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USER’S GUIDE
FDA Regulations
U.S. Food and Drug Administration (FDA) implemented regulations for laser products manufactured from 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 label shown on the back of the printer indicates compliance with the FDA regulations and must be attached to laser products marketed in the United States.
MANUFACTURED: BROTHER INDUSTRIES, LTD.
This product complies with FDA radiation performance standards, 21 CFR Subchapter J
Caution
Use of controls, adjustments or performance of procedures other than those specified in this manual may result in hazardous invisible radiation exposure.
For Your Safety
To ensure safe operation the
Extension cords used with the equipment must be
The fact that the equipment operates satisfactorily does not imply that the power is grounded and that the installation is completely safe. For your safety, if in any doubt about the effective grounding of the power, consult a qualified electrician.
DECLARATION OF CONFORMITY (EUROPE)
We, Brother International Europe Ltd.,
Brother House 1 tame Street, Guide Bridge, Audenshaw, Manchester M34 5JE, UK.
declare that this product is in conformity with the following normative documents:
Safety: | EN 60950, | EN 60825 |
EMC: | EN 55022 Class B, | EN |
following the provisions of the Low Voltage Directive 73/23/EEC and the Electromagnetic Compatibility Directive 89/336/EEC (as amended by 91/263/EEC and 92/31/EEC).
Manufacture at the following facilities is carried out under a Quality System which is registered by BSI Quality Assurance and JQA Quality Assurance.
Brother Industries, Ltd., Kariya Plant
BSI Certificate of Registration No. FM27391
JQA Certificate of Registration No. 0340
Issued by :
Brother International Europe Ltd.
European Development and Technical Services Division
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