Platinum Series P4H Operator’s Manual Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
Operating Instructions Manual Instructions Before Use Platinum Series P4H Diode Laser Systems are for Professional Use Only according to the Indications for Use in this manual. The laser is to be used under the supervision of a trained medical professional. When receiving this product, please carefully check the integrity of the packaging. Refer to the packing list and carefully check the product components and their quantity.
SYMBOL DESCRIPTION SYMBOL Laser Danger DESCRIPTION Optical Fiber Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
Warning or precaution associated with the device Laser Stop which are not found on the label Class II medical Serial Number equipment and or B-Type Device Refer to the Instruction Manual Date of Manufacture Manufacturer Lithium Battery Hazard Symbol Battery.
IPX0 Transport Upright Fragile - Handle with Care Indicates the temperature limits to which the medical device can be safely exposed. device is not made with Indicates the range of atmospheric pressure to which the medical device can be safely exposed. Indicates the range of humidity to which the medical device can be safely exposed.
Indicates a medical device that is non-pyrogenic Label / Symbol Intentionally left blank Title Intentionally left blank Description / Explanatory Text Laser Danger Safety warning Optical Fiber Safety warning Laser Output Port Safety warning Class 4 Laser Product Explanatory Safety warning Safety Interlock Indicates the presence of interlock to prevent human access to Class 3 or Class 4 laser radiation when that portion of the housing is removed.
CONTENTS 1 INTRODUCTIONS .............................................................................................................................................. 11 1.1 Device Description ................................................................................................................................ 11 1.2 Indication .............................................................................................................................................. 12 1.3 Intended User .......
5 CONTENTS OF PLATINUM SERIES P4H laser ................................................................................................ 34 6 SET‐UP INFORMATION ................................................................................................................................ 37 6.1 Platinum Series P4H Set-up................................................................................................................... 37 6.2 Operation Instructions ........................................
12.1 RF Transmitting ................................................................................................................................... 68 12.2 Electromagnetic Immunity.................................................................................................................. 68 12.3 Electromagnetic Immunity.................................................................................................................. 69 12.
Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
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.
medical personnel. Note Every clinic and hospital utilizing this device is encouraged to adopt a Laser Training and Safety Program. 1.2 Indication Platinum Series P4H is indicated for temporary relief of minor muscle and joint pain, stiffness, minor arthritis pain, muscle spasm, temporary increase in local blood circulation, and temporary relaxation of muscles by means of topical elevated tissue temperature from infrared spectral emissions. 1.
Do not apply the laser on patients with active cancer. Do not apply the laser to patients with a compromised immune system Do not apply the laser to patients with concerns of anticoagulation or thromboembolic disorders Do not apply the laser to patients with herpes simplex 1.5.2 Relative Contraindications Do not apply the laser over a working spinal cord stimulator (SCS) Do not apply the laser directly over a pacemaker or implanted electronic device.
Do not use the laser on patients with meningitis or encephalitis. 1.6 Warnings and Precautions For medico-legal reasons, the practitioner should know the patients‟ medical history and must weigh the benefit versus risk when providing laser therapy. Use caution when applying the laser over areas where sensory perception is absent or diminished. Use caution when applying the laser to patients who are sensitive to light exposure.
The device is lightweight, easy to carry and can be used with power adapter or rechargeable battery. 1.8 Usage Prerequisites Every clinic and hospital utilizing this device is encouraged to adopt a Laser Training and Safety Program. If there are any questions or needed assistance during the use, please contact the designated dealer or our company. Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
2 SAFETY PRECAUTION WARNING: Before using this product, please read this section carefully and strictly observe the safety information. This device is for Professional Use Only and its therapy uses shall only be administered by or under the supervision of a trained professional. 2.1 Safety Instruction Platinum Series P4H is a Class 4 laser product. Before use, users must read and familiarize the instruction manual, and strictly follow the instructions in the manual to operate and maintain the device.
hazard. No highly reflective material should be found in the therapy room, such as mirrors and chrome-plated glass. WARNING: Avoid contact of the laser and laser beam with flammable, explosive, anesthetic or other flammable solvents. Do not put paper or plastic products in the area of laser treatment to prevent fire. 2.
