Arthrex AR-3200-1018, Instructions For Use Manual

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5.0 APPENDIX [Detailed
EMC Information]
DETAILED EMC INFORMATION
NOTE: CE marked equipment has been tested
and found to comply with the EMC limits for the
Medical Device Directive 93/42/EEC [EN 55011
Class A and IEC 60601-1-2]. These limits are
designed to provide reasonable protection
against harmful interference in a typical medical
installation.
The Equipment generates and can radiate radio
frequency energy and, if not installed and used in
accordance with the instructions, may cause
harmful interference to other devices in the vicinity.
However, there is no guarantee that interference
will not occur in a particular installation. If this
equipment does cause harmful interference with
other devices, 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 device.
• Increase the separation between the
equipment.
• Connect the equipment to an outlet on a
circuit different from that to which the other
device(s) is connected.
• Consult the manufacturer or a field service
technician for assistance.
NOTE: The EMC tables and other guidelines that
are included in the Instruction Manual provide
information to the customer or user that is
essential in determining the suitability of the
Equipment or System for the Electro-magnetic
Environment of use, and in managing the
Electromagnetic Environment of use to permit
the Equipment or System to perform its
intended use without
disturbing other Equipment and Systems or
non-medical electrical equipment.
NOTE: Medical Electrical Equipment needs
special precautions regarding EMC and needs
to be installed and put into service according to
the EMC information provided in the
Accompanying Documents.
WARNINGS:
1. Portable and mobile RF communications
equipment can affect Medical Electrical
Equipment.
2. Use of accessories, transducers, and cables
other than those specified, with the
exception of transducers and cables sold by
the manufacturer of the equipment as
replacement parts for internal components,
may result in increased emissions and
decreased immunity of the equipment or
system.
3. The video equipment / system should not be
used adjacent to or stacked with other
equipment, and that if adjacent or stacked
use is necessary, the equipment or system
should be observed to verify normal
operation in the configuration in which it is
intended to be used.