that the RF emissions from our wireless power devices meet the basic
exposure restrictions set forth in ICNIRP or IEEE or similar international RF safety standards. Based on
readily available information, Intel’s wireless power device should not cause interference with any
implantable cardiac device. However because each cardiac device can be different and some may be
affected by low powered RF fields, individuals wearing implantable cardiac devices should not be in
very close proximity ( or direct contact) with the wireless power device. Individuals should discuss any
concerns about the compatibility of their medical device with their physician or medical device
manufacturer.