DO NOT remove the protective goggles until the operator returns to the "Standby" mode. DO NOT leave the laser in READY mode. DO NOT allow non-personnel to enter the therapy area during laser treatment. DO NOT wear any reflective jewelry or items during treatment. Avoid scattering or reflecting laser energy that may cause damage to eyes or skin. Turn the power switch to off when not using the laser device.
WARNING: If the device does not work normally, please contact the designated dealer or the company immediately for consultation. Unauthorized users are not allowed to open the device without permission. Unauthorized opening of the device presents a risk of electric shock, as well as severe or irreversible injury or damage to user or device. 2.
generated by the laser equipment being used. Solvents and flammable solutions used for cleaning and disinfection should be volatilized before using the equipment. There is a risk the internal gas may be ignited. WARNING: Diode lasers are attracted to melanin and hemoglobin. Power levels are inversely related to the amount of pigmentation and vascular of the targeted tissue.
the user's 4-digit security PIN identification for permissions. Emergency Stop The emergency stop switch is used to immediately stop the laser emitting output. When the device is powered on and operating, if an abnormal function (such as no display, and light abnormality, etc.) occurs during the course of treatment, immediately press the emergency stop switch to stop the laser output. Identify and correct the cause prior to resuming use.
When the device is turned on, the power indicator light is green. When the laser is outputting, the corresponding indicator light is yellow. When the alarm state occurs, the corresponding indicator light is red. Alarm Prompt When the system detects an abnormal or a non-normal working state, the equipment will provide alarm notifications by sound, light, graphic text alerts on the LCD screen that would inform the user the system is in an abnormal state.
3 INSTALLATION WARNING: The acceptance and set up of the P4H medical laser device should be done with the assistance and guidance of our authorized technicians or agents. 3.1 Check the Appearance and Packing Items Platinum Series P4H is packed and inspected strictly at the factory. After you receive the product, please check the box for damage. After unpacking, please check the boxing items are complete according to the packing list.
Laser is designed to fit perfectly Remove the foam on the right to in the left portion of the foam. All access the accessories. accessories fit on the right. Installation Site and Platform Selection The Platinum Series P4H has an air cooling design system. The system consists of a closed loop, liquid filled, heat pipe thermal transfer system with fan and air assistance. Heat is transferred to the system and dissipated across a framework of fins where it is released to the ambient atmosphere.
Do not touch end of the Insert fiber into laser port and Insert the black cable into the fiber. Place immediately into screw it until fastened tight. finger switch by aligning red the laser port, and when dots. Push in and Do not removing twist. the fiber place screw cap back on without touching end. WARNING: In order to avoid dust contamination, do not touch the laser port and the handle port by hand when connecting the handle. Dust cap should be placed and stored on the chain of the fiber.
Insert the plastic protrusion Fiber and black cable inserted Insert interlock on the other into the handle fiber optic cap correctly. side of the laser. Attach the base to the laser. Insert fiber below coupler into fiber clip on pedestal of laser. This will secure the fiber. to prevent dust contamination. Complete view. Do not twist to tighten. Wrap fiber counterclockwise leaving enough slack to move Complete view with the hand piece in the cradle the hand piece to the cradle.
The hand piece connector is located directly above the device. Remove the handle and laser port dust cap before installing the handle. Gently insert the handle connector into the laser port and tighten it by turning the fastening nut clockwise. Remove the black protective cap and place into case. Select the treating head and screw it to the base of the hand piece. Insert fiber into laser port and screw it until fastened tight. Remove black protective cap and place into case.
Internal power supply: When using the internal power supply, the power switch can be turned directly to the ON position. When the battery power is less than 1%, the laser stops working, and users will be informed of the sound and light that they should charge the device. When connecting an external power supply, use the provided power adapter. WARNING: Only use the rechargeable battery specified by our company to supply power.
accessories neatly in edge of the cutout, and wind position. When putting fiber counterclockwise. away unscrew tips and place black cap back on hand piece. Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
4 PRODUCT SPECIFICATION 4.1 Technical Parameters Feature Platinum P4H Diode GaAlAs Laser Source 4 Number of Diode Housing Color Black 650nm±20nm, 810nm±10nm, 915nm±10nm, 980nm± Wavelength 10nm Average Energy Output (Don‟t turn on ISP in pulse mode） Average Energy Output (Turn on ISP in pulse mode） CW Power (W) 14 W ± 1.4 W 20W±2W 28W±2.8W Intense Super Pulse (ISP) Max Output power NOHD (*) 30W±3W 3.
