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 MFC indicates compliance with the FDA regulations and must be attached to laser products marketed in the United States.
Manufactured:
BROTHER CORP. (ASIA) LTD.
BROTHER BUJI NAN LING FACTORY
Gold Garden Industry, Nan Ling Village, Buji, Rong Gang, Shenzhen, China.
This product complies with FDA radiation performance standards, 21 CFR Subchapter J.
WARNING
Use of controls, adjustments or performance of procedures other than those specified in this guide may result in hazardous invisible radiation exposure.
WARNING
Changes or modifications not expressly approved by Brother Industries, Ltd. may void the user’s authority to operate the equipment.
Internal laser radiation |
|
Max. Radiation Power | 5 mW |
Wave Length | 760 - 810 nm |
Laser Class | Class IIIb (Accordance with 21 CFR |
| Part 1040.10) |
11 - 6 IMPORTANT INFORMATION