BEUDAMED
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    DERMAFILE (CAT. # 38

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M3848133600·Xpress® Screwdriver Handle Only

    DFINER UROLOGICAL CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MEDICAL IMAGE PROCESSING UNIT

    FDA 510(k)
    FDA Class 2 ·Dental

    RECIPROC BLUE FILES, 6X, STERILE

    FDA Adverse Event
    Malfunction ·VDW GMBH·Product code EKS·September 18, 2023

    RINGLOC BI-POLAR CUP 28X49MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 15, 2014

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 31, 2012

    INTELLIVUE MP2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·August 20, 2010