Operator's Manual

Rev. 0 7/16/2020
11
Summus Medical Laser, LLC 1185 West Main St. Franklin, TN 37064 TEL: [phone]
1 INTRODUCTIONS
This manual applies to Platinum Series

P4H model.
The Platinum Series P4H is a portable laser product designed for medical
laser therapy. This device is for Professional Use Only and its therapy uses shall
only be administered by or under the supervision of a trained professional. The
product is dedicated to clinicians and patients with a safe and effective treatment
experience.
1.1 Device Description
The Platinum Series P4H uses Gallium Aluminum Arsenide (GaAlAs)
semiconductor diode as the lasers source. The laser energy is delivered to the
therapy area by an optical path transmission system consisting of a flexible quartz
fiber connecting the laser source and hand piece. Activation occurs when the
operator enables the laser and presses the finger switch on the distal end of the
probe. When the switch is activated, the message “LASER EMITTING” appears
on the LCD screen. When the finger switch is pressed a second time and
released, the laser is deactivated. The laser light is applied to the target area on
the patient with the hand piece either in contact or slightly off contact with the
patient‟s skin.
The light is an invisible non-ionizing thermal radiation that does not create
changes in cellular DNA. The P4H‟s continuous output power is 28W and 30W
with intense super pulse (ISP) mode . The output spot size and the power density
of the applied laser light is achieved with the 25mm and the 50mm broad beam
open end and curved contact hand piece tips respectively. In addition, the P4H
has been preset with a variety of reasonable and effective treatments in the
system for clinicians as a reference.
The user needs to carry out appropriate clinical and technical training before
using this product and should strictly follow the operation instruction manual
during the operation of the device. Before treatment, professional users should
choose the reasonable treatment parameters for the treatment according to the
patient's condition and treatment.
Note
The manufacturer assumes no responsibility for the direct effects or side effects that
arise from therapeutic or use of the system. The sole responsibility lies with the