Safety Information; Denmark Safety Certification; Laser Warning; Fda Class 1 Laser Device - 3Com 4007 Getting Started Manual

34 C 3: I
HAPTER NSTALLING THE

Safety Information

This section lists warning notices to read before you
install the Switch 4007 and its components.
WARNING: The Switch 4007 must be installed only
by trained service personnel.
WARNING: To maintain proper cooling in the chassis
and maintain safety compliance, make certain that
blank faceplates cover any empty slots.
WARNING: Hazardous energy levels exist inside of
the Switch. Do not place hands or objects into the
switch or touch components on an inserted module.
WARNING: Safety regulations state that the selected
table, shelf, or rack must be able to support at least
three times the weight of a fully loaded Switch. A
fully loaded Switch 4007 chassis weighs
approximately 38.55 kg (85 lb). Therefore, the
selected table or shelf must support at least 115.65
kg (255 lb).

Denmark Safety Certification

The following warning is required for Denmark safety
certification:
WARNING: For use in Denmark, each 3CB9EP9
power supply must receive power from a separately
dedicated socket outlet having a 16-ampere fuse in
the installation. This product must be mounted in a
fixed installation such as a permanent rack.
S 4007
WITCH
WARNING: Ved brug i Danmark, skal hver 3CB9EP9
stromforsyning modtage strom fra en separat,
dedikeret stikkontakt med en 16-ampere sikring i
installationen.

Laser Warning

The following warning is required when you install
fiber-optic communication modules into the
Switch 4007:
WARNING: To ensure optical safety when you install
a fiber-optic interface module, comply with the
following precaution:
Although the data communication LEDs and Lasers
used in this product meet the regulatory
requirements for casual exposure to the eye, as with
any source of bright light, 3Com
you do not look into the light source.
Laser Safety Information: IEC 825 and EN60825,
Class 1 Laser Device. For connection only to Class 1
Laser Devices.
CLASS 1
LASER PRODUCT

FDA Class 1 Laser Device

This product complies with U.S. Department of Health
and Human Services Rules 21 CFR Subchapter J
applicable at date of manufacture.
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recommends that