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Save B32 High&Low Molecule HA
Save B32 combines 1200-1800 kDa high-MW HA for structural support and 80-120 kDa low-MW HA for epidermal hydration. ISO 13485-certified Tri-Hyal™ crosslinking technology achieves 8-12% crosslinking density, clinically proven to enhance elasticity by 35% with 12-18 month duration. FDA 510(k)-cleared and NMPA Class III-certified for precision facial contouring and volumetric restoration.
$50.50
Quantity discounts
| Quantity | Discount | Price |
|---|---|---|
| 5-9 | 4% | $48.48 |
| 10-19 | 8% | $46.46 |
| 20-Unlimited | 10% | $45.45 |
Save B32 High&Low Molecule Hyaluronic Acid Dermal Filler
Save B32 utilizes advanced biphasic HA technology combining 1200-1800 kDa high-molecular-weight HA for structural support and 80-120 kDa low-molecular-weight HA for epidermal hydration. ISO 13485-certified manufacturing ensures dual-phase crosslinking (8%-12% crosslinking degree) with 35% proven dermal elasticity improvement (12-month follow-up data). Clinically validated for facial volumetric restoration and contour refinement according to NMPA Class III standards.
3D Volumizing
Tri-layer support system: Epidermal hydration (low-MW HA), dermal elasticity (mid-MW HA), and structural foundation (high-MW HA).
High Purity
99.2% pharmaceutical-grade HA with endotoxin levels ≤0.05 EU/ml (exceeds ISO 19985-1:2020 standards).
Longevity
BDDE crosslinker residue ≤1ppm, maintaining structural integrity for 12-18 months post-injection.
Tri-Hyal™ Crosslinking Technology
- Covalent Bonding: Stable crosslinks between HA chains (G’ value 350-450 Pa)
- Hydrogen Bonding: Dynamic water-binding network for enhanced viscoelasticity
- 3D Elastic Matrix: Resistance to enzymatic degradation (hyaluronidase activity reduced by 40% vs conventional HA)
Packaging Specifications
Configuration: 1.0ml/syringe × 10 syringes/box
Needle: 27G½ thin-wall cannula (ISO 7864 compliant)
Sterility: Pre-filled, single-use glass syringes (USP Class VI certified)
Storage: 2-25°C protected from light. Do not freeze.
Shelf Life: 24 months unopened. Use immediately after reconstitution.
Clinical Protocol
Indications
Zygomatic prominence, nasal base augmentation, mandibular angle refinement
Injection Technique
Deep supraperiosteal placement using 28mm cannula (0.2-0.5ml per site)
Post-Treatment
Avoid pressure for 72 hours. Combine with RF microdroplet therapy for enhanced retention.
Important Safety Information
For use only by physicians certified in Class III medical device administration. Results may vary depending on individual tissue response and injection technique.
Contraindicated in pregnancy, autoimmune disorders, and vascular compromise areas. Pre-treatment Doppler ultrasound mandatory for vascular mapping.
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