Laser Safety - Omron ZS-L User Manual

Laser Safety

Various safety standards regarding laser devices are stipulated depending on the country
of use.
(1) Using in U.S.
When using devices in which this product is installed in U.S., the devices are subjected
to the U.S. FDA (Food and Drug Administration) laser regulations.
The ZS-LD20ST/LD50S/LD130/LD350S/LD10GT/LD15GT is scheduled to by regis-
tered to CDRH (Center for Devices and Radiological Health).
Please inquire about details like export to the foreign country.
Labels relating to laser use on this product
The product is provided with labels that comply with FDA technical guidelines. When
using this product in the United States, swap the warning labels on the sensor body
with the FDA labels provided. Attach the labels at the correct locations as indicated in
the figure below.
The ZS-LD_ _ _ is intended to be installed in final system devices. When installing on
these devices, follow these technical guidelines.
∗ US Federal Law: 21CFR 1040.10 and 1040.11
Laser emission
opening label Warning label
Certification Label
(2) Using in a country other than U.S.
For countries other than Japan and U.S., warning labels must be replaced by English
ones (supplied with the product).
EN 60825 is provided for product exported to Europe, and the content of this standard
differs.
The ZS-L Series is categorized as a Class II device as stipulated in EN60825-1
(IEC60825-1).
Technical Guidelines Relating to Laser Products and "Specific-
application Laser Products"
Laser emission
opening label
Warning label
Certification Label
Section 6
APPENDIX
ZS-L
6-23
User's Manual