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USER’S GUIDE
vi
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.
15-1 Naeshiro-cho Mizuho-ku Nagoya, 467 Japan
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 three-pin plug supplied must be inserted only into a standard
three-pin power point which is effectively grounded through the normal household wiring.
Extension cords used with the equipment must be three-conductor and be correctly wired to
provide connection to ground. Incorrectly wired extension cords are a major cause of
fatalities.
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.