Effect of procedure
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Neuramis Volume Lidocaine is intended to fill the volume of regions on the face. It is appropriate for filling in medium-deep, deep skin folds and facial contouring.
Cheek and chin augmentation
Contours of the face
Applied Area
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• Cheek
• Chin
• Nose
• Forehead
• Nasolabial folds
• Marionette lines
• Lips
Recommended Treatment Policy
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• Needle : 27g x 1/2"(13mm) UTW (Ultra thin wall needle)
• Injection depth : Mid - Deep dermis
• Injection interval : 3-6months
Specifications
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• Type : Monophasic
• Ingredients : Hyaluronic acid, Lidocaine
• HA Composition : 20mg/mL
• Lidocaine : 0.3%
• Aesthetic effect : 6-12 months
• Packaging : 1 x 1ml
• Storage : 2-25℃
Features
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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
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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.
BDDE Standard solution
Neuramis series
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