Transmission System 600um Timer 0-3600s Fiber Quartz CW or chopped (0 – 20000 Hz) Emission 100 – 240V 50-60HZ Operating Voltage Closed loop, liquid filled, heat pipe thermal transfer system Cooling Method with fan/air assist. 1.2-0.5A Current 10.8V Operating Parameters User Interface 7-inch touch screen color display Laser Activation Finger switch, optional Foot pedal Laser Stop Yes Fiber Detection Yes Interlock Yes Input 100-240VAC, 50/60Hz Power Supply Output 18 VDC, 5.
Model Average Power 251 253 501 502 8S in CW and ISP 25mm tip* 25mm tip* 50mm tip 50mm tip 8mm tip (W) (W/cm2) (W/cm2) (W/cm ) (W/cm ) (W/cm ) 0.5 0.10 0.10 0.03 0.03 0.248 7 1.43 1.43 0.36 0.36 / 15 3.06 3.06 0.77 0.77 / 28 5.70 5.70 1.43 1.43 / 2 2 2 P4H * The laser device limits the 25mm tip to a maximum of 15W. * The laser device limits the 8mm tip to a maximum of 3W.
Avoid storing in explosive, corrosive gases, excessive dust or salt of the environment The battery may be stored within an environmental range of -100C to 450C for short term storage. Should the battery need to be stored for an extended period of time (over 3-months), provide battery with a full charge and the environmental condition shall be 23±50C and 65±20% RH. Battery shall be charged every three-months when in long term storage.
5 CONTENTS OF PLATINUM SERIES P4H laser NUMBER # ITEM DESCRIPTION 1 Diode Laser Therapeutic laser device 1 2 Hand Piece Treatment Hand Piece 1 25mm Open 4 25mm Curved Contact 3 Hand Piece Tips 50mm Curved Contact 50mm Broad Beam Open 4 Fiber Laser energy is transported through the Connects Power Supply to the Unit 5 DC Power Connector 1 fiber 1 Power supply - Input 100-240VAC, 50/60Hz Output 18 VDC, 5.
Component Description Platinum P4H is Black Side view showing hand piece in cradle and emergency shut off Hand piece in cradle and the zoom distal part Sinmpro external AC power adapter for all the models Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
Battery pack (included in the main unit) Protective goggle Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
6 SET‐UP INFORMATION 6.1 Platinum Series P4H Set-up Reference Contents and Accessories section of the Platinum Series P4H for identification of components and Installation section for pictured diagrams for assembly.
Turn power switch to the ON position User interface login system to enter 4-digit security PIN enter the main interface Enter 1111 for super administrative privileges i. Summus Medical Laser highly recommends changing the super administrative password to a unique 4-digit PIN applicable to your establishment. Entering a wrong security PIN will elicit a temporary “PIN error” message requiring the user to re-enter the correct secure PIN.
Navigate through the Home Interface settings for appropriate protocol selections. Administrative Settings The user can change the parameters for adding and removing users, volume, LCD brightness, language, date, time (standard or military), Wi-Fi connection, etc., for desired setting. Add New User Add, Edit or Remove User Adjust Volume, Brightness, Date, and Time Select Wi-Fi Settings Select Language Device Information Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
Device Information New Treatment The user can choose and program the parameters for initial treatment according to the needs of the patient. Select a Body Region: The user can choose between 5 body regions (Head, Spine, Upper Extremity, Torso and Lower Extremity) and Additional Treatments. Select a Body Part: The user can choose body parts for each body region previously chosen. Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
Select a Condition: The user can choose a general treatment or a specific condition to be treated for the body part previously chosen. Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
Customize Treatment by: The user can customize the treatment by the following variable. Body Type Skin Tone Pain Level Pain may be assessed by the numerical rating scale which is one of the most used pain scales in health care. The patient has the option to verbally rate their pain from 0 to 10. Zero indicates the absence of pain while ten represents the most intense pain possible. Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
Skin tone of the patient is based upon the Fitzpatrick scale. A recognized tool for dermatological assessment to skin pigmentation and how the skin responds to light. The scale is a numerical classification scheme for human skin color by six types. Type I indicates light skin color and Type IV indicates dark skin color. Thermal effects vary with skin pigmentation – darker absorbs more. If you get a withdrawal response, increase distance and/or move the beam more rapidly and/or reduce power.
