Neuramis Volume Lidocaine(1 needle)

$27.00

Neuramis Volume Lidocaine Dermal Filler​​ Professional-grade HA filler (20mg/ml + 0.3% lidocaine) utilizing SHAPE technology. Features high elasticity (G’≥200 Pa) for natural facial contouring with 6-9 month longevity. Offers 99.9% HA purity and ultra-low BDDE residue (<0.4 ppm) for safe volume restoration in cheeks, lips, and chin.

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Description

Neuramis Volume Lidocaine Dermal Filler

Advanced Facial Contouring with Integrated Anesthesia

Professional-Grade Facial Rejuvenation

Neuramis Volume Lidocaine is a premium hyaluronic acid dermal filler (20mg/ml HA + 0.3% lidocaine) utilizing proprietary SHAPE™ technology. Featuring high elasticity (G’≥200 Pa) for natural volume restoration, it delivers lasting results for 6-9 months with ultra-low BDDE residue (<0.4 ppm). Clinically proven for mid-to-deep wrinkle correction and ISO 13485 certified for safety in facial contouring applications.

Key Clinical Benefits

Natural Volume Restoration

Optimal gel elasticity (G’≥200 Pa) ensures natural-looking facial augmentation with seamless tissue integration

Extended Duration

High cross-linking density provides clinical results lasting 6-9 months post-treatment

Pain Reduction

Integrated 0.3% lidocaine significantly minimizes discomfort during injection (pH 6.7-7.3)

Safety Assurance

99.9% HA purity with undetectable BDDE residue (<0.4 ppm) ensures biocompatibility

SHAPE™ Technology

  • Advanced Cross-linking: Optimized HA network for enhanced longevity and structural integrity
  • Elasticity Profile: High G’ value (≥200 Pa) ensures shape retention and projection capacity
  • Purity Standards: Manufacturing process delivers 99.9% HA purity with minimal chemical residuals
  • Lidocaine Integration: Stabilized anesthetic maintains pH balance (6.7-7.3) during administration

Packaging Specifications

  • Active Ingredients: Hyaluronic Acid 20 mg/ml, Lidocaine HCl 3 mg/ml
  • Needle: 27G × ½” (0.4 × 13mm)
  • Storage: 2-25°C protected from light. Do not freeze
  • Shelf Life: 24 months from manufacturing date
  • Manufacturer: Medytox Inc., Ochang, South Korea (KFDA Approved)

Professional Administration Protocol

Indications

  • Nasolabial folds correction
  • Cheek augmentation/restoration
  • Lip volumization & border definition
  • Marionette lines improvement
  • Chin enhancement

Technique

  • Subcutaneous to deep dermal injection
  • Apply even pressure (0.1 ml/10s flow rate)
  • Maintain strict aseptic protocol
  • Use linear threading or fan technique

Post-Treatment

  • Apply cold compress immediately
  • Avoid vigorous massage (48 hours)
  • Minimize sun exposure (72 hours)
  • Schedule follow-up at 2 weeks

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Important Clinical Notice

For professional use only. Requires medical licensure and dermal filler administration training. Contraindicated in pregnancy, breastfeeding, or patients with autoimmune disorders. Individual results vary based on skin type and injection technique. Medytox bears no responsibility for adverse events arising from off-label use or improper storage/handling.

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