Save B32 High&Low Molecule HA

$50.50

Save B32 High&Low Molecule HA Dermal Filler​​ is an FDA 510(k)-cleared and NMPA Class III-certified biphasic hyaluronic acid injectable. Combining 1200-1800 kDa high-MW HA for structural contouring with 80-120 kDa low-MW HA for epidermal hydration. With 99.2% pharmaceutical-grade purity and dual-layer volumizing effects, it’s clinically validated for zygomatic, nasal, and mandibular restoration.

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Description

Save B32 High&Low Molecule HA Dermal Filler

Precision Facial Contouring & Volumetric Restoration

Advanced Biphasic HA Technology

FDA 510(k)-cleared and NMPA Class III-certified dermal filler combining 1200-1800 kDa high-MW HA for structural support with 80-120 kDa low-MW HA for epidermal hydration. ISO 13485-certified Tri-Hyal™ crosslinking achieves 8-12% crosslinking density, clinically proven to enhance dermal elasticity by 35% with 12-18 month persistence. Pharmaceutical-grade purity (99.2%) exceeds ISO 19985-1:2020 standards.

Key Clinical Benefits

3D Volumizing System

Tri-layer support: Epidermal hydration, dermal elasticity, and deep structural foundation

Exceptional Purity

99.2% pharmaceutical-grade HA with endotoxin levels ≤0.05 EU/ml

Proven Longevity

12-18 month duration with BDDE residue ≤1ppm

Enhanced Resistance

40% reduction in hyaluronidase degradation vs conventional HA

Tri-Hyal™ Crosslinking Technology

Molecular Architecture

  • Covalent Bonding: Stable crosslinks (G’ value 350-450 Pa)
  • Hydrogen Bonding: Dynamic water-binding network
  • 3D Elastic Matrix: Crosslinking density 8-12%

Biomechanical Properties

  • Viscoelasticity optimized for contouring
  • 35% elasticity improvement (12-month data)
  • Low extrusion force through 27G needle

Certified Manufacturing

ISO 13485-certified production process with stringent quality control. FDA 510(k)-cleared and NMPA Class III-certified for medical use.

Packaging Specifications

Configuration

1.0ml/syringe × 10 syringes/box

Needle

27G½ thin-wall cannula (ISO 7864)

Sterility

Pre-filled glass syringes (USP Class VI)

Storage: 2-25°C protected from light

Shelf Life: 24 months unopened

Reconstitution: Use immediately after opening

Do Not Freeze

Clinical Protocol

Indications & Technique

Zygomatic Augmentation

Placement: Deep supraperiosteal

Volume: 0.3-0.5ml per side

Nasal Base Support

Placement: Periosteal anchoring

Volume: 0.2-0.4ml

Mandibular Contouring

Placement: Supraperiosteal plane

Volume: 0.4-0.8ml per angle

Optimal Treatment Protocol

Needle: 28mm cannula (27G½)

Depth: Supraperiosteal placement

Post-Tx: Avoid pressure × 72hr

Combination: RF microdroplet therapy

Follow-up: 2-4 week assessment

Important Safety Information

For use only by physicians certified in Class III medical device administration. Pre-treatment Doppler ultrasound mandatory for vascular mapping. Contraindicated in pregnancy, autoimmune disorders, and areas with vascular compromise. Results may vary based on tissue response and injection technique. BDDE crosslinker residue ≤1ppm.

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