Non-Contact Non-contact treatments are almost always done in a scanning mode. Scan 1-2 cm from the surface with slow passage (about 3 cm/second) over the affected area and 1-2 inches of surrounding healthy tissue. Used over an injured area or where any other inflamed condition may be present. Also used on very painful/sensitive areas. Again, it can be done in conjunction with stretching or ROM. Keep in mind your “Line of Drive”. Make sure the laser beam is being directed towards the target tissue.
Custom treatment List Note Delete ISP peak power is delivered only in pulsed mode. The laser delivers the following average power in pulse mode: Platinum P4H Max avg. output = 0.1 to 20 W ± 2 W Note The frequency in Continuous Wave (CW) is automatically converted into 0 Hz. The frequency in ISP modality is defined between 1–20000 Hz. Note A 25 mm tips diameter is is 2.5 cm and has a 1.25 cm radius. Its area is 4.9 cm2. A 50 mm tips diameter is 5.0 cm and has a 2.5 cm radius. Its area is 19.6 cm2.
Inflammation >5,000 Hz Average power remains constant during emission in CW or Pulse respectively. Refer to Recommended Treatment Protocol tables for light or dark skin below for average power. Recommended Treatment Protocol for Light Skin Fitzpatrick scale 0 through 3 Total Average Power Treatment Body Power, Density, time, part Watts Watts/cm2 seconds Cervical 7 0.36 360 2520 400 6.3 * Thoracic 8.5 0.43 420 3570 500 7.14 * Lumbar 12 0.61 420 5040 500 10.
Recommended Treatment Protocol for Dark Skin Fitzpatrick scale 4 through 10 Total Average Power Treatment Power, Density, time, part Watts Watts/cm2 seconds Cervical 3.5 0.18 720 2520 400 6.3 * Thoracic 4 0.20 840 3570 500 7.14 * Lumbar 6 0.31 840 5040 500 10.08 * Shoulder 4 0.20 720 2880 400 7.2 * Elbow 3 0.15 360 1080 200 5.4 * Forearm 2.5 0.13 480 1200 300 4 * Wrist 2 0.10 240 480 100 4.8 * Hand 2 0.10 180 360 100 3.
Treatment areas The shaded areas on the figures below indicate the area to be treated for the listed body parts in the recommended values table above. The shaded areas represent the proper area to treat, to deliver the proper laser dosage. Cervical Shoulder Thoracic Elbow Hip and Lumbar Knee Ankle Leg Foot Forearm Hand and Wrist Toe Finger Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
Acute injuries use shorter times and/or lower power (Lower Total Dosage/Joules). Some injuries may respond to a graduated treatment from lower to higher frequencies. Example: Start with CW then go to 20 Hertz followed by 500 Hertz followed by 2500-5000 Hertz. The protocols programmed into the Summus lasers will do this for you automatically. However, if the user wants to adjust the set protocols then following these guidelines would assist them in safely doing so.
gradually until acceptable patient comfort is maintained. Treatments every 3-4 weeks may be adequate for maintenance in many patients. Most patients will show at least a mild positive response in 1-2 treatments. If positive response is not noticed in 3-4 treatments, re-evaluate condition/treatment or protocol/diagnosis. If diagnosis is correct, you may need to increase dosage (Time and/or Power). Increase dosage by 25%-50% per treatment episode until a positive response is observed.
Press and release finger switch a second time stop the laser from emitting during treatment if needed. Laser emission will automatically stop at the end of the selected protocol treatment time. Performance Tracker The user can review the online Performance Tracker for usage history, treatments provided by day, treatments by body part, and revenue generation.
