The MIRODERM® family of products consist of a non-crosslinked acellular wound matrix derived from porcine liver for the management of wounds including:
- Partial and full-thickness wounds
- Pressure ulcers
- Venous ulcers
- Chronic vascular ulcers
- Diabetic ulcers
- Tunneled and undermined wounds
- Trauma wounds (abrasions, lacerations, second-degree burns, skin tears)
- Drainage wounds and surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence)
One surface of MIRODERM retains the native liver capsule (an epithelial basement membrane) and the opposite surface is comprised of open liver matrix. The capsule surface of MIRODERM is placed outwards by placing the “L” notch in the upper right hand corner in an ”L” orientation.
The MIRODERM PRODUCT PORTFOLIO includes:
- MIRODERM Fenestrated (Medium expansion)
- MIRODERM Fenestrated Plus (Large expansion)
Our perfusion decellularization technology is in contrast to immersion decellularization and overcomes the hurdles of immersion by facilitating rapid access to the whole organ through the native vasculature by cannulating the vasculature and perfusing a mild detergent solution through the native blood vessels as opposed to immersing the organ.
MIRODERM, MIRODERM Fenestrated and MIRODERM Fenestrated Plus are processed and stored in a phosphate buffered aqueous solution, packaged in an inner sterile pouch and outer non-sterile pouch, and sterilized with electron beam irradiation. The product comes in a variety of sizes and is intended for use only by trained medical professionals who are familiar with wound procedures and techniques involving the use of a wound matrix. Federal (U.S.A.) law restricts this product to sale by or on the order of a physician.
See MIRODERM IFU for full prescribing information and warnings.