Compaq ProLiant 800 Manual page 208

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F-4
Regulatory Notices
CDRH Regulations
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.
This device is classified as a Class 1 laser product as defined by the CDRH regulations (CFR 1040.10,
para. b, item 5). This means that this is a Class of laser products that does not emit hazardous laser
radiation; this is possible only because the laser beam is totally enclosed during all modes of customer
operation.
The laser produces a beam that, if looked into, could cause eye damage. Installation and Service
procedures must be followed exactly as written without change.
WARNING:
!
open the cabinet. Wearing glasses and contact lenses, etc., increases the hazard.
All maintenance should be performed by an Authorized Compaq Service Provider.
WARNING:
!
than those specified herein or in the CD ROM installation guide may result in
hazardous radiation exposure.
International Regulations
This device is designed to comply with the appropriate safety standards, including IEC950 and
IEC825. This device is classified as a Class 1 laser product as defined by IEC825. The following label
(or equivalent) is located on the surface of your CD-ROM drive.
Laser Product Label
Because the internal laser beam may cause eye damage, do not
Use of controls or adjustments or performance of procedures other
This system is classified as a CLASS 1 LASER
PRODUCT. This label is located on the outside of your
system. A similar label also appears on the internal CD-
ROM installed in your system.
Writer: Project: Regulatory Notices Comments:
File Name: P-appf.doc Last Saved On: 4/24/97 10:53 AM

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