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Product Type: Acellular matrix
Other related brands
Parametrics Medical | |
HCPCS : (Medicare DME co-payment per billable unit min / max: $0.00 / $0.00)

Resolve Matrix is an acellular biologic dermal substitute derived from porcine peritoneum membrane.

INTENDED USES: Resolve Matrix™ is indicated for the management of topical wounds, including: partial and full-thickness wounds, pressure ulcers, venous ulcers, diabetic ulcers, chronic vascular ulcers, surgical wounds, trauma wounds, draining wounds, and tunneled or undermined wounds.

CLAIMED BENEFITS: Thin, flexible, yet strong biologic collagen matrix that's suturable, with ideal handling properties. Highly comfortable to the wound bed, allowing for optimal contact during the healing process. A potential need for fewer applications compared to thinner dermal substitutes. Preserves natural components such as growth factors, proteins, proteoglycans and glycosaminoglycans. In the body, these types of molecules are known to play an important role in tissue generation. Allows for cellular infiltration and migration. The scaffold is not crosslinked which may have negative biological consequences. Favorable safety profile. In vitro studies showed applied cells produced more growth factors in Resolve Matrix than in other scaffolds. Resolve Matrix allows more rapid angiogenesis than dermis in a CAM model. May be applied dry, hydrated in sterile saline, blood, BMA or PRP. Absence of stabilizers and preservatives avoids a potential foreign-body inflammatory response. Lyophilized, packaged and terminally sterilized. Stored at ambient temperature with a 3-year shelf life.

OPTIONS: Per Square Centimeter

RMAD22: Resolve Matrix Biologic Membrane, 2x2 cm: A2024

RMAD23: Resolve Matrix Biologic Membrane, 2x3 cm: A2024

RMAD24: Resolve Matrix Biologic Membrane, 2x4 cm: A2024

RMAD3535: Resolve Matrix Biologic Membrane, 3.5x3.5 cm: A2024

RMAD45: Resolve Matrix Biologic Membrane, 4x5 cm: A2024

RMAD55: Resolve Matrix Biologic Membrane, 5x5cm: A2024

RMAD68: Resolve Matrix Biologic Membrane, 6x8cm: A2024

Wound Reference does not produce, market, re-sell or distribute health care goods or services consumed by, or used on, patients.
Composition: Animal-derived
Composition: Human dermis with/without epidermis
Composition: Human placenta or umbilical cord
Composition: Viable (living) cells
Configuration: Fenestrated/ meshed
Configuration: Flowable
Configuration: Sheet
May apply on full-thickness wounds
May apply over exposed tendon/ bone/ muscle
May apply over infected tissue
Processing: Cryopreserved
Processing: Decellularized or irradiated
Processing: Dehydrated
Processing: Fresh (limited shelf life)
Processing: Hydrated
Processing: Minimally manipulated
Shelf life: Greater than 2 years
Storage: refrigeration needed
Storage: room temp

The addition of Skin Substitutes or Cellular or Tissue Based Products (CTPs) to certain wounds may afford a healing advantage over dressings and conservative treatments when these options appear insufficient to affect complete healing, after at least a 30 day period of comprehensive conservative therapy. There are currently a wide variety of bioengineered products available for soft tissue coverage to affect closure. • Human skin allografts are derived from donated human skin (cadavers) • Allogeneic matrices are derived from human tissue (fibroblasts or membrane) • Composite matrices are derived from human keratinocytes, fibroblasts and xenogeneic collagen • Acellular matrices are derived from allogeneic (non-related human donors) or xenogeneic (other species) collagen, membrane, or cellular remnants

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.

Important Notice: The product information contained on this page, including the product images and additional product materials, was collected from various supplier sources. All product claims and specifications are those of the product suppliers. Every effort has been made to ensure the accuracy of the product information, however on occasion manufacturers may alter their products or packaging without notice. Wound Reference assumes no liability for inaccuracies or misstatements about products. The properties of a product may change or be inaccurate following the posting or printing of the product information in the document, either in the print or online version. Due to product changes, information listed in this document is subject to change without notice. We recommend that you always read labels, warnings and instructions for use before using a product. Content on this site is for reference purposes and is not intended to be a substitute for professional advice given by a physician or other licensed healthcare professional.