Device typeWound-nonadherent dressing, permeable, antimicrobial: A wound covering typically in the form of a porous material (e.g., a fine mesh) impregnated/coated with a substance (e.g., petrolatum, silicone) or made of a material that prevents adherence to the wound bed, thereby decreasing the potential for trauma to the wound and surrounding skin, and that contains an antimicrobial agent (e.g., silver (Ag), honey). Its pores permit the drainage of exudates from, and application of medication to, the wound. This device may be used with other wound-care products to help heal chronic/infected and postoperative wounds, burns, skin grafts, cuts, or abrasions; it is not a dedicated burn dressing. This is a single-use device.
FDA categoryDressing, wound and burn, hydrogel w/drug and/or biologic
Device ID00749756940429
Catalog number46-712G
AvailabilityPrescription
SterileYes
MRI safetyLabeling does not contain MRI Safety Information