Plum A+
®
Infusion Systems
430-95597-001 (Rev. 06/05) 1- 13
generator, it is possible that the normal operation of a sensor
or microcomputer might be disrupted. Even in this event, the
outcome would likely be a false alarm or detected system
malfunction and would not result in a hazard to patient or
operator.
• This equipment has been tested and found to comply with the
EMC limits for the Medical Device Directive 93/42/EEC (EN
55011 Class B and IEC/EN 60601-1-2:2001). These limits
are designed to provide reasonable protection against
harmful interference in a typical medical installation. The
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 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 into an outlet on a circuit
different from that to which the other device(s) is
connected
• Consult the manufacturer or field service technician for
help
• Portable and mobile RF communications equipment, such as
cellular telephones, 2-way radios, Bluetooth devices,
microwave ovens, in close proximity to this device may affect
wireless and wired communications with the Infusion pump
and/or the operation of the Infusion pump. Special
precautions need to be exercised regarding EMC, These
include:
• Use of a shielded Ethernet cable (CAT5 STP or better)
for plugging into the RJ45 Ethernet connector. Using
an unshielded Ethernet cable may result in increased
emissions.
sec01.fm Page 13 Thursday, June 23, 2005 9:36 AM
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