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Operation Manual MA 28
8506915 Rev. 5
9
05/05/2021
2.7 Device Control
The user of the device should perform a subjective device check once a week
according to ISO 8253-1. See section 6.7 for a checklist.
For annual calibration please see sections 2.5 and 3.1
2.8 Electromagnetic Compatibility (EMC)
This device is suitable in hospital environments except for
near active HF surgical equipment and RF shielded rooms of
systems for magnetic resonance imaging, where the intensity
of electromagnetic disturbance is high.
The device fulfills the relevant EMC requirements. Avoid
unnecessary exposure to electromagnetic fields, e.g. from
mobile phones etc.
Use of this device adjacent to or stacked with other
equipment should be avoided because it could result in
improper operation. If such use is necessary, this device and
the other equipment should be observed to verify that they
are operating normally.
Use of accessories, transducers and cables other than those
specified or provided by the manufacturer of this equipment
could result in increased electromagnetic emissions or
decreased electromagnetic immunity of this equipment and
result in improper operation.
The list of accessories, transducers and cables can be found
in the section 6.5 of this instruction.
Portable
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 MA 28, including cables specified by the manufacturer.
Otherwise, degradation of the performance of this equipment
could result in improper operation.
WARNING
WARNING
WARNING