2.8
Warning signs on the device
A class 2 laser is installed in the device. The housing is labeled with a warning sign.
1
2
LASER
2
EN/IEC 60825-1:2014
for laser products except for conformance with IEC 60825-1 Ed.3.,
Complies with FDA performance standards
as described in Laser Notice No.56, dated May 8, 2019.
Ptotal < 22mW, DC or pulsed; λ = 660±15nm; P < C6*1mW within 7mm aperture
Figure 1: Warning sign on the device: Laser class 2 (EN/IEC 60825-1:2014)
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Laser radiation – Never look into the light beam – Laser class 2 (EN/IEC 60825-1:2014)
2
EN/IEC 60825-1:2014
Complies with the FDA performance requirements for laser products except for conform‐
ance with IEC 60825-1 Ed.3., as described in Laser Notice 56 dated May 8, 2019.
Ptotal < 22mW, DC or pulsed; λ = 660±15nm; P < C6*1mW within 7mm aperture
If the device itself is installed in a way that obscures the attached warning labels,
additional, clearly visible labels must be attached.
2.9
Note on laser radiation
This laser product corresponds to laser class 2 after having been assessed on the
basis of the Low Voltage Directive 2014/35/EU, which applies to all manufacturers
placing products on the market, in conjunction with EN 60825-1:2014 in the currently
applicable version. Due to the differing statutory requirements on occupational safety
according to guideline 2006/25/EC, this product has to be assessed based on the
older standard EN 60825-1:2007. Employers therefore need to instead base their
occupational safety measures on laser class 2M. Please observe the national regula‐
tions in relation to this.
SAFETY INFORMATION
2
8026049//2021-04 | SICK
O P E R A T I N G I N S T R U C T I O N S | Ruler3000
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Subject to change without notice
