Product information
of NEURAMIS Light (Lidocaine)
Basic information
Effect of procedure
Neuramis Light Lidocaine is intended for prolonged skin biorevitalization, correction of fine wrinkles, long-lasting renewal of skin hydrobalance and moisturizing the lips.
Correction of fine wrinkles
Moisturizing the lips
Applied Area
Forehead
Glabella line
Nose
Temples
Cheeks
Nasolabial fold
Neck
Decolletage
Recommended Treatment Policy
Needle : 2 needles 30G x 3/16"(4mm)
Injection depth : Mid layer of the dermis
Injection interval : 3-6months
Specifications
Type : Monophasic
Ingredients : Hyaluronic acid, Lidocaine
HA Composition : 20mg/mL
Lidocaine : 0.3%
Aesthetic effect : 6 - 12 months
Package : 1ml
Storage : 2-25
Features
Enhanced Safety
The origin of HA, microbial fermentation, and animal-free, ensures its safety. HA material with molecular weight, approved by EDQM and US FDA, is reliable and trustworthy.
Long-lasting effect
Neuramis's 2-step cross-linking process ensures long-lasting effect.
High satisfaction
Patients are satisfied with the natural results right after the treatment.
Description
High-quality Raw materials
Neuramis® is manufactured using a high-quality hyaluronic acid.
That is registered in the DMFs of the FDA and certified by the EDQM.
Hyaluronic Acid Raw Materials Managenment Standards
Ph. Eur
Neuramis
Residual protein
Maximum 0.3% or 0.1%
Maximum 0.1%
Endotoxin
< 0.5 or 0.05IU/mg
< 0.04IU/mg
Improved Refining Process with SHAPE technology
SHAPE(Stabilized Hyaluronic Acid and Purification Enhancement)technology is the exclusive technology of Neuramis®.
It stabilizes crosslinking and enhances the purification process.
Step1. Cross-linking with BDDE
Step2. Purification process
In-house quality-control
The general industry standard for the amount of residual BDDE is less than 2 ppm;
However, Medytox only sells products after complying with rigorous in-house quality-control standards which require products with a non-detectable level of BDDE.