BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    OPT80 THE TRANSPORTABLE (OPT80)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    M2A-MAGNUM PF CUP 58OD/52ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·July 5, 2017

    PRONTO LOW PROFILE (LP) EXTRACTION CATHETER, MODEL 5010

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PORT-X IV

    FDA 510(k)
    FDA Class 2 ·Dental

    FLOGARD

    FDA Adverse Event
    Malfunction ·SHARP CORPORATION OSAKA JAPAN·Product code FRN·February 21, 2013

    SPECTRA OPTIA EXCHANGE SET

    FDA Adverse Event
    Other ·CARIDIANBCT·Product code LKN·January 14, 2011

    QUANTA SYSTEM S.P.A.

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM, S.P.A.·Product code GEX·July 25, 2014

    XP-XP Tibial Tray - Interlok 75 mm Item # 195757

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·September 18, 2019