Plejuv 365 mg - next generation PLLA inducer
Plejuv 365 mg - next generation PLLA inducer

Plejuv 365 mg - next generation PLLA inducer

In Stock
zł690.00
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The lowest price of the product zł469.00 in day 07.01.2026

Plejuv is a sterile, biocompatible, and biodegradable Class III medical device in the form of a powder for injectable suspension. The preparation is based on Poly-L-Lactic Acid (PLLA), a synthetic polymer from the alpha-hydroxy acid group. The mechanism of action is based on inducing a controlled tissue response, leading to neocollagenesis (the stimulation of endogenous collagen production).

 

indications and intended use

The device is intended for use in adult patients for:

  • correction of deep wrinkles and furrows

  • restoration of soft tissue volume in cases of lipoatrophy (loss of adipose tissue)

  • improvement of skin density and structure through the stimulation of collagen biosynthesis

  • contouring of facial areas requiring structural support

treatment areas

  • face (cheeks, temples, jawline)

  • neck and décolletage

  • note: Do not use in the red border of the lips or in the immediate vicinity of the eyes

mechanism of action

Upon implantation into the deep layers of the dermis or subcutaneous tissue, PLLA particles act as a mechanical scaffold. This process induces a physiological defense response from the body, stimulating fibroblasts to produce new collagen fibers. The volume-increasing effect develops gradually over time. Clinical results are dependent on the regenerative capacity of the patient's organism.

composition

(Per 365 mg vial)

  • Poly-L-Lactic Acid (PLLA): 150 mg (active stimulating ingredient)

  • Sodium Carboxymethylcellulose: 90 mg (suspending agent)

  • Mannitol: 125 mg (isotonizing and stabilizing agent)

administration protocol

The number of treatment sessions is determined by the physician based on an individual assessment of the patient's skin condition. The standard protocol typically involves 2 to 3 treatments at intervals recommended by the manufacturer. The product requires proper preparation (reconstitution) before administration, in accordance with the Instructions for Use (IFU).

contents

  • 1 glass vial containing 365 mg of lyophilized powder

 

med

VIAL

Info

The product may only be used by professionals.

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