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Philips Lumify - Page 54

Philips Lumify
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Safety Electromagnetic Compatibility
54 Lumify Ultrasound System
Philips Healthcare 4535 618 58571_A/795 * MAY 2016
The transducer and representative Android device are classified as Group 1, Class A equipment
in accordance with international standard CISPR 11 for radiated and conducted electromagnetic
disturbances. Compliance with this standard allows the system to be used in all establishments
except domestic establishments and those directly connected to the public low-voltage power
supply network that supplies buildings used for domestic purposes. If the system is used in a
residential environment (for which CISPR 11 Class B is normally required), you may need to
relocate or reorient the system to offer adequate protection from radio frequency
communication services.
WARNING
Using cables, transducers, or accessories other than those specified for use with the system
may result in increased emissions or decreased immunity of the system.
CAUTION
Medical equipment has special precautions regarding EMC and must be installed and put
into service according to the EMC information provided in the system’s accompanying
documents.
This section includes information on electromagnetic emissions and immunity as it applies to
the system. Ensure that the operating environment of your system meets the conditions
specified in the referenced information. Operating the system in an environment that does not
meet these conditions may degrade system performance.
The information and warnings contained in this and other sections should be observed when
installing and using the system to ensure its EMC.
NOTE
See the other electrical-safety warnings and cautions in this section.

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