UL/EN Statement
This equipment has been tested and found to comply with the limits for
medical devices in UL/EN 60601-1, 60601-1-2 and FCC/CE.
These limits
are designed to provide reasonable protection against harmful interference in
a typical medical installation.
This 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 to 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) are connected.
Consult the manufacturer or field service technician for help.
Type of protection against electric shock: Class I equipment
Degree of protection against electric shock: Not classified - no applied
parts
Classification according to the degree of protection against ingress of
water as detailed in the current edition of IEC 529: IPX0, ordinary
equipment
This equipment is not suitable for use in the presence of flammable
anesthetics or oxygen
Mode of operation: continuous operation
Certification of Eye Safety
This laser product is inside implemented by using 1310/1550nm optical
module, manufactured by Opticis Co., Ltd., which are all certified by UL/EN
60601-1, 60601-1-2 referred in Accession Number 07-1334-0217 as classified
in Class1 LASER eye safety.
1-9 Regulatory Statements
© 2011 Opticis Co., Ltd. All Rights Reserved
Revision 1.0, .Mar. 04, 2011
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