USER MANUAL Page
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10.1 Components information
Power cord and adapter cord
Note
Portable and mobile radio frequency communication equipment may affect
the normal use of S3 medical diode laser device.Hospitals except for near
active HF SURGICAL and the RF shielded room of an ME SYSTEM for
magnetic resonance imaging,where the intensity of EM DISTURBANCES is
high. Please use the recommended electromagnetic environment during
use of the S3 medical diode laser instrument.
The use of non-specified accessories and cables may result in an increase
in the emission or immunity of the S3 medical diode laser treatment
instrument.PIOON cannot guarantee that accessories, lines and
transformers acquired outside of and not delivered from PIOON, will
correspond with EMC requirements of IEC 60601-1-2.
Note
The diode laser medical system is exclusively intended for use by medical
professionals. In residential areas, the diode laser medical system may
cause radio interference in certain circumstances so that it may be
necessary to undertake suitable measures such as realigning, rearranging
or screening the diode laser medical system, or filtering the connection with
the public power supply.
Note
The EMISSIONS characteristics of this equipment make it suitable for use
in industrial areas and hospitals (CISPR 11 class A). If it is used in a
residential environment (for which CISPR 11 class B is normally required)
this equipment might not offer adequate protection to radio-frequency
communication services. The user might need to take mitigation
measures,such as relocating or re-orienting the equipment.
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