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United States
This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to
Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful
interference in a residential installation. This equipment generates, uses and can radiate radio frequency
energy and, if not installed and used in accordance with the manufacturer's 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.
n
Increase the separation between the equipment and receiver.
n
Connect the equipment to an outlet on a circuit different from that to which the receiver is connected.
n
Consult the dealer or an experienced radio or TV technician for help.
n
Improper termination of access points installed in the United States configured to a non-US model controller is
a violation of the FCC grant of equipment authorization. Any such willful or intentional violation may result in a
requirement by the FCC for immediate termination of operation and may be subject to forfeiture (47 CFR
1.80).
The network administrator(s) is/are responsible for ensuring that this device operates in accordance with
local/regional laws of the host domain.
FCC regulations restrict the operation of this device to indoor use only.
The operation of this device is prohibited on oil platforms, cars, trains, boats, and aircraft, except that operation of this
device is permitted in large aircraft while flying above 10,000 feet.
Operation in the 5.9725-7.125GHz band is prohibited for control of or communication with unnamed aircraft systems.
Medical
1. Equipment not suitable for use in the presence of flammable mixtures.
2. Connect to only IEC 60950-1 or IEC 60601-1 certified products and power sources. The end user is
responsible for the resulting medical system complies with the requirements of IEC 60601-1.
3. Wipe with a dry cloth, no additional maintenance required.
4. No serviceable parts, the unit must be sent back to the manufacturer for repair.
5. No modifications are allowed without Aruba approval.
12
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Rev 01|March 2022
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