Frequently Asked Questions
EZDebride is a Class 1 Medical Device that is registered, listed and made in the U.S.A.
Yes: the EZDebride Wound Instrument is a sharp debridement tool that will effectively debride biofilm, bio-burden, and tissue slough from the surface of the wounds. It’s unique cutting flute system along with a broad head provides precise controlled depth sharp debridement with minimal to no injury or insult to the underlying healthy tissue.
EZDebride comes in a box containing 8 sterile EZDebrides.
The EZDebride Wound Instrument unlike scalpels or curettes provides for a uniform, controlled depth sharp debridement. The EZDebride instrument has been shown to be less painful with a decrease in wound surface hemorrhaging.
Although EZDebride heavily reduces the amount of pain endured by a patient receiving sharp debridement, topical anesthesia can be used depending on the comfort level of the patient.
No: the EZDebride Wound Instrument is a single use, FDA approved class 1 device and is sterilized. It is packaged as a single unit.
It can be used for callous however the condition and amount of callous will determine the best tool to use.
The EZDebride Wound Instrument is a sharp debridement instrument and the clinician can be reimbursed under the debridement codes: 97597, 97598 (superficial to dermis and subcutaneous respectfully), 11042, and 11043. It is also recommended that all necessary documentation is completed and expressed under Medicare/Medicaid standards such as wound dimensions, objective findings, and wound details, etc. prior.