Brother International DCP-L2550DW Product Safety Guide - Page 19

FDA Regulations (for 110-120V Models Only), For Use in the USA or Canada Only

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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 product during any phase of user operation. FDA Regulations (for 110-120V Models Only) U.S. Food and Drug Administration (FDA) has implemented regulations for laser products manufactured on or after August 2, 1976. Compliance is mandatory for products marketed in the United States. One of the following labels on the back of the product indicates compliance with the FDA regulations and must be attached to laser products marketed in the United States. Manufactured: BROTHER INDUSTRIES (VIETNAM) LTD. Phuc Dien Industrial Zone Cam Phuc Commune, Cam Giang District Hai Duong Province, Vietnam This product complies with FDA performance standards for laser products except for deviations pursuant to Laser Notice No. 50, dated June 24, 2007. WARNING Use of controls, adjustments, or performance of procedures other than those specified in this manual may result in hazardous invisible radiation exposure. Internal laser radiation: Max. Radiation Power: 25 mW Wave Length: 770 - 800 nm Laser Class: Class 3B For Use in the USA or Canada Only These products are made for use in the USA and Canada only. We cannot recommend using them overseas because it may violate the Telecommunications Regulations (MFC models only) of that country and the power requirements of your product may not be compatible with the power available in foreign countries. Using USA or Canada models overseas is at your own risk and may void your warranty. 19

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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 product during any phase of user
operation.
FDA Regulations (for 110-120V Models Only)
U.S. Food and Drug Administration (FDA) has implemented regulations for laser products
manufactured on or after August 2, 1976. Compliance is mandatory for products marketed in the
United States. One of the following labels on the back of the product indicates compliance with
the FDA regulations and must be attached to laser products marketed in the United States.
Manufactured:
BROTHER INDUSTRIES (VIETNAM) LTD.
Phuc Dien Industrial Zone Cam Phuc Commune, Cam Giang District Hai Duong Province,
Vietnam
This product complies with FDA performance standards for laser products except for
deviations pursuant to Laser Notice No. 50, dated June 24, 2007.
WARNING
Use of controls, adjustments, or performance of procedures other than those specified in this
manual may result in hazardous invisible radiation exposure.
Internal laser radiation:
Max. Radiation Power: 25 mW
Wave Length: 770 - 800 nm
Laser Class: Class 3B
For Use in the USA or Canada Only
These products are made for use in the USA and Canada only. We cannot recommend using
them overseas because it may violate the Telecommunications Regulations (MFC models only)
of that country and the power requirements of your product may not be compatible with the
power available in foreign countries. Using USA or Canada models overseas is at your own risk
and may void your warranty.
19