Prevena Plus™ 125 Therapy Unit Electromagnetic Compatibility - KCI PREVENA PLUS DUO Manual Del Usuario

PREVENA PLUS™ 125 THERAPY UNIT ELECTROMAGNETIC
COMPATIBILITY
The following are guidance and manufacturer's declarations regarding EMC for the PREVENA PLUS™
125 Therapy Unit.
•
The PREVENA PLUS™ 125 Therapy Unit needs special precautions regarding EMC and needs to
be installed and put into service according to the EMC information provided in the following
pages.
WARNING: This equipment is intended for use by healthcare professionals only. As
with all electrical medical equipment, this equipment may cause radio interference or
may disrupt the operation of nearby equipment. It may be necessary to take mitigation
measures such as re-orienting or relocating the PREVENA PLUS™ 125 Therapy Unit or
shielding the location.
•
Portable and Mobile RF communications equipment, RFID readers, electronic article
surveillance (anti-theft) equipment and metal detectors can affect the performance of the
PREVENA PLUS™ 125 Therapy Unit. Please use the guidelines and recommendations specified
in Tables 204 and 206.
•
Other medical equipment or systems can produce electromagnetic emissions and therefore
can interfere with the functionality of the PREVENA PLUS™ 125 Therapy Unit. Care should
be used when operating the PREVENA PLUS™ 125 Therapy Unit adjacent to or stacked with
other equipment. If adjacent or stacked use is necessary, the PREVENA PLUS™ 125 Therapy
Unit and the other equipment should initially be observed to verify normal operation in the
configuration in which it will be used.
•
The electrical cables, external power supplies and accessories listed or referenced in this
manual have been shown to comply with the test requirements listed in the following tables.
Care should be taken to use only manufacturer-recommended cables, power supplies and
accessories with the PREVENA PLUS™ 125 Therapy Unit. If a third-party supplier offers cables,
external power supplies and electrical accessories for use with the PREVENA PLUS™ 125
Therapy Unit and they are not listed or referenced in this manual, it is the responsibility of that
third-party supplier to determine compliance with the standards and tests in the following
tables.
•
The use of electrical cables and accessories other than those specified in this manual or
referenced documents may result in increased electromagnetic emissions from the PREVENA
PLUS™ 125 Therapy Unit or decreased electromagnetic immunity of the PREVENA PLUS™ 125
Therapy Unit.
•
Portable and mobile 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 PREVENA PLUS™ 125 Therapy Unit including cables specified by the manufacturer.
Otherwise, degredation of the performance of this equipment could result. More precisely,
the minimum recommended separation distance should be calculated from the equation
applicable to the frequency of the transmitter, as noted in the guidance below.
•
NOTE: This equipment has been tested and found to comply with the limits for medical
devices to IEC 60601-1-2: 2014 4th edition. These limits and test levels are intended to provide
reasonable safety with regard to electromagnetic disturbances when the device is used in a
typical medical installation.
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