BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    TEM-STIK

    FDA 510(k)
    FDA Class 2 ·Dental

    DYNALINK .035 BILIARY SELF-EXPANDING STENT SYSTEM, MODELS 1010102-38,1010102-56,1010102-80,1010103-38,1010103-56, 101010

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

    ALGINOR ALGINELLE TYPE 1 AND 2 MILLENIUM KROMOPAN 1 AND 2

    FDA 510(k)
    FDA Class 2 ·Dental

    ASKU

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·August 11, 2011

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·August 11, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·August 11, 2011

    PRIMEADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 20, 2014

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 6, 2012

    ACCU-CHEK ULTRAFLEX INFUSION SET

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code FPA·August 26, 2010