Laser Safety; Label Replacement; Standards - Omron ZX-GT User Manual

Laser Safety

Various safety standards regarding laser products are stipulated depending on the
country of use.
Take safety measures according to each standard.
Classification
Standards and classification (*1)
JIS C 6802 2005 (Japan)
EN60825/IEC60825-1 (Europe)
Class 1
*1 For products exported to the countries other than Japan and Europe, different safety standards are applied
according to the countries. Check the LED safety regulations and standards of the relevant country.

Label Replacement

The warning label written in Japanese is affixed to the Sensor unit. For countries other
than Japan, warning labels must be replaced by English ones (supplied with the Sensor).
● Use in the United States
When exporting devices in which this product is installed to the U.S., the devices are
subjected to the U.S. FDA (Food and Drug Administration) laser regulations, and is
classified as Class II specified by the U.S. FDA.
This product has already been registered with the CDRH (Center for Devices and
Radiological Health).
Labels in compliance with FDA laser regulations are attached to devices subjected to
these regulations. When exporting devices to the U.S., replace the labels on the Sensor
body referring to the figure below. Attach the labels at the correct positions marked in the
following figure.
These labels also show that the device will be installed in the end system. Follow the
following technical standards when installing the device in the end system.
* FDA standards: 21 CFR 1040.10 and 1040.11
Technical standards relating to "Laser products" and "Specific purpose laser products"
For details, consult us separately.
144
Laser Safety
Maximum output of
laser beam
FDA
(the United
States)
Class II Max. output 0.2 mW
ZX-GT User's Manual