
EBOX-335xDX3 Series
User Manual
DMP Electronics Inc.
3
Regulatory
FCC Class A Note
This equipment has been tested and found to comply with the limits for a Class A digital device,
pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful
interference when equipment is operated in a commercial environment. This equipment generates, uses and
can radiate radio frequency energy and, if not installed and used in accordance with the instruction manual,
may cause harmful interference in which case user will be required to correct interference at his own expense.
Testing was done with shielded cables. Follow FCC regulations, user must use shielded cables with installation.
WARNING
This product complies with EN55032 class A. In a domestic environment, may cause radio interference
in which case the user may be required to take adequate measures.
Changes or modifications to this unit not expressly approved by the party responsible for compliance could void
the user’s authority to operate the equipment.
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.
This digital apparatus does not exceed Class A limits for radio noise emissions from digital apparatus as set out in
interference - causing equipment standard “Digital Apparatus”, ICES-003 of the Department of Communications.
Manufacturer’s Declaration of Conformity
This equipment has been tested and found to comply with the requirements of European Community Council
Directives 2014/30/EU & 2014/35/EU relating to electromagnetic compatibility and product safety respectively.
Attention
This product has been designed and certified to comply with certain regulatory requirements pertaining to
Information Technology Equipment. This product has not been designed for use as a medical device.
Without limitation of the foregoing, this product is not intended and has not been certified for use in a hospital
or clinical environment to diagnose, treat, or monitor patients under medical supervision, and is not intended
and has not been certified to make physical or electrical contact with patients, nor to transfer energy to or from
patients and/or to detect such energy transfer to or from patients.
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