Product Description

HyaRegen is an anti-adhesion material widely used in pelvic cavity and abdominal cavity. It uses sodium hyaluronate as raw material and is prepared by the exclusive technology of the company. According to the data of secondary laparoscopy results of several clinical projects of China and Europe, HyaRegen can significantly and effectively prevent pelvic and abdominal adhesion, thus reducing the complications such as pain, intestinal obstruction and infertility. 

HyaRegen has now obtained the CE certification, and sales in more than 10 countries in the EU.

1) Adequate viscosity and hydrophilic property: creation of moist enviroment facilitating scar free tissue regeneration.

2) Controlled degradation profile: physical barrier during the tissue healing critical period to prevent adhesion and scar formation 

3) Terminal sterilization: maximized safety after application.

4) Degradable and completely bioresorbable: avoid secondary damage to the regenerated tissue.

5) Easy to use: no mixing requred, flexible delivery cannula to facilitate aplication and to reach the desired location.

6) Non-animal-sourced hyaluronic acid raw material used for production: avoid potential reactions to xenogeneic proteins.

Instruction For Use

1) Open the protection bax and pull the product out.

2) Follow the indication, peel-open the blister tray, remove the HyaRegen Gel syringe and place on sterile field.

3) Remove the tip cap from the syringe; attach a large-bore sterile delivery cannula with a standard luer lock.

4) Upon completion of the prcedures in the abdominal or the pelvic cavity, simply instill the HyaRegen Gel into the cavity via the delivery cannula to completely cover the surface of the organs.

5) In order to achieve the best adhesion prevention results, the gel should not only applied to the organs that are operated on but organs away from the surgical area should be also covered as much as possible.

6) The maimum volume of HyaRegen Gel used for one patient is  upto 2.0ml per kg of bodyweight.

7) Upon completion of the gel application, withdraw the catheter. Do not lavis the cavity.