BIONEXT
The
Bionext® wound healing product is a Class III medical device with the
equivalent of a 510K Clearance in Latin America. The Bionext® product
was developed to address key problems with current wound dressing
technologies. Specifically: pain, infection, and inefficiency of
changing wound dressing and overall cost to the healthcare system are
all bi-products of suboptimal wound protection and treatment systems.
The Bionext® product protects and treats post-traumatic wounds and can
easily be used at “in-the field triage centers”, outpatient clinics,
hospitals, emergency rooms or a physician’s office without the need for
surgery or complicated procedures. The Bionext®
technology deploys a bacterial biocellulose film to catalyze and
accelerate wound healing through dermal cell regeneration. This biocellulose film (BF) is synthesized by Acetobacter xylinum
bacteria and has been clinically proven to aid in wound healing. It is a
biocompatible dressing that temporarily replaces the skin in lesions
caused by burns, trauma and chronic ulcers associated to venous
insufficiency, diabetes and other diseases.
MDI has the rights to the Bionext technology for the United States territory.
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