Brivo OEC 715/785/865 Mobile C-Arm X-Ray Product Service Manual
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This label warns the operator or
the patient not to look at the laser
1
beams directly. (The label will only
be required if there is laser aimer)
This label indicates the
equipment was tested by a
Notified Body and was found to
be in compliance with the
2
requirements of all relevant
directives and standards in effect
within the European Union at the
time of manufacture.
This label indicates that waste
electronic and electrical
equipment must not be disposed
of as unsorted municipal waste
and must be collected separately.
1
Please contact an authorized
representative of the
manufacturer for information
concerning the decommissioning
of your equipment.
2
This is the label of branding.