Rejeunesse Deep HA Dermal Fillers
High-density cross-linked hyaluronic acid fillers with UPHEC™ purification technology, containing 24mg/ml medical-grade HA and 0.3% lidocaine for prolonged aesthetic correction (12-18 months duration)
Advanced Dermal Formulation Technology
Developed by Newmedic Co., Ltd (Seoul, KR), Rejeunesse utilizes SMART-Crosslinking™ technology achieving 92% BDDE elimination and endotoxin levels <0.05 EU/ml. The 3D matrix structure demonstrates 85% viscoelasticity retention at 12 months with particle size optimized for tissue integration (180-250μm). Clinically proven to maintain 94.7% HA integrity post-6 months in subcutaneous tissue.
Clinical Advantages
Superior Safety Profile
0.02% adverse reaction rate in 12,000 clinical cases (vs industry average 2.1%)
Precision Viscosity
G’ 350Pa optimal for mid-deep dermal placement with 0.68N extrusion force
Extended Duration
18-month persistence in 83% of patients (12-month follow-up study)
Pain Minimization
VAS score reduction of 78% with integrated anesthetic
Product Specifications
- Active Components: HA 24mg/ml + Lidocaine 0.3%
- Crosslinker: SMART-BDDE™ (residual <0.5ppm)
- Particle Size: 180-250μm monodisperse
- Viscosity: G’ 350Pa | G” 85Pa
- pH Level: 7.2±0.3
- Sterility: Gamma-irradiated 25kGy
Professional Protocols
- Needle: 27G×13mm (included)
- Injection Depth: Mid-deep dermis (2.5-4mm)
- Max Volume/Site: 0.2ml per linear thread
- Anesthesia: Not required (integrated lidocaine)
- Aftercare: Avoid pressure ×48hrs
- Storage: 2-25°C protected from light
Clinical Indications
Nasolabial Fold Correction
Recommended 0.8-1.2ml per side using linear threading technique. 94% patient satisfaction at 6 months.
Lip Enhancement
0.5-0.8ml per lip segment with 29G needle. Maintains 82% volume retention at 12 months.
Facial Contouring
Jawline augmentation: 2-3ml per side deposited supraperiosteally. CT scan shows 12-month persistence.
Medical Practitioner Notice
Important: Results may vary ±23% based on individual tissue response and injection technique. For use only by licensed practitioners with Level 3 aesthetic certification. Contraindicated in patients with autoimmune conditions or hypersensitivity to gram-positive bacterial proteins.
Proper aspiration technique must be employed to avoid vascular complications. Not for periocular or frontal region use. Report adverse events to local health authority and manufacturer. Batch-specific TSE/BSE certificates available upon request.
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