BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    THE MAGNUM CHIN IMPLANT

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

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112335·SURG-I-BAND LIME GREEN

    V-808 ATOM TRANSCAPSULE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW (0.5g)

    FDA 510(k)
    FDA Class 2 ·Dental

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·January 16, 2013

    BIPOL LEAD MODEL 300

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·January 12, 2011

    75MM SELECTABLE NEW TLC

    FDA Adverse Event
    ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 28, 2014

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·February 27, 2024

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·March 21, 2024