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Revitrane Filler 20 mg/ml

$36.50

REVITRANE HA10 Volume Filler​​ is a KMFDS-certified dermal filler (No. KMFDS-2023-14572) containing 20mg/ml medical-grade cross-linked hyaluronic acid. Featuring ≤2ppm BDDE residue and 93.4% viscosity retention, this lip-enhancing formulation delivers ≤12 month results through ISO-13485 manufacturing. Advanced cohesive matrix technology ensures natural volumizing with minimal migration risk when administered by professionals.

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Description

REVITRANE HA10 Volume Filler

Professional-Grade Lip Enhancement Solution

Advanced Dermal Filler

KMFDS-certified dermal filler (No. KMFDS-2023-14572) with 20mg/ml medical-grade hyaluronic acid. Features G50/G60 cross-linking technology with ≤2 ppm BDDE residue and 93.4% viscosity retention. Delivers ≤12 months duration using 27G/30G needles. Manufactured under ISO-13485 standards with 85% cohesion index to prevent migration.

Core Advantages

High Purity Formula

≤2 ppm BDDE residue
Nano-filtration technology

Optimal Performance

93.4% viscosity retention
350-450Pa G’-value

Longevity & Safety

≤12 months duration
ISO-13485 certified

Enhanced Stability

24-month shelf life
200-500μm particle size

Advanced Technologies

3D Matrix Cross-linking

Optimized G’-value (350-450Pa) for natural volumizing

Cohesive Polydensified Matrix

85% cohesion index prevents migration

Hybrid Particle Technology

200-500μm particles for layered correction

Nano-Filtration System

BDDE residue reduced to pharmacopeia standards

Packaging Specifications

Product Type

Revitrane HA10 Volume Filler

Concentration

20 mg/ml cross-linked HA

Needle Gauge

27G & 30G sterile needles

Unit Size

1 ml pre-filled syringe

Professional Application Protocol

  • Pre-treatment: Cleanse with chlorhexidine (0.05%) solution
  • Injection Depth: 2-4mm (epidermal layer)
  • Pressure Control: Maintain ≤0.3N injection pressure
  • Post-treatment: Apply 4°C cooling for 10 minutes
  • Follow-up: Assessment at 14-day intervals
  • Volume: 0.5-1ml per treatment area (adjust for anatomy)

Clinical Notice

KMFDS-certified (No. KMFDS-2023-14572). Contraindications: pregnancy, autoimmune disorders, active skin infections. Results may vary ±15% based on metabolic rate (2.3-4.2μL/h HA absorption). For professional use only. Not for self-administration. Storage: 2-25°C. BR Pharm manufacturing certification applies.

Additional information
ProType

Classic

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