LIGHTMED TruScan Pro – Operator’s Manual Rev. No. 01 Page 75 of 109
Section 5 Installation
5.1 Introduction and Requirements
It is strongly recommended that the TruScan Pro laser system be installed by the Manufacturer
or its authorized Service Technicians to ensure that the system is installed, aligned, and calibrated
correctly according to the manufacturer’s specifications. The user is responsible for ensuring that
the laser system is operating and operated appropriately, especially when the laser is moved or
relocated.
Please use the installation procedures mentioned in this section as reference to ensure a
successful installation process. A copy of the complete and signed Installation Record Sheet
(page 91) must be sent to the Manufacturer upon each installation completion. Both the installer
and customer are advised to keep a copy the Installation Record Sheet for future reference. If the
Installation Record Sheet is not sent to the Manufacturer, the Manufacturer reserves the
right to decline any warranty claims.
When installing the TruScan Pro laser system, all safety precautions must be observed to prevent
the risk of exposure to laser radiation.
CAUTION! Always wear laser safety glasses that are suitable for the appropriate wavelength(s)
to protect your eyes!
5.1.1 Requirements Prior to Installation
• 100 to 240 V, 50 or 60 Hz., AC mains power supply with an earth ground connection. This is
a single-phase outlet capable of delivering up to 400 W.
• A mains power cable is supplied but the connector may not suit the outlet that is available in
the treatment room. It is recommended to have a spare locally compatible cable available.
The cable assembly must be CE approved for use in EU countries.
• It is recommended that the main power cable of the ophthalmic table be plugged into multiple
portable socket outlet with more than 400 W loading capability.
• The laser system should be placed in a treatment room that provides a safe operating
environment. A dark room or surgery room would be preferred.
• Position the laser in such a way that the treatment beam does not interact with any windows,
doors, reflective surfaces (mirrors, metals, etc.).
• A laser safety sign must be posted on the treatment door or entrance.
• The laser is designed to be compatible with a remote door interlock, which disables the system
when the treatment room door is opened. This feature should be wired by an electrician with
the instructions from the Manufacturer or an authorized Service Technician.
• The remote door interlock is provided with an interlock key, which enables the system normally
despite the treatment room door being open or closed. Please keep the interlock key inserted
into the console If the remote door interlock feature is not used.
• If the laser needs to be relocated, please lock all the locking screws on the slit lamp to prevent
it from moving during transport. Moving the laser to a new facility that is not in walking distance
is a big task—the user should consider repacking the laser into its original foam packaging to
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