Collimated Ultrasound Maximum application time: 30 [min] - 1 to 30 [min] - 1[min] increments; • Ultrasound Frequency 3 MHz ±15%; • Maximum power [57 W] ±20%; • Flat or collimated beam; • 19 [cm2] beam input area; • Maximum input intensity 3 [W/cm2] ±30% - 0.1 [W/cm2] increments; • BNR (Beam Nonuniformity Ratio): Nd; • ERA (Effective Radiation Area): 19 [cm2] ±10%; • CONTINUOUS and PULSED mode; • Pulse frequency: 16 [Hz], 48 [Hz] or 100 [Hz]; • Duty cycle for PULSED mode: 5 [%], 10 [%], 20 [%] and 50[%]; • Pulse duration: 100 [Hz] (0.5 / 1.0 / 2.0 / 5) [ms]; 48 [Hz] (1.0 / 2.1/4.2 / 10.4) [ms]; 16 [Hz] (3.1 / 6.2/12.5 / 31.2) [ms]; • Pulse Repetition Period: 100 [Hz] 10 [ms]; 48 [Hz] 21 [ms]; 16 [Hz] 62.5 [ms]

1. Hygienization: Apply the body scrub to the site to be treated. Exfoliate for 3 minutes each side. Remove all the exfoliator with a moistened towel. Hygienization: Skin hygienization must be performed before any procedure, using products specific to the skin type of each patient. 2. Application of Ultrasound Select the program for cellulite. Insert the measurements found with the adipometer and the size of the area to be treated. Apply gel to the treatment area and start ultrasound application. The power and time of the ultrasound will vary according to the parameters informed (Velox Formula) Contact gel with active ingredients can be used. After the end of the treatment time, automatically the lymphatic drainage function will be activated with the same treatment time as the ultrasound. Drainage should be performed by moving the transducer towards the lymphatic vessels. 3. Finalize the procedure with the application of specific cosmetics for the treatment of cellulite.

The Velox Cavitational Ultrasound Machine contraindicated the use of any of the technologies of the ultrasound equipment referred to in this manual, in some specific regions, pathologies or conditions listed: pregnancy, infectious processes and/or acute allergic reactions, on regions with signs of vascular changes such as deep vein thrombosis and phlebitis, on the face, reproductive organs, eyes, ears and cardiac region, on malignant and/or pre-cancerous lesions, on epiphyseal plaques and bone prominences, on 63 hypoesthetic areas, on patients with diabetes mellitus, on patients under the age of 18, on regions with altered sensitivity, on regions treated by procedures such as abrasive or acid peels or skin lesions. These factors may increase the chances of chemical burns in procedures with combination therapies, in patients with metabolic or liver diseases that compromise the metabolism of fats, in patients with metal implants in the region to be treated, in chronic renal patients, in patients using corticosteroids and anticoagulants, in patients with cardiac pacemakers or other cardiac disorders, in patients with osteomyelitis and idiopathic pain, in patients with erysipelas, in patients with tuberculosis. NOTE: In addition, the use of Focused Ultrasound in patients with an adipose layer less than 2.0 cm (two centimeters) thick is contraindicated.Technical

Electrical Features: Network Voltage Range: 120 - 220 VAC, Power Frequency: 50-60 Hz, 2 x 2.5 A Fuse; Average Consumption Power: 200W; Maximum Peak Power: 300VA. Maximum ambient operating temperature: 35oC CLASS I equipment – Requires protective grounding circuit. Other electrical requirements: Power cable (with 2 pins + T) used for connection to alternating voltage mains. Equipment with applied part of type BF. IP20: Equipment not protected against harmful penetration of water and dust. Operation mode: Continuous operation; Equipment not suitable for use in the presence of a flammable anesthetic mixture with air, O2 or N2O. • Pollution Degree: II. Overvoltage Category II.

number 10411520024

Velox Cavitation Ultrasound Machine offers 2-year warranty