HP P4000 9.0.01 HP P4800 G2 SAN Solution for BladeSystem Maintenance Guide (BV - Page 40

Laser compliance notices, English laser notice - installation guide

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Laser compliance notices English laser notice This device may contain a laser that is classified as a Class 1 Laser Product in accordance with U.S. FDA regulations and the IEC 60825-1. The product does not emit hazardous laser radiation. WARNING! Use of controls or adjustments or performance of procedures other than those specified herein or in the laser product's installation guide may result in hazardous radiation exposure. To reduce the risk of exposure to hazardous radiation: • Do not try to open the module enclosure. There are no user-serviceable components inside. • Do not operate controls, make adjustments, or perform procedures to the laser device other than those specified herein. • Allow only HP Authorized Service technicians to repair the unit. The Center for Devices and Radiological Health (CDRH) of the U.S. Food and Drug Administration implemented regulations for laser products on August 2, 1976. These regulations apply to laser products manufactured from August 1, 1976. Compliance is mandatory for products marketed in the United States. Dutch laser notice French laser notice 40 Regulatory compliance notices

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Laser compliance notices
English laser notice
This device may contain a laser that is classified as a Class 1 Laser Product in accordance with
U.S. FDA regulations and the IEC 60825-1. The product does not emit hazardous laser radiation.
WARNING!
Use of controls or adjustments or performance of procedures other than those
specified herein or in the laser product's installation guide may result in hazardous radiation
exposure. To reduce the risk of exposure to hazardous radiation:
•
Do not try to open the module enclosure. There are no user-serviceable components inside.
•
Do not operate controls, make adjustments, or perform procedures to the laser device other
than those specified herein.
•
Allow only HP Authorized Service technicians to repair the unit.
The Center for Devices and Radiological Health (CDRH) of the U.S. Food and Drug Administration
implemented regulations for laser products on August 2, 1976. These regulations apply to laser
products manufactured from August 1, 1976. Compliance is mandatory for products marketed in
the United States.
Dutch laser notice
French laser notice
40
Regulatory compliance notices