EPIEFFECT™ is a minimally manipulated, lyophilized, non-viable cellular allograft derived from human amniotic membrane.
• Lyophilized human placental-based allograft membrane that includes the amnion layer, intermediate layer, and chorion layer
• Provides a biocompatible human extracellular matrix (ECM) and contains 300+ regulatory proteins
• Easy to apply
• Can be repositioned after hydrating
• Compatible with compression therapy, negative pressure wound therapy (NPWT), and hyperbaric oxygen therapy (HBOT)
• Terminally sterilized
• Shelf-stable
• 5-year shelf life
EPIEFFECT™ is a barrier intended for use in the treatment of acute and chronic wounds, providing a protective environment to support the healing process.
EPIEFFECT™ should not be used on: (1) areas with active or latent infection and/or (2) a patient with a disorder that would create an unacceptable risk of post-operative complications.
EPIEFFECT™ allografts remain suitable for transplantation in an unopened, undamaged package, under proper storage conditions.
Please inspect the integrity of the package upon receipt. If package and contents appear defective or damaged in any way, immediately contact the distributor.
This allograft is intended for single-patient use only. Discard all unused material.
The procedure should be performed by an authorized medical professional.
Strict donor screening and laboratory testing, along with dedicated processing and sterilization methods, are employed to reduce the risk of any disease transmission. However, as with all biological implants, an absolute guarantee of tissue safety is not
possible. This allograft has the potential to transmit infectious disease to the recipient.
The reaction of the body to any biological implant is not completely understood.
Caution should be used when treating patients with a known sensitivity to aminoglycoside antibiotics.
Discard all damaged, mishandled or potentially contaminated tissue.
As with any procedure, the possibility of infection exists.
Proprietary processing and validated sterilization methods are employed to eliminate potential deleterious components of the allograft. However, as with all biological implants, the possibility of rejection exists.
Any adverse reactions, including the suspected transmission of disease attributable to this allograft, should be reported immediately to MIMEDX®.
It is the responsibility of the distributor and/or end-user clinician to store EPIEFFECT™ allografts in a clean, dry environment between 2-30°C prior to further distribution or transplant. EPIEFFECT™ allografts have a 5-year shelf life. Check the label for the expiration date.
Acute Wounds
Chronic Wounds
Deep Wounds
Dehisced Wounds
Diabetic Foot
Granulating/Epithelializing Wounds
Moderate/Highly Exudating Wounds
Non/Minimally Exudating Wounds
Pressure Ulcers
Superficial Wounds
Venous Ulcers
Preparation, Reconstitution and Surgical Use: Prior to implantation, carefully follow the EPIEFFECT™ allograft preparation steps below using aseptic technique: Wound Bed Preparation Ensure the wound is free from clinical sign of infection. Prepare wound bed as needed. Removing EPIEFFECT™ from Packaging The outer peel pouch is not sterile. The inner pouch that contains EPIEFFECT™ is sterile (unless the pouches are damaged or compromised). Carefully open the peelable corner of the outer pouch and extract the inner pouch using aseptic technique. Ensure the inner pouch does not come in contact with any portions of non-sterile surface of the outer pouch. Using aseptic technique, slowly peel a corner of the inner peel pouch and allow the authorized medical professional to grasp EPIEFFECT™ with fingers or non-toothed, sterile forceps. Use EPIEFFECT™ promptly after opening the inner, sterile pouch. Please take great care when removing EPIEFFECT™ from the internal pouch. EPIEFFECT™ is thin and extremely lightweight. EPIEFFECT™ Preparation In a dry state, use sterile dry scissors to cut EPIEFFECT™ to fit within the wound margins. It is acceptable to overlap the wound margins with EPIEFFECT™ by 1mm. If needed, EPIEFFECT™ can be fenestrated to accommodate wounds that produce copious amounts of exudate. EPIEFFECT™ can be applied wet or dry. EPIEFFECT™ can be hydrated while on the wound site with sterile saline solution. Simply apply several drops of sterile solution to EPIEFFECT™. During and following hydration, the embossment on EPIEFFECT™ will begin to fade. EPIEFFECT™ Orientation & Application EPIEFFECT™ should be placed on the wound site, using the orientation of the embossment lettering as a guide. Proper orientation of EPIEFFECT™ can be noted when the embossment nomenclature reads correctly from left to right. Absorbable, non-absorbable suture material and/or tissue adhesives can be used to fixate EPIEFFECT™ to the site of application or itself if desired. Support Therapies EPIEFFECT™ is compatible with offloading/compression/negative pressure therapies. EPIEFFECT™ can be used in conjunction with hyperbaric oxygen therapy.
Primary Dressing EPIEFFECT™ should be covered with a non-adherent contact layer. EPIEFFECT™ should not be disturbed, if possible, for several days or before the next application, if needed. If an infection occurs at the graft site, treat infection per institution's protocol. Secondary Dressing EPIEFFECT™ requires a moist wound environment. Use appropriate moisture management dressings for the wound type and treatment ideology.
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