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10
INTRODUCT
ION
Laser Safety
Z500
Setup Manual
INTRODUCTION
Use in the U.S.
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.
FDA Labels
Be sure to attach FDA labels; do not attach EN/IEC WARNING label by mistake.
21CFR1040.10 and 1040.11
DANGER
DANGER
PEAK POWER
PULSE DURATION
WAVE LENGTH
15000
25000
658
µ
w
µ
s
Class III B Caution logo type
Aperture Label
Certification and Identification Label
AVOID
EXPOSURE
This laser product complies with
21 CFR 1040.10 and 1040.11.
Shiokoji Horikawa, Shimogyo-ku,
Kyoto 600-8530 JAPAN
OMRON Corporation
AYABE Factory, OMRON Corp.
Place of manufacture:
Manufactured in
Laser radiation
is emitted from
this aperture
15000
25000
658
µ
w
µ
s