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

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    ENTERNAL Y EXTENSION SET RECORDER

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

    MODIFICATION TO SMITH & NEPHEW INTRAMEDULLARY HIP SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    A-GENT QUANTICHROM THROMBIGEN-E

    FDA 510(k)
    FDA Class 2 ·Hematology

    TAXUS EXPRESS2 PACLITAXEL ELUTING STENT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·June 27, 2006

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·May 13, 2014

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·November 20, 2012

    EON MINI 16-CHANNEL IPG

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·September 17, 2010