WARNING: Verify that the fiber optic assembly is not twisted when returning the hand piece to the cradle. Fiber may break if it is twisted or crimped. WARNING: Do not leave the system in an uncontrolled environment where the temperature or humidity is too low or too high. Environmental conditions too low or too high will affect the stability of laser output power. 6.
5 Date and time display found in customizations: Users can set the date and time in the settings interface.
due to misuse. 6.4 Emergency Troubleshooting When the device is powered on and operating, if there is abnormal function (such as no display, light abnormal, etc.), immediately press the emergency stop switch to stop the laser output. Identify and correct the cause prior to resuming use. Reference Alarm Function and Fault Diagnosis and Analysis sections. If necessary, please notify the dealer or the company for help.
7 Control Instruction for Use 7.1 Finger Switch Connect the connector of the finger switch cable to the device. Place the finger switch on the platform floor. Set up appropriate parameters according to patient needs. Apply pressure to enclosed finger switch with your foot. The yellow LED Indicator light glows to indicate that the finger switch is operating when pressure is applied on the pedal to emit laser. Insert the black cable into the Complete view.
MUST wear the appropriate laser goggles for protection of emitting diode lasers with an optical density (OD) of 7.0 or greater for the infrared (810, 915, 980nm) wavelengths and 2.0 or greater for the visible red (650nm) wavelength emitted by the Platinum Series P4H device. Class IV laser radiation is hazardous to the eye from the direct beam and diffuse reflections. Laser radiation also represents a significant skin and fire hazard.
8 ALARM FUNCTION DESCRIPTION 8.1 Alarm Type The system provides five alarm prompts, namely: High temperature alarm Remote interlock alarm Hand piece switch alarm Laser alarm Fiber alarm All of the above alarms are technical alarms. When the alarm occurs, the user should follow the appropriate safety precaution procedures defined in Alarm Function section according to the priority of the alarm to prevent personnel and device damage. 8.
8.3 Alarm Function The Platinum Series P4H Laser monitors the operating status of the system in real time. Sounds, indicators, and graphical warning signs alert the system to unusual events with different priorities while interrupting the laser outputting. Alarm Types High Temperature Alarm Triggering conditions 1.Laser temperature exceeds 45 °C 2. Fiber coupler temperature exceeds 60 ℃; 3.
8.4 Alarm System Detection The device will determine the alarm status. When the device detects an alarm, the system will emit a sound, the alarm red LED indicator will illuminate, and graphical warning signs will appear on the LCD screen. 8.5 Fault Diagnosis and Analysis WARNING: Do not use the device for treatment when the device is malfunctioning or in other abnormal conditions. Promptly follow in accordance with the instructions for troubleshooting and contact the company for after-sales advice.
2. Laser attenuation the instructions. 3. Contact the company for after-sales maintenance. 1.The coupler is damaged No power outputting 2. Optical fiber is damaged 3.Laser is damaged Contact the company for after-sales maintenance. 4. System failure WARNING: Users can perform general troubleshooting according to the above scenarios. If you cannot solve the problem, Do Not disassemble the device to check and contact the designated dealer or company for maintenance. Rev.
9 POST TREATMENT CLEANING Appropriate steps shall be taken by the operator between treatments of the laser device and components to ensure the distal parts coming into direct or indirect contact with the patient such as the applicator treating head/ hand piece tips receive a thorough cleaning process.
Clean the applicator treating head/ hand piece tips between uses with products that are commonly used to disinfect medical electrical equipment, e.g. high purity alcohol, lens paper and/or Caviwipes TM. Observe the directions for intended use provided by the manufacturers of these products. Do not overly saturate the area being cleaned and wipe off any excess liquid to prevent the liquid from penetrating the optical fiber. Allow the liquid to volatize before reattaching the tip to the hand piece.
10 MAINTENANCE WARNING: This product is a Class 4 laser product. During use and maintenance, do not look into the laser or direct beam to avoid irreversible damage to the eyes. It is strongly recommended that users carefully read the instructions to avoid injury to the patient and damage to the device caused by possible harmful laser radiation. 10.1 Daily Maintenance 1) Check the optical fiber before each treatment to ensure the fiber is not bent or broken.
