Panasonic HL-C1-WL Series, User Manual

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2. FDA

Export to US
To export the laser product to the US installed on equipment, it is restricted by
the regulation of the USA Food and Drug Administration (FDA).
In case this product is used as a FDA conformity product, be sure to change
the warning label to the English version label and affix the Certifi-
cate/identification label, which are enclosed in the package of this product.

The FDA establishes the standard below to prevent problems to the user pre-
viously due to laser product.
PART1040 (PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS)
– Execution standard for laser beam emitting product –

This standard classifies the laser product based on the level of laser danger
and stipulates preventive safety measures to be executed for each class (21
CER 1040.10 and 1040.11).
Furthermore, the guidance of Laser Products-Conformance with IEC 60825-1,
2007 and IEC 60601-2-22; Final Guidance for Industry and FDA (Laser No-
tice No. 50) are applied to this product.
The classification of equipment type is as follows:
Classification of HL-C135C-BK10 (FDA)
Class IIIB