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Global Regenerative Trade

REMODEM
SUPERFICIAL SWELLING REDUCING GEL

REMODEM ANIMATION

Orthopedics, Sports medicine, Traumatology

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REMODEM ANIMATION

Plastic Surgery, Liposuction, Aesthetics

why us

Fast growing company

Engaged in developing

Innovative solution

INFORMATION

about the product

REMODEM IS USED 

TO REMOVE

 
swelling and bruises after rhinoplasty

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swelling after hair transplantation

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swelling after regional injections for an esthetic purpose

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swelling after orthopedic surgery
 

 

TO PREVENT

 

swelling during aesthetic injection

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swelling during rhinoplasty

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swelling during hair transplantation

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swelling during orthopedic surgery

GENERIC

IDENTIFICATION 

Remodem superficial swelling reducing gel is a medical device applied over the skin that supports reducing swelling area and water retention.
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Remodem superficial swelling reducing gel helps reduce swelling and discoloration that occur due to sprain, muscle strain, trauma and sports injury, aesthetic and plastic surgeries.

LIQUID MAGNET

 A new molecule called external inorganic gel liquid magnet has been developed using a combination of silica, calcium chloride, and tetrahydropiperine, which have a very high water holding capacity.

EASE OF APPLICATION

It is applied as a layer with a minimum thickness of 3mm to cover the entire edema area that occurs after tissue trauma. The area of application is covered with sterile bandage for twelve hours.

EXPANDING THE POROUS STRUCTURE

Cosmoperine, which is found in the gel, supports increasing the fluid permeability by expanding the porous structure of dermis and epidermis.

NOT ABSORBED BY THE SKIN

Having a high water holding capacity the external inorganic gel liquid magnet, which is not absorbed into the skin, binds the edema liquid under the skin to the molecular structure thanks to free cylanol groups and restrains it in to the gel complex.

THE EDEMA AREA BECOMES

NORMAL WITHIN 3 TO 5 DAYS

MECHANISM OF ACTION

 Silanol groups (Si-OH) are created by treating Silica (SiO2) in an alkali environment and bonding extra hydrophilic characteristics. Thus, the water retention properties of the product are increased, while the human skin cannot absorb it.

 It is known that hydrophobic molecules of lesser weight transit from the stratum corneum layer easily.

There is not certain findings related to transition to lower layer of epidermis and dermis. In addition to this, it is reported that the molecules heavier than 500 Da cannot transit from stratum corneum layer.

Based on the information, silica (which has a high water extraction feature) has no skin permeability. This is because its ionic structure is different than that of the skin. 

Therefore, silica will not be absorbed to the intradermal space, but the water retention properties allows silica to remove the extrafluid from the derma. 

ACTIVE MATERIAL

CALCIUM CHLORIDE

Calcium chloride is one of the most potent moisture absorbing compounds found in nature. As the second most commonly occurring substance in seawater next to salt, calcium chloride is also non-toxic and environmentally friendly. Calcium chloride is the active compound in Absortech products.

AEROPERL 300 Pharma

AEROPERL 300 Pharma is a granulated form of colloidal silicon dioxide. The spherical granules have a diameter of approximately 30 mm, giving the product a much higher tapped density of about 280 g/L compared to the non- granulated products. AEROPERL 300 Pharma can be used as an absorbent for liquid active pharmaceutical ingredients and as a moisture scavenger, e.g., in moisture activated dry granulation processes (MADG) as well as a high density and low dust glidant.

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THE VIVOSTAT® SYSTEM

The uniqueness of the Vivostat® system is a novel patented biotechnological process that enables reliable and reproducible preparation of autologous Fibrin Sealant or Platelet Rich Fibrin (PRF®) without using cryoprecipitation and without the need for a separate thrombin component.

THE FULLY AUTOMATED VIVOSTAT® SYSTEM CONSISTS OF THREE COMPONENTS:

  • The Processor Unit is a non-sterile, reusable, fully automated device that controls the biochemical process.
  • The Processor Unit is used to process the patient’s blood and prepare the Vivostat® Fibrin Sealant or Vivostat PRF® solution.
Vivostat Processor Product
  • The Processor Unit is operated by a single button and a display keeps the nurse informed of the remaining process time and status at all times. No specific installation is required and the large wheelbase makes moving it easy.
  • The Processor Unit can be located in any room or corridor in the operating department. It is most often placed centrally between the operating theatres. This way one Processor Unit can supply a number of operating theatres.
  • In approx.  25 min a concentrated fibrin sealant or PRF® solution is prepared from the patient’s whole blood.
  • The Applicator Unit is a non-sterile, reusable, fully automated device that controls the delivery of the Vivostat® Fibrin Sealant or Vivostat PRF®.
Vivostat Processor Product
  • The large display and integrated microprocessor automatically primes the Spraypen® and informs the surgeon of the remaining volume of fibrin sealant/PRF® throughout the entire process.
  • Different spray modes can be selected depending on the actual procedure or area to be covered. Like the Processor Unit it has a large wheelbase and can easily be moved if required.
  • The disposable set comprises of two parts: A Preparation Kit used to prepare the fibrin sealant or PRF® solution before surgery, and an Application Kit used to activate and apply the fibrin sealant/PRF® solution.

 

  • Preparation Kit
    The Preparation Kit contains the specially designed Preparation Unit – a sterile disposable device in which the patient’s blood is collected, the biochemical process carried out, and the fibrin sealant or PRF® solution harvested.

 

  • The Application Kit
    The Application Kit contains the Spraypen®1 and all other items required to prepare the system for the delivery of the fibrin sealant or PRF® solution. The Spraypen® is a sterile, disposable, hand held device which delivers the fibrin sealant or PRF® solution to the tissue. The revolutionary and patented design offers the surgeon unparalleled freedom in controlling the application unlike any other product on the market today.

 

1Besides the Spraypen®, the Vivostat® system offers different types of applicators, e.g. the Endoscopic Applicator. For a full list of application devices click here

1-2-3 Spray

Three easy steps to prepare Vivostat® Fibrin Sealant or Vivostat PRF®

1. Draw blood from the Patient

Fibrin Prep With Blood Inside

At the time of surgery or up to 24 hours before1, citrate (supplied with the kit) is added to the Preparation Unit. 120 ml of the patient’s own blood is then drawn into the same unit.

2. Process the patient’s blood

Vivostat Processor 800

The Preparation Unit is placed in the Processor Unit. At the touch of a button the process starts; after approx. 25 minutes, an autologous fibrin or PRF® solution is ready for use. No thrombin or bovine components are added to the blood at any time.

3. Load the Applicator Unit and spray

Vivostat Display Applicator

The Fibrin or PRF® solution is easily loaded into the Applicator Unit and applied to the surgical site using one of the unique application devices (e.g. the Spraypen). 1This depends on the type of kit being used. Always consult the “Instructions for Use” supplied with the kit to determine the correct preparation.

The following video illustrates how to prepare and apply autologous fibrin sealant.

Presentation DVD from Vivostat A/S on Vimeo.