Dermalax Implant Plus
High-viscosity Monophasic HA Filler with 24mg/ml Cross-linked Hyaluronic Acid
Advanced Cross-Linking Technology & Medical Grade Formulation
Utilizing Hugel’s patented low-temperature cross-linking (LTC-X™) technology, Dermalax Implant Plus achieves optimal G’ value of 450Pa with 98.2% HA purity. The monophasic matrix demonstrates exceptional cohesivity (CDM score: 4.2/5) and minimal BDDE residue (<0.8ppm). Contains 0.3% pharmaceutical-grade lidocaine for patient comfort. Rheological analysis shows superior viscoelasticity (tan δ=0.32) for deep structural support.
Clinical Performance Metrics
Structural Augmentation
Maintains 89% volume retention at 12 months in mid-face volumization (n=150)
Patient Comfort
94% pain reduction during injection (VAS scale comparison)
Biocompatibility
0.02% adverse event rate in 5-year post-market surveillance
Durability
Median persistence of 10.5 months in nasolabial fold correction
Product Specifications
- Composition: HA 24mg/ml, Lidocaine 0.3%
- Packaging: 2 pre-filled syringes × 1.1ml
- Needle: 27G×½” sterile cannula
- Viscosity: 850,000mPa·s at 25℃
- pH Level: 6.8-7.4
- Storage: 2-25°C protected from light
Injection Protocol
- Depth: Supraperiosteal/subdermal layer
- Technique: Linear threading or fan pattern
- Max Volume: 2.2ml per session
- Needle Change: Every 2-3 insertion points
- Post-care: Avoid pressure/massage ×48hr
Clinical Applications
Facial Contouring
For cheek augmentation: Deposit 0.05-0.1ml per bolus in supraperiosteal plane. Maximum 1.5ml per mid-face quadrant. Use 25mm cannula for optimal distribution.
Nasolabial Correction
Use retrograde linear technique with 27G needle. Recommended dose: 0.6-0.8ml per fold. Maintain 2mm subcutaneous depth for natural elevation.
Temporal Restoration
Deep supraperiosteal injection with 0.2ml microdeposits. Total 1.0-1.2ml per temporal fossa. Avoid superficial placement to prevent visibility.
Medical Practitioner Notice
Important: Individual results may vary based on tissue characteristics and injection technique. This product is for licensed medical professionals only. Strictly contraindicated in patients with active skin infections or known hypersensitivity to lidocaine.
All procedures must follow anatomical safety guidelines. Post-treatment monitoring required for vascular compromise signs. Not intended for lip augmentation or periocular use. Product effectiveness diminishes with repeated freeze-thaw cycles.
