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[HIFU] Shurink Universe with no wifi authentification version

[HIFU] Shurink Universe with no wifi authentification version

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LinearFirm Product Detailed Description

  • Product Name: SHURINK Universe
  • Manufacturer: CLASSYS Inc.
  • Device Type: Non-invasive focused ultrasound (HIFU) stimulation system for skin tightening and lifting
  • Principle of Operation: Utilizes ultrasound energy generated by a transducer with piezoelectric ceramics; electrical energy converts to ultrasound, focused at specific skin depths via geometric curvature, creating thermal coagulation points (TCP) that induce collagen regeneration for improved elasticity and wrinkle reduction
  • Key Modes:
    • MP Mode: Enables dense, uniform TCP generation without gaps, allowing treatments twice as fast as standard mode
    • Standard (Dot) Mode: Supports bidirectional treatment for reduced procedure time
  • Cartridges:
    • Ultra F Cartridges: Available for face at depths of 1.5 mm, 2.0 mm, 3.0 mm, 4.5 mm; tailored for specific concerns by treatment area
    • Ultra Booster Cartridges: Available at depths of 1.5 mm, 3.0 mm, 4.5 mm; designed for detailed and seamless treatments
  • User Features:
    • Intuitive GUI for easy operation
    • Lightweight handpiece for improved handling
    • Thin cartridges for better visibility during procedures
  • Benefits:
    • Promotes collagen regeneration through thermal coagulation, enhancing skin elasticity and reducing wrinkles
    • Customizable treatments based on patient needs with dual modes
    • Faster treatment speeds for efficiency, especially in MP mode and bidirectional operations
  • Target Applications: Primarily for eyebrow lifting by coagulating tissue; suitable for non-invasive skin lifting and tightening
  • Technical Specifications:
    • Rated Voltage/Frequency: 100~240VAC, 50/60Hz
    • Power Consumption: 400VA
    • Dimensions: 570 x 630 x 1330 mm (W x D x H)
    • Weight: 37 kg
    • Display: 10.4-inch LCD touch screen
  • Regulatory Details: Classified as a medical device (Product Approval No. 21-831); users must follow precautions and instructions for use

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