6) Please contact the company or the designated dealer to repair and maintain the device when the power is reduced. Do not disassemble the device without guidance of Summus Medical Laser personnel or designated dealers to avoid injury to the patient and damage to the device caused by possible harmful laser radiation.
damage to the device from harmful laser radiation. We recommend that you have your P4H laser calibrated every 24 months. Contact the Summus Medical Laser Service Center to schedule the calibration. Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
11 WASTE DISPOSAL Medical equipment is considered for disposal because of its natural obsolescence and failure to meet current treatment standards, uneconomic or poor serviceability, lack of spare parts, etc. Fibers, batteries and other discarded items, should be disposed of in accordance with Waste Disposal Policies and local laws and regulations for processing. The end user has an obligation to ensure the safe and responsible disposition of the medical laser device and battery.
12 ELECTROMAGNETIC COMPATIBILITY Platinum Series P4HTM semiconductor laser treatment instrument is the basic performance of the laser output power accuracy. Note: 1) The purchaser or user of the P4H semiconductor laser treatment instrument should use the instrument in the electromagnetic environment specified in this section. Otherwise, the Platinum Series semiconductor laser treatment instrument may not work properly.
12.1 RF Transmitting Guidance and manufacturer's declaration - Electromagnetic emission The Therapy laser is intended for use in the electromagnetic environment specified below, and the purchaser or user shall ensure that it is used in such an electromagnetic environment. Emission Tests Compliance Electromagnetic environment - guidance RF Emissions Group 1 The Therapy laser uses RF energy only for its internal functions.
Power dips, interruption short and voltage variations on power supply input lines <5% U T for 0.5 cycles (On U T ,> 95% of the sag) The network power supply should Applicable EN 61000-4-11 have a typical commercial or hospital environmental quality. If the user needs to run continuously 40% U T during for 5 cycles power interruption, it is recommended that the Therapy (On U T , 60% of the sag) laser be powered by uninterruptible Applicable power supply.
Level Not Portable and mobile RF communication equipment shall not be Applicable used within the recommended distance (unit: m) of any part of The Therapy laser (including cable). The recommended separation distance is calculated using the equation for the frequency of the transmitter. Recommended Interval Distance 3.5 d P V1 150KHz ~80MHz 3.5 d P E1 Conduction RF 3V(Valid values) 3V/m 80 MHz ~800MHz 7 d P E1 150KHz~80MHz EN 61000-4-6 800MHz ~2.
semiconductor laser treatment instrument. b In the frequency range of 150KHz ~ 80MHz, the field strength should be less than [V1] V / m. 12.4 The Spacing Distance Between RF Communication Equipment and The Therapy laser Portable and mobile is the recommended distance between RF communication equipment And the Therapy laser The Therapy laser is intended to be used in radioactive radiation harassment in controlled electromagnetic environments.
13 SERVICE 13.1 Quality Commitment Summus Medical Laser guarantees the factory technical parameters of Platinum Series P4H semiconductor laser device is in line with the product standard requirements of the medical device, is regulatory approved, and provides a lifetime diode warranty and a 3-year manufacturer warranty. 1) To provide laser training and clinical guidance 2) To provide parts or machine spare parts 3) Product maintenance and technical advice 13.
14 FCC STATEMENT This equipment has been tested and found to comply with the limits for a Class A digital device requirement of 47 CFR, pursuant to Part 15 of the FCC Rules. The device contains 20 and 40 MHz signal band width. The device must be placed at a minimum separation distance of at least 20cm from all persons and must not be located or operating in conjunction with any other antenna or transmitter.
15 CONTACT INFORMATION If you have any difficulties in the use of your P4H therapy laser, or have any questions and suggestions, please visit www.summuslaser.com, call or write to us. Manufacturer: Summus Medical Laser, LLC 1185 West Main St. Franklin TN 37064 Tel: 866-595-7749 Fax: -261-3535 Email: service@summuslaser.
60878. No part of this publication may be reproduced, transmitted, stored or translated into any language, in any form or through any electronic, magnetic, optical, chemical, manual, physical device or other means, without written consent. Right reservation to correct or modify the present document without prior notice. Rev. 0 7/16/2020 Summus Medical Laser, LLC 1185 West Main St.
