BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SOLITAIRE 2 REVASCULARIZATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ZEWA MFM-007 BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HEART START XL

    FDA Adverse Event
    Malfunction ·AGILENTTECHNOLOGIES, INC·Product code MKJ·August 9, 2011

    CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code LWR·November 21, 2008

    GYNECARE MORCELLEX TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code HET·July 22, 2013