Important—About the Interface Cable
A shielded interface cable, which is included with your machine, should be used to ensure compliance with the limits for a Class B digital device.
Caution
Changes or modifications not expressly approved by Brother Industries, Ltd. could void the user’s authority to operate the equipment.
Industry Canada Compliance Statement (For Canada Only)
This Class B digital apparatus complies with Canadian
Cet appareil numérique de la classe B est conforme à la norme
Laser Safety (For 110-120V Models Only)
This equipment is certified as a Class I 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
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.
Manufacturing Information
BROTHER CORP. (ASIA) LTD.
BROTHER BUJI NAN LING FACTORY
Gold Garden Industry, Nan Line Village, Buji,
Rona Gana, Shenzhen, China
This product complies with FDA radiation performance standards, 21 CFR Subchapter J.
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