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 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.
IEC 825 Laser Class (For 220–240 V Model Only)
CLASS 1 LASER PRODUCT.
APPAREIL Å LASER DE CLASSE 1.
LASER KLASSE 1
LUOKAN 1 LASERLAITE
KLASS 1 LASER APPARAT
KLASS 1 : LASER
KLASSE 1 LASER PRODUKT
For Finland and Sweden
Varoitus! Laitteen käyttäminen muulla kuin tässä käyttöohjeessa mainitulla tavalla saattaa altistaa käyttäjän turvallisuusluokan 1 ylittävälle näkymättömälle lasersäteilylle.
Varning – Om apparaten används på annat sätt än i denna Bruksanvisning specificerats, kan användaren utsättas för osynlig laserstrålning, som överskrider gränsen för laserklass 1.
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