The collagen preparation, which is applied during the GUNAPHORESIS procedure, is a class III medical device containing tropocollagen type I and active ingredients that support cellular metabolism.
The device used during the GUNAPHORESIS treatment increases the permeability of cell membranes and intensifies the action of the sodium-potassium pump, allowing the transport of molecules into the dermis and lower tissues.
Once it enters the cellular matrix, tropocollagen type I immediately strengthens and remodels tissue biorestructures. In addition, its increased concentration stimulates the process of neosynthesis of the body's own collagen fibers. As a result, the treatment leads to the stimulation of autologous mechanisms of repair and remodeling of damaged tissues.
Both before and immediately after undergoing GUNAPHORESIS collagen therapy, the patient can freely use the sauna, swimming pool or balneotherapy. The product has no interaction with other therapeutic substances, moreover, it has clinically proven efficacy and good tolerance. The treatment is non-injectable, non-invasive and painless.
Contraindications to GUNAPHORESIS collagen therapy:
The device used during the treatment produces an extremely low-frequency magnetic field that poses no danger to the patient or the operator. Magnetophoresis treatments are not indicated for pregnant women, for patients who have a pacemaker, or who have dental implants of a very old type, made of magnetic iron.
