Introduction And Operation; Intended Use; System Features; General Warnings - ConMed Linvatec LS7500 Instruction Manual

1.0
INTRODUCTION and
OPERATION
t is recommended that personnel study this
I
manual before attempting to operate or
clean the Linvatec LS7500 Xenon 300 Watt
Light Source. The safe and effective use of this
equipment requires the understanding of and
compliance with all warnings, cautionary
notices, and instructions marked on the product
and included in this manual. Improper use or
set-up of the light source may cause damage not
covered by the warranty.
1.1

Intended Use

The Linvatec LS7500 Xenon Light Source is
intended to be used with an endoscope to
provide illumination during endoscopic
procedures.
1.2

System Features

• Ultraviolet and infrared filters to prohibit
harmful radiation from entering the fiber
optic cable.
• A fully adjustable shutter to attenuate light
output intensity from 0-100%.
• Universal front panel receptacle that allows
the light source to be utilized with many
Light Guide Adapters (please refer to sec-
tion 1.4.1 for specific details).
• Lamp life indicator on front panel to indi-
cate the total hours of elapsed use.
• Stand-by feature blocks light from exiting
light guide port until selected.
• Auto and manual shutter modes to increase
/ decrease lamp intensity via serial commu-
nication link.
1.3

General Warnings

1. This equipment is designed for use by
medical professionals completely familiar
with the required techniques and
instructions for use of the equipment. Read
and follow all warning and cautionary
notices and instructions marked on the
product and included in this manual .
2. Do not attempt to open or service
the Light Source, as this may void
your warranty. There are no user-
serviceable parts inside. Remov-
ing the cover may introduce an
electric shock hazard by exposing
you to dangerous high voltages or other
risks. If the system malfunctions, return it
for service immediately.
3. Dangerous voltages are present in many
system assemblies. The unit should be used
only in rooms that comply with recommen-
dations concerning electrical safety when
used for medical purposes (as stated in
IEC 60601 Series, Title 21 CFR and
UL 2601-1).
4. System installation shall be in accordance
with the requirements of IEC 60601-1, The
Standard for Safety Requirements of Medi-
cal Electrical Systems.
5. Patients should only be connected to
applied parts complying with IEC 60601-1.
Other equipment used in the system should
comply with relevant IEC or ISO Standards.
6. Do not expose the Light Source to moisture,
operate in wet areas, or place liquids on or
above the unit.
7. Never insert foreign objects into the Light
Source.
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