Liporase Dissolve Hyaluronic Acid Hyaluronidase Liporase Injection to Remove Filler

• Supply Type: OEM/ODM
• Usage Mode: For external use
• Suitable for: Adult
• Model NO.: Hyaluronidase
• Application: for Prevention
• Form: Powder
• Product Name: Liporase Hyaluronidase
• Use: Dissolves Hyaluronic Acid
• Other Type: 1500iu Powder
• Item: Butt Face Lift
• Item1: 150mg Powder
• Transport Package: Box
• Specification: 10vials/Box
• Origin: China
• Production Capacity: 100000

Product Description

Liporase Hyaluronidase 1500iu Dissolves Hyaluronic Acid

 

Product Description

LIPORASE is also used where dermal filler has been inadvertently placed causing occlusion of the blood supply - indicated by blanching of skin at injection site and/or changes in skin color and/or tenderness that does not go away.

KIT INCLUDES:

• 1 box of 10 vials LIPORASE - Each vial contains 1,500 I.U. of hyaluronidase (in dry powder form) 
• 30mL sterile mixing solution + draw-up syringes for reconstituting LIPORASE
• 30 medical-grade syringes/sharps 30 gauge for most comfortable treatment
• Instructions + Techniques for Successful Use of LIPORASE

What is Hyaluronidase? (active ingredient in LIPORASE)
Hyaluronidase is an enzyme that causes cross-linked hyaluronic acid to dissolve immediately. It is often referred to as a reversal agent for dermal fillers. When the enzyme is injected it dissolves the dermal filler around the injection site(s) immediately and continues to work for 48 hours. 

HOW TO USE:
The reconstitution/mixing methods commonly used by experts are as follows: 1500IU (1 vial LIPORASE) + 3ml sterile mixing solution (included in kit).

The amount of dissolving serum is usually a one to one ratio as compared to the amount of filler previously injected. For example, if the client wishes to remove 2mL of dermal filler, then 2mL of the LIPORASE mixture should be used in the treatment area.

- Expiration Date and Lot Number printed on packaging.

sodium hyaluronate acid, which derived from fermentation, and cross-linked with 1,4butyl glycol two glycidyl ether (BDDE) in alkaline conditions, after a series of neutralization, dialysis to generate this product. And this product is limited to be used in the national formally approved medical establishment and related professional doctor with  qualification, according to different parts of the organization, to choose different types of  cross-linked sodium hyaluronate gel and be in strict  accordance with the requirements of the package insert.

Characterics
1.Raw material is approved by American FDA and European EDQM
2.Non-animal suorce hyaluronic acid,no risk of allergy reaction.
3.Strong anti-degradation capacity&stability
4.Low toxicity& rare side effects
5. Best price and stable quality because produced in our own factory