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

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    EMBOLECTOMY CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Continuum®

    FDA UDI
    Zimmer, Inc.·00889024153981·

    Continuum®

    FDA UDI
    Zimmer, Inc.·00889024153998·

    Momentum Spine

    FDA 510(k)
    FDA Unclassified ·Unknown

    W.O.M. LASER U100PLUS

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

    RESTORELLE A TRAP

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code FTL·February 7, 2014

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 9, 2012

    V-LOC 180 ABS CLOS DEVICE 3-0 CL 6 P-12

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GAM·September 8, 2010

    ONYX

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·July 13, 2023

    UNKNOWN SMARTPILL

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD., YOQNEAM·Product code NYV·February 13, 2023