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ZENTIA Special/Premium
  • ZENTIA Special/Premium
  • ZENTIA Special/Premium

ZENTIA Special/Premium

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Product Details
DescriptionZentia Cross-Linked Hyaluronic Acid

Performance: Hyaluronic acid is a high molecular substance composed of repeated disaccharides of N-acetyl glucosamin and glucuronic acid. Zentia has realized a stable gel through precision cross-linking technology. The stable stucture of hyaluronic acid gel fills the space, supports the structure, protects the cell, replenishes the volume of wrinkled skin and keeps it natural.

Safety: The active ingredient used in Zentia is non-animal. It is a human-adapted component, contains high-purity hyaluronic acid and naturally decomposed over time. Hyaluronic acid cross-linking gel can be corrected through hyaluronidase when a problem occurs. It is safe by providing the level of endotoxin and crosslinking agent below the detection limit through strict manufacturing process management.

Usability: Precisely designed handles and push rods keep the pressure at the time of injection evenly, enabling stable treatment. The monophasic structure is a regular and stable gel structure, and it is a specialized technology applied to Zentia that realizes natural volume and soft injection feeling.

Pain relief: Zentia contains Li docaine to improve pain-related discomfort during the treatment.

Product NameSPECIALPREMIUM
Injection SiteMid to deep dermisMid to deep dermis subcutaneous layer
HA Concentration24 mg / ml
Visco-elasticityMidHigh
Duration9-18 months12-24 months
Packaging unit27G*225G*2
Injection AreaNasolabial folds, forehead, marionette lines and face liftingFacial contouring, chin and chick augmentation
Syringe Volume1.1ml * 3syr
Li docaine0.3%
Shelf Life24 months
StorageStore in 2 – 25°C. Protect from direct sunlight and freezing

The durations are depends on age, lifestyle and the skill of a practitioner.

Cross-Linked Hyaluronic acid ZentiaHigh Quality Raw materials

Zentia is manufactured using 100% authentic high-quality hyaluronic acid, every Finished product complies with European Pharmacopoeia on the endotoxin level.

Test items – Endotoxin. Acceptance Criteria – Not more than 12.5 EU/ml. Results – Less than 0.5 EU/ml

High purification Process

10 steps only Zentia’s unique manufacturing technology enables high elasticity with lower amount of cross-linking agent and residual BDDE

Test items – BDDE. Acceptance Criteria –

Dermakor
South Korea

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Dermakor

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