Fi-VISION MAC – Biotechnological Supplement Clone

150,00

Innovative technology for neuroprotection and retinaprotection through electromagnetic induction.

INNOVATIVE
Wearable electromagnetic inductor, stimulated by body heat.

ADJUVANT
It can be used alongside traditional therapies in degenerative diseases (Glaucoma, Maculopathy).

SPECIFIC
The electromagnetic signals, appropriately set, induce biological effects on specific targets (FI VISION GL specific for GLAUCOMA, FIVISION MAC specific for MACULOPATHY).

NON-INVASIVE
Thin disc 26mm in diameter, applied to the skin with a transparent adhesive plaster.

EFFECTIVE
It induces a reduction of oxidative stress in vitro and promotes a positive reduction of functional parameters at the retinal level.

WELL TOLERATED
Applied to more than 500 patients in 3 years, with good satisfaction and compliance.

FREE FROM KNOWN SIDE EFFECTS

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Description

Fi-VISION MAC

Designed for patients with macular degeneration (AMD – Age-Related Macular Degeneration)

 

MACULOPATHY

It is a degenerative disease that affects the macula, the region of the retina responsible for clear vision, and can lead to serious visual impairment.

Patients with a family history of macular degeneration should undergo regular check-ups and tests, including electrophysiology tests (M-ERG*, F-ERG*): discovering the disease in its early stages has a significant impact on its prognosis. In case of altered results, the use of FI-VISION MAC.

 

WHAT IS IT?

The device (DM) is presented as a thin disk of 26 mm in diameter. It is packaged together with the relative instructions for use and two Tegaderm Film 4.4×4.4cm patches, necessary for its application on the skin. The DM is composed of a support in Polyethylene terephthalate (Mylar) on which an amalgam is layered containing, as main elements, micronized aluminum and fluorescent nanocrystals of graphene called Quantum Dots. The device, in contact with the skin, by potential difference, sends the patient very weak electromagnetic signals capable of inducing biological effects, in particular: reduction of oxidative stress and stabilization of functional parameters at the level of the retina. The DM is registered as a Class I Medical Device, with CE certification according to regulation (EU) 2017/745.

Example of DM application on the wrist.

Please note! The choice of application point is at the discretion of the patient.

 

HOW TO USE

1. The DM is applied to the skin, so that the logo is visible and the satin side is in contact with the skin.

2. The DM is then fixed to the skin with the transparent Tegaderm Film adhesive, supplied in the package: the application points are chosen at the patient's discretion.

3. For best results, it is recommended to keep the DM applied for a period of 30 days.

4. During the period of use of DM, especially during the first week, it is recommended to maintain high levels of hydration.

 

FINAL NOTES

1. DM causes no known side effects;

2. It can be used continuously according to individual needs.

3. It is advisable to monitor, at the end of the first month of application, the parameters of visual function (visual acuity, perimetry, electrofunctional tests).

4. It does not interact with other pharmacological treatments, but is used alongside them.

5. Since the intensity of the electromagnetic field transmitted by the DM is extremely low, it does not interfere with normal cardiac activity, nor with cardiac electrostimulators (pacemakers).

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