10
ZX2 User’s Manual
INTRODUCTION
MAIN
APPLICATIONS
& SETTING
METHODS
SPECIFI-
CATIONS
INDEX
SETTING
TRANSITION
CHARTS
DETAILED
SETTINGS
FLOW OF
OPERATION
CONTENTS
PREPARATION
FOR
MEASUREMENT
BASIC
SETUP
TROUBLE-
SHOOTING
Height
Double
Sheet
Detection
Positioning
Eccentricity
and Surface
Deflection
Steps
and
Warpage
Thickness
In Europe, diffuse-reflective models in the ZX2 Series are categorized as Class 2 laser
products and the regular-reflective model is classified as a Class 1 laser product
according to EN60825-1 (see note).
The CE markings on the products also reflect these categorizations.
In the U.S.A., diffuse-reflective models in the ZX2 Series are categorized as Class II laser
products, and the regular-reflective model is classified as a Class I laser product
according to IEC60825-1 criteria, in accordance with the stipulations of the FDA standard
Laser Notice No. 50 (see note).
This product has already been registered with the CDRH (Center for Devices and
Radiological Health). (Accession Number: 1020665)
Place the laser warning label and the FDA label on the sensor.
The ZX2 Series is meant to be built into final system equipment. Pay special attention to
the following precautions for the safe use of the product:
Note:
Europe: Class 1 and Class 2 of EN 60825-1: 1994 +A11:1996 +A2:2001
= IEC 60825-1:1993 +A1:1997 +A2:2001
U.S.A.: Class I and Class II of FDA (21 CFR1040.10)
(1) ZX2-LD
emits visual laser beam. Do not stare directly into the laser.
Make sure that the laser beam path is terminated. If specular objects are present in
the laser beam path, make sure that they are prevented from reflecting the laser
beam.
When used without an enclosure, make sure the laser path from eye level is avoided.
(2) To avoid exposure to hazardous laser radiation, do not displace nor remove the
protective housing during operation, maintenance, and any other servicing.
(3) As for countries other than those of Europe and the U.S.A., observe the regulations
and standards specified by each country.
(4) Label Indications
The EN and FDA labels are supplied with the product.
Replace the current labels with them according to the instructions given in the
manuals.
