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Monalisa Hard Dermal Filler

$28.90

Monalisa Hard Dermal Filler is a medical-grade hyaluronic acid injectable containing ​​24mg/ml cross-linked HA with 0.3% lidocaine​​. Clinically proven to deliver ​​89% improvement in glabellar lines​​ with ​​12-18 month longevity​​. Manufactured to ​​KGMP standards​​ with ​​<2% BDDE residues​​ for safe volumizing and contouring.

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Description

Monalisa Hard Dermal Filler

Precision Treatment for Medium-Deep Facial Wrinkles & Lip Enhancement

Professional Grade Filler

Medical-grade hyaluronic acid dermal filler containing 24mg/ml cross-linked HA with 0.3% lidocaine. Clinically proven to deliver 89% improvement in glabellar lines (Phase III trials) with longevity of 12-18 months. KGMP-certified formulation exceeds EU Medical Device Directive 93/42/EEC standards with <2% BDDE residues and <0.5 EU/ml endotoxins for enhanced safety profile.

Key Advantages

Optimal HA Density

24mg/ml concentration for superior volume restoration

Integrated Anesthetic

0.3% lidocaine for enhanced patient comfort

Precision Delivery

1.0ml syringe with 25G/27G needles

Extended Stability

24-month shelf life at 2-25°C

Core Technology

HyaluroLock™ Cross-Linking

Patented cross-linking technology achieves optimal G-prime value (450-550Pa) for:

  • Volume maintenance lasting 12+ months
  • Natural tissue integration
  • Minimal swelling propensity

ISO 13485 Certified | <2% BDDE residues | <0.5 EU/ml endotoxins

Medical Packaging

Packaging Details

  • Batch-tracked sterile packaging
  • Pre-filled 1.0ml precision syringe

Storage Requirements

  • 2-25°C temperature stability
  • 24-month shelf life

Clinical Protocol

Injection Technique

  • Subcutaneous injection method
  • 30°-45° needle angle insertion
  • Retrograde linear threading technique

Dosage Guidelines

  • Maximum 0.2ml per injection pass
  • 25G/27G needle selection
  • Staged treatment approach recommended

⚠️ Contraindication: Not for use during pregnancy

Medical Practice Notice

For licensed practitioners only. Not FDA-approved. Adverse event rate: 0.37% in clinical trials (temporary erythema/swelling possible). Genoss Co. certifies compliance with ISO 9001:2015 (QMS) and ISO 13485:2016 (Medical Devices). Results vary based on injection technique and patient physiology. Batch-specific data available upon request.

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