Description
The SK-360-MAX is a professional multi-technology desktop workstation designed for cosmetic clinics and aesthetic practices. Combining High-Intensity Focused Ultrasound, 6.78MHz radiofrequency, and EMS microcurrent, the system delivers customizable energy to the epidermis, dermis, superficial musculoaponeurotic system (SMAS), and subcutaneous layers across facial, ocular, and body areas.
Specifications
- System Type: Desktop multi-handle beauty device
- Operating Handles: 15RS, 36RS, 18RS
- Display: 15.1-inch touch screen
- Total Power Consumption: 1180W
- Power Input: AC 100–240V, 50/60Hz (grounding required)
- Ultrasound Output Range: 0.1–3.0 (0.1 step adjustment)
- RF Frequency: 6.78MHz
- Pulse Repeat Time: 0.1–1.0 sec (0.1 sec step adjustment)
- Scan Length: 5–25mm (5mm step adjustment)
- Point Pitch: 0.1–2.0mm (0.1mm step adjustment)
- Standard Probes Included: 9 total (15RS: 1.5mm, 2.0mm, 3.0mm, 4.5mm; 36RS: 1.5mm, 3.0mm, 4.5mm; 18RS: 8.0mm, 13.0mm)
- Optional Probes Supported: 7 total (15RS: 6.0mm, 9.0mm, 13.0mm; 18RS: 6.0mm, 10.0mm, 16.0mm, 18.0mm)
- Probe Mechanism: Detachable consumable cartridges with integrated shot tracking
Application Scenarios and Contraindications
The system is designed for multi-layer aesthetic procedures. Typical applications include targeted skin tightening on the facial epidermis and dermis (1.5mm and 3.0mm probes), deep facial and submental contouring targeting the SMAS layer (4.5mm and 6.0mm probes), dedicated peri-orbital treatments (2.0mm eye probe), and localized body tightening across the arms, abdomen, thighs, and buttocks (8.0mm to 18.0mm probes). Operators can select between Stamp mode for precise spot treatment or Slide mode for continuous sweeping coverage on body zones.
This device must not be used on individuals who are pregnant, children, or anyone with implanted electronic devices, metal stents, or metallic implants in the treatment area. It is strictly contraindicated over open wounds, severe active acne, folliculitis, or systemic/localized skin diseases that impair tissue healing. It must never be applied directly over the eyeballs. Clients with bleeding disorders, cardiovascular disease, recent chemical peels, or keloid tendencies require professional clinical clearance prior to procedure consideration.
Frequently Asked Questions
Which cartridges are included in the standard configuration?
The standard system package includes 9 consumable cartridges: four cartridges for the 15RS handle (1.5mm, 2.0mm eye-dedicated, 3.0mm, and 4.5mm), three cartridges for the 36RS handle (1.5mm, 3.0mm, and 4.5mm), and two cartridges for the 18RS handle (8.0mm and 13.0mm abdominal probes).
How are the three handles operated during a procedure?
Energy delivery is activated differently depending on the handpiece: the 15RS handle utilizes a built-in handle trigger button; the 36RS handle operates via an external foot switch; and the 18RS body handle supports both handle button and foot switch triggering.
What contact medium is required for treatments?
Procedures must strictly be performed using bubble-free, water-soluble ultrasound gel applied thinly over the cartridge acoustic window and across the targeted skin zone. Using oils, unapproved lotions, or dry contact can cause acoustic reflection and damage the cartridge.
How do operators track cartridge lifespan?
Each treatment cartridge is a consumable component equipped with usage monitoring. The remaining shot count is detected and displayed directly on the 15.1-inch control screen, allowing the operator to replace cartridges when lines are depleted.
What post-treatment care is required following a session?
Post-care protocols require washing with lukewarm water at or below 35 degrees Celsius, avoiding saunas, heat exposure, facial massages, heavy cosmetics, and direct sun exposure for at least one week. Operators must advise clients to avoid laser, light, or other energy-based treatments on the treated zone for two to four weeks.
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