BEUDAMED
    8 results · 36ms · Sources: EU EUDAMED, US FDA

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    NEURO N 50 LESION GENERATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    INTERMEDICS APR(TM) II FEMORAL COMPONENT

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

    MODIFIED SUTURE USED IN CATHETER INSERTION TRAYS

    FDA 510(k)
    FDA Class 1 ·General Hospital

    HEARTWARE VENTRICULAR ASSIST SYSTEM - SHOULDER PACK

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC.·Product code DSQ·March 27, 2018

    REALSEAL SE

    FDA Adverse Event
    Injury ·SYBRONENDO·Product code KIF·June 26, 2014

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2010

    AVAULTA PLUS BIOSTYNTHETIC SUPPORT SYSTEM - POSTERIOR

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON)·Product code FTL·December 28, 2012

    HEARTWARE VENTRICULAR ASSIST SYSTEM - SHOULDER PACK

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC.·Product code DSQ·October 4, 2018