BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    COAGULATION FACTOR IX DEFICIENT SUBSTRATE PLASMA

    FDA 510(k)
    FDA Class 2 ·Hematology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209120413·

    MALLINCKRODT

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code BTR·August 16, 2012

    Guide wire for Edi Catheter 6 Fr, Guide wire for Edi Catheter 8 Fr, 100 cm, Guide wire for Edi Catheter 8 Fr, 125 cm

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

    EZLOC FEMORAL FIXATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MALLINKRODT

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code JOH·August 17, 2010

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOUR·Product code CBK·April 4, 2014

    ELECTRODE, PACEMAKER, PERMANENT

    FDA Adverse Event
    Death ·MPRI·Product code DTB·November 30, 2012

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·September 28, 2010

    MUST MINI ROD REDUCTION DEVICE

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·September 27, 2019