Natalin is a tri-layer, decellularized, dehydrated human amniotic membrane allograft.
INTENDED USES: Natalin is intended for use as a wound covering or surgical barrier for acute and chronic wounds, including diabetic, venous, arterial, and pressure ulcers, burns, surgical
sites (including Mohs), and complex wounds with exposed structures (tendon, bone, muscle).
CLAIMED BENEFITS: Natalin serves as a biological membrane covering to protect wounds and surgical sites from the surrounding environment and support healing. It is trimmed and applied directly to the wound or surgical site. Natalin acts as a protective barrier, supporting wound coverage and healing.
Application of Skin Substitutes (also known as Cellular and/or Tissue Based Products) to certain wounds may help these wounds heal faster than conventional dressings and conservative treatments. Usually skin substitutes are used if conventional treatment has been tried for at least 30 days and the wound has not healed as quickly as expected. Human skin allografts are a type of skin substitute. They are made of skin donated by human donors that have had intact cells removed or treated to avoid immunologic rejection (a process in which the body of the person receiving the skin substitute kills the cells of the skin substitute).
For Medicare to cover this product, it needs to be ordered and applied by your clinician. A patient cannot purchase it directly from a Durable Medical Equipment (DME) store and receive reimbursement for it.
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