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INTRODUCTION
Use in the U.S.
Z500
10
Setup Manual
When a laser product mounted on a certain device is to be used in the U.S., it has
to meet the requirements set forth by the FDA (regulations for laser products set
forth by the Food and Drug Administration). Three different FDA labels are
enclosed in the sensor package. Attach them to the sensor body.
Applications have been approved by CDRH (Center for Devices and Radiological
Health) for Z500-SW6 and Z500-SW17. Z500-SW2T should not be used in the
U.S. at this moment since the application for this model has not been approved
yet.
FDA Labels for Laser Products
The Z500 is designed to be built into the finished system unit. Refer to the
following technical standard for installation.
21CFR1040.10 and 1040.11
FDA Labels
Class III B Caution logo type
DANGER
DANGER
µw
PEAK POWER
15000
µs
PULSE DURATION
25000
WAVE LENGTH
658
Aperture Label
AVOID
EXPOSURE
Laser radiation
is emitted from
this aperture
Be sure to attach FDA labels; do not attach EN/IEC WARNING label by mistake.
µw
15000
µs
25000
658
Certification and Identification Label
This laser product complies with
21 CFR 1040.10 and 1040.11.
OMRON Corporation
Shiokoji Horikawa, Shimogyo-ku,
Kyoto 600-8530 JAPAN
Place of manufacture:
AYABE Factory, OMRON Corp.
Manufactured in
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