Brother WL660 manual FDA Regulations For 110-120 V Model Only, Declaration of Conformity Europe

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REGULATIONS

FDA Regulations (For 110-120 V Model Only)

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.

15-1 Naeshiro-cho Mizuho-ku Nagoya, 467 Japan

This product complies with FDA radiation performance standards, 21 CFR chapter 1 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.

DECLARATION OF CONFORMITY (EUROPE)

We, Brother International Europe Ltd.,

Brother House 1 Tame Street, Guide Bridge, Audenshaw, Manchester M34 5JE, UK.

declare that this products is in conformity with the following normative documents.

Safety:	EN 60950,	EN 60825
EMC:	EN 55022 Class B,	EN 50082-1

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

1-5, Kitajizoyama, Noda-cho, Kariya-shi,

Aichi-ken 448, Japan

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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