Safety and Legal
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Industry Canada Compliance Statement (Canada only) A
This Class B digital apparatus complies with Canadian ICES–003.
Cet appareil numérique de la classe B est conforme à la norme NMB–003 du Canada.
Disconnect device A
This product must be installed near an electrical jack that is easily accessible. In case of
emergencies, you must disconnect the power cord from the electrical jack to shut off power
completely.
LAN connection A
CAUTION
Do not connect this product to a LAN connection that is subject to over-voltages.
Laser safety A
This equipment is certified as a Class 1 laser product under the U.S. Department of Health and
Human Services (DHHS) Radiation Performance Standard according to the Radiation Control for
Health and Safety Act of 1968. This means that the equipment does not produce hazardous laser
radiation.
Since radiation emitted inside the equipment is completely confined within protective housings
and external covers, the laser beam cannot escape from the machine during any phase of user
operation.
FDA regulations A
U.S. Food and Drug Administration (FDA) has implemented regulations for laser products
manufactured on and after August 2, 1976. Compliance is mandatory for products marketed in the
United States. The following label on the back of the machine indicates compliance with the FDA
regulations and must be attached to laser products marketed in the United States.
Manufactured:
Océ Imagistics Inc.
100 Oakview Drive Trumbull, CT 06611, U.S.A
This product complies with FDA performance standards for laser products except for deviations
pursuant to Laser Notice No. 50, dated July 26, 2001.
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