Avisos reglamentarios de dispositivo láser, Aviso de láser en inglés, Aviso de láser en holandés – HP Sistemas de almacenamiento de red HP StorageWorks X3000 Manual del usuario

Página 126: 126 aviso de láser en holandés

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Avisos reglamentarios de dispositivo láser

Aviso de láser en inglés

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.

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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.

Aviso de láser en holandés

Avisos sobre cumplimiento normativo

126

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