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CDRH Regulations (nur USA)
The Center for Devices and Radiological Health (CDRH) of the U.S. Food
and Drug Administration implemented regulations for laser products on
August 2, 1976. These regulations apply to laser products manufactured
from August 1, 1976. Compliance is mandatory for products marketed in
the United States. The labels and artwork shown below indicate
compliance with CDRH regulations and must be attached to laser
products marketed in the United States.
Use of controls, adjustments or performing procedures other
ACHTUNG
than those specified in this manual may result in hazardous
laser radiation exposure.
HINWEIS
Complies with 21 CFR Chapter 1 Subchapter J.
Laser Class Information: A black on yellow label which reads, "Class 1
Laser Product" printed in English, French, German, Finnish, Japanese,
and Spanish.
Anhang C
Sicherheitshinweise und behördliche Informationen
CDRH Regulations (nur USA)
C-3
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