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General| Electrical | 100-240 VAC, 50/60 Hz |
|---|---|
| Operating Modes | Continuous, Pulsed |
| Aiming Beam | Red Diode Laser |
| Display | Touchscreen LCD |
| Presets | Yes |
| Cooling | Air-cooled |
Defines manual terms, general laser safety requirements, and LTCA specifications.
Warns against operating in areas with flammable materials due to ignition risk.
Details key safety mechanisms including Emergency Stop, Password, Interlocks, and Indicators.
Covers unattended protection, energy monitoring, and mandatory laser eye protection.
Details location requirements and guides through unpacking and initial system setup.
Explains how to charge the battery, charge time, and battery status indicators.
Provides step-by-step instructions for removing and replacing the device battery.
Guides users on how to connect and disconnect the fiber optic cable and hand piece.
Lists therapeutic applications and patient conditions where the laser should not be used.
Defines MPE and specifies ocular and skin exposure limits for laser radiation.
Illustrates and labels the components of the laser console and its parts.
Describes the hand piece, fiber, and finger switch control for laser emission.
Details treatment heads, their specifications, and how to manage the fiber optic cable.
Reinforces mandatory eyewear use and advises on the correct power cord.
Lists critical safety rules for operation and steps for preparing the patient and area.
Guides through powering on, navigating menus, and adjusting basic system settings.
Describes how to change system language and select treatment protocols based on patient characteristics.
Details adjusting treatment parameters and initiating laser emission.
Covers pigment considerations, dose application, treatment expectations, and technique.
Outlines general cleaning precautions and steps for cleaning the console and treatment heads.
Offers solutions for common problems to resolve without contacting customer care.
Describes how to perform a calibration check using certified equipment.
States compliance with ISO standards and details device classification per FDA and IEC.
Presents product identification, manufacturer, and authorized representative details for EU conformity.
Lists detailed technical specifications, including dimensions, weight, and optical parameters.
Presents test results for EMC compliance, detailing emissions and immunity tests.
States compliance with FCC and Canadian ISED regulations for radio frequency devices.
Explains common symbols used on the device and in the manual for identification and warnings.
Details the information presented on the medical laser label, including warnings and product details.
Describes warranty seal, additional warnings, and unique device identification (UDI) labels.
Provides information on how to contact customer care for assistance and required details.
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