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Vitaran i PN 2% 1ml*1

$45.80

Vitaran I (BLUE) is a CE-certified medical-grade polynucleotide injectable containing 20mg/ml (2%) ultra-purified salmon DNA fragments. Clinically proven to increase collagen synthesis by 42% and elastin regeneration by 37%, this specialized treatment targets periorbital wrinkles while delivering anti-inflammatory benefits and combating free radical damage for revitalized under-eye skin.

Quantity discounts
QuantityDiscountPrice
5-9 3% $44.43
10-19 5% $43.51
20-Unlimited 8% $42.14
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Vitaran i PN 2% 1ml*1

VITARAN I represents cutting-edge biotechnology with 20mg/ml (2%) medical-grade Polynucleotides derived from ultra-purified salmon DNA. Clinically formulated to enhance dermal density by 28.3%* through fibroblast activation and collagen type I/III synthesis. This CE-certified solution delivers quantified bio-revitalization for periocular rejuvenation with anti-inflammatory benefits. (*Journal of Aesthetic Dermatology 2023)

Therapeutic Advantages

✓ Increases collagen synthesis by 42%*
✓ 37% elastin regeneration*
✓ Anti-inflammatory cytokine modulation
✓ Combats ROS free radical damage
✓ Bio-compatible with other injectables
✓ CE-marked safety certification

Molecular Technology

• 100% purified salmon DNA fragments
• Size-calibrated 500-1500bp polynucleotides
• ISO 13485 manufacturing process
• Triple-filtration sterilization protocol
• 0.22μm terminal filtration
• PCR-tested for biological safety

Clinical Packaging

▫️ 1 x 1ml sterile glass syringe
▫️ Polynucleotide sodium 20mg/ml (PN 2%)
▫️ 1 x sterile 34G ultra-fine needle
▫️ Batch-controlled manufacturing
▫️ Tamper-evident packaging
▫️ 24-month refrigerated stability

Application Protocol

① Cleanse with chlorhexidine solution
② Periorbital region injection (0.8-1.2ml)
④ 30G-34G needle, 2-3mm depth
⑤ Fanning technique: 0.05ml per point
⑥ Optimal interval: 3-4 weeks
⑦ Post-treatment cooling recommended
For certified practitioners only

MEDICAL DISCLAIMER:

For professional cosmetic use by qualified practitioners only. Individual treatment results vary based on skin condition, biological response, and technique. Not recommended during pregnancy or with active infections. Full medical history must be assessed prior to treatment. Clinical studies demonstrate 89% patient satisfaction at 3-month follow-up (Dermatologic Surgery, 2024).

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